OncoMatch/Clinical Trials/NCT07100392
Tauroursodeoxycholic Acid (TUDCA) Plus Camrelizumab and Regorafenib in Hepatocellular Carcinoma Previously Treated With Anti-PD1/PD-L1 and Bevacizumab
Is NCT07100392 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies multiple treatments including tauroursodeoxycholic acid (TUDCA) and Camrelizumab for hepatocellular carcinoma (hcc).
Treatment: tauroursodeoxycholic acid (TUDCA) · Camrelizumab · Regorafenib — To evaluate the efficacy and safety of Tauroursodeoxycholic Acid (TUDCA) plus Camrelizumab and Regorafenib for patients with advanced hepatocellular carcinoma (HCC) who have progressed on prior systemic treatment with Anti-PD1/PD-L1 plus bevacizumab combination.
Check if I qualifyExtracted eligibility criteria
Cancer type
Hepatocellular Carcinoma
Performance status
ECOG 0–2(Ambulatory, capable of self-care)
Prior therapy
Must have received: anti-PD-1 therapy — combination with bevacizumab
Disease progression following prior anti-PD1/PD-L1 plus bevacizumab combination treatment for HCC.
Lab requirements
Blood counts
absolute neutrophil count ≥ 1,500/L, platelets ≥60 x10^3/L
Kidney function
Serum Creatinine ≤ 1.5 x institutional ULN or creatinine clearance (CrCl) ≥ 30 mL/min (if using the Cockcroft-Gault formula)
Liver function
Total bilirubin ≤ 3x upper normal limit; AST/ALT ≤ 5x upper normal limit; INR ≤1.25; Albumin ≥ 31 g/dL; Child-Pugh scores 5-7
Adequate blood count, liver-enzymes, and renal function: absolute neutrophil count ≥ 1,500/L, platelets ≥60 x103/L; Total bilirubin ≤ 3x upper normal limit; Aspartate Aminotransferase (SGOT), Alanine aminotransferase (SGPT) ≤ 5 x upper normal limit (ULN); International normalized ratio (INR) ≤1.25; Albumin ≥ 31 g/dL; Serum Creatinine ≤ 1.5 x institutional ULN or creatinine clearance (CrCl) ≥ 30 mL/min (if using the Cockcroft-Gault formula)
Structured fields extracted by AI. May contain errors — verify against the official protocol.
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