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OncoMatch/Clinical Trials/NCT04742634

Pre-emptive Therapy With DEC-C to Improve Outcomes in MDS Patients With Measurable Residual Disease Post Allogeneic Hematopoietic Cell Transplant

Is NCT04742634 recruiting? Yes, currently enrolling (May 2026). This Phase 1/2 trial studies multiple treatments including DEC-C and MyeloSeq-HD for myelodysplastic syndromes.

Phase 1/2RecruitingWashington University School of MedicineNCT04742634Data as of May 2026

Treatment: DEC-C · MyeloSeq-HDThe investigators hypothesize that early measurable residual disease (MRD)-guided pre-emptive therapy with decitabine + cedazaridine (DEC-C) will decrease the risk of progression in post-transplant myelodysplastic syndromes (MDS) patients with persistent mutations (molecular MRD). To detect molecular MRD, the investigators will perform ultra-deep, error-corrected panel-based sequencing (MyeloSeq-HD) at Day 30 in post-transplant MDS patients. The investigators will treat patients with detectable molecular MRD with DEC-C to determine if pre-emptive, MRD-guided therapy with DEC-C decreases relapse rates and improves progression-free survival.

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Extracted eligibility criteria

Cancer type

Myelodysplastic Syndrome

Performance status

ECOG 0–2(Ambulatory, capable of self-care)

Prior therapy

Must have received: allogeneic hematopoietic cell transplant

who have received an allogeneic hematopoietic cell transplant

Cannot have received: investigational agent

Not currently receiving any investigational agents

Lab requirements

Blood counts

Absolute neutrophil count (ANC) ≥ 1.0 X 10^9/L and platelets ≥ 50 X 10^9/L

Kidney function

Creatinine clearance ≥ 30 mL/min using Cockcroft-Gault Formula

Liver function

Total bilirubin ≤ 1.5 x IULN (unless due to hemolysis or Gilbert's disease, per PI discretion); AST(SGOT)/ALT(SGPT) ≤ 3.0 IULN

Absolute neutrophil count (ANC) ≥ 1.0 X 10^9/L and platelets ≥ 50 X 10^9/L. Total bilirubin ≤ 1.5 x IULN. AST(SGOT)/ALT(SGPT) ≤ 3.0 IULN. Creatinine clearance ≥ 30 mL/min using Cockcroft-Gault Formula.

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

US trial sites

  • Washington University School of Medicine · St Louis, Missouri

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