A Phase 3, multicenter, randomized, double-blind, 48-week study of the clinical and antiviral effect of S-217622 compared with placebo in non-hospitalized high-risk participants with COVID-19
This Study is
No Longer Enrolling
Participation in the study will last about 24 weeks and participants will have at least 8 study visits. Participants will be randomly assigned to take the investigational drug or a placebo as 3 tablets on the first day of study treatment followed by 1 tablet a day for 4 days.
MoreAdult
You, or someone you know, may be able to take part if you/they: -are 18 years of age or older -have had a positive diagnosis of COVID-19 within the past 72 hours (3 days) -are experiencing COVID-19 symptoms such as coughing, shortness of breath, feeling feverish, fatigue, nausea, chills, headaches, or sore throat, among others, within the past 3 days (with one or more symptoms ongoing).
Treatment
National
Outpatient CTRC
Protocol Number: 22-0587
More information available at ClinicalTrials.gov: NCT05305547
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