drugset / Trial / NCT01493414

INC424 for Patients With Primary Myelofibrosis, Post Polycythemia Myelofibrosis or Post-essential Thrombocythemia Myelofibrosis.

NCT01493414

Phase 3 Completed 2233 enrolled Novartis Pharmaceuticals
NaSingle-groupOpen-labelTreatment

Summary

The primary objective of this study was to collect additional safety of INC424 in patients with Primary Myelofibrosis, Post Polycythemia Myelofibrosis or Post-essential Thrombocythemia Myelofibrosis, who either received prior treatment with commercially available agents or who have never received treatment.

Timeline

Start
2011-08-16
Primary completion
2017-01-26
Completion
2017-01-26

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Ruxolitinib Small molecule 5 mg Oral
Subject Ruxolitinib Small molecule 20 mg Oral
Subject Ruxolitinib Small molecule 25 mg Oral

Indications