CI

At a glance

ClinicalIndex Comparison Record
N/ARecruiting· 77 target
Drug / intervention
CAR-T cells +1 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/NCT06481241
NCT06481241N/ARecruitingMonitorUpdated 4mo ago · Completion was 1mo ago
Slow Enrollment
Monitor

Efficacy and Safety of Chemotherapy Combined With CAR-T Cells in Newly Diagnosed Adult Patients With Philadelphia Chromosome-Negative 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 and Venetoclax for Philadelphia Chromosome Negative ALL and Acute Lymphoblastic Leukemia, Adult. Currently recruiting, targeting 77 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 relapsed/refractory (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- B-ALL patients achieving complete remission (CR) with 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 10, 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

VEN