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Clinical trial intelligence report
Pilot Study of the Efficacy and Safety of CD38 Targeted Chimeric Antigen Receptor Engineered T-Cells in the Treatment of CD38 Positive Relapsed or Refractory Acute Myeloid Leukemia (AML)
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT04351022-Jul 28, 2026
NCT ID
NCT04351022
Status
UNKNOWN
Phase
Phase 1/2
Sponsor
The First Affiliated Hospital of Soochow University
Executive brief
Investment-Ready Snapshot
The pilot study evaluates CD38-targeted CAR T-cell therapy for relapsed or refractory acute myeloid leukemia (AML), a significant unmet medical need in hematological malignancies. The study's single-center design and open-label nature may limit generalizability but allows for focused data collection. The target population of CD38 positive AML patients presents a niche market opportunity, particularly as existing therapies may not effectively address relapsed cases. Competitive landscape analysis indicates a growing interest in CAR T-cell therapies, with several companies pursuing similar targets. Successful outcomes could position the sponsor favorably for partnerships or licensing agreements, enhancing their portfolio in immuno-oncology.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT04351022
Indication
Acute Myeloid Leukemia
Modality
protein therapy
Target
CD38
Intervention
CART-38
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.