drugset / Trial / NCT01616758

Phase II Study of GTx024 in Women With Metastatic Breast Cancer

NCT01616758

Phase 2 Terminated 22 enrolled GTx
NaSingle-groupOpen-labelTreatment

Summary

The primary efficacy analysis will be the clinical benefit at 6 months as measured by a modified Response Evaluation Criteria in Solid Tumors RECIST classification. Key secondary endpoints of objective response rate, progression free survival, time to progression, duration of response, effects on physical function, and effects on tumor progression in women with Androgen Receptor positive breast cancer will also be assessed.

Timeline

Start
2013-04
Primary completion
2014-06
Completion
2016-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Enobosarm Small molecule 9 mg

Indications