JP2017516781A5 - - Google Patents

Download PDF

Info

Publication number
JP2017516781A5
JP2017516781A5 JP2016569405A JP2016569405A JP2017516781A5 JP 2017516781 A5 JP2017516781 A5 JP 2017516781A5 JP 2016569405 A JP2016569405 A JP 2016569405A JP 2016569405 A JP2016569405 A JP 2016569405A JP 2017516781 A5 JP2017516781 A5 JP 2017516781A5
Authority
JP
Japan
Prior art keywords
formula
compound
treatment
acceptable salt
medicament
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
JP2016569405A
Other languages
English (en)
Japanese (ja)
Other versions
JP2017516781A (ja
JP6553092B2 (ja
Filing date
Publication date
Priority claimed from GBGB1409471.8A external-priority patent/GB201409471D0/en
Application filed filed Critical
Publication of JP2017516781A publication Critical patent/JP2017516781A/ja
Publication of JP2017516781A5 publication Critical patent/JP2017516781A5/ja
Application granted granted Critical
Publication of JP6553092B2 publication Critical patent/JP6553092B2/ja
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2016569405A 2014-05-28 2015-03-26 脳がんを治療するための化合物 Active JP6553092B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GBGB1409471.8A GB201409471D0 (en) 2014-05-28 2014-05-28 Pharmaceutical composition
GB1409471.8 2014-05-28
PCT/EP2015/056667 WO2015180865A1 (en) 2014-05-28 2015-03-26 Compounds for treating brain cancer

Publications (3)

Publication Number Publication Date
JP2017516781A JP2017516781A (ja) 2017-06-22
JP2017516781A5 true JP2017516781A5 (cg-RX-API-DMAC7.html) 2018-05-10
JP6553092B2 JP6553092B2 (ja) 2019-07-31

Family

ID=51177574

Family Applications (3)

Application Number Title Priority Date Filing Date
JP2016569405A Active JP6553092B2 (ja) 2014-05-28 2015-03-26 脳がんを治療するための化合物
JP2016569589A Pending JP2017518291A (ja) 2014-05-28 2015-05-26 癌を処置するための医薬組合せ
JP2020215170A Active JP7274450B2 (ja) 2014-05-28 2020-12-24 癌を処置するための医薬組合せ

Family Applications After (2)

Application Number Title Priority Date Filing Date
JP2016569589A Pending JP2017518291A (ja) 2014-05-28 2015-05-26 癌を処置するための医薬組合せ
JP2020215170A Active JP7274450B2 (ja) 2014-05-28 2020-12-24 癌を処置するための医薬組合せ

Country Status (22)

Country Link
US (8) US11419853B2 (cg-RX-API-DMAC7.html)
EP (4) EP3998068A1 (cg-RX-API-DMAC7.html)
JP (3) JP6553092B2 (cg-RX-API-DMAC7.html)
KR (2) KR102383794B1 (cg-RX-API-DMAC7.html)
CN (3) CN106659712A (cg-RX-API-DMAC7.html)
AU (2) AU2015266342B2 (cg-RX-API-DMAC7.html)
BR (2) BR112016027048B1 (cg-RX-API-DMAC7.html)
CA (2) CA2950374C (cg-RX-API-DMAC7.html)
DK (1) DK3148529T3 (cg-RX-API-DMAC7.html)
EA (2) EA037057B1 (cg-RX-API-DMAC7.html)
ES (2) ES2897727T3 (cg-RX-API-DMAC7.html)
GB (1) GB201409471D0 (cg-RX-API-DMAC7.html)
IL (2) IL249231B (cg-RX-API-DMAC7.html)
MX (2) MX376193B (cg-RX-API-DMAC7.html)
NZ (1) NZ725595A (cg-RX-API-DMAC7.html)
PH (2) PH12016502354A1 (cg-RX-API-DMAC7.html)
PT (1) PT3148529T (cg-RX-API-DMAC7.html)
SG (4) SG10201810397SA (cg-RX-API-DMAC7.html)
TW (1) TWI724990B (cg-RX-API-DMAC7.html)
UA (2) UA121311C2 (cg-RX-API-DMAC7.html)
WO (2) WO2015180865A1 (cg-RX-API-DMAC7.html)
ZA (2) ZA201607384B (cg-RX-API-DMAC7.html)

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TWI573792B (zh) 2012-02-01 2017-03-11 歐陸斯迪公司 新穎治療劑
GB201409488D0 (en) 2014-05-28 2014-07-09 Euro Celtique Sa Pharmaceutical composition
GB201409471D0 (en) 2014-05-28 2014-07-09 Euro Celtique Sa Pharmaceutical composition
GB201409485D0 (en) 2014-05-28 2014-07-09 Euro Celtique Sa Pharmaceutical composition
GB201601773D0 (en) 2016-02-01 2016-03-16 Renishaw Plc Method
TWI808055B (zh) 2016-05-11 2023-07-11 美商滬亞生物國際有限公司 Hdac 抑制劑與 pd-1 抑制劑之組合治療
TWI794171B (zh) 2016-05-11 2023-03-01 美商滬亞生物國際有限公司 Hdac抑制劑與pd-l1抑制劑之組合治療
US11266631B2 (en) 2016-10-11 2022-03-08 Purdue Pharmaceutical Products L.P. Hodgkin lymphoma therapy
TWI651088B (zh) 2017-03-23 2019-02-21 國立東華大學 用於治療癌症的Scalarane二倍半萜類、醫藥組合物及拓樸異構酶II與 Hsp90抑制劑及其用途與製備方法
GB201709402D0 (en) 2017-06-13 2017-07-26 Euro Celtique Sa Compounds for treating t-pll
GB201709405D0 (en) * 2017-06-13 2017-07-26 Euro Celtique Sa Compounds for treating ovarian cancer
GB201709406D0 (en) 2017-06-13 2017-07-26 Euro-Cletique S A Compounds for treating TNBC
GB201709403D0 (en) 2017-06-13 2017-07-26 Euro Celtique Sa Compounds for treating sarcoma
WO2019053611A1 (en) * 2017-09-14 2019-03-21 Glaxosmithkline Intellectual Property Development Limited POLY THERAPY FOR THE TREATMENT OF CANCER
KR20210105380A (ko) * 2018-12-18 2021-08-26 먼디파머 인터내셔널 코포레이션 리미티드 다발성 골수종을 치료하기 위한 화합물
CN112023022A (zh) * 2020-10-20 2020-12-04 澳门大学 卡非佐米在制备治疗抗药肿瘤的药物中的新的应用
JP7600020B2 (ja) 2021-03-31 2024-12-16 株式会社小糸製作所 画像投影装置

Family Cites Families (71)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE34727C (de) Ch. H. TH. HAVEMANN in Paris, 16 rue Bleue Verfahren zur direkten Gewinnung metallischen Bleis
DD34727A1 (de) 1963-12-21 1964-12-28 Dietrich Krebs Verfahren zur Herstellung von 1-Stellung substituierten [5-Bis-(chloräthyl)-amino-benzimidazolyl-(2)]-alkancarbonsäuren
US4522811A (en) 1982-07-08 1985-06-11 Syntex (U.S.A.) Inc. Serial injection of muramyldipeptides and liposomes enhances the anti-infective activity of muramyldipeptides
US6407079B1 (en) 1985-07-03 2002-06-18 Janssen Pharmaceutica N.V. Pharmaceutical compositions containing drugs which are instable or sparingly soluble in water and methods for their preparation
GB8926612D0 (en) 1989-11-24 1990-01-17 Erba Farmitalia Pharmaceutical compositions
US5376645A (en) 1990-01-23 1994-12-27 University Of Kansas Derivatives of cyclodextrins exhibiting enhanced aqueous solubility and the use thereof
KR0166088B1 (ko) 1990-01-23 1999-01-15 . 수용해도가 증가된 시클로덱스트린 유도체 및 이의 용도
US5369108A (en) 1991-10-04 1994-11-29 Sloan-Kettering Institute For Cancer Research Potent inducers of terminal differentiation and methods of use thereof
GB9126209D0 (en) 1991-12-10 1992-02-12 Orion Yhtymae Oy Drug formulations for parenteral use
US5602112A (en) 1992-06-19 1997-02-11 Supergen, Inc. Pharmaceutical formulation
US5882941A (en) 1994-05-04 1999-03-16 Massachusette Institute Of Technology Programmable genotoxic agents and uses therefor
US5874418A (en) 1997-05-05 1999-02-23 Cydex, Inc. Sulfoalkyl ether cyclodextrin based solid pharmaceutical formulations and their use
US6046177A (en) 1997-05-05 2000-04-04 Cydex, Inc. Sulfoalkyl ether cyclodextrin based controlled release solid pharmaceutical formulations
ATE253941T1 (de) 1997-06-13 2003-11-15 Cydex Inc Zusammensetzung mit erhöhter lagerstabilität enthaltend cyclodextrin und wirkstoffe oder wirkstoff-vorstufen, die in wasserunlösliche komponenten zersetzt werden
US6040321A (en) * 1997-11-12 2000-03-21 Bristol-Myers Squibb Company Aminothiazole inhibitors of cyclin dependent kinases
US6214852B1 (en) 1998-10-21 2001-04-10 Bristol-Myers Squibb Company N-[5-[[[5-alkyl-2-oxazolyl]methyl]thio]-2-thiazolyl]-carboxamide inhibitors of cyclin dependent kinases
US6392053B2 (en) 1999-12-15 2002-05-21 Bristol-Myers Squibb Company Process for preparing arylacetylaminothiazoles
AU2001273413A1 (en) 2000-07-12 2002-01-21 Immunex Corporation Method for treating cancer using an interleukin- 4 antagonist
PE20020354A1 (es) 2000-09-01 2002-06-12 Novartis Ag Compuestos de hidroxamato como inhibidores de histona-desacetilasa (hda)
DE60115279T2 (de) 2000-09-29 2006-12-28 Topotarget Uk Ltd., Abingdon Carbaminsäurederivate enthaltend eine amidgruppe als hdac-inhibitoren
WO2002055017A2 (en) 2000-11-21 2002-07-18 Wake Forest University Method of treating autoimmune diseases
CN1764648A (zh) 2003-01-13 2006-04-26 安斯泰来制药有限公司 作为组蛋白脱乙酰酶(hdac)抑制剂的异羟肟酸衍生物
US7652036B2 (en) 2003-02-25 2010-01-26 Topotarget Uk Limited Carbamic acid compounds comprising a bicyclic heteroaryl group as HDAC inhibitors
JP2007501775A (ja) 2003-08-07 2007-02-01 ノバルティス アクチエンゲゼルシャフト 免疫抑制剤としてのヒストンデアセチラーゼ阻害剤
US7223745B2 (en) 2003-08-14 2007-05-29 Cephalon, Inc. Proteasome inhibitors and methods of using the same
CA2561617A1 (en) 2004-04-05 2005-10-20 Aton Pharma, Inc. Histone deacetylase inhibitor prodrugs
WO2007134169A2 (en) 2006-05-10 2007-11-22 Nuada, Llc Indole, benzimidazole, and benzolactam boronic acid compounds, analogs thereof and methods of use thereof
US8436190B2 (en) 2005-01-14 2013-05-07 Cephalon, Inc. Bendamustine pharmaceutical compositions
ZA200710313B (en) 2005-05-13 2009-05-27 Topotarget Uk Ltd Pharmaceutical formulations of HDAC inhibitors
US7399956B2 (en) 2005-11-28 2008-07-15 Avago Technologies Ecbuip Pte Ltd Optical encoder with sinusoidal photodetector output signal
CA2673483C (en) 2006-10-20 2014-04-08 Icos Corporation Compositions of chk1 inhibitors
GB0621160D0 (en) 2006-10-24 2006-12-06 Imp College Innovations Ltd Compounds and uses thereof
AR063869A1 (es) 2006-11-20 2009-02-25 Cephalon Inc Metodo de radiosensibilizacion de tumores usando un agente radiosensibilizante
EP2099489B1 (en) * 2006-12-11 2014-05-21 Genentech, Inc. Compositions and methods for treating a neoplasm
CN101084876A (zh) 2007-07-11 2007-12-12 济南康泉医药科技有限公司 一种含苯达莫司汀的抗癌组合物
TW200922564A (en) 2007-09-10 2009-06-01 Curis Inc CDK inhibitors containing a zinc binding moiety
WO2009067453A1 (en) 2007-11-19 2009-05-28 Syndax Pharmaceuticals, Inc. Combinations of hdac inhibitors and proteasome inhibitors
WO2009100045A1 (en) 2008-02-04 2009-08-13 Translational Genomics Research Institute Compounds, pharmaceutical compositions and methods of use of hydroxamic acid derivatives
JP5670335B2 (ja) 2008-09-25 2015-02-18 セファロン、インク. ベンダムスチン液体製剤
MX2011003751A (es) 2008-10-08 2011-04-27 Cephalon Inc Procesos para preparar bendamustina.
WO2010075542A1 (en) 2008-12-23 2010-07-01 Curis, Inc. Cdk inhibitors
HUE025349T2 (en) 2009-01-23 2016-02-29 Euro Celtique Sa Hydroxamic acid derivatives
HUE038234T2 (hu) 2009-02-25 2018-10-29 Softkemo Pharma Corp Bendamusztin és ciklopoliszacharid kompozíciók
US8603521B2 (en) 2009-04-17 2013-12-10 Pharmacyclics, Inc. Formulations of histone deacetylase inhibitor and uses thereof
WO2011017448A1 (en) 2009-08-05 2011-02-10 The Trustees Of The University Of Pennsylvania Use of histone deacetylase inhibitors for treatment of autoimmune diseases
CN101928234B (zh) 2010-01-15 2012-12-12 北京欧凯纳斯科技有限公司 6/7-(杂)芳基-n-羟基己/庚酰胺化合物及其制备方法
US20130030237A1 (en) 2010-04-15 2013-01-31 Charles Theuer Potentiation of anti-cancer activity through combination therapy with ber pathway inhibitors
JP5727000B2 (ja) 2010-04-16 2015-06-03 ツェルアクト ファーマ ゲーエムベーハー 腫瘍の処置のためのエポトシドのアナログ
JO3659B1 (ar) 2010-06-02 2020-08-27 Astellas Deutschland Gmbh أشكال جرعات بينداموستين عن طريق الفم وإستخداماته العلاجية
US8748470B2 (en) 2011-03-17 2014-06-10 The University Of Chicago Methods for treating ovarian cancer by inhibiting fatty acid binding proteins
RU2609833C2 (ru) 2011-09-13 2017-02-06 Фармасайкликс Элэлси Лекарственные формы ингибитора гистондиацетилазы в комбинации с бендамутином и их применение
CN102993102B (zh) 2011-09-16 2016-08-24 杭州民生药业有限公司 [1-甲基-2-(7’-庚异羟肟酸基)-5-n,n-二(2’-氯乙基)]-1h-苯并咪唑的合成方法
ME03088B (me) * 2011-09-18 2019-01-20 Euro Celtique Sa Postupak za proizvodnju stabilnog, injektabilnog rastvora noradrenalina niske koncentracije
ES2616242T3 (es) 2011-09-28 2017-06-12 Euro-Celtique S.A. Derivados de mostaza de nitrógeno
TWI573792B (zh) 2012-02-01 2017-03-11 歐陸斯迪公司 新穎治療劑
EP3076963A4 (en) 2013-12-06 2017-09-13 Millennium Pharmaceuticals, Inc. Combination of aurora kinase inhibitors and anti-cd30 antibodies
NZ630314A (en) 2014-02-18 2016-03-31 Celgene Corp Combination therapy for hematological malignancies
GB201409471D0 (en) 2014-05-28 2014-07-09 Euro Celtique Sa Pharmaceutical composition
GB201409488D0 (en) 2014-05-28 2014-07-09 Euro Celtique Sa Pharmaceutical composition
GB201409485D0 (en) 2014-05-28 2014-07-09 Euro Celtique Sa Pharmaceutical composition
US9937174B2 (en) 2014-12-05 2018-04-10 University of Modena and Reggio Emilia Combinations of histone deacetylase inhibitors and bendamustine
JP2016109634A (ja) 2014-12-09 2016-06-20 株式会社安川電機 エンコーダ及びエンコーダ付きモータ
WO2017067474A1 (zh) 2015-10-20 2017-04-27 杭州民生药物研究院有限公司 一种药物组合物及其制备方法
US20180098969A1 (en) 2016-10-11 2018-04-12 Purdue Pharmaceutical Products L.P. Hodgkin lymphoma therapy
US11266631B2 (en) 2016-10-11 2022-03-08 Purdue Pharmaceutical Products L.P. Hodgkin lymphoma therapy
GB201709405D0 (en) 2017-06-13 2017-07-26 Euro Celtique Sa Compounds for treating ovarian cancer
GB201709403D0 (en) 2017-06-13 2017-07-26 Euro Celtique Sa Compounds for treating sarcoma
GB201709406D0 (en) 2017-06-13 2017-07-26 Euro-Cletique S A Compounds for treating TNBC
GB201709402D0 (en) 2017-06-13 2017-07-26 Euro Celtique Sa Compounds for treating t-pll
KR20210105380A (ko) 2018-12-18 2021-08-26 먼디파머 인터내셔널 코포레이션 리미티드 다발성 골수종을 치료하기 위한 화합물
US20240252472A1 (en) 2023-01-25 2024-08-01 Purdue Pharma L.P. Combinations for treating cancer

Similar Documents

Publication Publication Date Title
JP2017516781A5 (cg-RX-API-DMAC7.html)
CN102740851B (zh) Pi3k抑制剂和mek抑制剂的组合
CN106470696B (zh) 用于治疗癌症的药物组合
US20120045524A1 (en) Combination therapy with parp inhibitors
JP2006503919A5 (cg-RX-API-DMAC7.html)
RU2018105655A (ru) Комбинированная терапия с применением липосомального иринотекана и ингибитора parp для лечения рака
JP2013525291A (ja) 肝がんの治療に使用するための有機化合物
JP2015534578A5 (cg-RX-API-DMAC7.html)
JP2013507415A5 (cg-RX-API-DMAC7.html)
JP2012512158A5 (cg-RX-API-DMAC7.html)
JP2017518291A5 (cg-RX-API-DMAC7.html)
JP2015096544A5 (cg-RX-API-DMAC7.html)
CN102006875A (zh) 吡铂和贝伐单抗治疗结直肠癌的用途
WO2015097621A3 (en) Pharmaceutical combinations
Doghman et al. Efficacy of the novel dual PI3-kinase/mTOR inhibitor NVP-BEZ235 in a preclinical model of adrenocortical carcinoma
US20140093585A1 (en) Parp inhibitors for the treatment of cipn
JP2016525097A5 (cg-RX-API-DMAC7.html)
JP2016522202A5 (cg-RX-API-DMAC7.html)
JP2020523354A5 (cg-RX-API-DMAC7.html)
FI3463345T3 (fi) Farmaseuttisia yhdistelmiä
JP2017518292A5 (cg-RX-API-DMAC7.html)
US20150005354A1 (en) Combination Therapy With Parp Inhibitors
JP2009506054A5 (cg-RX-API-DMAC7.html)
ES2956411T3 (es) Combinaciones farmacéuticas
CN103889409A (zh) N-羟基-4-{2-[3-(n,n-二甲基氨基甲基)苯并呋喃-2-基羰基氨基]乙氧基}苯甲酰胺的给药方案