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Clinical trial

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

NCT00545246 is registered in ClinicalTrials.gov with Sanofi as lead sponsor.

NCT NCT00545246
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Registry record

As filed in ClinicalTrials.gov.

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
Lead sponsor
Sanofi
Phase
Phase 1
Overall status
Completed
Start date
October 31, 2007
Completion date
July 31, 2012
Enrollment
12 (actual)
Sites
2

Conditions

As the registry lists them; a condition with its own page is linked.

neoplasms