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A Single-center, Prospective, Exploratory Clinical Study

StatusNot Yet Recruiting
PhaseNot applicable
Started2026-08
View on ClinicalTrials.gov ↗
This study is designed as a prospective, single-arm, exploratory clinical trial based on lishatoclax, enrolling three independent cohorts of patients with Philadelphia chromosome-positive (Ph⁺) ALL, Philadelphia chromosome-negative (Ph-) ALL, and T-cell ALL (T-ALL). By investigating the combination of lishatoclax with established standard chemotherapy, targeted agents (e.g., tyrosine kinase inhibitors, TKIs), or immunotherapies, this study aims to further improve the remission rates across all ALL subtypes, and to develop a more effective and less toxic novel therapeutic strategy for ALL, thereby addressing the unmet clinical needs in current practice.
Trial Details
NCT Number NCT07795099
Lead Sponsor LanZhou University
Conditions Acute Lymphoblastic Leukemia
Enrollment 30 participants
Start Date 2026-08
Primary Completion 2029-08 (estimated)
Study Completion 2029-08 (estimated)
Updated on ClinicalTrials.gov 2026-08-31