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ACTIVE NOT RECRUITING
NCT05256537
PHASE2

Fludarabine and Total Body Irradiation 800 Centigray (cGy) or 1125 cGy For Allogeneic Stem Cell Transplant Using Graft Versus Host Disease Prophylaxis With Post-Transplant Cyclophosphamide and Tacrolimus, Without Mycophenolate Mofetil

Sponsor: Ronald Paquette

View on ClinicalTrials.gov

Summary

This is a pilot study to evaluate the feasibility, safety and potential benefits of removing one immune suppressive drug called mycophenolate mofetil (MMF) from the standard allogenic stem cell transplant treatment protocol. MMF will be omitted from the transplant regimen in 60 eligible patients with hematologic malignancies. Participants will be followed for up to 2 years post standard of care transplant at Cedars-Sinai.

Official title: IIT2021-11-PAQUETTE-OmitMMF: Fludarabine and Total Body Irradiation 800 cGy or 1125 cGy For Allogeneic Stem Cell Transplant Using Graft Versus Host Disease Prophylaxis With Post-Transplant Cyclophosphamide and Tacrolimus, Without Mycophenolate Mofetil

Key Details

Gender

All

Age Range

18 Years - 75 Years

Study Type

INTERVENTIONAL

Enrollment

60

Start Date

2022-04-26

Completion Date

2026-03-07

Last Updated

2025-12-08

Healthy Volunteers

No

Interventions

OTHER

Omission of the drug mycophenolate mofetil

Elimination of the immunosuppressive drug mycophenolate mofetil (MMF) from the post-transplant regimen.

Locations (1)

Cedars-Sinai Medical Center

Los Angeles, California, United States