drugset / Trial / NCT03757936

A Phase I Clinical Study to Evaluate the Safety, Tolerability and Pharmacokinetics of Anti-PD-1 Antibody (HLX10) in Combination With Avastin Biosimilar (HLX04) in Patients With Advanced Solid Tumors

NCT03757936

Phase 1 Unknown 30 enrolled Shanghai Henlius Biotech
NaSingle-groupOpen-labelTreatment

Summary

This is a single-center, open-label, dose-escalation Phase I clinical trial to evaluate the safety and the tolerability of HLX10-HLX04 combination therapy in patients with advanced solid tumors after failure of standard of care.

Timeline

Start
2018-11-27
Primary completion
2019-09-27
Completion
2020-12-27

Drugs

EvaluationDrugModalityDoseRoute
Subject Bevacizumab Monoclonal antibody 5 mg/kg Intravenous
Subject Serplulimab Monoclonal antibody 1 mg/kg Intravenous
Subject Serplulimab Monoclonal antibody 3 mg/kg Intravenous
Subject Serplulimab Monoclonal antibody 10 mg/kg Intravenous

Indications