OncoMatch

OncoMatch/Clinical Trials/NCT06927466

A Clinical Study to Evaluate the Safety, Tolerability, and Preliminary Efficacy of B019 Injection in Subjects With Relapsed or Refractory B-cell Acute Lymphoblastic Leukemia.

Is NCT06927466 recruiting? Yes, currently enrolling (Jun 2026). This Phase 1 trial studies B019 for relapsed or refractory b-cell acute lymphoblastic leukemia.

Phase 1RecruitingShanghai Pharmaceutical Group Biological Therapy Technology Co., Ltd.NCT06927466Data as of Jun 2026Location: China

Treatment: B019The purpose of the study is to evaluate the safety and tolerability of B019 in subjects.

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Extracted eligibility criteria

Treatments studied

Other

B019

Cancer type

Acute Lymphoblastic Leukemia

Biomarker criteria

Required: CD19 expression

Required: CD22 expression

Demographics

Ages 3–25

Prior therapy

Cannot have received: CAR-T cell therapy

Has had treatment with any prior CAR-T therapy

Lab requirements

Kidney function

Liver function

Cardiac function

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

Frequently asked questions

Is NCT06927466 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior CAR-T cell therapy disqualifies patients from enrollment.

Does this trial require CD19?

Yes, CD19 expression is a required biomarker for enrollment.

Does this trial require CD22?

Yes, CD22 expression is a required biomarker for enrollment.

Is there an age limit?

Yes. Patients must be 25 years or younger and at least 3 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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