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Study identifier: NCT07413094 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Efficacy and Safety of YD0743 Treatment for Sepsis-Associated ARDS

Condition: Sepsis  ·  Sponsor: Shanghai Yidian Pharmaceutical Technology Development Co., Ltd.

PhasePhase 2
Planned participants309
Who can joinAll sexes, 18 Years to 75 Years
Healthy volunteersNo

About this study

The goal of this clinical trial is to learn if YD0743 works to treat sepsis-associated acute respiratory distress syndrome (ARDS) in adult patients admitted to the Intensive Care Unit. It will also learn about the safety of drug YD0743. The main questions it aims to answer are: Does YD0743 injection shorten the ventilator-using days in sepsis-associated ARDS patients? What medical problems do participants have when accepting YD0743 treatment? Researchers will compare YD0743 to a placebo (a look-alike substance that contains no active drug) to see if YD0743 works to treat sepsis-associated ARDS. Participants will: Accepting YD0743 injection at least for 7 days. Visit the clinic in person at the Day 28 to receive the follow-up check (D1 is defined as the first day starting the YD0743 or placebo treatment) .

This description comes directly from the study's public registry record.

Talk to the study team

WenJing Zhang  ·  021-64311017  ·  zhang_wenjing1@hllife.com.cn

Always discuss trial participation with your own doctor first.

Locations (1)

Chinese Academy of Medical Sciences & Peking Union Medical College HospitalBeijing, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT07413094