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NCT04506983SUSPENDEDanonymous

The Phase I Efficacy and Safety Clinical Study of GPC3-CAR-T Cells in Hepatocellular Carcinoma Patients

Sponsor

Source record

Beijing Tsinghua Chang Gung Hospital

Phase

Source record

Phase 1

Modality

AI-normalized

protein therapy

Target

AI-normalized

Glypican-3 (GPC3), a cell membrane protein associated with hepatocellular carcinoma.

Indication / condition

AI-normalized

Hepatocellular Carcinoma

Intervention

Source record

GPC3-CAR-T cells

Source & freshness

Source record

NCT ID

NCT04506983

Original source

ClinicalTrials.gov

Source last updated

Feb 14, 2022

Ingested at

Jun 19, 2026

Internal sync

Jun 19, 2026

Model version

trialsignal-ai-v1

Normalized confidence

96%

Validation status

validated

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NCT ID

NCT04506983

Title

The Phase I Efficacy and Safety Clinical Study of GPC3-CAR-T Cells in Hepatocellular Carcinoma Patients

Sponsor

Beijing Tsinghua Chang Gung Hospital

Status

SUSPENDED

Phase

Phase 1

Condition raw

Hepatocellular Carcinoma

Condition normalized

Hepatocellular Carcinoma

Modality raw

protein therapy

Modality normalized

protein therapy

Target raw

Glypican-3 (GPC3), a cell membrane protein associated with hepatocellular carcinoma.

Target normalized

Glypican-3 (GPC3), a cell membrane protein associated with hepatocellular carcinoma.

Interventions

GPC3-CAR-T cells

Public preview

Source record

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.

AI-generated analysis supports research triage only. Verify source records, publications, sponsor disclosures and IP databases before making diligence decisions. Model: trialsignal-ai-v1.

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