Safety and Efficacy of Hepatitis B Virus (HBV)-Specific T Cell Receptor (TCR)-T Cell Therapy Combined With Nucleos(t)Ide Analogues (NAs) in HBeAg-Positive Chronic Hepatitis B Patients

Status: Recruiting
Location: See location...
Intervention Type: Biological
Study Type: Interventional
Study Phase: Phase 1
SUMMARY

This is a open-label study to evaluate the safety and efficacy of autologous T-cells transfected with messenger ribonucleic acid (mRNA) encoding Hepatitis-B virus (HBV) antigen specific T cell receptor (TCR) in combination with nucleos(t)ide analogues (NAs) in HBeAg-positive and negative chronic hepatitis B patients.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 65
Healthy Volunteers: f
View:

• CHB infection (Serum HBsAg-positive for ≥ 6 months)

• Serum HBeAg-positive or negative

• HLA class 1 profile matching HLA-class I restriction element of the available T cell receptors (restricted by either HLA-A\*02:01, A\*11:01 or A\*24:02).

• Liver biopsy, Fibroscan or equivalent test obtained within the past 6 months demonstrating liver disease consistent with chronic HBV infection without evidence of bridging fibrosis or cirrhosis (≥Metavir 3).

Locations
Other Locations
China
Changhai Hospital
RECRUITING
Shanghai
Time Frame
Start Date: 2024-12-31
Estimated Completion Date: 2028-12-01
Participants
Target number of participants: 19
Treatments
Experimental: LioCyx-M (Autologous T-cells transfected with mRNA encoding HBV antigen specific TCR)
Escalating doses of LioCyx-M from 5×10E05 to 50×10E06 cells/kg body weight (BW), administered every two weeks.
Related Therapeutic Areas
Sponsors
Collaborators: Guangzhou Lion TCR Co Ltd
Leads: Changhai Hospital

This content was sourced from clinicaltrials.gov