15
Participants
Start Date
May 7, 2025
Primary Completion Date
December 31, 2026
Study Completion Date
December 31, 2026
Combining the QH-1A bioartificial liver device with mesenchymal stem cells for blood purification(4 hours)
The 4-hour group treatment session lasts 4 hours (±15 minutes). In the HBAL mode of the combined bioartificial liver device QH-1A, blood is initially filtered to separate the plasma, which is then pumped into a bioreactor. In this study, this bioreactor is uniquely filled with immortalized mesenchymal stem cells (PT-MSCs) optimized for blood purification. These cells are cultured to adhere to the outer surface of hollow fibers within the bioreactor, creating a stable and efficient living interface that continuously secretes bioactive factors such as exosomes.After passing through the bioreactor, the plasma is re-filtered and then returned to the patient's circulation via a dedicated pump.
Combining the QH-1A bioartificial liver device with mesenchymal stem cells for blood purification(6 hours)
After the three subjects in the 4-hour group completed their 4-week follow-up, the Safety Evaluation Committee convened a meeting to review the safety data and determine whether to proceed with the recruitment for the 6-hour group.The 6-hour group treatment session lasts 6 hours (±15 minutes).The treatment procedure is identical to that of the 4-hour group.
Combining the QH-1A bioartificial liver device with mesenchymal stem cells for blood purification(8 hours)
After the three subjects in the 6-hour group completed their 4-week follow-up, the Safety Evaluation Committee convened a meeting to review the safety data and determine whether to proceed with the recruitment for the 8-hour group. The 8-hour group treatment session lasts 8 hours (±15 minutes).The treatment procedure is identical to that of the 4-hour group.
Combining the QH-1A bioartificial liver device with mesenchymal stem cells for blood purification(Multiple-treatment)
Subjects in the multiple-treatment group will receive 2-3 sessions of bioartificial liver treatment; the number of sessions will be determined by the investigators based on the subjects' clinical needs. The treatment duration for each session will be set as the maximum tolerable period, as confirmed by the Safety Evaluation Committee based on 28-day safety observations from the 4-hour, 6-hour, and 8-hour groups. Each treatment session is administered following the procedure applied to patients in the group with the optimal tolerability duration.
Third Affiliated Hospital, Sun Yat-sen University, Guangzhou
Guangdong Qianhui Biotechnology Co., Ltd
UNKNOWN
Third Affiliated Hospital, Sun Yat-Sen University
OTHER