drugset / Trial / NCT05185739

Perioperative Pembrolizumab and Lenvatinib in Resectable Hepatocellular Carcinoma (HCC)

NCT05185739

RandomizedParallel-groupOpen-labelTreatment

Summary

This is a multicentre randomised 3-arm phase II clinical trial in patients with resectable Hepatocellular Carcinoma (HCC). Sixty patients will be randomized 1:1:1 to 6 weeks of pre-operative therapy with: pembrolizumab, lenvatinib or the combination of pembrolizumab and lenvatinib followed by up to 12 months treatment with post-operative pembrolizumab. The aim of the study is to compare the efficacy of pembrolizumab combined with lenvatinib with that of pembrolizumab and lenvatinib alone in terms of major pathological response in patients with resectable HCC. Major pathological response will be defined by the proportion of patients with less than 10% viable tumour at resection.

Timeline

Start
2022-08-25
Primary completion
2028-07
Completion
2030-07

Drugs

EvaluationDrugModalityDoseRoute
Comparator Lenvatinib Small molecule 8 mg Oral
Comparator Lenvatinib Small molecule 12 mg Oral
Comparator Pembrolizumab Monoclonal antibody 200 mg Intravenous