drugset / Trial / NCT01460979

Efficacy,Tolerability,Safety of Temsirolimus in Women With Platinum-refractory Ovarian Carcinoma or Advanced Endometrial Carcinoma

NCT01460979

Phase 2 Completed 47 enrolled AGO Study Group
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to determine the activity, tolerability and safety of Temsirolimus in women with ovarian cancer who progressed during the previous platinum chemotherapy alternatively within 6 months from completion of therapy or advanced endometrial carcinoma.

Timeline

Start
2011-10
Primary completion
2015-06
Completion
2015-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Temsirolimus Small molecule 25 mg Intravenous