drugset / Trial / NCT00931762

A Study to Evaluate Safety and Efficacy of Panobinostat in Participants With Primary Myelofibrosis

NCT00931762

Phase 2 Terminated 35 enrolled Novartis Pharmaceuticals
NaSingle-groupOpen-labelTreatment

Summary

This study assessed the safety and efficacy of Panobinostat as a single agent in the treatment of Primary Myelofibrosis, Post-Polycythemia Vera and Post-Essential Thrombocythemia. There were two cohorts - participants with JAK2 mutation and participants without JAK2 mutation.

Timeline

Start
2009-08-31
Primary completion
2011-08-29
Completion
2011-08-29

Drugs

EvaluationDrugModalityDoseRoute
Subject Panobinostat Small molecule 40 mg Oral