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NCT06973668

A Randomized Study to Compare Post-transplant Cyclophosphamide, Sirolimus, Ruxolitinib and Post-transplant Cyclophosphamide, Sirolimus, Mycophenolate Mofetil to Prevent Graft Versus Host Disease

Recruiting now Phase 2 Last updated 16 April 2026
What this trial tests

Phase 2 trial testing Mycophenolate Mofetil in AML in 80 participants. Currently enrolling.

Timeline
22 July 2025
Primary endpoint
31 January 2028
31 January 2030

Quick facts

Lead sponsorM.D. Anderson Cancer Center
PhasePhase 2
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment80
Start date22 July 2025
Primary completion31 January 2028
Estimated completion31 January 2030
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

M.D. Anderson Cancer Center — full company profile →

Who can join

Adults 65 to 75, any sex, with AML. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The goal of this clinical research study is to compare the effects of these drug combinations (cyclophosphamide, sirolimus, and MMF vs cyclophosphamide, sirolimus, and ruxolitinib) on the prevention of GVHD after a stem cell transplant.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Mycophenolate Mofetil

Trials testing the same drug.

Other recruiting trials for AML

Currently open trials in the same condition.

Other M.D. Anderson Cancer Center trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06973668.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing