Malignant Solid Tumor Clinical Trial
Official title:
A Study to Evaluate the Potential of Concomitant Ramucirumab to Affect the Pharmacokinetics of Docetaxel in Patients With Advanced Malignant Solid Tumors
The purpose of this study is to assess the effect of concomitant ramucirumab on the
pharmacokinetics of docetaxel in participants with advanced malignant solid tumors.
Participants who do not complete both Cycle 1, Day 1, and Cycle 2, Day 1 according to
schedule will be replaced for the purpose of analysis; these participants may continue to
receive study therapy. No dose reductions, delayed or missed doses are allowed during Cycles
1 and 2.
n/a
Endpoint Classification: Pharmacokinetics Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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