OncoMatch

OncoMatch/Clinical Trials/NCT07249346

Dose-Expansion Study of Low Dose Post-Transplant Cyclophosphamide/Tacrolimus/Ruxolitinib for Graft-versus-Host Disease (GVHD) Prophylaxis in Myeloablative Allogeneic Peripheral Blood Stem Cell Transplantation

Is NCT07249346 recruiting? Yes, currently enrolling (Jun 2026). This Phase 2 trial studies multiple treatments including Ruxolitinib and Myeloablative conditioning regimen for leukemia.

Phase 2RecruitingHannah Choe, MDNCT07249346Data as of Jun 2026

Treatment: Ruxolitinib · Myeloablative conditioning regimen · Cyclophosphamide · TacrolimusThis is an open label, non-randomized, multicenter, pilot, dose expansion study of low dose post-transplant cyclophosphamide (25 mg/kg on Days +3 and +4)/tacrolimus/ruxolitinib in the setting of myeloablative conditioning (MAC) allogeneic peripheral blood stem cell transplantation (PBSCT).

Check if I qualify

Extracted eligibility criteria

Treatments studied

Targeted therapy

Ruxolitinib

Chemotherapy

Cyclophosphamide

Other

Myeloablative conditioning regimenTacrolimus

Cancer type

Acute Myeloid Leukemia

Prior therapy

Must have received: myeloablative conditioning regimen — planned

Planned myeloablative (MAC) conditioning regimen

Cannot have received: allogeneic transplant

Prior allogeneic transplant

Cannot have received: ruxolitinib (ruxolitinib)

Prior use of ruxolitinib

Cannot have received: immune checkpoint inhibitor

Prior use of immune checkpoint inhibitors (i.e., PD1, PDL1, CTLA4 modulators) within six (6) months prior to conditioning

Lab requirements

Kidney function

Estimated creatinine clearance >60 ml/min (C-G formula)

Liver function

AST/ALT <3x ULN; Total bilirubin <2 mg/dL excluding Gilbert's syndrome or hemolysis

Cardiac function

Left ventricular ejection fraction at least 45%

Cardiac function: Left ventricular ejection fraction at least 45%; Estimated creatinine clearance greater than 60 ml/min (C-G formula); Liver function: AST/ALT <3x ULN; Total bilirubin <2 mg/dL excluding Gilbert's syndrome or hemolysis; There are no restrictions based on blood counts

Structured fields extracted by AI. May contain errors — verify against the official protocol.

US trial sites

  • Ohio State University Comprehensive Cancer Center · Columbus, Ohio

Showing up to 5 US sites.

See all sites on ClinicalTrials.gov →

Frequently asked questions

Is NCT07249346 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior allogeneic transplant, ruxolitinib, immune checkpoint inhibitor disqualifies patients from enrollment.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

Check if I qualify