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NCT06796803RecruitingPhase 2/3

Camrelizumab Combined With Rivoceranib and Hepatic Arterial Infusion Chemotherapy (HAIC) as Conversion Therapy for Potentially Resectable Hepatocellular Carcinoma(HCC)

Camrelizumab and Rivoceranib Plus HAIC as Conversion Therapy for Potentially Resectable Intermediate-advanced Hepatocellular Carcinoma: a Multicenter, Open-label, Randomized, Phase 2/3 Study

Source: ClinicalTrials.gov · Last updated 17 Jul 2026

Brief summary (registry, in English)

The purpose of this phase 2/3 study is to investigate the efficacy and safety of camrelizumab combined with rivoceranib and hepatic arterial infusion chemotherapy (HAIC) as conversion therapy for Potentially Resectable HCC.

Status (registry)
Recruiting
Phase (registry)
Phase 2/3
Study type
Interventional
Enrollment
398 (estimated)
First submitted
22 Jan 2025
Start date
20 Feb 2025
Primary completion date
20 Feb 2028
Lead sponsor
Shanghai Zhongshan Hospital
NCT number
NCT06796803

What you commit to

  • Study type: Interventional · Phase 2/3
  • Planned participants: 398
  • From 20 Feb 2025 to the primary completion date, 20 Feb 2028
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Prior locoregional therapy (such as TACE、TAE、HAIC、TARE)
  • Prior allogeneic stem cell or solid organ transplantation

Other illness

  • Other active malignant tumor except HCC within 5 years or simultaneously
  • History of hepatic encephalopathy

Other

  • Known fibrolamellar HCC, sarcomatoid HCC, or mixed cholangiocarcinoma and HCC
  • There is an absolute contraindication to HAIC
  • Diffuse HCC, intrahepatic tumor burden \> 50%
  • PVTT reaching the superior mesenteric vein, and bilateral PVTT are present
  • Clinically significant ascites

Who the study is looking for

  • Signed Informed Consent Form (ICF)
  • Aged ≥18 years and ≤75 years at time of signing ICF
  • Documented diagnosis of HCC confirmed by histology/cytology or clinically
  • Patients with BCLC stage B (the sum of number of tumors and the maximum diameter of the largest tumor exceeding Up-to-7 criteria) and BCLC stage C without extrahepatic metastasis: ① tumors confined to one lobe (left, right, or middle lobe), or tumors in one lobe are present alongside a single tumor with diameter ≤5 cm or up to three tumors each with diameter ≤3 cm in the remaining lobes; ②No PVTT involving the contralateral liver lobe or reaching the superior mesenteric vein. And no tumor thrombus of the inferior vena cava reaching right atrium
  • Patients with recurrence following prior radical surgical resection must have undergone the initial surgery at least 5 years prior to study entry
  • At least one measurable lesion (per RECIST v1.1) untreated lesion
  • ECOG performance status of 0 or 1
  • Child-Pugh ≤7 score
  • Life expectancy ≥12 weeks
  • Adequate organ function
  • No prior anti-tumor systemic therapies for HCC

Age in the registry: 18 years to 75 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Harbin Medical University Cancer Hospital
Coordinator of this site? Confirm its status
HarbinChinaRecruiting
Zhongshan Hospital
Coordinator of this site? Confirm its status
ShanghaiChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.