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Clinical trial intelligence report
Prospective Non-randomized Phase I Study Investigating the Safety of CD19 CAR-T Cells in Patients With Refractory/Relapsed AML Expressing CD19.
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jun 19, 2026
NCT ID
NCT06649227
Status
RECRUITING
Phase
Phase 1
Sponsor
University Hospital, Lille
Executive brief
Investment-Ready Snapshot
The ongoing Phase I study at University Hospital, Lille, aims to evaluate the safety and efficacy of CD19 CAR-T cell therapy in patients with refractory/relapsed acute myeloid leukemia (AML) expressing CD19. Given the high unmet medical need in this patient population, particularly for those with the t(8;21) translocation, successful outcomes could position this therapy as a viable treatment option, potentially capturing a significant share of the AML market. The competitive landscape includes existing therapies such as bispecific monoclonal antibodies targeting CD19, but CAR-T therapies may offer a more durable response. The study's results could influence future investment and partnership opportunities, particularly with stakeholders interested in advanced cellular therapies.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT06649227
Indication
Relapsed Adult AML
Modality
gene therapy
Target
CD19 B-cell antigen
Intervention
CAR-T cell therapy
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.