Stopped: Termination of the clinical trial by sponsor.
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.
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Percentage of Polycythemia Vera Participants With a Confirmed Clinical Partial Response (PR) or Complete Response (CR)
Timeframe: Assessed after 2 cycles (56 days) of treatment on Day 1 of Cycle 3
Percentage of Essential Thrombocythemia (ET) Participants With a Confirmed Clinical Partial Response (PR) or Complete Response (CR)
Timeframe: Assessed after 2 cycles (56 days) of treatment on Day 1 of Cycle 3.