drugset / Trial / NCT07471503

Gecacitinib Pre-, During- and Post-HSCT for Patients With Primary or Secondary Myelofibrosis

NCT07471503

Phase 2 Not yet recruiting 39 enrolled Institute of Hematology & Blood Diseases Hospital, China
NaSingle-groupOpen-labelPrevention

Summary

The investigators evaluate the efficacy and safety of Gecacitinib in patients with myelofibrosis (MF) before, during, and after allogeneic hematopoietic stem cell transplantation (allo-HSCT).

Timeline

Start
2026-03-16
Primary completion
2029-04-01
Completion
2030-04-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Gecacitinib Unknown 100 mg

Indications