Trials / Recruiting
RecruitingNCT06961617
Autologous HBV-TCR T Cell Therapy (LioCyx-M) for the Treatment of Hepatocellular Carcinoma
Safety and Efficacy of Autologous HBV-TCR T Cell Therapy (LioCyx-M) for the Treatment of Hepatocellular Carcinoma
- Status
- Recruiting
- Phase
- Phase 1
- Study type
- Interventional
- Enrollment
- 10 (estimated)
- Sponsor
- Lion TCR Pte. Ltd. · Industry
- Sex
- All
- Age
- 18 Years – 70 Years
- Healthy volunteers
- Not accepted
Summary
This is a single center and open-label study to determine the safety and efficacy of mRNA HBV-TCR redirected T-cells in HBV-related HCC who are not amenable to/failed conventional treatment.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | LioCyx-M, HBV antigen-specific TCR-redirected T cells | Via intravenous (IV) infusion |
Timeline
- Start date
- 2024-06-01
- Primary completion
- 2027-12-01
- Completion
- 2028-12-01
- First posted
- 2025-05-08
- Last updated
- 2025-05-08
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT06961617. Inclusion in this directory is not an endorsement.