drugset / Trial / NCT04405570

Safety, Tolerability and Efficacy of Molnupiravir (EIDD-2801) to Eliminate Infectious Virus Detection in Persons With COVID-19

NCT04405570 ↗

RandomizedParallel-groupDouble-blindTreatment

Summary

This was a phase IIa, double-blind, placebo-controlled, randomized trial, designed to compare the safety, tolerability, and antiviral activity of EIDD-2801 (molnupiravir) versus placebo as measured by SARS-CoV-2 viral RNA detection in symptomatic adult outpatients with COVID-19.

Timeline

Start
2020-06-19
Primary completion
2021-02-21
Completion
2021-02-21

Outcome

Met primary endpoint

registry analysis (superiority test); Molnupiravir 800 mg; p = 0.0128; Log Rank NCT04405570 ↗

paper Time to viral RNA clearance was decreased and a greater proportion overall achieved clearance in participants administered 800 mg molnupiravir versus placebo (p = 0.01). PMID 34159342 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Molnupiravir Small molecule 200 mg Oral
Subject Molnupiravir Small molecule 400 mg Oral
Subject Molnupiravir Small molecule 800 mg Oral

Indications