A Study to Assess the Efficacy and Safety of XC221 in Patients With Mild COVID-19

PHASE3CompletedINTERVENTIONAL
Enrollment

274

Participants

Timeline

Start Date

June 26, 2021

Primary Completion Date

August 26, 2022

Study Completion Date

November 14, 2022

Conditions
Sars-CoV-2 Infection
Interventions
DRUG

XC221

Participants will receive XC221 100 mg 2 times a day during 14 full days

DRUG

Placebo

Participants will receive Placebo 2 times a day during 14 full days

Trial Locations (11)

117556

"State Budgetary Institution of Healthcare of Moscow City Polyclinic No. 2 of the Moscow Department of Healthcare", Moscow

125212

"Federal Budgetary Institution of Science Moscow Research Institute of Epidemiology and Microbiology named after G.N. Gabrichevsky of the Federal Service for the Oversight of Consumer Protection and Welfare", Moscow

153025

"Regional Budgetary Institution of Healthcare Ivanovskaya Clinical Hospital named after Kuvaevykh", Ivanovo

190013

"Limited Liability Company Medical Center Capital-Policy", Saint Petersburg

196143

"Limited Liability Company Research Center Eco-Safety", Saint Petersburg

197342

"LLC Sphere-Med", Saint Petersburg

199106

"Saint Petersburg State Budgetary Institution of Healthcare City Pokrovskaya Hospital (4th Cardiology Department)", Saint Petersburg

199178

"Saint Petersburg State Budgetary Institution of Healthcare City Polyclinic No. 4", Saint Petersburg

346918

"Municipal Budgetary Institution of Healthcare Central City Hospital of Novoshakhtinsk", Novoshakhtinsk

620000

"LLC Family Clinic", Yekaterinburg

634040

"Regional State Budgetary Institution of Healthcare Medical-Sanitary Unit No. 2", Tomsk

All Listed Sponsors
lead

RSV Therapeutics LLC

INDUSTRY