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Clinical Trial Summary

This is a randomized, double-blind, placebo-controlled, single dose escalation phase 1 study. The objective of this study is to evaluate the safety, tolerability, pharmacokinetics pharmacodynamics and immunogenicity of subcutaneous administered SHR-1703 in healthy subjects.


Clinical Trial Description

The study will consist of one dose esclation part with a total of 3 dose levels. The Subjects will be randomized to receive SHR-1703 as reflected by the guiding principle for the dose esclation/expansion phase. Each dose group includes a screening period, a baseline period, an observational period, and a safety follow-up period. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04855591
Study type Interventional
Source Atridia Pty Ltd.
Contact
Status Terminated
Phase Phase 1
Start date June 14, 2021
Completion date November 18, 2021

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