{"classes":[{"categories":[{"measurements":[{"groupId":"OG000","value":"7.3"},{"groupId":"OG001","value":"0.9"}]}],"title":"Complete response rate"},{"categories":[{"measurements":[{"groupId":"OG000","value":"50.9"},{"groupId":"OG001","value":"0.9"}]}],"title":"Partial response rate"}],"denoms":[{"counts":[{"groupId":"OG000","value":"110"},{"groupId":"OG001","value":"112"}],"units":"Participants"}],"description":"Durable Complete or Partial Clinicohematologic Response was defined as any participant who achieved complete or partial clinicohematologic response per the European LeukemiaNet modified criteria for response in polycythemia vera at Week 32 and maintained that response 48 weeks after randomization.","groups":[{"description":"Starting dose of 10 mg BID with individualized dose titration ranging from 5 mg QD to 25 mg BID based on safety and efficacy","id":"OG000","title":"Ruxolitinib"},{"description":"Best Available Therapy (BAT) will be selected by the Investigator for each participant. BAT may not include experimental agents (i.e. those not approved for the treatment of any indication) as well as a limited number of other selected drugs in accordance with the protocol-defined requirements.","id":"OG001","title":"Best Available Therapy"}],"paramType":"NUMBER","populationDescription":"Full Analysis Set (FAS) comprises all participants to whom study treatment had been assigned by randomization.","reportingStatus":"POSTED","timeFrame":"48 Weeks","title":"The Percentage of Participants Achieving a Durable Complete or Partial Clinicohematologic Response at Week 48","type":"SECONDARY","unitOfMeasure":"percentage of participants"}