A Multiple-Dose Clinical Study to Evaluate Safety, Tolerability, and Pharmacokinetics of MK-8527 in Healthy Participants

2022-502081-24-00 Protocol MK-8527-005 Human pharmacology (Phase I) - Other Expired

Status Expired · 1 EU/EEA countries · 1 sites · Protocol MK-8527-005

Overview

Sponsor-declared trial summary

Phase Human pharmacology (Phase I) - Other
Status Expired
Participants planned 28
Countries 1
Sites 1

HIV-1 (Human Immunodeficiency Virus Type 1)

Key facts

Sponsor
Merck Sharp & Dohme LLC
Participant type
Healthy volunteers
Age range
18-64 years
Gender
Male and Female
Therapeutic area
Diseases [C] - Virus Diseases [C02]
Decision date (initial)
2022-12-14
Transition trial
No
Low-intervention
No
Rare-disease indication
No
Vulnerable population
Yes

Trial design

CTIS Part I — objectives, methods, condition coding

Conditions and MedDRA coding

HIV-1 (Human Immunodeficiency Virus Type 1)

VersionLevelCodeTermSystem organ class
20.1 LLT 10068341 HIV-1 infection 10021881

Sponsors and contacts

Sponsor organisations, regulatory contacts, third parties

Merck Sharp & Dohme LLC

Sponsor organisation
Merck Sharp & Dohme LLC
Address
126 East Lincoln Avenue
City
Rahway
Postcode
07065-4607
Country
United States

Scientific contact point

Organisation
Merck Sharp & Dohme LLC
Contact name
Russ Carstens

Public contact point

Organisation
Merck Sharp & Dohme LLC
Contact name
Russ Carstens

Locations

1 EU/EEA country · 1 investigational sites

By country

CountryMS statusPlanned subjectsSites
Belgium Expired 28 1
Rest of world 0

Investigational sites

Belgium

1 site · Expired
Advanced Technology Corporation
Clinical Pharmacology Unit, Avenue De L'hopital 1, Etage 2e Tour 2 Route 124, Liege

Application history

1 submissions — initial application plus substantial / non-substantial modifications

#TypeCodeSubmittedReference MSConclusionDecision date
1 INITIAL IN 2022-10-28 Belgium Acceptable
2022-12-13
2022-12-14