JP2012504560A5 - - Google Patents

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Publication number
JP2012504560A5
JP2012504560A5 JP2011529448A JP2011529448A JP2012504560A5 JP 2012504560 A5 JP2012504560 A5 JP 2012504560A5 JP 2011529448 A JP2011529448 A JP 2011529448A JP 2011529448 A JP2011529448 A JP 2011529448A JP 2012504560 A5 JP2012504560 A5 JP 2012504560A5
Authority
JP
Japan
Prior art keywords
disorder
formula
abuse
schizophrenia
depression
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
JP2011529448A
Other languages
English (en)
Japanese (ja)
Other versions
JP2012504560A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/DK2009/050258 external-priority patent/WO2010037398A1/en
Publication of JP2012504560A publication Critical patent/JP2012504560A/ja
Publication of JP2012504560A5 publication Critical patent/JP2012504560A5/ja
Pending legal-status Critical Current

Links

JP2011529448A 2008-10-03 2009-10-01 経口製剤 Pending JP2012504560A (ja)

Applications Claiming Priority (9)

Application Number Priority Date Filing Date Title
US10237708P 2008-10-03 2008-10-03
US61/102,377 2008-10-03
DKPA200801392 2008-10-03
DKPA200801392 2008-10-03
US17639209P 2009-05-07 2009-05-07
DKPA200900591 2009-05-07
DKPA200900591 2009-05-07
US61/176,392 2009-05-07
PCT/DK2009/050258 WO2010037398A1 (en) 2008-10-03 2009-10-01 Oral formulation

Publications (2)

Publication Number Publication Date
JP2012504560A JP2012504560A (ja) 2012-02-23
JP2012504560A5 true JP2012504560A5 (show.php) 2012-11-15

Family

ID=41217546

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2011529448A Pending JP2012504560A (ja) 2008-10-03 2009-10-01 経口製剤

Country Status (16)

Country Link
US (1) US20110178094A1 (show.php)
EP (1) EP2344163A1 (show.php)
JP (1) JP2012504560A (show.php)
KR (1) KR20110081176A (show.php)
CN (1) CN102170884A (show.php)
AR (1) AR073755A1 (show.php)
AU (1) AU2009298264A1 (show.php)
BR (1) BRPI0919165A2 (show.php)
CA (1) CA2732613A1 (show.php)
CO (1) CO6321158A2 (show.php)
EA (1) EA201170512A1 (show.php)
IL (1) IL210235A0 (show.php)
MX (1) MX2011001044A (show.php)
NZ (1) NZ590897A (show.php)
WO (1) WO2010037398A1 (show.php)
ZA (1) ZA201102446B (show.php)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE602004000260T2 (de) 2003-07-22 2006-08-24 Arena Pharmaceuticals, Inc., San Diego Diaryl- und arylheteroarylharnstoffderivate als modulatoren des 5-ht2a-serotoninrezeptors, die sich zur prophylaxe und behandlung von damit im zusammenhang stehenden erkrankungen eignen
EP2254564A1 (en) 2007-12-12 2010-12-01 Glaxo Group Limited Combinations comprising 3-phenylsulfonyl-8-piperazinyl-1yl-quinoline
WO2009123714A2 (en) 2008-04-02 2009-10-08 Arena Pharmaceuticals, Inc. Processes for the preparation of pyrazole derivatives useful as modulators of the 5-ht2a serotonin receptor
NZ589571A (en) * 2008-05-07 2012-07-27 Lundbeck & Co As H Method for treating cognitive deficits using trans-4-((1r,3s)-6-chloro-3-phenylindan-1-yl)-1,2,2-trimethylpiperazine
US9126946B2 (en) 2008-10-28 2015-09-08 Arena Pharmaceuticals, Inc. Processes useful for the preparation of 1-[3-(4-bromo-2-methyl-2H-pyrazol-3-yl)-4-methoxy-phenyl]-3-(2,4-difluoro-phenyl)urea and crystalline forms related thereto
LT2720989T (lt) 2011-06-20 2016-11-25 H. Lundbeck A/S Deuterinti 1-piperazin-3-fenilindanai, skirti šizofrenijos gydymui
TWI552751B (zh) * 2011-06-20 2016-10-11 H 朗德貝克公司 投予4-((1r,3s)-6-氯-3-苯基-二氫茚-1-基)-1,2,2-三甲基-哌及其鹽用於治療精神分裂症的方法
RU2017145976A (ru) 2015-06-12 2019-07-15 Аксовант Сайенсиз Гмбх Производные диарил- и арилгетероарилмочевины, применимые для профилактики и лечения нарушения поведения во время REM-фазы сна
TW201720439A (zh) 2015-07-15 2017-06-16 Axovant Sciences Gmbh 用於預防及治療與神經退化性疾病相關的幻覺之作為5-ht2a血清素受體的二芳基及芳基雜芳基脲衍生物
JP7442538B2 (ja) 2018-10-29 2024-03-04 ハー・ルンドベック・アクチエゼルスカベット 非晶性の式(i)の化合物及び非晶性の式(i)の化合物塩
EP3891134A1 (en) 2018-12-03 2021-10-13 H. Lundbeck A/S Prodrugs of 4-((1r,3s)-6-chloro-3-phenyl-2,3-dihydro-1h-inden-1-yl)-1,2,2-trimethylpiperazine and 4-((1/r,3s)-6-chloro-3-(phenyl-d5)-2,3-dihydro-1h-inden-1-yl)-2,2-dimethy-1-(methyl-d3)piperazine

Family Cites Families (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4031216A (en) * 1974-08-12 1977-06-21 Knoll A.G. Chemische Fabriken 3-(3,4-Dialkoxy-benzyl)-3-methyl-piperazines
NZ196284A (en) * 1980-02-29 1983-12-16 Kefalas As 1-piperazino-3-phenylindane derivatives:pharmaceutical compositions
DE3139970A1 (de) * 1981-10-08 1983-04-28 Boehringer Mannheim Gmbh, 6800 Mannheim Neue carbonsaeurederivate, verfahren zu ihrer herstellung sowie diese verbindungen enthaltende arzneimittel
US5026853A (en) * 1987-04-01 1991-06-25 Janssen Pharmaceutica N.V. 4-substituted-2(or 3)aminocarbonyl-1-piperazineacetamide
US5466806A (en) * 1989-02-08 1995-11-14 Biochem Pharma Inc. Processes for preparing substituted 1,3-oxathiolanes with antiviral properties
CA2091204C (en) * 1992-03-11 1997-04-08 Ronald J. Mattson Antiischemic-piperazinyl and piperidinyl-cyclohexanes
DK55192D0 (da) * 1992-04-28 1992-04-28 Lundbeck & Co As H 1-piperazino-1,2-dihydroindenderivater
CA2132411A1 (en) * 1994-09-19 1996-03-20 Michael Trani Enzymatic esterification of long-chain racemic acids and alcohols
US6410794B1 (en) * 1994-12-16 2002-06-25 Uop Llc Process for preparation of pharmaceutically desired chiral tetralone from tetralones
US6455736B1 (en) * 1994-12-16 2002-09-24 Uop Llc Process for preparation of pharmaceutically desired sertraline and sertraline analogs
US5807897A (en) * 1996-03-01 1998-09-15 Zeneca Limited Aminotetralin derivative and compositions and method of use thereof
EP1073618B1 (en) * 1998-05-01 2003-12-03 Pfizer Products Inc. Process for the production of enantiomerically pure or optically enriched sertraline-tetralone using continuous chromatography
IN187170B (show.php) * 2000-01-04 2002-02-23 Sun Pharmaceutical Ind Ltd
IL162458A0 (en) * 2001-12-28 2005-11-20 Teva Pharma A stable pharmaceutical formulation of paroxetine hydrochloride anhydrous and a process for preparation thereof
JP5043429B2 (ja) * 2003-08-18 2012-10-10 ハー・ルンドベック・アクチエゼルスカベット トランス−4−((1r,3s)−6−クロロ−3−フェニルインダン−1−イル)−1,2,2−トリメチルピペラジンのコハク酸塩およびマロン酸塩、および薬剤としての使用方法
TWI376373B (en) * 2005-02-16 2012-11-11 Lundbeck & Co As H Crystalline base of a pharmaceutical compound
JP2008530039A (ja) * 2005-02-16 2008-08-07 ハー・ルンドベック・アクチエゼルスカベット トランス−1−((1r,3s)−6−クロロ−3−フェニルインダン−1−イル)−3,3−ジメチルピペラジンの酒石酸塩およびリンゴ酸塩
BRPI0714265A2 (pt) * 2006-08-10 2013-04-16 Cipla Ltd composiÇço oral sàlida, processo para preparar uma composiÇço oral sàlida, uso de uma composiÇço e mÉtodo para tratar hiv
NZ589571A (en) * 2008-05-07 2012-07-27 Lundbeck & Co As H Method for treating cognitive deficits using trans-4-((1r,3s)-6-chloro-3-phenylindan-1-yl)-1,2,2-trimethylpiperazine

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