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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)

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NCT06615050 · readout in 1,612 d

Sponsored by Incyte Corporation (industry) · INCY — their whole pipeline →. With Blood and Marrow Transplant Clinical Trials Network, National Institutes of Health (NIH), National Heart, Lung, and Blood Institute (NHLBI), National Cancer Institute (NCI).

Phase
Phase 3
Status
Recruiting
Study type
Interventional
Design
Randomized · None · Treatment
Enrollment
572estimated
Sites
30
Country
United States

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2025-04-02actualWhen the study began enrolling
Primary completion2031-01-17estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2031-01-17estimatedThe whole study's end, after follow-up
First posted2024-09-26actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-05-20actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Graft-versus-host Disease (GVHD)

Interventions

  • Drug: Tacrolimus (Tac)
  • Drug: Methotrexate (MTX)
  • Drug: Ruxolitinib (Rux) — also filed as Jakafi, INCB018424
  • Drug: Cyclophosphamide
  • Drug: Mycophenolate mofetil (MMF)

Primary outcome

what the primary-completion date above is the date OF
GVHD-free survival (GFS)
measured Up to 24 months post-transplant (Day 0)

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