drugset / Trial / NCT00667862
Efficacy and Safety Study of Panobinostat in Participants With Metastatic Hormone Refractory Prostate Cancer
NaSingle-groupOpen-labelTreatment
Summary
This Phase II single dose study was designed to characterize the safety, tolerability, and efficacy of intravenous (i.v.) panobinostat as a single-agent treatment in participants with hormone refractory prostate cancer.
Timeline
- Start
- 2008-03-18
- Primary completion
- 2010-11-05
- Completion
- 2010-11-05
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Panobinostat | Small molecule | 20 mg/m2 | Intravenous |