AU772228B2 - Topical treatment or prevention of ocular infections - Google Patents
Topical treatment or prevention of ocular infections Download PDFInfo
- Publication number
- AU772228B2 AU772228B2 AU39203/00A AU3920300A AU772228B2 AU 772228 B2 AU772228 B2 AU 772228B2 AU 39203/00 A AU39203/00 A AU 39203/00A AU 3920300 A AU3920300 A AU 3920300A AU 772228 B2 AU772228 B2 AU 772228B2
- Authority
- AU
- Australia
- Prior art keywords
- process according
- eye
- azalide antibiotic
- suspension
- antibiotic
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired
Links
- 230000000699 topical effect Effects 0.000 title claims abstract description 25
- 208000001860 Eye Infections Diseases 0.000 title claims abstract description 10
- 238000011282 treatment Methods 0.000 title claims description 11
- 230000002265 prevention Effects 0.000 title description 4
- 230000003115 biocidal effect Effects 0.000 claims abstract description 93
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- 239000000203 mixture Substances 0.000 claims description 72
- 238000000034 method Methods 0.000 claims description 45
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- 239000000725 suspension Substances 0.000 claims description 37
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 37
- 230000008569 process Effects 0.000 claims description 36
- -1 antifungals Substances 0.000 claims description 30
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Classifications
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- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/56—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
- A61K31/57—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane or progesterone
- A61K31/573—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane or progesterone substituted in position 21, e.g. cortisone, dexamethasone, prednisone or aldosterone
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- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/7042—Compounds having saccharide radicals and heterocyclic rings
- A61K31/7048—Compounds having saccharide radicals and heterocyclic rings having oxygen as a ring hetero atom, e.g. leucoglucosan, hesperidin, erythromycin, nystatin, digitoxin or digoxin
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- A61K31/7042—Compounds having saccharide radicals and heterocyclic rings
- A61K31/7052—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
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- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/26—Carbohydrates, e.g. sugar alcohols, amino sugars, nucleic acids, mono-, di- or oligo-saccharides; Derivatives thereof, e.g. polysorbates, sorbitan fatty acid esters or glycyrrhizin
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- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/30—Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
- A61K47/36—Polysaccharides; Derivatives thereof, e.g. gums, starch, alginate, dextrin, hyaluronic acid, chitosan, inulin, agar or pectin
- A61K47/38—Cellulose; Derivatives thereof
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- Y—GENERAL 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
Landscapes
- Health & Medical Sciences (AREA)
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- General Health & Medical Sciences (AREA)
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- Molecular Biology (AREA)
- Organic Chemistry (AREA)
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- General Chemical & Material Sciences (AREA)
- Ophthalmology & Optometry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicinal Preparation (AREA)
- Saccharide Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US28216599A | 1999-03-31 | 1999-03-31 | |
| US09/282165 | 1999-03-31 | ||
| US09/346,923 US6239113B1 (en) | 1999-03-31 | 1999-07-02 | Topical treatment or prevention of ocular infections |
| US09/346923 | 1999-07-02 | ||
| PCT/US2000/007924 WO2000057866A2 (en) | 1999-03-31 | 2000-03-27 | Use of azalide antibiotics for the topical treatment or prevention of ocular infections |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU3920300A AU3920300A (en) | 2000-10-16 |
| AU772228B2 true AU772228B2 (en) | 2004-04-22 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU39203/00A Expired AU772228B2 (en) | 1999-03-31 | 2000-03-27 | Topical treatment or prevention of ocular infections |
Country Status (15)
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|---|---|
| US (5) | US6239113B1 (https=) |
| EP (2) | EP1165058B1 (https=) |
| JP (1) | JP4904621B2 (https=) |
| KR (1) | KR100701721B1 (https=) |
| AT (1) | ATE296093T1 (https=) |
| AU (1) | AU772228B2 (https=) |
| CA (1) | CA2368637C (https=) |
| CY (1) | CY1107259T1 (https=) |
| DE (2) | DE60020351T2 (https=) |
| DK (1) | DK1165058T3 (https=) |
| ES (1) | ES2244421T3 (https=) |
| HK (1) | HK1041642B (https=) |
| MX (1) | MXPA01009718A (https=) |
| PT (1) | PT1165058E (https=) |
| WO (1) | WO2000057866A2 (https=) |
Families Citing this family (153)
| Publication number | Priority date | Publication date | Assignee | Title |
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| US6045815A (en) * | 1997-08-15 | 2000-04-04 | Board Of Regents, The University Of Texas System | Parenteral pimaricin as treatment of systemic infections |
| US6844004B2 (en) * | 1997-08-15 | 2005-01-18 | Board Of Regents, The University Of Texas System | Topical formulations of natamycin/pimaricin |
| US6699492B2 (en) * | 1999-03-31 | 2004-03-02 | Insite Vision Incorporated | Quinolone carboxylic acid compositions and related methods of treatment |
| US7056893B2 (en) | 1999-03-31 | 2006-06-06 | Insite Vision, Inc. | Topical treatment for prevention of ocular infections |
| US6239113B1 (en) * | 1999-03-31 | 2001-05-29 | Insite Vision, Incorporated | Topical treatment or prevention of ocular infections |
| US6685958B2 (en) * | 2001-04-25 | 2004-02-03 | Insite Vision Incorporated | Quinolone carboxylic acid compositions and related methods of treatment |
| JP3502574B2 (ja) | 1999-06-29 | 2004-03-02 | 東亜薬品株式会社 | 眼感染症治療用眼軟膏剤 |
| HU230030B1 (hu) | 1999-10-08 | 2015-05-28 | Debiopharm International Sa | Fab I inhibitorok |
| US7141607B1 (en) | 2000-03-10 | 2006-11-28 | Insite Vision Incorporated | Methods and compositions for treating and inhibiting retinal neovascularization |
| US6914051B1 (en) * | 2000-06-28 | 2005-07-05 | David M Allen | Penetrating antibiotic gel for soft tissue diseases |
| WO2002007736A1 (en) * | 2000-07-24 | 2002-01-31 | Cadila Pharmaceuticals Limited | The process for manufacturing of clear liquid pharmaceutical composition of azithromycin |
| EP1560584B1 (en) * | 2001-04-06 | 2009-01-14 | Affinium Pharmaceuticals, Inc. | Fab i inhibitors |
| FR2823441B1 (fr) * | 2001-04-12 | 2004-09-10 | Thea Lab | Composition pharmaceutique a base de macrolides pour application locale en ophtalmologie et son procede de preparation |
| KR100431431B1 (ko) * | 2001-04-25 | 2004-05-14 | 한미약품 주식회사 | 아지트로마이신 수화물의 1,2-프로필렌글리콜 내포화합물,그의 제조방법 및 그의 약학적 조성물 |
| JP2004529178A (ja) * | 2001-05-11 | 2004-09-24 | パシフィック・ファーマシューティカルズ・リミテッド | 味遮蔽医薬組成物 |
| CA2458135A1 (en) * | 2001-08-21 | 2003-03-06 | Pfizer Products Inc. | Single dose azithromycin for treating respiratory infections |
| US20080149521A9 (en) * | 2001-10-18 | 2008-06-26 | Michael Pesachovich | Methods of stabilizing azithromycin |
| ES2324527T3 (es) * | 2001-10-18 | 2009-08-10 | Teva Pharmaceutical Industries Ltd. | Composiciones de azitromicina estabilizadas. |
| WO2003041500A1 (en) * | 2001-11-14 | 2003-05-22 | Board Of Regents, The University Of Texas System | Topical formulations of natamycin/pimaricin |
| US20050209446A1 (en) * | 2002-02-26 | 2005-09-22 | Meiji Seika Kaisha Ltd. | Novel 15-membered cyclic azalide, novel 16-membered cyclic diazalide derivative, and process for producing these |
| AU2003214133A1 (en) * | 2002-03-18 | 2003-09-29 | Novartis Ag | Topical composition comprising a cyclofructan, a carrier and a drug |
| US7354574B2 (en) * | 2002-11-07 | 2008-04-08 | Advanced Ocular Systems Limited | Treatment of ocular disease |
| EP1575951B1 (en) * | 2002-12-06 | 2014-06-25 | Debiopharm International SA | Heterocyclic compounds, methods of making them and their use in therapy |
| WO2004082586A2 (en) | 2003-03-17 | 2004-09-30 | Affinium Pharmaceuticals, Inc. | Phamaceutical compositions comprising inhibitors of fab i and further antibiotics |
| US20050085446A1 (en) * | 2003-04-14 | 2005-04-21 | Babu M.K. M. | Fluoroquinolone formulations and methods of making and using the same |
| US20040202687A1 (en) * | 2003-04-14 | 2004-10-14 | Babu M.K. Manoj | Ciprofloxacin formulations and methods of making and using the same |
| US7125497B1 (en) * | 2003-05-22 | 2006-10-24 | Sandia Corporation | Reactive formulations for a neutralization of toxic industrial chemicals |
| US7083802B2 (en) * | 2003-07-31 | 2006-08-01 | Advanced Ocular Systems Limited | Treatment of ocular disease |
| KR20060085246A (ko) * | 2003-09-18 | 2006-07-26 | 마커사이트, 인코포레이티드 | 경공막 전달 |
| US7083803B2 (en) * | 2003-09-19 | 2006-08-01 | Advanced Ocular Systems Limited | Ocular solutions |
| US7087237B2 (en) * | 2003-09-19 | 2006-08-08 | Advanced Ocular Systems Limited | Ocular solutions |
| US20050181018A1 (en) * | 2003-09-19 | 2005-08-18 | Peyman Gholam A. | Ocular drug delivery |
| US20050095205A1 (en) * | 2003-10-31 | 2005-05-05 | Ramesh Krishnamoorthy | Combination of loteprednol etabonate and tobramycin for topical ophthalmic use |
| DK1828167T3 (da) * | 2004-06-04 | 2014-10-20 | Debiopharm Int Sa | Acrylamidderivater som antibiotiske midler |
| JP3933683B2 (ja) | 2004-07-02 | 2007-06-20 | わかもと製薬株式会社 | アジスロマイシン含有水性医薬組成物及びその調製方法 |
| US20060046970A1 (en) * | 2004-08-31 | 2006-03-02 | Insite Vision Incorporated | Topical otic compositions and methods of topical treatment of prevention of otic infections |
| ATE429921T1 (de) * | 2005-01-14 | 2009-05-15 | Glaxosmithkline Zagreb | 9a-carbamoyl- und thiocarbamoylazalide mit antimalariawirkung |
| US8663639B2 (en) * | 2005-02-09 | 2014-03-04 | Santen Pharmaceutical Co., Ltd. | Formulations for treating ocular diseases and conditions |
| DK1848431T3 (en) * | 2005-02-09 | 2016-04-18 | Santen Pharmaceutical Co Ltd | LIQUID FORMULATIONS FOR TREATMENT OF DISEASES OR CONDITIONS |
| AU2006227116A1 (en) * | 2005-03-21 | 2006-09-28 | Santen Pharmaceutical Co., Ltd. | Drug delivery systems for treatment of diseases or conditions |
| FR2884716B1 (fr) * | 2005-04-22 | 2009-08-21 | Thea Sa Lab | Utilisation de l'azithromycine pour la fabrication d'un medicament destine au traitement des infections oculaires |
| CN100393738C (zh) * | 2005-07-05 | 2008-06-11 | 广州市微生物研究所 | 纳他霉素的提取纯化方法 |
| EP1904056B1 (en) | 2005-07-18 | 2009-04-29 | Minu, L.L.C. | Use of a macrolide to restore corneal sensation |
| US20070014760A1 (en) * | 2005-07-18 | 2007-01-18 | Peyman Gholam A | Enhanced recovery following ocular surgery |
| US20070048389A1 (en) * | 2005-08-26 | 2007-03-01 | Fu-Pao Tsao | Stabilized and preserved ketotifen ophthalmic compositions |
| KR20080075027A (ko) * | 2005-12-05 | 2008-08-13 | 아피늄 파마슈티컬스, 인크. | Ｆａｂｉ 억제제 및 항박테리아제로서의헤테로시클릴아크릴아미드 화합물 |
| SG10202003901UA (en) | 2005-12-13 | 2020-05-28 | Incyte Holdings Corp | Heteroaryl substituted pyrrolo[2,3-b]pyridines and pyrrolo[2,3-b]pyrimidines as janus kinase inhibitors |
| JPWO2007074904A1 (ja) * | 2005-12-28 | 2009-06-04 | わかもと製薬株式会社 | 水性医薬組成物 |
| US20100130580A1 (en) * | 2006-01-25 | 2010-05-27 | Aciex Therapeutics, Inc. | Formulations and Methods for Treating Dry Eye |
| KR20140093764A (ko) | 2006-02-09 | 2014-07-28 | 산텐 세이야꾸 가부시키가이샤 | 안정한 제제와 그 제조 및 사용 방법 |
| US7767217B2 (en) | 2006-03-14 | 2010-08-03 | Foresight Biotherapeutics | Ophthalmic compositions comprising povidone-iodine |
| ES2563288T3 (es) | 2006-03-23 | 2016-03-14 | Santen Pharmaceutical Co., Ltd | Rapamicina en dosis bajas para el tratamiento de enfermedades relacionadas con la permeabilidad vascular |
| US7758553B2 (en) * | 2006-04-03 | 2010-07-20 | Insight Vision Incorporated | Drop dispenser for the delivery of uniform droplets of viscous liquids |
| US20070249546A1 (en) * | 2006-04-22 | 2007-10-25 | Sawaya Assad S | Ophthalmic and related aqueous solutions containing antifungal agents, uses therefor and methods for preparing them |
| JP2009539866A (ja) * | 2006-06-05 | 2009-11-19 | オースペックス・ファーマシューティカルズ・インコーポレイテッド | 置換エリスロマイシンアナログの調製および有用性 |
| JP5468899B2 (ja) | 2006-07-20 | 2014-04-09 | アフィニウム ファーマシューティカルズ， インク． | Ｆａｂｉインヒビターとしてのアクリルアミド誘導体 |
| EP2089035A1 (en) * | 2006-11-02 | 2009-08-19 | Riolan Technologies, Inc. | Method for treating blepharitis |
| WO2008085913A1 (en) * | 2007-01-04 | 2008-07-17 | Rib-X Pharmaceuticals, Inc. | Methods for treating, preventing, or reducing the risk of opthalmic, otic, and nasal infections |
| EP2125802A4 (en) | 2007-02-16 | 2014-08-20 | Debiopharm Int Sa | SALTS, PRODRUGS AND POLYMORPHES OF FAB I INHIBITORS |
| US20080265343A1 (en) * | 2007-04-26 | 2008-10-30 | International Business Machines Corporation | Field effect transistor with inverted t shaped gate electrode and methods for fabrication thereof |
| KR20150036210A (ko) | 2007-06-13 | 2015-04-07 | 인사이트 코포레이션 | 야누스 키나제 억제제（Ｒ）―３―（４―（７Ｈ―피롤로［２，３－ｄ］피리미딘―4―일）―1Ｈ―피라졸―1―일）―３―사이클로펜틸프로판니트릴의 염 |
| DK2079441T3 (da) | 2007-07-25 | 2010-12-13 | Ixodes Gmbh | Topisk antibiotisk sammensætning til forebyggelse af Lyme's sygdom |
| US7795231B2 (en) * | 2007-10-04 | 2010-09-14 | Insite Vision Incorporated | Concentrated aqueous azalide formulations |
| EP2222299B1 (en) * | 2007-11-19 | 2011-11-23 | Bausch & Lomb Incorporated | Use of levocabastine for modulating generation of pro-inflammatory cytokines |
| EP2098219A1 (en) | 2008-03-05 | 2009-09-09 | PARI Pharma GmbH | Macrolide compositions having improved taste and stability |
| US8030297B2 (en) | 2008-05-14 | 2011-10-04 | Otonomy, Inc. | Controlled release corticosteroid compositions and methods for the treatment of OTIC disorders |
| US9006210B2 (en) * | 2008-06-13 | 2015-04-14 | Case Western Reserve University | Compositions and methods for treating corneal inflammation |
| EP2310008A4 (en) * | 2008-07-09 | 2014-03-05 | Aspreva Internat Ltd | MYCOPHENOLIC SODIUM ACID SOLUTIONS WITH PH SPECIFIC FOR THE TREATMENT OF OCULAR DISORDERS |
| JP2011527709A (ja) | 2008-07-10 | 2011-11-04 | インスパイアー ファーマシューティカルズ，インコーポレイティド | 眼瞼炎の治療方法 |
| US8318817B2 (en) | 2008-07-21 | 2012-11-27 | Otonomy, Inc. | Controlled release antimicrobial compositions and methods for the treatment of otic disorders |
| CL2009001884A1 (es) * | 2008-10-02 | 2010-05-14 | Incyte Holdings Corp | Uso de 3-ciclopentil-3-[4-(7h-pirrolo[2,3-d]pirimidin-4-il)-1h-pirazol-1-il)propanonitrilo, inhibidor de janus quinasa, y uso de una composición que lo comprende para el tratamiento del ojo seco. |
| US20100158821A1 (en) * | 2008-12-22 | 2010-06-24 | Eastman Chemical Company | Antimicrobial agents, compositions and products containing the same, and methods of using the compositions and products |
| EP2393355A4 (en) * | 2009-01-23 | 2012-07-25 | Inspire Pharmaceuticals Inc | METHOD FOR TREATING A DRY EYE WITH AZITHROMYCIN |
| US10201548B2 (en) * | 2009-03-06 | 2019-02-12 | Sun Pharma Global Fze | Methods for treating ocular inflammatory diseases |
| US20170128481A9 (en) * | 2009-03-06 | 2017-05-11 | Insite Vision Corporation | Ocular treatment with reduced intraocular pressure |
| US10980818B2 (en) * | 2009-03-06 | 2021-04-20 | Sun Pharma Global Fze | Methods for treating ocular inflammatory diseases |
| US20120114637A1 (en) * | 2009-05-04 | 2012-05-10 | Santen Pharmaceutical Co., Ltd. | Mtor pathway inhibitors for treating ocular disorders |
| US8106111B2 (en) * | 2009-05-15 | 2012-01-31 | Eastman Chemical Company | Antimicrobial effect of cycloaliphatic diol antimicrobial agents in coating compositions |
| AR076794A1 (es) | 2009-05-22 | 2011-07-06 | Incyte Corp | Derivados de n-(hetero)aril-pirrolidina de pirazol-4-il-pirrolo [2,3-d]pirimidinas y pirrol-3-il-pirrolo [2,3-d ]pirimidinas como inhibidores de la quinasa janus y composiciones farmaceuticas que los contienen |
| SI2432472T1 (sl) * | 2009-05-22 | 2019-11-29 | Incyte Holdings Corp | 3-(4-(7H-pirolo(2,3-d)pirimidin-4-il)-1H-pirazol-1-il)oktan- ali heptan-nitril kot inhibitorji JAK |
| TW201113285A (en) * | 2009-09-01 | 2011-04-16 | Incyte Corp | Heterocyclic derivatives of pyrazol-4-yl-pyrrolo[2,3-d]pyrimidines as janus kinase inhibitors |
| EP2490722A4 (en) * | 2009-10-21 | 2014-03-05 | Otonomy Inc | MODULATION OF THE TEMPERATURE OF GELIFICATION OF FORMULATIONS CONTAINING POLOXAMERS |
| ES2758554T3 (es) | 2009-12-08 | 2020-05-05 | Univ Case Western Reserve | Aminoácidos gama para tratamiento de trastornos oculares |
| EP3354652B1 (en) | 2010-03-10 | 2020-05-06 | Incyte Holdings Corporation | Piperidin-4-yl azetidine derivatives as jak1 inhibitors |
| PL2547323T3 (pl) | 2010-03-17 | 2016-07-29 | Novaliq Gmbh | Kompozycja farmaceutyczna do leczenia podwyższonego ciśnienia wewnątrzgałkowego |
| PE20130216A1 (es) | 2010-05-21 | 2013-02-27 | Incyte Corp | Formulacion topica para un inhibidor de jak |
| USD640554S1 (en) | 2010-06-30 | 2011-06-28 | Inspire Pharmaceuticals, Inc. | Medicine dispenser |
| EP2444063A1 (en) | 2010-10-20 | 2012-04-25 | Novaliq GmbH | Liquid pharmaceutical compositions for the delivery of active ingredients |
| EP2462921A1 (en) | 2010-11-11 | 2012-06-13 | Novaliq GmbH | Liquid pharmaceutical compositions for the treatment of a posterior eye disease |
| US9034884B2 (en) | 2010-11-19 | 2015-05-19 | Incyte Corporation | Heterocyclic-substituted pyrrolopyridines and pyrrolopyrimidines as JAK inhibitors |
| PE20140146A1 (es) | 2010-11-19 | 2014-02-06 | Incyte Corp | Derivados de pirrolopiridina y pirrolopirimidina sustituidos con ciclobutilo como inhibidores de jak |
| JP6023181B2 (ja) | 2011-05-25 | 2016-11-09 | ノバリック ゲーエムベーハー | 爪に投与するための医薬組成物 |
| DK2714010T3 (en) | 2011-05-25 | 2017-06-12 | Novaliq Gmbh | TOPICAL PHARMACEUTICAL COMPOSITION BASED ON SEMIFLUORED ALKANES |
| CN103797010B (zh) | 2011-06-20 | 2016-02-24 | 因塞特控股公司 | 作为jak抑制剂的氮杂环丁烷基苯基、吡啶基或吡嗪基甲酰胺衍生物 |
| CA2840626A1 (en) * | 2011-06-29 | 2013-01-03 | Insite Vision Incorporated | Methods of treating recurrent meibomian glands disorder and thereby decreasing the frequency of recurrence |
| CN102352058B (zh) * | 2011-08-04 | 2013-04-24 | 华南农业大学 | 稳定水溶性纤维素水凝胶粘度的复合添加剂及应用 |
| TW201313721A (zh) | 2011-08-18 | 2013-04-01 | Incyte Corp | 作為ｊａｋ抑制劑之環己基氮雜環丁烷衍生物 |
| UA111854C2 (uk) | 2011-09-07 | 2016-06-24 | Інсайт Холдінгс Корпорейшн | Способи і проміжні сполуки для отримання інгібіторів jak |
| WO2013065029A1 (en) * | 2011-11-04 | 2013-05-10 | Micro Labs Limited | Fixed dose combination containing moxifloxacin and prednisolone for treatment of ocular infections |
| KR101989648B1 (ko) | 2012-01-23 | 2019-06-14 | 노바리크 게엠베하 | 부분불소화 알칸에 기초한 안정화된 단백질 조성물 |
| TW201406761A (zh) | 2012-05-18 | 2014-02-16 | Incyte Corp | 做爲ｊａｋ抑制劑之哌啶基環丁基取代之吡咯并吡啶及吡咯并嘧啶衍生物 |
| AU2013279021C1 (en) | 2012-06-19 | 2017-03-16 | Debiopharm International Sa | Prodrug derivatives of (E)-N-methyl-N-((3-methylbenzofuran-2-yl)methyl)-3-(7-oxo-5,6,7,8-tetrahydro-1,8-naphthyridin-3-yl)acrylamide |
| KR20140009819A (ko) * | 2012-07-13 | 2014-01-23 | 주식회사유한양행 | 반코마이신 또는 그의 염 및 덱사메타손 포스페이트 또는 그의 염을 포함하는 국소투여용 약학 조성물 |
| AU2013314303B2 (en) | 2012-09-12 | 2018-01-18 | Novaliq Gmbh | Semifluorinated alkane compositions |
| CN113679699B (zh) | 2012-09-12 | 2022-10-28 | 诺瓦利克有限责任公司 | 包含半氟化烷烃的混合物的组合物 |
| PH12020551186B1 (en) | 2012-11-15 | 2024-03-20 | Incyte Holdings Corp | Sustained-release dosage forms of ruxolitinib |
| RS62867B1 (sr) | 2013-03-06 | 2022-02-28 | Incyte Holdings Corp | Postupci i intermedijeri za dobijanje inhibitora jak |
| WO2014152661A1 (en) | 2013-03-14 | 2014-09-25 | Panoptica, Inc. | Ocular formulations for drug-delivery to the posterior segment of the eye |
| US9044508B2 (en) | 2013-03-15 | 2015-06-02 | Insite Vision Corporation | Concentrated aqueous azalide formulations |
| WO2014160579A1 (en) * | 2013-03-25 | 2014-10-02 | Insite Vision Incorporated | Combination anti-inflammatory ophthalmic compositions |
| PT3024484T (pt) | 2013-07-23 | 2018-10-24 | Novaliq Gmbh | Composições de anticorpo estabilizadas |
| SMT202000315T1 (it) | 2013-08-07 | 2020-07-08 | Incyte Corp | Forme di dosaggio a rilascio prolungato per un inibitore di jak1 |
| JP2016534121A (ja) | 2013-08-27 | 2016-11-04 | オトノミ—，インク． | 小児の耳の病気の処置 |
| US9498467B2 (en) | 2014-05-30 | 2016-11-22 | Incyte Corporation | Treatment of chronic neutrophilic leukemia (CNL) and atypical chronic myeloid leukemia (aCML) by inhibitors of JAK1 |
| GB2541840B (en) | 2014-06-20 | 2017-09-06 | Coopervision Int Holding Co Lp | Ophthalmic composition for the treatment of ocular infection |
| US9241971B1 (en) | 2014-07-18 | 2016-01-26 | Kurobe, Llc | Topical vancomycin formulation and methods of use |
| RU2580631C1 (ru) * | 2015-03-19 | 2016-04-10 | Общество с ограниченной ответственностью "Научно-внедренческий центр Агроветзащита" | Антибактериальное лекарственное средство в форме мази для лечения глазных болезней у животных |
| US11154513B2 (en) | 2015-09-30 | 2021-10-26 | Novaliq Gmbh | Semifluorinated compounds |
| CN110403923B (zh) | 2015-09-30 | 2021-09-21 | 诺瓦利克有限责任公司 | 半氟化化合物和其组合物 |
| RU2610408C1 (ru) * | 2016-01-11 | 2017-02-09 | Акционерное общество "Екатеринбургский центр МНТК "Микрохирургия глаза" | Способ лечения острых бактериальных послеоперационных эндофтальмитов |
| RS61312B1 (sr) | 2016-02-26 | 2021-02-26 | Debiopharm Int Sa | Lek za lečenje infekcija dijabetskog stopala |
| PT3442480T (pt) | 2016-06-23 | 2019-12-23 | Novaliq Gmbh | Método de administração tópica |
| CN109789125B (zh) | 2016-08-16 | 2022-10-18 | 罗切斯特大学 | 含有基于多粘菌素b/甲氧苄啶的治疗剂的药物组合物 |
| CA3036297C (en) | 2016-09-22 | 2023-09-05 | Novaliq Gmbh | Pharmaceutical compositions for use in the therapy of blepharitis |
| WO2018055101A1 (en) | 2016-09-23 | 2018-03-29 | Novaliq Gmbh | Ophthalmic compositions comprising ciclosporin |
| EP4374851B1 (en) | 2016-12-23 | 2026-04-15 | Novaliq GmbH | Ophthalmic composition for treatment of dry eye disease |
| EP3576755A4 (en) | 2017-02-02 | 2020-12-02 | McMaster University | BICARBONATE AS A POTENTIALIZER OF ANTIMICROBIAL AGENTS |
| CA3058097C (en) | 2017-04-21 | 2024-01-02 | Novaliq Gmbh | Iodine compositions |
| US11278503B2 (en) | 2017-05-12 | 2022-03-22 | Novaliq Gmbh | Pharmaceutical compositions comprising semifluorinated alkanes for the treatment of contact lense-related conditions |
| WO2018213389A1 (en) * | 2017-05-17 | 2018-11-22 | Nextcea Inc. | Inducing phospholipidosis for enhancing therapeutic efficacy |
| WO2018215638A1 (en) | 2017-05-26 | 2018-11-29 | Novaliq Gmbh | Pharmaceutical compositions comprising azithromycin |
| MX2020003534A (es) | 2017-09-27 | 2020-07-29 | Novaliq Gmbh | Composiciones oftalmicas que comprenden latanoprost para usarse en el tratamiento de las enfermedades oculares. |
| WO2019068763A1 (en) | 2017-10-04 | 2019-04-11 | Novaliq Gmbh | OPHTHALMIC COMPOSITIONS COMPRISING F6H8 |
| WO2019113487A1 (en) | 2017-12-08 | 2019-06-13 | Incyte Corporation | Low dose combination therapy for treatment of myeloproliferative neoplasms |
| SG11202007164UA (en) | 2018-01-30 | 2020-08-28 | Incyte Corp | Processes for preparing (1 -(3-fluoro-2-(trifluoromethyl)isonicotinyl)piperidine-4-one) |
| KR20200128407A (ko) | 2018-03-02 | 2020-11-12 | 노바리크 게엠베하 | 네비볼롤을 포함하는 약제학적 조성물 |
| SG11202007860XA (en) | 2018-03-28 | 2020-09-29 | Novaliq Gmbh | Pharmaceutical composition comprising timolol |
| SMT202400306T1 (it) | 2018-03-30 | 2024-09-16 | Incyte Corp | Trattamento dell'idrosadenite suppurativa utilizzando inibitori di jak. |
| CN112153970A (zh) | 2018-04-27 | 2020-12-29 | 诺瓦利克有限责任公司 | 用于治疗青光眼的包含他氟前列素的眼用组合物 |
| EP3829640A4 (en) | 2018-08-01 | 2022-05-25 | McMaster University | Methods for inhibiting microbe growth |
| AU2019343188A1 (en) * | 2018-09-21 | 2021-05-20 | Aufbau Medical Innovations Limited | Compositions and methods for glaucoma |
| SG11202102820VA (en) | 2018-10-12 | 2021-04-29 | Novaliq Gmbh | Ophthalmic composition for treatment of dry eye disease |
| EP3923907B1 (en) | 2019-02-13 | 2024-09-25 | Novaliq GmbH | Compositions and methods for the treatment of ocular neovascularization |
| TN2021000159A1 (en) | 2019-02-14 | 2023-04-04 | Debiopharm Int Sa | Afabicin formulation, method for making the same and uses thereof |
| JP7700045B2 (ja) | 2019-04-18 | 2025-06-30 | アズーラ オフサルミックス エルティーディー． | 眼障害を処置するための化合物および方法 |
| EP3955937A4 (en) | 2019-04-18 | 2023-01-18 | Azura Ophthalmics Ltd. | COMPOUNDS AND COMPOSITIONS FOR THE TREATMENT OF EYE DISEASES |
| JP7696697B2 (ja) * | 2019-06-13 | 2025-06-23 | 千寿製薬株式会社 | アジスロマイシン含有眼科用剤 |
| SG11202113174SA (en) | 2019-06-14 | 2021-12-30 | Debiopharm Int Sa | Medicament and use thereof for treating bacterial infections involving biofilm |
| KR20220058577A (ko) | 2019-09-06 | 2022-05-09 | 노바리크 게엠베하 | 포도막염 치료를 위한 안과용 조성물 |
| US11833155B2 (en) | 2020-06-03 | 2023-12-05 | Incyte Corporation | Combination therapy for treatment of myeloproliferative neoplasms |
| US20220160668A1 (en) * | 2020-11-23 | 2022-05-26 | Sight Sciences, Inc. | Formulations and methods for treating conditions of the eye |
| US11459351B1 (en) | 2021-04-05 | 2022-10-04 | Azura Ophthalmics Ltd. | Compounds and methods for the treatment of ocular disorders |
| WO2024216070A1 (en) | 2023-04-14 | 2024-10-17 | University Of Rochester | Combinatorial pharmaceutical compositions for treatment of bacterial infections |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4512982A (en) * | 1984-04-13 | 1985-04-23 | Pfizer Inc. | 9α-Aza-9α-homoerythromycin compounds, pharmaceutical composition and therapeutic method |
| WO1995009601A1 (en) * | 1993-10-01 | 1995-04-13 | The Procter & Gamble Company | Use of azithromycin for the treatment of adult periodontitis and topical compositions for this use |
Family Cites Families (47)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SI8110592A8 (en) | 1981-03-06 | 1996-06-30 | Pliva Pharm & Chem Works | Process for preparing of n-methyl-11-aza-10-deoxo-10-dihydroerythromycine a and derivatives thereof |
| US4474768A (en) | 1982-07-19 | 1984-10-02 | Pfizer Inc. | N-Methyl 11-aza-10-deoxo-10-dihydro-erytromycin A, intermediates therefor |
| CA1224148A (en) | 1983-05-16 | 1987-07-14 | John L. Haslam | Drug delivery system utilizing thermosetting gels |
| US4551456A (en) | 1983-11-14 | 1985-11-05 | Merck & Co., Inc. | Ophthalmic use of norfloxacin and related antibiotics |
| US4692454A (en) | 1986-02-03 | 1987-09-08 | Warner-Lambert Company | Opthalmic use of quinolone antibiotics |
| WO1989000576A1 (en) | 1987-07-09 | 1989-01-26 | Pfizer Inc. | Azithromycin dihydrate |
| KR920003601B1 (ko) | 1987-09-03 | 1992-05-04 | 유니버시티 어브 죠지아 리서취 화운데이션 인코포레이티드 | 점안 싸이클로스포린(cyclosporin)의 조성물 |
| US5807830A (en) | 1987-12-30 | 1998-09-15 | Cytoven J.V. | Method for treatment of purulent inflammatory diseases |
| US5192535A (en) | 1988-02-08 | 1993-03-09 | Insite Vision Incorporated | Ophthalmic suspensions |
| US5188826A (en) | 1988-02-08 | 1993-02-23 | Insite Vision Incorporated | Topical ophthalmic suspensions |
| YU45590A (sh) | 1990-03-07 | 1992-07-20 | PLIVA FARMACEVTSKA, KEMIJSKA, PREHRAMBENA I KOZMETIČKA INDUSTRIJA s.p.o. | Novi kompleksi odnosno helati antibiotika s dvovalentnim i/ili trovalentnim metalima i postupci za njihovo dobijanje |
| US5124154A (en) | 1990-06-12 | 1992-06-23 | Insite Vision Incorporated | Aminosteroids for ophthalmic use |
| SI9011409A (en) | 1990-07-18 | 1995-10-31 | Pliva Pharm & Chem Works | O-methyl azitromycin derivates, methods and intermediates for their preparation and methods for preparation of pharmaceuticals products which comprise them |
| US5912331A (en) | 1991-03-15 | 1999-06-15 | Merck & Co., Inc. | Process for the preparation of 9-deoxo-9(Z)-hydroxyiminoerythromycin A |
| US5225399A (en) | 1991-04-15 | 1993-07-06 | The Children's Hospital Of Philadelphia | Antimicrobial amphiphilic peptides |
| US5239059A (en) | 1991-05-10 | 1993-08-24 | The Children's Hospital Of Philadelphia | Ion-channel forming peptides |
| JP2880338B2 (ja) * | 1991-10-25 | 1999-04-05 | 株式会社森組 | 圧搾気体による被移送物の圧送方式 |
| ES2079994B1 (es) * | 1992-10-07 | 1996-08-01 | Cusi Lab | Formulacion farmaceutica a base de polimixina-trimetoprim y un agente antiinflamatorio para su utilizacion topica oftalmica y otica. |
| US5424290A (en) | 1992-10-26 | 1995-06-13 | Magainin Pharmaceuticals Inc. | Biologically active peptides and uses therefor |
| US5340572A (en) | 1993-02-08 | 1994-08-23 | Insite Vision Incorporated | Alkaline ophthalmic suspensions |
| US5804558A (en) | 1993-07-20 | 1998-09-08 | University Of California | Protegrins |
| US5631004A (en) | 1993-09-30 | 1997-05-20 | Alcon Laboratories, Inc. | Use of sustained release antibiotic compositions in ophthalmic surgical procedures |
| ATE219684T1 (de) | 1994-01-14 | 2002-07-15 | Xoma Technology Ltd | Anti gram positive bakterielle verfahren und mittel |
| US5441939A (en) | 1994-03-04 | 1995-08-15 | Pfizer Inc. | 3"-desmethoxy derivatives of erythromycin and azithromycin |
| US5610198A (en) | 1994-03-18 | 1997-03-11 | The United States Of America As Represented By The Department Of Health And Human Services | Anti-mycobacterial compositions and their use for the treatment of tuberculosis and related diseases |
| HRP940251B1 (en) | 1994-04-15 | 1998-12-31 | Stjepan Mutak | Process for the preparation of azithromycin dihydrochloride |
| US5605889A (en) | 1994-04-29 | 1997-02-25 | Pfizer Inc. | Method of administering azithromycin |
| ES2079320B1 (es) * | 1994-05-17 | 1996-10-16 | Cusi Lab | Disolucion oftalmica a base de un diclofenaco y tobramicina y sus aplicaciones. |
| US6309630B1 (en) | 1994-05-24 | 2001-10-30 | Insite Vision Incorporated | Non-steroidal anti-inflammatory ophthalmic suspensions |
| AU4399396A (en) | 1994-12-19 | 1996-07-10 | Russinsky Limited | Compounds |
| US5872104A (en) | 1994-12-27 | 1999-02-16 | Oridigm Corporation | Combinations and methods for reducing antimicrobial resistance |
| US5747058A (en) | 1995-06-07 | 1998-05-05 | Southern Biosystems, Inc. | High viscosity liquid controlled delivery system |
| US5767153A (en) | 1995-06-07 | 1998-06-16 | Insite Vision Incorporated | Sustained release emulsions |
| EP1006935B1 (en) | 1995-06-07 | 2005-01-26 | Southern Biosystems, Inc. | High viscosity liquid controlled delivery system |
| US5888973A (en) | 1996-08-09 | 1999-03-30 | Xoma Corporation | Anti-chlamydial uses of BPI protein products |
| GB9621771D0 (en) | 1996-10-18 | 1996-12-11 | St George S Enterprises Ltd | Method of treatment of heart disease |
| US5814655A (en) | 1996-11-14 | 1998-09-29 | Insite Vision Incorporated | Non-steroidal ophthalmic mixtures |
| PT102006B (pt) | 1997-05-19 | 2000-06-30 | Hovione Sociedade Quimica S A | Novo processo de preparacao de azitromicina |
| US6265444B1 (en) | 1997-05-23 | 2001-07-24 | Insite Vision Incorporated | Ophthalmic composition |
| US6159458A (en) | 1997-11-04 | 2000-12-12 | Insite Vision | Sustained release ophthalmic compositions containing water soluble medicaments |
| EP0925789B2 (en) * | 1997-12-02 | 2009-06-17 | Pfizer Products Inc. | Use of azithromycin in the topical treatment of ocular infections |
| US6861411B1 (en) | 1997-12-02 | 2005-03-01 | Pfizer, Inc. | Method of treating eye infections with azithromycin |
| US6378526B1 (en) | 1998-08-03 | 2002-04-30 | Insite Vision, Incorporated | Methods of ophthalmic administration |
| US6239113B1 (en) | 1999-03-31 | 2001-05-29 | Insite Vision, Incorporated | Topical treatment or prevention of ocular infections |
| US7056893B2 (en) | 1999-03-31 | 2006-06-06 | Insite Vision, Inc. | Topical treatment for prevention of ocular infections |
| IT1313610B1 (it) * | 1999-08-09 | 2002-09-09 | S I F I Societa Ind Farmaceuti | Processo per la preparazione di formulazioni acquose per uso oftalmico |
| AU2002317415A1 (en) | 2001-08-01 | 2003-02-17 | Pfizer Products Inc. | Azalide antibiotic compositions |
-
1999
- 1999-07-02 US US09/346,923 patent/US6239113B1/en not_active Expired - Lifetime
-
2000
- 2000-03-27 DK DK00918382T patent/DK1165058T3/da active
- 2000-03-27 PT PT00918382T patent/PT1165058E/pt unknown
- 2000-03-27 AT AT00918382T patent/ATE296093T1/de active
- 2000-03-27 JP JP2000607617A patent/JP4904621B2/ja not_active Expired - Lifetime
- 2000-03-27 KR KR1020017012268A patent/KR100701721B1/ko not_active Expired - Lifetime
- 2000-03-27 CA CA2368637A patent/CA2368637C/en not_active Expired - Lifetime
- 2000-03-27 DE DE60020351T patent/DE60020351T2/de not_active Expired - Lifetime
- 2000-03-27 WO PCT/US2000/007924 patent/WO2000057866A2/en not_active Ceased
- 2000-03-27 DE DE1165058T patent/DE1165058T1/de active Pending
- 2000-03-27 ES ES00918382T patent/ES2244421T3/es not_active Expired - Lifetime
- 2000-03-27 MX MXPA01009718A patent/MXPA01009718A/es active IP Right Grant
- 2000-03-27 EP EP00918382A patent/EP1165058B1/en not_active Expired - Lifetime
- 2000-03-27 AU AU39203/00A patent/AU772228B2/en not_active Expired
- 2000-03-27 EP EP05011127A patent/EP1588702A1/en not_active Withdrawn
- 2000-03-27 HK HK02103311.4A patent/HK1041642B/en not_active IP Right Cessation
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2001
- 2001-01-24 US US09/767,943 patent/US6569443B1/en not_active Expired - Lifetime
-
2003
- 2003-04-07 US US10/407,425 patent/US7749970B2/en not_active Expired - Fee Related
-
2004
- 2004-07-26 US US10/898,170 patent/US7732415B2/en not_active Expired - Fee Related
-
2005
- 2005-08-24 CY CY20051101022T patent/CY1107259T1/el unknown
-
2007
- 2007-05-08 US US11/801,345 patent/US20080161250A1/en not_active Abandoned
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4512982A (en) * | 1984-04-13 | 1985-04-23 | Pfizer Inc. | 9α-Aza-9α-homoerythromycin compounds, pharmaceutical composition and therapeutic method |
| WO1995009601A1 (en) * | 1993-10-01 | 1995-04-13 | The Procter & Gamble Company | Use of azithromycin for the treatment of adult periodontitis and topical compositions for this use |
Non-Patent Citations (1)
| Title |
|---|
| DAWSON C R ET AL CLIN. INFEC. DISEASES (1997)VOL.24 PP 363-8 * |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2000057866A2 (en) | 2000-10-05 |
| KR20020005634A (ko) | 2002-01-17 |
| US20080161250A1 (en) | 2008-07-03 |
| JP4904621B2 (ja) | 2012-03-28 |
| EP1588702A1 (en) | 2005-10-26 |
| CY1107259T1 (el) | 2012-11-21 |
| PT1165058E (pt) | 2005-10-31 |
| US6569443B1 (en) | 2003-05-27 |
| DE1165058T1 (de) | 2002-10-02 |
| HK1041642A1 (en) | 2002-07-19 |
| ES2244421T3 (es) | 2005-12-16 |
| KR100701721B1 (ko) | 2007-03-29 |
| DE60020351T2 (de) | 2006-01-26 |
| US7749970B2 (en) | 2010-07-06 |
| DK1165058T3 (da) | 2005-09-19 |
| US7732415B2 (en) | 2010-06-08 |
| MXPA01009718A (es) | 2002-08-12 |
| EP1165058A2 (en) | 2002-01-02 |
| US20030206956A1 (en) | 2003-11-06 |
| EP1165058B1 (en) | 2005-05-25 |
| ATE296093T1 (de) | 2005-06-15 |
| JP2002540147A (ja) | 2002-11-26 |
| US20040266702A1 (en) | 2004-12-30 |
| CA2368637C (en) | 2011-01-18 |
| AU3920300A (en) | 2000-10-16 |
| DE60020351D1 (de) | 2005-06-30 |
| US6239113B1 (en) | 2001-05-29 |
| WO2000057866A3 (en) | 2001-08-16 |
| CA2368637A1 (en) | 2000-10-05 |
| HK1041642B (en) | 2005-12-23 |
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