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Clinical trial intelligence report
A Phase I/II Study to Evaluate the Safety and Efficacy of Anti-CLL1-CD33-NKG2D Bicephali CAR-T Cells in Patients With Relapsed/Refractory Acute Myeloid Leukemia
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT07370064-Jul 28, 2026
NCT ID
NCT07370064
Status
NOT_YET_RECRUITING
Phase
Phase 1/2
Sponsor
Xuzhou Medical University
Executive brief
Investment-Ready Snapshot
The clinical trial sponsored by Xuzhou Medical University aims to evaluate a novel CAR-T cell therapy targeting relapsed/refractory acute myeloid leukemia (AML). Given the high unmet medical need in this patient population, successful outcomes could position this therapy as a competitive alternative to existing treatments, potentially capturing significant market share in the CAR-T space. The collaboration with Yake Biotechnology Ltd. may enhance development capabilities and commercialization prospects. However, the trial's not-yet-recruiting status indicates that market entry is still several years away, with estimated completion in 2029. Stakeholders should monitor the evolving landscape of AML therapies and the competitive positioning of this asset as it progresses through clinical development.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT07370064
Indication
AML (Acute Myeloid Leukemia)
Modality
protein therapy
Target
Anti-CLL1, CD33, NKG2D receptors on leukemia cells
Intervention
CAR-T
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.