drugset / Trial / NCT05078593

A Clinical Study to Evaluate the Safety, Tolerability and Pharmacokinetic Characteristics of HLX26 Monoclonal Antibody Injection in Patients With Solid Tumor or Lymphoma

NCT05078593

Phase 1 Completed 18 enrolled Shanghai Henlius Biotech
NaSingle-groupOpen-labelTreatment

Summary

This study is a first-in-class open-label phase I human clinical study to evaluate the safety and tolerability of HLX26 with escalated doses in the treatment of patients with advanced/metastatic solid tumors or lymphomas.

Timeline

Start
2021-10-11
Primary completion
2023-08-18
Completion
2023-08-18

Drugs

EvaluationDrugModalityDoseRoute
Subject HLX26 Monoclonal antibody 60 mg Intravenous
Subject HLX26 Monoclonal antibody 150 mg Intravenous
Subject HLX26 Monoclonal antibody 300 mg Intravenous
Subject HLX26 Monoclonal antibody 500 mg Intravenous
Subject HLX26 Monoclonal antibody 800 mg Intravenous
Subject HLX26 Monoclonal antibody 1200 mg Intravenous
Subject HLX26 Monoclonal antibody 1600 mg Intravenous

Indications