JP2013503134A5 - - Google Patents

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Publication number
JP2013503134A5
JP2013503134A5 JP2012526048A JP2012526048A JP2013503134A5 JP 2013503134 A5 JP2013503134 A5 JP 2013503134A5 JP 2012526048 A JP2012526048 A JP 2012526048A JP 2012526048 A JP2012526048 A JP 2012526048A JP 2013503134 A5 JP2013503134 A5 JP 2013503134A5
Authority
JP
Japan
Prior art keywords
compound
formula
anhydrous crystalline
crystalline form
pharmaceutical composition
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
JP2012526048A
Other languages
English (en)
Japanese (ja)
Other versions
JP2013503134A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/EP2010/062420 external-priority patent/WO2011023733A1/en
Publication of JP2013503134A publication Critical patent/JP2013503134A/ja
Publication of JP2013503134A5 publication Critical patent/JP2013503134A5/ja
Pending legal-status Critical Current

Links

JP2012526048A 2009-08-27 2010-08-25 無水形態のピリジン誘導体 Pending JP2013503134A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US23743509P 2009-08-27 2009-08-27
US61/237,435 2009-08-27
PCT/EP2010/062420 WO2011023733A1 (en) 2009-08-27 2010-08-25 Anhydrate forms of a pyridine derivative

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2015139845A Division JP6404186B2 (ja) 2009-08-27 2015-07-13 無水形態のピリジン誘導体

Publications (2)

Publication Number Publication Date
JP2013503134A JP2013503134A (ja) 2013-01-31
JP2013503134A5 true JP2013503134A5 (enExample) 2013-09-19

Family

ID=42790943

Family Applications (3)

Application Number Title Priority Date Filing Date
JP2012526048A Pending JP2013503134A (ja) 2009-08-27 2010-08-25 無水形態のピリジン誘導体
JP2015139845A Active JP6404186B2 (ja) 2009-08-27 2015-07-13 無水形態のピリジン誘導体
JP2017114602A Pending JP2017193564A (ja) 2009-08-27 2017-06-09 無水形態のピリジン誘導体

Family Applications After (2)

Application Number Title Priority Date Filing Date
JP2015139845A Active JP6404186B2 (ja) 2009-08-27 2015-07-13 無水形態のピリジン誘導体
JP2017114602A Pending JP2017193564A (ja) 2009-08-27 2017-06-09 無水形態のピリジン誘導体

Country Status (17)

Country Link
US (1) US8796269B2 (enExample)
EP (1) EP2470545B1 (enExample)
JP (3) JP2013503134A (enExample)
KR (1) KR20120056258A (enExample)
CN (1) CN102639536B (enExample)
AU (1) AU2010288502B2 (enExample)
CA (1) CA2772168C (enExample)
DK (1) DK2470545T3 (enExample)
EA (1) EA021411B1 (enExample)
ES (1) ES2440938T3 (enExample)
IL (1) IL217922A (enExample)
IN (1) IN2012DN01292A (enExample)
MX (1) MX2012002369A (enExample)
PL (1) PL2470545T3 (enExample)
SG (1) SG178231A1 (enExample)
WO (1) WO2011023733A1 (enExample)
ZA (1) ZA201200812B (enExample)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2440938T3 (es) * 2009-08-27 2014-01-31 Nerre Therapeutics Limited Formas anhidrato de un derivado de piridina
US10314835B2 (en) 2014-06-25 2019-06-11 Emory University Methods of managing conditioned fear with neurokinin receptor antagonists
AU2016264034B2 (en) * 2015-05-18 2020-03-05 KaNDy Therapeutics Limited Dual NK-1/NK-3 receptor antagonists for the treatment of sex-hormone-dependent diseases
AU2017376900A1 (en) * 2016-12-15 2019-05-23 Glaxosmithkline Intellectual Property Development Limited NRF2 compounds
EA202092131A1 (ru) 2018-03-14 2020-11-27 Кэнди Терапьютикс Лимитед Новый фармацевтический препарат, содержащий двойные антагонисты рецептора nk-1/nk-3
WO2021030335A1 (en) * 2019-08-12 2021-02-18 Millendo Therapeutics, Inc. A stereoisomerically pure nk-3 receptor antagonist and crystalline forms thereof
EP4058433A1 (en) 2019-11-15 2022-09-21 KaNDy Therapeutics Limited New chemical process for making 6-chloro-4-(4-fluoro-2-methylphenyl)pyridin-3-amine a key intermediate of nt-814
EP4431512A1 (en) 2023-03-16 2024-09-18 Bayer Consumer Care AG Novel dual nk-1/nk-3 receptor antagonists
WO2025242584A1 (en) 2024-05-24 2025-11-27 Bayer Consumer Care Ag A stable soft gelatin capsule formulation for elinzanetant
WO2025242583A1 (en) 2024-05-24 2025-11-27 Bayer Consumer Care Ag Novel formulation comprising elinzanetant in a solid dispersion
WO2025242585A1 (en) 2024-05-24 2025-11-27 Bayer Consumer Care Ag Crystalline forms of salts of elinzanetant and compositions containing salts of elinzanetant
TW202604529A (zh) * 2024-06-18 2026-02-01 瑞士商拜耳保健消費品股份有限公司 用於製造依林奈坦(elinzanetant)前驅物之改良方法
US12533358B1 (en) 2025-05-14 2026-01-27 Bayer Consumer Care Ag Methods of treatment with elinzanetant

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1035115B1 (en) * 1999-02-24 2004-09-29 F. Hoffmann-La Roche Ag 4-Phenylpyridine derivatives and their use as NK-1 receptor antagonists
GB0203022D0 (en) * 2002-02-08 2002-03-27 Glaxo Group Ltd Chemical compounds
HRP20050664A2 (en) * 2003-01-31 2006-12-31 F. Hoffmann - La Roche Ag NEW CRYSTALLINE MODIFICATION OF 2-(3,5-BIS-TRIFLUOROMETHYL-PHENYL)-N-[6-(1,1-DIOXO-1λ6-THIOMORPHOLIN-4-YL)-A(4-FLUORO-2-METHYL-PHENYL)-PYRIDIN-3-YL]-N-METHYL-ISOBUTYRAMIDE
ES2291891T3 (es) * 2003-07-03 2008-03-01 F. Hoffmann-La Roche Ag Antagonistas duales de nk1/nk3 para tratamiento de esquizofrenia.
DK1928886T3 (da) * 2005-09-09 2011-07-11 Glaxosmithkline Llc Pyridin-derivater og deres anvendelse i behandlingen af psykotiske lidelser
AU2008346110A1 (en) * 2007-12-11 2009-07-16 Cipla Ltd. Crystalline polymorphic forms of zopiclone, processes for their preparation and their pharmaceutical compositions
GB0814340D0 (en) * 2008-08-05 2008-09-10 Smithkline Beecham Corp Anhydrous crystol form fo a pyridine derivative
ES2440938T3 (es) * 2009-08-27 2014-01-31 Nerre Therapeutics Limited Formas anhidrato de un derivado de piridina
JP6342662B2 (ja) * 2014-01-29 2018-06-13 京セラ株式会社 ドリルおよびそれを用いた切削加工物の製造方法

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