PL3964503T3 - Krystaliczna postać inhibitora magl - Google Patents

Krystaliczna postać inhibitora magl

Info

Publication number
PL3964503T3
PL3964503T3 PL21199077.5T PL21199077T PL3964503T3 PL 3964503 T3 PL3964503 T3 PL 3964503T3 PL 21199077 T PL21199077 T PL 21199077T PL 3964503 T3 PL3964503 T3 PL 3964503T3
Authority
PL
Poland
Prior art keywords
crystalline form
magl inhibitor
magl
inhibitor
crystalline
Prior art date
Application number
PL21199077.5T
Other languages
English (en)
Inventor
Cheryl A. Grice
Todd K. Jones
Kurt G. GRIMM
Jacqueline Lorayne BLANKMAN
Channing Rodney Beals
Original Assignee
H. Lundbeck A/S
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by H. Lundbeck A/S filed Critical H. Lundbeck A/S
Publication of PL3964503T3 publication Critical patent/PL3964503T3/pl

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/10Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing aromatic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D295/00Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/16Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
    • C07D295/20Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carbonic acid, or sulfur or nitrogen analogues thereof
    • C07D295/205Radicals derived from carbonic acid
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/496Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/08Antiepileptics; Anticonvulsants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C57/00Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms
    • C07C57/02Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms with only carbon-to-carbon double bonds as unsaturation
    • C07C57/13Dicarboxylic acids
    • C07C57/15Fumaric acid
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/13Crystalline forms, e.g. polymorphs

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Neurology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Biomedical Technology (AREA)
  • Neurosurgery (AREA)
  • Pain & Pain Management (AREA)
  • Hospice & Palliative Care (AREA)
  • Rheumatology (AREA)
  • Psychiatry (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Plural Heterocyclic Compounds (AREA)
PL21199077.5T 2016-11-16 2017-11-15 Krystaliczna postać inhibitora magl PL3964503T3 (pl)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US201662423126P 2016-11-16 2016-11-16

Publications (1)

Publication Number Publication Date
PL3964503T3 true PL3964503T3 (pl) 2024-04-02

Family

ID=62145805

Family Applications (2)

Application Number Title Priority Date Filing Date
PL21199077.5T PL3964503T3 (pl) 2016-11-16 2017-11-15 Krystaliczna postać inhibitora magl
PL17872429T PL3541807T3 (pl) 2016-11-16 2017-11-15 Krystaliczna postać inhibitora magl

Family Applications After (1)

Application Number Title Priority Date Filing Date
PL17872429T PL3541807T3 (pl) 2016-11-16 2017-11-15 Krystaliczna postać inhibitora magl

Country Status (38)

Country Link
US (2) US11142517B2 (pl)
EP (2) EP3541807B1 (pl)
JP (2) JP7042548B2 (pl)
KR (1) KR102508739B1 (pl)
CN (2) CN110291083B (pl)
AU (1) AU2017361257B2 (pl)
BR (1) BR112019010003A2 (pl)
CA (1) CA3043610A1 (pl)
CL (1) CL2019001340A1 (pl)
CO (1) CO2019005045A2 (pl)
CR (1) CR20190242A (pl)
CY (1) CY1124870T1 (pl)
DK (1) DK3541807T3 (pl)
DO (1) DOP2019000120A (pl)
EA (1) EA201991086A1 (pl)
EC (1) ECSP19035171A (pl)
ES (2) ES2966939T3 (pl)
GE (2) GEAP202315091A (pl)
HR (2) HRP20211863T1 (pl)
HU (2) HUE056973T2 (pl)
IL (1) IL266548A (pl)
JO (1) JOP20190109B1 (pl)
LT (1) LT3541807T (pl)
MA (2) MA46866B1 (pl)
MX (2) MX389459B (pl)
MY (1) MY199386A (pl)
NI (1) NI201900053A (pl)
PE (1) PE20191239A1 (pl)
PH (1) PH12019501068A1 (pl)
PL (2) PL3964503T3 (pl)
PT (1) PT3541807T (pl)
RS (2) RS62665B1 (pl)
SI (1) SI3541807T1 (pl)
SM (2) SMT202300494T1 (pl)
TN (1) TN2019000151A1 (pl)
UA (1) UA124585C2 (pl)
WO (1) WO2018093953A1 (pl)
ZA (1) ZA201903093B (pl)

Families Citing this family (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2793148T3 (es) 2012-01-06 2020-11-13 Lundbeck La Jolla Research Center Inc Compuestos de carbamato y métodos para fabricarlos y usarlos
CA2984480A1 (en) 2015-05-11 2016-11-17 Abide Therapeutics, Inc. Methods of treating inflammation or neuropathic pain
US10899737B2 (en) 2016-09-19 2021-01-26 Lundbeck La Jolla Research Center, Inc. Piperazine carbamates and methods of making and using same
EP3541807B1 (en) 2016-11-16 2021-09-29 H. Lundbeck A/S A crystalline form of a magl inhibitor
JOP20190107A1 (ar) 2016-11-16 2019-05-09 Lundbeck La Jolla Research Center Inc مثبطات أحادي أسيل جليسرول ليباز (magl)
AU2017361254B2 (en) 2016-11-16 2021-09-23 H. Lundbeck A/S. Pharmaceutical formulations
US10266497B2 (en) 2017-05-23 2019-04-23 Abide Therapeutics, Inc. Pyrazole MAGL inhibitors
US10927105B1 (en) 2017-05-23 2021-02-23 Lundbeck La Jolla Research Center, Inc. Pyrazole MAGL inhibitors
CA3072923A1 (en) 2017-08-29 2019-03-07 Lundbeck La Jolla Research Center, Inc. Spirocycle compounds and methods of making and using same
CR20200545A (es) 2018-05-15 2020-12-17 Lundbeck La Jolla Research Center Inc Inhibidores magl
US20210309669A1 (en) * 2018-07-19 2021-10-07 Pfizer Inc. Heterocyclic Spiro Compounds As MAGL Inhibitors
EP3837263B1 (en) 2018-08-13 2024-07-03 F. Hoffmann-La Roche AG New heterocyclic compounds as monoacylglycerol lipase inhibitors
EP3883936B1 (en) 2018-11-22 2023-07-12 F. Hoffmann-La Roche AG New heterocyclic compounds
EP3914589A4 (en) * 2019-01-25 2022-11-30 H. Lundbeck A/S Methods of treating disease with magl inhibitors
AU2020383502A1 (en) * 2019-11-15 2022-06-30 H. Lundbeck A/S Crystalline forms of a MAGL inhibitor
CN115427403A (zh) * 2020-04-21 2022-12-02 H.隆德贝克有限公司 单酰基甘油脂肪酶抑制剂的合成
WO2023092079A1 (en) * 2021-11-19 2023-05-25 Bryant Cynthia W Use of cannabinoid compounds to treat gastrointestinal disorders
CA3242372A1 (en) 2021-12-29 2023-07-06 Psy Therapeutics, Inc. Inhibiting monoacylglycerol lipase (magl)
AU2023264787A1 (en) 2022-05-04 2024-10-31 H. Lundbeck A/S Crystalline form of 1,1,1,3,3,3-hexafluoropropan-2-yl (s)-1-(pyridazin-3-ylcarbamoyl)-6 azaspiro[2.5]octane-6-carboxylate as monoacylglycerol lipase inhibitor.
CN117665187B (zh) * 2023-11-23 2024-08-16 宁波大红鹰药业股份有限公司 一种舒林酸中间体杂质的测定方法

Family Cites Families (41)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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
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
EP0580860B2 (en) 1991-04-16 2004-12-15 Nippon Shinyaku Company, Limited Method of manufacturing solid dispersion
CA2122479C (en) 1991-11-22 1998-08-25 Richard John Dansereau Risedronate delayed-release compositions
US5461140A (en) 1992-04-30 1995-10-24 Pharmaceutical Delivery Systems Bioerodible polymers for solid controlled release pharmaceutical compositions
US5323907A (en) 1992-06-23 1994-06-28 Multi-Comp, Inc. Child resistant package assembly for dispensing pharmaceutical medications
DE69332291T2 (de) 1992-10-16 2003-07-31 Nippon Shinyaku Co., Ltd. Verfahren zur herstellung von wachsmatrizes
US5686105A (en) 1993-10-19 1997-11-11 The Procter & Gamble Company Pharmaceutical dosage form with multiple enteric polymer coatings for colonic delivery
KR19990014865A (ko) 1995-05-17 1999-02-25 피터 이. 브래이브맨 소장에서의 소화 및 흡수를 증진시키기 위한, 지방산을 함유한조성물들
US6395300B1 (en) 1999-05-27 2002-05-28 Acusphere, Inc. Porous drug matrices and methods of manufacture thereof
JP2004516266A (ja) 2000-12-18 2004-06-03 ノバルティス アクチエンゲゼルシャフト アムロジピンおよびベナゼブリルの治療的組み合わせ
US6465014B1 (en) 2001-03-21 2002-10-15 Isp Investments Inc. pH-dependent sustained release, drug-delivery composition
CA2476936A1 (en) 2002-02-20 2003-08-28 Chih-Hung Lee Fused azabicyclic compounds that inhibit vanilloid receptor subtype 1 (vr1) receptor
US7074805B2 (en) 2002-02-20 2006-07-11 Abbott Laboratories Fused azabicyclic compounds that inhibit vanilloid receptor subtype 1 (VR1) receptor
CN101128189A (zh) 2005-02-25 2008-02-20 弗·哈夫曼-拉罗切有限公司 药物物质分散性改善的片剂
CN101583620B (zh) 2005-11-28 2016-08-17 马里纳斯医药公司 加奈索酮组合物及其制备和使用方法
EP1938804A1 (en) 2006-12-22 2008-07-02 Novartis AG Pharmaceutical formulation comprising neurokinin antagonist
FR2938341A1 (fr) 2008-11-13 2010-05-14 Galderma Res & Dev Modulateurs de la monoglyceride lipase dans le traitement de l'acne, d'une dermatite seborrheique ou de l'hyperseborrhee
WO2010063802A1 (en) 2008-12-05 2010-06-10 Novartis Ag 3, 4-di-substituted cyclobutene- 1, 2 -diones as cxcr2 receptor antagonists
CN101530399B (zh) 2009-04-15 2011-01-26 江苏中兴药业有限公司 一种水飞蓟宾固体自乳化片
ES2793148T3 (es) 2012-01-06 2020-11-13 Lundbeck La Jolla Research Center Inc Compuestos de carbamato y métodos para fabricarlos y usarlos
WO2013142307A1 (en) 2012-03-19 2013-09-26 Abide Therapeutics Carbamate compounds and of making and using same
WO2013159095A1 (en) 2012-04-20 2013-10-24 Anderson Gaweco Ror modulators and their uses
SMT202500078T1 (it) 2012-11-02 2025-03-12 Vertex Pharma Composizioni farmaceutiche per il trattamento di malattie mediate da cftr
TW201446286A (zh) 2013-01-31 2014-12-16 Gilead Pharmasset Llc 抗病毒化合物之固態分散調製劑
US9551036B2 (en) 2013-02-25 2017-01-24 Whitehead Institute For Biomedical Research Metabolic gene mesenchymal signatures and uses thereof
JP6647592B2 (ja) 2013-07-03 2020-02-14 ルンドベック ラ ホーヤ リサーチ センター,インク. ピロロピロールカルバメート、および関連する有機化合物、医薬組成物、ならびにその医学的使用
WO2015030854A1 (en) 2013-08-27 2015-03-05 Gilead Pharmasset Llc Solid dispersion formulation of an antiviral compound
CN103893258B (zh) 2013-12-05 2017-09-29 人福医药集团股份公司 含有广金钱草总黄酮的口服固体制剂及其应用
WO2015164160A1 (en) 2014-04-21 2015-10-29 Merck Sharp & Dohme Corp. Pharmaceutical salts of an orexin receptor antagonist
WO2015179559A2 (en) * 2014-05-21 2015-11-26 Abide Therapeutics, Inc. Pyrazole compounds and methods of making and using same
CA2979537C (en) 2015-03-18 2023-08-29 Abide Therapeutics, Inc. Piperazine carbamates and methods of making and using same
CA2984480A1 (en) 2015-05-11 2016-11-17 Abide Therapeutics, Inc. Methods of treating inflammation or neuropathic pain
US10463753B2 (en) 2016-02-19 2019-11-05 Lundbeck La Jolla Research Center, Inc. Radiolabeled monoacylglycerol lipase occupancy probe
JOP20190105A1 (ar) 2016-11-16 2019-05-09 Lundbeck La Jolla Research Center Inc مثبطات أحادي أسيل جليسرول ليباز (magl)
AU2017361254B2 (en) 2016-11-16 2021-09-23 H. Lundbeck A/S. Pharmaceutical formulations
JOP20190106A1 (ar) 2016-11-16 2019-05-09 Lundbeck La Jolla Research Center Inc مثبطات أحادي أسيل جليسرول ليباز (magl)
JOP20190107A1 (ar) 2016-11-16 2019-05-09 Lundbeck La Jolla Research Center Inc مثبطات أحادي أسيل جليسرول ليباز (magl)
EP3541807B1 (en) 2016-11-16 2021-09-29 H. Lundbeck A/S A crystalline form of a magl inhibitor

Also Published As

Publication number Publication date
RS65016B1 (sr) 2024-01-31
CY1124870T1 (el) 2022-11-25
ES2966939T3 (es) 2024-04-25
EP3541807A1 (en) 2019-09-25
JP7042548B2 (ja) 2022-03-28
IL266548A (en) 2019-07-31
AU2017361257A1 (en) 2019-05-30
HUE064559T2 (hu) 2024-03-28
JP7350117B2 (ja) 2023-09-25
EP3541807A4 (en) 2020-04-22
US11993588B2 (en) 2024-05-28
RS62665B1 (sr) 2021-12-31
ZA201903093B (en) 2020-11-25
CO2019005045A2 (es) 2019-05-31
CN110291083B (zh) 2022-06-17
SMT202300494T1 (it) 2024-01-10
EP3964503B1 (en) 2023-11-08
AU2017361257B2 (en) 2022-02-10
MA46866A (fr) 2021-06-02
US20220235037A1 (en) 2022-07-28
SMT202100675T1 (it) 2022-01-10
RU2019116689A3 (pl) 2021-02-26
CN110291083A (zh) 2019-09-27
MY199386A (en) 2023-10-25
JOP20190109B1 (ar) 2022-09-15
NZ753241A (en) 2021-06-25
PL3541807T3 (pl) 2022-01-17
EP3964503A1 (en) 2022-03-09
HRP20211863T1 (hr) 2022-03-04
CN115093382A (zh) 2022-09-23
DK3541807T3 (da) 2021-12-06
GEAP202315091A (en) 2023-05-10
LT3541807T (lt) 2021-12-27
DOP2019000120A (es) 2019-09-30
US20200190063A1 (en) 2020-06-18
NI201900053A (es) 2019-10-30
ECSP19035171A (es) 2019-05-31
RU2019116689A (ru) 2020-12-17
CL2019001340A1 (es) 2019-10-04
EP3964503C0 (en) 2023-11-08
SI3541807T1 (sl) 2022-01-31
MX389459B (es) 2025-03-20
BR112019010003A2 (pt) 2019-08-20
PH12019501068A1 (en) 2019-08-19
MX2019005767A (es) 2019-12-05
PE20191239A1 (es) 2019-09-16
KR102508739B1 (ko) 2023-03-09
EA201991086A1 (ru) 2019-11-29
JP2019537596A (ja) 2019-12-26
CR20190242A (es) 2019-07-09
KR20190077561A (ko) 2019-07-03
CA3043610A1 (en) 2018-05-24
MX2022000249A (es) 2022-02-03
US11142517B2 (en) 2021-10-12
WO2018093953A1 (en) 2018-05-24
MA46866B1 (fr) 2021-11-30
EP3541807B1 (en) 2021-09-29
ES2900016T3 (es) 2022-03-15
GEP20237559B (en) 2023-10-25
MA58133B1 (fr) 2024-02-29
HRP20231697T1 (hr) 2024-03-15
JP2022084717A (ja) 2022-06-07
HUE056973T2 (hu) 2022-04-28
TN2019000151A1 (en) 2020-10-05
JOP20190109A1 (ar) 2019-05-09
PT3541807T (pt) 2021-12-09
UA124585C2 (uk) 2021-10-13

Similar Documents

Publication Publication Date Title
ZA201903093B (en) Crystalline forms of a magl inhibitor
IL263824A (en) Crystals in solid form in the presence of an inhibitor
ZA201903099B (en) Magl inhibitors
ZA201903100B (en) Magl inhibitors
IL266550A (en) Magl inhibitors
LT3831833T (lt) Pi3k inhibitoriaus gamybos būdai
ZA201802267B (en) Salts of a pim kinase inhibitor
IL267393B1 (en) Crystal forms of a Janus kinase inhibitor
GB201505658D0 (en) Inhibitor compounds
GB201522771D0 (en) Crystalline form of a phosphate derivative
PL3529236T4 (pl) Krystaliczne formy erawacykliny
IL254115A0 (en) Crystalline forms of a pyrrolpyridine compound
ZA201607107B (en) Salts and polymorphs of a substituted imidazopyridinyl-aminopyridine compound
GB201621619D0 (en) Inhibitor compounds
EP3256481A4 (en) Novel crystalline form of a proteasome inhibitor
GB201500644D0 (en) Inhibitor compounds