drugset / Trial / NCT06742892

A Phase II Clinical Study to Evaluate HLX43 in Patients With Locally Advanced or Metastatic HCC Failed or Intolerance to Standard Therapy

NCT06742892

Phase 2 Recruiting 90 enrolled Shanghai Henlius Biotech
RandomizedParallel-groupOpen-labelTreatment

Summary

The study is being conducted to to explore the reasonable dosage and evaluate the efficacy, safety and tolerability of HLX43 (Anti-PD-L1 ADC) in Patients with Locally Advanced or Metastatic Hepatocellular Carcinoma (HCC) Failed or Intolerance to Standard Therapy

Timeline

Start
2025-03-03
Primary completion
2026-10-31
Completion
2027-06-05

Drugs

EvaluationDrugModalityDoseRoute
Subject HLX43 Other / unclassified Intravenous