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Phase I dose escalation study of telatinib, a tyrosine kinase inhibitor of vascular endothelial growth factor receptor 2 and 3, platelet-derived growth factor receptor beta, and c-Kit, in patients with advanced or metastatic solid tumors

, , , , , , , , , , , and . J.Clin.Oncol., 27 (25): 4169-4176 (2009)

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Towards new methods for the determination of dose limiting toxicities and the assessment of the recommended dose for further studies of molecularly targeted agents--dose-Limiting Toxicity and Toxicity Assessment Recommendation Group for Early Trials of Targeted therapies, an European Organisation for Research and Treatment of Cancer-led study, , , , , , , , , and 7 other author(s). Eur J Cancer, 50 (12): 2040-2049 (August 2014)Phase I dose escalation study of telatinib, a tyrosine kinase inhibitor of vascular endothelial growth factor receptor 2 and 3, platelet-derived growth factor receptor beta, and c-Kit, in patients with advanced or metastatic solid tumors, , , , , , , , , and 2 other author(s). J.Clin.Oncol., 27 (25): 4169-4176 (2009)The clinical toxicity profile of vascular endothelial growth factor (VEGF) and vascular endothelial growth factor receptor (VEGFR) targeting angiogenesis inhibitors; a review, and . Eur.J.Cancer, 42 (18): 3127-3139 (2006)Defining dose-limiting toxicity for phase 1 trials of molecularly targeted agents: results of a DLT-TARGETT international survey, , , , , , , , , and 4 other author(s). Eur J Cancer, 50 (12): 2050-2056 (August 2014)Time-dependent effects of fixed covariates in Cox regression, and . Biometrics, 51 (4): 1550-1556 (December 1995)Analysis and design of production and control structures., and . APMS, volume 114 of IFIP Conference Proceedings, page 171-182. Chapman & Hall, (1996)