drugset / Trial / NCT05722691

Study for Efficacy and Safety Assessment of the Drug RADAMIN®VIRO for COVID-19 Postexposure Prophylaxis

NCT05722691 ↗

Phase 3 Completed 800 enrolled Promomed, LLC
RandomizedParallel-groupSingle-blindTreatment

Summary

This is Double-Blind, Placebo-Controlled Multicentre Clinical Phase III Study conducted in 10 medical facilities. The objective of the study is to evaluate efficacy and safety of the drug Drug RADAMIN®VIRO, Lyophilisate for Preparation of Solution for Intramuscular and Subcutaneous Administration for COVID-19 Postexposure Prophylaxis

Timeline

Start
2022-06-09
Primary completion
2022-11-22
Completion
2023-01-17

Drugs

EvaluationDrugModalityDoseRoute
Subject Double-Stranded RNA sodium salt Unknown 5 mg Intramuscular

Indications