drugset / Trial / NCT00493766

Safety of LBH589 Alone and in Combination With IV Docetaxel and Prednisone

NCT00493766

Phase 1 Terminated 16 enrolled Novartis Pharmaceuticals
Non-randomizedParallel-groupOpen-labelTreatment

Summary

This is a parallel, two-arm, open-label, multicenter phase IA/IB study of LBH589 (oral formulation) alone and in combination with docetaxel in patients with progressing hormone refractory prostate cancer. This study is designed to determine the maximum tolerated dose of LBH589 as a single agent and in combination with docetaxel and prednisone 5 mg two times a day , and to characterize the safety, tolerability, biologic activity and pharmacokinetic profile

Timeline

Start
2006-05
Primary completion
2008-07
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Panobinostat Small molecule Oral