CI

At a glance

ClinicalIndex Comparison Record
Phase 3Recruiting· 154 target
Drug / intervention
targeted drugdrug
Likely dose
targeted drug 100mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT07203352
NCT07203352Phase 3RecruitingOn TrackUpdated 8mo ago

Efficacy and Safety of Targeted Drugs Combined With Chemotherapy in the Treatment of Patients With Newly Diagnosed Acute T-lymphocytic Leukemia

Nanfang Hospital, Southern Medical University·interventional·Posted Oct 2, 2025·Updated Oct 2, 2025

In Brief

A Phase 3 clinical trial evaluating targeted drug for Acute Lymphoblastic Leukemia. Currently recruiting, targeting 154 participants across 1 site.

Detailed Summary

This prospective, randomized, controlled trial evaluates the efficacy and safety of a new targeted drug combined with chemotherapy versus standard chemotherapy alone. Eligible patients were randomized 1:1 to either the treatment or control group.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesChina
Collaborators--

Timeline

Phase 3Recruiting
20262027
First PostedOct 2, 2025
Enrollment StartOct 1, 2025
Primary CompletionDec 1, 2026
Study CompletionDec 30, 2026
TodayJul 1, 2026
Enrollment to primary: 1.2 yearsPosted 9 months agoPrimary completion in 5 months

Interventions

targeted drugdrug

Patients randomly assigned to the control group will receive standard chemotherapy treatment, but they cannot use targeted drugs in combination.The subjects randomly assigned to the experimental group received targeted drug treatment in addition to the chemotherapy regimen during the second course. Based on the results of bone marrow PCR, subjects with molecular typing of ABL1/ABL2/PDGFRB fusion were to receive chemotherapy combined with dasatinib 100mg orally once a day; subjects with molecular typing of FLT3-ITD positive were to receive chemotherapy combined with sorafenib 400mg orally twice a day.