drugset / Trial / NCT04948697

A Study Investigating the Efficacy and Safety of Ociperlimab and Tislelizumab and BAT1706 Combinations in Patients With Advanced HCC

NCT04948697

Phase 2 Completed 94 enrolled BeiGene
RandomizedParallel-groupOpen-labelTreatment

Summary

This was a Phase 2, randomized, multicenter, open-label, 2-arm study to investigate the efficacy and safety of ociperlimab in combination with tislelizumab plus BAT1706, and tislelizumab plus BAT1706, as first-line treatment in participants with advanced Hepatocellular Carcinoma (HCC).

Timeline

Start
2021-08-20
Primary completion
2024-02-01
Completion
2024-02-01

Drugs

EvaluationDrugModalityDoseRoute
Subject BAT1706 Unknown 15 mg/kg Intravenous
Subject Ociperlimab Monoclonal antibody 900 mg Intravenous
Subject Tislelizumab Monoclonal antibody 200 mg Intravenous