drugset / Trial / NCT03916094

Evaluate Safety, Tolerability and Pharmacokinetics of HLX22 in Patients With Advanced Solid Tumors Overexpressing HER2

NCT03916094

Phase 1 Completed 11 enrolled Shanghai Henlius Biotech
NaSingle-groupOpen-labelTreatment

Summary

a single-center, open-label, dose-escalation Phase I clinical trial to evaluate the safety and the tolerability of HLX22 in patients with advanced solid tumors overexpressing HER2 after failure of standard of care.

Timeline

Start
2019-07-31
Primary completion
2021-01-04
Completion
2021-12-27

Drugs

EvaluationDrugModalityDoseRoute
Subject HLX22 Monoclonal antibody 3 mg/kg Intravenous
Subject HLX22 Monoclonal antibody 10 mg/kg Intravenous
Subject HLX22 Monoclonal antibody 25 mg/kg Intravenous

Indications