drugset / Trial / NCT07302776

TACrolimus Targeted Immunosuppression Cessation in ALlogeneic HCT

NCT07302776

Phase 1 Not yet recruiting 50 enrolled Stanford University Eurofins Viracor Biopharma · collab
NaSingle-groupOpen-labelSupportive care

Summary

The purpose of this study is to test the feasibility and safety of early cessation of tacrolimus following allogeneic hematopoietic cell transplantation (HCT). Post-HCT tacrolimus is given to prevent graft-vs-host-disease (GVHD), but with the use of post-transplant cyclophosphamide (PTCy), the modern approach to GVHD prevention, GVHD rates have reduced markedly.

Timeline

Start
2026-06
Primary completion
2028-02
Completion
2028-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Tacrolimus Small molecule 0.5 mg Oral