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Melanotan-I

Afamelanotide, MT-I, [Nle4-D-Phe7]-α-MSH, Scenesse, CUV-1647

Quick Stats
Studies 225
Trials 100
Completed PHASE3 INTERVENTIONAL NCT04939428

Study of MK-4482 for Prevention of Coronavirus Disease 2019 (COVID-19) in Adults (MK-4482-013)

View on ClinicalTrials.gov Updated Dec 15, 2025

Brief Summary

The purpose of the study is to assess if the study medication (molnupiravir, MK-4482) will prevent symptomatic coronavirus disease 2019 (COVID-19) in adults who live with someone with confirmed COVID-19 infection. This is a phase 3, multicenter, randomized, double-blind, placebo-controlled study; half of the study participants will receive molnupiravir twice daily by mouth and the other half will receive a placebo. The primary objectives of the study are to determine if molnupiravir prevents symptomatic COVID-19 disease and to evaluate its safety and tolerability. All participants who develop COVID-19 during the study are still eligible for any COVID-19 treatment recommended by their doctor.

Interventions

Name: Molnupiravir
Type: DRUG
Description: Four molnupiravir 200 mg capsules taken by mouth.
Name: Placebo
Type: DRUG
Description: Placebo capsule matched to molnupiravir 200 mg capsules taken by mouth.

Primary Outcomes

Measure: Percentage of Participants Who Had Undetectable SARS-CoV-2 in Baseline Nasopharyngeal (NP) Swabs and Developed COVID-19 (Laboratory-Confirmed SARS-CoV-2 Infection With Symptoms) Through Day 14
TimeFrame: Day 14
Description: Percentage of participants who had undetectable SARS-CoV-2 in baseline NP swabs and developed COVID-19 (laboratory-confirmed SARS-CoV-2 infection with symptoms) through Day 14 were reported.
Measure: Percentage of Participants With ≥1 Adverse Event
TimeFrame: 29 days
Description: An AE is any untoward medical occurrence in a clinical study participant, temporally associated with the use of study intervention, whether or not considered related to the study intervention.
Measure: Percentage of Participants Discontinuing From Study Therapy Due to AE
TimeFrame: Up to 5 days
Description: An AE is any untoward medical occurrence in a clinical study participant, temporally associated with the use of study intervention, whether or not considered related to the study intervention.

Trial Information

NCT ID

NCT04939428

Status

Completed

Study Type

INTERVENTIONAL

Phases

PHASE3

Sponsor

Merck Sharp & Dohme LLC

Last Updated

December 15, 2025

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