JP2012167125A5 - - Google Patents

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Publication number
JP2012167125A5
JP2012167125A5 JP2012131109A JP2012131109A JP2012167125A5 JP 2012167125 A5 JP2012167125 A5 JP 2012167125A5 JP 2012131109 A JP2012131109 A JP 2012131109A JP 2012131109 A JP2012131109 A JP 2012131109A JP 2012167125 A5 JP2012167125 A5 JP 2012167125A5
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JP
Japan
Prior art keywords
formulation
phenyl
capsule
diazaspiro
decan
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.)
Granted
Application number
JP2012131109A
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English (en)
Japanese (ja)
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JP5415587B2 (ja
JP2012167125A (ja
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Publication of JP2012167125A publication Critical patent/JP2012167125A/ja
Publication of JP2012167125A5 publication Critical patent/JP2012167125A5/ja
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Publication of JP5415587B2 publication Critical patent/JP5415587B2/ja
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

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JP2012131109A 2006-04-05 2012-06-08 薬学的処方物:8−[{1−(3,5−ビス−(トリフルオロメチル)フェニル)−エトキシ}−メチル]−8−フェニル−1,7−ジアザ−スピロ[4.5]デカン−2−オンの塩およびそれを使用した処置方法 Expired - Fee Related JP5415587B2 (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US78951406P 2006-04-05 2006-04-05
US60/789,514 2006-04-05

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
JP2009504270A Division JP5155998B2 (ja) 2006-04-05 2007-04-04 薬学的処方物:8−[{1−(3,5−ビス−(トリフルオロメチル)フェニル)−エトキシ}−メチル]−8−フェニル−1,7−ジアザ−スピロ[4.5]デカン−2−オンの塩およびそれを使用した処置方法

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2012268500A Division JP5640065B2 (ja) 2006-04-05 2012-12-07 薬学的処方物:8−[{1−(3,5−ビス−(トリフルオロメチル)フェニル)−エトキシ}−メチル]−8−フェニル−1,7−ジアザ−スピロ[4.5]デカン−2−オンの塩およびそれを使用した処置方法

Publications (3)

Publication Number Publication Date
JP2012167125A JP2012167125A (ja) 2012-09-06
JP2012167125A5 true JP2012167125A5 (OSRAM) 2013-01-31
JP5415587B2 JP5415587B2 (ja) 2014-02-12

Family

ID=38441502

Family Applications (4)

Application Number Title Priority Date Filing Date
JP2009504270A Expired - Fee Related JP5155998B2 (ja) 2006-04-05 2007-04-04 薬学的処方物:8−[{1−(3,5−ビス−(トリフルオロメチル)フェニル)−エトキシ}−メチル]−8−フェニル−1,7−ジアザ−スピロ[4.5]デカン−2−オンの塩およびそれを使用した処置方法
JP2012131109A Expired - Fee Related JP5415587B2 (ja) 2006-04-05 2012-06-08 薬学的処方物:8−[{1−(3,5−ビス−(トリフルオロメチル)フェニル)−エトキシ}−メチル]−8−フェニル−1,7−ジアザ−スピロ[4.5]デカン−2−オンの塩およびそれを使用した処置方法
JP2012268500A Expired - Fee Related JP5640065B2 (ja) 2006-04-05 2012-12-07 薬学的処方物:8−[{1−(3,5−ビス−(トリフルオロメチル)フェニル)−エトキシ}−メチル]−8−フェニル−1,7−ジアザ−スピロ[4.5]デカン−2−オンの塩およびそれを使用した処置方法
JP2014218278A Expired - Fee Related JP6035305B2 (ja) 2006-04-05 2014-10-27 薬学的処方物:8−[{1−(3,5−ビス−(トリフルオロメチル)フェニル)−エトキシ}−メチル]−8−フェニル−1,7−ジアザ−スピロ[4.5]デカン−2−オンの塩およびそれを使用した処置方法

Family Applications Before (1)

Application Number Title Priority Date Filing Date
JP2009504270A Expired - Fee Related JP5155998B2 (ja) 2006-04-05 2007-04-04 薬学的処方物:8−[{1−(3,5−ビス−(トリフルオロメチル)フェニル)−エトキシ}−メチル]−8−フェニル−1,7−ジアザ−スピロ[4.5]デカン−2−オンの塩およびそれを使用した処置方法

Family Applications After (2)

Application Number Title Priority Date Filing Date
JP2012268500A Expired - Fee Related JP5640065B2 (ja) 2006-04-05 2012-12-07 薬学的処方物:8−[{1−(3,5−ビス−(トリフルオロメチル)フェニル)−エトキシ}−メチル]−8−フェニル−1,7−ジアザ−スピロ[4.5]デカン−2−オンの塩およびそれを使用した処置方法
JP2014218278A Expired - Fee Related JP6035305B2 (ja) 2006-04-05 2014-10-27 薬学的処方物:8−[{1−(3,5−ビス−(トリフルオロメチル)フェニル)−エトキシ}−メチル]−8−フェニル−1,7−ジアザ−スピロ[4.5]デカン−2−オンの塩およびそれを使用した処置方法

Country Status (19)

Country Link
US (4) US7563801B2 (OSRAM)
EP (2) EP2997964A1 (OSRAM)
JP (4) JP5155998B2 (OSRAM)
KR (1) KR20080108319A (OSRAM)
CN (2) CN103751186B (OSRAM)
AR (1) AR060303A1 (OSRAM)
AU (1) AU2007233389C1 (OSRAM)
BR (1) BRPI0710577A2 (OSRAM)
CA (2) CA2648640C (OSRAM)
CL (1) CL2007000945A1 (OSRAM)
ES (1) ES2553805T3 (OSRAM)
MX (1) MX2008012936A (OSRAM)
NO (1) NO342810B1 (OSRAM)
NZ (1) NZ571693A (OSRAM)
PE (2) PE20080054A1 (OSRAM)
SG (1) SG10201500028RA (OSRAM)
TW (1) TWI332836B (OSRAM)
WO (1) WO2007114921A2 (OSRAM)
ZA (1) ZA200808465B (OSRAM)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PE20030762A1 (es) 2001-12-18 2003-09-05 Schering Corp Compuestos heterociclicos como antagonistas nk1
CN102276606B (zh) 2006-04-05 2013-06-12 欧科生医股份有限公司 8-[{1-(3,5-双-(三氟甲基)苯基)-乙氧基}-甲基]-8-苯基-1,7-二氮杂-螺[4.5]癸-2-酮的甲苯磺酸盐及其制备方法
CL2007000945A1 (es) * 2006-04-05 2008-01-25 Schering Corp Formulacion farmaceutica que comprende una sal cristalina de monohidrato de hidrocloruro de (5s,8s)-8-[[(1r)-1-(3,5-bistrifluorometil)fenil]-etoximetil]-8-fenil-1,7-diaza-espiro[4.5]decan-2-ona; capsula que la contiene; y uso en el tratamiento de la emesis y nausea.
PE20081891A1 (es) 2007-03-22 2008-12-27 Opko Health Inc Formulaciones de comprimidos que contienen sales de 8-[{1-(3,5-bis-(trifluorometil)fenil)-etoxi}-metil]-8-fenil-1,7-diaza-spiro[4.5]decan-2-ona y comprimidos elaborados a partir de estas
AR066191A1 (es) 2007-03-22 2009-08-05 Schering Corp Proceso e intermediarios para la sintesis de compuestos 8- [ ( 1- (3,5- bis- ( trifluorometil) fenil) - etoxi ) - metil]- 8 fenil - 1,7- diaza - espiro (4, 5) decan -2 ona
AU2009289598B2 (en) 2008-09-05 2014-09-11 Opko Health, Inc. Process and intermediates for the synthesis of 8-[{1-(3,5-Bis-(trifluoromethyl)phenyl) -ethoxy}-methyl]-8-phenyl-1,7-diaza-spiro[4.5]decan-2-one compounds
WO2010077669A2 (en) * 2008-12-08 2010-07-08 Teva Pharmaceutical Industries Ltd. Palonosetron formulation
MX336071B (es) * 2009-08-14 2016-01-06 Opko Health Inc Formulaciones intravenosas de antagonistas de neurocinina 1.
EP3002005A1 (en) 2014-09-30 2016-04-06 Molkerei Meggle Wasserburg GmbH & Co. Kg Direct compression excipient based on lactose, cellulose and starch
CN104473887A (zh) * 2014-11-12 2015-04-01 广东东阳光药业有限公司 一种提高利伐沙班片溶出曲线重现性的方法
CN106866669A (zh) * 2017-04-19 2017-06-20 成都百特万合医药科技有限公司 一种合成罗拉吡坦中间体的方法

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FR2678971B1 (fr) * 1991-07-08 1998-04-10 Andre Giraud Elements de structure composite transparents et leurs procedes de fabrication.
US5830548A (en) * 1992-08-11 1998-11-03 E. Khashoggi Industries, Llc Articles of manufacture and methods for manufacturing laminate structures including inorganically filled sheets
US5665450A (en) * 1992-08-21 1997-09-09 The Curators Of The University Of Missouri Optically transparent composite material and process for preparing same
JPH08502510A (ja) 1992-10-28 1996-03-19 メルク シヤープ エンド ドーム リミテツド タキキニン拮抗剤としてのアリールメチルオキシメチルピペリジン
US5661162A (en) 1992-12-14 1997-08-26 Merck Sharp & Dohme Limited 4-aminomethyl/thiomethyl/sulfonylmethyl-4-phenylpiperdines as tachykinin receptor antagonists
US5760018A (en) 1994-01-13 1998-06-02 Merck Sharp & Dohme Ltd. Gem-disubstituted azacyclic tachykinin antagonists
US5733659A (en) * 1995-02-27 1998-03-31 Mitsubishi Engineering-Plastics Corporation Transparent rigid resin molded product and process for producing the same
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DE69616367T2 (de) 1995-08-28 2002-06-27 Schering Corp., Kenilworth Kombinationstherapie für fortgeschrittenes krebsstadium mit temozolomid und cisplatin
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EP1830845A2 (en) 2004-11-09 2007-09-12 Shering Corporation Improved dosing regimen of temozolomide for treating cancer based on the patient's mgmt level
CN102276606B (zh) 2006-04-05 2013-06-12 欧科生医股份有限公司 8-[{1-(3,5-双-(三氟甲基)苯基)-乙氧基}-甲基]-8-苯基-1,7-二氮杂-螺[4.5]癸-2-酮的甲苯磺酸盐及其制备方法
CL2007000945A1 (es) * 2006-04-05 2008-01-25 Schering Corp Formulacion farmaceutica que comprende una sal cristalina de monohidrato de hidrocloruro de (5s,8s)-8-[[(1r)-1-(3,5-bistrifluorometil)fenil]-etoximetil]-8-fenil-1,7-diaza-espiro[4.5]decan-2-ona; capsula que la contiene; y uso en el tratamiento de la emesis y nausea.
AR066191A1 (es) 2007-03-22 2009-08-05 Schering Corp Proceso e intermediarios para la sintesis de compuestos 8- [ ( 1- (3,5- bis- ( trifluorometil) fenil) - etoxi ) - metil]- 8 fenil - 1,7- diaza - espiro (4, 5) decan -2 ona
PE20081891A1 (es) 2007-03-22 2008-12-27 Opko Health Inc Formulaciones de comprimidos que contienen sales de 8-[{1-(3,5-bis-(trifluorometil)fenil)-etoxi}-metil]-8-fenil-1,7-diaza-spiro[4.5]decan-2-ona y comprimidos elaborados a partir de estas
AU2009289598B2 (en) 2008-09-05 2014-09-11 Opko Health, Inc. Process and intermediates for the synthesis of 8-[{1-(3,5-Bis-(trifluoromethyl)phenyl) -ethoxy}-methyl]-8-phenyl-1,7-diaza-spiro[4.5]decan-2-one compounds
MX336071B (es) 2009-08-14 2016-01-06 Opko Health Inc Formulaciones intravenosas de antagonistas de neurocinina 1.

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