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)
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 |