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Clinical Trial Summary

This is a randomized, double-blind, placebo-controlled phase I clinical study with the primary objective of evaluating the safety and tolerability of SHR-2106 in healthy subjects after a single intravenous or subcutaneous administration.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05948059
Study type Interventional
Source Guangdong Hengrui Pharmaceutical Co., Ltd
Contact
Status Enrolling by invitation
Phase Phase 1
Start date July 11, 2023
Completion date June 15, 2024

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