drugset / Trial / NCT04973189

A Study of SHR-1707 in Healthy Young Adult and Elderly Subjects

NCT04973189 ↗

Phase 1 Completed 63 enrolled Shanghai Hengrui Pharmaceutical Co., Ltd.
RandomizedParallel-groupDouble-blindBasic science

Summary

The study is being conducted to evaluate the safety, tolerability, pharmacokinetics and pharmacodynamics of single intravenous administration of SHR-1707 in healthy young adult and elderly subjects.

Timeline

Start
2021-05-08
Primary completion
2022-01-13
Completion
2022-01-13

Drugs

EvaluationDrugModalityDoseRoute
Subject SHR-1707 Monoclonal antibody 2 mg/kg Intravenous
Subject SHR-1707 Monoclonal antibody 6 mg/kg Intravenous
Subject SHR-1707 Monoclonal antibody 20 mg/kg Intravenous
Subject SHR-1707 Monoclonal antibody 40 mg/kg Intravenous
Subject SHR-1707 Monoclonal antibody 60 mg/kg Intravenous

Indications