OA16458A

OA16458A - Encased tamper resistant controlled release dosage forms.

Info

Publication number: OA16458A
Application number: OA1201300254
Authority: OA
Inventors: Haiyong Hugh. Huang
Original assignee: Purdue Pharma L.P.
Priority date: 2010-12-22
Filing date: 2011-12-21
Publication date: 2015-10-15

Abstract

In certain embodiments, the present invention is directed to a solid controlled release dosage form comprising: a core comprising a first portion of an opioid analgesic dispersed in a first matrix material; and a shell encasing the core and comprising a second portion of the opioid analgesic dispersed in a second matrix material; wherein the amount of opioid analgesic released from the dosage form is proportional within 20% to elapsed time from 8 to 24 hours, as measured by an in- vitro dissolution in a USP Apparatus 1 (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37 C.

Description

ENCASED TAMPER RESISTANT CONTROLLED RELEASE

DOSAGE FORMS

FIELD OFTHE INVENTION [0001) The présent invention relates to multi-layered pharmaceutical dosage forms that are tamper-resistant and preferably provide substantially zero-order release of the active agent contained therein.

BACKGROUND OF THE INVENTION |0002| Pharmaceutical products are sometimes the subject of abuse. For example, a particular dose of opioid agonist may be more potent when administered parenterally as compared to the same dose administered orally. Some formulations can be tampered with to provide the opioid agonist contained therein for illicit use. Controlled release opioid agonist formulations are sometimes crushed or subject to extraction with solvents (e.g., éthanol) by drug abusers to provide the opioid contained therein for immédiate release upon oral or parentéral administration.

[0003] Controlled release opioid agonist dosage forms that can liberate a portion of the opioid upon exposure to éthanol can also resuit in a patient receiving the dose more rapidly than intended if a patient disregards instructions for use and concomitantly uses alcohol with the dosage form.

[0004] U.S. Patent Application Publication No. 2009/0081290 discloses tamper-resistant dosage forms that, in certain embodiments, are directed to a solid, oral, extended-rclease pharmaceutical dosage form comprising an extended-release matrix formulation in the form of a tablet or multi-particulates. The tablet or the individual multi-particulates can be at least flattened without breaking, characterized by a thickness of the tablet or of the individual multi-particulates after flattening which corresponds to no more than about 60% of the thickness of the tablet or the individual multi-particulates before flattening, and wherein the flattened tablet or the flattened multi-particulates provide an in-vitro dissolution rate, when measured in a USP Apparatus 1 (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37° C, having a percent amount of active

-216458

I t released at 0.5 hours of dissolution that deviates no more than about 20% points from the corresponding in-vitro dissolution rate of a non-flattened reference tablet or reference multi-particulates.

|0005] There continues to exist a need in the art for tamper-resistant pharmaceutical oral dosage forms, wherein said dosage forms preferably provide a release profile of the active agent that is substantially zéro order.

{0006] Ail references and publications cited herein are hereby incorporated by reference in their entireties for ail purposes.

OBJECTS AND SUMMARY OF THE INVENTION [0007] It is an object of certain embodiments of the présent invention to provide a solid controlled release dosage form comprising an active agent (e.g., an opioid analgésie), which is tamper résistant.

[0008] It is an object of certain embodiments of the présent invention to provide a solid controlled release dosage form comprising an active agent (e.g., an opioid analgésie), which is résistant to crushing.

[0009] It is an object of certain embodiments of the présent invention to provide a solid controlled release dosage form comprising an opioid analgésie, which is subject to less parentéral abuse than other dosage forms.

[0010] It is an object of certain embodiments of the présent invention to provide a solid controlled release dosage form comprising an opioid analgésie, which is subject to less intranasal abuse than other dosage forms.

[0011] It is an object of certain embodiments of the présent invention to provide a solid controlled release dosage form comprising an opioid analgésie, which is subject to less oral abuse than other dosage forms. φ/~

-316458 [0012] It is a further object of certain embodiments of the présent invention to provide a solid controlled release dosage form comprising an opioid analgésie, which is subject to less diversion than other dosage forms.

[0013] It is a further object of certain embodiments of the présent invention to provide a method of treating pain in human patients with a solid controlled release dosage form comprising an opioid analgésie while reducing the abuse potential of the dosage form.

[0014] It is a further object of certain embodiments of the présent invention to treat a disease or condition (e.g., pain) by administering a solid controlled release dosage form as disclosed herein to a patient in need thereof.

]0015] It is a further object of certain embodiments of the présent invention to provide a 15 method of manufacturing an oral dosage form of an active agent (e.g., an opioid analgésie) as disclosed herein.

[0016] It is a further object of certain embodiments of the présent invention to provide a use of a médicament (e.g., an opioid analgésie) in the manufacture of a dosage form for 20 the treatment of a disease state (e.g., pain).

]0017| These objects and others are accomplished by the présent invention, which in certain embodiments is directed to a solid controlled release dosage form comprising a core comprising a first portion of an active agent (e.g., an opioid analgésie) dispersed in a 25 first matrix material; and a shell encasing the core and comprising a second portion of the active agent dispersed in a second matrix material; wherein the amount of active agent released from the dosage form is proportional within 20% to elapsed time from 8 to 24 hours, as measured by an in-vitro dissolution in a USP Apparatus 1 (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37°C.

[0018] In certain other embodiments, the amount of active agent released from the dosage form is proportional within 30% to elapsed time in at least one of (i) from 4 to 24

-416458 hours, (ii) from 8 to 24 hours, (iii) from 12 to 24 hours, (iv) from 18 to 24 hours, (v) from 4 to 8 hours, (vi) from 4 to 12 hours, (vii) from 4 to I8 hours, (viii) from 8 to 12 hours, (ix) from 8 to 18 hours, or (x) from 12 to 18 hours, as measured by an in-vitro dissolution in a USP Apparatus l (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37°C. In alternate embodiments, the amount of active agent released from the dosage form is proportîonal within 30% to elapsed time in ail of (i) from 8 to 24 hours, (ii) from 8 to 12 hours, and (iii) from 8 to 18 hours, as measured by an in-vitro dissolution in a USP Apparatus l (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37°C.

[0019| In certain other embodiments, the amount of active agent released from the dosage form is proportîonal within 25% to elapsed time in at least one of (i) from 4 to 24 hours, (ii) from 8 to 24 hours, (iii) from 12 to 24 hours, (iv) from 18 to 24 hours, (v) from 4 to 8 hours, (vi) from 4 to 12 hours, (vii) from 4 to 18 hours, (viii) from 8 to 12 hours, (ix) from 8 to 18 hours, or (x) frotn 12 to 18 hours, as measured by an in-vitro dissolution in a USP Apparatus l (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37°C. In alternate embodiments, the amount of active agent released from the dosage form is proportîonal within 25% to elapsed time in ail of (i) from 8 to 24 hours, (ii) from 8 to 12 hours, and (iii) from 8 to 18 hours, as measured by an in-vitro dissolution in a USP Apparatus l (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37°C.

|0020) In certain other embodiments, the amount of active agent released from the dosage form is proportîonal within 20% to elapsed time in at least one of (i) from 4 to 24 hours, (fl) from 8 to 24 hours, (iii) from I2 to 24 hours, (iv) from 18 to 24 hours, (v) from 4 to 8 hours, (vi) from 4 to 12 hours, (vii) from 4 to 18 hours, (viii) from 8 to 12 hours, (ix) from 8 to 18 hours, or (x) from 12 to 18 hours, as measured by an in-vitro dissolution in a USP Apparatus l (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37°C. In alternate embodiments, the amount of active agent released from the dosage form is proportîonal within 20% to elapsed time in ail of (i) from 8 to 24 hours, (ii) from 8 to 12 hours, and (iii) from 8 to 18 hours, as measured by an in-vitro

-516458 dissolution in a USP Apparatus l (basket) at I00 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37°C.

[0021| In certain other embodiments, the amount of active agent released from the dosage form is proportional within 10% to elapsed time in at least one of (i) from 4 to 24 hours, (ii) from 8 to 24 hours, (iii) from 12 to 24 hours, (iv) from 18 to 24 hours, (v) from 4 to 8 hours, (vi) from 4 to 12 hours, (vii) from 4 to 18 hours, (vîii) from 8 to 12 hours, (ix) from 8 to 18 hours, or (x) from 12 to 18 hours, as measured by an in-vitro dissolution in a USP Apparatus 1 (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37°C. In alternate embodiments, the amount of active agent released from the dosage form is proportional within 10% to elapsed time in ail of (i) from 8 to 24 hours, (ii) from 8 to 12 hours, and (iii) from 8 to 18 hours, as measured by an in-vitro dissolution in a USP Apparatus 1 (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37°C.

[0022) In certain other embodiments, the amount of active agent released from the dosage form is proportional within 5% to elapsed time in at least one of (î) from 4 to 24 hours, (ii) from 8 to 24 hours, (iii) from 12 to 24 hours, (iv) from 18 to 24 hours, (v) from 4 to 8 hours, (vi) from 4 to 12 hours, (vii) from 4 to 18 hours, (viii) from 8 to 12 hours, (ix) from 8 to 18 hours, or (x) from 12 to 18 hours, as measured by an in-vitro dissolution in a USP Apparatus 1 (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37°C. In alternate embodiments, the amount of active agent released from the dosage form is proportional within 5% to elapsed time in ail of (i) from 8 to 24 hours, (ii) from 8 to 12 hours, and (iii) from 8 to 18 hours, as measured by an in-vitro dissolution in a USP Apparatus 1 (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37°C.

[0023| In certain embodiments, the présent invention is directed to a solid controlled release dosage form comprising a core comprising a first portion of an active agent (e.g., an opioid analgésie) dispersed in a first matrix material comprising polyethylene oxide;

and a shell encasing the core and comprising a second portion of the active agent dispersed in a second matrix material comprising polyethylene oxide. In alternative einbodiments, v/

-616458 only the first matrix material comprises polyethylene oxide or only the second matrix material comprises polyethylene oxide.

[0024] In certain embodiments, the présent invention is directed to a solid controlled release dosage form comprising a compressed core comprising a first portion of an active agent (e.g., an opioid analgésie) dispersed in a first matrix material comprising polyethylene oxide; and a compression coating encasing the core and comprising a second portion of the active agent dispersed in a second matrix material comprising polyethylene oxide.

|0025| In certain embodiments, the présent invention is directed to a solid controlled release dosage form comprising a core comprising a first portion of an active agent (e.g., an opioid analgésie) dispersed in a first matrix material; and a shell encasing the core and comprising a second portion of the active agent dispersed in a second matrix material; wherein the amount of active agent released from the dosage form at 2 hours is less than about 25%; the amount of active agent released front the dosage form at 4 hours is from about 10% to about 30%; the amount of active agent released front the dosage form at 8 hours is from about 20% to about 60%; the amount of active agent released from the dosage form at 12 hours is from about 40% to about 90%; and the amount of active agent released from the dosage form at 18 hours is greater than about 70%; as measured by an în-vitro dissolution in a USP Apparatus 1 (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37° C.

[0026] In certain embodiments, the présent invention is directed to a solid controlled release dosage form comprising a core comprising a first portion of an active agent (e.g., an opioid analgésie) dispersed in a first matrix material; and a shell encasing the core and comprising a second portion of the active agent dispersed in a second matrix material; wherein the amount of active agent released from the dosage form at 2 hours is less than about 20%; the amount of active agent released from the dosage form at 4 hours is from about 10% to about 30%; the amount of active agent released from the dosage form at 8 hours is from about 30% to about 60%; the amount of active agent released from the dosage form at 12 hours is from about 50% to about 90%; and the amount of active agent /

-716458 released from the dosage form at 18 hours is greater than about 80%; as measured by an în-vitro dissolution in a US P Apparatus l (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37°C.

[0027] In certain embodiments, the présent invention is directed to a solid controlled release dosage form comprising a core comprising a first portion of an active agent (e.g., an opioid analgésie) dispersed in a first matrix material; and a shell encasing the core and comprising a second portion of the active agent dispersed in a second matrix material; wherein the amount of active agent released from the dosage form at 2 hours is less than about 15%; the amount of active agent released from the dosage form at 4 hours is from about 8% to about 20%; the amount of active agent released from the dosage form at 8 hours is from about 20% to about 50%; the amount of active agent released from the dosage form at 12 hours is from about 40% to about 70%; the amount of active agent released from the dosage form at 18 hours is greater than about 70%; and the amount of active agent released from the dosage form at 24 hours is greater than about 90%;as measured by an in-vitro dissolution in a USP Apparatus 1 (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37°C.In certain embodiments, the présent invention is directed to a solid controlled release dosage form comprising a therapeutically effective amount of hydrocodone or a pharmaceutically acceptable sait thereof, and a controlled release excipient; wherein the amount of opioid analgésie released from the dosage form is proportional within 20% to elapsed time from 8 to 24 hours, as measured by an in-vitro dissolution in a USP Apparatus 1 (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37°C; and the dosage form can be flattened without breaking, wherein the thickness of the dosage form after flattening corresponds to no more than about 20% of the thickness of the dosage form before flattening; and the amount of hydrocodone or sait thereof released at 0.5 hour from a flattened dosage form deviates no more than about 20% points from a non-flattened dosage form as measured by an in-vitro dissolution in a USP Apparatus 1 (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37°C.

[0028] In certain embodiment, the présent invention is directed to a solid controlled release dosage form comprising a therapeutically effective amount of hydrocodone or a

-816458 pharmaceutically acceptable sait thereof, and a controlled release excipient; wherein the amount of hydrocodone or sait thereof released from the dosage form at 2 hours is less than about 25%; the amount of hydrocodone or sait thereof released from the dosage form at 4 hours is from about 10% to about 30%; the amount of hydrocodone or sait thereof released from the dosage form at 8 hours is from about 20% to about 60%; the amount of hydrocodone or sait thereof released from the dosage form at 12 hours is from about 40% to about 90%; and the amount of hydrocodone or sait thereof released from the dosage form at 18 hours is greater than about 70%; as measured by an in-vitro dissolution in a USP Apparatus l (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37°C; and the dosage form can be flattened without breaking, wherein the thickness of the dosage form after flattening corresponds to no more than about 20% of the thickness of the dosage form before flattening; and the amount of hydrocodone or sait thereof released at 0.5 hour from a flattened dosage form deviates no more than about 20% points from a non-flattened dosage form as measured by an in-vitro dissolution in a USP Apparatus l (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37°C.

[0029] In certain embodiments, the présent invention is directed to a solid controlled release dosage form comprising a therapeutically effective amount of hydrocodone or a pharmaceutically acceptable sait thereof dispersed in a controlled release excipient; wherein the inner 60% of the dosage form contains at least 80% of the hydrocodone or sait thereof; wherein the amount of hydrocodone or sait thereof released from the dosage form is proportional within 20% to elapsed time from 8 to 24 hours, as measured by an in-vitro dissolution in a USP Apparatus l (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37°C.

[0030] In certain embodiments, the présent invention is directed to a method of preparing a solid controlled release dosage form comprising preparing a core comprising a first portion of an active agent (e.g., an opioid analgésie) dispersed in a first matrix material; and encasing the core in a shell comprising a second portion of the active agent dispersed in a second matrix material; wherein the amount of active agent released from the dosage form is proportional within 20% to elapsed time from 8 to 24 hours, as v/

-916458 measured by an in-vitro dissolution in a USP Apparatus l (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37°C.

[0031] In certain embodiments, the présent invention is directed to a method of preparing a solid controlled release dosage form comprising preparing a core comprising a first portion of an active agent (e.g., an opioid analgésie) dispersed in a first matrix material comprising polyethylene oxide; and encasing the core in a shell comprising a second portion of the active agent dispersed in a second matrix material comprising polyethylene oxide. In alternative embodiments, corresponding dosage forms are prepared such that only the first matrix material comprises polyethylene oxide or only the second matrix material comprises polyethylene oxide.

[0032] In certain embodiments, the présent invention is directed to a method of preparing a solid controlled release dosage form comprising preparing a compressed core comprising a first portion of an active agent (e.g., an opioid analgésie) dispersed in a first matrix material comprising polyethylene oxide; and encasing the core by compression coating a second portion of the active agent dispersed in a second matrix material comprising polyethylene oxide over the core. In alternative embodiments, corresponding compression coated dosage forms are prepared such that only the first matrix material comprises polyethylene oxide or only the second matrix material comprises polyethylene oxide.

|0033] In certain embodiments, the présent invention is directed to a method of preparing a solid controlled release dosage form comprising preparing a core comprising a first portion of an active agent (e.g., an opioid analgésie) dispersed in a first matrix material; and encasing the core in a shell comprising a second portion of the active agent dispersed in a second matrix material over the core; wherein the amount of active agent released from the dosage form at 2 hours is less than about 25%; the amount of active agent released from the dosage form at 4 hours is from about 10% to about 30%; the amount of active agent released from the dosage form at 8 hours is from about 20% to about 60%; the amount of active agent released from the dosage form at 12 hours is from about 40% to about 90%; and the amount of active agent released from the dosage form at f

- ιοί 6458 hours is greater than about 70%, as measured by an in-vitro dissolution in a USP Apparatus 1 (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at37°C.

|0034| In certain embodiments, the présent invention is directed to a method of preparing a solid controlled release dosage form comprising combining a therapeutïcally effective amount of hydrocodone or a pharmaceutically acceptable sait thereof, and a controlled release excipient; wherein the amount of hydrocodone or sait thereof released from the dosage form at 2 hours is less than about 25%; the amount of hydrocodone or sait thereof released from the dosage form at 4 hours is from about 10% to about 30%; the amount of hydrocodone or sait thereof released from the dosage form at 8 hours is from about 20% to about 60%; the amount of hydrocodone or sait thereof released from the dosage form at 12 hours is from about 40% to about 90%; and the amount of hydrocodone or sait thereof released from the dosage form at 18 hours is greater than about 70%; as measured by an in-vitro dissolution in a USP Apparatus 1 (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37°C; and the dosage form can be flattened without breaking, wherein the thickness of the dosage form after flattening corresponds to no more than about 20% of the thickness of the dosage form before flattening; and the amount of hydrocodone or sait thereof released at 0.5 hour from a flattened dosage form deviates no more than about 20% points from a non-flattened dosage form as measured by an in-vitro dissolution in a USP Apparatus 1 (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37°C.

[0035] In certain embodiment, the présent invention is directed to a method of preparing a solid controlled release dosage form comprising combining a therapeutïcally effective amount of hydrocodone or a pharmaceutically acceptable sait thereof, and a controlled release excipient; wherein the amount of hydrocodone or sait thereof released from the dosage form is proportional within 20% to elapsed time, at any two time points from 8 to 24 hours, as measured by an in-vitro dissolution in a USP Apparatus 1 (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37° C; and the dosage form can be flattened without breaking, wherein the thickness of the dosage form after flattening corresponds to no more than about 20% of the thickness of the dosage form before flattening; and the amount of hydrocodone or sait thereof released at 0.5 hour from a flattened dosage form deviates no more than about 20% points from a non-flattened dosage form as measured by an in-vitro dissolution in a USP Apparatus l (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37°C.

|0036| In certain embodiments, the présent invention is directed to a method of preparing a solid controlled release dosage form comprising dispersing a therapeutically effective amount of hydrocodone or a pharmaceutically acceptable sait thereof in a controlled release excipient; wherein the inner 60% of the dosage form contains at least 80% of the hydrocodone or sait thereof; wherein the amount of hydrocodone or sait thereof released from the dosage form is proportional within 20% to elapsed time from 8 to 24 hours, as measured by an in-vitro dissolution in a USP Apparatus l (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37°C.

(0037] In certain embodiments, the présent invention is directed to a method of treating pain in a patient or subject comprising administering a solid controlled release dosage form comprising an opioid analgésie as disclosed herein.

[0038] In preferred embodiments, the présent invention is directed to a dosage form of the présent invention which exhibits a substantially zero-order release rate after administration to a patient or subject.

[0039] The term “zero-order release rate” refers to the rate of active agent release from a dosage form which is independent of remaining active agent concentration in the dosage form, such that the rate is relatively constant over a period of time. A dosage form exhibiting zéro order release rate would exhibit a relatively straight line in a graphical représentation of percent active agent released versus time. In certain embodiments of the présent invention, substantial zéro order release is defined as a dosage form having an amount of active agent released which is proportional within 20% to elapsed time from 8 to 24 hours or 4 to 12 hours, as measured by an in-vitro dissolution in a USP Apparatus 1 (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37°C. For example, an amount released from a dosage form in-vitro at 8 hours of 20%, and an

- 1216458 amount released at 24 hours of 60% (±12) would literally meet the définition of proportional within 20% to elapsed time from 8 to 24 hours. This is demonstrated by the latter elapsed time (24 hours) and the latter release (60%) being the same multiple (3) of the former time (8 hours) and the former release (20%). To meet the définition of proportional within 20% to elapsed time from 8 to 24 hours (or any other time period) it is only necessary to consider the endpoints of the numerical values, although the définition does not preclude that other time points within the endpoints may be proportional as well.

|0040J In other embodiments of the présent invention, substantial zéro order release is defined as a dosage form wherein the amount of active agent released at 2 hours is less than about 25%; the amount of active agent released from the dosage form at 4 hours is from about 10% to about 30%; the amount of active agent released from the dosage form at 8 hours is from about 20% to about 60%; the amount of active agent released from the dosage form at 12 hours is from about 40% to about 90%; and the amount of active agent released from the dosage form at 18 hours is greater than about 70%; as measured by an in-vitro dissolution in a USP Apparatus l (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37°C.

[0041 ] The term “polyethylene oxide” is defined for purposes of the présent invention as a composition of polyethylene oxide (PEO) having a molecular weight of at least 25,000, measured as is conventional in the art, and preferably having a molecular weight of at least 100,000. Compositions with lower molecular weight are usually referred to as polyethylene glycols.

[0042| The term “high molecular weight polyethylene oxide (PEO)” is defined for proposes of the présent invention as having an approximate molecular weight of at least 1,000,000, based on rheological measurements.

[00431 The term “low molecular weight polyethylene oxide (PEO)” is defined for purposes of the présent invention as having an approximate molecular weight of less than

1,000,000, based on rheological measurements.

- 13 16458 [0044] The term “direct compression” is defined for purposes of the présent invention as referring to a process wherein the dosage form is made by a process comprising the steps of blending the ingrédients and compressing the blend to form the dosage form, e.g., by using a diffusion blend and/or convection mixing process (e.g., Guidance for Industry, SUPAC-IR/MR: Immédiate Release and Modified Release Solid Oral Dosage Forms, Manufacturing Equipment Addendum).

[0045] The terni “flattening” and related terms as used in the context of flattening a dosage form in accordance with the présent invention means that the dosage form is subjected to force applied from a direction substantially in line with the smallest diameter (i.e., the thickness) of the dosage form when the shape is other than spherical, and from any direction when the dosage fonn shape is spherical.

[0046] The term “résistant to crushing” is defined for the purposes of certain embodiments of the présent invention as referring to dosage forms that can at least be flattened with a bench press as described herein without breaking.

[0047] For purposes of the présent invention, the term “opioid analgésie” means one or more compounds selected from base opioid agonists, mixed opioid agonist-antagonists, partial opioid agonists, pharmaceutically acceptable salts, complexes, stereoîsomers, ethers, esters, hydrates and solvatés thereof and mixtures thereof.

[0048| The term simulated gastric fluid or “SGF” used herein refers to an aqueous solution utilized in dissolution testing to mimic the conditions of the stomach, e.g., a solution of 0.1 N HCl.

[0049] The term “percentage points” in the context of, e.g., “the amount of active agent released at 0.5 hour from a flattened dosage form deviates no more than about 20% points from a non-flattened dosage form” means that the différence in the % release prior to flattening and the % release after flattening is no more than 20 (i.e., 20 or less). For example, 60% release from a flattened dosage form is no more than about 20 % points from the 40% release of a non-flattened dosage form. va/

- 1416458 [0050] The term “percentage” or the use of “%” without reference to “percentage (or %) points” is the ordinary meaning of percent. For example, 48% release is within 20% of 60% release, whereas 40% would not literally be within 20% of 60% release.

[0051] The term “patient” means a subject (preferabiy a human) who has presented a clinical manifestation of a particular symptom or symptoms suggesting the need for treatment, who is treated preventatively or prophylactically for a condition, or who has been diagnosed with a condition to be treated.

]0052] The term “subject” is inclusive of the définition of the term “patient” and inclusive of the term “healthy subject” (i.e., an individual (e.g., a human) who is entîrely normal in ail respects or with respect to a particular condition.

[0053] As used herein, the term “stereoisomers” is a general term for ail isomers of individual molécules that differ only in the orientation of their atoms in space. It includes enantiomers and isomers of compounds with more than one chiral center that are not mirror images of one another (diastereomers).

[0054] The term “chiral center refers to a carbon atom to which four different groups are attached.

|0055| The term “enantiomer” or “enantioineric” refers to a molécule that is nonsuperimposable on its mirror image and hence optically active wherein the enantiomer rotâtes the plane of polarized light in one direction and its mirror image rotâtes the plane of polarized light in the opposite direction.

|0056] The term “racemic” refers to a mixture of enantiomers.

|0057| The tenu “resolution” refers to the séparation or concentration or déplétion of one of the two enantiomeric forms of a molécule.

- 1516458 |0058| “Hydrocodone” is defined for purposes of the invention as including hydrocodone free base, as well as pharmaceutically acceptable salts, complexes, stereoisomers, ethers, esters, hydrates and solvatés thereof and mixtures thereof.

|0059| The term “USP Paddle or Basket Method” is the Paddle and Basket Method described, e.g., in U,S, Pharmacopoeia XII (1990).

[0060] The term “pH-dependent” for purposes of the présent invention is defined as having characteristics (e.g., dissolution) which vary according to environmental pH.

|00611 The term “pH-independent” for purposes of the présent invention is defined as having characteristics (e.g., dissolution) which are substantially unaffected by pH.

[0062] The term “bioavailabîlity” is defined for purposes of the présent invention as the relevant extent to which the drug (e.g., hydrocodone) is absorbed from the unit dosage forms. Bioavailabîlity is also referred to as AUC (i.e., area under the plasma concentration/time curve).

[0063] The term “controlled-release”, extended-release or “sustained release” are interchangeable and are defined for purposes of the présent invention as the release of the drug (e.g., hydrocodone) at such a rate that blood (e.g., plasma) concentrations are maintained within the therapeutic range but below toxic concentrations over a period of time of at least about 12 hours or longer, or at least 24 hours or longer. Preferably, a controlled release dosage form can provide once daily or twice daily dosing.

[0064] The term “C_max” dénotés the maximum plasma concentration obtained during the dosing interval.

[0065] The term “C24” as it is used herein is the plasma concentration of the drug at 24 hours after administration.

[0066] The term “T_mox” dénotés the time to maximum plasma concentration (C_niax).

- 1616458 [0067] The term “C24/C_max ratio” is defined for purposes of the présent invention as the ratio of the plasma concentration of the drug at 24 hours after administration to the highest plasma concentration of the drug attained within the dosing interval.

[0068] The term “T|_ng” dénotés the time point immediately prior to the first measurable plasma concentration.

[0069] The tenu “Τ^” dénotés the plasma half-life of the terminal phase. This is the time it takes for any concentration in the terminal phase to decrease by half. The term “minimum effective analgésie concentration” or MEAC with respect to concentrations of opioids such as hydrocodone is very difficult to quantify. However, there is generally a minimally effective analgésie concentration of plasma hydrocodone below which no analgesia is provided. While there is an indirect relationship between, e.g., plasma hydrocodone levels and analgesia, higher and prolonged plasma levels are generally associated with superior pain relief. There is a delay (or hystérésis) between the time of peak plasma hydrocodone-levels and the time of peak drug effects. This holds true for the treatment of pain with opioid analgésies in general.

[0070] For purposes of the présent invention, unless further specified, the term “a patient” or “a subject” means that the discussion (or claim) is directed to the pharmacokinetic parameters of an individual patient or subject.

[0071] The term “population of patients” or “population of subjects” or “population of healthy subjects” means that the discussion (or claim) is directed to the mean pharmacokinetic parameters of at least two patients, subjects, or healthy subjects; at least six patients, subjects or healthy subjects; or at least twelve patients, subjects or healthy subjects.

[0072] For purposes of the présent invention, the controlled release formulations disclosed herein are preferably dose proportional. In dose proportional formulations, the pharmacokinetic parameters (e.g., AUC and C,_nax) and/or in-vitro release increase linearly v^/^-

- 1716458 from one dosage strength to another. Therefore, the pharmacokinetic and în-vitro parameters of a particular dose can be inferred from the parameters of a different dose of the same formulation.

|0073J The term “first administration” means a single dose of the présent invention at the initiation of therapy to an individual subject, patient, or healthy subject or a subject population, patient population, or healthy subject population.

[0074] The term “steady state” means that the amount of the drug reaching the System is 10 approximately the same as the amount of the drug leaving the System. Thus, at steadystate, the patient's body éliminâtes the drug at approximately the same rate that the drug becomes available to the patient's System through absorption into the blood stream.

BRIEF DESCRIPTION OF THE DRAWINGS

I0075] FIG. I is a graph that depicts the dissolution of the compositions of Examples l-

4.

|0076| FIG. 2 is a graph that depicts the dissolution of the compositions of Examples 5 20 and 6.

[0077] FIG. 3 is a graph that depicts the dissolution of the compositions of Examples 712.

[0078]

FIG. 4 is a graph that depicts the mean plasma concentration time curve of

Itération l of Example 13.

[0079] FIG. 5 is a graph that depicts the mean plasma concentration time curve of Itération 2 of Example 13.

[00801 FIG. 6 is a graph that depicts the mean plasma concentration time curve of

Itération 3 of Example 13. \a/

- 1816458 [0081] FIG. 7 is a graph that depicts the plasma concentrations of the compositions of Examples 14-20.

DETAÏLED DESCRIPTION |0082| The présent invention is directed to controlled release pharmaceutical formulations that in certain embodiments comprise a higher concentration of drug in an inner région of the dosage form as compared to an outer région. Preferably, the inner and outer régions are configured as an inner core (e.g., a compressed tablet) and a shell encasing the core (e.g., a compression coating). The active agent can be contaîned solely in the core or contained in both the core and the shell. In preferred embodiments, the release of the active agent from the dosage form is substantially zéro order, which provides dosing certainty and reduced plasma fluctuations as compared to alternative treatments (e.g., immédiate release dosage forms).

[0083] The dosage forms of the présent invention are preferably tamper résistant as they are difficult to crush or grind (e.g., in accordance with the flattening criteria disclosed herein). This characteristic makes them especially suitable for controlled release opioid analgésie products that hâve a large dose of opioid analgésie intended to be released over a period of time from each dosage unit. Drug abusers typically may take a controlled-release product and crush, shear, grind, chew, dissolve, heat, extract or otherwise damage the product so that a large portion or the full contents of the dosage form becomes available for immédiate absorption by injection, inhalation, and/or oral consumption.

(0084| The shell of the dosage form of the présent invention is preferably difficult to physically separate from the core. This is particularly useful in embodiments that hâve an increased amount of active agent in the core as compared to the shell, as abusers will hâve difficulty in accessing the greater drug payload of the core.

[0085| In certain embodiments, the présent invention is directed to a solid controlled release dosage form comprising: a core comprising a first portion of an opioid analgésie

- 1916458 dtspersed in a first matrix material; and a shell encasing the core and comprising a second portion of the opioid analgésie dispersed in a second matrix material.

[0086J The core of the dosage form can be formed, e.g., by direct compression, extrusion or molding. Preferably, the inner core provides a controlled release excipient and is in the form of a compressed tablet.

|0087| The shell of the dosage form can be formed, e.g., by compression coating, molding, spraying one or more layers onto the core, dipping one or more layers onto the core or a combination thereof. Preferably, the shell contains a controlled release excipient and is a compression coating.

[0088| In preferred embodiments, the weight ratio of the core to the shell of the dosage forms described herein is from about 1:0.5 to about 1:5; from about 1:0.5 to about 1:2; from about 1:0.6 to about 1:1.5; or from about 1:0.8 to about 1:1.2.

[0089] In preferred embodiments, the core and the shell are visually indistinguishable (e.g., by color) and there is not a clear démarcation between each component. This contributes to tamper résistance of the dosage form by hindering efforts to access the core, which in certain embodiments will contain the bulk of the active agent. One measurement that can be utilized in order to evaluate the color of the shell and the core is CIE L*A*B* value. Preferably, the CIE L*A*B* value of the core and the shell are within 10% of each other. Another measurement to evaluate color is the use of a RYB or RGB color wheel, where the core and shell preferably correspond to the same hue or adjacent hues.

|0090] In certain embodiments, the first matrix material comprises PEO. In other embodiments, the second matrix material comprises PEO. In yet other embodiments, the first matrix material comprises PEO and the second matrix material comprises PEO.

Preferably, polyethylene oxide is contained in both components. In such embodiments, the molecular weight of the PEO in the first matrix material is the same or different than the average molecular weight in the second matrix material. In certain embodiments, —

-20molecular weight of the PEO contained in both components is within 20%, within 10% or within 5% of each other.

|00911 In preferred embodiments of the présent invention, when polyethylene oxide is présent in both the first and second matrices, the molecular weight of the polyethylene oxide used in the first matrix (in the core) is lower than the molecular weight of the polyethylene oxide used in the second matrix material (in the shell). For example, in preferred embodiments, the polyethylene oxide in the first matrix material may hâve a molecular weight from about 300,000 to about 10,000,000 and the polyethylene oxide in the second matrix material may hâve a molecular weight from about 1,000,000 to about 10,000,000. In other preferred embodiments, the polyethylene oxide in the first matrix material may hâve a molecular weight from about 300,000 to about 3,000,000 and the polyethylene oxide in the second matrix material may bave a molecular weight from about 4,000,000 to about 10,000,000. In other preferred embodiments, the polyethylene oxide in the first matrix material may hâve a molecular weight from about 500,000 to about 1,000,000 and the polyethylene oxide in the second matrix material may hâve a molecular weight from about 6,000,000 to about 8,000,000.

|0092] In certain embodiments, the active agent (e.g., opioid analgésie) in the first portion (in the core) is the same as the active agent in the second portion (in the shell). In other embodiments, the active agent in the first portion is different than the active agent in the second portion.

[0093| In certain embodiments, the ratio of active agent (e.g., opioid analgésie) in the core to the ratio of active agent in the shell is from about 1 il to about 10:1 ; from about 2:1 to about 8:1; from about 2:1 to about 5:1 or about 4:1.

(0094| In certain embodiments, the weight ratio of the first portion of active agent (e.g., opioid analgésie) to polyethylene oxide in the first matrix material is from about 1:0.25 to about 1:30; from about 1:0.5 to about 1:100; from about 1:0.5 to about 1:20; from about 1:1 to about 1:10; from about 1:15 to about 1:20; from about 1:1.5 to about 1:4; about 1:18 or about 1:2.

-21 16458 [0095] In alternative embodiments, the weight ratio of the second portion of active agent (e.g., opioid analgésie) to polyethylene oxide in the second matrix material is from about l : l to about 1:200; from about 1:1 to about 1:125; from about 1:2 to about 1:100; from 5 about 1:5 to about 1:50; from about 1:12 to about 1:25; about 1:98 or about 1:15.

(0096] In certain embodiments, the amount of active agent (e.g., opioid analgésie) released from the dosage form is proportional within 20%, or within 10%, or within 5% to elapsed time from 8 to 24 hours, as measured by an in-vitro dissolution in a USP 10 Apparatus 1 (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at37°C.

[0097] In certain embodiments, the amount of active agent (e.g., opioid analgésie) released from the dosage form is proportional within 20%, or within 10%, or within 5% to 15 elapsed time from 8 to 18 hours, as measured by an in-vitro dissolution in a USP

Apparatus 1 (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37°C.

[0098] In certain embodiments, the amount of active agent (e.g., opioid analgésie) 20 released from the dosage form is proportional within 20%, or within 10%, or within 5% to elapsed time from 8 to 12 hours, as measured by an in-vitro dissolution in a USP Apparatus 1 (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37°C.

(0099] In certain embodiments, the amount of active agent (e.g., opioid analgésie) released from the dosage form is proportional within 20%, or within 10%, or within 5% to elapsed time from 12 to 24 hours, as measured by an in-vitro dissolution in a USP Apparatus 1 (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37°C.

100100] In certain embodiments, the amount of active agent (e.g., opioid analgésie) released from the dosage form is proportional within 20%, or within 10%, or within 5% to

-2216458 elapsed time from 12 to 18 hours, as measured by an in-vitro dissolution in a USP Apparatus l (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37°C.

[00101] In certain embodiments, the amount of active agent (e.g., opioid analgésie) released from the dosage form is proportional within 20%, or within 10%, or within 5% to elapsed time from 4 to 20 hours, as measured by an in-vitro dissolution in a USP Apparatus 1 (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37°C.

[00102] In certain embodiments, the amount of active agent (e.g., opioid analgésie) released from the dosage form is proportional within 20%, or within 10%, or within 5% to elapsed time from 4 to 15 hours, as measured by an in-vitro dissolution in a USP Apparatus 1 (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37°C.

[00103] In certain embodiments, the amount of active agent (e.g., opioid analgésie) released from the dosage form is proportional within 20%, or within 10%, or within 5% to elapsed time from 4 to 10 hours, as measured by an in-vitro dissolution in a USP Apparatus 1 (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37° C.

|00104] In certain embodiments, the amount of active agent (e.g., opioid analgésie) released from the dosage form is proportional within 20%, or within 10%, or within 5% to elapsed time from 8 to 20 hours, as measured by an in-vitro dissolution in a USP Apparatus 1 (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37°C.

[00105] In certain embodiments, the amount of active agent (e.g., opioid analgésie) released from the dosage form is proportional within 20%, or within 10%, or within 5% to elapsed time from 10 to 15 hours, as measured by an in-vitro dissolution in a USP

-2316458

Apparatus l (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37°C.

(00106) In certain embodiments, the amount of active agent (e.g., opioid analgésie) released at 2 hours is less than about 25%; the amount of active agent released from the dosage form at 4 hours is from about 10% to about 30%; the amount of active agent released from the dosage form at 8 hours is from about 20% to about 60%; the amount of active agent released from the dosage form at 12 hours is from about 40% to about 90%;

and the amount of active agent released from the dosage form at 18 hours is greater than 10 about 70%; as measured by an in-vitro dissolution in a USP Apparatus 1 (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37°C.

(00107) In certain embodiments, the amount of active agent (e.g., opioid analgésie) released at 2 hours is less than about 15%; the amount of active agent released from the 15 dosage form at 4 hours is from about 10% to about 20%; the amount of active agent released from the dosage form at 8 hours is from about 30% to about 45%; the amount of active agent released from the dosage form at 12 hours is from about 50% to about 70%;

and the amount of active agent released from the dosage form at 18 hours is greater than about 90%; as measured by an in-vitro dissolution in a USP Apparatus 1 (basket) at 100 20 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37° C.

(00108) In certain embodiments, the amount of active agent (e.g., opioid analgésie) released at 2 hours is less than about 10%; the amount of active agent released from the dosage form at 4 hours is from about 20% to about 30%; the amount of active agent 25 released from the dosage form at 8 hours is from about 45% to about 60%; the amount of active agent released from the dosage form at 12 hours is from about 70% to about 90%; and the amount of active agent released from the dosage form at 18 hours is greater than about 95%; as measured by an in-vitro dissolution in a USP Apparatus 1 (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37°C.

[00109| In certain embodiments, the amount of active agent (e.g., opioid analgésie) released from the dosage form is proportional within 20% to elapsed time from 8 to 24 * t

hours, as measured by an in-vitro dissolution in a USP Apparatus l (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37°C and at least one of the following is exhibited: (i) the amount of opioid analgésie released at 2 hours is less than about 20%, (ii) the amount of opioid analgésie released at 4 hours is from about 10% to about 30%, (iii) the amount of opioid analgésie released at 8 hours is from about 30% to about 60%, (iv) the amount of opioid analgésie released at 12 hours is from about 50% to about 90%, or (v) the amount of opioid analgésie released at 18 hours is greater than about 80%.

[00110] In certain embodiments, the amount of active agent (e.g., opioid analgésie) released from the dosage form is proportional within 20% to elapsed time from 8 to 24 hours, as measured by an in-vitro dissolution in a USP Apparatus 1 (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37°C and at least one of the following is exhibited: (i) the amount of opioid analgésie released at 2 hours is less than about 15%, (ii) the amount of opioid analgésie released at 4 hours is from about 10% to about 20%, (iii) the amount of opioid analgésie released at 8 hours is from about 30% to about 45%, (iv) the amount of opioid analgésie released at 12 hours is from about 50% to about 70%, or (v) the amount of opioid analgésie released at 18 hours is greater than about 90%.

(00111] In certain embodiments, the amount of active agent (e.g., opioid analgésie) released from the dosage form is proportional within 20% to elapsed tîme from 8 to 24 hours, as measured by an in-vitro dissolution in a USP Apparatus 1 (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37°C and at least one of the following is exhibited: (i) the amount of opioid analgésie released at 2 hours is less than about 10%, (ii) the amount of opioid analgésie released at 4 hours is from about 20% to about 30%, (iii) the amount of opioid analgésie released at 8 hours is from about 45% to about 60%, (iv) the amount of opioid analgésie released at 12 hours is from about 70% to about 90%, or (v) the amount of opioid analgésie released at 18 hours is greater than about 95%.

e

-25 16458 |00ll2] In certain embodiments, the amount of active agent (e.g., opioid analgésie) released from the dosage form is proportional within 20% to elapsed time from 8 to 24 hours, as measured by an in-vitro dissolution in a USP Apparatus l (basket) at 100 rpm in 900 ml sïmulated gastric fluid without enzymes (SGF) at 37°C and at least one of the following is exhibited: (i) the amount of opioid analgésie released at 2 hours is less than about 15%, (ii) the amount of opioid analgésie released at 4 hours is from about 8% to about 20%, (iii) the amount of opioid analgésie released at 8 hours is from about 20% to about 50%, (iv) the amount of opioid analgésie released at 12 hours is from about 40% to about 70%, (v) the amount of opioid analgésie released at 18 hours is greater than about 70% or (vi) the amount of opiid analgésie released from the dosage form at 24 hours is greater than about 90%.

DOSAGE FORMS [00113] In certain embodiments, the core may be prepared by dry blending a controlled release material, an active agent, and optionally other excipients, followed by granulating the mixture until proper granulation is obtained. The process can be performed by dry or wet granulation methods. Typically with a wet granulation, the wet granules are dried in a fluid bed dryer, and sifted and ground to appropriate size. Lubricating agents are typically mixed with the granulation to obtain the final core formulation.

[00114] A non-limiting list of suitable controlled release materials which may be selected for inclusion in a formulation according to the présent invention includes hydrophilic and hydrophobie materials such as sustained release polymers, gums, acrylic resins, proteinderived materials, waxes, shellacs, and oils such as hydrogenated castor oil and hydrogenated vegetable oil. More specifically, the controlled release materials can be, e.g., alkylcelluloses such as ethylcellulose, acrylic and methacrylic acid polymers and copolymers, and cellulose ethers, such as hydroxyalkylcelluloses (e.g., hydroxypropylmethyicellulose) and carboxyalkylcelluloses. Waxes include, e.g., natural and synthetîc waxes, fatty acids, fatty alcohols, and mixtures of the same (e.g., beeswax, camauba wax, stearic acid and stearyl alcohol). Certain embodiments utilize mixtures of two or more of the foregoing controlled release materials in the matrix of the core. However, any pharmaceutically acceptable hydrophobie or hydrophilic controlled release

-2616458 material which is capable of imparting controlled release of the active agent may be used in accordance with the présent invention.

[00115] The cores may also contain suitable quantities of additional excipients, e.g., lubricants, binders, granulating aids, diluents, colorants, flavorants (e.g., bittering agents) and glidants, ail of which are conventional in the pharmaceutical art.

|00116] Spécifie examples of pharmaceutically acceptable diluents and excipients that may be used in formulating the cores are described in the Handbook of Pharmaceutical Excipients, American Pharmaceutical Association (1986), incorporated by reference herein.

[00117] In preferred embodiments, matrices of the dosage forms of the présent invention incorporate polyethyiene oxide (e.g., high and/or low molecular weight PEO).

[00118] Polyethyiene oxide is considered to hâve an approximate molecular weight of 1,000,000 when a 2% (by wt) aqueous solution of the PEO using a Brookfield viscometer Model RVF, spindle No. 1, at 10 rpm, at 25°C shows a viscosity range of 400 to 800 mPas (cP).

[00119] Polyethyiene oxide is considered to hâve an approximate molecular weight of 2,000,000 when a 2% (by wt) aqueous solution of the PEO using a Brookfield viscometer Model RVF, spindle No. 3, at 10 rpm, at 25°C shows a viscosity range of 2000 to 4000 mPa-s (cP).

[00120] Polyethyiene oxide is considered to hâve an approximate molecular weight of 4,000,000 when a 1% (by wt) aqueous solution of the polyethyiene oxide using a Brookfield viscometer Model RVF, spindle No. 2, at 2 rpm, at 25°C shows a viscosity range of 1650 to 5500 mPa-s (cP).

[00121] Polyethyiene oxide is considered to hâve an approximate molecular weight of

5,000,000 when a 1% (by wt) aqueous solution of the polyethyiene oxide using a

-2716458

Brookfield viscometer Model RVF, spindle No. 2, at 2 rpm, at 25°C shows a viscosity range of 5500 to 7500 mPa-s (cP).

[00122] Polyethylene oxide is considered to hâve an approximate molecular weight of 5 7,000,000 when a 1% (by wt) aqueous solution of the polyethylene oxide using a

Brookfield viscometer Model RVF, spindle No. 2, at 2 rpm, at 25°C shows a viscosity range of 7500 to 10,000 mPa-s (cP).

[00123] Polyethylene oxide is considered to hâve an approximate molecular weight of 10 8,000,000 when a 1% (by wt) aqueous solution of the polyethylene oxide using a

Brookfield viscometer Model RVF, spindle No, 2, at 2 rpm, at 25°C shows a viscosity range of 10,000 to 15,000 mPa-s (cP).

|00124] Regarding the lower molecular weight polyethylene oxides, polyethylene oxide is 15 considered to hâve an approximate molecular weight of 100,000 when a 5% (by wt) aqueous solution of the polyethylene oxide using a Brookfield viscometer Model RVT, spindle No. 1, at 50 rpm, at 25°C shows a viscosity range of 30 to 50 mPa-s (cP).

[00125) Polyethylene oxide is considered to hâve an approximate molecular weight of 20 900,000 when a 5% (by wt) aqueous solution of the polyethylene oxide using a Brookfield viscometer Model RVF, spindle No. 2, at 2 rpm, at 25°C shows a viscosity range of 8800 to 17,600 mPa-s (cP).

COMPRESSION COATED DOSAGE FORMS [00126} In embodiments utilizing compression coating, it is preferred that ail or part of the pharmaceutically acceptable excipient(s) in the coating should impart sufficient compressibility to provide a pharmaceutically acceptable product. The compression coating onto the pre-formed core is dépendent in part on the individual characteristics of 30 the selected excipients and the active agent, e.g., in terms of polymer solubility, flowability, glass transition température, etc.

-2816458 |00127| Compression coated dosage forms can be prepared, e.g., by utilizing a premanufactured core or preparing a core (e.g., by compression) prior to the coating. The inner core can be prepared by wet or dry granulating active agent together with the pharmaceutically acceptable excipients; followed by drying and milling as necessary to 5 obtain a granulate; adding optional extragranular excipients and/or active agent with appropriate blending; adding a lubricant as needed; and compressing the granulate with a tablet press. The résultant compressed core can be optionally coated with a functional coating or film coating prior to compression coating.

(00128] The blend for compression coating can be prepared by a similar process as the blend for the core utilizing any of the controlled release materiais disclosed above. Preferably, the compression coating includes polyethylene oxide. The blend can be coated onto the core by compression. The compression of the core and/or the coating can utilize a Killion or Fette rotary press at a compression force, e.g., from about 1 to about 20 15 kilonewtons.

[00129] In certain embodiments, a Manesty Dry-Cota press (e.g., Model 900) can be utilized. This apparatus consists of two side by side interconnected tablet presses where the core is made on one press and then mechanically transferred to the next press for 20 compression coating. Each press has an independent powder feed mechanism so that the core blend is loaded on one machine, and the coating blend is loaded on the other machine. Mechanical transfer arms rotate between the machines to remove cores from the core press and transfer them to the coating press. Other presses which may be used to préparé the dosage forms of the présent invention include Elizabeth Hata HT-AP44-MSU25 C; Killian RLUD; and Fette PT 4090, each of which has a dual feed system for coating blend and pre-made cores. Utilizing these presses allows multiple compression coatinglayers to be achieved by recycling tablets that hâve already been compression-coated. Ail of these presses hâve mechanisms to center the tablet within the coating blend both vertically and radially.

[00130] In certain embodiments, the compression coating is not applied at the same thickness at ail points around the inner core, but instead is applied at different thicknesses

-2916458 around the inner core. Thinner areas of coating will produce areas of the compressed dosage form that will release drug from the inner core sooner than other areas. This may be simply accomplished, e.g., by having the core to which the compression coating is being applied not being centered in the press at the time of coating.

[00131] In certain embodiments, the compression coated dosage form can be further overcoated with a hydrophobie or enteric coating material. In other embodiments, the compression coated dosage forms can be coated with a hydrophilic coating in addition to or instead of the hydrophobie or enteric coating.

[00132| In still further embodiments, an optional coat (e.g., hydrophobie, hydrophilic or enteric) may be alternatively or additionally applied as an intermediate layer between the core and the compression coating.

ACTIVE AGENTS [00133] Opioid analgésies useful in the présent invention include, but are not limited to, alfentanil, allylprodine, alphaprodine, anileridine, benzyl morphine, bezitramide, buprénorphine, butorphanol, clonitazene, codéine, desomorphine, dextromoramide, dezocine, diampromide, diamorphone, dihydrocodéine, dihydromorphine, dimenoxadol, dimepheptanol, dimethylthiambutene, dioxaphetyl butyrate, dipipanone, eptazocine, ethoheptazine, ethylmethylthiambutene, ethylmorphine, etonitazene, etorphine, dihydroetorphine, fentanyl and dérivatives, hydrocodone, hydromorphone, hydroxypethidine, isomethadone, ketobemidone, levorphanol, levophenacylmorphan, lofentanil, meperidine, meptazinol, metazocine, methadone, metopon, morphine, myrophine, narceine, nicomorphine, norlevorphanol, normethadone, nalorphine, nalbuphene, normorphine, norpipanone, opium, oxycodone, oxymorphone, papaveretum, pentazocine, phenadoxone, phenomorphan, phenazocine, phenoperidine, piminodine, piritramide, propheptazine, promedol, properidine, propoxyphene, sufentanil, tilidine, tramadol, pharmaceutically acceptable salts, complexes (e.g., with a cyclodextrin), stereoisomers, ethers, esters, hydrates, solvatés, and mixtures thereof.

-3016458 [00134| Preferably, the opioid analgésie is selected from the group consisting of codeine, hydrocodone, hydromorphone, morphine, oxycodone, oxymorphone, tramadol, pharmaceutically acceptable salts, complexes, stereoisomers, ethers, esters, hydrates, solvatés, and mixtures thereof.

[00135] In certain embodiments, the opioid analgésie is selected from the group consisting of hydrocodone, pharmaceutically acceptable salts, complexes, stereoisomers, ethers, esters, hydrates, solvatés, and mixtures thereof. Preferably, the opioid analgésie is hydrocodone bitartrate.

|00136] The opioids used according to the présent invention may contain one or more asymmetric centers and may give rise to enantiomers, diastereomers, or other stereoisomeric forms. The présent invention is meant to encompass the use of ail such possible forms as well as their racemic and resolved forms and compositions thereof.

When the compounds described herein contain olefinic double bonds or other centers of géométrie asymmetry, it is intended to include both E and Z géométrie isomers. Ail tautomers are intended to be encompassed by the présent invention as well.

[00137] Pharmaceutically acceptable salts include, but are not limited to, inorganic acid salts such as hydrochloride, hydrobromide, sulfate, phosphate and the like; organic acid salts such as formate, acetate, trifluoroacetate, maleate, tartrate and the like; sulfonates such as methanesulfonate, benzenesulfonate, p-toluenesulfonate, and the like; amino acid salts such as arginate, asparaginate, glutamate and the like; métal salts such as sodium sait, potassium sait, césium sait and the like; alkaline earth metals such as calcium sait, magnésium sait and the like; and organic amine salts such as triethylamine sait, pyridine sait, picoline sait, ethanolamine sait, triethanolamine sait, dicyclohexylamine sait, N,Ndibenzylethylenediamine sait and the like.

[00138| Additionally, active agents other than opioid analgésies that are potentially subject to abuse may be used in accordance with the présent invention. Such agents include, e.g., tranquilizers, CNS depressants, CNS stimulants, sédatives, hypnotics, stimulants (including appetite suppressants such as phenylpropanolamine), and

-31 16458 cannabinoids, among others. More specifically, the active agent can be selected ÎTom barbiturates such as phénobarbital, secobarbital, pentobarbital, butabarbital, talbutal, aprobarbital, mephobarbital, butalbital, pharmaceutically acceptable salts thereof, and the like; benzodiazépines such as diazepam, chlordiazepoxide, alprazolam, triazolam, estazolam, clonazepam, flunitrazepam, pharmaceutically acceptable salts thereof, and the like; stimulants such as gamma-hydroxybutyrate, dextroamphétamine, methylphenidate, sibutramine, methylenedioxymethamphetamine, pharmaceutically acceptable salts thereof, and the like; other agents such as marinol, meprobamate and carisoprodol; and ail pharmaceutically acceptable salts, complexes, stereoisomers, ethers, esters, hydrates, solvatés, and mixtures thereof.

[00139] In further embodiments, other therapeutically active agents may be used in accordance with the présent invention, either alone or in combination with opioids. Examples of such therapeutically active agents include antihistamines (e.g., dimenhydrinate, diphenhydramine, chlorpheniramine and dexchlorpheniramine maleate), non-steroidal anti-inflammatory agents (e.g., naproxen, diclofenac, indomethacin, ibuprofen, sulindac, Cox-2 inhibitors), acetaminophen, anti-emetics (e.g., metoclopramide, methylnaltrexone), anti-epiieptics (e.g., phenyloin, meprobmate and nitrazepam), vasodilators (e.g., nifedipine, papaverine, diltiazem and nicardipine), anti-tussive agents and expectorants, anti-asthmatics (e.g. theophylline), antacids, anti-spasmodics (e.g., atropine, scopolamine), antidiabetics (e.g., insulin), diuretics (e.g., ethacrynic acid, bendrofluthiazide), anti-hypotensives (e.g., propranolol, clonidine), antihypertensives (e.g., clonidine, methyldopa), bronchodilators (e.g., albuterol), steroids (e.g., hydrocortisone, triamcinolone, prednisone), antibiotics (e.g., tétracycline), antihemonhoidals, psychotropics, anti-diarrheals, mucolytics, decongestants (e.g., pseudoephedrine), laxatives, vitamins, and the pharmaceutically acceptable salts, complexes, stereoisomers, ethers, esters, hydrates, solvatés, and mixtures thereof.

-32 16458

HYDROCODONE EMBODIMENTS [00140] The controlled release oral dosage forms of the présent invention preferably include from about 0.5 mg to about 1250 mg hydrocodone or an équivalent amount of a pharmaceutically acceptable sait thereof. In other embodiments, the dosage forms contain from about 2 mg to about 200 mg hydrocodone or an équivalent amount of a pharmaceutically acceptable sait thereof, or from about 16 mg to about 120 mg hydrocodone or an équivalent amount of a pharmaceutically acceptable sait thereof. In certain preferred embodiments, the dosage form eontains about 20 mg, about 30 mg, about 40 mg, about 60 mg, about 80 mg, about 100 mg or about 120 mg hydrocodone bitartrate.

[00141| Suitable pharmaceutically acceptable salts ofhydrocodone include hydrocodone bitartrate, hydrocodone bitartrate hydrate, hydrocodone hydrochloride, hydrocodone ptoluenesulfonate, hydrocodone phosphate, hydrocodone thiosemicarbazone, hydrocodone sulfate, hydrocodone trifluoroacetate, hydrocodone hemipentahydrate, hydrocodone pentafluoropropionate, hydrocodone p-nitrophenylhydrazone, hydrocodone omethyloxime, hydrocodone semicarbazone, hydrocodone hydrobromide, hydrocodone mucate, hydrocodone oleate, hydrocodone phosphate dibasic, hydrocodone phosphate monobasic, hydrocodone inorganic sait, hydrocodone organic sait, hydrocodone acetate trihydrate, hydrocodone bis(heptafuorobutyrate), hydrocodone bis(methylcarbamate), hydrocodone bis(pentafluoropropionate), hydrocodone bisfpyridine carboxylate), hydrocodone b is(tri fl uoro acetate), hydrocodone chlorhydrate, and hydrocodone sulfate pentahydrate. Preferably, the hydrocodone is présent as the bitartrate sait.

|00142] A hydrocodone dosage form of the présent invention may further include one or more additional drugs, which may or may not act synergistically with the hydrocodone contained therein. Examples of such additional drugs include non-steroidal antiinflammatory agents, including ibuprofen, diclofenac, naproxen, benoxaprofen, flurbiprofen, fenoprofen, flubufen, ketoprofen, indoprofen, piroprofen, carprofen, oxaprozin, pramoprofen, muroprofen, trioxaprofen, suprofen, aminoprofen, tiaprofenic acid, fluprofen, bucloxic acid, indomethacin, sulindac, tolmetin, zomepirac, tiopinac, zidometacin, acemetacin, fentiazac, clidanac, oxpinac, mefenamic acid, meelofenamie

-33 16458 acid, flufenamic acid, niflumic acid tolfenamic acid, diflurisal, flufenisal, piroxicam, sudoxicam, isoxicam and the pharmaceutically acceptable salts, complexes, stereoisomers, ethers, esters, hydrates, solvatés, and mixtures thereof. Such non-steroidal antiinflammatory agents also include cyclo-oxygenase inhibitors such as celecoxib, meloxicam, nabumetone, nimesulide and the pharmaceutically acceptable salts, complexes, stereoisomers, ethers, esters, hydrates, solvatés, and mixtures thereof.

|001431 Other additional drugs that can be co-formulated with hydrocodone include NMDA receptor antagonists such as dextrorphan, dextromethorphan, 3-(l-naphthalennyl)-

5-(phosphonomethyl)-L-phenylalanine, 3-( 1 -naphthalenyl)-5-(phosphonomethyl)-DLphenylalanine, l-(3,5-dimethylphenyl)naphthalene, 2-(3,5-dimethylphenyl) naphthalene, 2SR,4RS-4-(((lH-Tetrazol-5-yl)methyl)oxy)piperidine-2-carboxylic acid, 2SR,4RS-4((((lH-Tetrazol-5-yl)methyi)oxy)methyl)piperidine-2-carboxylic acid, E and Z 2SR-4-(O(1 H-Tetrazol-5-yl)methyl)ketoximino)piperidine-2-carboxylic acid, 2SR,4RS-4-((l HTetrazol-5-yl)thio)piperidine-2-carboxylic acid, 2SR,4RS-4-((lH-Tetrazol-5yl)thio)piperidine-2-carboxylic acid, 2SR,4RS-4-(5-mercapto-1 H-Tetrazol-1 yl)piperidine-2-carboxylic acid, 2SR,4RS-4-(5-mercapto-2IT-Tetrazol-2-yl)piperidine-2carboxylic acid, 2SR,4RS-4-(5-mercapto-l H-Tetrazol-l-yl) piperidine-2-carboxylic acid, 2SR,4RS-4-(5-mercapto-2H-Tetrazol-2-yl) piperidine-2-carboxylic acid, 2SR,4RS-4(((1 H-Tetrazol-5-yl)thio)methyl)piperidine-2-carboxylic acid, 2SR,4RS-4-((5-mercapto1 H-Tetrazol- l-yl)methyl) piperidine-2-carboxylic acid, 2SR,4RS-4-((5-mercapto-2HTetrazol-2-yl)methyl)piperidîne-2-carboxylic acid, and the pharmaceutically acceptable salts, complexes, stereoisomers, ethers, esters, hydrates, solvatés, and mixtures thereof.

|00144] Other suitable drugs which may be included in the hydrocodone dosage forms of the présent invention include acetaminophen and aspirin.

[00145] In preferred embodiments, the hydrocodone formulations of the présent invention are suitable for once-a-day administration and provide a relatively fiat plasma profile, meaning that the plasma level of the hydrocodone provides a C24/C_max ratio of about 0.55 to about 1.0 after administration. In certain embodiments, the CîVCmax ratio is about 0.55 va/”'

-3416458 to about 0.85, about 0.55 to about 0.75 or about 0,60 to about 0.70 after administration of the dosage form.

[00146] In preferred embodiments, the hydrocodone formulations of the présent invention provide a T_max (h) of hydrocodone from about 4 to about 20 hours after administration. In certain embodiments, the T_max is about 6 to about 12 hours, about 8 to about 10 hours, about 4 to about 10 hours, about 8 to about 14 hours, or about 14 to about 20 hours after administration of the dosage form.

[00147] In still other embodiments, a solid controlled release dosage form of the présent invention provides an AUC (ng*h/mL) after administration of about 200 to 450 or about 250 to 400 per each 20 mg hydrocodone or pharmaceutically acceptable sait thereof included in the dosage form.

[00148] In certain embodiments, a solid controlled release dosage form that contains 20 mg hydrocodone or a pharmaceutically acceptable sait thereof provides an AUC (ng*li/mL) after administration of about 200 to about 450, about 250 to about 400, about 275 to about 350, about 300 to 330 or about 280 to about 320.

[00149] In certain embodiments, a solid controlled release dosage form that contains 120 mg hydrocodone or a pharmaceutically acceptable sait thereof provides an AUC (ng*h/mL) after administration of about 1000 to about 3000, about 1500 to about 2400, about 1700 to about 2200, about 1800 to about 2100 or about 1900 to about 2100.

|00150] In other embodiments, a solid controlled release dosage form of the présent invention provides a C_max (ng/mL) after administration of about 5 to about 40, about 10 to about 30 per each 20 mg hydrocodone included in the dosage form.

|00151] In certain embodiments, a solid controlled release dosage form that contains 20 mg hydrocodone or a pharmaceutically acceptable sait thereof provides a C_inax (ng/mL) after administration of about 5 to about 40, about 10 to about 30, about 12 to about 25, about 14 to about 18 or about 12 to about 17.

-3516458 [00152] In certain embodiments, a solid controlled release dosage form that contains 120 mg hydrocodone or a pharmaceutically acceptable sait thereof provides a C_lllax (ng/mL) after administration of about 30 to about 120, about 60 to about 180, about 100 to about 160, about 110 to about 150 or about 100 to about 140.

[00153] In certain embodiments, a solid controlled release dosage form of the présent invention provides a T_max (h) of hydrocodone after administration of about 7 to about 22, 10 to about 20, about 12 to about 18, about 13 to about 17 or about 14 to about 16.

[00154] In other embodiments, a solid controlled release dosage form of the présent invention provides a Tj/2 (h) of hydrocodone after administration of about 5 to about 10, about 6 to about 9, about 7 or about 8.

[00155] In other embodiments, a solid controlled release dosage form of the présent invention provides a T|_ag (h) of hydrocodone after administration of about 0.01 to about 0.2, about 0.1 to about 0.18, about 0.3 to about 0.17 or about 0.06 t about 0.15.

[00156] In other embodiments, a solid controlled release dosage form of the présent invention provides a C24/C_niax ratio of hydrocodone of about 0.2 to about 0.8, about 0.3 to about 0.7 or about 0.4 to about 0.6.

[00157] In certain embodiments, any one or ail of the above mean in vivo parameters are achieved after administration in the fasted state.

[00158[ In certain embodiments, the mean AUC (ng*h/mL) of hydrocodone after administration in the fed state is less than 20% higher, less than 16% higher or less than 12% higher than the AUC (ng*h/mL) of hydrocodone after administration in the fasted state.

-3616458 (00159] In certain embodiments, the mean C_inax (ng/mL) of hydrocodone after administration in the fed state is less than 80% higher, less than 70% higher or less than 60% higher than the C_tnax of hydrocodone after administration in the fasted state.

[00160] In certain embodiments, the mean T_max (h) of hydrocodone after administration in the fed state is within 25%, within 20% or within 15% of the T_mux of hydrocodone after administration in the fasted state.

(00161) In certain embodiments, the mean T1/2 (h)of hydrocodone after administration in the fed state is within 8%, within 5% or within 2% of the T1/2 after administration in the fasted state.

[00162| In certain embodiments, the mean T|_ng of hydrocodone after administration in the fed state is less than 150% higher, less than 125% higher or less than 100% higher than the T[/2 after administration in the fasted state.

(00163) In certain embodiments, any one or ail of the above in vivo parameters are achieved after a first administration of the dosage form to a human subject, patient, or healthy subject (individual data) or a population of human subjects, patients or healthy subjects (mean data).

)00164) In certain alternative embodiments, any one or ail of the above in vivo parameters are achieved after steady state administration of the dosage form to a human subject, patient or healthy subject or a population of human subjects, patients or healthy subjects.

CURED FORMULATIONS [00165| In certain embodiments, a process of the présent invention further comprises the step of curing the final dosage form.

(00166) For embodiments comprising polyethylene oxide în a controlled release formulation, the curing step may comprise at least partially melting the polyethylene oxide v/^

-3716458 in the formulation. In certain embodiments, at least about 20% or at least about 30% of the polyethylene oxide in the formulation melts. Preferably, at least about 40%, or at least about 50%, or at least about 60%, or at least about 75%, or at least about 90% of the polyethylene oxide in the formulation melts during the curing step. In a preferred embodiment, about 100% of the polyethylene oxide melts.

[00167] In other embodiments, the curing step comprises subjecting the formulation to an elevated température for a certain period of time. In such embodiments, the curing température is at least as high as the softening température of the polyethylene oxide. According to certain embodiments, the curing température is at least about 60°C, at least about 62°C, ranges from about 62°C to about 90°C, from about 62°C to about 85°C, from about 62°C to about 80°C, from about 65°C to about 90°C, from about 65°C to about 85°C, or from about 65°C to about 80°C. The curing température preferably ranges from about 68°C to about 90°C, from about 68°C to about 85°C, from about 68°C to about 80°C, from about 70°C to about 90°C, from about 70°C to about 85°C, from about 70°C to about 80°C, from about 72°C to about 90°C, from about 72°C to about 85°C or from about 72°C to about 80°C. The curing température may be at least about 60°C, at least about 62°C, less than about 90°C or less than about 80°C. Preferably, it is in the range of from about 62°C to about 72°C or from about 68°C to about 72°C. Preferably, the curing température is at least as high as the lower limit of the softening température range of the polyethylene oxide, or at least about 62°C, or at least about 68°C. More preferably, the curing température is within the softening température range of the polyethylene oxide, or at least about 70°C, In further embodiments, the curing température is at least as high as the upper limit of the softening température range of the polyethylene oxide, or at least about 72^qC. In further embodiments, the curing température is higher than the upper limit of the softening température range of the polyethylene oxide, or at least about 75°C, or at least about 80°C.

[00168] In those embodiments where the curing step invoives subjecting the formulation to an elevated température for a certain period of time, this period of time is hereinafter referred to as the curing time. For the measurement of the curing time, a starting point and an end point of the curing step are defined. For the purposes of the présent invention, the m/'

-3816458 starting point of the curing step is defined to be the point in time when the curing température is reached.

|00169] In certain embodiments, the température profile during the curing step shows a plateau-like form between the starting point and the end point of the curing. In such embodiments, the end point of the curing step is defined to be the point in time when the heating is stopped or at least reduced, e.g. by terminating or reducing the heating and/or by starting a subséquent cooling step, and the température subsequently drops below the curing température by more than about 1O°C and/or below the lower limit of the softening température range of polyethylene oxide, for example, below about 62°C. When the curing température is reached and the curing step is thus started, déviations from the curing température in the course of the curing step can occur. Such déviations are tolerated as long as they do not exceed a value of about ± 1O°C, preferably about ± 6°C, and more preferably about ± 3°C. For example, if a curing température of at least about 75°C is to be maintained, the measured température may temporarily increase to a value of about 85°C, about 8l°C, or about 78^qC, and the measured température may also temporarily drop down to a value of about 65°C, about 69^qC or about 72°C. In the cases of a larger decrease of the température and/or in the case that the température drops below the lower limit of the softening température range of polyethylene oxide, for example below about 62°C, the curing step is discontinued, i.e. an end point is reached. Curing can be restarted by again reaching the curing température.

[00I70J In other embodiments, the température profile during the curing step shows a parabolic or triangular form between the starting point and the end point of the curing. This means that after the starting point, i.e., the point in time when the curing température is reached, the température further increases to reach a maximum, and then decreases. In such embodiments, the end point of the curing step is defined to be the point in time when the température drops below the curing température.

[00171] Depending on the apparatus used for the curing (i.e., curing device), different températures within the curing device can be measured to characterize the curing température.

-3916458 [00172| In certain embodiments, the curing step may take place in an oven. In such embodiments, the température inside the oven is measured. Based thereon, when the curing step takes place in an oven, the curing température is defined to be the target inside température of the oven and the starting point of the curing step is defined to be the point in time when the inside température of the oven reaches the curing température. The end point of the curing step is defined to be (1) the point in time when the heating is stopped or at least reduced and the température inside the oven subsequently drops below the curing température by more than about 10°C and/or below the lower limit of the softening 10 température range of high molecular weight polyethylene oxide , for example below about

62°C, in a plateau-like température profile or (2) the point in time when the température inside the oven drops below the curing température in a parabolic or triangular température profile. Preferably, the curing step starts when the température inside the oven reaches a curing température of at least about 62°C, at least about 68°C, at least 15 about 70°C, at least about 72°C or at least about 75°C. In preferred embodiments, the température profile during the curing step shows a plateau-like form, wherein the curing température, i.e. the inside température of the oven, is at least about 68°C, about 70°C, about 72°C, about 73°C, or lies within a range of from about 70°C to about 75°C, and the curing time is preferably in the range of from about 30 minutes to about 20 hours, from 20 about 30 minutes to about 15 hours, from about 30 minutes to about 4 hours, or from about 30 minutes to about 2 hours. In certain embodiments, the curing time is in the range of from about 30 minutes to about 90 minutes.

|00173] in certain other embodiments, the curing takes place in curing devices that are 25 heated by an air flow and comprise a heated air supply (inlet) and an exhaust, e.g., a coating pan or fluidized bed. Such curing devices will hereinafter be called convection curing devices. In such curing devices, it is possible to measure the température of the inlet air, i.e., the température of the heated air entering the convection curing device and/or the température of the exhaust air, i.e., the température of the air leaving the convection 30 curing device. It is also possible to déterminé or at least estimate the température of the formulations inside the convection curing device during the curing step, e.g., by using infrared température measurement instruments (such as an IR gun) or by measuring the

-40 16458 température using a température probe that was placed inside the curing device near the formulations. Based thereon, when the curing step takes place in a convection curing device, the curing température can be defined and the curing time can be measured as follows.

[00174] In one embodiment (method l), the curing température is defined to be the target inlet air température and the starting point of the curing step is defined to be the point in time when the inlet air température reaches the curing température. The end point of the curing step is defined to be (l) the point in time when the heating is stopped or at least reduced and the inlet air température subsequently drops below the curing température by more than about l0°C and/or below the lower limit of the softening température range of high molecular weight polyethylene oxide, for example below about 62°C, in a plateaulike température profile, or (2) the point in time when the inlet air température drops below the curing température in a parabolic or triangular température profile. Preferably, the curing step starts according to method l, when the inlet air température reaches a curing température of at least about 62°C, at least about 68°C, at least about 70°C, at least about 72°C or at least about 75°C. In a preferred embodiment, the température profile during the curing step shows a plateau-like form, wherein the curing température, i.e. the target inlet air température, is preferably at least about 72°C, for example, about 75°C, and the curing time which is measured according to method l is preferably in the range of from about 15 minutes to about 2 hours, for example, about 30 minutes or about l hour.

|00175| In another embodiment (method 2), the curing température is defined to be the target exhaust air température, and the starting point of the curing step is defined to be the point in time when the exhaust air température reaches the curing température. The end point of the curing step is defined to be (l) the point in time when the heating is stopped or at least reduced and the exhaust air température subsequently drops below the curing température by more than about l0°C and/or below the lower limit of the softening température range of high molecular weight polyethylene oxide, for example below about 62°C, in a plateau-like température profile, or (2) the point in time when the exhaust air température drops below the curing température in a parabolic or triangular température profile. Preferably, the curing step starts according to method 2, when the exhaust air

-41 16458 température reaches a curing température of at least about 62°C, at least about 68°C, at least about 70°C, at least about 72°C or at least about 75°C. In preferred embodiments, the température profile during the curing step shows a plateau-like form, wherein the curing température, i.e. the target exhaust air température, is preferably at least about 5 68°C, at least about 70°C or at least about 72°C, for example the target exhaust air température is about 68°C, about 70°C, about 72°C, about 75°C or about 78°C, and the curing time which is measured according to method 2 is preferably in the range of from about l minute to about 2 hours or from about 5 minutes to about 90 minutes, for example, the curing time is about 5 minutes, about 10 minutes, about 15 minutes, about 30 minutes, 10 about 60 minutes, about 70 minutes, about 75 minutes or about 90 minutes. In a more preferred embodiment, the curing time which is measured according to method 2 is in the range of from about 15 minutes to about l hour.

(00176] In a further embodiment (method 3), the curing température is defined to be the target température of the formulations and the starting point of the curing step is defined to be the point in time when the température of the formulations, which can be measured for example by an IR gun, reaches the curing température. The end point of the curing step is defined to be (1) the point in time when the heating is stopped or at least reduced and the température of the formulations subsequently drops below the curing température by more 20 than about 10°C and/or below the lower limit of the softening température range of high molecular weight polyethylene oxide, for example below about 62°C, in a plateau-like température profile or (2) the point in time when the température of the formulations drops below the curing température in a parabolic or triangular température profile. Preferably, the curing step starts according to method 3, when the température of the formulations 25 reaches a curing température of at least about 62°C, at least about 68°C, at least about 70°C, at least about 72°C or at least about 75°C.

[00177] In still another embodiment (method 4), the curing température is defined to be the target température measured using a température probe, such as a wire thermocouple, that is placed inside the curing device near the formulations, and the starting point of the curing step is defined to be the point in time when the température measured using the température probe reaches the curing température. The end point of the curing step is

-4216458 defined to be (l) the point in time when the heating is stopped or at least reduced and the température measured using the température probe subsequently drops below the curing température by more than about l0°C and/or below the lower limit of the softening température range of polyethylene oxide, for example below about 62°C, in a plateau-like température profile, or (2) the point in time when the température measured using the température probe drops below the curing température in a parabolic or triangular température profile. Preferably, the curing step starts when the température measured using a température probe registers a température in the curing device of at least about 62°C, at least about 68°C, at least about 70°C, at least about 72°C or at least about 75°C. In a preferred embodiment, the température profile during the curing step shows a plateaulike form, wherein the curing température is at least about 68°C, for example, about 70°C, and the curing time which is measured according to method 4 is preferably in the range of from about 15 minutes to about 2 hours or about 60 minutes or about 90 minutes.

[001781 If curing takes place in a convection curing device, the curing time can be measured by any of the methods described above.

[00179] In certain embodiments, the curing température is defined as a target température range, for example, the curing température is defined as a target inlet air température range or a target exhaust air température range. In such embodiments, the starting point of the curing step is defined to be the point in time when the lower limit of the target température range is reached, and the end point of the curing step is defined to be the point in time when the heating is stopped or at least reduced, and the température subsequently drops below the lower limit of the target température range by more than about 10°C and/or below the lower limit of the softening température range of polyethylene oxide, for example, below about 62°C.

[00180] The curing time, i.e., the time period the formulation is subjected to the curing température, which can, for example, be measured according to the methods described above, is at least about 1 minute or at least about 5 minutes. The curing time may vary from about 1 minute to about 24 hours, from about 5 minutes to about 20 hours, from about 10 minutes to about 15 hours, from about 15 minutes to about 10 hours, or from

-43 16458 about 30 minutes to about 5 hours depending on the spécifie formulation and the curing température. According to certain embodiments, the curing time varies from about 15 minutes to about 30 minutes. According to further embodiments, wherein the curing température is at least about 60°C, at least about 62°C, at least about 68°C, at least about 70°C, at least about 72°C or at least about 75°C, or varies from about 62°C to about 85°C or from about 65°C to about 85°C, then the curing time is preferably at least about 15 minutes, at least about 30 minutes, at least about 60 minutes, at least about 75 minutes, at least about 90 minutes or at least about 120 minutes. In preferred embodiments, wherein the curing température is, for example, at least about 62°C, at least about 68°C, at least about 70°C, at least about 72°C or at least about 75°C, or ranges from about 62°C to about 80°C, from about 65°C to about 80°C, from about 68°C to about 80°C, from about 70°C to about 80°C or from about 72°C to about 80°C, then the curing time is preferably at least about l minute, at least about 5 minutes, at least about 10 minutes, at least about 15 minutes or at least about 30 minutes. In certain such embodiments, the curing time can be chosen to be as short as possible while still achieving the desired resuit (e.g., increased tamper résistance). For example, the curing time preferably does not exceed about 5 hours, does not exceed about 3 hours or does not exceed about 2 hours. Preferably, the curing time is in the range of from about l minute to about 5 hours, from about 5 minutes to about 3 hours, from about 15 minutes to about 2 hours, or from about 15 minutes to about l hour. Any combination of the curing températures and the curing times as disclosed herein lies within the scope of the présent invention.

[00181] In certain embodiments, the composition is only subjected to the curing température until the polyethyiene oxide présent in the formulation has reached its softening température and/or at least partially melts. In certain such embodiments, the curing time may be less than about 5 minutes, for example the curing time may vary from greater than 0 minutes to about 3 hours, from about 1 minute to about 2 hours or from about 2 minutes to about 1 hour. Instant curing is possible by choosing a curing device which allows for an instant heating of the polyethyiene oxide in the formulation to at least its softening température, so that the high molecular weight polyethyiene oxide at least partially melts. Such curing devices are, for example, microwave ovens, ultrasound \λ/~~

-4416458 devices, light irradiation apparatus such as UV-irradiatîon apparatus, ultra-high frequency (UHF) fields or any other apparatus known to the person skilled in the art.

|00182| The size of the formulation may détermine the required curing time and curing température to achieve the desired tamper résistance.

[00183] In certain embodiments, the curing step leads to a decrease in the density of the formulation, such that the density of the cured formulation is lower than the density of the formulation prior to the curing step. Preferably, the density of the cured formulation in comparison to the density of the uncured formulation decreases by at least about 0.5%. More preferably, the density of the cured formulation in comparison to the density of the uncured formulation decreases by at least about 0.7%, at least about 0.8%, at least about 1.0%, at least about 2.0% or at least about 2.5%.

[00184] In certain embodiments, the solid controlled release dosage form is cured at a température of at least the softening point of the polyethylene oxide for at least 1 minute, at least 5 minutes or at least 15 minutes.

100185| In other embodiments, the solid controlled release dosage form is cured at a température of at least the softening point of the polyethylene oxide from about 1 minute to about 48 hours, from about 5 minutes to about 24 hours, from about 15 minutes to about 1 hour or about 30 minutes.

[00186] The solid controlled release dosage form can be cured, e.g., at a température of at least about 60°C, at least about 65°C, at least about 70°C, at least about 75°C or at a température of about 72°C.

100187] In alternative embodiments, the solid controlled release dosage form can be cured at a température from about 60°C to about 90°C, from about 62°C to about 72°C, from about 65°C to about 85°C, from about 70°C to about 80°C, from about 75° C to about 80°C or from about 70° C to about 75°C. άΑ”

-45 FLATTENING PROCEDURES [00l88| In certain embodiments, dosage forms of the présent invention may be flattened without substantially compromising the release of the active or the integrity of the dosage 5 form. Flatness is described in terms of the thickness of the smallest diameter of the flattened shape compared to the thickness of the smallest diameter of the non-flattened shape. This comparison is expressed in % thickness, based on either (i) the thickness of the smallest diameter of the non-flattened shape when the initial shape is non-spherical or (ii) the thickness of the diameter when the initial shape is spherical. The thickness may be 10 measured using a thickness gauge (e.g., a digital thickness gauge or digital caliper). The flattening force may be applied by any possible method. For purposes of testing the dosage forms of the présent invention, a carver style bench press may be used (unless otherwise specified) so as to achieve the target flatness or reduced thickness. According to certain embodiments of the invention, the flattening does not resuit in breaking of the 15 dosage form into separate pièces; however, edge splits and cracks may occur.

[00189] In certain embodiments of the invention, a hammer can be used for flattening a dosage form. In such a process, hammer strikes can be manually applied from a direction substantially normal to the thickest dimension of the dosage form. The flatness is then 20 described in the same manner as disclosed above.

|00190) In other embodiments, flattening can be measured relative to breaking strength or hardness tests, as described in Remington's Pharmaceutical Sciences, I8th édition, 1990, Chapter 89 Oral Solid Dosage Forms, pages 1633-1665, using the Schleuniger 25 Apparatus. In such an embodiment, the dosage form is pressed between a pair of fiat plates arranged in parallel such that the force is applied substantially normal to the thickest dimension of the dosage form, thereby flattening the dosage form. The flattening of the dosage form may be described in terms of % flattening, based on the thickness of the dimension being flattened before conducting the breaking strength test. The breaking 30 strength (or hardness) is defined as the force at which the tested dosage form breaks.

Dosage forms that do not break, but which are deformed due to a force applied are considered to be break-resîstant at that particular force,

-4616458 [00191] A further test to quantify the strength of dosage forms îs the indentation test using a Texture Analyzer, such as the TA-XT2 Texture Analyzer (Texture Technologies Corp., 18 Fairview Road, Scarsdale, N.Y. 10583). In this method, a dosage form is placed on top of a stainless steel stand with a slightly concave surface and penetrated by the descending probe of the Texture Analyzer, such as a TA-8A 1/8 inch diameter stainless steel bail probe. Before starting the measurement, the dosage form is alîgned directly under the probe, such that the descending probe will penetrate the tablet pivotally, i.e., in the center of the dosage form, and such that the force of the descending probe is applied substantially perpendicular to the diameter and substantially in line with the thickness of the dosage form. First, the probe of the Texture Analyzer starts to move towards the dosage form sample at the pre-test speed. When the probe contacts the dosage form surface and the trigger force set is reached, the probe continues its movement with the test speed and pénétrâtes the dosage form. For each pénétration depth or distance of the probe, the corresponding force is measured. When the probe has reached the desired maximum pénétration depth, it changes direction and moves back at the post-test speed, while further measurements are taken. The cracking force is defined to be the force of the first local maximum that is reached in the corresponding force/distance diagram and is calculated using, for example, the Texture Analyzer software Texture Expert Exceed, Version 2.64 English.

[00192J The term résistant to crushing is defined for the purposes of certain embodiments of the présent invention as referring to dosage forms that can at least be flattened with a bench press as described above without breaking to no more than about 60% thickness, preferably no more than about 50% thickness, more preferred no more than about 40% thickness, even more preferred no more than about 30% thickness and most preferred no more than about 20% thickness, 10% thickness or 5% thickness.

[00193] In certain embodiments, the amount of active agent (e.g., opioid analgésie) released at 0.5 hour from a flattened dosage form deviates no more than about 10 % points, 15 % points or 20% points from the amount released at 0.5 hour from a non-4716458 flattened dosage form as measured by an in-vitro dissolution in a USP Apparatus l (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37°C.

|00194] In alternative embodiments, the solid controlled release dosage form can be flattened without breaking, wherein the thickness of the dosage form after flattening corresponds to no more than about 60% of the thickness of the dosage form before flattening, no more than about 50% of the thickness of the dosage form before flattening, no more than about 40% of the thickness of the dosage form before flattening, no more than about 30% of the thickness of the dosage form before flattening or no more than about 20% of the thickness of the dosage form before flattening.

[00195] The following examples are set forth to assist in understanding the invention and should not be construed as specifically limiting the invention described and claimed herein. Such variations of the invention, including the substitution of ail équivalents now known or later developed, which would be within the purview of those skilled in the art, and changes in formulation or minor changes in experimental design, are to be considered to fall within the scope of the invention incorporated herein.

EXAMPLES |00196] The présent invention will now be more fully described with reference to the accompanying examples. It should be understood, however, that the following description is illustrative only and should not be taken in any way as a restriction of the invention,

EXAMPLE 1 |00197] A 400 mg tablet (Tablet A) including 20 mg of hydrocodone bitartrate was prepared using high molecular weight polyethylene oxide (PEO 303 - MW 7,000,000), as set forth in Table 1 below.

-48 16458

Table 1 (Tablet A)

	Hydrocodone (mg)	Total wt	% Hydrocodone	of Tooling Size (mm)
Core	16	200	8	7.94
Shell	4	200	2	10.32
Total	20	400	10

[00198] To préparé the core, a single station Manesty Type F 3 tablet press was equipped with 7,94 mm, round, standard concave plain tooling, A powdered aliquot of the core blend, as set forth above in Table 1, was weighed out to target weight of 200 mg, charged into the die, and compressed to form the core of Tablet A.

[00199] To préparé the shell, the single station Manesty Type F 3 tablet press was equipped with 10.32 mm, round, standard concave plain tooling. 100 mg of the shell blend, as set forth in Table 1, was placed in the die. The tablet core as prepared above was manually centered in the die (on top of the powder bed), and an additional 100 mg of the shell blend was placed on top of the tablet in the die. The materials were then manually compressed by turning the compression wheel to form compression coated Tablet A.

[00200] Several compression coated Tablet A tablets prepared as above were placed onto a tray, which was placed in a Hotpack model 435304 oven targeting 72°C for 30 minutes to cure.

[00201] Dissolution of cured Tablet A tablets was then tested in a USP Apparatus 1 (basket) at 100 rpm in 900 ml simulatcd gastric fluid without enzymes (SGF) at 37 °C. Results are shown against the results of the formulations of Examples 2-4 in Figure 1.

EXAMPLE 2 |00202] A 500 mg tablet (Tablet B) including 20 mg of hydrocodone bitartrate was prepared using high molecular weight polyethylene oxide (PEO 303 - MW 7,000,000), as set forth in Table 2 below.

-49Table 2 (Tablet B)

	Hydrocodone (mg)	Total wt	% Hydrocodone	of Tooling Size (mm)
Core	16	300	5.3	8.73
Shell	4	200	2	11.Il
Total	20	500	4

[00203] To préparé the core, a single station Manesty Type F 3 tablet press was equipped with 8.73 mm, round, standard concave plain tooling. A powdered aliquot of the core blend, as set forth above in Table 2, was weighed out to target weight of 300 mg, charged into the die and compressed to form the core of Tablet B.

[00204) To préparé the shell, the single station Manesty Type F 3 tablet press was equipped with l l.l l mm, round, standard concave plain tooling. The first portion of the 200 mg shell blend, as set forth in Table 2, was placed in the die. The tablet core as prepared above was manually centered in the die (on top of the powder bed), and the remaining portion of the 200 mg shell blend was placed on top of the tablet in the die. The materiais were then manually compressed by tuming the compression wheel to form compression coated Tablet B.

[002051 Several compression coated Tablet B tablets prepared as above were placed onto a tray, which was placed in a Hotpack model 435304 oven targeting 72°C for 30 minutes to cure.

[00206] Dissolution of cured Tablet B tablets was then tested in a USP Apparatus l (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37 °C. Results are shown against the results of the formulations of Examples l and 3-4 in Figure l. yS'

-5016458

EXAMPLE 3 [00207] A 500 mg tablet (Tablet C) including 20 mg of hydrocodone bitartrate was prepared using high molecular weight polyethylene oxide (PEO 303 - MW 7,000,000), as set forth in Table 3 below.

Table 3 (Tablet C)

	Hydrocodone (mg)	Total wt	% Hydrocodone	of Tooling Size (mm)
Core	16	300	5.3	9.53
Shell	4	200	2	11.11
Total	20	500	4

[00208) To préparé the core, a single station Manesty Type F 3 tablet press was equipped with 9.53mm, round, standard concave plain tooling. A powdered aliquot of the core blend, as set forth above in Table 3, was weighed out to target weight of 300 mg, charged into the die and compressed to form the core of Tablet C.

[00209] To préparé the shell, the single station Manesty Type F 3 tablet press was equipped with 11.11 mm, round, standard concave plain tooling. A first portion of the 200 mg shell blend, as set forth in Table 3, was placed in the die. The tablet core as prepared above was manually centered in the die (on top of the powder bed), and the remaining portion of the 200 mg shell blend was placed on top of the tablet in the die. The materials were then manually compressed by tuming the compression wheel to form compression coated Tablet C.

[00210] Several compression coated Tablet C tablets prepared as above were placed onto a tray, which was placed in a Hotpack model 435304 oven targeting 72°C for 30 minutes to cure.

[00211] Dissolution of cured Tablet C tablets was then tested in a USP Apparatus 1 (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37 °C.

Results are shown against the results of the formulations of Examples 1-2 and 4 in Figure

1.

>

-51 16458

EXAMPLE 4 (00212] A 475 mg tablet (Tablet D) including 20 mg of hydrocodone bitartrate was prepared using high molecular weight polyethylene oxide (PEO 303 - MW 7,000,000), as set forth in Table 4 below.

Table 4 (Tablet D)

	Hydrocodone (mg)	Total wt	% Hydrocodone	of Tooling Size (mm)
Core	14	175	8	7.94
Shell	6	300	2	11.Il
Total	20	475	4.2

[00213] To préparé the core, a single station Manesty Type F 3 tablet press was equipped with 7.94 mm, round, standard concave plain tooling. A powdered aliquot of the core blend, as set forth in Table 4, was weîghed out to target weight of 175 mg, charged into the die and compressed to form the core of Tablet D.

[00214] To préparé the shell, the single station Manesty Type F 3 tablet press was equipped with 11.11 mm, round, standard concave plain tooling. A first portion of the 300 mg shell blend, as set forth in Table 4, was placed in the die. The tablet core as prepared above was manually centered in the die (on top of the powder bed), and the remaining portion of the 300 mg shell blend was placed on top of the tablet in the die. The materials were then manually compressed by tuming the compression wheel to form compression coated Tablet D.

[00215] Several compression coated Tablet D tablets prepared as above were then placed onto a tray, which was placed in a Hotpack model 435304 oven targeting 72°C for 30 minutes to cure.

[00216] Dissolution of cured Tablet D tablets was then tested in a USP Apparatus 1 (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37 °C.

Results are shown against the results ofthe formulations ofExamples 1-3 in Figure 1.

» ι

-5216458

EXAMPLE 5 [00217] A 500 mg tablet (Tablet E) including 120 mg of hydrocodone was prepared using low molecular weight polyethylene oxide (PEO 205 - MW 600,000) for the core and using high molecular weight polyethylene oxide (PEO 303 - MW 7,000,000) for the shell, as set forth in Table 5 below.

Table 5 (Tablet E)

	Hydrocodone (mg)	Total wt	% Hydrocodone	of Tooling Size (mm)
Core	96	300	32	8.73
Shell	24	200	12	11.11
Total	120	500	24

[00218] To préparé the core, a single station Manesty Type F 3 tablet press was equipped with 8.73 mm, round, standard concave plain tooling. A powdered aliquot of the core blend, as set forth in Table 5, was weighed out to target weight of 300 mg, charged into the die and compressed to form the core of Tablet E.

[00219] To préparé the shell, the single station Manesty Type F 3 tablet press was equipped with 11.11 mm, round, standard concave plain tooling. A first portion of the 200 mg shell blend, as set forth in Table 5, was placed in the die. The tablet core as prepared above was manually centered in the die (on top of the powder bed), and the remaining portion of the 200 mg shell blend was placed on top of the tablet in the die. The materials were manually compressed by tuming the compression wheel to form compression coated Tablet E.

[00220] Several compression coated Tablet E tablets prepared as above were then placed onto a tray, which was placed in a Hotpack model 435304 oven targeting 72°C for 30 minutes to cure.

[00221] Dissolution of cured Tablet E tablets was then tested in a USP Apparatus 1 (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37 °C.

Results are shown against the results of the formulations of Examples 5 and 6 in Figure 2.

-53 16458

EXAMPLE 6 [00222] A 500 mg tablet (Tablet F) including 120 mg of hydrocodone was prepared using high molecular weight polyethylene oxide (PEO 303 - MW 7,000,000), as set forth in Table 6 below.

Table 6 (Tablet F)

	Hydrocodone (mg)	Total wt	% Hydrocodone	of Tooling Size (mm)
Core	96	300	32	8.73
Shell	24	200	12	11.Il
Total	120	500	24

[00223] To préparé the core, a single station Manesty Type F 3 tablet press was equipped with 8.73 mm, round, standard concave plain tooling. A powdered aliquot of the core blend, as set forth in Table 6, was weighed out to target weight of 300 mg, charged into the die and compressed to form the core of Tablet F.

[00224] To préparé the shell, the single station Manesty Type F 3 tablet press was equipped with 11 ,l l mm, round, standard concave plain tooling. A first portion of the 200 mg shell blend, as set forth in Table 6, was placed in the die. The tablet core as prepared above was manually centered in the die (on top of the powder bed), and the remaining portion of the 200 mg shell blend was placed on top of the tablet in the die. The materials were manually compressed by tuming the compression wheel to form compression coated Tablet F.

[00225] Several compression coated Tablet F tablets prepared as above were then placed onto a tray, which was placed in a Hotpack mode! 435304 oven targeting 72°C for 30 minutes to cure.

[00226] Dissolution of Tablet F tablets was then tested in a USP Apparatus l (basket) at

100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37 °C. Results are shown against the results of the formulations of Examples 5 and 6 in Figure 2. v/

- 5416458

EXAMPLES 7-12 [00227] Six different compression coated tablets (designated as Tablets G-L) containing a total of either 20 mg of hydrocodone bitartrate (Tablets G, H and I) or

120 mg of hydrocodone bitartrate (Tablets J, K and L) were prepared according to

Table 7 (20 mg) or Table 8 (120 mg) below.

Table 7 (Tablets G, H, I)
20mg	Formulation G	Formulation H	Formulation 1
Component	mg/tablet	mg/tablet	mg/tablet
Core
Hydrocodone Bitartate	16	16	16
Microcrystalline Cellulose, Avicel PH 101	1.09	1.09	1.09
Hydroxypropyl Cellulose, Klucel EXF	1.09	1.09	1.09
PEO (Mw=600,000) POLYOX WSR 205	280.32	280.32	280.32
Magnésium Stéarate	1.5	1.5	1.5
Subtotal	300	300	300
Dry Coal
Hydrocodone Bitartate	4	4	4
Microcrystalline Cellulose, Avicel PH 101	0.27	0.27	0.27
Hydroxypropyl Cellulose, Klucel EXF	0.27	0.27	0.27
PEO (Mw=7,000,000) POLYOX WSR
303 FP	393.26	293.81	194.36
Magnésium Stéarate	2	1.5	1
D&C Yellow No. 10 Aluminum Lake	0.2	0.15	0.1
Subtotal	400	300	200
Cosmetic Coat
Opadry White Y-5-18024-A	28	24	20
Total	728	624	520

Table 8 (Tablets J, K, L)

120mg	Formulation J	Formulation K	Formulation L
Component	mg/tablet	mg/tablet	mg/tablet
Core
Hydrocodone Bitartate	96	96	96
Microcrystalline Cellulose, Avicel PH
101	6.54	6.54	6.54
Hydroxypropyl Cellulose, Klucel EXF	6.54	6.54	6.54
PEO (Mw=600,000) POLYOX WSR
205	189.42	189.42	189.42
Magnésium Stéarate	1.5	1.5	1.5
Subtotal	300	300	300

Dry Coat

Hydrocodone Bitartate	24	24	24
Microcrystalline Cellulose, Avicel PH
101	1.64	1.64	1.64
Hydroxypropyl Cellulose, Klucel EXF	1.64	1.64	1.64
PEO (Mw=7,000,000) POLYOX WSR
303 FP	370.52	271.07	171.62
Magnésium Stéarate	2	1.5	1
D&C Red No. 30 Aluminum Lake	0.2	0.15	0.1
Subtotal	400	300	200
Cosmetic Coat
OpadryPink Y-S-1-14518A	28	24	20
Total	728	624	520

[00228] A high-shear granulator (Collette 75 L) was charged with the hydrocodone bitartrate, the microcrystalline cellulose and the hydroxypropylcellulose. Water was added to the mixture (e.g., 8-15%) with the propeller and chopper on. The wet granulation was passed through the coarse screen of a Quadro Comil milling device. The screened wet granulation was dried in a Vector VFC-3 fluid bed dryer. The dried granulation was passed through the fine screen of the Quadro Comil milling device.

|00229] A 16 Q “V” blender was charged with the PEO POLYOX WSR 205 and the milled granulation, and blended for 5 minutes. Screened magnésium stéarate was added to the mixture and blended for 1 minute to préparé the core blend.

|00230] A 16 Q “V” blender was charged with the PEO POLYOX WSR 303, the D&C Red No. 30 aluminum lake, and the milled granulation, and blended for 5 minutes. Screened magnésium stéarate was added to the mixture and blended for 1 minute to préparé the dry coat blend.

|00231] The core blend and dry coat blend were compressed into dry coated tablets on a DryCota Press. The core blend was loaded into the side one hopper and the core weight was adjusted to target 300 mg. Then the dry coat blend was loaded into the side two hopper and the total tablet weight was adjusted to target. \a/

-5616458

After weight adjustment, the compression run was started and the press was run at, e.g., 6 rpm.

[002321 Approximately 10 kg of the compression coated tablets were weighed out and spray-coated with the Opadry coating suspension to a target weight gain of about 1.0 % (by wt.) in a perforated 24 inch Compu-Lab pan coater. The spraycoating was carried out as follows. The tablet bed was warmed by setting the inlet air température to 55° C. Once the exhaust température reached 39° C, the film coating began at a pan speed of 12 rpm and a spray rate of approximately 44 mL/min. Film coating was continued until the target 1% weight gain was achieved (this was a partial coating prior to the curing in step x, as the final coating of 4% weight gain in step xii would become sticky during curing).

[00233] The partially coated tablets were cured in the perforated pan coater. The 15 inlet température was set to 85 °C at a pan speed of approximately 10 rpm. The tablets were cured at an exhaust température of 72 °C for approximately 30 minutes.

[00234| After curing, the tablets were cooled in the rotating pan by setting the 20 inlet température to 22 °C. Cooling was continued until the exhaust température was less than 28 °C.

[00235) The cured tablets were then spray-coated with additional coating suspension to attain a target final weight gain of 4.0 % (by wt., inclusive of the 25 previous 1% coating) in the perforated pan coater at a pan speed of 12 rpm and spray rate of approximately 44 mL/min.

[00236] The film coated tablets were transferred into a tared polyethylene lined drum.

»

-5716458 [00237] The dissolution results (% active released over time) for these compression coated 20 mg and 120 mg tablets are presented in Figure 3 and Tables 9 and 10 below.

Table 9

Dîsso Time (h)	20mg Slow (G) % active released	20mg Med. (H) % active released	20mg Fast (I) % active released
1	5	6	8
2	8	10	14
4	14	19	28
8	33	43	55
12	56	66	81
18	81	91	106
24	99	102	107

Table 10

Disso Time (h)	120mg Slow (J) % active released	120mg Med. (K) % active released	120mg Fast (L) % active released
1	5	6	8
2	8	10	15
4	14	20	29
8	35	47	57
12	59	72	82
18	86	100	98
24	102	103	100

[00238] As indicated by the dissolution of the above examples, factors which influence the dissolution of active agent from the dosage forms are the core:shell weight ratio and the tablet weight. Further, dissolution data presented above demonstrates that formulations of the présent invention exhibit substantially zéro order release as disclosed herein.

EXAMPLE 13 |00239] A randomized, open-label, crossover study in healthy adult male and female subjects was conducted with the hydrocodone formulations (HYD) of Examples 7-12. The study was comprised of Itérations (a process of repeating the study design each time with a unique group of subjects undergoing a set of predefined treatments). The following Itérations were conducted:

Itération 1 :

N=36

Randomized, single-dose, 3 treatment, 3 period crossover.

• HYD 20 mg, slow release tablet, fasted state (Tablet G) • HYD 20 mg, medium release tablet, fasted state (Tablet H) • HYD 20 mg, fast release tablet, fasted state (Tablet I)

Itération 2:

N=36

Randomized, single-dose, 3 treatment, 3 period crossover.

• HYD 120 mg, slow release tablet, fasted state (Tablet J) • HYD 120 mg, medium release tablet, fasted state (Tablet K) • HYD 120 mg, fast release tablet, fasted state (Tablet L)

Itération 3:

N=16

Randomized, single-dose, 2 treatment, 2 period crossover.

• HYD 120 mg, slow release tablet, fasted state (Tablet J) • HYD 120 mg, slow release tablet, fed state (Tablet J) [00240] The formulations were each administered orally with 8 oz. (240 mL) water as a single dose in the fasted or fed state as indicated.

[00241] As this study was conducted in healthy human subjects, the opioid antagonist naltrexone hydrochloride was administered to minimize opioid-related adverse events.

Screening procedures

The following screening procedures were performed for ail potential subjects at a screening visit conducted within 28 days prior to first dose administration:

-Infoimed consent.

-Informed consent for optional pharmacogenomic sampling.

-Infoimed consent for optional hair sampling.

-Weight, height, body mass index (BMI), and démographie data.

-Evaluation of inclusion/exclusion criteria.

-Medical and médication history, including concomitant médication, vZ

-59-Vital signs (systolic/diastolic blood pressure, puise rate, respiration rate, oral température) after being seated for approximately 5 minutes and SpOi

-Additional vital signs (systolic/diastolic blood pressure, and puise rate) after standing for approximately 2 minutes.

-HDYF? Inquiry was performed at the same time vital signs were measured.

-Routine physical examination.

-Clinical laboratory évaluations following at least a 4 hour fast (including biochemistry, hematology, and urinalysis).

-12-lead ECG. QTcF not to exceed 450 msec.

-Screens for hepatitis (including hepatitis B surface antigen [HBsAg], hepatitis C antibody [anti-HCV]).

-Screens for alcohol, cotinine, and selected drugs of abuse.

-Sérum pregnancy test, female subjects only; Sérum follicle stimulating hormone (FSH) postmenopausal females only;.

-Sérum pregnancy test (female subjects only).

-Sérum follicle stimulating hormone (FSH) test (postmenopausal females only).

Inclusion criteria

-Subjects who met the following criteria were included in the study.

-Provided written informed consent.

-Males and females aged 18 to 50, inclusive.

-Body weight ranging from 50 to 100 kg (l 10 to 220 Ibs) and a BMI 18 to 34 (kg/m²), inclusive.

-Healthy and free of significant abnormal findings as determined by medical history, physical examination, vital signs, and ECG.

-Females of child-bearing potentîal must be using an adéquate and reliable method of contraception (i.e, barrier with additional spermicidal foam or jelly, intra-uterine

-60device, hormonal contraception). Females who are post-menopausal must hâve been postmenopausal > l year and hâve elevated sérum FSH.

-Willing to eat the food supplied during the study.

-Will refrain from strenuous exercise during the entire study. Subjects will not begin a new exercise program nor participate in any unusually strenuous physical exertion.

Exclusion criteria

The following criteria excluded potential subjects from the study.

-Females who are prégnant (positive beta human chorionic gonadotropin test) or lactating.

-Current or recent (within 5 years) history of drug or alcohol abuse.

-History or any current conditions that might interfère with drug absorption, distribution, metabolism or excrétion.

-Use of an opioid-containing médication in the past 30 days preceding the initial dose in this study.

-History of known sensitivity to hydrocodone, naltrexone or related compounds.

-Any history of frequent nausea or emesis regardless of etiology.

-Any history of seizures or head trauma with sequelae.

-Participation in a clinical drug study during the 30 days preceding the initial dose in this study.

-Any signifîcant illness during the 30 days preceding the initial dose in this study.

-Use of any médication including thyroid hormonal therapy (hormonal contraception is allowed), vitamins, herbal and/or minerai suppléments during the 7 days preceding the initial dose.

-Abnormal cardiac conditions including any of the following:

-6l - • QTc interval > 450 msec (calculated using Fridericia’s correction) at screening.

• QTc interval > 480 msec (calculated using Fridericia’s correction) during Treatment period,

-Refusa! to abstain from food 10 hours preceding and 4 hours following study drug administration and to abstain from caffeine or xanthine containing beverages entirely during each confinement.

-Refusai to abstain from consumption of alcoholic beverages 48 hours prior to initial study drug administration (day l ) and anytime during study.

-History of smoking or use of nicotine products within 45 days of study drug administration or a positive urine cotinine test.

-Blood or blood products donated within 60 days prior to study drug administration or anytime during the study and for 30 days after completion of the study, except as required by this protocol.

-Plasma donated within 14 days prior to study drug administration or any time during the study, except as required by this protocol.

-Positive results of urine drug screen or alcohol screen.

-Positive results of HBsAg, anti-HCV.

-Positive naloxone HCl challenge test.

-Presence of Gilbert’s Syndrome, or any known hepatobiliary abnormalities.

-For the optional hair sampling portion of the study only, an insufficient amount of scalp hair to provide an adéquate sample.

-The investigator believes the subject to be unsuitable for reason(s) not specifically stated in the exclusion criteria.

[00242| Subjects meeting ail the inclusion criteria and none of the exclusion criteria were randomized into the study.

-6216458 [00243] Each subject was assigned a unique subject number at screening. Assignaient of subject numbers was in ascending order and no nuinbers were omitted. Subject numbers were used on ail study documentation.

CHECK-ÏN PROCEDURES [00244] On Day -l of Period l only, subjects were admitted to the study unit and received a Naloxone HCl challenge test. The results of the test had to be négative for subjects to continue in the study. Vital signs and SPO2 were measured prior to and following the Naloxone HCl.

[002451 The following procedures were also performed for ail subjects at Check-in for each period:

-Vérification of inclusion/exclusion criteria, including vérification of willingness to comply with caffeine and xanthine restriction criteria.

-Vital signs (after being seated for approximately 5 minutes) and SpO2.

-HDYF(How do you feel) ? Inquiry was performed at the same time vital signs were measured.

-Clinical laboratory évaluations (day -1, period 1 only) including biochemistry (fasting for at least 4 hours), hematology and urinalysis) were collected after vital signs and SpCh were measured.

-Screen for alcohol (via urine or blood alcohol or breathalyzer test), cotinine, and selected drugs of abuse (via urine testing).

-Urine pregnancy test (for ail female subjects).

-Concomitant médication monitoring and recording.

-AE monitoring and recording.

[002461 Foi^- subjects to continue their participation in the study, the results of the drug screen (including alcohol and cotinine) had to be available and négative prior to dosing. In addition, contînued compliance with concomitant médication and other restrictions were verified at Check-in and throughout the study in the appropriate source documentation.

-63TREATMENT PERIOD PROCEDURES

Treatments to be studied were predetermined for each Itération. Within an Itération, as data became available, treatments were dropped between cohorts. Dropped treatments were replaced with repeats of remaining treatments.

-Prior to the first dose in period l, subjects were randomized to a treatment sequence.

-Subjects received naltrexone HCl tablets (50 mg) with 240 mL of water at -12 h prior to study drug dosing.

-Prior to study drug administration (except period l), subjects had chemistry (fasting for at least 4 hours), hematology and urinalysis tests performed.

-Subjects were adminîstered the study drug with 240 mL of water as follows:

• For Fasted Treatment:

Following a I0-hour overnight fast, subjects were adminîstered study drug with 240 mL of water. Subjects receiving fasted treatment continued fasting from food for 4 hours following dosing.

• For Fed Treatments:

Following a I0-hour overnight fast, the subjects were fed a standard meal (FDA high-fat breakfast) 30 minutes prior to administration of study drug with 240 mL of water. No food was allowed for at least 4 hours post-dose. It was made very clear to the subjects that ail ofthe meal should be consumed within the designated time-frame.

• Subjects were standing or in an upright sitting position while receiving their dose of study drug.

• Fasting was not required for nondosing study days.

-Subjects received naltrexone HCl 50-mg tablets with 240 mL of water at -12, 0, 12, 24, and 36 hours relative to each study drug dosing.

-For subjects receiving hydrocodone doses of 60 mg or more, SpCb was monitored continuously beginning prior to dosing and continuing through 24 hours post-dose.

-6416458

-Vital signs (after being seated for approximately 5 minutes) and SpOi, were obtained pre-dose and at hour l, 2, 4, 6, 8, 12, 24, 36, 48, and 72 hour post dose for each period.

-HDYF (How do you feel) ? Inquiry was performed at the same time vital signs were measured.

-Subjects had biochemistry (fasting for at least 4 hours), hematology, and urinalysis tests performed 24 hours post-dose.

-In addition, 12-lead ECGs were performed for each subject pre-dose and approximately 12, 24 and 48 hours post-dose. If QTcF exceeded 480 msec the subject was discontinued due to the reason of Adverse Event.

-Blood samples for determining hydrocodone plasma concentrations were obtained for each subject at pre-dose and at 0.5, l, 1.5, 2, 2.5, 3,3.5, 4, 5, 6, 8, 10, 12,14, 18 24, 36, 48, and 72 hours post-dose for each period.

-Subjects were confined to the unit from check-in to the unit on the day before dosing until the time that their 48 h procedures were completed. The subjects retumed to the unit for the 72 h procedures.

-During the study, AEs and concomitant médications were recorded.

[00247| In addition, the subjects were infortned that it is very important to report any/ail épisodes of emesis to the study staff immediately and that this information is crucial to the proper conduct and outcome of the trial. The subjects were informed that they would not be penalized in any way due to reporting cases of emesis. The study staff was instructed to carefully document any/all cases of emesis.

STUDY COMPLETION PROCEDURES [00248] The following procedures were performed at the study site for ail subjects at endof-study (study completion), 7 to 10 days after receiving their last dose of study drug or upon early discontinuation from the study. -γκ/

-6516458

-Concomitant médication évaluation.

-Vital signs (after being seated for approximately 5 minutes) and SpO2.

-HDYF? Inquiry was performed at the same time vital signs are measured. -Physicaï examination.

-12-Lead ECG.

-Clinical laboratory évaluations (including biochemistry [fasted at least 4 hours], hematology, and urinalysis).

-AE évaluations.

-Sérum pregnancy test (for female subjects only).

[00249] The draft results are set forth in Figures 4-6 and Table 13 below;

Table 13 Summary of Draft Plasma Hydrocodone Pharmacokinetic Parameters

	Itération 1 : I-IYD 20 mg	Itération 2: HYD 120 mg
Slow (G)	Mediu m(I-I)	Fast (I)	Slow (J)	Mediu m(K)	Fast (L) Faste
Parameler	Statist	Fasted	Fasted	Fasted	Fasted	Fasted	d (N=3
(Unit)	ic	(N=36)	(N=36)	(N=36)	(N=36)	(N=36)	6)

Itération 3:

H YD 120 mg Slow Slow (J) (J)

Fasted Fed (N=14 (N=16 ) )

MEA

AUCt	N	302	323	330	2028	2074	2048	1921	2025
(ng*li/mL )	SD	138	101	90	439	440	514	369	420
	MIN	43	95	78	1315	1043	430	1417	1135
	MAX	619	557	499	2911	2869	2917	2586	2716
AUCinf	Mean	312	326	329	2037	2083	2055	1933	2032
(ng*h/mL )	SD	142	102	90	442	443	516	374	420
	Min	44	97	83	1320	1046	430	1427	1136
	Max	623	564	507	2935	2908	2924	2594	2717
Cmax	Mean	15.0	17.4	20.9	119	138	142	110	166
(ng/mL)	SD	6.4	5.8	7.2	35.8	35.3	39.3	30	34.2
	Min	4.3	7.5	7.7	55.2	76.7	35.6	67	96.2
	Max	30.7	31.3	39.0	227	241	239	162	240 va/~

-6616458

Tmax (h)	Mean	15.2	13.7	11.4	15.4	12.7	10.7	15	12.0
	SD	4.7	2.6	3.5	2.9	1.7	2.0	3	1.0
	Min	5	8	6	10	10	6	12	10
	Media
	n	14	14	12	14	12	10	14	12
	Max	24	18	24	24	18	14	24	14
Tl/2 (h)	Mean	8.3	7.6	9.0	7.1	7.6	7.1	7.7	7.8
	SD	3.1	2.9	4.9	2.4	3.3	2.5	2.4	4.6
	Min	4.1	4.5	4.4	4.5	4.2	4.1	4.0	3.8
	Max	15.3	17.3	25.2	16.0	17.9	13.4	12.4	21.4
Tlag (h)	Mean	0.15	0.11	0.13	0.06	0.03	0.01	0.03	0.06
	SD	0.23	0.21	0.22	0.16	0.12	0.09	0.13	0.17
	Min	0	0	0	0	0	0	0	0
	Max	0.5	0.5	0.5	0.5	0.5	0.5	0.5	0.5

C24/Cma

x	Mean	0.57	0.45	0.30	0.52	0.32	0.23	N/A	N/A
	SD	0.28	0.20	0.18	0.21	0.15	0.10	N/A	N/A
	Min	0.03	0.10	0.06	0.17	0.11	0.07	N/A	N/A
	Max	1.00	0.84	1.00	1.00	0.74	0.48	N/A	N/A

EXAMPLES 14-20 |00250] Seven different compression coated tablets (designated as Tablets M-S) containing a total of 20, 30, 40, 60, 80, 100 or 120 mg of hydrocodone bitartrate, respectively, were prepared according to Tables 14 (Tablets M, N, O, P) and 15 (Tablets Q, R, S) below. xrX~

-67Table 14 (Tablets M, N, O, P)

	Formulation M (20 mg)	Formulation N (30 mg)	Formulation O (40 mg)	Formulation P (60 mg)
Componcnt	mg/tablet	nig/tnblct	mg/tablet	mg/tablet
Core
Hydrocodone Bitartate	16.000	24.000	32.000	48.000
Microcrystalline
Cellulose, Avicel PH 101	1.091	1.636	2.182	3.273
Hydroxypropyl Cellulose,
Klucel EXF	1.091	1.636	2.182	3.273
Purified Water
PEO (Mw=600,000)
POLYOX WSR 205 FP	279.918	270.827	261.736	243.555
Magnésium Stéarate	1.500	1.500	1.500	1.500
FD&C Yellow No. 6
Aluminutn Lake	0.400	0.400	0.400	0,400
Subtotal	300	300	300	300
Dry Coat
Hydrocodone Bitartate	4.000	6.000	8.000	12.000
Microcrystalline
Cellulose, Avicel PH 101	0.273	0.409	0.545	0.818
Hydroxypropyl Cellulose,
Klucel EXF	0.273	0.409	0.545	0.818
Purified Water
PEO (Mw=7,000,000)
POLYOX WSR 303 FP	393.455	391.182	388.909	384.364
Magnésium Stéarate	2.000	2.000	2.000	2.000
Subtotal	400	400	400	400
Cosmetic Coat
Opadry Clear 85F19250	14	14	14	14
Opadry Green
85F110049	21
Opadry Yellow
85F120034		21
Opadry Gray 85F175009			21
Opadry Beige 85F170015				21
Opadry Pink 85F140044
Opadry Blue 85F105039
Opadry White 85F18422
Total	735	735	735	735 fw'

-68Table 15 (Tablets Q, R, S)

	Formulation Q (80 mg)	Formulation R (100 mg)	Formulation S (120 mg)
Component	mg/tablet	mg/tablet	mg/tablet
Cote
Hydrocodone Bitartate	64.000	80.000	96.000
Microcrystalline Cellulose,
Avicel PH 101	4.364	5.455	6.545
Hydroxypropyl Cellulose,
Klucel EXF	4.364	5.455	6.545
Purified Water
PEO (Mw=600,000)
POLYOX WSR 205 FP	225.373	207.191	189.009
Magnésium Stéarate	1.500	1.500	1.500
FD&C Yellow No. 6
Aluminum Lake	0.400	0.400	0.400
Subtotal	300	300	300
Dry Coat
Hydrocodone Bitartate	16.000	20.000	24.000
Microcrystalline Cellulose,
Avicel PH 101	1.091	1.364	1.636
Hydroxypropyl Cellulose,
Klucel EXF	1.091	1.364	1.636
Purified Water
PEO (Mw=7,000,000)
POLYOX WSR 303 FP	379.818	375.273	370.727
Magnésium Stéarate	2.000	2.000	2.000
Subtotal	400	400	400
Cosmetic Coat
Opadry Clear 85F19250	14	14	14
Opadry Green 85F110049
Opadry Yellow 85F120034
Opadry Gray 85F175009
Opadry Beige 85F170015
Opadry Pink 85F140044	21
Opadry Blue 85F105039		21
Opadry White 85F18422			21
Total	735	735	735 χαΛ~

-6916458 [00251] A high shear mixer was charged with the hydrocodone bitartrate, the microcrystalline cellulose, and the hydroxypropyl cellulose.

|00252] The dry mix mixture was mixed for one (1) minute at low speed and the chopper off, then mixed at high speed with the chopper on. Water was added to the mixture until the desired amount of water had been added, producing a wet granulation.

[00253| The wet granulation was then passed through a screening mill to de-lump, and transferred to a fluid bed dryer to dry.

[00254] The dry mixture was then passed through a fine mesh screen until the target particle size range was achieved (< 1.0%).

[00255] The dried screened granulation was then passed through a screening mill and the active granulation was collected in stainless steel containers.A V-blender was charged with approximately half of the polyethylene oxide (POLYOX WSR-205); the appropriate amount of active granulation (adjusted for assay); the aluminum lake; and the remaining polyethylene oxide (POLYOX WSR-205), and the mixture was blended for 10 minutes.

[00256] The V-blender was then charged with the magnésium stéarate and the mixture was blended for 2 minutes and discharged into stainless steel drums.

[00257] A V-blender was charged with approximately half of the polyethylene oxide (POLYOX WSR-303); the appropriate amount of active granulation (adjusted for assay); and the remaining polyethylene oxide (POLYOX WSR-303), and the mixture was blended for 10 minutes.

|00258| The V-blender was then charged with the magnésium stéarate; blended for 2 minutes and discharged into stainless steel drums.

-70[00259] The left side of the press was set up with 8.75 mm, round, shallow concave tooling, and the right side of the press with 12 mm, round, shallow concave, bevel edge tooling.

[00260] The core blend (colored) was then charged into the left side hopper (gravity feed systern) to initiate core compression.

[00261 ] The core weight was adjusted to the target weight (300 mg, +/- 5%).

[00262] The dry coat blend (white to off white) was then charged into the right side hopper (gravity feed systern) to initiate tablet compression.

[00263] The initial dry coat fill and subséquent dry coat fill were adjusted after core placement to the target total tablet weight of 700 mg (300 mg core + 400 mg dry coat).

[00264] For the Opadry color dispersion (target 20% solids), a mixing vessel was charged with the appropriate amount of purified water the mixer speed was adjusted to form a vortex. Opadry color powder was added to the vessel over a period of 2 - 5 minutes, and mixed until a homogenous dispersion is produced (minimum 1 hour).

|002651 For the Opadry clear dispersion (target 7.5% solids) a separate mixing vessel was charged with the appropriate amount of purified water and the mixer speed was adjusted to form a vortex. Opadry clear powder was added to the vessel over a period of 2 - 5 minutes (target 3 min), and mixed until a homogenous dispersion is produced (minimum 1 hour).

100266] The compression coated tablets were then transferred to a perforated coating pan and film-coated with the Opadry color dispersion to a target weight gain of 0.7% - 1.5%.

[00267] The heating température was increased and the tablets were cured to a target exhaust température of 72° C for approximately 30 minutes, then cooled. v\Z

-71 16458 [00268] The tablet coating was continuée! with the Opadry color dispersion to a target weight gain of 3% including the weight gain from the previous coating.

[00269| The tablets were then film-coated with the Opadry clear dispersion to a final 5 target weight gain of 5%.

[00270] The dissolution results (% active released over time) for these compression coated 20 mg, 30 mg, 40 mg, 60 mg, 80 mg, 100 mg, and 120 mg tablets are presented in Table 16 below.

Table 16

The Dissolution Results of Compression Coated 20,40, 60, 80,120 mg Tablets (SGF, n=12)

Diss Time (h)	20 mg % active released	40 mg % active released	60 mg % active released	80 mg % active released	120 mg % active released
1	4	4	4	5	4
2	Ί	7	7	7	7
4	13	13	13	13	14
6	21	21	21	21	22
8	31	32	32	31	32
10	42	43	44	43	45
12	53	55	55	55	57
14	62	65	66	65	68
16	71	74	75	74	77
18	79	82	83	83	86
20	87	91	92	91	93
22	95	99	98	98	99
24	99	102	102	101	101

EXAMPLE 21 |00271] A randomized, open-label, single-dose, 5-treatment, 4-period crossover, incomplète block study in healthy adult male and female subjects was conducted with the hydrocodone formulations (HYD) of Examples 14-20. The study was comprised of a maximum of 5 treatments, across 4 periods.

[00272] The HYD tablet strength, or doses studied were:

-7216458 • lx 20 mg HYD tablet • l x 40 mg HYD tablet • lx 60 mgHYD tablet • lx 80 mg HYD tablet • lx 120 mg HYD tablet [00273] The treatments were each administered orally with 8 oz. (240 mL) water as a single dose in the fasted state.

[00274] As this study was conducted in healthy human subjects, the opioid antagonist naltrexone hydrochlorîde was administered to minimize opioîd-related adverse events.

SUBJECT SELECTION

Screening procedures

-Informed consent.

-Informed consent for optional pharmacogenomic sampling.

-Informed consent for optional hair sampling.

-Weight, height, body mass index (BMI), and démographie data.

-Evaluation of inclusion/exclusion criteria.

-Medical and médication history, including concomitant médication.

-Vital signs (systolic/diastolic blood pressure, puise rate, respiration rate, oral température) after being seated for approximately 5 minutes and SpC>2

-HDYF? Inquiry was performed at the same time vital signs were measured.

-Routine physical examination.

>

- 73 16458

-Clinical laboratory évaluations following at least a 4 hour fast (including biochemîstry, hematology, and urinalysis).

-12-lead ECG. QTcF not to exceed 450 msec.

-Screens for alcohol, cotinine, and selected drugs of abuse.

-Sérum pregnancy test (female subjects only).

-Sérum follicle stimulating hormone (FSH) test (postmenopausal females only).

Inclusion criteria

Subjects who met the following criteria were included in the study.

- Provide written informed consent.

- Males and Females aged 18 to 50, inclusive.

- Willing to eat the food supplied during the study.

Body weight ranging from 50 to 100 kg ( 110 to 220 Ibs) and a BMI of 18 to 30 (kg/m2), inclusive.

- Willing to refrain from strenuous exercise through the end of study visit. Subjects will not begin a new exercise program nor participate in any unusually strenuous physical exertion.

- Healthy and free of significant abnormal fmdings as determined by medical history, physical examination, clinical laboratory values, vital signs, and ECG.

- Females of child-bearing potential must be using an adéquate and reliable method of contraception (ie, barrier with additional spermicidal foam or jelly, intra-uterine \_k/~

-74device, hormonal contraception). Females who are postmenopausal must hâve been postmenopausal > l year and hâve elevated sérum FSH.

Exclusion criteria

The following criteria excluded potential subjects from the study.

Females who are prégnant (positive beta human chorionic gonadotropin test) or lactating.

Current or recent (within 5 years) history of drug or alcohol abuse.

History or any current conditions that might interfère with drug absorption, distribution, metabolism or excrétion.

Use of an opioid-containing médication in the past 30 days preceding the initial dose of study drug in this study.

History of known sensitivity to hydrocodone, naltrexone, or related compounds.

Any history of frequent nausea or emesis regardless of etiology.

Any history of seizures or head trauma with sequelae.

Participation in a clinical drug study during the 30 days preceding the initial dose of study drug in this study.

Any significant illness during the 30 days preceding the initial dose of study drug in this study.

Use of any médication including thyroid hormonal therapy (hormonal contraception and hormonal replacement therapy in the form of estrogen with or

-75without progestin is allowed), vitamins, herbal and/or minerai suppléments during the 7 days preceding the initial dose of study drug.

Any personal or family history of prolonged QT interval or disorders of cardiac rhythm.

Abnormal cardiac conditions including any of the following:

• QTc interval > 450 msec (calculated using Fridericia’s correction) at screening • QTc interval > 480 msec (calculated using Fridericia’s correction) during the treatment period.

-Refusai to abstain from food 10 hours preceding and 4 hours following study drug administration and to abstain from caffeine or xanthine containing beverages entirely during each confinement.

-Refusai to abstain from consumption of alcoholic beverages 48 hours prior to initial study drug administration (day l) and any time through the end of study visit.

-Blood or blood products donated within 30 days prior to initial study drug administration or anytime through the end of study visit, except as required by this protocol.

-History of smoking or use of nicotine products within 45 days of initial study drug administration or a positive urine cotinine test.

-Positive results of urine drug screen or alcohol screen.

-Positive results of HBsAg, anti-HCV.

-Positive naloxone HCl challenge test.

-Presence of Gilbert’s Syndrome, or any known hepatobiliary abnormalities.

-7616458

[00275| Subjects meeting ail the inclusion criteria and none of the exclusion criteria were randomized into the study.

[00276] Each subject was assigned a unique subject number at screening. Assignment of subject numbers was in ascending order and no numbers were omitted. Subject numbers were used on ail study documentation.

CHECK-IN PROCEDURES [00277) On Day -l of Period l only, subjects were admitted to the study unit and received a Naloxone HCl challenge test. The results of the test had to be négative for subjects to continue in the study. Vital signs and SPO2 were measured prior to and following the Naloxone HCl.

[00278] The following procedures were also performed for ail subjects at Check-in for each period:

-Vital signs (after being seated for approximately 5 minutes) and SpO2.

-Clinical laboratory évaluations (day -l, period l only) includingbiochemistry (fasting for at least 4 hours), hematology and urinalysis) were collected after vital signs and SpC>2 were measured.

-Urine pregnancy test (for ail female subjects). +/ »

-77-Concomitant médication monitoring and recording.

-AE monitoring and recording.

[00279] For subjects to continue their participation in the study, the results of the drug screen (including alcohol and cotinine) had to be available and négative prior to dosing. In addition, continued compliance with concomitant médication and other restrictions were verified at Check-in and throughout the study in the appropriate source documentation.

TREATMENT PERIOD PROCEDURES

-Subjects were administered the study drug with 240 mL of water as following a I0-hour overnight fast. Subjects continued fasting from food for 4 hours following dosing.

• Fasting was not required for nondosing study days.

-For subjects receiving hydrocodone doses of 60 mg or more, SpO₂ was monitored continuously beginning prior to dosing and continuing through 24 hours post-dose.

-78-Vital signs (after being seated for approximately 5 minutes) and SpCh, were obtained pre-dose and at hour l, 2.5, 4, 6, 8, 12, 24, 36, 48, and 72 hour post dose for each period.

- 12-lead ECGs were performed for each subject pre-dose and approximately 12, 24 and 48 hours post-dose.

-Blood samples for determining hydrocodone plasma concentrations were obtained for each subject at pre-dose and at 0.5, l, 2.5, 4, 6, 8, 10, 12, 14, 16, 18, 24, 36, 48, and 72 hours post-dose for each period.

-Subjects were confined to the unit from check-in to the unit on the day before dosing until the time that their 72 h procedures were completed.

-During the study, AEs and concomitant médications were recorded.

[00280] In addition, the subjects were informed that it is very important to report any/all épisodes of emesis to the study staff immediately and that this information is crucial to the proper conduct and outcome of the trial. The subjects were informed that they would not be penalized in any way due to reporting cases of emesis. The study staff was instructed to carefully document any/all cases of emesis.

STUDY COMPLETION PROCEDURES [002811 The following procedures were performed at the study site for ail subjects at endof-study (study completion), 7 to 10 days after receiving their last dose of study drug or upon early discontinuation from the study.

-Concomitant médication évaluation.

-Vital signs (after being seated for approximately 5 minutes) and SpOî.

-HDYF? Inquiry was performed at the same time vital signs are measured.

-Physical examination.

-12-Lead ECG.

-Ί916458

-AE évaluations.

-Sérum pregnancy test (for female subjects only).

[00282] The draft results are set forth in Figure 7 and Table 17 below:

Table 17 Summary of Draft Plasma Hydrocodone Pharmacokinetlc Parameters

Parameter	HYD 20 mg (N=29)	HYD 40 mg (N=30)	HYD 60 mg (N=28)	HYD 80 mg (N=30)	HYD 120 mg (N-29)
(Unit)	Statistic
AUCt	MEAN	281	618	1004	1298	1759
(ng*h/mL)	SD	127	255	292	373	671
	MIN	30	85	580	559	303
	MAX	591	1200	1724	2501	3324
AUCinf	Mean	284	622	1009	1304	1768
(ng*h/mL)	SD	128	256	294	375	674
	Min	31	86	583	564	305
	Max	595	1213	1742	2514	3347
Cmax	Mean	15	34	54	69	110
(ng/mL)	SD	5.5	12	15	17	44
	Min	3.5	7.6	33	40	28
	Max	26	54	83	109	199
Tmax (h)	Mean	15	16	16	15	15
	SD	4.5	4.5	4.7	2.6	4.4
	Min	6	6	10	10	6
	Médian	16	16	14	16	14
	Max	24	24	30	24	30

|00283| The présent invention is not to be limited in scope by the spécifie embodiments disclosed in the examples which are intended as illustrations of a few aspects of the 10 invention and any embodiments that are functionally équivalent are within the scope of this invention. Indeed, various modifications of the invention in addition to those shown and described herein will become apparent to those skilled in the art and are intended to fall within the scope of the appended claims. άΑ

-8016458 [00284] This application claims priority from U.S. Provîsional Application Serial No.

61/426,306, filed December 22, 2010, the disclosure of which is hereby incorporated by reference.

Sari

53

- 81 CLAIMS

Claims

1. A solid controlled release dosage form comprising:

a core comprising a first portion of an opioid analgésie dispersed in a first matrix material; and a shell encasing the core and comprising a second portion of the opioid analgésie dispersed in a second matrix material;

wherein the amount of opioid analgésie released from the dosage form is proportional within 20% to elapsed time from 8 to 24 hours, as measured by an in-vitro dissolution in a USP Apparatus l (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37°C.

2. The solid controlled release dosage form of claim l, wherein the core is a compressed tablet and/or wherein the shell is a compression coating.

3. The solid controlled release dosage form of claim l or 2, wherein the first matrix material comprises polyethylene oxide, preferably wherein the first matrix material comprises polyethylene oxide having an average molecular weight from about 300,000 to about 10,000,000, more preferably from about 500,000 to about 1,000,000.

4. The solid controlled release dosage form of claim 1 or 2, wherein the second matrix material comprises polyethylene oxide, preferably wherein the second matrix material comprises polyethylene oxide having an average molecular weight from about 1,000,000 to about 10,000,000, more preferably from about 6,000,000 to about 8,000,000.

5. The solid controlled release dosage form of claim 1 or 2, wherein both the first matrix material and the second matrix material comprise polyethylene oxide, preferably wherein the polyethylene oxide in the second matrix material has a higher viscosity than the polyethylene oxide in the first matrix material.

6. The solid controlled release dosage form of claim 5, wherein the polyethylene oxide in the second matrix material has an average molecular weight from about 4,000,000 to about 10,000,000 and the polyethylene oxide in the first matrix material has an average molecular weight from about 300,000 to about 3,000,000, or wherein the polyethylene oxide in the second matrix material has an average molecular weight from about 6,000,000 to about 8,000,000 and the polyethylene oxide in the first matrix material has an average molecular weight from about 500,000 to about l ,000,000.

7. The solid controlled release dosage form of any one of claims l to 6, wherein the weight ratio of the core to the shell is from about l :0.5 to about l :5, preferably from about l :0.6 to about l : l .5, more preferably from about l :0.8 to about l : l .2.

8. The solid controlled release dosage form of claim 3, wherein the weight ratio of the first portion of opioid analgésie to polyethylene oxide in the first matrix material is from about 1:0.5 to about 1:100, preferably from about 1:1 to about 1:10, more preferably from about 1:1.5 to about 1:4.

9. The solid controlled release dosage form of claim 4, wherein the weight ratio of the second portion of opioid analgésie to polyethylene oxide in the second matrix material is from about 1:2 to about 1:200, preferably from about 1:5 to about 1:50, more preferably from about 1:12 to about 1:25.

10. The solid controlled release dosage form of any one of claims 1 to 9, wherein the opioid analgésie in the first portion is the same as the opioid analgésie in the second portion, or wherein the opioid analgésie in the first portion is different than the opioid analgésie in the second portion.

11. The solid controlled release dosage form of any one of claims 1 to 10, wherein the ratio of opioid analgésie in the core to the ratio of opioid analgésie in the shell is from about 1:1 to about 10:1, preferably from about 2:1 to about 8:1, or preferably from about 2:1 to about 5:1.

12. The solid controlled release dosage form of any one of claims 1 to 11, wherein the opioid analgésie is selected from the group consisting of alfentanil, aliylprodine,

-83 16458 alphaprodine, anileridine, benzylmorphine, bczitramide, buprénorphine, butorphanol, clonitazene, codeine, desomorphine, dextromoramide, dezocine, diampromide, diamorphone, dihydrocodéine, dihydromorphine, dimenoxadol, dimepheptanol, dimethylthiambutene, dioxaphetyl butyrate, dipipanone, eptazocine, ethoheptazine,

5 ethylmethylthiambutene, ethylmorphine, etonitazene, etorphine, dihydroetorphine, fentanyl and dérivatives, hydrocodone, hydromorphone, hydroxypethidine, isomethadone, ketobemidone, levorphanol, levophenacylmorphan, lofentanil, meperidine, meptazinol, metazocine, methadone, metopon, morphine, myrophine, narceine, nicomorphine, norlevorphanol, normethadone, nalorphine, nalbuphene, normorphine, norpipanone, 10 opium, oxycodone, oxymorphone, papaveretum, pentazocine, phenadoxone, phenomorphan, phenazocine, phenoperidine, piminodine, piritramide, propheptazine, promedol, properidine, propoxyphene, sufentanil, tilidine, tramadol, pharmaceutically acceptable salts thereof, hydrates thereof, solvatés thereof, and mixtures thereof, preferably

15 wherein the opioid analgésie is selected from the group consisting of codeine, hydrocodone, hydromorphone, morphine, oxycodone, oxymorphone, tramadol, pharmaceutically acceptable salts thereof, hydrates thereof, solvatés thereof, and mixtures thereof.

20

13. The solid controlled release dosage form of claim 12, wherein the opioid analgésie is selected from the group consisting of hydrocodone, pharmaceutically acceptable salts thereof, hydrates thereof, solvatés thereof, and mixtures thereof.

14. The solid controlled release dosage form of claim 13, wherein the opioid analgésie 25 is hydrocodone bitartrate, wherein preferably the total amount of hydrocodone bitartrate in the dosage form is from about 0.5 mg to about 1250 mg, or from about 2 mg to about 200 mg, or from about 16 mg to about 120 mg.

15. The solid controlled release dosage form of any one of claims l to 14, wherein the 30 amount of opioid analgésie released is proportional within 10%, preferably within 5% to elapsed time from 8 to 24 hours and/or

-8416458 wherein the amount of opioid analgésie released is proportional within 20%, preferably within 10% or within 5% to elapsed time from 8 to 18 hours and/or wherein the amount of opioid analgésie released is proportional within 20%, preferably within 10% or within 5% to elapsed time from 8 to 12 hours and/or wherein the amount of opioid analgésie released is proportional within 20%, preferably within 10% or within 5% to elapsed time from 12 to 24 hours and/or wherein the amount of opioid analgésie released is proportional within 20%, preferably within 10%, or within 5% to elapsed time from 12 to 18 hours.

16. The solid controlled release dosage form of any one of claims 1 to 15, wherein the amount of opioid analgésie released at 2 hours is less than about 25%, or less than about 20%, or less than about 15%, and/or wherein the amount of opioid analgésie released at 4 hours is from about 10% to about 30%, or from about 10% to about 20%, or from about 20% to about 30%, and/or wherein the amount of opioid analgésie released at 8 hours is from about 20% to about

60%, or from about 20% to about 40%, or from about 45% to about 60%, and/or wherein the amount of opioid analgésie released at 12 hours is from about 40% to about 90%, or from about 40% to about 65%, or from about 70% to about 90%, and/or wherein the amount of opioid analgésie released at 18 hours is greater than about 70%, or greater than about 80%, or greater than about 90%.

17. The solid controlled release dosage form of claim 5, wherein the dosage form is cured at a température of at least the softening point of the polyethylene oxide for at least 1 minute, at least 5 minutes, or at least 15 minutes, or wherein the dosage form is cured at a température of at least the softening point of the polyethylene oxide from about 1 minute to about 48 hours, or from about 5 minutes to about 24 hours, or from about 15 minutes to about 1 hour.

18. The solid controlled release dosage form of claim 17, wherein the dosage form is cured at a température of at least about 60°C, at least about 65°C, at least about 70°C, at least about 75°C, or at a température of about 72°C. ά/’’

-8516458

19. The solid controlled release dosage form of any one of claims l to 18, wherein the core and the shell are visually indistinguishable, or wherein the core and the shell hâve a CIE L*A*B* value within 10% of each other.

20. The solid controlled release dosage form of any one of claims l to 19, wherein the dosage form can be flattened without breaking, wherein the thickness of the dosage form after flattening corresponds to no more than about 60% of the thickness of the dosage form before flattening, preferably the thickness of the dosage form after flattening corresponds to no more than about 50%, or to no more than about 40%, or to no more than about 30%, or to no more than about 20% of the thickness of the dosage form before flattening.

21. The solid controlled release dosage form of claim 20, wherein the amount of opioid analgésie released at 0.5 hour from a flattened dosage form deviates no more than about 20% points, or no more than about 15% points, or no more than about 10% points from a non-flattened dosage form as measured by an in-vitro dissolution in a USP Apparatus l (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37°C.

22. The solid controlled release dosage form of claim 13, that provides a C24/C_niax ratio of hydrocodone of about 0.55 to about l .0 after administration, preferably the C24/C_inaxratio is about 0.55 to about 0.85, or about 0.55 to about 0.75, or about 0.60 to about 0.70, and/or that provides a T_)nax (h) of hydrocodone from about 4 to about 20 hours after administration, preferably the T_max (h) is about 6 to about 12 hours, or about 8 to about 10 hours, or about 4 to about 10 hours, or about 8 to about 14 hours, or about 14 to about 20 hours after administration of the dosage form.

23. The solid controlled release dosage form of claim 22, wherein the administration is a first administration to a healthy subject or to a population of healthy subjects, or wherein the administration is steady state administration to a healthy subject or to a population of healthy subjects.

24. The solid controlled release dosage form of claim I3, that contains about 20 mg hydrocodone or a pharmaceutically acceptable sait thereof, and that preferably provides a mean AUC (ng*h/mL) after administration of about 250 to about 400, about 275 to about 350, about 300 to 330 or about 280 to about 320, and/or a mean C_max (ng/mL) after administration of about 10 to about 30, about 12 to about 25, about 14 to about 18 or about 12 to about 17.

25. The solid controlled release dosage form of claim 13, that contains about 120 mg hydrocodone or a pharmaceutically acceptable sait thereof, and that preferably provides a mean AUC (ng*h/mL) after administration of about 1500 to about 2400, about 1700 to about 2200, about 1800 to about 2100 or about 1900 to about 2100, and/or a mean C_inax(ng/mL) after administration of about 60 to about 180, about 100 to about 160, about 110 to about 150 or about 100 to about 140.

26. The solid controlled release dosage form of claim 13, that provides a mean AUC (ng*h/mL) after administration of about 250 to 400 per each 20 mg hydrocodone included in the dosage form, and/or that provides a mean C_max (ng/mL) after administration of about 10 to about 30 per each 20 mg hydrocodone included in the dosage form.

27. The solid controlled release dosage form of claim 13, that provides a mean T_max (h) after administration of about 10 to about 20, about 12 to about 18, about 13 to about 17 or about 14 to about 16, and/or that provides a mean Tj/2 (h) after administration of about 5 to about 10, about 6 to about 9, about 7 or about 8, and/or that provides a mean T]_ag (h) after administration of about 0,01 to about 0.2, about 0.1 to about 0.18, about 0.3 to about 0.17 or about 0.06 t about 0.15, and/or wherein the mean C2₄/C_mOx ratio is about 0.2 to about 0.8, about 0.3 to about 0.7 or about 0.4 to about 0.6.

28. The solid controlled release dosage form of claim 26 or 27, wherein the administration is in the fasted state.

29. The solid controlled release dosage form of claim 13, wherein the mean AUC (ng*h/mL) after administration in the fed state is less than 20% higher, less than 16%

-8716458 higher or less than 12% higher than the AUC (ng*h/mL) after administration in the fasted state, and/or wherein the mean C_max (ng/mL) after administration in the fed state is less than 80% higher, less than 70% higher or less than 60% higher than the Cma» after administration in the fasted state.

30. The solid controlled release dosage form of claim 13, wherein the mean T_max (h) after administration in the fed state is within 25%, within 20% or within 15% of the T_max(h) after administration in the fasted state, and/or wherein the mean T^ (h) after administration in the fed state is within 8%, within 5% or within 2% of the Ti/2 after administration in the fasted state, and/or wherein the mean Ti_ag (h) after administration in the fed state is less than 150% higher, less than 125% higher or less than 100% higher than the Ti/2 after administration in the fasted state.

31. A solid controlled release dosage form comprising:

a core comprising a first portion of an opioid analgésie dispersed in a first matrix material comprising polyethylene oxide; and a shell encasing the core and comprising a second portion of the opioid analgésie dispersed in a second matrix material comprising polyethylene oxide.

32. A solid controlled release dosage form comprising:

a compressed core comprising a first portion of an opioid analgésie dispersed in a first matrix material comprising polyethylene oxide; and a compression coating encasing the core and comprising a second portion of the opioid analgésie dispersed in a second matrix material comprising polyethylene oxide.

33. A solid controlled release dosage form comprising:

wherein the amount of opioid analgésie released from the dosage form at 2 hours is less than about 25%;

-8816458 the amount of opioid analgésie released from the dosage form at 4 hours is from about 10% to about 30%;

the amount of opioid analgésie released from the dosage form at 8 hours is from about 20% to about 60%;

the amount of opioid analgésie released from the dosage form at 12 hours is from about 40% to about 90%; and the amount of opioid analgésie released from the dosage form at 18 hours is greater than about 70%;

as measured by an in-vitro dissolution in a USP Apparatus l (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37°C.

34. A solid controlled release dosage form comprising:

a therapeutically effective amount of hydrocodone or a pharmaceutically acceptable sait thereof, and a controlled release excipient;

wherein the amount of hydrocodone or sait thereof released from the dosage form is proportional within 20% to elapsed time from 8 to 24 hours, as measured by an in-vitro dissolution in a USP Apparatus l (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37°C; and the dosage form can be flattened without breaking, wherein the thickness of the dosage form after flattening corresponds to no more than about 20% of the thickness of the dosage form before flattening; and the amount of hydrocodone or sait thereof released at 0.5 hour from a flattened dosage form deviates no more than about 20% points from a non-flattened dosage form as measured by an in-vitro dissolution in a USP Apparatus l (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37°C.

35. A solid controlled release dosage form comprising:

wherein the amount of hydrocodone or sait thereof released from the dosage form at 2 hours is less than about 25%;

-8916458 the amount of hydrocodone or sait thereof released from the dosage form at 4 hours îs from about 10% to about 30%;

the amount of hydrocodone or sait thereof released from the dosage form at 8 hours is from about 20% to about 60%;

the amount of hydrocodone or sait thereof released from the dosage form at 12 hours is from about 40% to about 90%; and the amount of hydrocodone or sait thereof released from the dosage form at 18 hours is greater than about 70%;

as measured by an in-vitro dissolution in a USP Apparatus l (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37°C; and the dosage form can be flattened without breaking, wherein the thickness of the dosage form after fiattening corresponds to no more than about 20% of the thickness of the dosage form before fiattening; and the amount of hydrocodone or sait thereof released at 0.5 hour from a flattened dosage form deviates no more than about 20% points from a non-flattened dosage form as measured by an in-vitro dissolution in a USP Apparatus l (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37°C.

36. A solid controlled release dosage form comprising:

a therapeutically effective amount of hydrocodone or a pharmaceutically acceptable sait thereof dispersed in a controlled release excipient; wherein the inner 60% of the dosage form contains at least 80% of the hydrocodone or sait thereof;

wherein the amount of hydrocodone or sait thereof released from the dosage form is proportional within 20% to elapsed time from 8 to 24 hours, as measured by an in-vitro dissolution in a USP Apparatus l (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37°C.

37. The solid controlled release dosage form of claim 36, wherein the inner 50% of the dosage form contains at least 80% of the hydrocodone or sait thereof.

38. Use of a solid controlled release dosage form according to any of claims l-37 in the manufacture of a médicament for treating pain in a subject in need thereof. γχχ'

-9016458

39. A method of preparing a solid controlled release dosage form comprising:

preparing a core comprising a first portion of an opioid analgésie dispersed in a first matrix material; and encasing the core with a shell comprising a second portion of the opioid analgésie dispersed in a second matrix material;

wherein the amount of opioid analgésie released from the dosage form is proportîonal within 20% to elapsed time from 8 to 24 hours, as measured by an in-vitro dissolution in a USP Apparatus l (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37°C.

40. A method of preparing a solid controlled release dosage form comprising:

preparing a core comprising a first portion of an opioid analgésie dispersed in a first matrix material comprising polyethylene oxide; and encasing the core in a shell comprising a second portion of the opioid analgésie dispersed in a second matrix material comprising polyethylene oxide.

41. A method of preparing a solid controlled release dosage form comprising:

preparing a compressed core comprising a first portion of an opioid analgésie dispersed in a first matrix material comprising polyethylene oxide; and encasing the core by compression coating a second portion of the opioid analgésie dispersed in a second matrix material comprising polyethylene oxide over the core.

42. A method of preparing a solid controlled release dosage fonn comprising:

preparing a core comprising a first portion of an opioid analgésie dispersed in a first matrix material; and encasing the core in a shell comprising a second portion of the opioid analgésie dispersed in a second matrix material over the core;

the amount of opioid analgésie released from the dosage form at 4 hours is from about 10% to about 30%;

-91 16458 the amount of opioid analgésie released from the dosage form at 8 hours is from about 20% to about 60%;

the amount of opioid analgésie released from the dosage form at 12 hours is from about 40% to about 90%; and the amount of opioid analgésie released from the dosage form at 18 hours is greater than about 70%.

43. A method of preparing a solid controlled release dosage form comprising:

combining a therapeutically effective amount of hydrocodone or a pharmaceutically acceptable sait thereof, and a controlled release excipient;

wherein the amount of hydrocodone or sait thereof released from the dosage form is proportional within 20% to elapsed time, at any two time points from 8 to 24 hours, as measured by an in-vitro dissolution in a USP Apparatus l (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37°C; and the dosage form can be flattened without breaking, wherein the thickness of the dosage form after flattening corresponds to no more than about 20% of the thickness of the dosage form before flattening; and the amount of hydrocodone or sait thereof released at 0.5 hour from a flattened dosage form deviates no more than about 20% points from a non-flattened dosage form as measured by an in-vitro dissolution in a USP Apparatus l (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37°C.

44. A method of preparing a solid controlled release dosage form comprising:

the amount of hydrocodone or sait thereof released from the dosage form at 4 hours is from about 10% to about 30%;

-9216458 the amount of hydrocodone or sait thereof released from the dosage form at 8 hours is from about 20% to about 60%;

as measured by an in-vitro dissolution in a USP Apparatus l (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37° C; and the dosage form can be flattened without breaking, wherein the thickness of the dosage form after flattening corresponds to no more than about 20% of the thickness of the dosage form before flattening; and the amount of hydrocodone or sait thereof released at 0.5 hour from a flattened dosage form deviates no more than about 20% points from a non-flattened dosage form as measured by an in-vitro dissolution in a USP Apparatus l (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37°C.

45. A method of preparing a solid controlled release dosage form comprising:

dispersing a therapeutically effective amount of hydrocodone or a pharmaceutically acceptable sait thereof in a controlled release excipient; wherein the inner 60% of the dosage form contains at least 80% of the hydrocodone or sait thereof;

wherein the amount of hydrocodone or sait thereof released from the dosage form is proportional within 20% to elapsed time from 8 to 24 hours, as measured by an in-vitro dissolution in a USP Apparatus l (basket) at 100 rpm in 900 ml simulated gastric fluid without enzymes (SGF) at 37°C. 4 7 JUIN