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OncoMatch/Clinical Trials/NCT06429098

Study of A Venetoclax-based, Anthracycline-free Regimen in Newly Diagnosed CBFβ::MYH11(+) AML

Is NCT06429098 recruiting? Yes, currently enrolling (Jun 2026). This Phase 2 trial studies multiple treatments including Venetoclax and azacitidine for acute myeloid leukemia.

Phase 2RecruitingThe First Affiliated Hospital of Soochow UniversityNCT06429098Data as of Jun 2026Location: China

Treatment: Venetoclax · azacitidine · decitabine · CytarabineThis investigator-initiated, single-arm, phase II trial is aimed to evaluate the efficacy and safety of a venetoclax-based, anthracycline-free regimen in patients with newly diagnosed CBFβ::MYH11-positive acute myeloid leukemia.

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Extracted eligibility criteria

Treatments studied

Targeted therapy

Venetoclax

Chemotherapy

azacitidinedecitabineCytarabine

Cancer type

Acute Myeloid Leukemia

Biomarker criteria

Required: CBFB cbfβ::myh11 fusion

Performance status

ECOG 0–3(Limited self-care)

Prior therapy

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

Cannot have received: hypomethylating agent

Exception: oral hydroxyurea and/or leukocytometry to reduce white blood cell count

Subject has received treatment with a hypomethylating agent and/or other chemotherapeutic agents either conventional or experimental or targeted drug therapy for AML (except oral hydroxyurea and/or leukocytometry to reduce white blood cell count)

Cannot have received: chemotherapeutic agent

Exception: oral hydroxyurea and/or leukocytometry to reduce white blood cell count

Subject has received treatment with a hypomethylating agent and/or other chemotherapeutic agents either conventional or experimental or targeted drug therapy for AML (except oral hydroxyurea and/or leukocytometry to reduce white blood cell count)

Cannot have received: targeted drug therapy

Exception: oral hydroxyurea and/or leukocytometry to reduce white blood cell count

Subject has received treatment with a hypomethylating agent and/or other chemotherapeutic agents either conventional or experimental or targeted drug therapy for AML (except oral hydroxyurea and/or leukocytometry to reduce white blood cell count)

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

Frequently asked questions

Is NCT06429098 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.

Does this trial require CBFB?

Yes, CBFB cbfβ::myh11 fusion is a required biomarker for enrollment.

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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