Official Title
An Open-label Study to Characterize the Pharmacokinetics, Safety and Tolerability of Single and Multiple Oral Doses of MK-4482 in Chinese Healthy Male Participants
Brief Summary

The goal of the study is to learn what happens to MK-4482 after single and multiple dosesin healthy Chinese participants over time. Researchers also want to learn about thesafety of MK-4482, including how well people tolerate it.

Detailed Description

Not Provided

Completed
Healthy

Drug: MK-4482

Participants in period 1 received, MK-4482 800 mg single oral dose in the morning on Day
1. Participants in period 2 received, MK-4482 800mg oral dose administered every 12 hours
(Q12H) on Day 1 through Day 6 for11 doses.

Eligibility Criteria

Inclusion Criteria:

The main inclusion criteria include but are not limited to the following:

- Has a Body Mass Index (BMI) of 19 to 24 weight (kg)/height (m)2, inclusive, and body
weight of ≥ 50 kg at the screening visit.

Exclusion Criteria:

The main exclusion criteria include but are not limited to the following:

- Has a history of clinically significant abnormalities or diseases.

- Has history of cancer.

- Has a history of significant multiple and/or severe allergies.

- Had any major surgery.

- Has participated in another investigational study within 3 months prior to the
screening visit.

Eligibility Gender
Male
Eligibility Age
Minimum: 18 Years ~ Maximum: 60 Years
Countries
China
Locations

Peking University Third Hospital (Site 0001)
Beijing 1816670, Beijing Municipality 2038349, China

Medical Director, Study Director
Merck Sharp & Dohme LLC

Merck Sharp & Dohme LLC
NCT Number
Keywords
Coronavirus disease (COVID-19)
MeSH Terms
COVID-19
Molnupiravir