drugset / Trial / NCT02690350

An Open Study Assessing the Safety and Tolerability of U3-1784

NCT02690350

Phase 1 Terminated 10 enrolled Daiichi Sankyo
Non-randomizedSequentialOpen-labelTreatment

Summary

The main objectives of the trial are: * To evaluate the safety and tolerability of U3-1784 in patients with advanced solid tumours * To determine the maximum tolerated dose (MTD) and or establish the safety and tolerability of the maximum administered dose (MAD) of U3-1784

Timeline

Start
2016-02-29
Primary completion
2017-02-28
Completion
2017-02-28

Drugs

EvaluationDrugModalityDoseRoute
Subject U3-1784 Unknown 2.5 mg/kg Intravenous
Subject U3-1784 Unknown 3.75 mg/kg Intravenous
Subject U3-1784 Unknown 5.6 mg/kg Intravenous
Background Cholestyramine Other / unclassified