drugset / Trial / NCT06907615

A Phase II Clinical Study to Evaluate HLX43 in Subjects With Advanced Non-small Cell Lung Cancer (NSCLC)

NCT06907615

Phase 2 Recruiting 243 enrolled Shanghai Henlius Biotech Henlius USA · collab
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 Advanced Non-small Cell Lung Cancer (NSCLC)

Timeline

Start
2025-06-09
Primary completion
2028-04-20
Completion
2028-06-04

Drugs

EvaluationDrugModalityDoseRoute
Subject HLX43 Other / unclassified 2 mg/kg Intravenous
Subject HLX43 Other / unclassified 2.5 mg/kg Intravenous