ME02608B - Kombinacija, komplet i postupak snižavanja intraokularnog pritiska - Google Patents

Kombinacija, komplet i postupak snižavanja intraokularnog pritiska

Info

Publication number
ME02608B
ME02608B MEP-2017-11A MEP1117A ME02608B ME 02608 B ME02608 B ME 02608B ME P1117 A MEP1117 A ME P1117A ME 02608 B ME02608 B ME 02608B
Authority
ME
Montenegro
Prior art keywords
combination
compound
eye
subject
use according
Prior art date
Application number
MEP-2017-11A
Other languages
German (de)
English (en)
French (fr)
Inventor
Norman N Kim
William K Mcvicar
Thomas Mccauley
Rudolf A Baumgartner
Original Assignee
Inotek Pharmaceuticals Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=44258984&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=ME02608(B) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Inotek Pharmaceuticals Corp filed Critical Inotek Pharmaceuticals Corp
Publication of ME02608B publication Critical patent/ME02608B/me

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/557Eicosanoids, e.g. leukotrienes or prostaglandins
    • A61K31/5575Eicosanoids, e.g. leukotrienes or prostaglandins having a cyclopentane, e.g. prostaglandin E2, prostaglandin F2-alpha
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/16Amides, e.g. hydroxamic acids
    • A61K31/165Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/185Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
    • A61K31/19Carboxylic acids, e.g. valproic acid
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/21Esters, e.g. nitroglycerine, selenocyanates
    • A61K31/215Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids
    • A61K31/216Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acids having aromatic rings, e.g. benactizyne, clofibrate
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/70Carbohydrates; Sugars; Derivatives thereof
    • A61K31/7042Compounds having saccharide radicals and heterocyclic rings
    • A61K31/7052Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
    • A61K31/706Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom
    • A61K31/7064Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines
    • A61K31/7076Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines containing purines, e.g. adenosine, adenylic acid
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • 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
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00Drugs for disorders of the senses
    • 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
    • A61P27/00Drugs for disorders of the senses
    • A61P27/02Ophthalmic agents
    • A61P27/06Antiglaucoma agents or miotics
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07HSUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H19/00Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
    • C07H19/02Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
    • C07H19/04Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
    • C07H19/16Purine radicals

Landscapes

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

Claims (10)

1.  Oftalmološka kombinacija koja obuhvata i) ((2R,3S,4R,5R)-5-(6-(ciklopentilamino)-9H-purin-9-il)-3,4-dihidroksitetrahidrofuran-2-il)metil nitrat,ili njegova farmaceutski prihvatljiva so, i ii) jedinjenje odabrano iz grupe koju čine latanoprost, travoprost, unoproston i bimatoprost, za upotrebu u snižavanju povišenog intraokularnog pritiska u oku nekog subjekta.
2.  Kombinacija za upotrebu prema zahtevu 1, u kojoj jedinjenje (ii) je latanoprost.
3. Kombinacija za upotrebu prema bilo kom od zahteva 1 do 2, u kojoj se jedinjenje (i) primenjuje na oko subjekta simultano, odvojeno ili sekvencijalno u odnosu na primenu jedinjenja (ii) na oko subjekta.
4.  Kombinacija za upotrebu prema zahtevu 1, u kojoj se jedna ili više kapi od oko 0,05 mg/ml do oko 7,0 mg/ml jedinjenja (i) nanose na oko subjekta sa oko 30 µg/ml do oko 50 µg/ml jedinjenja (ii) od 1 do 4 puta dnevno.
5.  Kombinacija za upotrebu prema zahtevu 4, u kojoj se oko 20-700 µg, ili 20-350 µg jedinjenja (i) nanosi na oko subjekta od 1 do 2 puta dnevno.
6.  Kombinacija za upotrebu prema bilo kom od zahteva 1 do 5, u kojoj se jedinjenje (i) i jedinjenje (ii) nanose topikalno na oko subjekta kao jedna ili više očnih kapi.
7.  Kombinacija za upotrebu prema bilo kom od zahteva 1 do 6 za upotrebu u tretiranju bolesti i stanja izazvanih povišenim intraokularnim pritiskom kod subjekta.
8.  Kombinacija za upotrebu prema zahtevu 7, u kojoj su bolesti i stanja izazvana povišenim intraokularnim pritiskom kod čoveka odabrana iz grupe koju čine očna hipertenzija, i primarni glaukom otvorenog ugla.
9.  Komplet koji obuhvata kombinaciju prema bilo kom od zahteva 1 do 8 za upotrebu u snižavanju povišenog intraokularnog pritiska u oku nekog subjekta.
10.  Kombinacija koja obuhvata i) ((2R,3S,4R,5R)-5-(6-(ciklopentilamino)-9H-purin-9-il)-3,4-dihidroksitetrahidrofuran-2-il)metil nitrat ili njegovu farmaceutski prihvatljivu so i ii) jedinjenje odabrano iz grupe koju čine latanoprost, travoprost, unoproston i bimatoprost za upotrebu kao lek.
MEP-2017-11A 2010-01-11 2011-01-11 Kombinacija, komplet i postupak snižavanja intraokularnog pritiska ME02608B (me)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US29380610P 2010-01-11 2010-01-11
PCT/US2011/020808 WO2011085361A1 (en) 2010-01-11 2011-01-11 Combination, kit and method of reducing intraocular pressure
EP11732309.7A EP2523669B1 (en) 2010-01-11 2011-01-11 Combination, kit and method of reducing intraocular pressure

Publications (1)

Publication Number Publication Date
ME02608B true ME02608B (me) 2017-06-20

Family

ID=44258984

Family Applications (1)

Application Number Title Priority Date Filing Date
MEP-2017-11A ME02608B (me) 2010-01-11 2011-01-11 Kombinacija, komplet i postupak snižavanja intraokularnog pritiska

Country Status (29)

Country Link
US (3) US8877732B2 (me)
EP (1) EP2523669B1 (me)
JP (2) JP2013516495A (me)
KR (1) KR20120115344A (me)
CN (1) CN102711771B (me)
AU (1) AU2011203897B2 (me)
BR (1) BR112012017106A2 (me)
CA (1) CA2784908A1 (me)
CL (1) CL2012001912A1 (me)
CO (1) CO6571924A2 (me)
CY (1) CY1118510T1 (me)
DK (1) DK2523669T3 (me)
EA (1) EA025415B1 (me)
ES (1) ES2613698T3 (me)
HR (1) HRP20170007T1 (me)
HU (1) HUE030566T2 (me)
IL (1) IL220604A (me)
IN (1) IN2012DN06592A (me)
LT (1) LT2523669T (me)
ME (1) ME02608B (me)
MX (1) MX2012007661A (me)
PH (1) PH12012501320A1 (me)
PL (1) PL2523669T3 (me)
PT (1) PT2523669T (me)
RS (1) RS55615B1 (me)
SG (2) SG182285A1 (me)
SI (1) SI2523669T1 (me)
SM (2) SMT201700017T1 (me)
WO (1) WO2011085361A1 (me)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PT2424546E (pt) * 2009-05-01 2015-12-23 Inotek Pharmaceuticals Corp Método de redução de pressão intraocular em seres humanos
LT2523669T (lt) * 2010-01-11 2017-04-25 Inotek Pharmaceuticals Corporation Akispūdžio mažinimo būdas, derinys ir rinkinys
AU2011230580A1 (en) 2010-03-26 2012-10-11 Inotek Pharmaceuticals Corporation Method of reducing intraocular pressure in humans using N6 -cyclopentyladenosine (CPA), CPA derivatives or prodrugs thereof
PL2807178T3 (pl) * 2012-01-26 2017-12-29 Inotek Pharmaceuticals Corporation Bezwodne polimorfy azotanu (2R,3S,4R,5R)-5-(6-(cyklopentyloamino)-9H-puryn-9-ylo)-3,4-dihydroksytetrahydrofuran-2-ylo)metylu i sposoby ich wytwarzania
MX2015013240A (es) * 2013-03-15 2016-04-07 Inotek Pharmaceuticals Corp Método para proporcionar neuroprotección ocular.
WO2014152723A1 (en) * 2013-03-15 2014-09-25 Inotek Pharmaceuticals Corporation Ophthalmic formulations
JP6217866B2 (ja) 2014-10-24 2017-10-25 小野薬品工業株式会社 Kcnq2〜5チャネル活性化剤
CN107406479A (zh) * 2014-12-03 2017-11-28 伊诺泰克制药公司 预防、减轻或治疗黄斑变性的方法

Family Cites Families (107)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4935635B1 (me) 1970-12-28 1974-09-25
CH563405A5 (me) 1971-09-10 1975-06-30 Duschinsky Robert Dr Schweiz I
DE2226295A1 (de) 1972-05-30 1973-12-20 Henning Berlin Gmbh Salpetersaeureester von purinnucleosiden und verfahren zur herstellung derselben
DE2342479A1 (de) 1973-08-23 1975-03-13 Merck Patent Gmbh Ribonucleosid-5'-nitrate und verfahren zu ihrer herstellung
GB2001976B (en) 1977-08-03 1982-03-10 Yamasa Shoyu Kk S-adenosyl-l-methionine compositions and production thereof
US4849311A (en) 1986-09-24 1989-07-18 Toa Nenryo Kogyo Kabushiki Kaisha Immobilized electrolyte membrane
US4968697A (en) 1987-02-04 1990-11-06 Ciba-Geigy Corporation 2-substituted adenosine 5'-carboxamides as antihypertensive agents
US5219840A (en) 1987-04-06 1993-06-15 Sandoz Ltd. Antihypertensive 9-(2,N6 -disubstituted adenyl) ribofuranuronic acid derivatives
US5221763A (en) * 1987-04-30 1993-06-22 R-Tech Ueno, Ltd. Prostaglandins of the F series
US5591887A (en) * 1987-04-30 1997-01-07 R-Tech Ueno, Ltd. Prostaglandins of the F series
US6187813B1 (en) 1990-04-10 2001-02-13 Pharmacia & Upjohn Aktiebolag Prostaglandin derivatives for the treatment of glaucoma or ocular hypertension
EP1348437A3 (en) 1988-09-06 2003-11-19 Pharmacia Aktiebolag Prostaglandin derivatives for the treatment of glaucoma or ocular hypertension
US5296504A (en) 1988-09-06 1994-03-22 Kabi Pharmacia Prostaglandin derivatives for the treatment of glaucoma or ocular hypertension
US5140015A (en) 1990-02-20 1992-08-18 Whitby Research, Inc. 2-aralkoxy and 2-alkoxy adenosine derivatives as coronary vasodilators and antihypertensive agents
US5280015A (en) 1990-09-05 1994-01-18 The United States Of America As Represented By The Department Of Health And Human Services 2-substituted adenosines and 2-substituted adenosine 5'-carboxamides
JP3020580B2 (ja) 1990-09-28 2000-03-15 株式会社日立製作所 マイクロ波プラズマ処理装置
US5206222A (en) 1991-05-22 1993-04-27 Vanderbilt University Methods for the reduction of myocardial reperfusion injury
HU212570B (en) * 1991-06-24 1996-08-29 Chinoin Gyogyszer Es Vegyeszet Process for producing 13,14-dihydro-15(r)-17-phenyl-18,19,20-trinor-pgf2alfa-isopropylester
US5407793A (en) 1991-10-18 1995-04-18 University Of Pittsburgh Of The Commonwealth System Of Higher Education An aqueous heart preservation and cardioplegia solution
US5278150A (en) 1992-04-24 1994-01-11 Whitby Research, Inc. 2-hydrazoadenosines and their utility for the treatmeat of vascular conditions
DK62692D0 (me) 1992-05-14 1992-05-14 Novo Nordisk As
WO1994002497A1 (en) 1992-07-15 1994-02-03 The United States Of America, Represented By The Secretary, Department Of Health And Human Services Sulfo-derivatives of adenosine
US5972991A (en) * 1992-09-21 1999-10-26 Allergan Cyclopentane heptan(ene) oic acid, 2-heteroarylalkenyl derivatives as therapeutic agents
US5338430A (en) 1992-12-23 1994-08-16 Minnesota Mining And Manufacturing Company Nanostructured electrode membranes
US5443836A (en) 1993-03-15 1995-08-22 Gensia, Inc. Methods for protecting tissues and organs from ischemic damage
EP0708781B1 (en) 1993-07-13 2001-10-04 THE UNITED STATES OF AMERICA, as represented by THE SECRETARY, Department of Health and Human Services A 3 adenosine receptor agonists
US5589467A (en) 1993-09-17 1996-12-31 Novo Nordisk A/S 2,5',N6-trisubstituted adenosine derivatives
WO1995011681A1 (en) 1993-10-29 1995-05-04 Merck & Co., Inc. Human adenosine receptor antagonists
US5620676A (en) 1994-03-08 1997-04-15 The United States Of America As Represented By The Department Of Health And Human Services Biologically active ATP analogs
EP0704215A3 (en) 1994-06-02 1998-04-01 Takeda Chemical Industries, Ltd. Inhibitor of vascular permeability enhancer
GB9414193D0 (en) 1994-07-14 1994-08-31 Glaxo Group Ltd Compounds
US5801159A (en) 1996-02-23 1998-09-01 Galileo Laboratories, Inc. Method and composition for inhibiting cellular irreversible changes due to stress
CN1164122A (zh) 1996-03-01 1997-11-05 株式会社日立制作所 等离子处理机及其处理方法
WO1997033590A1 (en) 1996-03-13 1997-09-18 Novo Nordisk A/S A method of treating disorders related to cytokines in mammals
WO1997033879A1 (en) 1996-03-15 1997-09-18 Merck & Co., Inc. Compounds and methods for selectively inhibiting activation of the human a3 adenosine receptor
US5789416B1 (en) 1996-08-27 1999-10-05 Cv Therapeutics Inc N6 mono heterocyclic substituted adenosine derivatives
TW528755B (en) 1996-12-24 2003-04-21 Glaxo Group Ltd 2-(purin-9-yl)-tetrahydrofuran-3,4-diol derivatives
AU750322B2 (en) 1997-05-09 2002-07-18 Trustees Of The University Of Pennsylvania, The Methods and compositions for reducing ischemic injury of the heart by administering adenosine receptor agonists and antagonists
EP1037621A4 (en) 1997-10-15 2004-01-21 Univ Jefferson NITROGEN OXYD DONOR COMPOSITIONS, METHODS, APPARATUS, AND KITS FOR PREVENTING OR REDUCING VASCARSIONS OR VASCULAR SPAS IN A MAMMAL
WO1999020284A1 (en) 1997-10-23 1999-04-29 Trustees Of The University Of Pennsylvania Methods for reducing ischemic injury of the heart via the sequential administration of monophosphoryl lipid a and adenosine receptor agents
GB9723590D0 (en) 1997-11-08 1998-01-07 Glaxo Group Ltd Chemical compounds
GB9723566D0 (en) 1997-11-08 1998-01-07 Glaxo Group Ltd Chemical compounds
FR2775901B1 (fr) 1998-03-13 2000-07-21 Logeais Labor Jacques Sels de cetoacides et de derives amines, et leur utilisation pour la preparation de medicaments
GB9813535D0 (en) 1998-06-23 1998-08-19 Glaxo Group Ltd Chemical compounds
EP1096975B1 (en) 1998-07-16 2005-03-16 The Trustees Of The University Of Pennsylvania Use of a3 adenosine receptor antagonists in the manufacture of a medicament for reducing intraocular pressure
BR9914526A (pt) 1998-10-16 2001-07-03 Pfizer Derivados de adenina
IL127947A0 (en) 1999-01-07 1999-11-30 Can Fite Technologies Ltd Pharmaceutical use of adenosine agonists
US6232297B1 (en) 1999-02-01 2001-05-15 University Of Virginia Patent Foundation Methods and compositions for treating inflammatory response
US6180615B1 (en) 1999-06-22 2001-01-30 Cv Therapeutics, Inc. Propargyl phenyl ether A2A receptor agonists
IL147194A0 (en) 1999-06-22 2002-08-14 Cv Therapeutics Inc Thiophene a2a receptor agonists
US6403567B1 (en) 1999-06-22 2002-06-11 Cv Therapeutics, Inc. N-pyrazole A2A adenosine receptor agonists
US6214807B1 (en) 1999-06-22 2001-04-10 Cv Therapeutics, Inc. C-pyrazole 2A A receptor agonists
IL133680A0 (en) 1999-09-10 2001-04-30 Can Fite Technologies Ltd Pharmaceutical compositions comprising an adenosine receptor agonist or antagonist
GB9924361D0 (en) 1999-10-14 1999-12-15 Pfizer Ltd Purine derivatives
US6368573B1 (en) 1999-11-15 2002-04-09 King Pharmaceuticals Research And Development, Inc. Diagnostic uses of 2-substituted adenosine carboxamides
US6258793B1 (en) 1999-12-03 2001-07-10 Cv Therapeutics, Inc. N6 heterocyclic 5′ modified adenosine derivatives
GB9930071D0 (en) 1999-12-20 2000-02-09 Glaxo Group Ltd Medicaments
GB0003960D0 (en) 2000-02-18 2000-04-12 Pfizer Ltd Purine derivatives
US20010051612A1 (en) 2000-02-23 2001-12-13 Gloria Cristalli 2-Thioether A2A receptor agonists
US20030010454A1 (en) 2000-03-27 2003-01-16 Bailey Andrew D. Method and apparatus for varying a magnetic field to control a volume of a plasma
US6534651B2 (en) 2000-04-06 2003-03-18 Inotek Pharmaceuticals Corp. 7-Substituted isoindolinone inhibitors of inflammation and reperfusion injury and methods of use thereof
US6753322B2 (en) 2000-06-06 2004-06-22 Pfizer Inc 2-aminocarbonyl-9H-purine derivatives
US6921753B2 (en) 2000-06-27 2005-07-26 Pfizer Inc Purine derivatives
MXPA03000729A (es) 2000-07-28 2004-11-01 Inspire Pharmaceuticals Inc Metodo para reducir la presion intraocular utilizando derivados de indol.
JP4012070B2 (ja) 2001-01-16 2007-11-21 カン−フィテ・バイオファーマ・リミテッド ウイルスの複製を阻害するためのアデノシンa3受容体アゴニストの使用
GB2372742A (en) 2001-03-03 2002-09-04 Univ Leiden C2,5'-Disubstituted and N6,C2,5'-trisubstituted adenosine derivatives and their different uses
EP1241176A1 (en) 2001-03-16 2002-09-18 Pfizer Products Inc. Purine derivatives for the treatment of ischemia
US20040204481A1 (en) 2001-04-12 2004-10-14 Pnina Fishman Activation of natural killer cells by adenosine A3 receptor agonists
US20030013675A1 (en) 2001-05-25 2003-01-16 Boehringer Ingelheim Pharma Kg Combination of an adenosine A2A-receptor agonist and tiotropium or a derivative thereof for treating obstructive airways and other inflammatory diseases
US7713946B2 (en) 2002-07-11 2010-05-11 Cv Therapeutics, Inc. Partial and full agonists A1 adenosine receptors
JP2004537401A (ja) 2001-08-08 2004-12-16 ブラウン ユニバーシティ リサーチ ファウンデーション 疎水性薬物の微粉砕方法
SG176313A1 (en) 2001-10-01 2011-12-29 Univ Virginia Patent Found 2-propynyl adenosine analogs having a2a agonist activity and compositions thereof
CN101385738A (zh) 2002-04-18 2009-03-18 Cv医药有限公司 包括给予A1腺苷激动剂以及β受体阻滞剂、钙通道阻滞剂、或强心苷的治疗心律失常的方法
US7351407B2 (en) 2002-04-30 2008-04-01 Alcon, Inc. Agents which regulate, inhibit, or modulate the activity and/or expression of connective tissue growth factor (CTGF) as a unique means to both lower intraocular pressure and treat glaucomatous retinopathies/optic neuropathies
GB0216416D0 (en) 2002-07-15 2002-08-21 Novartis Ag Organic compounds
GB2436255B (en) 2002-12-23 2007-11-28 Global Cardiac Solutions Pty L Organ preconditioning, arrest, protection, preservation and recovery
WO2004056180A1 (en) 2002-12-23 2004-07-08 Global Cardiac Solutions Pty Ltd Organ preconditioning, arrest, protection, preservation and recovery (1)
US8008338B2 (en) 2003-06-03 2011-08-30 Allergan, Inc. Ketorolac tromethamine compositions for treating or preventing ocular pain
US20090131342A1 (en) 2004-01-22 2009-05-21 Nitromed, Inc. Nitrosated and/or nitrosylated compounds, compositions and methods of use
US7423144B2 (en) * 2004-05-26 2008-09-09 Inotek Pharmaceuticals Corporation Purine Derivatives as adenosine A1 receptor agonists and methods of use thereof
CN101010085B (zh) 2004-05-26 2012-12-26 伊诺泰克制药公司 嘌呤衍生物作为腺苷a1受体激动剂及其用法
CA2573682A1 (en) 2004-07-12 2006-02-16 Cv Therapeutics, Inc. Process for the preparation of a1 adenosine receptor agonists
DK1802277T3 (da) * 2004-10-18 2010-05-17 Polymun Scient Immunbio Forsch Liposomal sammensætning indeholdende en aktiv bestanddel til relaksation af glat muskulatur og terapeutisk anvendelse af sammensætningen
US20090220516A1 (en) 2005-06-22 2009-09-03 Alan Laties Neuroprotection of retinal ganglion cells
BRPI0619261A2 (pt) * 2005-11-30 2011-09-27 Inotek Pharmaceuticals Corp derivados de purina e métodos de uso desses
US7964191B2 (en) 2006-02-02 2011-06-21 Allergan, Inc. Compositions and methods for the treatment of ophthalmic disease
US8784886B2 (en) 2006-03-09 2014-07-22 GlaxoSmithKline, LLC Coating capsules with active pharmaceutical ingredients
AU2007229463A1 (en) 2006-03-23 2007-10-04 Inotek New Zealand Limited Purine compounds and methods of use thereof
US8163737B2 (en) 2006-06-13 2012-04-24 Vertex Pharmaceuticals Incorporated CGRP receptor antagonists
AR062046A1 (es) 2006-07-25 2008-08-10 Osmotica Pharmaceutical Argentina S A Soluciones oftalmicas
WO2008045330A2 (en) 2006-10-06 2008-04-17 The Trustees Of The University Of Pennsylvania Effective delivery of cross-species a3 adenosine-receptor antagonists to reduce intraocular pressure
PT2083629E (pt) 2006-11-10 2011-09-01 Basf Se Modificação cristalina de fipronil
AU2007327990A1 (en) 2006-12-05 2008-06-12 The Royal Institution For The Advancement Of Learning/ Mcgill University Methods of use of TRK receptor modulators
JP2008266143A (ja) 2007-04-16 2008-11-06 Santen Pharmaceut Co Ltd アデノシン誘導体を有効成分として含有する緑内障治療剤
JP5674469B2 (ja) 2007-10-11 2015-02-25 バイオジェン・アイデック・エムエイ・インコーポレイテッド LINGO−1アンタゴニストおよびTrkBアゴニストの投与を介して圧力誘導性の視神経障害を処置し、神経変性を防ぎ、ニューロン細胞の生存を促進する方法
WO2009076580A2 (en) 2007-12-12 2009-06-18 Thomas Jefferson University Compositions and methods for the treatment and prevention of cardiovascular diseases
KR20100117105A (ko) 2008-02-07 2010-11-02 질레드 팔로 알토 인코포레이티드 Abca-1 상승 화합물 및 이의 용도
EP2349332B1 (en) 2008-11-13 2019-10-23 The General Hospital Corporation Methods and compositions for regulating iron homeostasis by modulation bmp-6
PT2424546E (pt) 2009-05-01 2015-12-23 Inotek Pharmaceuticals Corp Método de redução de pressão intraocular em seres humanos
EA201200635A1 (ru) 2009-10-26 2012-10-30 Инотек Фармасьютикалз Корпорейшн Глазной состав и способ его изготовления
WO2011077435A1 (en) 2009-12-22 2011-06-30 Bar-Ilan University Compositions and methods for reducing intraocular pressure
LT2523669T (lt) 2010-01-11 2017-04-25 Inotek Pharmaceuticals Corporation Akispūdžio mažinimo būdas, derinys ir rinkinys
US20110217262A1 (en) 2010-03-05 2011-09-08 Kornfield Julia A Treatment of Ocular Surface Disorders by Increasing Conjunctival Vascular Permeability
PL2555775T3 (pl) 2010-03-19 2017-08-31 Inotek Pharmaceuticals Corporation Kompozycje połączenia agonistów receptora adenozyny A<sub>1</sub> i inhibitorów anhydrazy węglanowej do obniżania ciśnienia wewnątrzgałkowego
SMT201700020T1 (it) * 2010-03-19 2017-03-08 Inotek Pharmaceuticals Corp Combinazione di composizioni di antagonisti di adenosina a1 e bloccanti di recettori non selettivi beta-adrenergici per ridurre la pressione intraoculare
US8501708B2 (en) 2010-03-26 2013-08-06 Inotek Pharmaceuticals Corporation Adenosine compounds and their use thereof
AU2011230580A1 (en) * 2010-03-26 2012-10-11 Inotek Pharmaceuticals Corporation Method of reducing intraocular pressure in humans using N6 -cyclopentyladenosine (CPA), CPA derivatives or prodrugs thereof

Also Published As

Publication number Publication date
ES2613698T3 (es) 2017-05-25
SMT201700017B (it) 2017-03-08
IN2012DN06592A (me) 2015-10-23
EA201201011A1 (ru) 2012-12-28
SI2523669T1 (sl) 2017-05-31
HRP20170007T1 (hr) 2017-03-10
PL2523669T3 (pl) 2017-06-30
SG10201502588UA (en) 2015-05-28
JP2016040320A (ja) 2016-03-24
EP2523669A1 (en) 2012-11-21
EP2523669B1 (en) 2016-12-07
JP2013516495A (ja) 2013-05-13
CN102711771A (zh) 2012-10-03
RS55615B1 (sr) 2017-06-30
PH12012501320A1 (en) 2013-01-21
US20110172177A1 (en) 2011-07-14
SG182285A1 (en) 2012-08-30
US20150038448A1 (en) 2015-02-05
CY1118510T1 (el) 2017-07-12
US9370530B2 (en) 2016-06-21
AU2011203897A1 (en) 2012-08-09
US8877732B2 (en) 2014-11-04
EP2523669A4 (en) 2013-08-28
AU2011203897B2 (en) 2016-11-17
KR20120115344A (ko) 2012-10-17
LT2523669T (lt) 2017-04-25
WO2011085361A1 (en) 2011-07-14
SMT201700017T1 (it) 2017-03-08
CO6571924A2 (es) 2012-11-30
BR112012017106A2 (pt) 2018-05-29
EA025415B1 (ru) 2016-12-30
IL220604A (en) 2017-01-31
HUE030566T2 (en) 2017-05-29
CL2012001912A1 (es) 2013-04-19
CA2784908A1 (en) 2011-07-14
PT2523669T (pt) 2017-01-31
DK2523669T3 (en) 2017-02-06
MX2012007661A (es) 2012-08-01
CN102711771B (zh) 2016-05-18
IL220604A0 (en) 2012-08-30
US20160367586A1 (en) 2016-12-22

Similar Documents

Publication Publication Date Title
HRP20170007T1 (hr) Kombinacija, komplet i metoda za smanjivanje intraokularnog tlaka
CA3045733A1 (en) Compositions comprising tacrolimus for the treatment of intraocular inflammatory eye diseases
HRP20151200T1 (hr) Metoda za snižavanje intraokularnog tlaka kod ljudi
MX2020009132A (es) Composiciones farmaceuticas que comprenden nebivolol.
Dams et al. Therapeutic uses of prostaglandin F2α analogues in ocular disease and novel synthetic strategies
JP2013542239A5 (me)
AU2011282681B2 (en) Preservative free bimatoprost and timolol solutions
ME02594B (me) Kombinovane kompozicje adenozinskih a1 agonista i ne-selektivnih beta- adrenergičnih receptor blokera za snižavanje intraokularnog pritiska
NI201100100A (es) Moduladores de aril metil benzoquinazolinona alostéricos positivos del receptor m1.
CN103191129A (zh) 治疗眼睛病症的脂氧化物类化合物
ES2711425T3 (es) Espesamiento de la córnea central reducido mediante el uso de profármacos de éster hidrófilos de beta-clorociclopentanos
IL274234B2 (en) Compositions and methods for the treatment of eye disorders
JP2013500977A5 (me)
JP2013528563A5 (me)
ME02593B (me) Kombinovane kompozicije adenozinskih a1 agonista i inhibitora ugljene anhidraze za snižavanje intraokularnog pritiska
AR062395A1 (es) Uso de derivados del 2.5-dihidroxibenceno para el tratamiento de enfermedades oculares
JP2022530471A (ja) 神経保護のためのカンナビノイドの組成物及び使用方法
NO20092764L (no) Isosorbid mononitrat derivater for behandling av okular hypertensjon
FI2765988T3 (fi) Silmäkoostumus, joka sisältää bromfenaakkia, jolla on parannettu biologinen hyötyosuus
ES2764654T3 (es) Combinaciones de prostaglandinas y donantes de óxido nítrico
WO2013184650A3 (en) Treatment of ocular inflammatory diseases using laquinimod
Bagnis et al. Antiglaucoma drugs: The role of preservative-free formulations
JP2017534658A5 (me)
JP2009500397A5 (me)
JP2009500398A5 (me)