RecruitingPhase 2NCT06360042

Anti-PD-1/PD-L1 Combined With Anti-angiogenic Agents as First-line Treatment for Unresectable HCC

Anti-PD-1/PD-L1 Combined With Anti-angiogenic Agents as First-line Therapy for Unresectable Hepatocellular Carcinoma: a Multicenter, Randomized, Open-label Trial


Sponsor

Peking University Cancer Hospital & Institute

Enrollment

111 participants

Start Date

Jan 1, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

This is a multicenter, randomized, open-label clinical study to evaluate the efficacy and safety of Adebrelimab plus Apatinib (cohort 1), or Adebrelimab plus Bevacizumab (cohort 2), or Camrelizumab plus Apatinib (cohort 3) as first-line treatment of unresectable HCC.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is examining the real-world effectiveness of combining immune checkpoint therapy (anti-PD-1 or anti-PD-L1 drugs) with drugs that cut off blood supply to tumors (anti-angiogenic agents) as a first-line treatment for advanced liver cancer (hepatocellular carcinoma or HCC) that cannot be surgically removed. **You may be eligible if...** - You have locally advanced or metastatic unresectable hepatocellular carcinoma (HCC) - You have not previously received systemic (body-wide) treatment for HCC - Your cancer is classified as BCLC Stage B or C - You have at least one measurable lesion - Your liver function is relatively preserved (Child-Pugh class A5–B7) - You are in good general health (ECOG 0–1) **You may NOT be eligible if...** - You have a mixed type of liver cancer (e.g., cholangiocarcinoma component) - You have had prior immunotherapy or anti-angiogenic treatment - You have uncontrolled hepatitis B or C - You have serious heart, kidney, or autoimmune conditions - You are pregnant or breastfeeding Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGAdebrelimab plus Apatinib

Adebrelimab 1200mg intravenously every 3 weeks plus Apatinib 250mg orally once daily

DRUGAdebrelimab plus Bevacizumab

Adebrelimab 1200mg intravenously plus Bevacizumab 15 mg/kg intravenously every 3 weeks

DRUGCamrelizumab plus Apatinib

camrelizumab 200mg intravenously every 2 weeks plus Apatinib 250mg orally once daily


Locations(1)

Beijing Cancer Hospital

Beijing, Beijing Municipality, China

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NCT06360042


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