RecruitingNCT06537908

Anti-PD-1/PD-L1 Antibodies Plus Anti-VEGF Antibody Treatment in Patients With Advanced-Stage HCC

Phase I/II Study of Anti-PD-1/PD-L1 Antibodies Combined With Anti-VEGF Antibody Treatment in Patients With Advanced-Stage Hepatocellular Carcinoma


Sponsor

Shanghai Zhongshan Hospital

Enrollment

50 participants

Start Date

Aug 1, 2024

Study Type

OBSERVATIONAL

Conditions

Summary

This study is being done to analyze the safety, tolerability, and efficacy of treatment using combination of anti-VEGF and anti-PD-1/PDL1 antibodies for patients with advanced hepatocellular carcinoma.


Eligibility

Min Age: 18 YearsMax Age: 90 Years

Plain Language Summary

Simplified for easier understanding

This study examines how well the combination of an immunotherapy drug (anti-PD-1/PD-L1) and an anti-VEGF drug (which blocks tumor blood vessel growth) works in patients with advanced liver cancer (hepatocellular carcinoma, or HCC) that cannot be surgically removed. **You may be eligible if...** - You are 18 or older with advanced HCC that is inoperable or has spread - You have at least one measurable tumor that has not been treated locally - Your liver function is classified as Child-Pugh A (well-preserved) - Your cancer stage is Barcelona B or C - You are in good physical condition (ECOG 0 or 1) **You may NOT be eligible if...** - Your liver function is significantly impaired - You have had prior treatments that would exclude you per study criteria - You are pregnant or need contraception but refuse to use it 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

DRUGAnti-PD-1/PD-L1 antibodies

Anti-PD-1/PD-L1 Intravenous injection for at least 6 months

DRUGAnti-VEGF

Anti-VEGF Intravenous injection for at least 6 months


Locations(1)

Zhongshan Hospital Fudan university

Shanghai, China

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NCT06537908


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