MA65149A1 - Formes cristallines à l'état solide d'un modulateur sélectif du canal potassique - Google Patents

Formes cristallines à l'état solide d'un modulateur sélectif du canal potassique

Info

Publication number
MA65149A1
MA65149A1 MA65149A MA65149A MA65149A1 MA 65149 A1 MA65149 A1 MA 65149A1 MA 65149 A MA65149 A MA 65149A MA 65149 A MA65149 A MA 65149A MA 65149 A1 MA65149 A1 MA 65149A1
Authority
MA
Morocco
Prior art keywords
solid
potassium channel
crystalline forms
channel modulator
selective potassium
Prior art date
Application number
MA65149A
Other languages
English (en)
Inventor
Paul Robert BICHLER
Jean-Jacques A. CADIEUX
Matthew David Tandy
Gregory N. Beatch
Original Assignee
Xenon Pharmaceuticals Inc.
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 Xenon Pharmaceuticals Inc. filed Critical Xenon Pharmaceuticals Inc.
Publication of MA65149A1 publication Critical patent/MA65149A1/fr

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/47—Quinolines; Isoquinolines
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/47—Quinolines; Isoquinolines
    • A61K31/472—Non-condensed isoquinolines, e.g. papaverine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/08—Antiepileptics; Anticonvulsants
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D217/00—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
    • C07D217/02—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with only hydrogen atoms or radicals containing only carbon and hydrogen atoms, directly attached to carbon atoms of the nitrogen-containing ring; Alkylene-bis-isoquinolines
    • C07D217/04—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with only hydrogen atoms or radicals containing only carbon and hydrogen atoms, directly attached to carbon atoms of the nitrogen-containing ring; Alkylene-bis-isoquinolines with hydrocarbon or substituted hydrocarbon radicals attached to the ring nitrogen atom
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00—Indexing scheme relating to specific properties of organic compounds
    • C07B2200/13—Crystalline forms, e.g. polymorphs

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Medicinal Chemistry (AREA)
  • Neurology (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pain & Pain Management (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Biomedical Technology (AREA)
  • Neurosurgery (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Peptides Or Proteins (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Medicinal Preparation (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Laminated Bodies (AREA)
  • Liquid Crystal Substances (AREA)
  • Transmitters (AREA)

Abstract

La présente invention concerne des formes à l'état solide d'un modulateur sélectif du canal potassique et des compositions pharmaceutiques comprenant les formes cristallines à l'état solide, ainsi que des excipients pharmaceutiquement acceptables, et des procédés de préparation et d'utilisation des formes à l'état solide et des compositions pharmaceutiques de celles-ci.
MA65149A 2019-10-10 2022-04-07 Formes cristallines à l'état solide d'un modulateur sélectif du canal potassique MA65149A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201962913574P 2019-10-10 2019-10-10
PCT/US2020/055129 WO2021072307A1 (fr) 2019-10-10 2020-10-09 Formes cristallines à l'état solide d'un modulateur sélectif du canal potassique

Publications (1)

Publication Number Publication Date
MA65149A1 true MA65149A1 (fr) 2026-03-31

Family

ID=73040296

Family Applications (2)

Application Number Title Priority Date Filing Date
MA56288A MA56288A1 (fr) 2019-10-10 2020-10-09 Formes cristallines à l'état solide d'un modulateur sélectif du canal potassique
MA65149A MA65149A1 (fr) 2019-10-10 2022-04-07 Formes cristallines à l'état solide d'un modulateur sélectif du canal potassique

Family Applications Before (1)

Application Number Title Priority Date Filing Date
MA56288A MA56288A1 (fr) 2019-10-10 2020-10-09 Formes cristallines à l'état solide d'un modulateur sélectif du canal potassique

Country Status (30)

Country Link
US (4) US11091441B2 (fr)
EP (2) EP4523687A3 (fr)
JP (1) JP2022552187A (fr)
KR (1) KR20220080119A (fr)
CN (4) CN120157617A (fr)
AU (1) AU2020364142A1 (fr)
BR (1) BR112022006583A2 (fr)
CA (1) CA3153752A1 (fr)
CL (1) CL2022000881A1 (fr)
CO (1) CO2022005890A2 (fr)
CR (1) CR20220187A (fr)
DK (1) DK4041713T3 (fr)
ES (1) ES3014703T3 (fr)
FI (1) FI4041713T3 (fr)
GE (2) GEAP202415926A (fr)
HR (1) HRP20250134T1 (fr)
HU (1) HUE070295T2 (fr)
IL (2) IL292005B2 (fr)
LT (1) LT4041713T (fr)
MA (2) MA56288A1 (fr)
MX (3) MX2022004209A (fr)
PE (1) PE20221023A1 (fr)
PH (1) PH12022550854A1 (fr)
PL (1) PL4041713T3 (fr)
PT (1) PT4041713T (fr)
RS (1) RS66531B1 (fr)
SI (1) SI4041713T1 (fr)
SM (1) SMT202500101T1 (fr)
TW (1) TWI886158B (fr)
WO (1) WO2021072307A1 (fr)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TWI886158B (zh) * 2019-10-10 2025-06-11 加拿大商再諾製藥公司 選擇性鉀通道調節劑之固態晶型
WO2021092439A1 (fr) 2019-11-08 2021-05-14 Xenon Pharmaceuticals Inc. Méthodes de traitement de troubles dépressifs
IL304920A (en) 2021-02-09 2023-10-01 Xenon Pharmaceuticals Inc A voltage-gated potassium channel opener for use in the treatment of anhedonia
EP4074696B1 (fr) 2021-10-27 2026-02-04 Shanghai Zhimeng Biopharma, Inc. N-[4-(6-fluoro-3,4-dihydro-2(1h)-isoquinolinyl)-2,6-diméthylphenyl]-1-méthyl-cyclopropane-acetamide, un régulateur du canal potassique pour le traitement d'épilepsie
CN113698345B (zh) * 2021-10-27 2022-02-01 上海挚盟医药科技有限公司 作为钾通道调节剂的化合物及其制备和应用
WO2025167886A1 (fr) * 2024-02-08 2025-08-14 上海挚盟医药科技有限公司 Forme cristalline d'un composé tétrahydroisoquinoléine et son utilisation
WO2025179128A1 (fr) 2024-02-22 2025-08-28 Xenon Pharmaceuticals Inc. Azétukalner destiné à être utilisé dans le traitement de la dépression, de l'anhédonie ou d'un trouble épileptique tel que l'épilepsie chez des sujets pédiatriques

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008024398A2 (fr) * 2006-08-23 2008-02-28 Valeant Pharmaceuticals International Dérivés de 4-(n-azacycloalkyl) anilides en tant que modulateurs du canal potassique
US20110003850A1 (en) * 2006-08-23 2011-01-06 Valeant Pharmaceuticals International, Inc. Derivatives of 4-(n-azacycloalkyl) anilides as potassium channel modulators

Family Cites Families (103)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3639385A (en) 1968-07-26 1972-02-01 Eastman Kodak Co Heterocyclic monoazo compounds from n n-diaralkyl anilines and polyester textile materials dyed therewith
US3845770A (en) 1972-06-05 1974-11-05 Alza Corp Osmatic dispensing device for releasing beneficial agent
US4181803A (en) 1973-12-14 1980-01-01 Eisai Co., Ltd. Propiophenone derivatives and preparation thereof
US4326525A (en) 1980-10-14 1982-04-27 Alza Corporation Osmotic device that improves delivery properties of agent in situ
DE3369315D1 (en) 1982-10-27 1987-02-26 Degussa Derivatives of 2-amino-3-acylamino-6-benzylamino pyridine with an anti-epileptic activity
DE3337593A1 (de) 1982-10-27 1984-05-03 Degussa Ag, 6000 Frankfurt 2-amino-3-acylamino-6-benzylamino-pyridin-derivate mit antiepileptischer wirkung
DE3665538D1 (en) 1985-01-23 1989-10-19 Asta Pharma Ag Synergistic combination of flupirtin and non-steroidal anti-phlogistics
DE3604575A1 (de) 1985-02-23 1986-08-28 Degussa Ag, 6000 Frankfurt Kombination von flupirtin und anticholinergisch wirkenden spasmolytika
EP0193056B1 (fr) 1985-02-23 1989-06-07 ASTA Pharma Aktiengesellschaft Combinaison de la flupirtine avec des spasmolytiques à effet anticholinergique
JP2583067B2 (ja) 1987-08-04 1997-02-19 住友化学工業株式会社 モノアゾ化合物およびそれを用いて疎水性繊維材料を染色または捺染する方法
GB8800199D0 (en) 1988-01-06 1988-02-10 Beecham Group Plc Pharmaceutical preparation
MC2029A1 (fr) 1988-05-16 1990-04-25 Asta Pharma Ag (n-heterocyclyl)-3 diamino-2,6 pyridines substituees et leurs n-oxydes,preparation de ces composes et leur application comme medicaments
US5629307A (en) 1989-10-20 1997-05-13 Olney; John W. Use of ibogaine in reducing excitotoxic brain damage
US6004945A (en) 1990-05-10 1999-12-21 Fukunaga; Atsuo F. Use of adenosine compounds to relieve pain
IN172468B (fr) 1990-07-14 1993-08-14 Asta Medica Ag
US5643921A (en) 1990-09-26 1997-07-01 E.R. Squibb & Sons, Inc. Cardiopulmonary bypass and organ transplant using a potassium channel activator
US5234947A (en) 1991-11-07 1993-08-10 New York University Potassium channel activating compounds and methods of use thereof
DE4200259A1 (de) 1992-01-08 1993-07-15 Asta Medica Ag Neue 1,2,4-triaminobenzol-derivate und verfahren zu deren herstellung
US5262419A (en) 1992-06-11 1993-11-16 E. R. Squibb & Sons, Inc. Method for the prophylaxis and/or treatment of ulcerative gastrointestinal conditions using a potassium channel activator
CA2115792C (fr) 1993-03-05 2005-11-01 David J. Mayer Methode de traitement de la douleur
US5428039A (en) 1994-02-20 1995-06-27 The Center For Innovative Technology Method for electively achieving reversible hyperpolarized cardiac arrest
JP4097285B2 (ja) 1994-09-22 2008-06-11 リチャード・アラン・スミス 種々の頑固な疾患の治療のための医薬の製造に有用な組成物
US5679706A (en) 1994-09-30 1997-10-21 Bristol-Myers Squibb Company Combination of a potassium channel activator and an antiarrhythmic agent
EP2301562B1 (fr) 1994-12-12 2013-04-17 Omeros Corporation Solution d'irrigation et utilisation de celle-ci pour inhiber périopérativement la douleur, l'inflammation et/ou les spasmes
DE19539861A1 (de) 1995-10-26 1997-04-30 Asta Medica Ag Verwendung von 4-Amino-4-(4-fluorbenzylamino)-1-ethoxy-carbonylaminobenzen zur Prophylaxe und Behandlung der Folgen der akuten und chronischen zerebralen Minderdurchblutung sowie neurodegenerativer Erkrankungen
DE19701694A1 (de) 1997-01-20 1998-07-23 Asta Medica Ag Neue Modifikationen des 2-Amino-4-(4-fluorbenzylamino)-l-ethoxycarbonyl-aminobenzen sowie Verfahren zu ihrer Herstellung
US5760007A (en) 1997-07-16 1998-06-02 Ortho Pharmaceutical Corporation Anticonvulsant derivatives useful in treating neuropathic pain
EP1004316B1 (fr) 1997-08-08 2005-11-02 Chugai Seiyaku Kabushiki Kaisha Remedes contre les complications du diabete
US6265417B1 (en) 1997-12-18 2001-07-24 Abbott Laboratories Potassium channel openers
US6593335B1 (en) 1997-12-18 2003-07-15 Abbott Laboratories Potassium channel openers
US6211171B1 (en) 1998-05-19 2001-04-03 Dalhousie University Use of antidepressants for local analgesia
JP3441970B2 (ja) 1998-06-30 2003-09-02 株式会社サミー 豆腐の製造方法及び製造装置
JP2002542147A (ja) 1998-12-14 2002-12-10 セレジィ ファーマシューティカルス， インコーポレイテッド 肛門直腸障害の処置のための組成物および方法
US6281211B1 (en) 1999-02-04 2001-08-28 Euro-Celtique S.A. Substituted semicarbazides and the use thereof
GB9903476D0 (en) 1999-02-17 1999-04-07 Zeneca Ltd Therapeutic agents
US6451857B1 (en) 1999-03-10 2002-09-17 Warner-Lambert Company Analgesic compositions comprising anti-epileptic compounds and methods of using same
AU766648B2 (en) 1999-03-17 2003-10-23 Axys Pharmaceuticals, Inc. Compounds and methods for modulation of estrogen receptors
AT409083B (de) 1999-04-01 2002-05-27 Sanochemia Pharmazeutika Ag Pharmazeutische, tolperison enthaltende zubereitung zur oralen verabreichung
US6610324B2 (en) 1999-04-07 2003-08-26 The Mclean Hospital Corporation Flupirtine in the treatment of fibromyalgia and related conditions
GB9915414D0 (en) 1999-07-01 1999-09-01 Glaxo Group Ltd Medical use
EP1200073B1 (fr) 1999-07-06 2007-01-10 Eli Lilly And Company ANTAGONISTES SELECTIFS DU RECEPTEUR iGluR 5? UTILISES DANS LE TRAITEMENT DE LA MIGRAINE
US6472165B1 (en) 1999-08-03 2002-10-29 Arzneimittelwerk Dresden Gmbh Modulatory binding site in potassium channels for screening and finding new active ingredients
NZ527771A (en) 1999-08-04 2005-04-29 Icagen Inc Methods for treating or preventing anxiety
US6495550B2 (en) 1999-08-04 2002-12-17 Icagen, Inc. Pyridine-substituted benzanilides as potassium ion channel openers
NZ516610A (en) 1999-08-04 2004-05-28 Icagen Inc Benzanilides as potassium channel openers
US6117900A (en) 1999-09-27 2000-09-12 Asta Medica Aktiengesellschaft Use of retigabine for the treatment of neuropathic pain
US6383511B1 (en) 1999-10-25 2002-05-07 Epicept Corporation Local prevention or amelioration of pain from surgically closed wounds
US6538004B2 (en) 2000-03-03 2003-03-25 Abbott Laboratories Tricyclic dihydropyrazolone and tricyclic dihydroisoxazolone potassium channel openers
US20020015730A1 (en) 2000-03-09 2002-02-07 Torsten Hoffmann Pharmaceutical formulations and method for making
TWI287984B (en) 2000-10-17 2007-10-11 Wyeth Corp Pharmaceutical composition for modulating bladder function
US6589986B2 (en) 2000-12-20 2003-07-08 Wyeth Methods of treating anxiety disorders
US6469042B1 (en) 2001-02-20 2002-10-22 Bristol-Myers Squibb Company Fluoro oxindole derivatives as modulators if KCNQ potassium channels
AR033095A1 (es) 2001-04-04 2003-12-03 Wyeth Corp Metodos para el tratamiento de motilidad gastrica hiperactiva
GB0119711D0 (en) 2001-08-13 2001-10-03 Unilever Plc Process for the production of detergent granules
GB0121214D0 (en) 2001-08-31 2001-10-24 Btg Int Ltd Synthetic method
WO2003068769A1 (fr) 2002-02-12 2003-08-21 Pfizer Inc. Composes non-peptidiques influant sur l'action de la gnrh
WO2003097586A1 (fr) 2002-05-17 2003-11-27 Janssen Pharmaceutica N.V. Modulateurs de l'uree derives de l'aminotetraline du recepteur vanilloide vr1
AUPS312602A0 (en) 2002-06-21 2002-07-18 James Cook University Organ arrest, protection, preservation and recovery
US7419981B2 (en) 2002-08-15 2008-09-02 Pfizer Inc. Synergistic combinations of an alpha-2-delta ligand and a cGMP phosphodieterse 5 inhibitor
EP1581510A4 (fr) 2002-11-22 2006-08-30 Bristol Myers Squibb Co 1-aryl-2-hydroxyethyle amides ouvreurs de canaux potassiques
EP1585522B1 (fr) 2002-12-23 2010-11-17 Icagen, Inc. Quinazolinones comme modulateurs de canaux potassiques
MXPA05006463A (es) 2002-12-27 2005-08-26 Lundbeck & Co As H Derivados de 1,2,4-triaminobenceno, utiles para tratar transtornos del sistema nervioso central.
WO2004080950A1 (fr) 2003-03-14 2004-09-23 H. Lundbeck A/S Derives d'aniline substitues
BRPI0408437A (pt) 2003-03-21 2006-04-04 Lundbeck & Co As H derivados de p-diaminobenzeno substituìdos, composição farmacêutica, e, uso da mesma
EP1631546A1 (fr) 2003-04-25 2006-03-08 H. Lundbeck A/S Derives indole et indoline substitues
JP2006528231A (ja) 2003-05-27 2006-12-14 アルタナ　ファルマ　アクチエンゲゼルシャフト プロトンポンプ阻害剤と胃腸運動性を変更する化合物との医薬品組合せ物
US20050070570A1 (en) 2003-06-18 2005-03-31 4Sc Ag Novel potassium channels modulators
US20050089473A1 (en) 2003-09-10 2005-04-28 Cedars-Sinai Medical Center Potassium channel mediated delivery of agents through the blood-brain barrier
US20050089559A1 (en) 2003-10-23 2005-04-28 Istvan Szelenyi Combinations of potassium channel openers and sodium channel inhibitors or sodium channel-influencing active compounds for treating pains
DE10359335A1 (de) 2003-10-23 2005-05-25 Viatris Gmbh & Co. Kg Kombinationen aus Kaliumkanalöffnern und Natriumkanalinhibitoren oder Natriumkanal beeinflussenden Wirkstoffen zur Behandlung von Schmerzzuständen
ES2235626B1 (es) 2003-11-10 2006-11-01 Almirall Prodesfarma, S.A. Formas de administracion masticables, no comprimidas dosificadas individualmente.
US7553858B2 (en) 2003-12-17 2009-06-30 Meda Pharma Gmbh & Co. Kg Combination of flupirtine and tramadol
US8236861B2 (en) 2004-02-13 2012-08-07 Hormos Medical Corporation Method for enhancing the bioavailablity of ospemifene
TWI357901B (en) 2004-03-12 2012-02-11 Lundbeck & Co As H Substituted morpholine and thiomorpholine derivati
KR20070030196A (ko) 2004-04-13 2007-03-15 이카겐, 인코포레이티드 칼륨 이온 채널 조절제로서의 폴리시클릭 피리딘
CA2565154A1 (fr) 2004-05-03 2005-11-24 Duke University Compositions influant sur la perte de poids
UA89503C2 (uk) 2004-09-13 2010-02-10 Х. Луннбек А/С Заміщені похідні аніліну
CA2589001A1 (fr) 2004-11-19 2006-05-26 Kissei Pharmaceutical Co., Ltd. Agent preventif ou therapeutique pour la douleur neuropathique
EP1688141A1 (fr) 2005-01-31 2006-08-09 elbion AG Utilisation de flupirtine pour le traitement de la vessie hyperactive et des maladies associées et pour le traitement du syndrome du colon irritable
EP1861394A1 (fr) 2005-03-03 2007-12-05 H.Lundbeck A/S Derives de pyridine substitues
US7683058B2 (en) 2005-09-09 2010-03-23 H. Lundbeck A/S Substituted pyrimidine derivatives
EP2012769A1 (fr) 2006-05-02 2009-01-14 Rundfeldt, Chris Activateurs de canaux potassiques pour la prévention et le traitement de la dystonie et des systèmes assimilés à la dystonie
CA2670966A1 (fr) 2006-11-28 2008-06-05 Valeant Pharmaceuticals International Analogues de 1,4-diamino retigabine bicycliques en tant que modulateurs de canaux potassiques
US20090018154A1 (en) 2007-05-17 2009-01-15 Endo Pharmaceuticals, Inc., A Corporation Of Delaware Opioid and methods of making and using the same
CN101790374A (zh) 2007-08-01 2010-07-28 H.隆德贝克有限公司 Kcnq钾通道开放剂用于减轻多巴胺能系统受到干扰的障碍或病症的症状或治疗这种障碍或病症的用途
WO2009074594A1 (fr) 2007-12-11 2009-06-18 Neurosearch A/S Nouveaux dérivés de 2-éthyl-méthyl-amino-3-amido-6-amino-pyridine utiles en tant d'activateurs de canaux potassiques
US20100297181A1 (en) 2007-12-26 2010-11-25 Eisai R&D Management Co., Ltd. AMPA Receptor Antagonists for Epilepsy, Mental Disorders or Deficits in Sensory Organ
US20100323016A1 (en) 2008-07-18 2010-12-23 Biljana Nadjsombati Modified release formulation and methods of use
EP2525788A2 (fr) 2010-01-20 2012-11-28 Glaxo Group Limited Nouvelle composition du retigabine
WO2012027247A2 (fr) 2010-08-23 2012-03-01 Vertex Pharmaceuticals Incorporated Composition pharmaceutique à base de (r)-1-(2,2-difluorobenzo[d][1,3]dioxol-5-yl)-n-(1-(2,3-dihydroxypropyl)-6-fluoro-2-(1-hydroxy-2-méthylpropan-2-yl)-1h-indol-5-yle)cyclopropane carboxamide et son administration
JP5248585B2 (ja) * 2010-12-15 2013-07-31 ゼノン・ファーマシューティカルズ・インコーポレイテッド 治療薬としてのニコチンアミド誘導体およびそれらの使用
WO2013067591A1 (fr) 2011-11-10 2013-05-16 Relevare Australia Pty Ltd Formulations topiques pour gestion de la douleur
US10500216B2 (en) 2011-11-18 2019-12-10 Corcept Therapeutics, Inc. Optimizing mifepristone absorption
ES2919923T3 (es) 2012-03-01 2022-07-29 Array Biopharma Inc Formas cristalinas de clorhidrato de 1-(3-tert-butil-1-p-tolil-1H-pirazol-5-il)-3-(5-fluoro-2-(1-(2-hidroxietil)-1H-indazol-5-iloxi)urea
WO2013167999A2 (fr) 2012-05-10 2013-11-14 Mahesh Kandula Compositions et méthodes de traitement d'affections neurologiques
US9248122B2 (en) 2012-11-28 2016-02-02 Grünenthal GmbH Heteroquinoline-3-carboxamides as KCNQ2/3 modulators
EP2970188A4 (fr) 2013-03-15 2016-10-19 Vm Therapeutics Llc Nouvelles formes cristallines
AU2015364640B2 (en) 2014-12-16 2020-08-13 Ptc Therapeutics, Inc. Polymorphic and amorphous forms of (R)-2-hydroxy-2-methyl-4-(2,4,5-trimethyl-3,6-dioxocyclohexa-1,4-dienyl)butanamide
KR20200139127A (ko) 2017-10-10 2020-12-11 카울라 아부-이짜 설파살라진 염 조성물 및 이의 사용 방법
HRP20230808T1 (hr) 2018-02-20 2023-11-10 H. Lundbeck A/S Derivati alkohola kao otvarači kv7 kalijevih kanala
FI3790548T3 (fi) 2018-05-11 2023-11-17 Xenon Pharmaceuticals Inc Menetelmiä jänniteriippuvaisen kaliumkanavan avaajan biosaatavuuden ja eksposition tehostamiseksi
TWI886158B (zh) * 2019-10-10 2025-06-11 加拿大商再諾製藥公司 選擇性鉀通道調節劑之固態晶型
EP4074696B1 (fr) 2021-10-27 2026-02-04 Shanghai Zhimeng Biopharma, Inc. N-[4-(6-fluoro-3,4-dihydro-2(1h)-isoquinolinyl)-2,6-diméthylphenyl]-1-méthyl-cyclopropane-acetamide, un régulateur du canal potassique pour le traitement d'épilepsie

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008024398A2 (fr) * 2006-08-23 2008-02-28 Valeant Pharmaceuticals International Dérivés de 4-(n-azacycloalkyl) anilides en tant que modulateurs du canal potassique
US20110003850A1 (en) * 2006-08-23 2011-01-06 Valeant Pharmaceuticals International, Inc. Derivatives of 4-(n-azacycloalkyl) anilides as potassium channel modulators

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