TrialSignal
Clinical trial intelligence report
First-in-Human (FIH), Open-Label, Non-Randomized, Single-Arm Phase 1 Study to Evaluate the Safety and Tolerability of Donor-Derived CD5 CAR T Cells in Subjects with Relapsed or Refractory T-Cell Acute Lymphoblastic Leukemia
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jun 24, 2026
Report code
NCT05032599-Jun 24, 2026
NCT ID
NCT05032599
Status
TERMINATED
Phase
Phase 1
Sponsor
Beijing Boren Hospital
Executive brief
Investment-Ready Snapshot
The trial, sponsored by Beijing Boren Hospital, focuses on the use of donor-derived CD5 CAR T cells for treating relapsed or refractory T-cell acute lymphoblastic leukemia (T-ALL). Given the limited treatment options for this patient population, the asset addresses a significant unmet medical need. The competitive landscape includes other CAR T therapies targeting different antigens; however, CD5-targeted therapies may offer a unique approach in this niche. The termination of the trial due to an ethics committee decision raises concerns regarding regulatory and ethical compliance, which could impact future development and investor confidence. Further diligence is required to assess the implications of this termination on the asset's viability and potential market entry.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT05032599
Indication
T-Cell Acute Lymphoblastic Leukemia
Modality
protein therapy
Target
CD5 (Cluster of Differentiation 5)
Intervention
CD5 CART
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.