CI

At a glance

ClinicalIndex Comparison Record
N/ARecruiting· 82 target
Drug / intervention
CAR-T cells +2 morecombination
Likely dose
Not stated in 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/NCT06481228
NCT06481228N/ARecruitingMonitorUpdated 4mo ago · Completion was 1mo ago
Slow Enrollment
Monitor

Efficacy and Safety of Molecular Targeted Therapy Combined With Chemotherapy and Sequential CAR-T Cells in Newly Diagnosed Adult Patients With Philadelphia Chromosome-Positive B-cell Acute Lymphoblastic Leukemia

Institute of Hematology & Blood Diseases Hospital, China·interventional·Posted Jul 1, 2024·Updated Mar 2, 2026

In Brief

A clinical study evaluating CAR-T cells, Venetoclax, and 1 other intervention for Philadelphia Positive Acute Lymphoblastic Leukemia and Acute Lymphoblastic Leukemia, Adult. Currently recruiting, targeting 82 participants across 1 site.

Signals

Enrolling slower than its timeline implies

Detailed Summary

In recent years, immunotherapy (eg. blinatumomab, inotuzumab ozogamicin, CAR-T cells) has demonstrated a high safety and efficacy profile in relapsed/refractory (R/R)B-ALL. The available data suggest that the advancement of immunotherapy from R/R field to the frontline setting may be an important approach to increase the depth of remission, which ultimately translates into a survival benefit. In this study, the investigators propose a treatment regimen using CAR-T cell therapy as a consolidation method for Ph+ ALL patients achieving complete remission (CR) with overembatinib, venetoclax and reduced-intensity chemotherapy, aiming to reduce the total cycles of chemotherapy and related toxicities, shorten length of hospitalization, and ultimately improve patients' survival and quality of life.The study endpoints include 2-year disease-free survival (DFS) rate, overall survival (OS) rate, event-free survival (EFS) rate, cumulative molecular remission rate, immune repertoire-minimal residual disease (MRD) remission rate, cumulative relapse rate, treatment-related toxicities, and quality of life. Additionally, an interim analysis will be conducted, with the 1-year DFS rate as the key index for this analysis.

Study Details

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

Timeline

N/ARecruiting
2025202620272028
First PostedJul 1, 2024
Enrollment StartJun 4, 2024
Primary CompletionJun 1, 2026
Study CompletionJun 1, 2028
TodayJul 1, 2026
Enrollment to primary: 2.0 yearsPosted 2 years ago

Interventions

CAR-T cellscombination

CAR-T cells as consolidation therapy

Venetoclaxdrug

BCL2 inhibitor

Olverembatinibdrug

TKI