TerminatedPhase 3NCT04551053

To Evaluate Efficacy and Safety of Parsaclisib and Ruxolitinib in Participants With Myelofibrosis Who Have Suboptimal Response to Ruxolitinib (LIMBER-304)

Studying Essential thrombocythemia

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Key facts

Sponsor
Incyte Corporation
Principal Investigator
Albert Assad, M.D., MD
Incyte Corporation
Intervention
parsaclisib(drug)
Enrollment
177 enrolled
Eligibility
18 years · All sexes
Timeline
20212024

Study locations (30)

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT04551053 on ClinicalTrials.gov

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