JP2014503499A5 - - Google Patents

Download PDF

Info

Publication number
JP2014503499A5
JP2014503499A5 JP2013540060A JP2013540060A JP2014503499A5 JP 2014503499 A5 JP2014503499 A5 JP 2014503499A5 JP 2013540060 A JP2013540060 A JP 2013540060A JP 2013540060 A JP2013540060 A JP 2013540060A JP 2014503499 A5 JP2014503499 A5 JP 2014503499A5
Authority
JP
Japan
Prior art keywords
cancer
ldh
ldh5
ldh4
tumor
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.)
Pending
Application number
JP2013540060A
Other languages
English (en)
Japanese (ja)
Other versions
JP2014503499A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2011/061440 external-priority patent/WO2012068483A1/en
Publication of JP2014503499A publication Critical patent/JP2014503499A/ja
Publication of JP2014503499A5 publication Critical patent/JP2014503499A5/ja
Pending legal-status Critical Current

Links

JP2013540060A 2010-11-18 2011-11-18 低酸素状態に基づく治療に適した被験体の事前選択 Pending JP2014503499A (ja)

Applications Claiming Priority (21)

Application Number Priority Date Filing Date Title
US41515810P 2010-11-18 2010-11-18
US41515510P 2010-11-18 2010-11-18
US41515610P 2010-11-18 2010-11-18
US41512210P 2010-11-18 2010-11-18
US41513610P 2010-11-18 2010-11-18
US41514710P 2010-11-18 2010-11-18
US41513910P 2010-11-18 2010-11-18
US61/415,155 2010-11-18
US61/415,139 2010-11-18
US61/415,156 2010-11-18
US61/415,147 2010-11-18
US61/415,158 2010-11-18
US61/415,122 2010-11-18
US61/415,136 2010-11-18
US201161510648P 2011-07-22 2011-07-22
US201161510660P 2011-07-22 2011-07-22
US201161510653P 2011-07-22 2011-07-22
US61/510,660 2011-07-22
US61/510,648 2011-07-22
US61/510,653 2011-07-22
PCT/US2011/061440 WO2012068483A1 (en) 2010-11-18 2011-11-18 Preselection of subjects for therapeutic treatment based on hypoxic status

Publications (2)

Publication Number Publication Date
JP2014503499A JP2014503499A (ja) 2014-02-13
JP2014503499A5 true JP2014503499A5 (enExample) 2015-01-15

Family

ID=45217699

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2013540060A Pending JP2014503499A (ja) 2010-11-18 2011-11-18 低酸素状態に基づく治療に適した被験体の事前選択

Country Status (7)

Country Link
US (2) US20120128665A1 (enExample)
EP (1) EP2640385A1 (enExample)
JP (1) JP2014503499A (enExample)
CN (1) CN103327976A (enExample)
AU (1) AU2011329681A1 (enExample)
CA (1) CA2817564A1 (enExample)
WO (1) WO2012068483A1 (enExample)

Families Citing this family (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8053456B2 (en) 2006-05-25 2011-11-08 Synta Pharmaceuticals Corp. Triazole compounds that modulate Hsp90 activity
EP2323737A2 (en) 2008-08-08 2011-05-25 Synta Pharmaceuticals Corp. Triazole compounds that modulate hsp90 activity
EP2560640A1 (en) 2010-04-19 2013-02-27 Synta Pharmaceuticals Corp. Cancer therapy using a combination of a hsp90 inhibitory compounds and a egfr inhibitor
JP2014534228A (ja) 2011-11-02 2014-12-18 シンタ ファーマシューティカルズ コーポレーション 白金含有剤とhsp90阻害剤の組合せ療法
JP2014532712A (ja) 2011-11-02 2014-12-08 シンタ ファーマシューティカルズ コーポレーション トポイソメラーゼi阻害剤とhsp90阻害剤の組合せを使用する癌療法
AU2012339679A1 (en) 2011-11-14 2014-06-12 Synta Pharmaceuticals Corp. Combination therapy of Hsp90 inhibitors with BRAF inhibitors
WO2013170182A1 (en) * 2012-05-11 2013-11-14 Synta Pharmaceuticals Corp. Treating cancer with an hsp90 inhibitory compound
CA2872942A1 (en) * 2012-05-16 2013-11-21 Synta Pharmaceuticals Corp. Pre-selection of subjects for therapeutic treatment with an hsp90 inhibitor based on hypoxic status
US20160022757A1 (en) * 2013-03-15 2016-01-28 Icahn School Of Medicine At Mount Sinai Therapeutic methods for treating solid tumors and related diagnostic methods
US9927437B2 (en) * 2013-12-12 2018-03-27 The Brigham And Women's Hospital, Inc. Treating neurodegenerative disease
LT3179991T (lt) 2014-08-11 2021-11-10 Acerta Pharma B.V. Terapiniai btk inhibitoriaus ir bcl-2 inhibitoriaus deriniai
WO2016024232A1 (en) 2014-08-11 2016-02-18 Acerta Pharma B.V. Therapeutic combinations of a btk inhibitor, a pi3k inhibitor, a jak-2 inhibitor and/or a cdk 4/6 inhibitor
US20170239351A1 (en) 2014-08-11 2017-08-24 Acerta Pharma B.V. Therapeutic Combinations of a BTK Inhibitor, a PI3K Inhibitor, a JAK-2 Inhibitor, a PD-1 Inhibitor, and/or a PD-L1 Inhibitor
CN104267191B (zh) * 2014-09-09 2016-03-23 北京大学口腔医学院 口腔鳞状细胞癌的生物标志物及其应用
WO2016073669A1 (en) * 2014-11-05 2016-05-12 Vojo Vukovic Combination therapy of hsp90 inhibitory compounds with mtor inhibitors
WO2017136326A1 (en) * 2016-02-01 2017-08-10 Board Of Regents, The University Of Texas System Using spectral ct to diagnose thyroid nodules
CN105709239A (zh) * 2016-03-22 2016-06-29 山东省肿瘤医院 一种非小细胞肺癌放疗相关的HIF-1α的抑制剂
JPWO2023276768A1 (enExample) * 2021-06-29 2023-01-05

Family Cites Families (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4250255A (en) 1977-07-11 1981-02-10 Eastman Kodak Company Assay method for isoenzyme activity
US6242208B1 (en) 1988-07-15 2001-06-05 International Reagents Corporation LDH1 assay
WO1994004679A1 (en) 1991-06-14 1994-03-03 Genentech, Inc. Method for making humanized antibodies
US5362718A (en) 1994-04-18 1994-11-08 American Home Products Corporation Rapamycin hydroxyesters
US5747498A (en) 1996-05-28 1998-05-05 Pfizer Inc. Alkynyl and azido-substituted 4-anilinoquinazolines
CO4950519A1 (es) 1997-02-13 2000-09-01 Novartis Ag Ftalazinas, preparaciones farmaceuticas que las comprenden y proceso para su preparacion
UA74803C2 (uk) 1999-11-11 2006-02-15 Осі Фармасьютікалз, Інк. Стійкий поліморф гідрохлориду n-(3-етинілфеніл)-6,7-біс(2-метоксіетокси)-4-хіназолінаміну, спосіб його одержання (варіанти) та фармацевтичне застосування
US7087613B2 (en) 1999-11-11 2006-08-08 Osi Pharmaceuticals, Inc. Treating abnormal cell growth with a stable polymorph of N-(3-ethynylphenyl)-6,7-bis(2-methoxyethoxy)-4-quinazolinamine hydrochloride
US7417055B2 (en) 2003-04-25 2008-08-26 Gilead Sciences, Inc. Kinase inhibitory phosphonate analogs
CN101072759B (zh) 2004-11-18 2013-06-19 Synta医药公司 调节hsp90活性的三唑化合物
GB0510390D0 (en) 2005-05-20 2005-06-29 Novartis Ag Organic compounds
WO2007123793A2 (en) * 2006-04-04 2007-11-01 Stc.Unm Swellable particles for drug delivery
GB0610925D0 (en) * 2006-06-02 2006-07-12 Novartis Ag Use of vascular endothelial growth factor receptor inhibitors for the treatment of cancer
SE530596C2 (sv) 2006-10-13 2008-07-15 Mathias Karlsson Metod att fastställa syrebrist i blod från skalpen under förlossning
US8592166B2 (en) 2006-11-21 2013-11-26 Beth Israel Deaconess Medical Center, Inc. Hypoxia related genes and proteins for the treatment and diagnosis of pregnancy related complications
US20080318241A1 (en) * 2007-06-18 2008-12-25 The Regents Of The University Of Michigan Methods and Systems for Detecting Antiangiogenesis

Similar Documents

Publication Publication Date Title
JP2014503499A5 (enExample)
JP2014503500A5 (enExample)
JP2013545759A5 (enExample)
Varey et al. VEGF165b, an antiangiogenic VEGF-A isoform, binds and inhibits bevacizumab treatment in experimental colorectal carcinoma: balance of pro-and antiangiogenic VEGF-A isoforms has implications for therapy
AU2017205101B2 (en) Inhibitors of ataxia-telangiectasia mutated and Rad3-related protein kinase (ATR) for use in methods of treating cancer
JP6066421B2 (ja) 癌の治療のための低酸素活性化プロドラッグおよび血管新生阻害剤の投与方法
JPWO2020130125A1 (ja) 抗体−薬物コンジュゲートとキナーゼ阻害剤の組み合わせ
AU2015317327B9 (en) Pyridinyl quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
Speranza et al. BKM-120 (Buparlisib): A phosphatidyl-inositol-3 kinase inhibitor with anti-invasive properties in glioblastoma
KR20200028047A (ko) 항 trop2 항체-약물 컨쥬게이트
JP2013543011A (ja) 癌の治療法
CN116635082A (zh) 抗体-药物缀合物和atr抑制剂的组合
WO2020106304A1 (en) Topical formulations
WO2015104292A2 (en) Compounds for use in treating or preventing cancerous diseases
RU2015105786A (ru) Комбинированная терапия ингибиторами igf1r и pi3k
JP2017526662A5 (enExample)
JP2014513097A5 (enExample)
KR20240130087A (ko) 항체-약물 접합체와 atr 저해제의 조합
Brandl et al. Targeting c-MYC through Interference with NAMPT and SIRT1 and their association to oncogenic drivers in murine serrated intestinal tumorigenesis
Chiacchiera et al. Signal-dependent regulation of gene expression as a target for cancer treatment: inhibiting p38α in colorectal tumors
US20240398767A1 (en) Inhibitors of the mtdh-snd1 protein complex for cancer therapy
Lian et al. RJT-101, a novel camptothecin derivative, is highly effective in the treatment of melanoma through DNA damage by targeting topoisomerase 1
US9844552B2 (en) Methods of treating fibrosis
JP2018528949A5 (enExample)
TW202423446A (zh) 用於治療實性瘤之包含 krasg12c 抑制劑及 egfr 抑制劑之組成物及方法