drugset / Trial / NCT01445769

Alternative Dosing Strategy of Ruxolitinib in Patients With Myelofibrosis

NCT01445769 ↗

Phase 2 Completed 45 enrolled Incyte Corporation
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study was to evaluate the effect of an alternative dosing strategy of ruxolitinib in subjects with primary myelofibrosis (PMF), post-polycythemia vera-myelofibrosis (PPV-MF) and post essential thrombocythemia-myelofibrosis (PET-MF) in order to minimize the development of anemia and thrombocytopenia.

Timeline

Start
2011-09
Primary completion
2013-03
Completion
2013-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Ruxolitinib Small molecule 10 mg —
Subject Ruxolitinib Small molecule 15 mg —
Subject Ruxolitinib Small molecule 20 mg —