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Brief Title: A Phase I Study of Intravenous Aflibercept in Combination With Docetaxel in Japanese Cancer Patients
Official Title: A Phase I, Dose-Escalation Study of the Safety, Tolerability, and Pharmacokinetics of Intravenous Aflibercept in Combination With Intravenous Docetaxel Administered Every 3 Weeks in Patients With Advanced Solid Malignancies
Study ID: NCT00545246
Brief Summary: The primary objective of this study is to determine the dose of aflibercept to be further studied in combination with docetaxel in Japanese cancer patients. The secondary objectives of this study are to assess the safety profile of aflibercept, to determine the pharmacokinetics of aflibercept, to make a preliminary assessment of antitumor effects.
Detailed Description:
Minimum Age: 20 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Sanofi-Aventis Investigational Site Number 392002, Iruma-gun, , Japan
Sanofi-Aventis Investigational Site Number 392001, Sunto-Gun, , Japan
Name: Clinical Sciences & Operations
Affiliation: Sanofi
Role: STUDY_DIRECTOR