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A Clinical Study on the Safety and Effectiveness of Donor Derived CD19 CAR-T Cells in the Treatment of R/R B-cell Acute Lymphoblastic Leukemia
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jun 24, 2026
Report code
NCT06793241-Jun 24, 2026
NCT ID
NCT06793241
Status
RECRUITING
Phase
Early Phase 1
Sponsor
Zhejiang University
Executive brief
Investment-Ready Snapshot
The clinical trial is sponsored by Zhejiang University and aims to evaluate the safety and effectiveness of donor-derived CD19 CAR-T cells in treating relapsed or refractory B-cell acute lymphoblastic leukemia (R/R B-ALL). Given the increasing prevalence of R/R B-ALL and the growing demand for innovative therapies, this trial positions itself in a competitive landscape dominated by established CAR-T therapies such as Kymriah (Novartis) and Yescarta (Gilead). The trial's focus on donor-derived cells may offer a novel approach that could address limitations associated with autologous CAR-T therapies, such as preparation failures and patient eligibility. Successful outcomes could enhance market positioning and attract potential partnerships or acquisitions, particularly from companies looking to expand their oncology portfolios.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT06793241
Indication
B-cell Acute Lymphoblastic Leukemia
Modality
protein therapy
Target
CD19 (Chimeric Antigen Receptor T-cell therapy)
Intervention
CD19 B-cell Acute Lymphoblastic Leukemia Targeted CAR T-cells injection
Source record
Protocol Description
Detailed source ingestion pending.
Source record
Outcome Measures
Detailed source ingestion pending.
Source record
Eligibility
Detailed source ingestion pending.
AI analysis
Known Results And Readout Context
Detailed source ingestion pending.
IP intelligence
Patent And IP Landscape
Detailed source ingestion pending.
Source record
Contacts
Detailed source ingestion pending.