A Phase 1, Open-Label, Safety and Tolerability Study of INCB057643 in Participants With Myelofibrosis and Other Advanced Myeloid Neoplasms (LIMBER)
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- STATUS
- Recruiting
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- End date
- Nov 11, 2024
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- participants needed
- 39
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- sponsor
- Incyte Corporation
Summary
The purpose of this study is to evaluate the safety, tolerability, and preliminary efficacy of INCB057643 as monotherapy or combination with ruxolitinib for participants with myelofibrosis and other myeloid neoplasms.
Details
| Condition | Myelofibrosis, Myelodysplastic Syndrome, Myelodysplastic/Myeloproliferative Neoplasm Overlap Syndrome, Myeloproliferative Neoplasm, Relapsed or Refractory Primary Myelofibrosis, Secondary Myelofibrosis (Post-Polycythemia Vera Myelofibrosis, Post-Essential Thrombocythemia Myelofibrosis) |
|---|---|
| Treatment | Ruxolitinib, INCB057643 |
| Clinical Study Identifier | NCT04279847 |
| Sponsor | Incyte Corporation |
| Last Modified on | 24 October 2022 |
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