CI

At a glance

ClinicalIndex Comparison Record
Phase 3Recruiting· 150 target
Drug / intervention
olverembatinibdrug
Likely dose
olverembatinib 1 gfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

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Search/NCT07152041
NCT07152041Phase 3RecruitingOn TrackUpdated 9mo ago

A Phase 3, Multicenter Trial for Pediatric Philadelphia Chromosome-positive B-Acute Lymphoblastic Leukemia -2025 Project

Institute of Hematology & Blood Diseases Hospital, China·interventional·Posted Sep 3, 2025·Updated Sep 3, 2025

In Brief

A Phase 3 clinical trial evaluating olverembatinib for Acute Lymphoblastic Leukemia (ALL) Philadelphia Chromosome-positive (Ph+) and Childhood Leukemia, Acute Lymphoblastic. Currently recruiting, targeting 150 participants across 24 sites in 2 countries.

Detailed Summary

This 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

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesChina, Hong Kong
Collaborators--

Timeline

Phase 3Recruiting
20262027202820292030
First PostedSep 3, 2025
Enrollment StartMar 28, 2025
Primary CompletionDec 1, 2029
Study CompletionJun 1, 2030
TodayJul 1, 2026
Enrollment to primary: 4.7 yearsPosted 10 months agoPrimary completion in 3.4 years

Interventions

olverembatinibdrug

All Ph+-ALL patients will uniformly use the 3rd generation of TKI olverembatinib (OVB) instead of dasatinib throughout the regimen. OVB is combined with Vincristine and Prednisone (VP) during the first 2 weeks and with blinatumomab during the last 4 weeks of remission induction in this protocol. Patients will receive blinatumomab for 28 days as induction instead of CAT to improve induction response and avoid toxicity. All patients will receive two cycles of HDMTX+Blina-14 and 4 times of triple intrathecal therapy (TIT) throughout the consolidation 1 phase. To decrease the toxicities of high-dose AraC, the dosage will be reduced to 1 g/m2 in the consolidation 2 phase in contrast to 2 g/m2 in 2020 protocol. Throughout the early Maintenance Therapy, dexamethasone and vincristine combination will be added with either venetoclax or daunorubicin alternatively for five cycles, given after MTX and 6-MP.