MA35662B1 - Administration d'un inhibiteur d'enzyme activant nedd8 et agent d'hypométhylation - Google Patents
Administration d'un inhibiteur d'enzyme activant nedd8 et agent d'hypométhylationInfo
- Publication number
- MA35662B1 MA35662B1 MA37066A MA37066A MA35662B1 MA 35662 B1 MA35662 B1 MA 35662B1 MA 37066 A MA37066 A MA 37066A MA 37066 A MA37066 A MA 37066A MA 35662 B1 MA35662 B1 MA 35662B1
- Authority
- MA
- Morocco
- Prior art keywords
- administration
- enzyme inhibitor
- activating enzyme
- treatment
- hypomethylation agent
- Prior art date
Links
- 239000003795 chemical substances by application Substances 0.000 title abstract 2
- 229940123621 Nedd 8 activating enzyme inhibitor Drugs 0.000 title 1
- 206010028980 Neoplasm Diseases 0.000 abstract 2
- 201000011510 cancer Diseases 0.000 abstract 2
- 238000000034 method Methods 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- XAUDJQYHKZQPEU-KVQBGUIXSA-N 5-aza-2'-deoxycytidine Chemical compound O=C1N=C(N)N=CN1[C@@H]1O[C@H](CO)[C@@H](O)C1 XAUDJQYHKZQPEU-KVQBGUIXSA-N 0.000 abstract 1
- NMUSYJAQQFHJEW-KVTDHHQDSA-N 5-azacytidine Chemical compound O=C1N=C(N)N=CN1[C@H]1[C@H](O)[C@H](O)[C@@H](CO)O1 NMUSYJAQQFHJEW-KVTDHHQDSA-N 0.000 abstract 1
- 229960002756 azacitidine Drugs 0.000 abstract 1
- 229960003603 decitabine Drugs 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 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
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/7042—Compounds having saccharide radicals and heterocyclic rings
- A61K31/7052—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
- A61K31/706—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom
-
- 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
- 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
-
- 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
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Molecular Biology (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
La présente invention concerne des procédés pour le traitement du cancer dans des patients en besoin reconnu d'un tel traitement. Les procédés comprennent l'administration à un tel patient d'un inhibiteur de nae ou d'un sel pharmaceutiquement acceptable de celui-ci, tel que le sulfamate de ((1s,2s,4r)-4-(4-((1s)-2,3-dihydro-1h-indén-1-ylamino)-7h-pyrrolo[2,3 d]pyrimidin 7-yl)-2-hydroxycyclopentyl)méthyle (mln4924) ou le sulfamate de {(1s,2s,4r)-4-[(6-{[(1r,2s)-5-chloro-2 méthoxy-2,3-dihydro-1h-indén-1-yl]amino}pyrimidin-4-yl)oxy]-2-hydroxycyclopentyl}-méthyle (i-216), et un agent d'hypométhylation ou un sel pharmaceutiquement acceptable de celui-ci, tel que l'azacitidine ou la décitabine. L'invention porte également sur des médicaments destinés à être utilisés dans le traitement du cancer.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201161555049P | 2011-11-03 | 2011-11-03 | |
| PCT/US2012/063382 WO2013067396A2 (fr) | 2011-11-03 | 2012-11-02 | Administration d'un inhibiteur d'enzyme activant nedd8 et agent d'hypométhylation |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA35662B1 true MA35662B1 (fr) | 2014-11-01 |
Family
ID=48193039
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA37066A MA35662B1 (fr) | 2011-11-03 | 2014-05-26 | Administration d'un inhibiteur d'enzyme activant nedd8 et agent d'hypométhylation |
Country Status (23)
| Country | Link |
|---|---|
| US (2) | US8980850B2 (fr) |
| EP (1) | EP2773360B1 (fr) |
| JP (2) | JP6231988B2 (fr) |
| KR (1) | KR101987861B1 (fr) |
| CN (1) | CN104245699B (fr) |
| AU (1) | AU2012321106C1 (fr) |
| BR (1) | BR112014010699B1 (fr) |
| CA (1) | CA2854461C (fr) |
| EA (1) | EA028380B1 (fr) |
| ES (1) | ES2668272T3 (fr) |
| GE (2) | GEP20186940B (fr) |
| HK (1) | HK1201733A1 (fr) |
| IL (1) | IL232353B (fr) |
| MA (1) | MA35662B1 (fr) |
| MX (1) | MX357835B (fr) |
| MY (1) | MY176125A (fr) |
| PH (1) | PH12014501001B1 (fr) |
| PL (1) | PL2773360T3 (fr) |
| SG (1) | SG11201401895WA (fr) |
| TN (1) | TN2014000194A1 (fr) |
| TR (1) | TR201807342T4 (fr) |
| UA (1) | UA114414C2 (fr) |
| WO (1) | WO2013067396A2 (fr) |
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| UA108986C2 (uk) | 2009-05-14 | 2015-07-10 | Мілленніум Фармасьютікалз, Інк. | Кристалічна форма гідрохлориду ((1s,2s,4r)-4-{4-[(1s)-2,3-дигідро-1h-інден-1-іламіно]-7h-піроло[2,3-d]піримідин-7іл}-2-гідроксициклопентил)метилсульфамату (варіанти) |
| SG11201400102WA (en) * | 2011-08-24 | 2014-03-28 | Millennium Pharm Inc | Inhibitors of nedd8-activating enzyme |
| EP2764866A1 (fr) * | 2013-02-07 | 2014-08-13 | IP Gesellschaft für Management mbH | Inhibiteurs de l'enzyme activant nedd8 |
| CA2923752A1 (fr) | 2013-05-14 | 2014-11-20 | Millennium Pharmaceuticals, Inc. | Administration d'inhibiteur d'enzyme d'activation de la nedd8 et d'agents chimiotherapeutiques |
| CA2919296A1 (fr) * | 2013-07-26 | 2015-01-29 | Boehringer Ingelheim International Gmbh | Volasertib en combinaison avec de l'azacitidine pour le traitement de la leucemie aigue myeloide et du syndrome myelodysplasique ii |
| JP6783224B2 (ja) | 2014-04-04 | 2020-11-11 | デル マー ファーマシューティカルズ | 肺の非小細胞癌腫及び卵巣癌を処置するためのジアンヒドロガラクチトール及びその類縁体又は誘導体の使用 |
| CN103948590A (zh) * | 2014-05-22 | 2014-07-30 | 中国药科大学 | Nedd8激活酶抑制剂及其医药用途 |
| MX381582B (es) * | 2015-10-15 | 2025-03-12 | Celgene Corp | Terapia de combinacion para el tratamiento de neoplasias malignas. |
| WO2018218119A1 (fr) * | 2017-05-25 | 2018-11-29 | The Board Of Trustees Of The Leland Stanford Junior University | Combinaison d'une faible dose d'il-2 et d'un inhibiteur de la désensibilisation treg il-2 r pour traiter des maladies inflammatoires auto-immunes et allergiques |
| US11124519B2 (en) * | 2017-09-21 | 2021-09-21 | Millennium Pharmaceuticals, Inc. | Cocrystal forms of ((1S,2S,4R)-4-{4-[(1S)-2,3-dihydro-1H-inden-1-ylamino]-7H-pyrrolo [2,3-d]pyrimidin-7-yl}-2-hydroxycyclopentyl) methyl sulfamate, formulations and uses thereof |
| US20220017908A1 (en) * | 2018-11-20 | 2022-01-20 | Fulcrum Therapeutics, Inc. | Compositions and methods for increasing fetal hemoglobin and treating sickle cell disease |
| CA3133751A1 (fr) | 2019-03-15 | 2020-09-24 | Fulcrum Therapeutics, Inc. | Derives d'azolopyridine macrocycliques utilises en tant que modulateurs eed et prc2 |
| WO2023025668A1 (fr) | 2021-08-25 | 2023-03-02 | Asociación Centro De Investigación Cooperativa En Biociencias-Cic Biogune | Méthodes pour la génération de lymphocytes t à mémoire de cellules souches pour une thérapie adoptive par lymphocytes t |
| WO2023242235A1 (fr) * | 2022-06-14 | 2023-12-21 | Scandion Oncology A/S | Inhibiteur d'abcg2 et inhibiteur de nae pour le traitement du cancer |
| CN115007323B (zh) * | 2022-06-17 | 2024-01-23 | 中南大学 | 一种抑制矿物中黄铁矿浮选的方法 |
| WO2024012414A1 (fr) * | 2022-07-11 | 2024-01-18 | Westlake University | Utilisation d'un inhibiteur spécifique de fbxo42 dans le traitement d'une maladie dépendante de la signalisation notch |
Family Cites Families (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6943249B2 (en) | 2003-03-17 | 2005-09-13 | Ash Stevens, Inc. | Methods for isolating crystalline Form I of 5-azacytidine |
| US6887855B2 (en) | 2003-03-17 | 2005-05-03 | Pharmion Corporation | Forms of 5-azacytidine |
| US20060063735A1 (en) | 2004-09-17 | 2006-03-23 | Supergen, Inc. | Salts of 5-azacytidine |
| US20060128654A1 (en) | 2004-12-10 | 2006-06-15 | Chunlin Tang | Pharmaceutical formulation of cytidine analogs and derivatives |
| JP5048520B2 (ja) | 2005-02-04 | 2012-10-17 | ミレニアム ファーマシューティカルズ， インコーポレイテッド | Ｅ１活性化酵素の阻害剤 |
| SG169369A1 (en) | 2006-02-02 | 2011-03-30 | Millennium Pharm Inc | Inhibitors of e1 activating enzymes |
| ATE485276T1 (de) * | 2006-08-08 | 2010-11-15 | Millennium Pharm Inc | Heteroarylverbindungen als hemmer der e1- aktivierenden enzyme |
| US20080057086A1 (en) | 2006-09-01 | 2008-03-06 | Pharmion Corporation | Colon-targeted oral formulations of cytidine analogs |
| CA2742252A1 (fr) | 2007-11-01 | 2009-05-07 | Celgene Corporation | Analogues de la cytidine destines au traitement de syndromes myelodysplasiques |
| JP2011513274A (ja) * | 2008-02-26 | 2011-04-28 | ネルビアーノ・メデイカル・サイエンシーズ・エツセ・エルレ・エルレ | モルホリニルアントラサイクリン誘導体および脱メチル化剤を含む、抗腫瘍性組合せ |
| HUE055911T2 (hu) | 2008-05-15 | 2021-12-28 | Celgene Corp | Citidin-analógokat tartalmazó orális készítmények, és eljárások azok alkalmazására |
| KR101667641B1 (ko) * | 2008-06-09 | 2016-10-20 | 싸이클라셀 리미티드 | 데시타빈 및 프로카인과 같은 ｄｎａ 메틸전이효소 저해제와 사팍시타빈 또는 ｃｎｄａｃ의 조합 |
| AU2010228982B2 (en) * | 2009-03-23 | 2015-05-14 | Ambit Biosciences Corporation | Methods of treatment using combination therapy |
| UA108986C2 (uk) | 2009-05-14 | 2015-07-10 | Мілленніум Фармасьютікалз, Інк. | Кристалічна форма гідрохлориду ((1s,2s,4r)-4-{4-[(1s)-2,3-дигідро-1h-інден-1-іламіно]-7h-піроло[2,3-d]піримідин-7іл}-2-гідроксициклопентил)метилсульфамату (варіанти) |
| JP2014503597A (ja) | 2011-01-31 | 2014-02-13 | セルジーン コーポレイション | シチジンアナログの医薬組成物及びその使用方法 |
| TW201700103A (zh) | 2011-11-01 | 2017-01-01 | 西建公司 | 利用胞嘧啶核苷類似物之口服配方治療癌症的方法 |
-
2012
- 2012-11-02 US US13/667,641 patent/US8980850B2/en active Active
- 2012-11-02 CA CA2854461A patent/CA2854461C/fr not_active Expired - Fee Related
- 2012-11-02 TR TR2018/07342T patent/TR201807342T4/tr unknown
- 2012-11-02 EP EP12844799.2A patent/EP2773360B1/fr active Active
- 2012-11-02 MX MX2014005323A patent/MX357835B/es active IP Right Grant
- 2012-11-02 GE GEAP201813483A patent/GEP20186940B/en unknown
- 2012-11-02 ES ES12844799.2T patent/ES2668272T3/es active Active
- 2012-11-02 CN CN201280062112.9A patent/CN104245699B/zh active Active
- 2012-11-02 EA EA201400539A patent/EA028380B1/ru not_active IP Right Cessation
- 2012-11-02 MY MYPI2014001239A patent/MY176125A/en unknown
- 2012-11-02 WO PCT/US2012/063382 patent/WO2013067396A2/fr not_active Ceased
- 2012-11-02 KR KR1020147014236A patent/KR101987861B1/ko not_active Expired - Fee Related
- 2012-11-02 JP JP2014540146A patent/JP6231988B2/ja active Active
- 2012-11-02 BR BR112014010699-1A patent/BR112014010699B1/pt not_active IP Right Cessation
- 2012-11-02 UA UAA201405842A patent/UA114414C2/uk unknown
- 2012-11-02 AU AU2012321106A patent/AU2012321106C1/en not_active Ceased
- 2012-11-02 HK HK15102294.2A patent/HK1201733A1/xx unknown
- 2012-11-02 PL PL12844799T patent/PL2773360T3/pl unknown
- 2012-11-02 GE GEAP201213483A patent/GEP20196940B/en unknown
- 2012-11-02 SG SG11201401895WA patent/SG11201401895WA/en unknown
- 2012-11-02 PH PH1/2014/501001A patent/PH12014501001B1/en unknown
-
2014
- 2014-04-29 IL IL232353A patent/IL232353B/en active IP Right Grant
- 2014-04-30 TN TNP2014000194A patent/TN2014000194A1/en unknown
- 2014-05-26 MA MA37066A patent/MA35662B1/fr unknown
-
2015
- 2015-01-23 US US14/603,717 patent/US20150366886A1/en not_active Abandoned
-
2017
- 2017-10-20 JP JP2017203560A patent/JP2018009035A/ja active Pending
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