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Study identifier: NCT06615050 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

A Study of Tacrolimus/Methotrexate/Ruxolitinib Versus Post-Transplant Cyclophosphamide/Tacrolimus/Mycophenolate Mofetil in Non-Myeloablative/Reduced Intensity Conditioning Allogeneic Peripheral Blood Stem Cell Transplantation (BMT CTN 2203)

Condition: Graft-versus-host Disease (GVHD)  ·  Sponsor: Incyte Corporation

PhasePhase 3
Planned participants572
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The purpose of this study is to assess Tacrolimus/Methotrexate/Ruxolitinib versus Post-Transplant Cyclophosphamide/Tacrolimus/Mycophenolate Mofetil in Non-Myeloablative/Reduced Intensity Conditioning Allogeneic Peripheral Blood Stem Cell Transplantation

This description comes directly from the study's public registry record.

Talk to the study team

Incyte Corporation Call Center (US)  ·  1.855.463.3463  ·  medinfo@incyte.com

Incyte Corporation Call Center (ex-US)  ·  +800 00027423  ·  eumedinfo@incyte.com

Always discuss trial participation with your own doctor first.

Locations (30)

Stanford Cancer CenterPalo Alto, California, United StatesRecruiting
University of California San FranciscoSan Francisco, California, United StatesRecruiting
University of MiamiMiami, Florida, United StatesRecruiting
Moffitt Cancer CenterTampa, Florida, United StatesRecruiting
Blood and Marrow Transplant Group of GeorgiaAtlanta, Georgia, United StatesRecruiting
Indiana University Cancer CenterIndianapolis, Indiana, United StatesRecruiting
University of Kansas Hospital AuthorityKansas City, Kansas, United StatesRecruiting
Massachusetts General HospitalBoston, Massachusetts, United StatesRecruiting
Dana Farber Cancer InstituteBoston, Massachusetts, United StatesRecruiting
University of MichiganAnn Arbor, Michigan, United StatesRecruiting
Karmanos Cancer InstituteDetroit, Michigan, United StatesRecruiting
Henry Ford HospitalDetroit, Michigan, United StatesRecruiting

+ 18 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT06615050