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OncoMatch/Clinical Trials/NCT06990321

Effectiveness of Medium-Dose Cytarabine Combined With Venetoclax for Consolidation Therapy in Elderly Patients With Intermediate to High-Risk Acute Myeloid Leukemia

Is NCT06990321 recruiting? Yes, currently enrolling (Jun 2026). This Phase 3 trial studies Intermediate-dose Cytarabine in Combination with Venetoclax for acute myeloid leukemia (aml).

Phase 3RecruitingYehui TanNCT06990321Data as of Jun 2026Location: China

Treatment: Intermediate-dose Cytarabine in Combination with VenetoclaxA Single-center, Single-arm, Prospective Clinical Study of Intermediate-dose Cytarabine in Combination with Venetoclax for Consolidation Therapy of Middle- and High-risk Acute Myeloid Leukemia in the Elderly

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Extracted eligibility criteria

Treatments studied

Other

Intermediate-dose Cytarabine in Combination with Venetoclax

Cancer type

Acute Myeloid Leukemia

Performance status

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

Demographics

Ages 60–75

Prior therapy

Must have received: induction therapy

AML patients who achieve remission with morphologic assessment of bone marrow showing no leukemic involvement after induction therapy

Lab requirements

Kidney function

Serum creatinine < 2x ULN

Liver function

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

Cardiac function

Ejection fraction within normal limits as determined by echocardiogram

Total bilirubin ≤ 1.5x ULN; AST and ALT ≤ 2.5x ULN; Serum creatinine < 2x ULN; Cardiac ejection fraction within normal limits as determined by echocardiogram

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

Frequently asked questions

Is NCT06990321 currently recruiting?

Yes, this trial is currently recruiting patients.

Is prior treatment required for enrollment?

Yes. Patients must have previously received induction therapy.

Is there an age limit?

Yes. Patients must be 75 years or younger and at least 60 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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