drugset / Trial / NCT01605396

A Phase II Trial of Ridaforolimus and Exemestane, Compared to Ridaforolimus, Dalotuzumab and Exemestane in Participants With Breast Cancer (MK-8669-064)

NCT01605396

Phase 2 Completed 80 enrolled Merck Sharp & Dohme LLC
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of the study is to evaluate the efficacy of the triplet of ridaforolimus, dalotuzumab and exemestane compared to the combination of ridaforolimus and exemestane in post-menopausal participants with breast cancer. The primary hypothesis of the study is that the triplet of ridaforolimus, dalotuzumab and exemestane will improve progression free survival (PFS) compared to ridaforolimus and exemestane.

Timeline

Start
2012-07-04
Primary completion
2014-02-19
Completion
2018-03-15

Drugs

EvaluationDrugModalityDoseRoute
Subject dalotuzumab Monoclonal antibody 10 mg/kg Intravenous
Subject ridaforolimus Small molecule 10 mg Oral
Subject ridaforolimus Small molecule 30 mg Oral
Background Exemestane Small molecule 25 mg Oral

Indications