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Urokinase-Plasminogen Activator (uPA) Inhibitor WX-UK1 in Combination With Capecitabine in Advanced Malignancies

NCT00083525 Phase 1 COMPLETED

The purpose of this study is to determine the safety, tolerability, maximum tolerated dose (MTD), pharmacokinetics, and pharmacodynamics of the combination of WX-UK1 and capecitabine in patients with advanced malignancies.

Details

Lead sponsorHeidelberg Pharma AG
PhasePhase 1
StatusCOMPLETED
Enrolment33
Start date2004-05

Conditions

Interventions

Countries

United States