drugset / Trial / NCT04728321

A Study of Anti-PD-1/CTLA-4 Bispecific AK104 Alone or in Combination With Lenvatinib in Advanced Hepatocellular Carcinoma

NCT04728321 ↗

Phase 2 Completed 32 enrolled Akeso Akeso Pharmaceuticals, Inc. · collab
Non-randomizedSingle-groupOpen-labelTreatment

Summary

An open-label multi-center phase II study to evaluate the efficacy and safety of anti-PD-1/CTLA-4 bispecific antibody AK104 alone or in combination with lenvatinib in patients with advanced hepatocellular carcinoma.

Timeline

Start
2021-01-27
Primary completion
2022-08-02
Completion
2023-08-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Cadonilimab Monoclonal antibody 15 mg/kg Intravenous
Subject Lenvatinib Small molecule 8 mg Oral
Subject Lenvatinib Small molecule 12 mg Oral