drugset / Trial / NCT01832857
Phase 2 Safety, Tolerability and Efficacy Study of CPI-613 in Cancer Patients
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | CPI-613 | Small molecule | 3000 mg/m2 | Intravenous |