DK2903618T3 - Rho-kinase-inhibitorer - Google Patents
Rho-kinase-inhibitorer Download PDFInfo
- Publication number
- DK2903618T3 DK2903618T3 DK13843426.1T DK13843426T DK2903618T3 DK 2903618 T3 DK2903618 T3 DK 2903618T3 DK 13843426 T DK13843426 T DK 13843426T DK 2903618 T3 DK2903618 T3 DK 2903618T3
- Authority
- DK
- Denmark
- Prior art keywords
- kinase inhibitors
- rho kinase
- rho
- inhibitors
- kinase
- Prior art date
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic 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
- C07D403/12—Heterocyclic 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 chain containing hetero atoms as chain links
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- 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
- A61K31/495—Heterocyclic 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
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
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- A61P11/06—Antiasthmatics
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- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/32—One oxygen, sulfur or nitrogen atom
- C07D239/42—One nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201261710373P | 2012-10-05 | 2012-10-05 | |
US201361840288P | 2013-06-27 | 2013-06-27 | |
PCT/US2013/063752 WO2014055996A2 (en) | 2012-10-05 | 2013-10-07 | Rho kinase inhibitors |
Publications (1)
Publication Number | Publication Date |
---|---|
DK2903618T3 true DK2903618T3 (da) | 2022-08-22 |
Family
ID=50435589
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DK13843426.1T DK2903618T3 (da) | 2012-10-05 | 2013-10-07 | Rho-kinase-inhibitorer |
Country Status (16)
Country | Link |
---|---|
US (4) | US9815820B2 (da) |
EP (2) | EP2903618B1 (da) |
JP (2) | JP6419076B2 (da) |
CN (5) | CN113637008A (da) |
CA (2) | CA3151343A1 (da) |
DK (1) | DK2903618T3 (da) |
EA (1) | EA201500362A1 (da) |
ES (1) | ES2924915T3 (da) |
HR (1) | HRP20220913T1 (da) |
HU (1) | HUE059305T2 (da) |
LT (1) | LT2903618T (da) |
PL (1) | PL2903618T3 (da) |
PT (1) | PT2903618T (da) |
RS (1) | RS63503B1 (da) |
SI (1) | SI2903618T1 (da) |
WO (1) | WO2014055996A2 (da) |
Families Citing this family (40)
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US11008359B2 (en) * | 2002-08-23 | 2021-05-18 | Illumina Cambridge Limited | Labelled nucleotides |
HRP20220913T1 (hr) | 2012-10-05 | 2022-10-28 | Kadmon Corporation, Llc | Inhibitori rho kinaze |
US11311541B2 (en) * | 2014-04-09 | 2022-04-26 | Kadmon Corporation, Llc | Treatment of GVHD |
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CA2995344C (en) | 2014-10-07 | 2021-05-04 | Kadmon Corporation, Llc | Human anti-vegfr-2/kdr antibodies |
EP3262041A4 (en) | 2015-02-27 | 2018-08-01 | Lycera Corporation | Indazolyl thiadiazolamines and related compounds for inhibition of rho-associated protein kinase and the treatment of disease |
EP3283479B1 (en) * | 2015-04-01 | 2022-12-14 | Rigel Pharmaceuticals, Inc. | Tgf-beta inhibitors |
US9937154B2 (en) | 2015-06-10 | 2018-04-10 | Hackensak University Medical Center | Use of telmisartan to prevent and treat graft versus host disease and other alloimmune and autoimmune diseases |
EP3313825A4 (en) * | 2015-06-26 | 2019-03-13 | Kadmon Corporation, LLC | GLUCOSE ABSORPTION INHIBITORS |
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SG11201900027XA (en) * | 2016-08-05 | 2019-02-27 | Medimmune Llc | Anti-o2 antibodies and uses thereof |
EP3504204A4 (en) | 2016-08-26 | 2020-05-27 | Lycera Corporation | INDAZOLYL-L, 2,4-THIADIAZOLAMINE AND RELATED COMPOUNDS FOR INHIBITING RHO-ASSOCIATED PROTEIN KINASES AND FOR TREATING DISEASES |
CN109843917B (zh) | 2016-10-19 | 2023-10-03 | 免疫医疗有限责任公司 | 抗o1抗体及其用途 |
CN106916145B (zh) * | 2017-03-06 | 2019-06-04 | 上海应用技术大学 | SLx-2119的合成方法 |
IT201700047189A1 (it) * | 2017-05-02 | 2018-11-02 | Fondazione St Italiano Tecnologia | Composti e composizioni per il trattamento di cancro, disordini della retina e cardiomiopatie |
US10323023B2 (en) | 2017-06-30 | 2019-06-18 | Beijing Tide Pharmaceutical Co., Ltd. | Rho-associated protein kinase inhibitor, pharmaceutical composition comprising the same, as well as preparation method and use thereof |
US10329282B2 (en) | 2017-06-30 | 2019-06-25 | Beijing Tide Pharmaceutical Co., Ltd. | Rho-associated protein kinase inhibitor, pharmaceutical composition comprising the same, as well as preparation method and use thereof |
CN111217797B (zh) | 2017-06-30 | 2021-02-05 | 北京泰德制药股份有限公司 | Rho相关蛋白激酶抑制剂、包含其的药物组合物及其制备方法和用途 |
EA202090572A1 (ru) * | 2017-09-01 | 2020-07-06 | Кадмон Корпорейшн, Ллк | ИНГИБИТОРЫ Rho-АССОЦИИРОВАННОЙ, СОДЕРЖАЩЕЙ СУПЕРСПИРАЛЬ ПРОТЕИНКИНАЗЫ |
EP3676262A4 (en) | 2017-09-03 | 2021-03-31 | Angion Biomedica Corp. | VINYLHETEROCYCLENE AS RHO-ASSOCIATED COILED COIL KINASE (ROCK) INHIBITORS |
WO2019201297A1 (zh) | 2018-04-18 | 2019-10-24 | 南京明德新药研发有限公司 | 作为rho激酶抑制剂的苯并吡唑类化合物 |
US11248004B2 (en) | 2018-11-06 | 2022-02-15 | Cervello Therapeutics, Llc. | Substituted isoquinolines as rock kinase inhibitors |
KR20210093269A (ko) | 2018-11-06 | 2021-07-27 | 써벨로 테라퓨틱스, 엘엘씨 | Rock 키나아제 저해제 |
WO2020210382A1 (en) * | 2019-04-08 | 2020-10-15 | The General Hospital Corporation | Enhancement of melanocyte migration using rock inhibitors |
JP7252417B2 (ja) | 2019-10-18 | 2023-04-04 | メッドシャイン ディスカバリー インコーポレイテッド | Rhoキナーゼ阻害剤としてのベンゾピラゾール化合物の塩形、結晶形及びその製造方法 |
WO2021129589A1 (zh) * | 2019-12-27 | 2021-07-01 | 广东东阳光药业有限公司 | Kd-025的新晶型及其制备方法 |
IL299985A (en) * | 2020-07-22 | 2023-03-01 | Beijing Tide Pharmaceutical Co Ltd | A method for treating graft-versus-Maschen disease caused by hematopoietic stem cell transplantation |
CA3186800A1 (en) | 2020-07-22 | 2022-01-27 | Teva Pharmaceuticals International Gmbh | Solid state forms of belumosudil and belumosudil salts |
WO2022042666A1 (zh) * | 2020-08-28 | 2022-03-03 | 杭州邦顺制药有限公司 | 选择性rock2激酶抑制剂 |
JP2024503021A (ja) | 2021-01-11 | 2024-01-24 | インサイト・コーポレイション | Jak経路阻害剤及びrock阻害剤を含む併用療法 |
WO2022170864A1 (zh) * | 2021-02-09 | 2022-08-18 | 苏州科睿思制药有限公司 | Belumosudil甲磺酸盐的晶型及其制备方法和用途 |
WO2022229351A1 (en) | 2021-04-28 | 2022-11-03 | Graviton Bioscience Bv | Selective inhibitors of rock2 for the treatment of muscular dystrophy |
WO2023285706A1 (en) | 2021-07-16 | 2023-01-19 | Sandoz Ag | Solid-state forms of 2-(3-(4-(1h-indazol-5-ylamino)quinazolin-2-yl )phenoxy)-n- isopropylacetamide methane sulfonic acid salt |
WO2023205153A1 (en) | 2022-04-19 | 2023-10-26 | Kadmon Corporation, Llc | Belumosudil for treating chronic lung allograft dysfunction |
WO2024015068A1 (en) | 2022-07-14 | 2024-01-18 | Kadmon Corporation, Llc | Belumosudil metabolites and uses thereof in the treatment of chronic graft-versus-host disease |
WO2024015066A1 (en) | 2022-07-14 | 2024-01-18 | Kadmon Corporation, Llc | Methods of administering belumosudil in combination with cyp3a inducers and/or proton pump inhibitors |
WO2024015067A1 (en) | 2022-07-14 | 2024-01-18 | Kadmon Corporation, Llc | Methods of administering belumosudil for treatment of chronic graft versus host disease |
WO2024015065A1 (en) | 2022-07-14 | 2024-01-18 | Kadmon Corporation, Llc | Methods of administering belumosudil for treatment of chronic graft versus host disease in patient subpopulations |
WO2024023276A1 (en) | 2022-07-27 | 2024-02-01 | Graviton Bioscience Bv | Rock2 inhibitors for the treatment of viral infections |
WO2024063770A1 (en) * | 2022-09-21 | 2024-03-28 | Kadmon Corporation, Llc | Liquid formulation of belumosudil |
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CR9465A (es) * | 2005-03-25 | 2008-06-19 | Surface Logix Inc | Compuestos mejorados farmacocineticamente |
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PL2542528T3 (pl) * | 2010-03-02 | 2013-11-29 | Amakem Nv | Heterocykliczne amidy jako inhibitory ROCK |
US9079880B2 (en) * | 2010-07-07 | 2015-07-14 | Boehringer Ingelheim International Gmbh | Rho kinase inhibitors |
WO2012040499A2 (en) | 2010-09-22 | 2012-03-29 | Surface Logix, Inc. | Metabolic inhibitors |
AU2011329233A1 (en) | 2010-11-15 | 2013-05-23 | Abbvie Deutschland Gmbh & Co Kg | NAMPT and ROCK inhibitors |
GB201107223D0 (en) | 2011-04-29 | 2011-06-15 | Amakem Nv | Novel rock inhibitors |
GB201114854D0 (en) | 2011-08-29 | 2011-10-12 | Amakem Nv | Novel rock inhibitors |
CN103874683A (zh) | 2011-08-31 | 2014-06-18 | 阿玛克姆股份有限公司 | 新的rock激酶抑制剂 |
WO2014055999A2 (en) * | 2012-10-05 | 2014-04-10 | Kadmon Corporation, Llc | Treatment of ocular disorders |
HRP20220913T1 (hr) * | 2012-10-05 | 2022-10-28 | Kadmon Corporation, Llc | Inhibitori rho kinaze |
US11311541B2 (en) * | 2014-04-09 | 2022-04-26 | Kadmon Corporation, Llc | Treatment of GVHD |
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2013
- 2013-10-07 HR HRP20220913TT patent/HRP20220913T1/hr unknown
- 2013-10-07 CN CN202110707587.XA patent/CN113637008A/zh active Pending
- 2013-10-07 WO PCT/US2013/063752 patent/WO2014055996A2/en active Application Filing
- 2013-10-07 EP EP13843426.1A patent/EP2903618B1/en active Active
- 2013-10-07 PT PT138434261T patent/PT2903618T/pt unknown
- 2013-10-07 CA CA3151343A patent/CA3151343A1/en active Pending
- 2013-10-07 CN CN202110707555.XA patent/CN113637007A/zh active Pending
- 2013-10-07 CN CN202110707631.7A patent/CN113773308A/zh active Pending
- 2013-10-07 EP EP22175888.1A patent/EP4116293A3/en active Pending
- 2013-10-07 RS RS20220776A patent/RS63503B1/sr unknown
- 2013-10-07 DK DK13843426.1T patent/DK2903618T3/da active
- 2013-10-07 CN CN202110707706.1A patent/CN113620933A/zh active Pending
- 2013-10-07 JP JP2015535880A patent/JP6419076B2/ja active Active
- 2013-10-07 CA CA2926478A patent/CA2926478C/en active Active
- 2013-10-07 LT LTEPPCT/US2013/063752T patent/LT2903618T/lt unknown
- 2013-10-07 ES ES13843426T patent/ES2924915T3/es active Active
- 2013-10-07 CN CN201380063599.7A patent/CN105120869A/zh active Pending
- 2013-10-07 SI SI201332003T patent/SI2903618T1/sl unknown
- 2013-10-07 PL PL13843426.1T patent/PL2903618T3/pl unknown
- 2013-10-07 US US14/431,936 patent/US9815820B2/en active Active
- 2013-10-07 HU HUE13843426A patent/HUE059305T2/hu unknown
- 2013-10-07 EA EA201500362A patent/EA201500362A1/ru unknown
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2017
- 2017-11-10 US US15/809,460 patent/US10183931B2/en active Active
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2018
- 2018-10-09 JP JP2018191181A patent/JP6703075B2/ja active Active
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2019
- 2019-01-18 US US16/251,952 patent/US10696660B2/en active Active
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2020
- 2020-06-26 US US16/913,267 patent/US20210147391A1/en active Pending
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