JP2016512517A5 - - Google Patents

Download PDF

Info

Publication number
JP2016512517A5
JP2016512517A5 JP2016501158A JP2016501158A JP2016512517A5 JP 2016512517 A5 JP2016512517 A5 JP 2016512517A5 JP 2016501158 A JP2016501158 A JP 2016501158A JP 2016501158 A JP2016501158 A JP 2016501158A JP 2016512517 A5 JP2016512517 A5 JP 2016512517A5
Authority
JP
Japan
Prior art keywords
compound
pharmaceutical composition
disease
administered
dose
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.)
Granted
Application number
JP2016501158A
Other languages
English (en)
Japanese (ja)
Other versions
JP6527851B2 (ja
JP2016512517A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2014/023138 external-priority patent/WO2014164658A1/en
Publication of JP2016512517A publication Critical patent/JP2016512517A/ja
Publication of JP2016512517A5 publication Critical patent/JP2016512517A5/ja
Application granted granted Critical
Publication of JP6527851B2 publication Critical patent/JP6527851B2/ja
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2016501158A 2013-03-12 2014-03-11 ロイコトリエンa4加水分解酵素を阻害する方法 Active JP6527851B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201361776981P 2013-03-12 2013-03-12
US61/776,981 2013-03-12
PCT/US2014/023138 WO2014164658A1 (en) 2013-03-12 2014-03-11 Methods of inhibiting leukotriene a4 hydrolase

Publications (3)

Publication Number Publication Date
JP2016512517A JP2016512517A (ja) 2016-04-28
JP2016512517A5 true JP2016512517A5 (enExample) 2017-04-13
JP6527851B2 JP6527851B2 (ja) 2019-06-05

Family

ID=51658933

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2016501158A Active JP6527851B2 (ja) 2013-03-12 2014-03-11 ロイコトリエンa4加水分解酵素を阻害する方法

Country Status (8)

Country Link
US (3) US9820974B2 (enExample)
EP (1) EP2968359B1 (enExample)
JP (1) JP6527851B2 (enExample)
AU (1) AU2014249168B2 (enExample)
CA (1) CA2905340C (enExample)
ES (1) ES2864862T3 (enExample)
RU (1) RU2686101C2 (enExample)
WO (1) WO2014164658A1 (enExample)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3205644A1 (en) 2005-12-29 2017-08-16 Celtaxsys Inc. Diamine derivatives as inhibitors of leukotriene a4 hydrolase
WO2014164658A1 (en) * 2013-03-12 2014-10-09 Celtaxsys, Inc. Methods of inhibiting leukotriene a4 hydrolase
CA2906084A1 (en) 2013-03-14 2014-09-25 Celtaxsys, Inc. Inhibitors of leukotriene a4 hydrolase
EP2968264A4 (en) 2013-03-14 2016-11-02 Celtaxsys Inc INHIBITORS OF LEUCOTRIENE A4 HYDROLASE
CA2906086A1 (en) 2013-03-14 2014-09-25 Celtaxsys, Inc. Inhibitors of leukotriene a4 hydrolase
SG11202010115RA (en) * 2018-05-15 2020-11-27 Alkahest Inc Treatment of aging-associated disease with modulators of leukotriene a4 hydrolase
ES3014615T3 (en) * 2018-05-31 2025-04-23 Celltaxis Llc Method of reducing pulmonary exacerbations in respiratory disease patients
AU2020207638B2 (en) 2019-01-11 2023-04-13 Novartis Ag LTA4H inhibitors for the treatment of Hidradenitis Suppurativa
TW202122078A (zh) 2019-09-06 2021-06-16 瑞士商諾華公司 使用lta4h抑制劑治療肝臟疾病之方法
EP4196478A1 (en) 2020-08-14 2023-06-21 Novartis AG Heteroaryl substituted spiropiperidinyl derivatives and pharmaceutical uses thereof
AU2022376563A1 (en) 2021-11-01 2023-12-07 Alkahest, Inc. Benzodioxane modulators of leukotriene a4 hydrolase (lta4h) for prevention and treatment of aging-associated diseases
CA3239752A1 (en) * 2021-12-09 2023-06-15 Stanley Glenn Rockson Methods of treating lymphedema
WO2024254377A2 (en) * 2023-06-09 2024-12-12 Celltaxis, Llc Methods of treating lipedema and lymphatic disease of the subcutaneous tissue

Family Cites Families (85)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL6815872A (enExample) 1967-11-22 1969-05-27
JPS5614663B2 (enExample) 1971-08-21 1981-04-06
US4582833A (en) 1984-04-16 1986-04-15 American Cyanamid Company 2-(substituted-1-piperazinyl)[1,2,4]triazolo[1,5-a]pyrimidines
US4576943A (en) 1984-10-09 1986-03-18 American Cyanamid Company Pyrazolo[1,5-a]pyrimidines
US5308852A (en) 1992-06-29 1994-05-03 Merck Frosst Canada, Inc. Heteroarylnaphthalenes as inhibitors of leukotriene biosynthesis
US6506876B1 (en) 1994-10-11 2003-01-14 G.D. Searle & Co. LTA4 hydrolase inhibitor pharmaceutical compositions and methods of use
WO1997029774A1 (en) 1996-02-13 1997-08-21 G.D. Searle & Co. Combinations, having immunosuppressive effects, containing a cyclooxygenase-2 inhibitor and a leukotriene a4 hydrolase inhibitor
US5952349A (en) 1996-07-10 1999-09-14 Schering Corporation Muscarinic antagonists for treating memory loss
JP2000516611A (ja) 1996-08-14 2000-12-12 ワーナー―ランバート・コンパニー Mcp―1アンタゴニストとしての2―フェニルベンズイミダゾール誘導体
US6309561B1 (en) 1997-12-24 2001-10-30 3M Innovative Properties Company Liquid crystal compounds having a chiral fluorinated terminal portion
US6380203B1 (en) 1998-01-14 2002-04-30 Merck & Co., Inc. Angiogenesis inhibitors
GB9815880D0 (en) 1998-07-21 1998-09-16 Pfizer Ltd Heterocycles
GB9919776D0 (en) 1998-08-31 1999-10-27 Zeneca Ltd Compoujnds
AR023659A1 (es) 1998-09-18 2002-09-04 Vertex Pharma Un compuesto inhibidor de p38, una composicion farmaceutica que lo comprende y el uso de dicha composicion en el tratamiento y prevencion de estados patologicos
US6699873B1 (en) 1999-08-04 2004-03-02 Millennium Pharmaceuticals, Inc. Melanocortin-4 receptor binding compounds and methods of use thereof
US6924313B1 (en) 1999-09-23 2005-08-02 Pfizer Inc. Substituted tertiary-heteroalkylamines useful for inhibiting cholesteryl ester transfer protein activity
WO2001056990A2 (en) 2000-02-03 2001-08-09 Eli Lilly And Company Pyridine derivates as potentiators of glutamate receptors
US6451798B2 (en) 2000-02-22 2002-09-17 Cv Therapeutics, Inc. Substituted alkyl piperazine derivatives
US6552023B2 (en) 2000-02-22 2003-04-22 Cv Therapeutics, Inc. Aralkyl substituted piperazine compounds
JP2001354657A (ja) 2000-06-09 2001-12-25 Sds Biotech:Kk 置換ピペラジン誘導体及び農園芸用殺菌剤
DE60114518T2 (de) 2000-07-06 2006-08-10 Fuji Photo Film Co. Ltd., Minamiashigara Flüssigkristallzusammensetzung, die Flüssigkristallmoleküle und Ausrichtungsmittel enthält
WO2002064211A1 (en) 2001-02-09 2002-08-22 Merck & Co., Inc. Thrombin inhibitors
US7012075B2 (en) 2001-03-02 2006-03-14 Merck & Co., Inc. Cathepsin cysteine protease inhibitors
AUPR362001A0 (en) 2001-03-08 2001-04-05 Fujisawa Pharmaceutical Co., Ltd. New compound
FR2826011B1 (fr) 2001-06-14 2004-12-10 Oreal Nouveaux derives de la 7-oxo-dhea et utilisation cosmetique
SE0102616D0 (sv) 2001-07-25 2001-07-25 Astrazeneca Ab Novel compounds
AU2002336532C1 (en) 2001-09-14 2008-10-16 Amgen, Inc Linked biaryl compounds
WO2003037271A2 (en) 2001-10-30 2003-05-08 Millennium Pharmaceuticals,Inc. Compounds, pharmaceutical compositions and methods of use therefor
AU2003270291A1 (en) 2002-10-04 2004-04-23 Ucb 4-aminopiperidine derivatives, processes for their preparation and their use as medicaments
AU2003290527A1 (en) 2002-10-17 2004-05-04 Decode Genetics Ehf. Susceptibility gene for myocardial infarction
WO2005027886A2 (en) 2003-09-17 2005-03-31 Decode Genetics Ehf. Methods of preventing or treating recurrence of myocardial infarction
US7851486B2 (en) 2002-10-17 2010-12-14 Decode Genetics Ehf. Susceptibility gene for myocardial infarction, stroke, and PAOD; methods of treatment
AU2003300360A1 (en) 2002-12-20 2004-07-22 Migenix Corp. Ligands of adenine nucleotide translocase (ant) and compositions and methods related thereto
CA2521000A1 (en) 2003-04-03 2004-10-21 Kyowa Hakko Kogyo Co., Ltd. Preventive and/or therapeutic agent for neuropathic pain
WO2004099164A1 (en) 2003-05-02 2004-11-18 Rigel Pharmaceuticals, Inc. Substituted diphenyl isoxazoles, pyrazoles and oxadiazoles useful for treating hcv infection
JP2005008581A (ja) 2003-06-20 2005-01-13 Kissei Pharmaceut Co Ltd 新規なピラゾロ[1,5−a]ピリミジン誘導体、それを含有する医薬組成物およびそれらの用途
KR20060054408A (ko) 2003-07-28 2006-05-22 얀센 파마슈티카 엔.브이. 벤즈이미다졸, 벤즈티아졸 및 벤즈옥사졸 유도체 및lta4 h 조정자로서의 그의 용도
EP1669348A4 (en) 2003-09-30 2009-03-11 Eisai R&D Man Co Ltd NEW ANTIPILIC AGENT CONTAINING A HETEROCYCLIC COMPOUND
GB0326632D0 (en) * 2003-11-14 2003-12-17 Jagotec Ag Dry powder formulations
DE10356579A1 (de) 2003-12-04 2005-07-07 Merck Patent Gmbh Aminderivate
SE0303480D0 (sv) 2003-12-19 2003-12-19 Biovitrum Ab Benzofuranes
EP1699847B1 (en) * 2003-12-30 2011-04-13 3M Innovative Properties Company Method for the preparation of medicinal compositions
ATE437880T1 (de) 2004-02-04 2009-08-15 Neurosearch As Dimere azacyclische verbindungen und deren verwendung
WO2006033795A2 (en) 2004-09-17 2006-03-30 Wyeth Substituted pyrazolo [1, 5-a] pyrimidines for inhibiting abnormal cell growth
CA2595791C (en) * 2005-03-16 2013-10-08 Meda Pharma Gmbh & Co. Kg The combination of anticholinergics and leukotriene receptor antagonists for the treatment of respiratory diseases
KR20080003385A (ko) 2005-03-31 2008-01-07 얀센 파마슈티카 엔.브이. 페닐 및 피리딜 lta4h 조절제
GB0514018D0 (en) 2005-07-07 2005-08-17 Ionix Pharmaceuticals Ltd Chemical compounds
JP5133889B2 (ja) 2005-09-21 2013-01-30 デコード ジェネティクス イーエイチエフ 炎症治療のためのビアリール基置換複素環lta4h阻害剤
CN1947717B (zh) 2005-10-14 2012-09-26 卓敏 选择性抑制腺苷酸环化酶1的化合物在制备用于治疗神经性疼痛和炎性疼痛的药物中的应用
DE102005049954A1 (de) 2005-10-19 2007-05-31 Sanofi-Aventis Deutschland Gmbh Triazolopyridin-derivate als Inhibitoren von Lipasen und Phospholipasen
EP3205644A1 (en) * 2005-12-29 2017-08-16 Celtaxsys Inc. Diamine derivatives as inhibitors of leukotriene a4 hydrolase
AU2007215247B2 (en) 2006-02-10 2012-12-13 Transtech Pharma, Llc Benzazole derivatives, compositions, and methods of use as Aurora kinase inhibitors
WO2008016131A1 (en) 2006-08-04 2008-02-07 Takeda Pharmaceutical Company Limited Fused heterocyclic compound
CN101528709B (zh) 2006-10-19 2012-02-01 弗·哈夫曼-拉罗切有限公司 对痕量胺相关受体有亲和性的氨基甲基-2-咪唑类
US7893257B2 (en) 2006-12-14 2011-02-22 Janssen Pharmaceutica Nv Process for the preparation of piperazinyl and diazepanyl benzamide derivatives
FR2911139A1 (fr) 2007-01-05 2008-07-11 Sanofi Aventis Sa Nouveaux derives de phenyl-(4-phenyl-pyrimidin-2-yl)amines, leur preparation a titre de medicaments, compositions pharmaceutiques et notamment comme inhibiteurs de ikk
FR2911140B1 (fr) 2007-01-05 2009-02-20 Sanofi Aventis Sa Nouveaux derives de 2-anilino 4-heteroaryle pyrimides, leur preparation a titre de medicaments, compositions pharmaceutiques et notamment comme inhibiteurs de ikk
FR2911138B1 (fr) 2007-01-05 2009-02-20 Sanofi Aventis Sa Nouveaux derives de n, n'-2,4-dianilinopyrimidines, leur preparation a titre de medicaments, compositions pharmaceutiques et notamment comme inhibiteurs de ikk
CN101687844B (zh) 2007-07-02 2013-11-13 弗·哈夫曼-拉罗切有限公司 用作ccr2受体拮抗剂的咪唑衍生物
AR068498A1 (es) * 2007-09-27 2009-11-18 Merck & Co Inc Compuestos de oxadiazol para inhibicion de biosintesis de leucotrienos
AU2008334444B2 (en) 2007-12-12 2011-12-15 Astrazeneca Ab Peptidyl nitriles and use thereof as dipeptidyl peptidase I inhibitors
BRPI0908529A2 (pt) 2008-02-26 2015-09-29 Novartis Ag composto orgânicos
FR2928070A1 (fr) 2008-02-27 2009-09-04 Sumitomo Chemical Co Composition agricole, utilisation d'un compose pour sa production et procede pour matriser ou prevenir les maladies des plantes.
US20100029657A1 (en) 2008-02-29 2010-02-04 Wyeth Bridged, Bicyclic Heterocyclic or Spiro Bicyclic Heterocyclic Derivatives of Pyrazolo[1, 5-A]Pyrimidines, Methods for Preparation and Uses Thereof
KR101228378B1 (ko) 2008-04-11 2013-01-31 얀센 파마슈티카 엔.브이. 류코트리엔 α4 하이드롤레이즈의 조정제로서의 티아졸로피리딘-2-일옥시-페닐 및 티아졸로피라진-2-일옥시-페닐 아민
EP2110374A1 (en) 2008-04-18 2009-10-21 Merck Sante Benzofurane, benzothiophene, benzothiazol derivatives as FXR modulators
WO2010011912A1 (en) 2008-07-25 2010-01-28 Smithkline Beecham Corporation Trpv4 antagonists
GB2465897B (en) * 2008-08-07 2011-02-09 Argenta Discovery Ltd Respiratory disease treatment
RU2011145278A (ru) * 2009-04-09 2013-05-20 Алкермес Фарма Айэленд Лимитед Композиции клозапина с контролируемым высвобождением
CN102030700B (zh) 2009-09-30 2016-06-01 中国医学科学院药物研究所 苯甲酰胺基羧酸类化合物及其制法和药物用途
CN102741226B (zh) 2009-10-30 2016-01-06 詹森药业有限公司 4-取代的-2-苯氧基-苯胺δ阿片类受体调节剂
AU2010328419A1 (en) 2009-12-07 2012-06-21 Targacept, Inc. 3,6-diazabicyclo[3.1.1]heptanes as neuronal nicotinic acetylcholine receptor ligands
ES2823350T3 (es) 2010-07-29 2021-05-06 Rigel Pharmaceuticals Inc Compuestos heterocíclicos que activan AMPK y métodos de uso de los mismos
WO2012067822A1 (en) 2010-11-16 2012-05-24 Abbott Laboratories Pyrazolo [1, 5 -a] pyrimidin potassium channel modulators
TR201802550T4 (tr) 2011-03-14 2018-03-21 Boehringer Ingelheim Int Lökotrien üretiminin benzodioksan inhibitörleri.
SG193424A1 (en) 2011-03-15 2013-10-30 Rib X Pharmaceuticals Inc Antimicrobial agents
US9642888B2 (en) * 2011-04-12 2017-05-09 Moerae Matrix, Inc. Compositions and methods for preventing or treating diseases, conditions, or processes characterized by aberrant fibroblast proliferation and extracellular matrix deposition
ES2557450T3 (es) 2011-05-23 2016-01-26 Janssen Pharmaceutica, N.V. Derivados de ácido picolinamido-propanoico útiles como antagonistas de los receptores de glucagón
CN103159742B (zh) 2011-12-16 2015-08-12 北京韩美药品有限公司 5-氯嘧啶类化合物及其作为egfr酪氨酸激酶抑制剂的应用
US9006235B2 (en) 2012-03-06 2015-04-14 Bristol-Myers Squibb Company Inhibitors of human immunodeficiency virus replication
EP2827849A4 (en) 2012-03-23 2015-11-18 Univ Leland Stanford Junior TREATMENT OF PULMONARY HYPERTONIA WITH LEUKOTRIENHEMMERN
WO2014164658A1 (en) * 2013-03-12 2014-10-09 Celtaxsys, Inc. Methods of inhibiting leukotriene a4 hydrolase
CA2906084A1 (en) 2013-03-14 2014-09-25 Celtaxsys, Inc. Inhibitors of leukotriene a4 hydrolase
CA2906086A1 (en) 2013-03-14 2014-09-25 Celtaxsys, Inc. Inhibitors of leukotriene a4 hydrolase
EP2968264A4 (en) 2013-03-14 2016-11-02 Celtaxsys Inc INHIBITORS OF LEUCOTRIENE A4 HYDROLASE

Similar Documents

Publication Publication Date Title
JP2016512517A5 (enExample)
JP6527851B2 (ja) ロイコトリエンa4加水分解酵素を阻害する方法
JP6111202B2 (ja) 免疫抑制製剤
JP2017528507A5 (enExample)
JP2014532638A5 (enExample)
JP2018534348A5 (enExample)
JP2015145426A5 (enExample)
JP2016516808A5 (enExample)
JP2017222722A5 (enExample)
JP2024153665A (ja) P2x3調節剤としての置換イミダゾピリジン化合物の結晶形態およびそれらの使用
TW201417811A (zh) 脂質異常症治療劑
JP2005522449A (ja) Pde4阻害剤として有用なニコチンアミド誘導体
JP2015510916A5 (enExample)
JP5362151B2 (ja) Pgd2拮抗剤及びヒスタミン拮抗剤からなるアレルギー性鼻炎治療用医薬
JP4012935B2 (ja) Pde4阻害剤として有用なニコチンアミド誘導体
JP2020510027A5 (enExample)
JP2013516475A5 (enExample)
FI4426307T3 (fi) Uusi suun kautta otettava farmaseuttinen koostumus ja annosteluohjelma progressiivisen interstitiaalisen keuhkosairauden hoitoon
JP2015189677A (ja) ソリフェナシン非晶質体を含有する医薬組成物
JP2013177351A (ja) Pgd2拮抗剤及びロイコトリエン拮抗剤からなる喘息治療剤
EP3397285A1 (en) Tablet formulations of montelukast sodium and rupatadine fumarate
WO2011152808A1 (en) Formulation comprising cefpodoxime proxetil and clavulanic acid
CA3108713A1 (en) Methods of administering therapy
EP2575811A1 (en) Pharmaceutical formulation comprising cefpodoxime proxetil and clavulanic acid
JP2007008815A (ja) N−(ベンゾイル)アミノ酸誘導体を有効成分とする呼吸器疾患治療剤