BR112018007947A2 - uso de antagonistas de receptor ep4 para o tratamento de câncer de fígado associado a nash - Google Patents
uso de antagonistas de receptor ep4 para o tratamento de câncer de fígado associado a nashInfo
- Publication number
- BR112018007947A2 BR112018007947A2 BR112018007947A BR112018007947A BR112018007947A2 BR 112018007947 A2 BR112018007947 A2 BR 112018007947A2 BR 112018007947 A BR112018007947 A BR 112018007947A BR 112018007947 A BR112018007947 A BR 112018007947A BR 112018007947 A2 BR112018007947 A2 BR 112018007947A2
- Authority
- BR
- Brazil
- Prior art keywords
- treatment
- liver cancer
- cancer associated
- nash
- receptor antagonists
- Prior art date
Links
- 101150109738 Ptger4 gene Proteins 0.000 title abstract 2
- 201000007270 liver cancer Diseases 0.000 title abstract 2
- 208000014018 liver neoplasm Diseases 0.000 title abstract 2
- 239000002464 receptor antagonist Substances 0.000 title 1
- 229940044551 receptor antagonist Drugs 0.000 title 1
- 239000005557 antagonist Substances 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- 238000000034 method Methods 0.000 abstract 2
- 239000013543 active substance Substances 0.000 abstract 1
- 208000008338 non-alcoholic fatty liver disease Diseases 0.000 abstract 1
- 206010053219 non-alcoholic steatohepatitis Diseases 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 238000002560 therapeutic procedure Methods 0.000 abstract 1
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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4412—Non condensed pyridines; Hydrogenated derivatives thereof having oxo groups directly attached to the heterocyclic ring
-
- 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
-
- 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
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/192—Carboxylic acids, e.g. valproic acid having aromatic groups, e.g. sulindac, 2-aryl-propionic acids, ethacrynic acid
-
- 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
- A61K31/4353—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 ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
-
- 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
- A61K31/64—Sulfonylureas, e.g. glibenclamide, tolbutamide, chlorpropamide
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2300/00—Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Gastroenterology & Hepatology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Pyridine Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
essa invenção é voltada aos antagonistas de receptor 4 (ep4) de prostaglandina e2 úteis no tratamento de câncer de fígado associado à esteato-hepatite não alcoólica em um humano ou animal. o método compreende administrar um ou mais dentre o composto a, composto b ou composto c ou sais farmaceuticamente aceitáveis dos mesmos, como os antagonista(s) de ep4. o método pode incluir uma composição farmacêutica compreendendo o(s) antagonista(s) de ep4 e pode incluir um ou mais agentes ativos e/ou terapias.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US15/343,999 US10342785B2 (en) | 2016-11-04 | 2016-11-04 | Use of EP4 receptor antagonists for the treatment of NASH-associated liver cancer |
PCT/JP2017/039680 WO2018084230A1 (en) | 2016-11-04 | 2017-11-02 | Use of ep4 receptor antagonists for the treatment of nash-associated liver cancer |
Publications (1)
Publication Number | Publication Date |
---|---|
BR112018007947A2 true BR112018007947A2 (pt) | 2018-10-30 |
Family
ID=60582639
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BR112018007947A BR112018007947A2 (pt) | 2016-11-04 | 2017-11-02 | uso de antagonistas de receptor ep4 para o tratamento de câncer de fígado associado a nash |
Country Status (12)
Country | Link |
---|---|
US (2) | US10342785B2 (pt) |
EP (1) | EP3344296B1 (pt) |
JP (1) | JP6516341B2 (pt) |
KR (1) | KR20180064438A (pt) |
CN (1) | CN108289960B (pt) |
BR (1) | BR112018007947A2 (pt) |
CA (1) | CA3000237C (pt) |
ES (1) | ES2729961T3 (pt) |
HK (2) | HK1251162B (pt) |
MX (1) | MX2018005715A (pt) |
RU (2) | RU2717331C2 (pt) |
WO (1) | WO2018084230A1 (pt) |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU2019255196A1 (en) * | 2018-04-16 | 2020-11-12 | Arrys Therapeutics, Inc. | EP4 inhibitors and use thereof |
EP3820469A4 (en) * | 2018-07-11 | 2022-04-13 | Arrys Therapeutics, Inc. | EP4 INHIBITORS AND USE THEREOF |
KR20210117280A (ko) | 2019-01-22 | 2021-09-28 | 키테라 (쑤저우) 파마슈티컬스 컴퍼니 리미티드 | Pge2/ep4 신호 전달을 억제하기 위한 화합물, 이의 제조 방법, 및 이의 의약적 용도 |
EP3722319A1 (en) | 2019-04-09 | 2020-10-14 | Rottapharm Biotech S.r.l. | Pharmaceutical combination of an ep4 antagonist and immune checkpoint inhibitors for the treatment of tumours |
CN110386941A (zh) * | 2019-08-15 | 2019-10-29 | 上海邦耀生物科技有限公司 | Ep4受体拮抗剂和pd-1抑制剂联合用于癌症的治疗 |
CN110680555B (zh) * | 2019-11-12 | 2021-06-01 | 重庆医药高等专科学校 | 一种裸鼠皮下成瘤装置 |
WO2021205367A1 (en) * | 2020-04-08 | 2021-10-14 | Askat Inc. | Use of ep4 receptor antagonists for the treatment of liver cancer, melanoma, lymphoma and leukemia |
CN113577267B (zh) * | 2021-09-06 | 2022-04-08 | 江西北正干细胞生物科技有限公司 | Nk细胞和抗体的药物组合物及其在治疗癌症中的用途 |
Family Cites Families (28)
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ATE348608T1 (de) | 1999-08-10 | 2007-01-15 | Glaxo Group Ltd | Ep4 rezeptor ligand und verwendung gegen neuropatischen schmerzen, colon krebs, hiv und migräne |
EP1258473A4 (en) | 2000-02-22 | 2004-09-01 | Ono Pharmaceutical Co | BENZOIC ACID DERIVATIVES, PROCESS FOR PRODUCING THE SAME, AND MEDICINAL PRODUCT CONTAINING SUCH DERIVATIVES AS ACTIVE INGREDIENT |
US6710205B2 (en) | 2000-02-22 | 2004-03-23 | Ono Pharmaceutical Co., Ltd. | Benzoic acid derivatives, processes for producing the same and drugs containing the same as the active ingredient |
HN2001000224A (es) | 2000-10-19 | 2002-06-13 | Pfizer | Compuestos de imidazol condensado con arilo o heteroarilo como agentes anti - inflamatorios y analgesicos. |
AR036993A1 (es) | 2001-04-02 | 2004-10-20 | Wyeth Corp | Uso de agentes que modulan la interaccion entre pd-1 y sus ligandos en la submodulacion de respuestas inmunologicas |
MXPA04009961A (es) | 2002-04-12 | 2004-12-13 | Pfizer | Compuestos de imidazol como agentes anti-inflamatorios y analgesicos. |
JP2005526107A (ja) | 2002-04-16 | 2005-09-02 | 藤沢薬品工業株式会社 | 慢性拒絶反応を予防および/または処置するための医薬 |
CA2508660C (en) | 2002-12-23 | 2013-08-20 | Wyeth | Antibodies against pd-1 and uses therefor |
EP1663979B1 (en) | 2003-09-03 | 2013-10-09 | RaQualia Pharma Inc. | Phenyl or pyridyl amide compounds as prostaglandin e2 antagonists |
BRPI0509993A (pt) | 2004-04-20 | 2007-10-16 | Pfizer Prod Inc | combinações compreendendo ligandos de alfa-2-delta |
WO2005105733A1 (en) | 2004-05-04 | 2005-11-10 | Pfizer Japan Inc. | Ortho substituted aryl or heteroaryl amide compounds |
CN1950333A (zh) | 2004-05-04 | 2007-04-18 | 辉瑞大药厂 | 取代的甲基芳基或杂芳基酰胺化合物 |
BRPI0608819B8 (pt) | 2005-03-11 | 2021-05-25 | Askat Inc | formas cristalinas de um derivado de imidazol |
SI2439273T1 (sl) | 2005-05-09 | 2019-05-31 | Ono Pharmaceutical Co., Ltd. | Človeška monoklonska protitelesa za programirano smrt 1 (PD-1) in postopki za zdravljenje raka z uporabo protiteles proti PD-1 samostojno ali v kombinaciji z ostalimi imunoterapevtiki |
ATE533766T1 (de) | 2005-05-19 | 2011-12-15 | Merck Canada Inc | Chinolinderivate als ep4-antagonisten |
CN101248089A (zh) | 2005-07-01 | 2008-08-20 | 米德列斯公司 | 抗程序性死亡配体1(pd-l1)的人单克隆抗体 |
KR101586617B1 (ko) | 2007-06-18 | 2016-01-20 | 머크 샤프 앤 도메 비.브이. | 사람 프로그램된 사멸 수용체 pd-1에 대한 항체 |
US8119129B2 (en) | 2008-08-01 | 2012-02-21 | Bristol-Myers Squibb Company | Combination of anti-CTLA4 antibody with dasatinib for the treatment of proliferative diseases |
SI2342226T1 (sl) | 2008-09-26 | 2016-11-30 | Dana-Farber Cancer Institute Inc. | Humana protitelesa proti PD-1, PD-L1 in PD-L2 in njihove uporabe |
KR101050829B1 (ko) | 2008-10-02 | 2011-07-20 | 서울대학교산학협력단 | 항 pd-1 항체 또는 항 pd-l1 항체를 포함하는 항암제 |
UA109108C2 (uk) | 2008-12-09 | 2015-07-27 | Дженентек, Інк. | Антитіло до pd-l1 та його застосування для посилення функції t-клітин |
ES2698508T3 (es) * | 2009-04-22 | 2019-02-05 | Askat Inc | Sustancia antagonista del receptor EP4 selectivo para el tratamiento del cáncer |
AU2010303149B2 (en) | 2009-09-30 | 2016-08-04 | Board Of Regents, The University Of Texas System | Combination immunotherapy for the treatment of cancer |
CA2789665C (en) * | 2010-02-22 | 2020-06-16 | Raqualia Pharma Inc. | Use of ep4 receptor antagonists in the treatment of il-23 mediated diseases |
KR101974675B1 (ko) | 2011-09-16 | 2019-05-02 | 갈렉틴 테라퓨틱스, 인크. | 비알콜성 지방간염 및 비알콜성 지방간 질환의 치료를 위한 갈락토-람노갈락투로네이트 조성물 |
US20150004175A1 (en) | 2011-12-13 | 2015-01-01 | Yale University | Compositions and Methods for Reducing CTL Exhaustion |
CN106102774A (zh) * | 2013-12-17 | 2016-11-09 | 豪夫迈·罗氏有限公司 | 包含ox40结合激动剂和pd‑1轴结合拮抗剂的组合疗法 |
KR102535283B1 (ko) | 2014-05-23 | 2023-05-22 | 에자이 알앤드디 매니지먼트 가부시키가이샤 | 암의 치료를 위한 조합 요법 |
-
2016
- 2016-11-04 US US15/343,999 patent/US10342785B2/en active Active
-
2017
- 2017-11-02 KR KR1020187012103A patent/KR20180064438A/ko not_active Application Discontinuation
- 2017-11-02 MX MX2018005715A patent/MX2018005715A/es active IP Right Grant
- 2017-11-02 RU RU2018117891A patent/RU2717331C2/ru active
- 2017-11-02 CN CN201780004254.2A patent/CN108289960B/zh active Active
- 2017-11-02 BR BR112018007947A patent/BR112018007947A2/pt not_active Application Discontinuation
- 2017-11-02 ES ES17809396T patent/ES2729961T3/es active Active
- 2017-11-02 CA CA3000237A patent/CA3000237C/en active Active
- 2017-11-02 JP JP2018516877A patent/JP6516341B2/ja active Active
- 2017-11-02 WO PCT/JP2017/039680 patent/WO2018084230A1/en active Application Filing
- 2017-11-02 RU RU2020109376A patent/RU2762193C2/ru active
- 2017-11-02 EP EP17809396.9A patent/EP3344296B1/en active Active
-
2018
- 2018-08-20 HK HK18110632.3A patent/HK1251162B/zh unknown
- 2018-10-02 HK HK18112566.9A patent/HK1253277A1/zh unknown
-
2019
- 2019-05-21 US US16/417,870 patent/US10583129B2/en active Active
Also Published As
Publication number | Publication date |
---|---|
CA3000237C (en) | 2019-02-26 |
EP3344296B1 (en) | 2019-05-15 |
CN108289960A (zh) | 2018-07-17 |
HK1253277A1 (zh) | 2019-06-14 |
RU2762193C2 (ru) | 2021-12-16 |
RU2717331C2 (ru) | 2020-03-23 |
US20190269663A1 (en) | 2019-09-05 |
CA3000237A1 (en) | 2018-05-04 |
CN108289960B (zh) | 2021-07-09 |
US10583129B2 (en) | 2020-03-10 |
RU2020109376A3 (pt) | 2020-10-27 |
US10342785B2 (en) | 2019-07-09 |
WO2018084230A1 (en) | 2018-05-11 |
RU2018117891A (ru) | 2019-11-18 |
JP2018535939A (ja) | 2018-12-06 |
ES2729961T3 (es) | 2019-11-07 |
KR20180064438A (ko) | 2018-06-14 |
JP6516341B2 (ja) | 2019-05-22 |
US20180125832A1 (en) | 2018-05-10 |
EP3344296A1 (en) | 2018-07-11 |
HK1251162B (zh) | 2020-01-17 |
RU2018117891A3 (pt) | 2019-11-18 |
MX2018005715A (es) | 2018-08-09 |
RU2020109376A (ru) | 2020-04-29 |
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B06F | Objections, documents and/or translations needed after an examination request according [chapter 6.6 patent gazette] | ||
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Free format text: ANULADA A PUBLICACAO CODIGO 6.6.1 NA RPI NO 2631 DE 08/06/2021 POR TER SIDO INDEVIDA. |
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