JP6231988B2 - Nedd8活性化酵素阻害剤および低メチル化剤の投与 - Google Patents

Nedd8活性化酵素阻害剤および低メチル化剤の投与 Download PDF

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JP6231988B2
JP6231988B2 JP2014540146A JP2014540146A JP6231988B2 JP 6231988 B2 JP6231988 B2 JP 6231988B2 JP 2014540146 A JP2014540146 A JP 2014540146A JP 2014540146 A JP2014540146 A JP 2014540146A JP 6231988 B2 JP6231988 B2 JP 6231988B2
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pharmaceutically acceptable
acceptable salt
cancer
administered
hydroxycyclopentyl
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JP2015505816A (ja
JP2015505816A5 (OSRAM
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ピーター ジー. スミス,
ピーター ジー. スミス,
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Millennium Pharmaceuticals Inc
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/70Carbohydrates; Sugars; Derivatives thereof
    • A61K31/7042Compounds having saccharide radicals and heterocyclic rings
    • A61K31/7052Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
    • A61K31/706Compounds 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical & Material Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Molecular Biology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Hematology (AREA)
  • Oncology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
JP2014540146A 2011-11-03 2012-11-02 Nedd8活性化酵素阻害剤および低メチル化剤の投与 Active JP6231988B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201161555049P 2011-11-03 2011-11-03
US61/555,049 2011-11-03
PCT/US2012/063382 WO2013067396A2 (en) 2011-11-03 2012-11-02 Administration of nedd8-activating enzyme inhibitor and hypomethylating agent

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2017203560A Division JP2018009035A (ja) 2011-11-03 2017-10-20 Nedd8活性化酵素阻害剤および低メチル化剤の投与

Publications (3)

Publication Number Publication Date
JP2015505816A JP2015505816A (ja) 2015-02-26
JP2015505816A5 JP2015505816A5 (OSRAM) 2017-10-26
JP6231988B2 true JP6231988B2 (ja) 2017-11-15

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Family Applications (2)

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JP2014540146A Active JP6231988B2 (ja) 2011-11-03 2012-11-02 Nedd8活性化酵素阻害剤および低メチル化剤の投与
JP2017203560A Pending JP2018009035A (ja) 2011-11-03 2017-10-20 Nedd8活性化酵素阻害剤および低メチル化剤の投与

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JP2017203560A Pending JP2018009035A (ja) 2011-11-03 2017-10-20 Nedd8活性化酵素阻害剤および低メチル化剤の投与

Country Status (23)

Country Link
US (2) US8980850B2 (OSRAM)
EP (1) EP2773360B1 (OSRAM)
JP (2) JP6231988B2 (OSRAM)
KR (1) KR101987861B1 (OSRAM)
CN (1) CN104245699B (OSRAM)
AU (1) AU2012321106C1 (OSRAM)
BR (1) BR112014010699B1 (OSRAM)
CA (1) CA2854461C (OSRAM)
EA (1) EA028380B1 (OSRAM)
ES (1) ES2668272T3 (OSRAM)
GE (1) GEP20196940B (OSRAM)
HK (1) HK1201733A1 (OSRAM)
IL (1) IL232353B (OSRAM)
MA (1) MA35662B1 (OSRAM)
MX (1) MX357835B (OSRAM)
MY (1) MY176125A (OSRAM)
PH (1) PH12014501001B1 (OSRAM)
PL (1) PL2773360T3 (OSRAM)
SG (1) SG11201401895WA (OSRAM)
TN (1) TN2014000194A1 (OSRAM)
TR (1) TR201807342T4 (OSRAM)
UA (1) UA114414C2 (OSRAM)
WO (1) WO2013067396A2 (OSRAM)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BRPI1012142A2 (pt) 2009-05-14 2016-03-29 Millennium Pharm Inc sal cloridrato de ((1s,2s,4r)-4-{4-[(1s)-2,3-diidro-1h-inden-1-ilamino]-7h-pirrolo[2,3-d]pirimidin-7-il}-2-hidroxiciclopentil) metil sulfamato
PH12014500419A1 (en) * 2011-08-24 2020-06-22 Millennium Pharm Inc Inhibitors of nedd8-activating enzyme
EP2764866A1 (en) * 2013-02-07 2014-08-13 IP Gesellschaft für Management mbH Inhibitors of nedd8-activating enzyme
CA2923752A1 (en) 2013-05-14 2014-11-20 Millennium Pharmaceuticals, Inc. Administration of nedd8-activating enzyme inhibitor and chemotherapeutic agents
JP2016525531A (ja) * 2013-07-26 2016-08-25 ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング 急性骨髄性白血病及び骨髄異形成症候群の処置のためのアザシチジンと組み合わせたボラセルチブ
CA2946538A1 (en) 2014-04-04 2015-10-08 Del Mar Pharmaceuticals Use of dianhydrogalactitol and analogs or derivatives thereof to treat non-small-cell carcinoma of the lung and ovarian cancer
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
CA3002029A1 (en) * 2015-10-15 2017-04-20 Celgene Corporation Combination therapy for treating malignancies
WO2018218119A1 (en) * 2017-05-25 2018-11-29 The Board Of Trustees Of The Leland Stanford Junior University Combination of low dose il-2 and an inhibitor of treg il-2r desensitization to treat autoimmune and allergic inflammatory diseases
EP3684363A4 (en) * 2017-09-21 2021-05-12 Millennium Pharmaceuticals, Inc. CO-CRYSTALLINE FORMS OF ((1S, 2S, 4R) -4- {4 - [(1S) -2,3-DIHYDRO-1H-INDÉN-1-YLAMINO] -7H-PYRROLO [2,3-D] PYRIMIDIN -7-YL} -2-HYDROXYCYCLOPENTYL) METHYLSULFAMATE, THEIR FORMULATIONS AND USES
CA3119781A1 (en) * 2018-11-20 2020-05-28 Fulcrum Therapeutics, Inc. Compositions and methods for increasing fetal hemoglobin and treating sickle cell disease
KR20210151833A (ko) 2019-03-15 2021-12-14 풀크럼 쎄러퓨틱스, 인코포레이티드 Eed 및 prc2 조절제로서 마크로사이클릭 아졸로피리딘 유도체
WO2023025668A1 (en) 2021-08-25 2023-03-02 Asociación Centro De Investigación Cooperativa En Biociencias-Cic Biogune Methods for the generation of stem cell memory t cells for adoptive t cell therapy
WO2023242235A1 (en) * 2022-06-14 2023-12-21 Scandion Oncology A/S Abcg2 inhibitor and nae inhibitor for the treatment of 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
EP4554608A1 (en) * 2022-07-11 2025-05-21 Westlake University Use of a fbxo42 specific inhibitor in treating notch signaling-dependent disease

Family Cites Families (16)

* Cited by examiner, † Cited by third party
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
SI1848718T1 (sl) 2005-02-04 2012-12-31 Millennium Pharmaceuticals, Inc. Inhibitorji E1 aktivacijskih enzimov
JP5231251B2 (ja) 2006-02-02 2013-07-10 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
CA2659894C (en) * 2006-08-08 2018-03-27 Millennium Pharmaceuticals, Inc. Heteroaryl compounds useful as inhibitors of e1 activating enzymes
WO2008028193A2 (en) 2006-09-01 2008-03-06 Pharmion Corporation Colon-targeted oral formulations of cytidine analogs
CA2742252A1 (en) 2007-11-01 2009-05-07 Celgene Corporation Cytidine analogs for treatment of myelodysplastic syndromes
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
AU2009246926B2 (en) 2008-05-15 2014-06-26 Celgene Corporation Oral formulations of cytidine analogs and methods of use thereof
EP2307002B1 (en) * 2008-06-09 2013-01-02 Cyclacel Limited Combinations of sapacitabine or cndac with dna methyltransferase inhibitors such as decitabine and procaine
ES2681529T3 (es) * 2009-03-23 2018-09-13 Ambit Biosciences Corporation Métodos de tratamiento utilizando terapia de combinación
BRPI1012142A2 (pt) 2009-05-14 2016-03-29 Millennium Pharm Inc sal cloridrato de ((1s,2s,4r)-4-{4-[(1s)-2,3-diidro-1h-inden-1-ilamino]-7h-pirrolo[2,3-d]pirimidin-7-il}-2-hidroxiciclopentil) metil sulfamato
CN103338753A (zh) 2011-01-31 2013-10-02 细胞基因公司 胞苷类似物的药物组合物及其使用方法
HK1200716A1 (zh) 2011-11-01 2015-08-14 细胞基因公司 使用胞苷類似物的口服製劑治療癌症的方法

Also Published As

Publication number Publication date
US8980850B2 (en) 2015-03-17
JP2015505816A (ja) 2015-02-26
TN2014000194A1 (en) 2015-09-30
TR201807342T4 (tr) 2018-06-21
EP2773360A2 (en) 2014-09-10
CA2854461C (en) 2021-01-19
AU2012321106A1 (en) 2013-05-23
EA028380B1 (ru) 2017-11-30
WO2013067396A3 (en) 2014-10-16
PH12014501001B1 (en) 2018-05-04
JP2018009035A (ja) 2018-01-18
NZ624881A (en) 2016-10-28
AU2012321106B2 (en) 2016-08-04
US20130116208A1 (en) 2013-05-09
MY176125A (en) 2020-07-24
IL232353A0 (en) 2014-06-30
MX357835B (es) 2018-07-26
US20150366886A1 (en) 2015-12-24
MA35662B1 (fr) 2014-11-01
KR20140097229A (ko) 2014-08-06
BR112014010699B1 (pt) 2020-12-15
SG11201401895WA (en) 2014-05-29
MX2014005323A (es) 2014-06-05
UA114414C2 (uk) 2017-06-12
EA201400539A1 (ru) 2014-12-30
CN104245699A (zh) 2014-12-24
GEP20196940B (en) 2019-01-10
CN104245699B (zh) 2017-06-27
WO2013067396A2 (en) 2013-05-10
IL232353B (en) 2018-11-29
CA2854461A1 (en) 2013-05-10
PH12014501001A1 (en) 2014-06-09
EP2773360B1 (en) 2018-02-28
HK1201733A1 (en) 2015-09-11
PL2773360T3 (pl) 2018-09-28
KR101987861B1 (ko) 2019-06-11
AU2012321106C1 (en) 2016-11-24
ES2668272T3 (es) 2018-05-17
BR112014010699A2 (pt) 2017-04-25
EP2773360A4 (en) 2015-09-23

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