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SY-005 （Recombinant Human Annexin A5）in Patients With Sepsis

Sepsis Clinical Trial

Official title:
A Phase IIa Randomized, Double-blind, Parallel Group, Placebo-controlled, Multicenter Study to Evaluate Safety, Tolerability, Pharmacokinetics and Efficacy of Multiple Intravenous Injection of SY-005 in Sepsis Subjects

Clinical Trial Summary

This Phase IIa Randomized, Double-blind, Parallel Group, Placebo-controlled, multicenter Study to Evaluate Safety, Tolerability, Pharmacokinetics and Efficacy of Multiple Intravenous Injection of SY-005（recombinant human annexin A5） in Sepsis Subjects. 96 patients will be entered into the study and randomised in a 1:1:1:1 ratio to receive SY-005 2.5mg or SY-005 5mg or SY-005 10mg or placebo.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04898322
Study type Interventional
Source Suzhou Yabao Pharmaceutical R&D Co., Ltd.
Contact Yi Yang
Phone +86 025-83272015
Email yiyiyang2004@163.com
Status Recruiting
Phase Phase 2
Start date January 2, 2022
Completion date July 1, 2023
View Details
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