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
DKPA200801392 2008-10-03
DKPA200801392 2008-10-03
US61/102,377 2008-10-03
US17639209P 2009-05-07 2009-05-07
US61/176,392 2009-05-07
DKPA200900591 2009-05-07
DKPA200900591 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 (enExample) 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 (enExample)
EP (1) EP2344163A1 (enExample)
JP (1) JP2012504560A (enExample)
KR (1) KR20110081176A (enExample)
CN (1) CN102170884A (enExample)
AR (1) AR073755A1 (enExample)
AU (1) AU2009298264A1 (enExample)
BR (1) BRPI0919165A2 (enExample)
CA (1) CA2732613A1 (enExample)
CO (1) CO6321158A2 (enExample)
EA (1) EA201170512A1 (enExample)
IL (1) IL210235A0 (enExample)
MX (1) MX2011001044A (enExample)
NZ (1) NZ590897A (enExample)
WO (1) WO2010037398A1 (enExample)
ZA (1) ZA201102446B (enExample)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1558582B1 (en) 2003-07-22 2005-12-21 Arena Pharmaceuticals, Inc. Diaryl and arylheteroaryl urea derivatives as modulators of the 5-ht2a serotonin receptor useful for the prophylaxis and treatment of disorders related thereto
EP2254564A1 (en) 2007-12-12 2010-12-01 Glaxo Group Limited Combinations comprising 3-phenylsulfonyl-8-piperazinyl-1yl-quinoline
US20110021538A1 (en) 2008-04-02 2011-01-27 Arena Pharmaceuticals, Inc. Processes for the preparation of pyrazole derivatives useful as modulators of the 5-ht2a serotonin receptor
WO2009135495A1 (en) * 2008-05-07 2009-11-12 H. Lundbeck A/S Method for treating cognitive deficits
WO2010062321A1 (en) 2008-10-28 2010-06-03 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
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
PL3135656T3 (pl) 2011-06-20 2019-07-31 H. Lundbeck A/S Deuterowane 1-piperazyno-3-fenyloindany do leczenia schizofrenii
HK1245660A1 (zh) 2015-06-12 2018-08-31 Axovant Sciences Gmbh 有用於预防和治疗rem睡眠行为障碍的二芳基脲和芳基脲衍生物
WO2017011767A2 (en) 2015-07-15 2017-01-19 Axovant Sciences Ltd. Diaryl and arylheteroaryl urea derivatives as modulators of the 5-ht2a serotonin receptor useful for the prophylaxis and treatment of hallucinations associated with a neurodegenerative disease
US20210395208A1 (en) 2018-10-29 2021-12-23 H. Lundeck A/S Amorphous compounds of formula (i) and amorphous compounds of formula (i) salts
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
IE50867B1 (en) * 1980-02-29 1986-08-06 Kefalas As Indane derivatives
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
US6455736B1 (en) * 1994-12-16 2002-09-24 Uop Llc Process for preparation of pharmaceutically desired sertraline and sertraline analogs
US6410794B1 (en) * 1994-12-16 2002-06-25 Uop Llc Process for preparation of pharmaceutically desired chiral tetralone from tetralones
US5807897A (en) * 1996-03-01 1998-09-15 Zeneca Limited Aminotetralin derivative and compositions and method of use thereof
ATE255555T1 (de) * 1998-05-01 2003-12-15 Pfizer Prod Inc Verfahren zur herstellung von enantiomeren reinem oder optisch angereicherter sertraline-tetralon durch kontinuierliche chromatographie
IN187170B (enExample) * 2000-01-04 2002-02-23 Sun Pharmaceutical Ind Ltd
US7396542B2 (en) * 2001-12-28 2008-07-08 Teva Pharmaceutical Industries Ltd. Stable pharmaceutical formulation of paroxetine hydrochloride anhydrous and a process for preparation thereof
PL1658277T3 (pl) * 2003-08-18 2012-10-31 H Lundbeck As Sól bursztynianowa i malonianowa trans-4-((1R,3S)-6-chloro-3-fenyloindan-1-ylo)-1,2,2-tri-metylopiperazyny i zastosowanie jako lek
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
WO2008017867A2 (en) * 2006-08-10 2008-02-14 Cipla Limited Antiretroviral solid oral composition with at least one water insoluble polymer
WO2009135495A1 (en) * 2008-05-07 2009-11-12 H. Lundbeck A/S Method for treating cognitive deficits

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