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A phase I dose-escalation and pharmacokinetic study of enzastaurin and erlotinib in patients with advanced solid tumors
Authors:Sukhmani?K.?Padda,Yelena?Krupitskaya,Laveena?Chhatwani,George?A.?Fisher,Alexander?D.?Colevas,Melanie?San Pedro-Salcedo,Rodney?Decker,Jane?E.?Latz,Heather?A.?Wakelee  author-information"  >  author-information__contact u-icon-before"  >  mailto:Hwakelee@stanford.edu"   title="  Hwakelee@stanford.edu"   itemprop="  email"   data-track="  click"   data-track-action="  Email author"   data-track-label="  "  >Email author
Affiliation:(1) Department of Medicine, Division of Oncology, Stanford University, 875 Blake Wilbur Drive, Stanford, CA 94305-5826, USA;(2) Stanford Cancer Institute, Stanford, CA, USA;(3) Eli Lilly and Company, Indianapolis, IN, USA;(4) Present address: Department of Medicine, Division of Pulmonary and Critical Care Medicine, Virginia Commonwealth University Medical Center, Richmond, VA, USA;
Abstract:

Purpose  

Enzastaurin, an oral serine/threonine kinase inhibitor, targets the protein kinase C and AKT pathways with anti-tumor and anti-angiogenic effects. Erlotinib, an oral epidermal growth factor receptor (EGFR) inhibitor, has activity in solid tumors. Based on the promising combination of EGFR inhibitors and anti-angiogenic agents, this phase I trial was initiated.
Keywords:
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