JP2024534268A5 - - Google Patents

Info

Publication number
JP2024534268A5
JP2024534268A5 JP2024537805A JP2024537805A JP2024534268A5 JP 2024534268 A5 JP2024534268 A5 JP 2024534268A5 JP 2024537805 A JP2024537805 A JP 2024537805A JP 2024537805 A JP2024537805 A JP 2024537805A JP 2024534268 A5 JP2024534268 A5 JP 2024534268A5
Authority
JP
Japan
Prior art keywords
cocrystal
forming agent
aicd
nicotinamide
inhibitor
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
JP2024537805A
Other languages
English (en)
Japanese (ja)
Other versions
JP2024534268A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2022/041823 external-priority patent/WO2023034184A1/en
Publication of JP2024534268A publication Critical patent/JP2024534268A/ja
Publication of JP2024534268A5 publication Critical patent/JP2024534268A5/ja
Pending legal-status Critical Current

Links

JP2024537805A 2021-08-31 2022-08-29 共結晶 Pending JP2024534268A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US202163238928P 2021-08-31 2021-08-31
US63/238,928 2021-08-31
PCT/US2022/041823 WO2023034184A1 (en) 2021-08-31 2022-08-29 Co-crystals

Publications (2)

Publication Number Publication Date
JP2024534268A JP2024534268A (ja) 2024-09-18
JP2024534268A5 true JP2024534268A5 (https=) 2025-08-20

Family

ID=85411664

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2024537805A Pending JP2024534268A (ja) 2021-08-31 2022-08-29 共結晶

Country Status (11)

Country Link
US (4) US12226408B2 (https=)
EP (1) EP4395827A4 (https=)
JP (1) JP2024534268A (https=)
KR (1) KR20240054333A (https=)
CN (1) CN117897174A (https=)
AU (1) AU2022338032A1 (https=)
CA (1) CA3230151A1 (https=)
IL (1) IL310956A (https=)
MX (1) MX2024002472A (https=)
NO (1) NO20240297A1 (https=)
WO (1) WO2023034184A1 (https=)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2022338032A1 (en) * 2021-08-31 2024-03-07 Cerespir Incorporated Co-crystals
WO2025244939A1 (en) * 2024-05-18 2025-11-27 Cerespir Incorporated Polymorphs of co-crystals of itanapraced and nicotinamide

Family Cites Families (39)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US320706A (en) * 1885-06-23 Mechanical movement
CA1146866A (en) 1979-07-05 1983-05-24 Yamanouchi Pharmaceutical Co. Ltd. Process for the production of sustained release pharmaceutical composition of solid medical material
US4327725A (en) 1980-11-25 1982-05-04 Alza Corporation Osmotic device with hydrogel driving member
US4624848A (en) 1984-05-10 1986-11-25 Ciba-Geigy Corporation Active agent containing hydrogel devices wherein the active agent concentration profile contains a sigmoidal concentration gradient for improved constant release, their manufacture and use
GB8518301D0 (en) 1985-07-19 1985-08-29 Fujisawa Pharmaceutical Co Hydrodynamically explosive systems
US5011692A (en) 1985-12-28 1991-04-30 Sumitomo Pharmaceuticals Company, Limited Sustained pulsewise release pharmaceutical preparation
US4968509A (en) 1987-07-27 1990-11-06 Mcneilab, Inc. Oral sustained release acetaminophen formulation and process
IL92966A (en) 1989-01-12 1995-07-31 Pfizer Dispensing devices powered by hydrogel
US5017381A (en) 1990-05-02 1991-05-21 Alza Corporation Multi-unit pulsatile delivery system
WO1992018106A1 (fr) 1991-04-16 1992-10-29 Nippon Shinyaku Co., Ltd. Procede de production d'une dispersion solide
HU227530B1 (en) 1991-11-22 2011-07-28 Warner Chilcott Company Delayed-release compositions containing risedronate and process for their production
US5229135A (en) 1991-11-22 1993-07-20 Prographarm Laboratories Sustained release diltiazem formulation
US5340591A (en) 1992-01-24 1994-08-23 Fujisawa Pharmaceutical Co., Ltd. Method of producing a solid dispersion of the sparingly water-soluble drug, nilvadipine
US5461140A (en) 1992-04-30 1995-10-24 Pharmaceutical Delivery Systems Bioerodible polymers for solid controlled release pharmaceutical compositions
US5260068A (en) 1992-05-04 1993-11-09 Anda Sr Pharmaceuticals Inc. Multiparticulate pulsatile drug delivery system
AU4198793A (en) 1992-07-24 1994-01-27 Takeda Chemical Industries Ltd. Microparticle preparation and production thereof
US5700485A (en) 1992-09-10 1997-12-23 Children's Medical Center Corporation Prolonged nerve blockade by the combination of local anesthetic and glucocorticoid
JP2616252B2 (ja) 1992-10-16 1997-06-04 日本新薬株式会社 ワックスマトリックスの製法
US5260069A (en) 1992-11-27 1993-11-09 Anda Sr Pharmaceuticals Inc. Pulsatile particles drug delivery system
US5322655A (en) 1993-02-19 1994-06-21 Thomas Engineering, Inc. Method for monitoring and controlling the weights of each layer of a multilayer tablet
US5686105A (en) 1993-10-19 1997-11-11 The Procter & Gamble Company Pharmaceutical dosage form with multiple enteric polymer coatings for colonic delivery
US5567441A (en) 1995-03-24 1996-10-22 Andrx Pharmaceuticals Inc. Diltiazem controlled release formulation
JPH11505258A (ja) 1995-05-17 1999-05-18 セダーシナイ メディカル センター 小腸における消化および吸収を改善させる脂肪酸を含む組成物
US5837284A (en) 1995-12-04 1998-11-17 Mehta; Atul M. Delivery of multiple doses of medications
US5840329A (en) 1997-05-15 1998-11-24 Bioadvances Llc Pulsatile drug delivery system
ATE400252T1 (de) 1999-02-10 2008-07-15 Pfizer Prod Inc Pharmazeutische feste dispersionen
US6395300B1 (en) 1999-05-27 2002-05-28 Acusphere, Inc. Porous drug matrices and methods of manufacture thereof
US6465014B1 (en) 2001-03-21 2002-10-15 Isp Investments Inc. pH-dependent sustained release, drug-delivery composition
IL165383A0 (en) 2002-06-21 2006-01-15 Transform Pharmaceuticals Inc Pharmaceutical compositions with improved dissolution
JP4472691B2 (ja) 2003-02-21 2010-06-02 キエシ・フアルマチエウテイチ・ソチエタ・ペル・アチオニ 神経変性疾患の処置のための1−フェニルアルカンカルボン酸誘導体
WO2009133128A1 (en) 2008-04-29 2009-11-05 Pharnext Combination compositions for treating alzheimer disease and related disorders with zonisamide and acamprosate
EP2133322A1 (en) 2008-06-11 2009-12-16 CHIESI FARMACEUTICI S.p.A. Process of preparing derivatives of 1-(2-halobiphenyl-4-yl)-cyclopropanecarboxylic acid
ES2437163T3 (es) 2009-08-04 2014-01-09 Chiesi Farmaceutici S.P.A. Procesos para la preparación de derivados del ácido 1-(2-halobifenil-4-il)-ciclopropanocarboxílico
US9592210B2 (en) 2011-12-22 2017-03-14 Chiesi Farmaceutici S.P.A. 1-phenylalkanecarboxylic acid derivatives for the treatment of cognitive impairment
IN2014DN09031A (https=) 2012-03-30 2015-05-22 Nuformix Ltd
BR112015002309A2 (pt) 2012-08-07 2017-07-04 Buck Inst Res Aging formulação de múltiplos componentes para aprimorar a função neurológica
WO2014206898A1 (en) 2013-06-24 2014-12-31 Chiesi Farmaceutici S.P.A. Improved process for the preparation of derivatives of 1-(2-fluoro[1,1'-biphenyl]-4-yl)-cyclopropanecarboxylic acid
WO2015173133A1 (en) 2014-05-12 2015-11-19 Chiesi Farmaceutici S.P.A. Formulations and methods of treating alzheimer's disease and other proteinopathies by combination therapy
AU2022338032A1 (en) * 2021-08-31 2024-03-07 Cerespir Incorporated Co-crystals

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