JP2012523376A5 - - Google Patents

Download PDF

Info

Publication number
JP2012523376A5
JP2012523376A5 JP2011552217A JP2011552217A JP2012523376A5 JP 2012523376 A5 JP2012523376 A5 JP 2012523376A5 JP 2011552217 A JP2011552217 A JP 2011552217A JP 2011552217 A JP2011552217 A JP 2011552217A JP 2012523376 A5 JP2012523376 A5 JP 2012523376A5
Authority
JP
Japan
Prior art keywords
sns
pharmaceutical composition
composition according
cancer
dose
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
JP2011552217A
Other languages
English (en)
Japanese (ja)
Other versions
JP2012523376A (ja
JP5936862B2 (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2010/025737 external-priority patent/WO2010099526A1/en
Publication of JP2012523376A publication Critical patent/JP2012523376A/ja
Publication of JP2012523376A5 publication Critical patent/JP2012523376A5/ja
Application granted granted Critical
Publication of JP5936862B2 publication Critical patent/JP5936862B2/ja
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2011552217A 2009-02-27 2010-03-01 Brca2活性が低下した癌対象の治療のためのsns−595の使用方法 Expired - Fee Related JP5936862B2 (ja)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US15644909P 2009-02-27 2009-02-27
US61/156,449 2009-02-27
US17001309P 2009-04-16 2009-04-16
US61/170,013 2009-04-16
PCT/US2010/025737 WO2010099526A1 (en) 2009-02-27 2010-03-01 Methods of using sns-595 for treatment of cancer subjects with reduced brca2 activity

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2015060900A Division JP2015145396A (ja) 2009-02-27 2015-03-24 Brca2活性が低下した癌対象の治療のためのsns−595の使用方法

Publications (3)

Publication Number Publication Date
JP2012523376A JP2012523376A (ja) 2012-10-04
JP2012523376A5 true JP2012523376A5 (enExample) 2013-04-18
JP5936862B2 JP5936862B2 (ja) 2016-06-22

Family

ID=42224275

Family Applications (2)

Application Number Title Priority Date Filing Date
JP2011552217A Expired - Fee Related JP5936862B2 (ja) 2009-02-27 2010-03-01 Brca2活性が低下した癌対象の治療のためのsns−595の使用方法
JP2015060900A Pending JP2015145396A (ja) 2009-02-27 2015-03-24 Brca2活性が低下した癌対象の治療のためのsns−595の使用方法

Family Applications After (1)

Application Number Title Priority Date Filing Date
JP2015060900A Pending JP2015145396A (ja) 2009-02-27 2015-03-24 Brca2活性が低下した癌対象の治療のためのsns−595の使用方法

Country Status (14)

Country Link
US (3) US20120148564A1 (enExample)
EP (2) EP2400959A1 (enExample)
JP (2) JP5936862B2 (enExample)
KR (2) KR20110132400A (enExample)
CN (2) CN104688732A (enExample)
AU (2) AU2010217796B2 (enExample)
CA (1) CA2753261A1 (enExample)
IL (1) IL214784A0 (enExample)
MX (1) MX348412B (enExample)
NZ (1) NZ594829A (enExample)
RU (1) RU2558835C2 (enExample)
SG (2) SG10201400258SA (enExample)
WO (1) WO2010099526A1 (enExample)
ZA (1) ZA201106199B (enExample)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2005222622B2 (en) 2004-03-15 2011-04-07 Dainippon Sumitomo Pharma Co., Ltd. SNS-595 and methods of using the same
AU2008317400B2 (en) 2007-10-22 2014-10-02 Sunesis Pharmaceuticals, Inc. Methods of using (+)-1,4-dihydro-7-[(3S,4S)-3-methoxy-4-(methylamino) -1-pyrrolidinyl]-4-oxo-1-(2-thiazolyl)-1,8-naphthyridine-3- carboxylic acid in combination therapy
EP3284745A1 (en) 2008-12-31 2018-02-21 Sunesis Pharmaceuticals, Inc. Composition of (+)-1,4-dihydro-7-[(3s,4s)-3-methoxy-4-(methylamino)-1-pyrrolidinyl]-4-oxo-1-(2-thiazolyl)-1,8-naphthyridine-3-carboxylic acid
CN104688732A (zh) * 2009-02-27 2015-06-10 逊尼希思制药公司 利用sns-595治疗具有降低的brca2活性的癌症对象的方法
UA110465C2 (en) 2009-09-04 2016-01-12 Sunesis Pharmaceutecals Inc Stable sns-595 composition
US8470817B2 (en) 2009-10-26 2013-06-25 Sunesis Pharmaceuticals, Inc. Compounds and methods for treatment of cancer
WO2023110045A1 (en) 2021-12-15 2023-06-22 Y-Mabs Therapeutics, Inc. Scfv and antibodies with reduced multimerisation

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6024A (en) * 1849-01-09 Cast-iron gar-wheel
KR0166088B1 (ko) 1990-01-23 1999-01-15 . 수용해도가 증가된 시클로덱스트린 유도체 및 이의 용도
ATE209645T1 (de) 1994-06-14 2001-12-15 Dainippon Pharmaceutical Co Neue verbindung, verfahren zu ihrer herstellung und antitumormittel
JPH10173986A (ja) 1996-12-16 1998-06-26 Sony Corp 移動体撮影装置
CA2547077C (en) * 2003-12-01 2015-11-03 Kudos Pharmaceuticals Limited Dna damage repair inhibitors for treatment of cancer
AU2005222622B2 (en) 2004-03-15 2011-04-07 Dainippon Sumitomo Pharma Co., Ltd. SNS-595 and methods of using the same
AU2006287149B2 (en) * 2005-09-02 2013-05-23 Sunesis Pharmaceuticals, Inc. Methods of using (+)-1,4-dihydro-7-[(3S,4S)-3-methoxy-4-(methylamino)-1-pyrrolidinyl]-4-oxo-1-(2-thiazolyl)-1,8-naphthyridine-3-carboxylic acid for treatment of cancer
MX2008015775A (es) 2006-06-12 2009-04-17 Sunesis Pharmaceuticals Inc Compuestos y composiciones para tratamiento de cancer.
US7790274B2 (en) 2006-08-02 2010-09-07 High Impact Technology, Llc Layered panel structure including self-bonded thermoformable and non-thermoformable layer materials
EP2155897A2 (en) * 2007-03-30 2010-02-24 Source Precision Medicine, Inc. d/b/a Source MDX. Gene expression profiling for identification, monitoring, and treatment of prostate cancer
CN104688732A (zh) * 2009-02-27 2015-06-10 逊尼希思制药公司 利用sns-595治疗具有降低的brca2活性的癌症对象的方法

Similar Documents

Publication Publication Date Title
Topatana et al. Advances in synthetic lethality for cancer therapy: cellular mechanism and clinical translation
Wagner et al. Senescence as a therapeutically relevant response to CDK4/6 inhibitors
Hirpara et al. Metabolic reprogramming of oncogene-addicted cancer cells to OXPHOS as a mechanism of drug resistance
Huang et al. Palbociclib enhances radiosensitivity of hepatocellular carcinoma and cholangiocarcinoma via inhibiting ataxia telangiectasia–mutated kinase–mediated DNA damage response
Yan et al. Aurora‐A kinase: a potent oncogene and target for cancer therapy
Ganguly et al. Maternal embryonic leucine zipper kinase: key kinase for stem cell phenotype in glioma and other cancers
Rajeshkumar et al. MK-1775, a potent Wee1 inhibitor, synergizes with gemcitabine to achieve tumor regressions, selectively in p53-deficient pancreatic cancer xenografts
Wicki et al. First-in human, phase 1, dose-escalation pharmacokinetic and pharmacodynamic study of the oral dual PI3K and mTORC1/2 inhibitor PQR309 in patients with advanced solid tumors (SAKK 67/13)
Gild et al. Targeting mTOR in RET mutant medullary and differentiated thyroid cancer cells
JP2012523376A5 (enExample)
Patel et al. Enhancing direct cytotoxicity and response to immune checkpoint blockade following ionizing radiation with Wee1 kinase inhibition
Magnussen et al. Combined inhibition of the cell cycle related proteins Wee1 and Chk1/2 induces synergistic anti-cancer effect in melanoma
Cocco et al. Dual CCNE1/PIK3CA targeting is synergistic in CCNE1-amplified/PIK3CA-mutated uterine serous carcinomas in vitro and in vivo
Tryfonidis et al. A European Organisation for Research and Treatment of Cancer randomized, double-blind, placebo-controlled, multicentre phase II trial of anastrozole in combination with gefitinib or placebo in hormone receptor-positive advanced breast cancer (NCT00066378)
HRP20191145T1 (hr) Postupak predviđanja ishoda liječenja s afliberceptom kod pacijenta za kojeg se sumnja da ima rak
Lian et al. Anlotinib can overcome acquired resistance to EGFR‐TKIs via FGFR1 signaling in non‐small cell lung cancer without harboring EGFR T790M mutation
Yang et al. Perspectives on the combination of radiotherapy and targeted therapy with DNA repair inhibitors in the treatment of pancreatic cancer
Narayanan et al. Discovery and preclinical characterization of novel small molecule TRK and ROS1 tyrosine kinase inhibitors for the treatment of cancer and inflammation
Ma et al. Inhibition of farnesyltransferase potentiates NOTCH-targeted therapy against glioblastoma stem cells
RU2011139323A (ru) Способы применения sns-595 для лечения субъектов с онкологическими заболеваниями, имеющих сниженную активность brca2
Miyamoto et al. Synergistic effects of olaparib and DNA-damaging agents in oesophageal squamous cell carcinoma cell lines
Pan et al. An unbiased high‐throughput drug screen reveals a potential therapeutic vulnerability in the most lethal molecular subtype of pancreatic cancer
US10188666B2 (en) Dendrogenin A and antineoplastic agents for the treatment of chemosensitive or chemoresistant tumors
Mann et al. Combined inhibition of RAD51 and CHK1 causes synergistic toxicity in cisplatin resistant cancer cells by triggering replication fork collapse
Lin et al. Potent effects of roniciclib alone and with sorafenib against well-differentiated thyroid cancer