drugset / Trial / NCT00726232
Study to Determine the Safety and Efficacy of INCB018424 in Patients With Polycythemia Vera or Essential Thrombocythemia
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Ruxolitinib | Small molecule | 10 mg | Oral |
| Subject | Ruxolitinib | Small molecule | 25 mg | Oral |
| Subject | Ruxolitinib | Small molecule | 50 mg | Oral |