Clinical Trials Directory

Trials / Completed

CompletedNCT04393220

Combination of PD-1 and VEGFR-2 Blockade for Advanced Hepatocellular Carcinoma

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
60 (actual)
Sponsor
Fuda Cancer Hospital, Guangzhou · Academic / Other
Sex
All
Age
18 Years – 70 Years
Healthy volunteers
Not accepted

Summary

The aie of this clinical study is the safety and efficacy of combination therapy for HCC patients.

Detailed description

Activation of anti-tumor immune response using programmed death receptor-1 (PD-1)blockade showed benefit only in a fraction of hepatocellular carcinoma (HCC) patients. Specific blockade of vascular endothelial receptor 2 (VEGFR-2) using a murine antibody significantly delayed primary tumor growth but failed to prolong survival. Combining PD-1 blockade with antiangiogenesis has shown promise in substantially increasing the fraction of HCC patients who respond to treatment in vitro. Based on these clinical data, we are aimed to investigation the safety and efficacy of combination therapy for HCC patients.

Conditions

Interventions

TypeNameDescription
DRUGBevacizumab Injection15mg/kg (Q3W)
DRUGNivolumabnivolumab 480 mg IV infusions for 30 minutes q4w

Timeline

Start date
2020-05-11
Primary completion
2021-07-30
Completion
2021-08-31
First posted
2020-05-19
Last updated
2021-09-05

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT04393220. Inclusion in this directory is not an endorsement.