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Spots Global Cancer Trial Database for A Phase I Study of Intravenous Aflibercept in Combination With Docetaxel in Japanese Cancer Patients

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Trial Identification

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

Conditions

Neoplasms

Study Description

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:

Keywords

Eligibility

Minimum Age: 20 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Sanofi-Aventis Investigational Site Number 392002, Iruma-gun, , Japan

Sanofi-Aventis Investigational Site Number 392001, Sunto-Gun, , Japan

Contact Details

Name: Clinical Sciences & Operations

Affiliation: Sanofi

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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