Allogeneic Gamma-delta T Cells Combined With Targeted Therapy and Immunotherapy in a Phase 1 Clinical Trial for First-line Treatment of Hepatocellular Carcinoma - Trial NCT06364787
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.
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Study Focus
Sponsor & Location
Beijing 302 Hospital
Timeline & Enrollment
Phase 1
Apr 26, 2024
Sep 26, 2026
Primary Outcome
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)
Summary
The purpose of this study is to evaluate the safety and efficacy of allogeneic ฮณฮด T cells
 combined with targeted therapy and PD-1 monoclonal antibody in first-line treatment of
 patients with hepatocellular carcinoma.
ICD-10 Classifications
Data Source
ClinicalTrials.gov
NCT06364787
Non-Device Trial