AU2001284236A1

AU2001284236A1 - Pharmaceutical formulation of salmeterol and fluticasone propionate

Info

Publication number: AU2001284236A1
Application number: AU2001284236A
Authority: AU
Inventors: Donald Herbert Horstman; Claire Julia Maden
Original assignee: Glaxo Group Ltd
Current assignee: Glaxo Group Ltd
Priority date: 2000-08-31
Filing date: 2001-08-31
Publication date: 2002-03-13
Also published as: BG107596A; WO2002017894A2; NO20030899D0; US20040009963A1; NO20030899L; ZA200301475B; KR20030031997A; EP1313484A2; OA12370A; IL154403A0; MA25834A1; HUP0303755A2; MXPA03001752A; CA2420532A1; JP2004507494A; AR030516A1; WO2002017894A3; SK2302003A3; BR0113555A; PE20020387A1

Description

Use of saimeterol and fluticasone propionate combination

The present invention relates to the use of saimeterol and fluticasone propionate combinations for the treatment of chronic obstructive pulmonary disease.

The combination of the beta-2 adrenergic agonist saimeterol or a physiologically acceptable salt thereof and the corticosteroid fluticasone propionate has been described in GB 2 235 627 for use in the treatment of asthma and other respiratory disorders.

Fluticasone propionate is itself known from GB 2 088 877 to have anti- inflammatory activity and to be useful for the treatment of allergic and inflammatory conditions of the nose, throat, or lungs such as asthma and rhinitis, including hay fever. However, the clinical utility of inhaled corticosteroids in the treatment of chronic obstructive pulmonary disease is uncertain as discussed,, for example, in the editorials by Calverley and Barnes, American Journal of Respiratory and Critical Care Medicine, vol 161 , pp341- 344, 2000.

Saimeterol is known from GB 2 140 800 and is used clinically in the form of its xinafoate salt for the treatment of asthma and chronic obstructive pulmonary disease.

Chronic obstructive pulmonary disease (COPD) is a general term encompassing chronic bronchitis, emphysema, and chronic obstructive airways disease. COPD is a chronic slowly progressive disorder characterised by airways obstruction which does not change markedly over several months. Unlike asthma, airflow limitation in COPD as measured by FEV₁ (forced expiratory volume) can never be returned to normal values. Symptoms of COPD, which vary with the severity of the disease, include coughing with or without sputum, and breath lessness (dyspnea) with or without wheezing. In the UK during the period 1990 to 1992 there were 81,500 deaths attributable to COPD in people aged over 65. There still exists the need for further therapeutic agents which could be used in the clinical management of COPD.

In a more particular aspect, the present invention relates to treatment and alleviation of the symptoms associated with COPD, particularly of breathlessness, to improvement in health status and to a reduction in exacerbation rate including those requiring treatment with oral corticosteroids.

We now propose that the use of a combination of saimeterol or a physiologically acceptable salt thereof and fluticasone propionate may have clinical advantages in the treatment of COPD over the use of saimeterol alone.

Accordingly, the present invention provides a method for treatment of COPD in a mammal, such as a human, which comprises administering an effective amount of a combination of saimeterol or a physiologically acceptable salt thereof, such as the xinafoate salt, and fluticasone propionate.

In the alternative, there is provided the use of a combination of saimeterol or a physiologically acceptable salt thereof, such as the xinafoate salt, and fluticasone propionate for the manufacture of a medicament for treatment of COPD.

As used herein, the term "treatment" means the improvement of clinical outcome, for example, improvement of lung function and/or alleviation of symptoms such as breathlessness (dyspnea) with or without wheezing, and/or improvement in health status, and/or a reduction in exacerbation rate including those requiring treatment with oral corticosteroids. Health status may be measured using the St. George's Respiratory Questionnaire (Jones PW, Quirk FH, Baveystock CM, and Littlejohns P., A self-complete measure of health status for chronic airflow limitation. The St George's Respiratory Questionnaire, Am. Rev. Respir. Dis. , vol. 145, pp 1321-7, 1992).

Throughout the specification and the claims which follow, unless the context requires otherwise, the word 'comprise', and variations such as 'comprises' and 'comprising', will be understood to imply the inclusion of a stated integer or step or group of integers but not to the exclusion of any other integer or step or group of integers or steps.

It will be appreciated that the compounds of the saimeterol and fluticasone propionate combination may be administered simultaneously, either in the same or different pharmaceutical formulations, or sequentially. Where there is sequential administration, the delay in administering the second and any subsequent active ingredient should not be such as to lose the beneficial therapeutic effect of the combination of the active ingredients. In a preferred aspect of the invention, the saimeterol or its physiologically acceptable salt and the fluticasone propionate are administered as a combined pharmaceutical formulation. The weight/weight ratio of saimeterol to fluticasone administered according to the invention is preferably in the range 4:1 to 1:20.

The amount of saimeterol or a physiologically acceptable salt thereof, such as the xinafoate salt, and fluticasone propionate which is required to achieve a therapeutic effect will, of course, vary with the particular salt form, the route of administration, the subject under treatment, and the particular disorder or disease being treated. The combination of the invention may be administered by inhalation to an adult human at a dose of from 50μg to 2000μg per day, suitably 100μg to 1500μg per day, more suitably 500μg to 1000μg per day of fluticasone propionate and 50μg to 200μg per day, suitably 50μg to 100μg per day of saimeterol. Preferred combinations include 250μg or 500μg of fluticasone propionate and 50μg of saimeterol. The daily dose may be administered as several sub-doses, for example, twice daily.

While it is possible for saimeterol or a physiologically acceptable salt thereof, such as the xinafoate salt, and fluticasone propionate to be administered as raw drugs, it is preferable to present each of them as a pharmaceutical formulation.

Hereinafter, the term "active ingredient" means saimeterol or a physiologically acceptable salt thereof, such as the xinafoate salt, and/or fluticasone propionate.

Suitable formulations include those suitable for oral, parenteral (including subcutaneous, intradermal, intramuscular, intravenous and intraarticular), inhalation (including fine particle dusts or mists which may be generated by means of various types of metered dose pressurised aerosols, nebulisers or insufflators), rectal and topical (including dermal, buccal, sublingual and intraocular) administration although the most suitable route may depend upon for example the condition and disorder of the recipient. The formulations may conveniently be presented in unit dosage form and may be prepared by any of the methods well known in the art of pharmacy. All methods include the step of bringing the active ingredient into association with the carrier which constitutes one or more accessory ingredients. In general the formulations are prepared by uniformly and intimately bringing into association the active ingredient with liquid carriers or finely divided solid carriers or both and then, if necessary, shaping the product into the desired formulation. Preferably, the pharmaceutical formulations used in accordance with the present invention are suitable for administration by inhalation. Inhalation formulations may be in the form of powder compositions which will preferably contain lactose, or spray compositions which may be formulated, for example, as aqueous solutions or suspensions or as aerosols delivered from pressurised packs, with the use of a suitable propellant, e.g. dichlorodifluoromethane, trichlorofluoromethane, dichlorotetrafluoroethane, 1 ,1 ,1 ,2,3,3,3-heptafluoro- propane, 1 ,1 ,1 ,2-tetrafluoroethane, carbon dioxide or other suitable gas. Suitable aerosol spray compositions for use in accordance with the invention are described in WO 93/11743.

A preferred formulation is a powder composition comprising saimeterol or a physiologically acceptable salt thereof, such as the xinafoate salt, fluticasone propionate and lactose.

Another preferred formulation is an aerosol formulation consisting of saimeterol or a physiologically acceptable salt thereof, such as the xinafoate salt, fluticasone propionate, and 1 ,1 ,1 ,2,3,3,3-heptafluoropropane and/or 1 ,1 ,1 ,2- tetrafluoroethane as propellant.

Capsules and cartridges of for example gelatin, or blisters of for example laminated aluminium foil, for use in an inhaler or insuflator may be formulated containing a powder mix of a compound of the invention and a suitable powder base such as lactose or starch.

Solutions for inhalation by nebulation may be formulated with an aqueous vehicle with the addition of agents such as acid or alkali, buffer salts, isotonicity adjusting agents or antimicrobials. They may be sterilised by filtration or heating in an autoclave, or presented as a non-sterile product. It should be understood that in addition to the ingredients particularly mentioned above, the formulations used according to the invention may include other agents conventional in the art having regard to the type of formulation in question, for example those suitable for oral administration may include flavouring agents. Furthermore, the combination of saimeterol or a physiologically acceptable salt thereof, such as the xinafoate salt, and fluticasone propionate used according to the present invention may be used in combination with a further active ingredient, for example another bronchodilator suitably an anticholinergic such as ipratropium, tiotropium, or oxitropium, or a methylxanthine such as theophylline, another anti-inflammatory drug such as sodium cromoglycate or nedocromil sodium, an antihistamine or mucolytic.

Thus according to a further aspect of the invention, there is provided a pharmaceutical formulation for the treatment of COPD comprising saimeterol or a physiologically acceptable salt thereof, such as the xinafoate salt, and fluticasone propionate, and a pharmaceutically acceptable carrier or excipient, and optionally one or more other therapeutic agents. Preferably, the pharmaceutical formulation is in a form which is suitable for inhalation.

EXAMPLES

A randomised, double-blind, parallel group 6 month clinical trial was conducted to compare the effects of an inhaled saimeterol and fluticasone propionate combination product, inhaled saimeterol, inhaled fluticasone propionate, and placebo in COPD patients. Each group of patients was treated with either salmeterol/fluticasone propionate 50μg/500μg (165 patients), saimeterol 50μg (160 patients), fluticasone propionate 500μg (168 patients), or placebo (181 patients), all administered twice daily by a dry-powder inhaler (DISKUS™, Glaxo Wellcome). Saimeterol, both as part of the combination product and as a monotherapy, was administered as its xinafoate salt. 71% of the patients included in the study met the poorly reversible criteria for COPD, i.e. ΔFENΛ, less than 10% predicted following inhalation of 400μg salbutamol (a short-acting beta-2 agonist). The differences between the predose FEV₁ on the first day of treatment and predose FE^ at subsequent treatment visits was measured, the results of which are shown in Figure 1. Post-dose FEN/^ and PEFR were measured similarly giving the results shown in Figures 2 and 3 respectively. The Transitional Dyspnea Score (TDI) (see Mahler DA, Weinberg DH, Wells CK, and Feinstein AR; Chest, (1984) 85:751-8) was also measured at each visit and the results are shown in Figure 4.

In a further placebo-controlled clinical trial of 12 months treatment duration in patients with COPD, regular use of an inhaled saimeterol xinafoate and fluticasone propionate combination product rapidly improved lung function, reduced breathlessness and reduced the use of relief medication. Figure 5 shows the mean improvement in pre-dose FEV., over time for all the patients enrolled in the trial (the intent-to-treat population). Figure 6 shows the mean % days when no relief medication (Ventolin™ (salbutamol), Glaxo Wellcome) was required. In addition the risk of COPD exacerbation and the need for additional courses of oral corticosteroids was significantly reduced, as shown in Figure 7. There were also significant improvements in health status, as measured using the St. George's Respiratory Questionnaire (Jones PW, Quirk FH, Baveystock CM, and Littlejohns P., A self-complete measure of health status for chronic airflow limitation. The St George's Respiratory Questionnaire, Am. Rev. Respir. Dis. , vol. 145, pp 1321-7, 1992), and shown in Figure 8.

In Figures 1 to 8, the abbreviations used are as follows: Sal50: patients receiving saimeterol 50μg FP500: patients receiving fluticasone propionate 500μg

SFC50/500: patients receiving salmeterol/fluticasone propionate 50μg/500μg.

FEV.,: forced expiratory volume in one second

PEFR: peak expiratory flow rate EP: end point

PLA: placebo

OCS: oral corticosteroid

B/L: baseline (prior to commencement of trial)

SGQR: St George's Respiratory Questionnaire wks: weeks into trial

Claims

1. A method for treatment of COPD in a mammal, such as a human, which comprises administering an effective amount of a combination of saimeterol or a physiologically acceptable salt thereof and fluticasone propionate.

2. A method according to claim 1 wherein the saimeterol or physiologically acceptable salt thereof and fluticasone propionate are administered as a combined pharmaceutical formulation.

3. A method according to claim 1 or 2 in which the saimeterol or physiologically acceptable salt thereof and fluticasone propionate are administered by inhalation.

/ 4. A method according to any one of claims 1 to 3 in which the saimeterol is administered as the xinafoate salt.

5. Use of a combination of saimeterol or a physiologically acceptable salt thereof and fluticasone propionate for the manufacture of a medicament for the treatment of COPD.

6. Use according to claim 5 wherein the medicament is a combined pharmaceutical formulation.

7. Use according to claim 5 or 6 in which the medicament is suitable for inhalation therapy.

8. Use according to any one of claims 5 to 7 in which the saimeterol is in the form of the xinafoate salt.

9. A pharmaceutical formulation for the treatment of COPD comprising saimeterol or a physiologically acceptable salt thereof and fluticasone propionate, and a pharmaceutically acceptable carrier or excipient and optionally one or more other therapeutic agents.

10. A pharmaceutical formulation according to claim 9 which is in a form suitable for inhalation.

11. A pharmaceutical formulation according to either claim 9 or 10 in which the saimeterol is in the form of the xinafoate salt.