MX2020001602A - Inhibidor del antigeno-1 asociado a la funcion del linfocito (lfa-1) y polimorfo del mismo. - Google Patents

Inhibidor del antigeno-1 asociado a la funcion del linfocito (lfa-1) y polimorfo del mismo.

Info

Publication number
MX2020001602A
MX2020001602A MX2020001602A MX2020001602A MX2020001602A MX 2020001602 A MX2020001602 A MX 2020001602A MX 2020001602 A MX2020001602 A MX 2020001602A MX 2020001602 A MX2020001602 A MX 2020001602A MX 2020001602 A MX2020001602 A MX 2020001602A
Authority
MX
Mexico
Prior art keywords
lfa
polymorph
inhibitor
disclosed
intermediates
Prior art date
Application number
MX2020001602A
Other languages
English (en)
Inventor
Michael Hall
James Robert Zeller
Subashree Iyer
Sripathy Venkatraman
Elisabeth C A Brot
Original Assignee
Novartis Ag
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=MX2020001602(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Novartis Ag filed Critical Novartis Ag
Publication of MX2020001602A publication Critical patent/MX2020001602A/es

Links

Classifications

    • 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
    • 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
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/13Crystalline forms, e.g. polymorphs

Abstract

La presente invención se refiere a métodos de preparación y purificación de un compuesto, intermediarios del mismo, un polimorfo del mismo, y compuestos relacionados. También se describen las formulaciones y usos de las mismas en el tratamiento de enfermedades mediadas por LFA-1.
MX2020001602A 2012-07-25 2015-01-23 Inhibidor del antigeno-1 asociado a la funcion del linfocito (lfa-1) y polimorfo del mismo. MX2020001602A (es)

Applications Claiming Priority (3)

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

Publications (1)

Publication Number Publication Date
MX2020001602A true MX2020001602A (es) 2020-07-13

Family

ID=49995472

Family Applications (2)

Application Number Title Priority Date Filing Date
MX2015001098A MX2015001098A (es) 2012-07-25 2013-07-25 Inhibidor del antigeno-1 asociado a la funcion del linfocito (lfa-1) y polimorfo del mismo.
MX2020001602A MX2020001602A (es) 2012-07-25 2015-01-23 Inhibidor del antigeno-1 asociado a la funcion del linfocito (lfa-1) y polimorfo del mismo.

Family Applications Before (1)

Application Number Title Priority Date Filing Date
MX2015001098A MX2015001098A (es) 2012-07-25 2013-07-25 Inhibidor del antigeno-1 asociado a la funcion del linfocito (lfa-1) y polimorfo del mismo.

Country Status (13)

Country Link
US (4) US9085553B2 (es)
EP (2) EP2877465A4 (es)
JP (3) JP6607780B2 (es)
KR (2) KR20200108932A (es)
CN (2) CN110922393A (es)
AU (5) AU2013295706A1 (es)
BR (1) BR112015001608B1 (es)
CA (1) CA2879982C (es)
HK (2) HK1210145A1 (es)
IN (1) IN2015DN00847A (es)
MX (2) MX2015001098A (es)
RU (1) RU2658015C2 (es)
WO (1) WO2014018748A1 (es)

Families Citing this family (41)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SI2444079T1 (sl) * 2005-05-17 2017-05-31 Sarcode Bioscience Inc. Sestavki in postopki za zdravljenje očesnih motenj
EP2265125B1 (en) * 2008-04-15 2019-08-14 SARcode Bioscience Inc. Topical lfa-1 antagonists for use in localized treatment of immune related disorders
EP2877465A4 (en) 2012-07-25 2016-05-11 Sarcode Bioscience Inc LFA-1 HEMMER AND POLYMORPH THEREOF
EP3197454B1 (en) 2014-09-25 2021-01-06 Novartis AG Continuous flow carboxylation reaction
CA2973471A1 (en) 2015-01-12 2016-07-21 Kedalion Therapeutics, Inc. Micro-droplet delivery device and methods
US10799447B2 (en) 2016-03-04 2020-10-13 James M. Rynerson Method of treating an eye disorder by inhibiting or disrupting bacterial biofilm formation
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
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
JP7232780B2 (ja) * 2017-06-30 2023-03-03 サイノファーム タイワン,リミティド リフィテグラスト及びその中間体を調製するための方法
WO2019020580A1 (en) 2017-07-24 2019-01-31 Interquim, S.A. PROCESS FOR PREPARING AND PURIFYING LIFITEGRAST ANTAGONIST OF LFA-1
US20200369652A1 (en) * 2017-08-03 2020-11-26 Dr. Reddy's Laboratories Limited Processes for preparation of lifitegrast and intermediates thereof
WO2019053607A1 (en) * 2017-09-18 2019-03-21 Glenmark Pharmaceuticals Limited PROCESS FOR PREPARING LIFITEGRAST
EP3694499A4 (en) * 2017-10-10 2021-09-01 Mankind Pharma Ltd. NEW LIFITEGRAST PREPARATION PROCESS
WO2019097547A1 (en) 2017-11-15 2019-05-23 Cipla Limited An improved process for the preparation of lifitegrast or salts thereof
WO2019096996A1 (en) 2017-11-17 2019-05-23 Medichem, S.A. A process to obtain a tetrahydroisoquinoline derivative
KR20240045373A (ko) 2018-01-15 2024-04-05 코그니보티스 에이비 산업용 로봇 아암
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
IT201800006337A1 (it) * 2018-06-14 2019-12-14 Procedimento per la preparazione di lifitegrast
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
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
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
US11679028B2 (en) 2019-03-06 2023-06-20 Novartis Ag Multi-dose ocular fluid delivery system
KR20220003555A (ko) 2019-04-18 2022-01-10 아주라 오프탈믹스 엘티디 안구 장애의 치료를 위한 화합물 및 방법
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
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
US11938057B2 (en) 2020-04-17 2024-03-26 Bausch + Lomb Ireland Limited Hydrodynamically actuated preservative free dispensing system
CA3180199A1 (en) 2020-04-17 2021-10-21 Yehuda Ivri Hydrodynamically actuated preservative free dispensing system
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
CN113880819A (zh) * 2021-09-18 2022-01-04 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
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
CN115784950A (zh) * 2022-12-08 2023-03-14 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

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
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
US4668506A (en) 1985-08-16 1987-05-26 Bausch & Lomb Incorporated Sustained-release formulation containing and amino acid polymer
US5023252A (en) 1985-12-04 1991-06-11 Conrex Pharmaceutical Corporation Transdermal and trans-membrane delivery of drugs
US5001139A (en) 1987-06-12 1991-03-19 American Cyanamid Company Enchancers for the transdermal flux of nivadipine
US4992445A (en) 1987-06-12 1991-02-12 American Cyanamid Co. Transdermal delivery of pharmaceuticals
GB2209937B (en) 1987-09-21 1991-07-03 Depiopharm S A Water insoluble polypeptides
DE3852374T2 (de) 1987-11-02 1995-05-04 Baylor College Medicine Verwendung von ICAM-1 oder ihre funktionelle Derivate zur Behandlung unspezifischer Entzündungen.
US5236704A (en) 1988-01-28 1993-08-17 Sumitomo Pharmaceuticals Co., Ltd. Controlled release formulation
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
EP0362526B1 (en) 1988-08-23 1995-06-14 Dana Farber Cancer Institute The Alpha-subunit of the LFA-1 leukocyte adhesion receptor
DE68929096T2 (de) 1988-09-01 2000-05-11 Bayer Ag Menschliches Rhinovirusrezeptorprotein, das die Virusinfektionsanfälligkeit hemmt
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
AU5553290A (en) 1989-04-28 1990-11-29 Baylor College Of Medicine Dissemination of hiv-1 infected cells
CH679207A5 (es) 1989-07-28 1992-01-15 Debiopharm Sa
WO1991019511A1 (en) 1990-06-18 1991-12-26 The General Hospital Corporation CONTROLLING CELLULAR IMMUNE/INFLAMMATORY RESPONSES WITH β2 INTEGRINS
CA2046830C (en) 1990-07-19 1999-12-14 Patrick P. Deluca Drug delivery system involving inter-action between protein or polypeptide and hydrophobic biodegradable polymer
US5318965A (en) 1990-08-24 1994-06-07 Abbott Laboratories Quinobenzoxazine, antineoplastic agents
CA2090427A1 (en) 1990-08-27 1992-02-28 Cetus Oncology Corporation Cd18 peptide medicaments for the treatment of disease
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.
ATE180408T1 (de) 1991-10-04 1999-06-15 Us Health Herstellung eines arzneimittels zur behandlung von augenentzündung durch blockierung von zelladhäsionsmolekulen
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
ATE161192T1 (de) 1992-08-21 1998-01-15 Genentech Inc Verfahren zur behandlung einer durch lfa-1 vermittelten störung
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
US5672659A (en) 1993-01-06 1997-09-30 Kinerton Limited Ionic molecular conjugates of biodegradable polyesters and bioactive polypeptides
ATE236655T1 (de) 1993-01-06 2003-04-15 Kinerton Ltd Ionische molekularkonjugate von bioabbaubaren polyestern und bioaktiven polypeptiden
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
EP0656348B1 (de) 1993-12-03 2000-05-03 F. Hoffmann-La Roche Ag Essigsäurederivate als Arzneimittel
US5470953A (en) 1993-12-23 1995-11-28 Icos Corporation Human β2 integrin α subunit
EP0762886A4 (en) 1994-04-19 1999-03-31 Univ Kansas ICAM-1 / LFA-1 SHORT CHAIN PEPTIDES AND METHODS FOR USE THEREOF
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
ES2123889T3 (es) 1994-11-02 1999-01-16 Merck Patent Gmbh Antagonistas de receptores de adhesion.
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
EP1479708A3 (en) 1996-04-23 2005-05-25 Ipsen Manufacturing Ireland Limited Biodegradable polyesters and method for their preparation
HRP970493A2 (en) 1996-09-23 1998-08-31 Wienman E. Phlips Oral delayed immediate release medical formulation and method for preparing the same
CA2217134A1 (en) 1996-10-09 1998-04-09 Sumitomo Pharmaceuticals Co., Ltd. Sustained release formulation
EP0944619B1 (en) 1996-11-27 2006-10-11 Bristol-Myers Squibb Pharma Company Novel integrin receptor antagonists
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
DE69935133T2 (de) 1998-03-27 2007-11-22 Genentech, Inc., South San Francisco Antagonisten zur behandlung von cd11/cd18 adhäsionsrezeptor-vermittelten krankheiten
US6331640B1 (en) 1998-10-13 2001-12-18 Hoffmann-La Roche Inc. Diaminopropionic acid derivatives
EP1135112B1 (en) 1998-11-27 2004-10-20 TAKADA, Kanji An oral formulation for gastrointestinal drug delivery
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
CA2348488C (en) 1999-01-05 2011-03-01 The Flinders University Of South Australia Novel agents and methods for treatment and diagnosis of ocular disorders
AU2847200A (en) 1999-01-27 2000-08-18 G.D. Searle & Co. Novel hydroxyamidino carboxylate derivatives useful as nitric oxide synthase inhibitors
EP1028114A1 (en) 1999-02-13 2000-08-16 Aventis Pharma Deutschland GmbH Novel guanidine derivatives as inhibitors of cell adhesion
SK288541B6 (sk) 1999-03-31 2018-03-05 Janssen Pharmaceutica N. V. Predželatínovaný škrob v hydrofilnej formulácii s riadeným uvoľňovaním
EP1194128A2 (en) 1999-06-23 2002-04-10 Sedum Laboratories Ionically formulated biomolecule microcarriers
JP4303438B2 (ja) 1999-08-18 2009-07-29 ソシエテ・ドゥ・コンセイユ・ドゥ・ルシェルシュ・エ・ダプリカーション・シャンティフィック・エス・ア・エス ペプチドの持続放出製剤
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
KR100567292B1 (ko) 1999-12-14 2006-04-04 제넨테크, 인크. Lfa-1 또는 tnf-알파 매개 질환의 치료용tnf-알파 길항제 및 lfa-1 길항제
US7326425B2 (en) 1999-12-31 2008-02-05 Rutgers, The State University Pharmaceutical formulation composed of a polymer blend and an active compound for time-controlled release
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
JP2003519164A (ja) 1999-12-31 2003-06-17 ルトガーズ、ザ ステイト ユニバーシティ ポリマーマトリクスに基づく生理活性化合物徐放調節用医薬製剤
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
US6821986B2 (en) 2000-05-05 2004-11-23 Societe De Conseils De Recherchet Et E'applications Scientifiques (S.C.R.A.S.) Amino acid derivatives and their use as medicines
GB0011817D0 (en) 2000-05-16 2000-07-05 Pharmacia & Upjohn Spa Antagonists of integrin receptors
JP2004502681A (ja) 2000-06-29 2004-01-29 アボット・ラボラトリーズ アリールフェニル複素環スルフィド誘導体および細胞接着を阻止する抗炎症性および免疫抑制性物質としてのその使用
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
EP1323702A4 (en) * 2000-09-27 2005-12-07 Asahi Glass Co Ltd METHOD FOR THE PRODUCTION OF ACYL-FLUORIDES AND CARBOXYLIC ACID SALTS
AR030817A1 (es) 2000-10-02 2003-09-03 Novartis Ag Derivados de diazacicloalcanodiona
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
KR20030051882A (ko) 2000-11-28 2003-06-25 제넨테크, 인크. Lfa-1 대항제 화합물
US20030008848A1 (en) 2000-12-19 2003-01-09 Fleck Roman Wolfgang Small molecules useful in the treatment of inflammatory disease
CA2435415A1 (en) 2001-01-26 2002-08-01 Debio Recherche Pharmaceutique S.A. Microparticles of biodegradable polymer encapsulating a biologically active substance
ES2275808T3 (es) 2001-02-06 2007-06-16 Pfizer Products Inc. Composiciones farmaceuticas para el tratamiento de trastornos del snc y otros trastornos.
US20030044406A1 (en) 2001-03-02 2003-03-06 Christine Dingivan Methods of preventing or treating inflammatory or autoimmune disorders by administering CD2 antagonists in combination with other prophylactic or therapeutic agents
WO2002074247A2 (en) 2001-03-19 2002-09-26 Praecis Pharmaceuticals Incorporated Pharmaceutical formulations for sustained release
US6872382B1 (en) 2001-05-21 2005-03-29 Alcon, Inc. Use of selective PDE IV inhibitors to treat dry eye disorders
PT1392306E (pt) 2001-06-06 2008-03-07 Aventis Pharma Ltd Tetra-hidroisoquinolinas substituídas para utilização no tratamento de doenças inflamatórias
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
EP1480618B1 (en) 2002-03-04 2009-06-03 Ipsen Pharma Sustained release drug formulations containing a carrier peptide
CA2497977A1 (en) 2002-09-20 2004-04-01 Alcon, Inc. Use of cytokine synthesis inhibitors for the treatment of dry eye disorders
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
US7501538B2 (en) 2003-08-08 2009-03-10 Transtech Pharma, Inc. Aryl and heteroaryl compounds, compositions and methods of use
EP1660439A2 (en) 2003-08-08 2006-05-31 Transtech Pharma, Inc. Aryl and heteroaryl compounds, compositions, and methods of use
WO2005042710A1 (en) 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 Use of statin to kill ebv-transformed b cells
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
CN101166736B (zh) 2005-04-28 2013-02-06 惠氏公司 他那普戈特的多晶型ⅱ
SI2444079T1 (sl) 2005-05-17 2017-05-31 Sarcode Bioscience Inc. Sestavki in postopki za zdravljenje očesnih motenj
WO2007057919A2 (en) * 2005-10-25 2007-05-24 Alembic Limited An improved process for preparation of (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
CA2958665C (en) 2007-10-19 2021-03-02 Sarcode Bioscience Inc. Compositions and methods for treatment of diabetic retinopathy
CA2711043A1 (en) 2008-01-01 2009-07-09 Cipla Limited Method of synthesis of bosentan, its polymorphic forms and its salts
WO2009139817A2 (en) 2008-04-15 2009-11-19 Sarcode Corporation Crystalline pharmaceutical and methods of preparation and use thereof
US8378105B2 (en) * 2009-10-21 2013-02-19 Sarcode Bioscience Inc. Crystalline pharmaceutical and methods of preparation and use thereof
EP2877465A4 (en) 2012-07-25 2016-05-11 Sarcode Bioscience Inc LFA-1 HEMMER AND POLYMORPH THEREOF

Also Published As

Publication number Publication date
CN104797574A (zh) 2015-07-22
EP3715345B1 (en) 2024-04-10
US10906892B2 (en) 2021-02-02
HK1210145A1 (en) 2016-04-15
US9708303B2 (en) 2017-07-18
AU2020281063A1 (en) 2021-01-07
RU2018121523A3 (es) 2022-02-25
AU2019210525A1 (en) 2019-08-15
AU2017265071B2 (en) 2019-08-22
JP6607780B2 (ja) 2019-11-20
HK1210782A1 (en) 2016-05-06
US20140031387A1 (en) 2014-01-30
BR112015001608B1 (pt) 2022-08-23
RU2018121523A (ru) 2019-12-13
AU2023204287A1 (en) 2023-07-27
EP3715345A3 (en) 2020-11-11
CA2879982A1 (en) 2014-01-30
US20180118726A1 (en) 2018-05-03
US9085553B2 (en) 2015-07-21
CA2879982C (en) 2020-09-01
JP2018162313A (ja) 2018-10-18
CN104797574B (zh) 2019-11-22
KR102157608B1 (ko) 2020-09-18
JP2015523398A (ja) 2015-08-13
US10214517B2 (en) 2019-02-26
RU2015102926A (ru) 2016-09-20
IN2015DN00847A (es) 2015-06-12
KR20200108932A (ko) 2020-09-21
JP7008750B2 (ja) 2022-01-25
MX2015001098A (es) 2015-09-25
EP2877465A1 (en) 2015-06-03
US20150336939A1 (en) 2015-11-26
US20190382389A1 (en) 2019-12-19
CN110922393A (zh) 2020-03-27
EP3715345A2 (en) 2020-09-30
BR112015001608A2 (pt) 2017-07-04
AU2019210525B2 (en) 2020-12-17
WO2014018748A1 (en) 2014-01-30
JP2020128433A (ja) 2020-08-27
RU2658015C2 (ru) 2018-06-19
AU2017265071A1 (en) 2017-12-14
AU2013295706A1 (en) 2015-02-19
EP2877465A4 (en) 2016-05-11
KR20150067129A (ko) 2015-06-17

Similar Documents

Publication Publication Date Title
MX2020001602A (es) Inhibidor del antigeno-1 asociado a la funcion del linfocito (lfa-1) y polimorfo del mismo.
LTC2785706I2 (lt) Pakeistieji 4-fenil-piridinai, skirti su nk-receptoriumi susijusių ligų gydymui
IL235767A0 (en) Converted pyrrolidines as factor xia inhibitors for the treatment of thromboembolic diseases
EP2938616A4 (en) PROCESS FOR THE PREPARATION OF TOFACITINIB AND INTERMEDIATES
PH12015500376B1 (en) Novel bicyclic pyridinones
TN2012000414A1 (en) Forms of rifaximin and uses thereof
MX349004B (es) Nuevos compuestos.
EP2773342A4 (en) COMPOSITIONS USEFUL FOR THE TREATMENT OF VIRAL DISEASES
PL2925757T3 (pl) Związki i kompozycje do leczenia chorób pasożytniczych
EA201491028A1 (ru) Способ получения замещенных 5-фтор-1н-пиразолопиридинов
WO2013165921A3 (en) Therapeutic use of chardonnay seed products
EP2967049A4 (en) Methods, compounds, and compositions for the treatment of angiotensin-related diseases
HK1212628A1 (zh) 用於抑制炎症的抗- 、抗- 、抗- 、抗- 、抗- 和抗- 試劑
WO2012103810A1 (en) Certain chemical entities, compositions, and methods
WO2012104823A3 (en) Pyridopyrimidinone compounds in the treatment of neurodegenerative diseases
HK1206938A1 (en) Process for the preparation of 3-chloro-4,5,6-trifluoro- picolinonitrile 3--456--
MX2014010433A (es) Nueva forma cristalina de sulfato de sitagliptina.
GB201213484D0 (en) Pharmaceutical compositions comprising 15-OHEPA and methods of using the same
WO2012154879A3 (en) Autophagy inhibitors
MX2015007945A (es) Usos y métodos para el tratamiento de enfermedades o afecciones hepáticas.
WO2014008204A3 (en) Structures of proteasome inhibitors and methods for synthesizing and use thereof
MX2014002378A (es) Proceso para la preparacion de (r)-2-acetamido-n-bencil-3-metoxipr opionamida e intermediarios de la misma.
LT2855487T (lt) Junginiai, skirti ligų, susijusių su išemija-reperfuzija, gydymui
ES2421810A2 (es) Intermedios utiles para la sintesis de fexofenadina, procedimientos para su preparacion y para la preparacion de fexofenadina
TR201106224A2 (tr) Solunum yolu hastalıkları tedavisinde kullanılan farmasötik bileşimler.