JP2014526508A5 - - Google Patents

Download PDF

Info

Publication number
JP2014526508A5
JP2014526508A5 JP2014530765A JP2014530765A JP2014526508A5 JP 2014526508 A5 JP2014526508 A5 JP 2014526508A5 JP 2014530765 A JP2014530765 A JP 2014530765A JP 2014530765 A JP2014530765 A JP 2014530765A JP 2014526508 A5 JP2014526508 A5 JP 2014526508A5
Authority
JP
Japan
Prior art keywords
dosage form
oral dosage
disease
weight
dispersion
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.)
Ceased
Application number
JP2014530765A
Other languages
English (en)
Japanese (ja)
Other versions
JP2014526508A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2012/054990 external-priority patent/WO2013040120A1/en
Publication of JP2014526508A publication Critical patent/JP2014526508A/ja
Publication of JP2014526508A5 publication Critical patent/JP2014526508A5/ja
Ceased legal-status Critical Current

Links

JP2014530765A 2011-09-14 2012-09-13 シクロプロパンカルボン酸{2−[(1s)−1−(3−エトキシ−4−メトキシ−フェニル)−2−メタンスルホニル−エチル]−3−オキソ−2,3−ジヒドロ−1h−イソインドール−4−イル}−アミドの製剤 Ceased JP2014526508A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201161534841P 2011-09-14 2011-09-14
US61/534,841 2011-09-14
PCT/US2012/054990 WO2013040120A1 (en) 2011-09-14 2012-09-13 Formulations of cyclopropanecarboxylic acid {2-(1s)-1-(3-ethoxy-4-methoxy-phenyl)-2-methanesulfonyl-ethyl]-3-oxo-2,3-dihydro-1h-isoindol-4-yl}-amidecelgene corporation state of incorporation:delaware

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2017016400A Division JP6339251B2 (ja) 2011-09-14 2017-02-01 シクロプロパンカルボン酸{2−[(1s)−1−(3−エトキシ−4−メトキシ−フェニル)−2−メタンスルホニル−エチル]−3−オキソ−2,3−ジヒドロ−1h−イソインドール−4−イル}−アミドの製剤

Publications (2)

Publication Number Publication Date
JP2014526508A JP2014526508A (ja) 2014-10-06
JP2014526508A5 true JP2014526508A5 (OSRAM) 2015-11-05

Family

ID=46964044

Family Applications (3)

Application Number Title Priority Date Filing Date
JP2014530765A Ceased JP2014526508A (ja) 2011-09-14 2012-09-13 シクロプロパンカルボン酸{2−[(1s)−1−(3−エトキシ−4−メトキシ−フェニル)−2−メタンスルホニル−エチル]−3−オキソ−2,3−ジヒドロ−1h−イソインドール−4−イル}−アミドの製剤
JP2017016400A Active JP6339251B2 (ja) 2011-09-14 2017-02-01 シクロプロパンカルボン酸{2−[(1s)−1−(3−エトキシ−4−メトキシ−フェニル)−2−メタンスルホニル−エチル]−3−オキソ−2,3−ジヒドロ−1h−イソインドール−4−イル}−アミドの製剤
JP2017104141A Pending JP2017178961A (ja) 2011-09-14 2017-05-26 シクロプロパンカルボン酸{2−[(1s)−1−(3−エトキシ−4−メトキシ−フェニル)−2−メタンスルホニル−エチル]−3−オキソ−2,3−ジヒドロ−1h−イソインドール−4−イル}−アミドの製剤

Family Applications After (2)

Application Number Title Priority Date Filing Date
JP2017016400A Active JP6339251B2 (ja) 2011-09-14 2017-02-01 シクロプロパンカルボン酸{2−[(1s)−1−(3−エトキシ−4−メトキシ−フェニル)−2−メタンスルホニル−エチル]−3−オキソ−2,3−ジヒドロ−1h−イソインドール−4−イル}−アミドの製剤
JP2017104141A Pending JP2017178961A (ja) 2011-09-14 2017-05-26 シクロプロパンカルボン酸{2−[(1s)−1−(3−エトキシ−4−メトキシ−フェニル)−2−メタンスルホニル−エチル]−3−オキソ−2,3−ジヒドロ−1h−イソインドール−4−イル}−アミドの製剤

Country Status (15)

Country Link
US (1) US9884042B2 (OSRAM)
EP (1) EP2765993B1 (OSRAM)
JP (3) JP2014526508A (OSRAM)
KR (1) KR20140063808A (OSRAM)
CN (1) CN105142615A (OSRAM)
AU (1) AU2012308663B2 (OSRAM)
CA (1) CA2848493A1 (OSRAM)
CL (1) CL2014000623A1 (OSRAM)
ES (1) ES2803524T3 (OSRAM)
IL (1) IL231462A0 (OSRAM)
MX (1) MX356105B (OSRAM)
PH (1) PH12014500593A1 (OSRAM)
RU (2) RU2017121896A (OSRAM)
SG (1) SG11201400632YA (OSRAM)
WO (1) WO2013040120A1 (OSRAM)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PH12014500593A1 (en) 2011-09-14 2019-09-02 Celgene Corp Formulations of cyclopropanecarboxylic acid {2-(1s)-1-(3-ethoxy-4-methoxy-phenyl)-2-methanesulfonyl-ethyl]-3-oxo-2,3-dihydro-1h-isoindol-4-yl}-amidecelgene corporation state of incorporation:delaware
EP2764866A1 (en) 2013-02-07 2014-08-13 IP Gesellschaft für Management mbH Inhibitors of nedd8-activating enzyme
ES3041833T3 (en) 2013-12-31 2025-11-14 Ascendia Pharmaceuticals Llc Pharmaceutical compositions for poorly water-soluble compounds
WO2015175505A1 (en) * 2014-05-15 2015-11-19 Lundbeck Llc Tetrabenazine modified release formulation
EP3142663A1 (en) * 2014-05-16 2017-03-22 Celgene Corporation Compositions and methods for the treatment of atherosclerotic cardiovascular diseases with pde4 modulators
KR101722564B1 (ko) * 2014-09-16 2017-04-03 강원대학교산학협력단 수-난용성 약물을 포함하는 고체분산체
EP3308792A4 (en) * 2015-06-12 2018-09-12 Nissan Chemical Industries, Ltd. Calcium salt composition and filaggrin production promoter using same
KR20200043618A (ko) * 2018-10-18 2020-04-28 주식회사유한양행 아미노피리미딘 유도체 또는 이의 염을 포함하는 경구투여용 약학 조성물
CA3193661A1 (en) * 2020-10-01 2022-04-07 Amy TAPPER Pharmaceutical formulations for treating diseases mediated by kdm1a

Family Cites Families (45)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1995003009A1 (en) 1993-07-22 1995-02-02 Oculex Pharmaceuticals, Inc. Method of treatment of macular degeneration
WO1995003807A1 (en) 1993-07-27 1995-02-09 The University Of Sydney Treatment of age-related macular degeneration
US5801195A (en) * 1994-12-30 1998-09-01 Celgene Corporation Immunotherapeutic aryl amides
IT1274549B (it) 1995-05-23 1997-07-17 Indena Spa Uso di flavanolignani per la preparazione di medicamenti ad attivita' antiproliferativa nei tumori dell'utero,dell'ovaio e del seno
US5800819A (en) 1996-01-25 1998-09-01 National Institute For Pharmaceutical Research And Development Federal Ministry Of Science And Technology Piper guineense, pterocarpus osun, eugenia caryophyllata, and sorghum bicolor extracts for treating sickle cell disease
US5635517B1 (en) 1996-07-24 1999-06-29 Celgene Corp Method of reducing TNFalpha levels with amino substituted 2-(2,6-dioxopiperidin-3-YL)-1-oxo-and 1,3-dioxoisoindolines
US6281230B1 (en) 1996-07-24 2001-08-28 Celgene Corporation Isoindolines, method of use, and pharmaceutical compositions
CZ302378B6 (cs) 1996-07-24 2011-04-20 Celgene Corporation Optický izomer (S)-1,3-dioxo-2-(2,6-dioxopiperidin-3-yl)-4-aminoisoindolin a farmaceutická kompozice s jeho obsahem
HU228769B1 (en) 1996-07-24 2013-05-28 Celgene Corp Substituted 2(2,6-dioxopiperidin-3-yl)phthalimides and -1-oxoisoindolines and their use for production of pharmaceutical compositions for mammals to reduce the level of tnf-alpha
HN1998000115A (es) * 1997-08-21 1999-06-02 Warner Lambert Co Formas de dosificación farmacéuticas sólidas
US6015803A (en) 1998-05-04 2000-01-18 Wirostko; Emil Antibiotic treatment of age-related macular degeneration
US6225348B1 (en) 1998-08-20 2001-05-01 Alfred W. Paulsen Method of treating macular degeneration with a prostaglandin derivative
US6001368A (en) 1998-09-03 1999-12-14 Protein Technologies International, Inc. Method for inhibiting or reducing the risk of macular degeneration
US6667316B1 (en) * 1999-11-12 2003-12-23 Celgene Corporation Pharmaceutically active isoindoline derivatives
US7182953B2 (en) 1999-12-15 2007-02-27 Celgene Corporation Methods and compositions for the prevention and treatment of atherosclerosis restenosis and related disorders
CN1511420A (zh) 2001-11-09 2004-07-07 ���µ�����ҵ��ʽ���� 运动图像编码方法和装置
US7968569B2 (en) 2002-05-17 2011-06-28 Celgene Corporation Methods for treatment of multiple myeloma using 3-(4-amino-1-oxo-1,3-dihydro-isoindol-2-yl)-piperidine-2,6-dione
US7323479B2 (en) 2002-05-17 2008-01-29 Celgene Corporation Methods for treatment and management of brain cancer using 1-oxo-2-(2,6-dioxopiperidin-3-yl)-4-methylisoindoline
US7393862B2 (en) 2002-05-17 2008-07-01 Celgene Corporation Method using 3-(4-amino-1-oxo-1,3-dihydro-isoindol-2-yl)-piperidine-2,6-dione for treatment of certain leukemias
US20100129363A1 (en) 2002-05-17 2010-05-27 Zeldis Jerome B Methods and compositions using pde4 inhibitors for the treatment and management of cancers
US7189740B2 (en) 2002-10-15 2007-03-13 Celgene Corporation Methods of using 3-(4-amino-oxo-1,3-dihydro-isoindol-2-yl)-piperidine-2,6-dione for the treatment and management of myelodysplastic syndromes
US20050203142A1 (en) 2002-10-24 2005-09-15 Zeldis Jerome B. Methods of using and compositions comprising immunomodulatory compounds for treatment, modification and management of pain
US20040091455A1 (en) 2002-10-31 2004-05-13 Zeldis Jerome B. Methods of using and compositions comprising immunomodulatory compounds for treatment and management of macular degeneration
US7563810B2 (en) 2002-11-06 2009-07-21 Celgene Corporation Methods of using 3-(4-amino-1-oxo-1,3-dihydroisoindol-2-yl)-piperidine-2,6-dione for the treatment and management of myeloproliferative diseases
US20050100529A1 (en) 2003-11-06 2005-05-12 Zeldis Jerome B. Methods of using and compositions comprising immunomodulatory compounds for the treatment and management of asbestos-related diseases and disorders
CN1913896B (zh) 2003-12-02 2010-12-01 细胞基因公司 用于治疗和控制血红蛋白病和贫血病的方法和组合物
US20050143344A1 (en) 2003-12-30 2005-06-30 Zeldis Jerome B. Methods and compositions using immunomodulatory compounds for the treatment and management of central nervous system disorders or diseases
CN1956718A (zh) 2004-03-22 2007-05-02 细胞基因公司 用于治疗和控制皮肤疾病和病症的含免疫调节化合物的组合物和使用方法
US20050222209A1 (en) 2004-04-01 2005-10-06 Zeldis Jerome B Methods and compositions for the treatment, prevention or management of dysfunctional sleep and dysfunctional sleep associated with disease
KR20070010184A (ko) 2004-04-23 2007-01-22 셀진 코포레이션 폐 고혈압증의 치료 및 관리를 위한 면역조절 화합물의사용 방법 및 상기 화합물을 포함하는 조성물
EP1817008B1 (en) * 2004-11-09 2020-04-01 Board of Regents, The University of Texas System Stabilized hme composition with small drug particles
CN101098694A (zh) 2004-11-12 2008-01-02 细胞基因公司 使用免疫调节化合物治疗和控制寄生性疾病的方法和组合物
ZA200704890B (en) 2004-11-23 2008-09-25 Celgene Corp Methods and compositions using immunomodulatory compounds for treatment and management of central nervous system injury
ATE499112T1 (de) 2005-09-01 2011-03-15 Celgene Corp Immunologische verwendungen von immunmodulatorischen verbindungen für einen impfstoff und therapie gegen infektionskrankheiten
JP2010526848A (ja) * 2007-05-11 2010-08-05 エフ.ホフマン−ラ ロシュ アーゲー 難溶性薬物用の医薬組成物
JP4989733B2 (ja) * 2008-02-13 2012-08-01 大日本住友製薬株式会社 口腔内崩壊錠
CA2718412A1 (en) * 2008-03-24 2009-10-01 Celgene Corporation Treatment of psoriasis or psoriatic arthritis using cyclopropyl-n-{2-{(1s)-1-(3-ethoxy-4-methoxyphenyl)-2-(methylsulfonyl)ethyl]-3-oxoisoindoline-4-yl}carboxamide
US9192578B2 (en) * 2008-08-20 2015-11-24 Board Of Regents, The University Of Texas System Hot-melt extrusion of modified release multi-particulates
HRP20130356T1 (en) 2008-09-10 2013-05-31 Celgene Corporation Processes for the preparation of aminosulfone compounds
US20120149716A1 (en) 2009-02-10 2012-06-14 Zeldis Jerome B Methods of using and compositions comprising pde4 modulators for treatment, prevention and management of tuberculosis
ES2727733T3 (es) * 2009-11-10 2019-10-18 Celgene Corp Nanosuspensión de un fármaco poco soluble preparada por el proceso de microfluidización
JP5854476B2 (ja) 2009-11-30 2016-02-09 アデア ファーマスーティカルズ,インコーポレイテッド 圧縮性コーティングで被覆された医薬組成物及び錠剤並びに製造方法
ES2632979T3 (es) * 2011-01-10 2017-09-18 Celgene Corporation Formas de dosificación oral de {2-[(1S)-1-(3-etoxi-4-metoxi-fenil)-2-metanosulfonil-etil]-3-oxo-2,3-dihidro-1H-isoindol-4-il}-amida de ácido ciclopropanocarboxílico
PH12014500593A1 (en) 2011-09-14 2019-09-02 Celgene Corp Formulations of cyclopropanecarboxylic acid {2-(1s)-1-(3-ethoxy-4-methoxy-phenyl)-2-methanesulfonyl-ethyl]-3-oxo-2,3-dihydro-1h-isoindol-4-yl}-amidecelgene corporation state of incorporation:delaware
DK2797581T3 (da) 2011-12-27 2020-07-20 Amgen Europe Gmbh Formuleringer af (+)-2-[1-(3-ethoxy-4-methoxyphenyl)-2-methansulfonylethyl]-4-acetylaminoisoindolin-1,3-dion

Similar Documents

Publication Publication Date Title
JP2014526508A5 (OSRAM)
RU2014114499A (ru) Препараты {2-[(1s)-1-(3-этокси-4-метоксифенил)-2-метансульфонилэтил]-3-оксо-2,3-дигидро-1h-изоиндол-4-ил}амида циклопропанкарбоновой кислоты
JP6898960B2 (ja) 脳癌の治療
Schopf et al. Topical ocular drug delivery to the back of the eye by mucus-penetrating particles
HRP20171578T1 (hr) Čvrsta disperzija
CN107530348B (zh) 一种含有jak激酶抑制剂或其可药用盐的药物组合物
JP2012526855A5 (OSRAM)
DK2953948T3 (en) FLUORINATED INTEGRIN ANTAGONISTS
AU2012250862B2 (en) Rapid dissolve tablet compositions for vaginal administration
JP2016525102A5 (OSRAM)
JP2018507200A5 (OSRAM)
JP2015517976A5 (OSRAM)
FI3265084T3 (fi) Brutonin tyrosiinikinaasin estäjän lääkeformulaatioita
RU2017106795A (ru) Новые составы ингибитора тирозинкиназы брутона
JP2015524444A5 (OSRAM)
JP2017533968A5 (OSRAM)
JP2014532638A5 (OSRAM)
JP2010505958A5 (OSRAM)
JP2017505822A5 (OSRAM)
JP2019506387A5 (OSRAM)
BR122019027412B8 (pt) composição farmacêutica de liberação sustentada na forma de micropartículas, processo para preparação das ditas micropartículas, e kit de administração
RU2016136697A (ru) Комплексы сиролимуса и его производных, способ их получения и фармацевтические композиции, содержащие указанные комплексы
JP2017528497A5 (OSRAM)
JP2017527600A5 (OSRAM)
US20170368031A1 (en) Solid dispersion formulations of antiviral compounds