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Clinical Trial Summary

To compare the safety and efficacy of unmodified RAK cells and anti-TIM-3 blocked autologous RAK cells in preventing postoperative recurrence of HCC by postoperative TACE therapy combined with immune cell therapy.


Clinical Trial Description

Research process: Initial screening period (-7 to -1 days) • Sign an informed consent form; • Assign screening numbers; • Assessment of eligibility for initial screening. 1. Day 0 (period 1) - Reconfirm the inclusion and exclusion criteria; - 50-60ml of anticoagulant peripheral blood was sampled; Treatment time: 2. On (±2) days 15 and 16, Autologous RAK cells were reinfused for treatment (cycle 1). 3. TACE was performed on day 28 (±7). 4. Blood drawing from autologous RAK cells in the second cycle (week 10 ±7 days) 5. The second cycle of autologous RAK cell transfusion treatment (12 weeks ±7 days after hepatocellular carcinoma surgery); 6. Blood was drawn from autologous RAK cells in the third cycle (week 22 ±7 days); 7. Reinfusion of autologous RAK cells in the third cycle (week 24 ±7 days); After completing 3 cycles of treatment, the patients were assessed by the investigator to be under control or remission of disease after treatment, and then they were followed up for treatment ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05738980
Study type Interventional
Source Beijing Hospital
Contact Caixia Liu, master
Phone 010-85133662
Email liucxmm@163.com
Status Recruiting
Phase N/A
Start date February 1, 2023
Completion date December 31, 2026

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