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OncoMatch/Clinical Trials/NCT07152041

Newly-diagnosed Pediatric Ph-positive B-ALL Protocol

Is NCT07152041 recruiting? Yes, currently enrolling (Jun 2026). This Phase 3 trial studies olverembatinib for acute lymphoblastic leukemia (all) philadelphia chromosome-positive (ph+).

Phase 3RecruitingInstitute of Hematology & Blood Diseases Hospital, ChinaNCT07152041Data as of Jun 2026Location: China · Hong Kong

Treatment: olverembatinibThis prospective clinical trial evaluates the effectiveness and safety of "chemotherapy-light" regimen incorporating the third-generation TKI olverembatinib, the bi-specific CD3/CD19 T cell engager blinatumomab, and the BCL-2 selective inhibitor venetoclax for newly diagnosed pediatric/adolescent patients with Ph+ ALL. The CCCG-Ph+ B-ALL-2025 protocol will be modified as following compared to the CCCG-ALL-2020 protocol

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Extracted eligibility criteria

Treatments studied

Targeted therapy

olverembatinib

Cancer type

Acute Lymphoblastic Leukemia

Biomarker criteria

Required: ABL1 fusion

Required: BCR fusion

Demographics

Ages 0–18

Prior therapy

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

Cannot have received: glucocorticoid

Exception: less than 14 days within one month before enrollment

Treated with glucocorticoids for ≥14 days within one month before enrollment

Cannot have received: targeted inhibitor

Exception: less than or equal to 7 days within one month before enrollment

targeted inhibitor for > 7 days within one month before enrollment

Cannot have received: chemotherapy

any chemotherapy or any systemic anticancer therapy (including but not limited to any TKI) or radiotherapy within 3 months before enrollment (except for emergency radiotherapy to relieve airway compression)

Cannot have received: systemic anticancer therapy

any chemotherapy or any systemic anticancer therapy (including but not limited to any TKI) or radiotherapy within 3 months before enrollment (except for emergency radiotherapy to relieve airway compression)

Cannot have received: tyrosine kinase inhibitor

any chemotherapy or any systemic anticancer therapy (including but not limited to any TKI) or radiotherapy within 3 months before enrollment (except for emergency radiotherapy to relieve airway compression)

Cannot have received: radiotherapy

Exception: emergency radiotherapy to relieve airway compression

any chemotherapy or any systemic anticancer therapy (including but not limited to any TKI) or radiotherapy within 3 months before enrollment (except for emergency radiotherapy to relieve airway compression)

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

Frequently asked questions

Is NCT07152041 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 ABL1?

Yes, ABL1 fusion is a required biomarker for enrollment.

Does this trial require BCR?

Yes, BCR fusion is a required biomarker for enrollment.

Is there an age limit?

Yes. Patients must be 18 years or younger and at least 0 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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