drugset / Trial / NCT07487519

Phase II Study of HLX43 Monotherapy or Combined With Immune Checkpoint Inhibitors in Patients With Locally Advanced, Recurrent, or Metastatic Triple-negative Breast Cancer.

NCT07487519

Phase 2 Not yet recruiting 180 enrolled Shanghai Henlius Biotech
RandomizedParallel-groupOpen-labelTreatment

Summary

The study is being conducted to explore the reasonable dosage and evaluate the efficacy, safety and tolerability of HLX43 (Anti-PD-L1 ADC) as a monotherapy or in combination with immune checkpoint inhibitors in Subjects with locally advanced, recurrent or metastatic triple-negative breast cancer (TNBC).

Timeline

Start
2026-04-25
Primary completion
2027-05-15
Completion
2028-05-22

Drugs

EvaluationDrugModalityDoseRoute
Subject HLX43 Other / unclassified
Subject Serplulimab Monoclonal antibody