drugset / Trial / NCT00934544

Controlled Myelofibrosis Study With Oral Janus-associated Kinase (JAK) Inhibitor Treatment-II: The COMFORT-II Trial

NCT00934544

Phase 3 Completed 219 enrolled Novartis Pharmaceuticals
RandomizedCrossoverOpen-labelTreatment

Summary

This was an open label, randomized study comparing the efficacy and safety of randomized 2:1 Ruxolitinib tablets versus best-available therapy, as selected by the investigator. The purpose was to compare the efficacy, safety and tolerability of Ruxolitinib (INC424/INCB018424) given twice daily to the best-available therapy, in subjects with primary myelofibrosis (PMF), post polycythemia vera myelofibrosis (PPV-MF) or post essential thrombocythemia myelofibrosis (PET-MF).

Timeline

Start
2009-07-01
Primary completion
2015-03-04
Completion
2015-03-04

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Ruxolitinib Small molecule 15 mg Oral
Subject Ruxolitinib Small molecule 20 mg Oral

Indications