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Clinical trial

A 2-Part, Phase 2, Open-Label Study of the Safety, Tolerability, and Efficacy of Itacitinib Immediate Release in Participants With Primary Myelofibrosis or Secondary Myelofibrosis (Post-Polycythemia Vera Myelofibrosis or Post-Essential Thrombocythemia Myelofibrosis) Who Have Received Prior Ruxolitinib and/or Fedratinib Monotherapy

NCT04629508 is registered in ClinicalTrials.gov with Incyte Corporation as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
A 2-Part, Phase 2, Open-Label Study of the Safety, Tolerability, and Efficacy of Itacitinib Immediate Release in Participants With Primary Myelofibrosis or Secondary Myelofibrosis (Post-Polycythemia Vera Myelofibrosis or Post-Essential Thrombocythemia Myelofibrosis) Who Have Received Prior Ruxolitinib and/or Fedratinib Monotherapy
Lead sponsor
Incyte Corporation
Phase
Phase 2
Overall status
Completed
Start date
July 12, 2021
Completion date
August 24, 2023
Enrollment
4 (actual)
Sites
21

Conditions

As the registry lists them; a condition with its own page is linked.

myelofibrosis, polycythemia vera, thrombocythemia