drugset / Trial / NCT00667862

Efficacy and Safety Study of Panobinostat in Participants With Metastatic Hormone Refractory Prostate Cancer

NCT00667862

Phase 2 Completed 35 enrolled Novartis Pharmaceuticals
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

EvaluationDrugModalityDoseRoute
Subject Panobinostat Small molecule 20 mg/m2 Intravenous

Indications