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A Phase I Study to Evaluate the Safety and Maximum Tolerated Dose of Momelotinib Durind and Following Hematopoietic Cell Transplantation for Patients With Myelofibrosis
This is a single-center, open-label, phase I study to determine the safety and tolerability of momelotinib in patients with myelofibrosis during and after hematopoietic cell transplantation (HCT).
Details
| Lead sponsor | Massachusetts General Hospital |
|---|---|
| Phase | Phase 1 |
| Status | RECRUITING |
| Enrolment | 28 |
| Start date | 2026-02-23 |
| Completion | 2030-01 |
Conditions
- Myelofibrosis
- Hematopoietic Cell Transplantation (HCT)
Interventions
- Momelotinib
Primary outcomes
- Maximum Tolerated Dose (MTD) of Momelotinib — From start of study treatment (Day -7) through 28 days.
MTD is defined as the highest dose level at which 0 or 1 of 6 patients experience a Dose Limiting Toxicity (DLT). Toxicities will be graded and documented according to NCI CTCAE version 5.0.
Countries
United States