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HRP20220972T1 - Oftalmološki pripravci koji sadrže muskarinski antagonist i deuteriranu vodu - Google Patents

Oftalmološki pripravci koji sadrže muskarinski antagonist i deuteriranu vodu Download PDF

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Publication number
HRP20220972T1
HRP20220972T1 HRP20220972TT HRP20220972T HRP20220972T1 HR P20220972 T1 HRP20220972 T1 HR P20220972T1 HR P20220972T T HRP20220972T T HR P20220972TT HR P20220972 T HRP20220972 T HR P20220972T HR P20220972 T1 HRP20220972 T1 HR P20220972T1
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Croatia
Prior art keywords
ophthalmic preparation
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months
mass
ophthalmic
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HRP20220972TT
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English (en)
Inventor
Gregory I. Ostrow
Kenneth J. Widder
David S. Baker
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Sydnexis, Inc.
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First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=54868660&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=HRP20220972(T1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Sydnexis, Inc. filed Critical Sydnexis, Inc.
Publication of HRP20220972T1 publication Critical patent/HRP20220972T1/hr

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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/468-Azabicyclo [3.2.1] octane; Derivatives thereof, e.g. atropine, cocaine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/02Inorganic compounds
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/06Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
    • A61K47/08Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
    • A61K47/10Alcohols; Phenols; Salts thereof, e.g. glycerol; Polyethylene glycols [PEG]; Poloxamers; PEG/POE alkyl ethers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/06Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
    • A61K47/08Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
    • A61K47/12Carboxylic acids; Salts or anhydrides thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/06Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
    • A61K47/26Carbohydrates, e.g. sugar alcohols, amino sugars, nucleic acids, mono-, di- or oligo-saccharides; Derivatives thereof, e.g. polysorbates, sorbitan fatty acid esters or glycyrrhizin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/0012Galenical forms characterised by the site of application
    • A61K9/0048Eye, e.g. artificial tears
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/08Solutions
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00Drugs for disorders of the senses
    • A61P27/02Ophthalmic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/30Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Ophthalmology & Optometry (AREA)
  • Emergency Medicine (AREA)
  • Inorganic Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Organic Chemistry (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Biochemistry (AREA)
  • Molecular Biology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicinal Preparation (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Claims (18)

1. Oftalmološki pripravak, naznačen time, da sadrži muskarinski antagonist i deuteriranu vodu od 0,001% po masi do 0,05% po masi, na pD vrijednosti od 4,2 do 7,9, pri čemu muskarinski antagonist je atropin ili atropin sulfat.
2. Oftalmološki pripravak prema patentnom zahtjevu 1, naznačen time, da oftalmološki pripravak ima jednu od sljedećih pD vrijednosti: manje od 7,3, manje od 7,2, manje od 7,1, manje od 7, manje od 6,8, manje od 6,5, manje od 6,4, manje od 6,3, manje od 6,2, manje od 6,1, manje od 6, manje od 5,9, manje od 5,8, manje od 5,2, ili manje od 4,8 nakon produljenog vremenskog perioda pod skladišnim uvjetima.
3. Oftalmološki pripravak prema bilo kojem od patentnih zahtjeva 1 do 2, naznačen time, da oftalmološki pripravak ima jedan od sljedećih: najmanje 80%, najmanje 85%, najmanje 90%, najmanje 93%, najmanje 95%, najmanje 97%, najmanje 98%, ili najmanje 99% muskarinskog antagonista na temelju inicijalne koncentracije nakon produljenog vremenskog perioda pod skladišnim uvjetima.
4. Oftalmološki pripravak prema bilo kojem od patentnih zahtjeva 1 do 3, naznačen time, da oftalmološki pripravak nadalje ima potentnost kao jednu od sljedećih: najmanje 80%, najmanje 85%, najmanje 90%, najmanje 93%, najmanje 95%, najmanje 97%, najmanje 98%, ili najmanje 99% nakon produljenog vremenskog perioda pod skladišnim uvjetima.
5. Oftalmološki pripravak prema bilo kojem od patentnih zahtjeva 1 do 4, naznačen time, da je produljeni vremenski period jedan od sljedećih: 1 tjedan, 2 tjedna, 3 tjedna, 1 mjesec, 2 mjeseca, 3 mjeseca, 4 mjeseca, 5 mjeseci, 6 mjeseci, 8 mjeseci, 10 mjeseci, 12 mjeseci, 18 mjeseci, 24 mjeseca, 36 mjeseci, 4 godine, ili 5 godina.
6. Oftalmološki pripravak prema bilo kojem od patentnih zahtjeva 1 do 5, naznačen time, da skladišni uvjeti imaju temperaturu skladištenja od 2°C do 10°C ili od 16°C do 26°C.
7. Oftalmološki pripravak prema bilo kojem od patentnih zahtjeva 1 do 6, naznačen time, da se muskarinski antagonist nalazi u pripravku s koncentracijom koja je jedna od sljedećih: od 0,001% po masi do 0,03% po masi, od 0,001% po masi do 0,025% po masi, od 0,001% po masi do 0,02% po masi, od 0,001% po masi do 0,01% po masi, od 0,001% po masi do 0,008% po masi, ili od 0,001% po masi do 0,005% po masi.
8. Oftalmološki pripravak prema bilo kojem od patentnih zahtjeva 1 do 7, naznačen time, da oftalmološki pripravak nadalje sadrži: sredstvo za podešavanje osmolarnosti, poželjno natrijev klorid; konzervans, poželjno odabran od benzalkonij klorida, cetrimonija, natrijevog perborata, stabiliziranog oksikloro kompleksa, SofZia, polikvaternija-1, klorobutanola, edetat dinatrija, poliheksametilen bigvanida, ili njihovih kombinacija; puferski agens, poželjno odabran od borata, kompleksa borat-poliol, fosfatnih puferskih agensa, citratnih puferskih agensa, acetatnih puferskih agensa, karbonatnih puferskih agensa, organskih puferskih agensa, aminokiselinskih puferskih agensa, ili njihovih kombinacija; sredstvo za podešavanje toničnosti; ili njihove kombinacije.
9. Oftalmološki pripravak prema bilo kojem od patentnih zahtjeva 1 do 8, naznačen time, da je oftalmološki pripravak uglavnom oslobođen od prokaina i benaktizina, ili njihovih farmaceutski prihvatljivih soli.
10. Oftalmološki pripravak prema bilo kojem od patentnih zahtjeva 1 do 9, naznačen time, da oftalmološki pripravak nadalje sadrži sredstvo za podešavanje pD vrijednosti, koje se bira od deuterirane klorovodične kiseline (DCl), deuteriranog natrijevog hidroksida (NaOD), deuterirane octene kiseline (CD3COOD), i deuterirane limunske kiseline (C6D8O7).
11. Oftalmološki pripravak prema bilo kojem od patentnih zahtjeva 1 do 9, naznačen time, da oftalmološki pripravak nadalje sadrži sredstvo za podešavanje pH vrijednosti, koje se bira od HCl, NaOH, CH3COOH, i C6H8O7.
12. Oftalmološki pripravak prema bilo kojem od patentnih zahtjeva 1 do 11, naznačen time, da oftalmološki pripravak sadrži jedno od sljedećih: manje od 5% H2O, manje od 4% H2O, manje od 3% H2O, manje od 2% H2O, manje od 1% H2O, manje od 0,5% H2O, manje od 0,1% H2O, ili 0% H2O.
13. Oftalmološki pripravak prema bilo kojem od patentnih zahtjeva 1 do 12, naznačen time, da oftalmološki pripravak nije formuliran kao formulacija koja se može dati injekcijom.
14. Oftalmološki pripravak prema bilo kojem od patentnih zahtjeva 1 do 13, naznačen time, da je oftalmološki pripravak formuliran kao oftalmološka otopina za liječenje oftalmološkog poremećaja koji se bira od predmiopije, miopije, ili progresije miopije.
15. Oftalmološki pripravak prema bilo kojem od patentnih zahtjeva 1 do 14, naznačen time, da je za uporabu u postupku zaustavljanja razvoja miopije ili sprečavanja razvoja miopije, pri čemu postupak obuhvaća primjenu učinkovite količine navedenog oftalmološkog pripravka u oko pojedinca kojemu je to potrebno.
16. Oftalmološki pripravak za uporabu prema patentnom zahtjevu 15, naznačen time, da se oftalmološki pripravak prije prve uporabe skladišti između 2°C i 10°C.
17. Oftalmološki pripravak za uporabu prema patentnom zahtjevu 15, naznačen time, da se oftalmološki pripravak nakon prve uporabe skladišti između 16°C i 26°C.
18. Oftalmološki pripravak za uporabu prema patentnom zahtjevu 15, naznačen time, da je za uporabu u postupku smanjivanja stupnja pojačanja miopije.
HRP20220972TT 2014-06-24 2015-06-23 Oftalmološki pripravci koji sadrže muskarinski antagonist i deuteriranu vodu HRP20220972T1 (hr)

Applications Claiming Priority (6)

Application Number Priority Date Filing Date Title
US201462016502P 2014-06-24 2014-06-24
US201462096433P 2014-12-23 2014-12-23
US201562151926P 2015-04-23 2015-04-23
US14/726,139 US9421199B2 (en) 2014-06-24 2015-05-29 Ophthalmic composition
PCT/US2015/037249 WO2015200361A1 (en) 2014-06-24 2015-06-23 Ophthalmic composition
EP15811865.3A EP3160471B1 (en) 2014-06-24 2015-06-23 Ophthalmic compositions comprising a muscarinic antagonist and deuterated water

Publications (1)

Publication Number Publication Date
HRP20220972T1 true HRP20220972T1 (hr) 2022-11-25

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ID=54868660

Family Applications (1)

Application Number Title Priority Date Filing Date
HRP20220972TT HRP20220972T1 (hr) 2014-06-24 2015-06-23 Oftalmološki pripravci koji sadrže muskarinski antagonist i deuteriranu vodu

Country Status (20)

Country Link
US (11) US9421199B2 (hr)
EP (3) EP3689350A1 (hr)
JP (4) JP6678362B2 (hr)
KR (4) KR102506109B1 (hr)
CN (3) CN110638749A (hr)
BR (1) BR112016030368B1 (hr)
CA (1) CA2953363C (hr)
DK (1) DK3160471T3 (hr)
ES (1) ES2924243T3 (hr)
HR (1) HRP20220972T1 (hr)
HU (1) HUE059521T2 (hr)
IL (1) IL249643B (hr)
LT (1) LT3160471T (hr)
PL (1) PL3160471T3 (hr)
PT (1) PT3160471T (hr)
RS (1) RS63486B1 (hr)
SG (3) SG10201913976SA (hr)
SI (1) SI3160471T1 (hr)
TW (2) TWI763620B (hr)
WO (1) WO2015200361A1 (hr)

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