Allogeneic Gamma-delta T Cells Combined With Targeted Therapy and Immunotherapy in a Phase 1 Clinical Trial for First-line Treatment of Hepatocellular Carcinoma
- Disease/Condition
- Hepatocellular Carcinoma
- Drug/Device/Intervention
- γδ T cells
- Study type
- Interventional
- Intervention type
- biological
- Primary sponsor
- Beijing 302 Hospital
- Phase
- Phase 1
- Start date
- Apr 26, 2024
- End date
- Sep 26, 2026
- Enrollment
- 18 participants
Safety evaluation: Incidence of Adverse events (AEs),Safety evaluation: Dose limited toxicity (DLTs),Safety evaluation: Maximum-tolerated dose (MTD),Efficacy evaluation: Objective Response Rate(ORR),Efficacy evaluation: Duration of Response(DOR),Efficacy evaluation: Progress Free Survival(PFS),Efficacy evaluation: Overall Survival (OS)
The purpose of this study is to evaluate the safety and efficacy of allogeneic γδ T cells
 combined with targeted therapy and PD-1 monoclonal antibody in first-line treatment of
 patients with hepatocellular carcinoma.
- Registry
- ClinicalTrials.gov
- Trial ID
- NCT06364787
- Type
- Non-Device Trial
Access comprehensive clinical trial information for NCT06364787 through Pure Global AI's free database. This Phase 1 trial is sponsored by Beijing 302 Hospital and is currently Not yet recruiting. The study focuses on Hepatocellular Carcinoma. Target enrollment is 18 participants.
This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.