drugset / Trial / NCT06449859

A Clinical Trial of TQC2938 Injection in Healthy Adult Subjects

NCT06449859 ↗

RandomizedParallel-groupQuadruple-blindTreatment

Summary

The study is designed in two phases: single-dose administration and multiple-dose administration. A randomized, double-blind, placebo-controlled trial design was used to evaluate the safety, tolerability, pharmacokinetic characteristics and immunogenicity of TQC2938 injection in healthy adults.

Timeline

Start
2023-06-13
Primary completion
2024-11
Completion
2024-11

Drugs

EvaluationDrugModalityDoseRoute
Subject TQC2938 Monoclonal antibody 52.5 mg Subcutaneous
Subject TQC2938 Monoclonal antibody 210 mg Subcutaneous
Subject TQC2938 Monoclonal antibody 420 mg Subcutaneous
Subject TQC2938 Monoclonal antibody 630 mg Subcutaneous
Subject TQC2938 Monoclonal antibody 840 mg Subcutaneous
Subject TQC2938 Monoclonal antibody 1260 mg Subcutaneous

Indications