TrialSignal
Clinical trial intelligence report
The Phase I Efficacy and Safety Clinical Study of GPC3-CAR-T Cells in Hepatocellular Carcinoma Patients
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jun 19, 2026
NCT ID
NCT04506983
Status
SUSPENDED
Phase
Phase 1
Sponsor
Beijing Tsinghua Chang Gung Hospital
Executive brief
Investment-Ready Snapshot
The GPC3-CAR-T cell therapy is positioned to address a significant unmet need in hepatocellular carcinoma (HCC), particularly for patients who have failed or are intolerant to first-line treatments. The market for HCC therapies is growing, with increasing incidence rates globally, especially in regions with high hepatitis prevalence. Competitive landscape includes existing immunotherapies and emerging CAR-T therapies targeting various antigens. The suspension of the trial for plan adjustments may indicate strategic recalibrations to enhance efficacy or safety profiles, which could impact timelines and investor confidence. Diligence should focus on regulatory pathways and potential partnerships with biotech firms specializing in CAR-T technologies.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT04506983
Indication
Hepatocellular Carcinoma
Modality
protein therapy
Target
Glypican-3 (GPC3), a cell membrane protein associated with hepatocellular carcinoma.
Intervention
GPC3-CAR-T cells
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.