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OncoMatch/Clinical Trials/NCT06393985

Decitabine, Venetoclax and Blinatumomab for Maintenance Following HSCT in Patients With Ph-Negative B-ALL

Is NCT06393985 recruiting? Yes, currently enrolling (Jun 2026). This Phase 2 trial studies Decitabine, venetoclax and blinatumomab for b-cell acute lymphoblastic leukemia.

Phase 2RecruitingThe First Affiliated Hospital of Soochow UniversityNCT06393985Data as of Jun 2026Location: China

Treatment: Decitabine, venetoclax and blinatumomabThis study aims to evaluate whether maintenance therapy with decitabine, venetoclax and blinatumomab could improve the 2-year progression free survival (PFS) of patients with philadelphia chromosome-negative B-cell acute lymphoblastic leukemia who had recently received an allogeneic stem cell transplant and in measurable residual disease-negative remission.

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Extracted eligibility criteria

Treatments studied

Other

Decitabine, venetoclax and blinatumomab

Cancer type

Acute Lymphoblastic Leukemia

Biomarker criteria

Required: BCR fusion (negative)

fusion gene negative

Performance status

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

Demographics

Ages ≤ 65

Prior therapy

Must have received: allogeneic hematopoietic stem cell transplant

who underwent an alloHSCT

Lab requirements

Blood counts

hematopoietic reconstitution, i.e., ANC ≥0.5 x 10^9/L, and platelets >20 x 10^9/L

Kidney function

Creatinine clearance ≥ 30 mL/min

Liver function

Total serum bilirubin ≤ 3 x upper limit of normal (ULN), alanine aminotransferase (ALT) ≤ 5 x ULN, aspartate aminotransferase (AST) ≤ 5 x ULN

Cardiac function

left ventricular ejection fraction ≥ 0.5 by echocardiography; no grade III/IV cardiovascular dysfunction (NYHA)

hematopoietic reconstitution, i.e., ANC ≥0.5 x 10^9/L, and platelets >20 x 10^9/L. Total serum bilirubin ≤ 3 x upper limit of normal (ULN), alanine aminotransferase (ALT) ≤ 5 x ULN, aspartate aminotransferase (AST) ≤ 5 x ULN. Creatinine clearance ≥ 30 mL/min. left ventricular ejection fraction < 0.5 by echocardiography or grade III/IV cardiovascular dysfunction according to the New York Heart Association Classification [excluded].

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

Frequently asked questions

Is NCT06393985 currently recruiting?

Yes, this trial is currently recruiting patients.

Is prior treatment required for enrollment?

Yes. Patients must have previously received allogeneic hematopoietic stem cell transplant.

Does this trial require BCR?

Yes, BCR fusion is a required biomarker for enrollment.

Is there an age limit?

Yes. Patients must be 65 years or younger.

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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