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BMS 582664
Known as:
BMS-582664
, BMS582664
A vascular endothelial growth factor receptor 2 (VEGFR2) inhibitor with potential antineoplastic activity. BMS-582664 strongly binds to and inhibits…
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National Institutes of Health
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Related topics
Related topics
2 relations
Broader (2)
brivanib
brivanib alaninate
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
A phases II evaluation of brivanib in the treatment of persistent or recurrent carcinoma of the cervix: An NRG Oncology/Gynecologic Oncology Group study.
J. Chan
,
W. Deng
,
+6 authors
B. Monk
2015
Corpus ID: 87434694
e16599 Background: Brivanib (BMS582664) is an oral, multi-targeted tyrosine kinase inhibitor against vascular endothelial growth…
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2012
2012
Acid-catalyzed hydrolysis of BMS-582664: degradation product identification and mechanism elucidation.
F. Zhao
,
G. Derbin
,
Scott A. Miller
,
S. Badawy
,
M. Hussain
Journal of Pharmacy and Science
2012
Corpus ID: 1689110
BMS-582664 is an investigational drug intended for cancer treatment through oral administration. The preformulation studies…
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2011
2011
Brivanib (BMS-582664) in advanced soft-tissue sarcoma (STS): Biomarker and subset results of a phase II randomized discontinuation trial.
G. Schwartz
,
R. Maki
,
+15 authors
I. Walters
Journal of Clinical Oncology
2011
Corpus ID: 10337261
10000 Background: Pts with sarcomas, a family of >70 types of cancer, have limited options once cytotoxic agents fail. Brivanib…
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Review
2011
Review
2011
Brivanib (BMS-582664) in advanced solid tumors (AST): Results of a phase II randomized discontinuation trial (RDT).
M. Ratain
,
G. Schwartz
,
+16 authors
I. Walters
Journal of Clinical Oncology
2011
Corpus ID: 41693517
3079 Background: Brivanib (B) is an oral once daily selective dual inhibitor of FGF and VEGF signaling currently in phase III…
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2008
2008
A phase I study of brivanib alaninate (BMS-582664), an oral dual inhibitor of VEGFR and FGFR tyrosine kinases, in combination with full dose cetuximab (BC) in patients (pts) with advanced…
C. Garrett
,
L. Siu
,
+7 authors
D. Feltquate
2008
Corpus ID: 59106845
4111 Background: Brivanib alaninate (B) is an oral prodrug of BMS-540215, a dual tyrosine kinase inhibitor of VEGFR and FGFR…
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2007
2007
A phase I study of BMS-582664 (brivanib alaninate), an oral dual inhibitor of VEGFR and FGFR tyrosine kinases, in patients (pts) with advanced/metastatic solid tumors: Safety, pharmacokinetic (PK…
D. Jonker
,
L. Rosen
,
+7 authors
S. Galbraith
2007
Corpus ID: 74607729
3559 Background: Brivanib is an oral prodrug of BMS-540215, a dual tyrosine kinase inhibitor of VEGFR and FGFR signaling. Part A…
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2007
2007
A phase I study of BMS-582664 (brivanib alaninate), an oral dual inhibitor of VEGFR and FGFR tyrosine kinases, in combination with full-dose cetuximab in patients (pts) with advanced gastrointestinal…
C. Garrett
,
L. Siu
,
+7 authors
D. Feltquate
2007
Corpus ID: 75321639
14018 Background: Brivanib is an oral prodrug of BMS-540215, a dual tyrosine kinase inhibitor of VEGFR and FGFR signaling. Prior…
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2007
2007
BMS-582664, a dual inhibitor of VEGF and FGF signaling pathways, induces growth suppression and apoptosis in mouse models of hepatocellular carcinoma
H. Hung
,
Fargnoli Joseph
,
A. Mark
,
S. Chee
,
C. Pierce
,
Tran Evelyn
2007
Corpus ID: 89690895
A31 Hepatocellular carcinoma (HCC) is the fifth most common malignancy worldwide, with no effective treatment for most…
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2006
2006
Phase I dose escalation study to determine the safety, pharmacokinetics and pharmacodynamics of BMS-582664, a VEGFR/FGFR inhibitor in patients with advanced/metastatic solid tumors.
L. Rosen
,
G. Wilding
,
+6 authors
S. Galbraith
Journal of Clinical Oncology
2006
Corpus ID: 33588881
3051 Background: This is the first multiple-dose study with BMS-582664, an oral VEGFR/FGFR tyrosine kinase inhibitor (IC50 34, 10…
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2005
2005
Preclinical studies of BMS-582664, an alanine prodrug of BMS-540215, a potent, dual inhibitor of VEGFR-2 and FGFR-1 kinases
J. Fargnoli
,
R. Bhide
,
+11 authors
B. Henley
2005
Corpus ID: 71033331
Proc Amer Assoc Cancer Res, Volume 46, 2005 3033 The growth, survival and dissemination of tumors is critically dependent on…
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