IN2015DN00847A - - Google Patents

Info

Publication number
IN2015DN00847A
IN2015DN00847A IN847DEN2015A IN2015DN00847A IN 2015DN00847 A IN2015DN00847 A IN 2015DN00847A IN 847DEN2015 A IN847DEN2015 A IN 847DEN2015A IN 2015DN00847 A IN2015DN00847 A IN 2015DN00847A
Authority
IN
India
Prior art keywords
disclosed
lfa
polymorph
formulations
purification
Prior art date
Application number
Other languages
English (en)
Inventor
James Robert Zeller
Sripathy Venkatraman
Elisabeth C A Brot
Subashree Iyer
Michael Hall
Original Assignee
Sarcode Bioscience Inc
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=49995472&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=IN2015DN00847(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Sarcode Bioscience Inc filed Critical Sarcode Bioscience Inc
Publication of IN2015DN00847A publication Critical patent/IN2015DN00847A/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/10Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing aromatic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D407/00Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
    • C07D407/02Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings
    • C07D407/06Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • 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
    • A61K31/47Quinolines; Isoquinolines
    • A61K31/472Non-condensed isoquinolines, e.g. papaverine
    • A61K31/4725Non-condensed isoquinolines, e.g. papaverine containing further heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/14Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • 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
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • 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
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/06Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/13Crystalline forms, e.g. polymorphs
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B63/00Purification; Separation; Stabilisation; Use of additives

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Epidemiology (AREA)
  • Immunology (AREA)
  • Ophthalmology & Optometry (AREA)
  • Rheumatology (AREA)
  • Pain & Pain Management (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
IN847DEN2015 2012-07-25 2013-07-25 IN2015DN00847A (fr)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US201261675663P 2012-07-25 2012-07-25
US201261680099P 2012-08-06 2012-08-06
US201261729294P 2012-11-21 2012-11-21
PCT/US2013/052044 WO2014018748A1 (fr) 2012-07-25 2013-07-25 Inhibiteur de lfa-1 et polymorphe de celui-ci

Publications (1)

Publication Number Publication Date
IN2015DN00847A true IN2015DN00847A (fr) 2015-06-12

Family

ID=49995472

Family Applications (1)

Application Number Title Priority Date Filing Date
IN847DEN2015 IN2015DN00847A (fr) 2012-07-25 2013-07-25

Country Status (14)

Country Link
US (4) US9085553B2 (fr)
EP (3) EP3715345B8 (fr)
JP (3) JP6607780B2 (fr)
KR (2) KR20200108932A (fr)
CN (2) CN104797574B (fr)
AU (5) AU2013295706A1 (fr)
BR (1) BR112015001608B1 (fr)
CA (1) CA2879982C (fr)
HK (1) HK1210782A1 (fr)
IN (1) IN2015DN00847A (fr)
MX (2) MX2015001098A (fr)
RU (1) RU2658015C2 (fr)
SI (1) SI3715345T1 (fr)
WO (1) WO2014018748A1 (fr)

Families Citing this family (57)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8168655B2 (en) * 2005-05-17 2012-05-01 Sarcode Bioscience Inc. Compositions and methods for treatment of eye disorders
ES2763703T3 (es) * 2008-04-15 2020-05-29 Sarcode Bioscience Inc Antagonistas de LFA-1 tópicos utilizados en el tratamiento localizado de trastornos inmunes
SI3715345T1 (sl) * 2012-07-25 2024-07-31 Bausch + Lomb Ireland Limited Priprava zaviralca lfa-1
AU2015320349B2 (en) * 2014-09-25 2020-03-12 Bausch + Lomb Ireland Limited Continuous flow carboxylation reaction
KR101984116B1 (ko) 2015-01-12 2019-05-31 켄달리온 테라퓨틱스 인코포레이티드 마이크로-액적 전달 장치 및 방법
WO2017070561A1 (fr) 2015-10-23 2017-04-27 Pfizer Inc. Anticorps anti-il-2, compositions les contenant et leurs utilisations
JP2019507193A (ja) 2016-03-04 2019-03-14 ジェームズ・エム・ライナーソン 細菌のバイオフィルム形成を阻止又は妨害することによって眼障害を治療する方法
US11013736B2 (en) * 2016-07-29 2021-05-25 Wuhan Ll Science And Technology Development Co., Ltd. Oral solid preparation and use thereof
AU2017310520A1 (en) 2016-08-12 2019-03-21 Silk Technologies, Ltd. Silk-derived protein for treating inflammation
CN108084067B (zh) * 2016-11-22 2019-08-30 重庆圣华曦药业股份有限公司 一种立他司特中间体的制备方法
CA3039106A1 (fr) 2017-01-20 2018-07-26 Kedalion Therapeutics, Inc. Distributeur de fluide piezoelectrique
CN106947792A (zh) * 2017-03-07 2017-07-14 上海倍殊生物科技有限公司 一种间甲砜基‑l‑苯丙氨酸的制备方法
CA3068522A1 (fr) * 2017-06-30 2019-01-03 Scinopharm Taiwan, Ltd. Procede pour la preparation de lifitegrast et d'intermediaires de celui-ci
ES2876292T3 (es) 2017-07-24 2021-11-12 Interquim Sa Procedimiento de preparación y purificación del antagonista de LFA-1 lifitegrast
WO2019026014A1 (fr) * 2017-08-03 2019-02-07 Dr. Reddy's Laboratories Limited Procédés de préparation de lifitegrast et de ses intermédiaires
WO2019053607A1 (fr) * 2017-09-18 2019-03-21 Glenmark Pharmaceuticals Limited Procédé de préparation de lifitegrast
KR102716461B1 (ko) * 2017-10-10 2024-10-11 맨카인드 파마 리미티드 리피테그라스트의 신규 제조 방법
WO2019097547A1 (fr) * 2017-11-15 2019-05-23 Cipla Limited Procédé amélioré pour la préparation de lifitegrast ou de sels de celui-ci
US11001574B2 (en) 2017-11-17 2021-05-11 Medichem S.A. Process to obtain a tetrahydroisoquinoline derivative
JP7436363B2 (ja) 2017-12-08 2024-02-21 ノバルティス アーゲー 流体送達アライメントシステム
WO2019138025A1 (fr) 2018-01-15 2019-07-18 Cognibotics Ab Bras de robot industriel
US10435395B1 (en) 2018-03-30 2019-10-08 Scinopharm Taiwan, Ltd. Crystal forms of lifitegrast
US11345683B2 (en) * 2018-03-31 2022-05-31 Aurobindo Pharma Ltd Process for the preparation of lifitegrast
US12350194B1 (en) 2018-04-12 2025-07-08 Bausch + Lomb Ireland Limited Topical ocular delivery of fluids with controlled mass dosing and wireless communication
US20190314197A1 (en) 2018-04-12 2019-10-17 Kedalion Therapeutics, Inc. Topical Ocular Delivery Methods and Devices for Use in the Same
IT201800006337A1 (it) * 2018-06-14 2019-12-14 Procedimento per la preparazione di lifitegrast
CA3102410A1 (fr) 2018-07-03 2020-01-09 Kedalion Therapeutics, Inc. Dispositifs d'administration oculaire topique et leurs procedes d'utilisation
CN111100118A (zh) * 2018-10-29 2020-05-05 重庆圣华曦药业股份有限公司 一种立他司特杂质及其制备方法
CN109384717A (zh) * 2018-10-29 2019-02-26 广安凯特制药有限公司 5,7-二氯-1,2,3,4-四氢异喹啉-6-甲酸盐酸盐水合物及其制备方法和用途
CN111285855A (zh) * 2018-12-07 2020-06-16 苏州旺山旺水生物医药有限公司 一种制备化合物Lifitegrast的方法
CN111471003B (zh) * 2019-01-24 2022-09-23 上海皓元医药股份有限公司 一种立他司特中间体的制备方法
US12097145B2 (en) 2019-03-06 2024-09-24 Bausch + Lomb Ireland Limited Vented multi-dose ocular fluid delivery system
US11679028B2 (en) 2019-03-06 2023-06-20 Novartis Ag Multi-dose ocular fluid delivery system
EP3955926A4 (fr) 2019-04-18 2022-11-30 Azura Ophthalmics Ltd. Composés et procédés pour le traitement de troubles oculaires
CN110256343A (zh) * 2019-05-28 2019-09-20 苏州芝宇生物科技有限公司 3,5-二氯-4-溴异喹啉衍生物及其制备方法和应用
CN112409256B (zh) * 2019-08-21 2024-04-02 山东福长药业有限公司 5,7-二氯四氢异喹啉缩醛胺类化合物、其制备方法与应用
US12496218B1 (en) 2019-11-12 2025-12-16 Bausch + Lomb Ireland Limited Fractionated topical ocular drug delivery methods and devices for use in the same
WO2021141672A2 (fr) 2019-11-15 2021-07-15 Silk Technologies, Ltd. Formulations stables de protéine dérivée de la soie
CN111057003A (zh) * 2019-12-06 2020-04-24 广安凯特制药有限公司 一种立他司特中间体5,7-二氯-1,2,3,4-四氢异喹啉的合成方法
US12290472B2 (en) 2020-04-17 2025-05-06 Bausch + Lomb Ireland Limited Hydrodynamically actuated preservative free dispensing system
WO2021212038A1 (fr) 2020-04-17 2021-10-21 Kedalion Therapeutics, Inc. Système de distribution sans conservateur à actionnement hydrodynamique comprenant un réservoir de liquide pliable
US11938057B2 (en) 2020-04-17 2024-03-26 Bausch + Lomb Ireland Limited Hydrodynamically actuated preservative free dispensing system
JP7711090B2 (ja) 2020-04-17 2025-07-22 ボシュ + ロム アイルランド リミテッド 流体力学的に起動される防腐剤無添加分注システム
CN111205275A (zh) * 2020-04-22 2020-05-29 南京佰麦生物技术有限公司 立他司特晶型及其制备方法
CN112321506B (zh) * 2020-11-26 2021-12-24 江西天戌药业有限公司 一种5,7-二氯-1,2,3,4-四氢异喹啉的制备方法
CN112500343B (zh) * 2020-12-26 2023-04-07 山东金城柯瑞化学有限公司 5,7-二氯-1,2,3,4-四氢异喹啉盐酸盐的合成方法
CN112300139A (zh) * 2020-12-29 2021-02-02 南京佰麦生物技术有限公司 立他司特水合物晶型及其制备方法
US11459351B1 (en) 2021-04-05 2022-10-04 Azura Ophthalmics Ltd. Compounds and methods for the treatment of ocular disorders
CN119060022A (zh) * 2021-09-18 2024-12-03 浙江大学医学院附属第一医院 立他司特的制备方法及其中间体化合物
CN116063286A (zh) * 2021-10-29 2023-05-05 威智医药有限公司 一种立他司特及其中间体的制备方法
CN114524767B (zh) * 2022-03-11 2022-10-18 成都道合尔医药技术有限公司 立他司特中间体5,7-二氯-1,2,3,4-四氢异喹啉盐酸盐的合成方法
CN117186150B (zh) * 2022-05-30 2026-04-17 维眸生物科技(浙江)股份有限公司 一种lfa-1抑制剂的制备方法
CN115784950B (zh) * 2022-12-08 2024-06-28 广东先强药业有限公司 一种立他司特中间体的制备方法
CN116239532B (zh) * 2022-12-19 2023-11-07 浙江博崤生物制药有限公司 一种二氯四氢异喹啉羧酸的中间体及其制备方法和应用
CN116462644B (zh) * 2023-05-06 2024-11-19 上海华默西医药科技有限公司 一种2-(呋喃-2-基亚甲基)-4-硝基丁酸酯化合物及其制备方法和应用
IT202400005227A1 (it) * 2024-03-08 2025-09-08 Olon Spa Processo per preparare lifitegrast.
IT202400005224A1 (it) * 2024-03-08 2025-09-08 Olon Spa Processo per preparare lifitegrast.

Family Cites Families (113)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3773919A (en) 1969-10-23 1973-11-20 Du Pont Polylactide-drug mixtures
JPS5759843A (en) * 1980-09-30 1982-04-10 Neos Co Ltd Perfluoroalkyl ether amide derivative and its preparation
IE52535B1 (en) 1981-02-16 1987-12-09 Ici Plc Continuous release pharmaceutical compositions
US4931279A (en) 1985-08-16 1990-06-05 Bausch & Lomb Incorporated Sustained release formulation containing an ion-exchange resin
US4668506A (en) 1985-08-16 1987-05-26 Bausch & Lomb Incorporated Sustained-release formulation containing and amino acid polymer
US4713244A (en) 1985-08-16 1987-12-15 Bausch & Lomb Incorporated Sustained-release formulation containing an amino acid polymer with a lower alkyl (C1 -C4) polar solvent
US5023252A (en) 1985-12-04 1991-06-11 Conrex Pharmaceutical Corporation Transdermal and trans-membrane delivery of drugs
US4992445A (en) 1987-06-12 1991-02-12 American Cyanamid Co. Transdermal delivery of pharmaceuticals
US5001139A (en) 1987-06-12 1991-03-19 American Cyanamid Company Enchancers for the transdermal flux of nivadipine
GB2209937B (en) 1987-09-21 1991-07-03 Depiopharm S A Water insoluble polypeptides
EP0314863B1 (fr) 1987-11-02 1994-12-07 Baylor College Of Medicine Utilisation du ICAM-1 ou de ses derivés fonctionels pour le traitement des inflammations non spécifiques
EP0326151B1 (fr) 1988-01-29 1993-06-16 Sumitomo Pharmaceuticals Company, Limited Formulations perfectionnées à libération contrôlée
DE3802996A1 (de) 1988-02-02 1989-08-10 Cassella Ag Verwendung von 2-oxo-pyrrolidin-1-acetamid zur bestimmung der glomerulaeren filtrationsrate beim menschen
US5424399A (en) 1988-06-28 1995-06-13 The Children's Medical Center Corporation Human CR3α/β heterodimers
DE68923048T2 (de) 1988-08-23 1995-11-16 Dana Farber Cancer Inst Inc Alpha-Subeinheit des LFA-1-Leukocyt-Adhäsions-Rezeptors.
ES2141076T3 (es) 1988-09-01 2000-03-16 Bayer Ag Proteina del receptor de rinovirus humano que inhibe la infectividad del virus.
AU4412889A (en) 1988-09-28 1990-04-18 Dana-Farber Cancer Institute Intercellular adhesion molecules, and their binding ligands
US5149780A (en) 1988-10-03 1992-09-22 The Scripps Research Institute Peptides and antibodies that inhibit integrin-ligand binding
JPH04505009A (ja) 1989-03-09 1992-09-03 ダナ・ファーバー・キャンサー・インスティチュート クローニングlfa―1
ZA903223B (en) 1989-04-28 1991-02-27 Baylor College Medicine Dissemination of hiv-1 infected cells
CH679207A5 (fr) 1989-07-28 1992-01-15 Debiopharm Sa
WO1991019511A1 (fr) 1990-06-18 1991-12-26 The General Hospital Corporation LUTTE CONTRE LES REACTIONS IMMUNITAIRES/INFLAMMATOIRES CELLULAIRES DES INTEGRINES β2
CA2046830C (fr) 1990-07-19 1999-12-14 Patrick P. Deluca Systeme d'administration des medicaments comprenant une interaction entre une proteine ou une polypeptide et un polymere hydrophobe biodegradable
US5318965A (en) 1990-08-24 1994-06-07 Abbott Laboratories Quinobenzoxazine, antineoplastic agents
JPH06500555A (ja) 1990-08-27 1994-01-20 カイロン コーポレイション 病気の処置のためのペプチドの薬物
JP2995860B2 (ja) 1990-11-27 1999-12-27 味の素株式会社 新規ペプチド
US5288854A (en) 1990-11-28 1994-02-22 Center For Blood Research, Inc. Functional derivatives of ICAM-1 which are substantially capable of binding to LFA-1 but are substantially incapable of binding to MAC-1
CH683149A5 (fr) 1991-07-22 1994-01-31 Debio Rech Pharma Sa Procédé pour la préparation de microsphères en matériau polymère biodégradable.
JP3679112B2 (ja) 1991-10-04 2005-08-03 アメリカ合衆国 細胞接着分子の遮断による眼の炎症の治療
GB9211268D0 (en) 1992-05-28 1992-07-15 Ici Plc Salts of basic peptides with carboxyterminated polyesters
US5298492A (en) 1992-08-04 1994-03-29 Schering Corporation Diamino acid derivatives as antihypertensives
AU687755B2 (en) 1992-08-21 1998-03-05 Genentech Inc. Method for treating an LFA-1-mediated disorder
AU5466794A (en) 1992-11-18 1994-06-08 Helsinki University Licensing Ltd Oy Peptides from human icam-2 and from human icam-1 and their analogs for use in therapy and diagnosis
JPH08505395A (ja) 1993-01-06 1996-06-11 キナートン リミティド 生物分解性ポリエステルと生物活性ポリペプチドのイオン分子結合体
US5672659A (en) 1993-01-06 1997-09-30 Kinerton Limited Ionic molecular conjugates of biodegradable polyesters and bioactive polypeptides
US5424289A (en) 1993-07-30 1995-06-13 Alza Corporation Solid formulations of therapeutic proteins for gastrointestinal delivery
US5397791A (en) 1993-08-09 1995-03-14 Merck & Co., Inc. Fibrinogen receptor antagonists
SI0656348T1 (en) 1993-12-03 2000-08-31 F. Hoffmann-La Roche Ag Aceric acid derivatives as medicaments
US5470953A (en) 1993-12-23 1995-11-28 Icos Corporation Human β2 integrin α subunit
JPH09512021A (ja) 1994-04-19 1997-12-02 ザ ユニバーシティ オブ カンサス Icam−1/lfa−1 短鎖ペプチドおよび該ペプチドの使用方法
US5849327A (en) 1994-07-29 1998-12-15 Advanced Polymer Systems, Inc. Delivery of drugs to the lower gastrointestinal tract
US5510495A (en) * 1994-09-19 1996-04-23 The Du Pont Merck Pharmaceutical Company Process for the isolation and purification of ester functionalized imidazole intermediates by selective hydrolysis
US5585359A (en) 1994-09-29 1996-12-17 Merck & Co., Inc. Inhibitors of farnesyl-protein transferase
ATE170179T1 (de) 1994-11-02 1998-09-15 Merck Patent Gmbh Adhäsionsrezeptor-antagonisten
US5612052A (en) 1995-04-13 1997-03-18 Poly-Med, Inc. Hydrogel-forming, self-solvating absorbable polyester copolymers, and methods for use thereof
US5747035A (en) 1995-04-14 1998-05-05 Genentech, Inc. Polypeptides with increased half-life for use in treating disorders involving the LFA-1 receptor
US5877224A (en) 1995-07-28 1999-03-02 Rutgers, The State University Of New Jersey Polymeric drug formulations
US5980945A (en) 1996-01-16 1999-11-09 Societe De Conseils De Recherches Et D'applications Scientifique S.A. Sustained release drug formulations
US5840332A (en) 1996-01-18 1998-11-24 Perio Products Ltd. Gastrointestinal drug delivery system
JP3155013B2 (ja) 1996-04-23 2001-04-09 キナートン・リミテッド 酸性ポリ乳酸ポリマー
HRP970493A2 (en) 1996-09-23 1998-08-31 Wienman E. Phlips Oral delayed immediate release medical formulation and method for preparing the same
CA2217134A1 (fr) 1996-10-09 1998-04-09 Sumitomo Pharmaceuticals Co., Ltd. Formulation a liberation-retard
WO1998023608A1 (fr) 1996-11-27 1998-06-04 Dupont Pharmaceuticals Company Nouveaux antagonistes des recepteurs de l'integrine
US5968895A (en) 1996-12-11 1999-10-19 Praecis Pharmaceuticals, Inc. Pharmaceutical formulations for sustained drug delivery
US5893985A (en) 1997-03-14 1999-04-13 The Lincoln Electric Company Plasma arc torch
AR012443A1 (es) 1997-04-16 2000-10-18 Uriach & Cia Sa J Nuevas carboxamidas como inhibidores de la agregacion plaquetaria, procedimiento para su preparacion, composiciones farmaceuticas que loscontienen y uso de los mismos en la manufactura de medicamentos
WO1999049856A2 (fr) 1998-03-27 1999-10-07 Genentech, Inc. Antagonistes destines au traitement de troubles induits par le recepteur d'adhesion de cd11/cd18
US6331640B1 (en) 1998-10-13 2001-12-18 Hoffmann-La Roche Inc. Diaminopropionic acid derivatives
ID29085A (id) 1998-11-27 2001-07-26 Kanji Takada Suatu formulasi oral untuk penghantaran obat gastrointestinal
IT1304152B1 (it) 1998-12-10 2001-03-08 Mediolanum Farmaceutici Srl Composizioni comprendenti un peptide ed acido polilattico-glicolicoatte alla preparazione di impianti sottocutanei aventi un prolungato
US6670321B1 (en) 1998-12-30 2003-12-30 The Children's Medical Center Corporation Prevention and treatment for retinal ischemia and edema
ATE330631T1 (de) 1999-01-05 2006-07-15 Univ Southern Australia Antikörperfragmente zur lokalen behandlung von augenerkrankungen
WO2000044731A1 (fr) 1999-01-27 2000-08-03 G.D. Searle & Co. Nouveaux derives d'hydroamidino carboxylate utilise comme inhibiteurs de la synthase de l'oxyde nitrique
EP1028114A1 (fr) 1999-02-13 2000-08-16 Aventis Pharma Deutschland GmbH Nouveaux dérivés de guanidine et leur utilisation comme inhibiteurs de l'adhésion des cellules
PL198797B1 (pl) 1999-03-31 2008-07-31 Janssen Pharmaceutica Nv Zastosowanie wstępnie żelowanej skrobi
WO2001001964A2 (fr) 1999-06-23 2001-01-11 Sedum Laboratories, Inc. Micro-excipients de biomolecules a formulation ionique
ES2209948T3 (es) 1999-08-18 2004-07-01 Societe De Conseils De Recherches Et D'applications Scientifiques S.A.S. Formulacion de un peptico de liberacion sostenida.
ECSP003707A (es) 1999-10-13 2002-05-23 Novartis Ag Diazepanes
US6294522B1 (en) 1999-12-03 2001-09-25 Cv Therapeutics, Inc. N6 heterocyclic 8-modified adenosine derivatives
US6605597B1 (en) 1999-12-03 2003-08-12 Cv Therapeutics, Inc. Partial or full A1agonists-N-6 heterocyclic 5′-thio substituted adenosine derivatives
PT1237575E (pt) 1999-12-14 2008-11-17 Genentech Inc Antagonista de tnf-alfa e antagonista de lfa-1 para tratar a artrite reumatóide
US7521061B2 (en) 1999-12-31 2009-04-21 Rutgers, The State University Of New Jersey Pharmaceutical formulation for regulating the timed release of biologically active compounds based on a polymer matrix
AU775905B2 (en) 1999-12-31 2004-08-19 Rutgers, The State University Pharmaceutical formulation composed of a polymer blend and an active compound for time-controlled release
AU784226B2 (en) 1999-12-31 2006-02-23 Rutgers, The State University Pharmaceutical formulation for regulating the timed release of biologically active compounds based on a polymer matrix
US20030064105A1 (en) 2000-08-25 2003-04-03 Myung-Jin Kim Lipophilic-coated microparticle containing a protein drug and formulation comprising same
US6515124B2 (en) 2000-02-09 2003-02-04 Hoffman-La Roche Inc. Dehydroamino acids
EP1296943A1 (fr) 2000-05-05 2003-04-02 Societe De Conseils De Recherches Et D'applications Scientifiques S.A. (S.C.R.A.S.) Derives d'aminoacides et leur application a titre de medicaments
GB0011817D0 (en) 2000-05-16 2000-07-05 Pharmacia & Upjohn Spa Antagonists of integrin receptors
CN1705649A (zh) 2000-06-29 2005-12-07 艾伯特公司 芳基苯基杂环基硫醚衍生物及其作为抑制细胞粘附的抗炎和免疫抑制剂的用途
JP2002030052A (ja) * 2000-07-18 2002-01-29 Tosoh Corp ヒドロキシアミノカルボン酸、その用途、及びその製造法
JPWO2002026686A1 (ja) * 2000-09-27 2004-02-05 旭硝子株式会社 アシルフルオリド類およびカルボン酸塩類の製造方法
PE20020420A1 (es) 2000-10-02 2002-06-27 Novartis Ag Derivados de diazacicloalcanodiona como antagonistas del antigeno asociado a la funcion del linfocito-1 (lfa-1)
GB0025208D0 (en) 2000-10-13 2000-11-29 Euro Celtique Sa Delayed release pharmaceutical formulations
US6653478B2 (en) 2000-10-27 2003-11-25 Ortho-Mcneil Pharmaceutical, Inc. Substituted benzimidazol-2-ones as vasopressin receptor antagonists and neuropeptide Y modulators
DE10055857A1 (de) 2000-11-10 2002-08-22 Creative Peptides Sweden Ab Dj Neue pharmazeutische Depotformulierung
GB0028367D0 (en) 2000-11-21 2001-01-03 Celltech Chiroscience Ltd Chemical compounds
US6667318B2 (en) 2000-11-28 2003-12-23 Genentech, Inc. LFA-1 antagonist compounds
US20030008848A1 (en) 2000-12-19 2003-01-09 Fleck Roman Wolfgang Small molecules useful in the treatment of inflammatory disease
WO2002058672A2 (fr) 2001-01-26 2002-08-01 Debio Recherche Pharmaceutique S.A. Microparticules de polymere biodegradable encapsulant une substance biologiquement active et formulations pharmaceutiques a liberation prolongee contenant lesdites particules
ES2275808T3 (es) 2001-02-06 2007-06-16 Pfizer Products Inc. Composiciones farmaceuticas para el tratamiento de trastornos del snc y otros trastornos.
WO2002098370A2 (fr) 2001-03-02 2002-12-12 Medimmune, Inc. Methodes d'administration/dosage d'antagonistes de cd2 pour la prevention et le traitement des maladies auto-immunes ou inflammatoires
EP1383376A4 (fr) 2001-03-19 2006-03-08 Praecis Pharm Inc Formulations pharmaceutiques a liberation prolongee
US6872382B1 (en) 2001-05-21 2005-03-29 Alcon, Inc. Use of selective PDE IV inhibitors to treat dry eye disorders
ATE383858T1 (de) 2001-06-06 2008-02-15 Aventis Pharma Ltd Substituierte tetrhydroisochinolin-derivate zur behandlung von entzündlichen erkrankungen
CN1606432A (zh) 2001-12-19 2005-04-13 阿尔扎公司 用于增加亲水性大分子的口服生物利用度的制剂和剂型
DE60327843D1 (de) 2002-03-04 2009-07-16 Ipsen Pharma Arzneimittelformulierungen mit verzögerter freisetzung mit einem trägerpeptid
BR0314603A (pt) 2002-09-20 2005-07-26 Alcon Inc Uso de inibidores da sìntese de citoquina para o tratamento de distúrbios de olhos secos
US7785578B2 (en) 2002-10-11 2010-08-31 Aciont, Inc. Non-invasive ocular drug delivery
RU2005117343A (ru) * 2002-12-20 2006-01-27 Астразенека Аб (Se) Новые производные пиперидина в качестве модуляторов хемокинового рецептора ccr5
WO2005014533A2 (fr) 2003-08-08 2005-02-17 Transtech Pharma, Inc. Composes aryle et heteroaryle, compositions et procedes d'utilisation
US7501538B2 (en) 2003-08-08 2009-03-10 Transtech Pharma, Inc. Aryl and heteroaryl compounds, compositions and methods of use
WO2005042710A1 (fr) 2003-10-28 2005-05-12 The Government Of The United States Of America, As Represented By The Secretary, Department Of Health And Human Services Utilisation de statines pour detruire des cellules b transformees par virus d'epstein-barr (veb)
JP5105578B2 (ja) 2003-11-05 2012-12-26 サーコード バイオサイエンス インコーポレイテッド 細胞接着のモジュレーター
GT200500139A (es) 2004-06-08 2005-07-25 Metodo para la preparacion de acidos hidroxamicos
MX2007013469A (es) * 2005-04-28 2008-01-22 Wyeth Corp Forma ii polimorfa de tanaproget.
US8168655B2 (en) 2005-05-17 2012-05-01 Sarcode Bioscience Inc. Compositions and methods for treatment of eye disorders
WO2007057919A2 (fr) * 2005-10-25 2007-05-24 Alembic Limited Procede ameliore pour la preparation de (s)-n-(1-carboxy-2-methyl-prop-1-yl)-n-pentanoyl-n-[2'-(1h-tetrazol-5-yl)biphenyl-4-ylmethyl]-amine
JP4193895B2 (ja) 2006-10-12 2008-12-10 横河電機株式会社 欠陥検査装置
MX2010004281A (es) 2007-10-19 2010-09-10 Sarcode Corp Composiciones y metodos para el tratamiento de la retinopatia diabetica.
NZ586900A (en) * 2008-01-01 2012-10-26 Cipla Ltd Anhydrous polymorphic form b of bosentan and uses thereof
WO2009139817A2 (fr) * 2008-04-15 2009-11-19 Sarcode Corporation Produit pharmaceutique cristallin et ses procédés de préparation et d'utilisation
US8378105B2 (en) 2009-10-21 2013-02-19 Sarcode Bioscience Inc. Crystalline pharmaceutical and methods of preparation and use thereof
SI3715345T1 (sl) * 2012-07-25 2024-07-31 Bausch + Lomb Ireland Limited Priprava zaviralca lfa-1

Also Published As

Publication number Publication date
RU2658015C2 (ru) 2018-06-19
JP2020128433A (ja) 2020-08-27
BR112015001608B1 (pt) 2022-08-23
WO2014018748A1 (fr) 2014-01-30
MX2015001098A (es) 2015-09-25
CA2879982C (fr) 2020-09-01
RU2015102926A (ru) 2016-09-20
MX2020001602A (es) 2020-07-13
CN104797574A (zh) 2015-07-22
RU2018121523A (ru) 2019-12-13
JP2018162313A (ja) 2018-10-18
KR20150067129A (ko) 2015-06-17
AU2017265071A1 (en) 2017-12-14
US20190382389A1 (en) 2019-12-19
CN104797574B (zh) 2019-11-22
EP3715345B8 (fr) 2024-05-29
EP2877465A4 (fr) 2016-05-11
US9708303B2 (en) 2017-07-18
AU2017265071B2 (en) 2019-08-22
BR112015001608A2 (pt) 2017-07-04
SI3715345T1 (sl) 2024-07-31
AU2013295706A1 (en) 2015-02-19
AU2020281063A1 (en) 2021-01-07
CA2879982A1 (fr) 2014-01-30
EP3715345A3 (fr) 2020-11-11
EP2877465A1 (fr) 2015-06-03
AU2023204287B2 (en) 2025-08-21
AU2023204287A1 (en) 2023-07-27
US20150336939A1 (en) 2015-11-26
US20180118726A1 (en) 2018-05-03
US10906892B2 (en) 2021-02-02
AU2019210525A1 (en) 2019-08-15
HK1210782A1 (en) 2016-05-06
US20140031387A1 (en) 2014-01-30
JP2015523398A (ja) 2015-08-13
US10214517B2 (en) 2019-02-26
KR102157608B1 (ko) 2020-09-18
JP6607780B2 (ja) 2019-11-20
EP4406950A3 (fr) 2025-04-23
EP3715345B1 (fr) 2024-04-10
HK1210145A1 (en) 2016-04-15
AU2019210525B2 (en) 2020-12-17
RU2018121523A3 (fr) 2022-02-25
KR20200108932A (ko) 2020-09-21
EP4406950A2 (fr) 2024-07-31
JP7008750B2 (ja) 2022-01-25
US9085553B2 (en) 2015-07-21
EP3715345A2 (fr) 2020-09-30
CN110922393A (zh) 2020-03-27

Similar Documents

Publication Publication Date Title
MX2020001602A (es) Inhibidor del antigeno-1 asociado a la funcion del linfocito (lfa-1) y polimorfo del mismo.
IL274469A (en) Compositions, uses and methods for the treatment of metabolic disorders and diseases
ME03042B (fr) Composés et compositions pour le traitement de maladies parasitaires
ZA201402424B (en) 1- arylcarbonyl -4 - oxy - piperidine compounds useful for the treatment of neurodegenerative diseases
GB201021103D0 (en) New compounds for the treatment of neurodegenerative diseases
SG10201507120TA (en) Treatment of diseases
EP2938616A4 (fr) Procédé de préparation de tofacitinib et d'intermédiaires
IN2015DN01119A (fr)
WO2012104823A3 (fr) Composés pyridopyrimidinones dans le traitement de maladies neurodégénératives
EP2709632A4 (fr) Compositions et procédés pour le traitement de maladies de la peau
PL2892556T3 (pl) Kompozycje i sposoby odnoszące się do leczenia chorób
IL234796B (en) Compounds for the treatment of diseases related to ischemia-reperfusion
PL395469A1 (pl) Pochodne indoloamin do leczenia chorób osrodkowego ukladu nerwowego
GB201217331D0 (en) Novel compound useful for the treatment of infectious diseases
AU2011900644A0 (en) Therapeutic Uses of SLIRP
HK1182092A (en) Arylosulfonamides for the treatment of cns diseases
AU2011903764A0 (en) Treatment of bone diseases