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OncoMatch/Clinical Trials/NCT06886074

Efficacy of Short-course Blinatumomab for MRD Erradication in B-ALL

Is NCT06886074 recruiting? Yes, currently enrolling (Jun 2026). This Phase 2 trial studies Short course of blinatumomab for acute lymphoblastic leukemia.

Phase 2RecruitingHospital Universitario Dr. Jose E. GonzalezNCT06886074Data as of Jun 2026Location: Mexico

Treatment: Short course of blinatumomabDetectable measurable residual disease (MRD) is the most important prognostic factor for B-cell acute lymphoblastic leukemia (B-ALL) for overall survival (OS) and disease-free survival (DFS). Patients who are MRD positive and have no access to novel immunotherapies should receive an allogeneic hematopoietic stem cell transplantation (HSCT). Blinatumomab is considered a standard of care (SOC) for this group of patients, however, the ideal treatment dose for MRD is unknown as doses were adjusted from the relapsed/refractory setting. Preliminary data suggest short cycles of blinatumomab can also be effective in states of lower disease burden prior to transplant. Thus, the investigators are performing a phase 2 trial assessing 7 days of blinatumomab as a bridge to HSCT Primary endpoint is assessing the MRD response following a short-course blinatumomab infusion in patients with B-ALL with complete response (CR) and have detectable MRD disease who are candidates for HSCT. Secondary endpoints include incidence of adverse events, OS, DFS, percentage of patients who receive HSCT, incidence of cytokine release syndrome (CRS) and immune effector cell associated neurotoxicity syndrome (ICANS)

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Extracted eligibility criteria

Treatments studied

Other

Short course of blinatumomab

Cancer type

Acute Lymphoblastic Leukemia

Biomarker criteria

Required: BCR wild-type

Philadelphia chromosome-negative

Performance status

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

Demographics

Ages 16–60

Prior therapy

Cannot have received: bispecific antibody (blinatumomab)

Having previously received blinatumomab

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

Frequently asked questions

Is NCT06886074 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior bispecific antibody disqualifies patients from enrollment.

Does this trial require BCR?

Yes, BCR wild-type is a required biomarker for enrollment.

Is there an age limit?

Yes. Patients must be 60 years or younger and at least 16 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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