OncoMatch

OncoMatch/Clinical Trials/NCT06345365

MA+AZA Regimen for the Treatment of Newly Diagnosed Acute Myeloid Leukemia (AML)

Is NCT06345365 recruiting? Yes, currently enrolling (May 2026). This Phase 3 trial studies multiple treatments including mitoxantrone liposome, Ara-Cytarabine and azacitidine and Daunorubicin,Ara-Cytarabine, azacitidine for acute myeloid leukaemia.

Phase 3RecruitingZhongnan HospitalNCT06345365Data as of May 2026

Treatment: mitoxantrone liposome, Ara-Cytarabine and azacitidine · Daunorubicin,Ara-Cytarabine, azacitidineInvestigator proposed to apply the new dosage form of mitoxantrone hydrochloride liposomes to the clinical treatment of AML, while combining with cytarabine and azacitidine to form the MA+AZA treatment regimen(Mitoxantrone liposome +Ara-Cytarabine+Azacitidine), which would provide an optimal induction treatment regimen for patients with primary AML by comparing with the traditional chemotherapy regimen, DA+AZA (Daunorubicin+Ara-Cytarabine+Azacitidine).

Check if I qualify

Extracted eligibility criteria

Cancer type

Acute Myeloid Leukemia

Performance status

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

Lab requirements

Kidney function

serum creatinine <1.5 × uln, 80 ml/min ≤ creatinine clearance ≤120 ml/min

Liver function

serum total bilirubin ≤1.5 × uln, ast/alt <2 × uln

Cardiac function

ejection fraction ef ≥50%, ultrasensitive troponin and natriuretic peptide <1.5 × uln

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

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