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Clinical Trial Summary

The purpose of this study is to determine whether thymalfasin is safe and effective in patients who have sepsis


Clinical Trial Description

Our previous study reported that the 7-day treatment of Ta 1 demonstrated positive active effect as to the 28-day all-cause mortality and the augmentation of mHLA-DR (monocyte Human Leukocyte Antigen DR) at the secondary endpoint. Therefore, we intend to verify this finding through a randomized, double-blind and placebo-controlled clinical trial and the trail will include subjects with impaired immunologic functions. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02867267
Study type Interventional
Source Sun Yat-sen University
Contact
Status Completed
Phase Phase 3
Start date September 6, 2016
Completion date March 23, 2021

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