drugset / Trial / NCT05409326

A Study of TQH2722 Injection to Evaluate the Safety, Tolerability, Pharmacokinetics, Efficacy and Immunogenicity in Healthy Adult Subjects

NCT05409326 ↗

RandomizedParallel-groupQuadruple-blindTreatment

Summary

A randomized, double-blind, placebo-controlled trial design was used to assess the safety, tolerability, pharmacokinetics and pharmacodynamics characteristics, and immunogenicity of TQH2722 injection in healthy subjects.

Timeline

Start
2022-06
Primary completion
2023-06
Completion
2023-08

Drugs

EvaluationDrugModalityDoseRoute
Subject TQH2722 Monoclonal antibody 50 mg Subcutaneous
Subject TQH2722 Monoclonal antibody 150 mg Subcutaneous
Subject TQH2722 Monoclonal antibody 300 mg Subcutaneous
Subject TQH2722 Monoclonal antibody 600 mg Subcutaneous
Subject TQH2722 Monoclonal antibody 1200 mg Subcutaneous

Indications