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OncoMatch/Clinical Trials/NCT07132684

Comparison of VA and D/IA Induction Regimens in Elderly Fit Acute Myeloid Leukemia Patients

Is NCT07132684 recruiting? Yes, currently enrolling (Jun 2026). This Phase 3 trial studies multiple treatments including Daunorubicin/Idarubicin and Cytarabine for aml, adult.

Phase 3RecruitingInstitute of Hematology & Blood Diseases Hospital, ChinaNCT07132684Data as of Jun 2026Location: China

Treatment: Daunorubicin/Idarubicin · Cytarabine · Azacitidine · VenetoclaxThis study is a multicenter, randomized, controlled phase III clinical trial aimed at comparing the efficacy of two induction chemotherapy regimens-VA (Venetoclax + Azacitidine) and D/IA (Daunorubicin/Idarubicin + Cytarabine)-in elderly patients (aged 55-75) with acute myeloid leukemia (AML) who are fit for intensive chemotherapy.

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Extracted eligibility criteria

Treatments studied

Targeted therapy

Venetoclax

Chemotherapy

CytarabineAzacitidine

Other

Daunorubicin/Idarubicin

Cancer type

Acute Myeloid Leukemia

Biomarker criteria

Excluded: PML fusion with RARA

Acute promyelocytic leukemia with PML-RARA fusion gene

Excluded: RUNX1 fusion with RUNX1T1

AML with RUNX1-RUNX1T1 fusion gene

Excluded: CBFB fusion with MYH11

AML with CBFB-MYH11 fusion gene

Excluded: BCR fusion with ABL

AML with BCR-ABL fusion gene

Performance status

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

Demographics

Ages 55–75

Prior therapy

No prior treatment (treatment-naive required)
Max 0 prior lines

Cannot have received: induction chemotherapy

Exception: hydroxyurea is allowed

Relapsed or refractory AML (previously treated with induction chemotherapy, but hydroxyurea is allowed)

Lab requirements

Kidney function

Serum creatinine <2× ULN

Liver function

Total bilirubin ≤1.5× ULN; AST and ALT ≤2.5× ULN

Cardiac function

Cardiac enzymes <2× ULN; LVEF within normal range (by echocardiogram)

Adequate organ function: Total bilirubin ≤1.5× ULN; AST and ALT ≤2.5× ULN; Serum creatinine <2× ULN; Cardiac enzymes <2× ULN; LVEF within normal range

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

Frequently asked questions

Is NCT07132684 currently recruiting?

Yes, this trial is currently recruiting patients.

Can patients have received prior systemic therapy?

No. This trial requires treatment-naive patients — prior systemic therapy is an exclusion criterion.

Are patients with PML alterations eligible?

No. PML fusion with RARA is an exclusion criterion.

Are patients with RUNX1 alterations eligible?

No. RUNX1 fusion with RUNX1T1 is an exclusion criterion.

Is there an age limit?

Yes. Patients must be 75 years or younger and at least 55 years old.

Could you qualify for this trial?

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

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