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Clinical Trial Summary

This study aims to investigate the effects of SHR-1222 on vascular inflammatory factors in patients with low bone mass.


Clinical Trial Description

In this study, total 50 patients with low bone mass will be enrolled and divided into 5 dose groups. In the lowest dose group 6 subjects will be recruited, among whom 4 will receive SHR-1222 and the other 2 will receive placebo. In each of the other 4 groups, 11 subjects will be recruited, among whom 9 will be administered with SHR-1222 and the other 2 with placebo. Levels of nitric oxide (NO), Endothelin-1 (ET-1), plasminogen activator inhibitor-1 (PAI-1) and hypersensitivity C-reactive protein (hs-CRP) will be detected in patients before and after the SHR-1222 injection. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03898024
Study type Interventional
Source Second Xiangya Hospital of Central South University
Contact
Status Completed
Phase N/A
Start date April 15, 2019
Completion date August 15, 2020

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