drugset / Trial / NCT02202746

A Study to Assess the Safety and Efficacy of the VEGFR-FGFR-PDGFR Inhibitor, Lucitanib, Given to Patients With Metastatic Breast Cancer

NCT02202746

Phase 2 Terminated 178 enrolled Clovis Oncology, Inc.
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to determine whether lucitanib is safe and effective in the treatment of patients with FGF aberrant metastatic breast cancer, as well as in the treatment of patients with biomarker negative (FGF non-aberrant) metastatic breast cancer.

Timeline

Start
2014-09-09
Primary completion
2017-01-17
Completion
2017-01-18

Drugs

EvaluationDrugModalityDoseRoute
Subject Lucitanib Small molecule 10 mg Oral
Subject Lucitanib Small molecule 15 mg Oral