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NCT04430530 · ClinicalTrials.gov record · last posted 2026-08-24

4SCAR-T Therapy Post CD19-targeted Immunotherapy

StatusTerminated
PhasePhase 1/2
Started2026-06-01
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from the ClinicalTrials.gov record
This study will evaluate safety and efficacy of a combination of 4th generation chimeric antigen receptor gene-modified T cells (4SCAR-T) targeting CD19-negative B-ALL that express alternative surface antigens such as CD22, CD10, CD20, CD38, and CD123, as many patients relapse after anti-CD19 immunotherapy. Clinical response and optiminzation of a standardized lentiviral vector and cell production protocol will be investigated. This is a phase I/II trial enrolling patients from multiple clinical centers.

Protocol amendment history 3 changes detected by DataLookout

2026-08-25
critical
Trial terminated
2026-08-25
minor
Primary completion moved earlier: 2029-12-31 → 2026-07-01
2026-08-25
minor
Completion moved earlier: 2030-12-31 → 2026-07-31
Trial Details
NCT Number NCT04430530
Lead Sponsor Shenzhen Geno-Immune Medical Institute
Conditions CD19 Negative B-cell Malignancies
Enrollment 100 participants
Start Date 2026-06-01
Primary Completion 2026-07-01 (estimated)
Study Completion 2026-07-31 (estimated)
Updated on ClinicalTrials.gov 2026-08-24