CNClinicalTrials.govClinical trialPhase 3Not yet recruiting
A Study of TACE in Combination With SHR-8068, Adebrelimab, and Bevacizumab Versus TACE in Participants With Incurable Hepatocellular Carcinoma
Official record
- Identifier
NCT07691762- Recruiting locations
country
China- Interventions studied
- SHR-8068 + Adebrelimab + BevacizumabSHR-8068 Placebo + Adebrelimab Placebo + Bevacizumab PlaceboSHR-8068 Placebo + Adebrelimab + Bevacizumab
- Lead sponsor
- Suzhou Suncadia Biopharmaceuticals Co., Ltd.
- Target enrolment
- 690 participants
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Status
- Not yet recruiting
- First posted
- Jul 9, 2026
- Last updated on the registry
- Sep 28, 2026
- Age
- 18 Years – 75 Years
- Sex
- ALL
- Study contact
- The official record lists a study contact. Contact details are published there and are intentionally not copied to this page.
- Eligibility criteria
Reproduced verbatim from the official record. Eligibility is decided by the study team, never by this page.
Inclusion Criteria: 1. Age 18-75 years old, male or female; 2. Diagnosis confirmed HCC by pathologically or clinically; 3. At least one measurable lesion; 4. Child-Pugh liver function grade A; 5. ECOG-PS score: 0 or 1; 6. Eligible for TACE treatment as assessed by the investigator; 7. Participants with HBV or HCV infection must be on and remain on standard antiviral therapy throughout the study period; 8. Consent to contraception. Exclusion Criteria: 1. Fibrolamellar hepatocellular carcinoma, sarcomatoid hepatocellular carcinoma or mixed cholangiocarcinoma / hepatocellular carcinoma; Participants with other malignancies currently or within the past 5 years; 2. Participants with any active, known or suspected autoimmune disorder; 3. Participants with hypertension which cannot be well controlled by antihypertensives; 4. Uncontrolled cardiac diseases or symptoms; 5. Participants with hepatic encephalopathy; 6. Prior esophageal and/or gastric varices bleeding within 6 months prior to initiation of study treatment; 7. History of gastrointestinal perforation and/or fistula; 8. Participants with other potential factors that may affect the study results.
- Indexed under
- Liver Cancer