drugset / Trial / NCT01832857

Phase 2 Safety, Tolerability and Efficacy Study of CPI-613 in Cancer Patients

NCT01832857

Phase 2 Terminated 7 enrolled Cornerstone Pharmaceuticals
NaSingle-groupOpen-labelTreatment

Summary

This Phase II study is conducted to assess the safety and efficacy of CPI-613 in patients with advanced and/or metastatic solid tumors for whom there there is no available therapy to provide clinical benefit or for those who have refused further standard therapy. The primary outcome measure is Overall Survival (OS). The secondary outcome measures are: Response Rate (RR), Progression-Free Survival (PFS), and safety.

Timeline

Start
2013-06
Primary completion
2016-12
Completion
2016-12

Drugs

EvaluationDrugModalityDoseRoute
Subject CPI-613 Small molecule 3000 mg/m2 Intravenous

Indications