drugset / Trial / NCT00726232

Study to Determine the Safety and Efficacy of INCB018424 in Patients With Polycythemia Vera or Essential Thrombocythemia

NCT00726232 ↗

Phase 2 Terminated 73 enrolled Incyte Corporation
RandomizedParallel-groupOpen-labelTreatment

Summary

To evaluate the safety and efficacy profile of different treatment regimens of Ruxolitinib (INCB018424) administered to two groups of patients; those with polycythemia vera (PV) and those with essential thrombocythemia (ET). Patients in each group were refractory to hydroxyurea or for whom hydroxyurea is contraindicated.

Timeline

Start
2008-08-20
Primary completion
2010-06-20
Completion
2018-08-20

Outcome

Outcome not reported

Stopped: “Termination of the clinical trial by sponsor.”

Drugs

EvaluationDrugModalityDoseRoute
Subject Ruxolitinib Small molecule 10 mg Oral
Subject Ruxolitinib Small molecule 25 mg Oral
Subject Ruxolitinib Small molecule 50 mg Oral