JP2018065829A5 - - Google Patents

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Publication number
JP2018065829A5
JP2018065829A5 JP2017225061A JP2017225061A JP2018065829A5 JP 2018065829 A5 JP2018065829 A5 JP 2018065829A5 JP 2017225061 A JP2017225061 A JP 2017225061A JP 2017225061 A JP2017225061 A JP 2017225061A JP 2018065829 A5 JP2018065829 A5 JP 2018065829A5
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JP
Japan
Prior art keywords
pharmaceutical composition
composition according
treatment
subject
compound
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JP2017225061A
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English (en)
Japanese (ja)
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JP6419294B2 (ja
JP2018065829A (ja
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Publication of JP2018065829A5 publication Critical patent/JP2018065829A5/ja
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JP2017225061A 2010-07-20 2017-11-22 シグマ受容体に仲介される障害を処置するための環状アミド誘導体の使用の方法 Active JP6419294B2 (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US36608010P 2010-07-20 2010-07-20
US61/366,080 2010-07-20

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
JP2016135208A Division JP2016199578A (ja) 2010-07-20 2016-07-07 シグマ受容体に仲介される障害を処置するための環状アミド誘導体の使用の方法

Publications (3)

Publication Number Publication Date
JP2018065829A JP2018065829A (ja) 2018-04-26
JP2018065829A5 true JP2018065829A5 (enExample) 2018-07-05
JP6419294B2 JP6419294B2 (ja) 2018-11-07

Family

ID=45497167

Family Applications (3)

Application Number Title Priority Date Filing Date
JP2013520841A Pending JP2013531073A (ja) 2010-07-20 2011-07-20 シグマ受容体に仲介される障害を処置するための環状アミド誘導体の使用の方法
JP2016135208A Pending JP2016199578A (ja) 2010-07-20 2016-07-07 シグマ受容体に仲介される障害を処置するための環状アミド誘導体の使用の方法
JP2017225061A Active JP6419294B2 (ja) 2010-07-20 2017-11-22 シグマ受容体に仲介される障害を処置するための環状アミド誘導体の使用の方法

Family Applications Before (2)

Application Number Title Priority Date Filing Date
JP2013520841A Pending JP2013531073A (ja) 2010-07-20 2011-07-20 シグマ受容体に仲介される障害を処置するための環状アミド誘導体の使用の方法
JP2016135208A Pending JP2016199578A (ja) 2010-07-20 2016-07-07 シグマ受容体に仲介される障害を処置するための環状アミド誘導体の使用の方法

Country Status (15)

Country Link
US (4) US20130274290A1 (enExample)
EP (2) EP4070794A3 (enExample)
JP (3) JP2013531073A (enExample)
KR (1) KR101867634B1 (enExample)
CN (2) CN107007603A (enExample)
BR (1) BR112013001302A2 (enExample)
CA (2) CA2805904C (enExample)
DK (1) DK2595485T3 (enExample)
ES (1) ES2914120T3 (enExample)
HU (1) HUE058736T2 (enExample)
PL (1) PL2595485T3 (enExample)
PT (1) PT2595485T (enExample)
RU (2) RU2746871C2 (enExample)
TW (1) TWI520949B (enExample)
WO (1) WO2012012543A1 (enExample)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8937900B2 (en) 2010-07-20 2015-01-20 Qualcomm Incorporated Enhancing pilot channel transmission in TD-SCDMA multicarrier systems using secondary carrier frequencies
US10179776B2 (en) 2014-06-09 2019-01-15 Intra-Cellular Therapies, Inc. Compounds and methods of use to treat schizophrenia
IL301320B2 (en) 2014-12-02 2024-11-01 Minerva Neurosciences Inc Compositions comprising 2-((1-(2(4-fluorophenyl)-2-oxoethyl)piperidin-4-yl)methyl)isoindolin-1-one for treating schizophrenia
CN113694065A (zh) * 2016-05-25 2021-11-26 田边三菱制药株式会社 用于治疗非精神分裂症患者中的阴性症状的组合物和方法
JP2020525436A (ja) 2017-06-21 2020-08-27 ミネルバ・ニューロサイエンシズ・インコーポレイテッド 胃耐性制御放出経口剤形
EP3840835A1 (en) * 2018-08-21 2021-06-30 Minerva Neurosciences, Inc. Use of roluperidone to treat negative symptoms and disorders, increase neuroplasticity, and promote neuroprotection
IL298323B2 (en) 2020-05-20 2023-10-01 Univ Illinois A method for treating lysosomal storage disease using histatin peptides

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NZ235841A (en) * 1989-10-27 1993-03-26 Du Pont (n-phthalimidoalkyl) piperidine derivatives and pharmaceutical compositions
EP0497843A4 (en) * 1989-10-27 1992-09-23 The Du Pont Merck Pharmaceutical Company (n-phthalimidoalkyl) piperidines
JP3333878B2 (ja) * 1992-04-23 2002-10-15 メレルダウファーマスーティカルズ インコーポレイテッド セロトニン5ht2拮抗剤としての4‐イミドメチル‐1‐[2’フェニル‐2’オキソエチル‐]ピペリジン類,それらの製法及び治療用途
NZ521576A (en) * 2000-02-29 2005-06-24 Mitsubishi Pharma Corp Novel cyclic amide derivatives
TW200817400A (en) * 2006-05-30 2008-04-16 Elbion Ag Pyrido [3,2-e] pyrazines, their use as inhibitors of phosphodiesterase 10, and processes for preparing them

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