JP2018035160A5 - - Google Patents

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Publication number
JP2018035160A5
JP2018035160A5 JP2017172276A JP2017172276A JP2018035160A5 JP 2018035160 A5 JP2018035160 A5 JP 2018035160A5 JP 2017172276 A JP2017172276 A JP 2017172276A JP 2017172276 A JP2017172276 A JP 2017172276A JP 2018035160 A5 JP2018035160 A5 JP 2018035160A5
Authority
JP
Japan
Prior art keywords
pharmaceutical composition
hydrate
composition according
substantially pure
crystalline form
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.)
Pending
Application number
JP2017172276A
Other languages
English (en)
Japanese (ja)
Other versions
JP2018035160A (ja
Filing date
Publication date
Application filed filed Critical
Publication of JP2018035160A publication Critical patent/JP2018035160A/ja
Publication of JP2018035160A5 publication Critical patent/JP2018035160A5/ja
Pending legal-status Critical Current

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JP2017172276A 2008-11-11 2017-09-07 有機化合物 Pending JP2018035160A (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP08168865 2008-11-11
EP08168865.7 2008-11-11

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
JP2015173474A Division JP2016028056A (ja) 2008-11-11 2015-09-03 有機化合物

Publications (2)

Publication Number Publication Date
JP2018035160A JP2018035160A (ja) 2018-03-08
JP2018035160A5 true JP2018035160A5 (OSRAM) 2019-01-31

Family

ID=40521487

Family Applications (4)

Application Number Title Priority Date Filing Date
JP2011535130A Withdrawn JP2012508216A (ja) 2008-11-11 2009-11-10 有機化合物
JP2014020950A Withdrawn JP2014139179A (ja) 2008-11-11 2014-02-06 有機化合物
JP2015173474A Withdrawn JP2016028056A (ja) 2008-11-11 2015-09-03 有機化合物
JP2017172276A Pending JP2018035160A (ja) 2008-11-11 2017-09-07 有機化合物

Family Applications Before (3)

Application Number Title Priority Date Filing Date
JP2011535130A Withdrawn JP2012508216A (ja) 2008-11-11 2009-11-10 有機化合物
JP2014020950A Withdrawn JP2014139179A (ja) 2008-11-11 2014-02-06 有機化合物
JP2015173474A Withdrawn JP2016028056A (ja) 2008-11-11 2015-09-03 有機化合物

Country Status (14)

Country Link
US (2) US8530522B2 (OSRAM)
EP (1) EP2356090B1 (OSRAM)
JP (4) JP2012508216A (OSRAM)
KR (2) KR20130109254A (OSRAM)
CN (3) CN104788325A (OSRAM)
AU (1) AU2009315736B2 (OSRAM)
BR (1) BRPI0921826A2 (OSRAM)
CA (1) CA2743232C (OSRAM)
ES (1) ES2643161T3 (OSRAM)
MX (1) MX2011004962A (OSRAM)
PL (1) PL2356090T3 (OSRAM)
PT (1) PT2356090T (OSRAM)
RU (2) RU2015111229A (OSRAM)
WO (1) WO2010055028A2 (OSRAM)

Families Citing this family (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2621889B1 (en) 2010-10-01 2019-07-17 Synthon BV Process for making fingolimod hydrochloride crystals
US8735627B2 (en) 2010-10-28 2014-05-27 Mapi Pharma Ltd. Intermediate compounds and process for the preparation of fingolimod
WO2012071524A1 (en) 2010-11-24 2012-05-31 Ratiopharm Gmbh Arylsulfonate salts of fingolimod and processes for preparation thereof
US9266816B2 (en) 2010-11-25 2016-02-23 Shilpa Medicare Limited Fingolimod polymorphs and their processes
EP2658840B1 (en) 2010-12-28 2019-07-03 Synthon BV Process for making fingolimod hydrochloride crystals
WO2012097330A2 (en) * 2011-01-14 2012-07-19 University Of Washington Compositions and methods for treating degenerative muscle conditions
EP2702034A4 (en) 2011-04-29 2015-03-25 Reddys Lab Ltd Dr PREPARATION OF FINGOLIMOD AND ITS SALTS
US9751834B2 (en) 2011-05-26 2017-09-05 Gri Bio, Inc. Oxygenated amino- or ammonium-containing sulfonic acid, phosphonic acid and carboxylic acid derivatives and their medical use
WO2012160187A1 (en) * 2011-05-26 2012-11-29 Jado Technologies Gmbh Amino- or ammonium-containing sulfonic acid, phosphonic acid and carboxylic acid derivatives and their medical use
US9573886B2 (en) 2011-05-26 2017-02-21 Glycoregimmune, Inc. Hydroxy-substituted amino and ammonium derivatives and their medical use
US9186333B2 (en) 2011-08-01 2015-11-17 Teva Pharmaceutical Industries Ltd. Process for preparing pharmaceutical compositions of fingolimod
WO2013091704A1 (en) * 2011-12-22 2013-06-27 Synthon Bv Pharmaceutical composition comprising fingolimod
CN102887829B (zh) * 2012-09-05 2014-07-02 中国科学院上海药物研究所 芬戈莫德粘酸盐及其晶体的制备方法和用途
US9732030B2 (en) 2013-01-17 2017-08-15 Shilpa Medicare Limited Process for the preparation of fingolimod and its salts
EP2964210B1 (en) * 2013-03-05 2023-10-04 Biocon Limited A process for the preparation of 2-amino-1,3-propane diol compounds and salts thereof
EP3027174B1 (en) 2013-07-29 2019-07-24 Aizant Drug Research Solutions Private Limited Pharmaceutical compositions of fingolimod
WO2016042493A1 (en) 2014-09-19 2016-03-24 Aizant Drug Research Pvt. Ltd Pharmaceutical compositions of fingolimod
US9925138B2 (en) 2015-01-20 2018-03-27 Handa Pharmaceuticals, Llc Stable solid fingolimod dosage forms
RU2627691C1 (ru) * 2016-07-06 2017-08-10 Олег Ростиславович Михайлов Кристаллическая η-модификация 2-амино-2-(2-(4-октилфенил)этил)пропан-1,3-диол гидрохлорида, способ её получения и фармацевтическая композиция на её основе
CN106667981B (zh) * 2017-01-16 2019-05-14 南京医科大学第二附属医院 盐酸芬戈莫德在制备治疗药物性肝损伤药物中的应用
CN106860440A (zh) * 2017-01-16 2017-06-20 南京医科大学第二附属医院 盐酸芬戈莫德在制备治疗系统性红斑狼疮脑病药物中的应用
GR1009654B (el) 2018-08-31 2019-11-18 Φαρματεν Α.Β.Ε.Ε. Φαρμακευτικο σκευασμα που περιλαμβανει εναν ανοσοτροποποιητικο παραγοντα και μεθοδος για την παρασκευη αυτου
WO2020245775A1 (en) * 2019-06-05 2020-12-10 Biocon Limited Crystalline forms of 2-amino-2-(2-(4-octylphenyl) ethyl) propane-1,3-diol
CA3156298A1 (en) 2019-10-31 2021-05-06 Laetitia POUZOL Combination of a cxcr7 antagonist with an s1p1 receptor modulator
WO2022253077A1 (zh) 2021-05-31 2022-12-08 上海博志研新药物技术有限公司 芬戈莫德药用盐、制备方法、含其的药物组合物及应用
EP4212156A1 (en) 2022-01-13 2023-07-19 Abivax Combination of 8-chloro-n-(4-(trifluoromethoxy)phenyl)quinolin-2-amine and its derivatives with a s1p receptor modulator

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US5604229A (en) * 1992-10-21 1997-02-18 Yoshitomi Pharmaceutical Industries, Ltd. 2-amino-1,3-propanediol compound and immunosuppressant
US6476004B1 (en) * 1996-07-18 2002-11-05 Mitsubishi Pharma Corporation Pharmaceutical composition
JP4079505B2 (ja) * 1998-04-28 2008-04-23 田辺三菱製薬株式会社 2−アミノ−2−[2−(4−オクチルフェニル)エチル]プロパン−1,3−ジオールの新規な製造法
WO2000027798A1 (en) * 1998-11-11 2000-05-18 Novartis Ag Production of 2-amino-2-[2-(4-c2-20-alkyl-phenyl)ethyl]propane-1,3-diols
ATE216223T1 (de) * 1999-01-27 2002-05-15 Idea Ag Transnasaler transport bzw. impfung mit hochadaptierbaren trägern
AU2460600A (en) * 1999-02-10 2000-08-29 Mitsubishi Pharma Corporation Amide compounds and medicinal use thereof
CN1144779C (zh) * 1999-03-11 2004-04-07 杭州中美华东制药有限公司 制备2-[2-(4-烷基苯基)-乙基]-2-氨基-丙二醇的方法以及其中制得的中间产物
RU2003136730A (ru) * 2001-06-08 2005-05-20 Новартис АГ (CH) Лечение или профилактика отторжения инсулин-продуцирующего клеточного трансплантата
US20030144712A1 (en) * 2001-12-20 2003-07-31 Jackson Streeter, M.D. Methods for overcoming organ transplant rejection
NZ536513A (en) * 2002-05-16 2007-10-26 Novartis Ag Use of EDG receptor binding agents in cancer
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EP2008650A3 (en) 2003-04-08 2011-04-27 Novartis AG Solid oral composition comprising a S 1 P receptor agonist and a sugar alcohol
CN1212308C (zh) * 2003-07-24 2005-07-27 漆又毛 2-氨基-2-(2-(4-辛基苯基)乙基)-1,3-丙二醇盐酸盐的制备方法
CN1241903C (zh) * 2003-10-14 2006-02-15 马启明 制备2-对辛基苯乙基-2-氨基丙二醇的方法
TWI418350B (zh) * 2005-06-24 2013-12-11 Sankyo Co 含有ppar調節劑之醫藥組成物的用途
BRPI0616640A2 (pt) * 2005-09-30 2011-06-28 Novartis Ag combinação de compostos orgánicos
CN1310869C (zh) * 2005-11-22 2007-04-18 江苏吴中苏药医药开发有限责任公司 2-氨基-2-[2-(4-烷基苯基)乙基]-1,3-丙二醇的制备方法
CN100548968C (zh) * 2006-03-01 2009-10-14 徐州师范大学 一种制备2-对辛基苯乙基-2-氨基丙二醇盐酸盐的方法
ES2414205T3 (es) * 2006-06-02 2013-07-18 The Ohio State University Research Foundation Agentes terapéuticos para el tratamiento de linfoma de células del manto
KR102044064B1 (ko) * 2006-09-26 2019-11-12 노파르티스 아게 S1p 조정제를 포함하는 제약 조성물
EP2303250A1 (en) * 2008-06-20 2011-04-06 Novartis AG Paediatric compositions for treating1 multiple sclerosis
EP2621889B1 (en) 2010-10-01 2019-07-17 Synthon BV Process for making fingolimod hydrochloride crystals

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