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