Study to Assess the Efficacy and Safety of STI-1558 in Adult Subjects With Mild or Moderate (COVID-19)

PHASE3CompletedINTERVENTIONAL
Enrollment

1,218

Participants

Timeline

Start Date

February 8, 2023

Primary Completion Date

July 26, 2023

Study Completion Date

July 26, 2023

Conditions
COVID-19
Interventions
DRUG

STI-1558

STI-1558 will be orally administered under fasting condition twice daily (BID) for 5 days (10 doses in total) at a dose of 600 mg, respectively; the two doses administered will be at a minimum interval of 8 hours (≥8 h). Efficacy and safety will be assessed until D29 after the first dose.

DRUG

STI-1558 placebo

STI-1558 placebo will be orally administered under fasting condition twice daily (BID) for 5 days (10 doses in total) at a dose of 0 mg, respectively; the two doses administered will be at a minimum interval of 8 hours (≥8 h). Efficacy and safety will be assessed until D29 after the first dose.

Trial Locations (2)

Unknown

Beijing Ditan Hospital, Capital Medical University, Beijing

Shenzhen Third People 's Hospital, Shenzhen

All Listed Sponsors
lead

Zhejiang ACEA Pharmaceutical Co. Ltd.

INDUSTRY