A clinical study of MK-1403 in healthy men (MK-1403-004)

2024-514629-52-00 Protocol MK-1403-004 Human pharmacology (Phase I) - Other Ended

Start 28 Oct 2024 · End 18 Jul 2025 · Status Ended · 1 EU/EEA countries · 1 sites · Protocol MK-1403-004

Overview

Sponsor-declared trial summary

Phase Human pharmacology (Phase I) - Other
Status Ended
Participants planned 32
Countries 1
Sites 1

Atherosclerosis

Key facts

Sponsor
Merck Sharp & Dohme LLC
Participant type
Healthy volunteers
Age range
18-64 years
Gender
Male
Therapeutic area
Diseases [C] - Cardiovascular Diseases [C14]
Trial duration
28 Oct 2024 → 18 Jul 2025
Decision date (initial)
2024-10-15
Transition trial
No
Low-intervention
No
Rare-disease indication
No
Vulnerable population
No

External identifiers

EU CT number
2024-514629-52-00
WHO UTN
U1111-1308-1921

Trial design

CTIS Part I — objectives, methods, condition coding

Conditions and MedDRA coding

Atherosclerosis

VersionLevelCodeTermSystem organ class
26.0 LLT 10003601 Atherosclerosis 10047065

Sponsors and contacts

Sponsor organisations, regulatory contacts, third parties

Merck Sharp & Dohme LLC

Sponsor organisation
Merck Sharp & Dohme LLC
Address
126 East Lincoln Avenue, P. O. Box 2000 P. O. Box 2000
City
Rahway
Postcode
07065-4607
Country
United States

Scientific contact point

Organisation
Merck Sharp & Dohme LLC
Contact name
Kelly Duncan

Public contact point

Organisation
Merck Sharp & Dohme LLC
Contact name
Kelly Duncan

Locations

1 EU/EEA country · 1 investigational sites

By country

CountryMS statusPlanned subjectsSites
Belgium Ended 32 1
Rest of world 0

Investigational sites

Belgium

1 site · Ended
SGS Belgium
SGS Clinical Pharmacology Unit, Drie Eikenstraat 655, 2650, Edegem

Country notifications

Trial-start, recruitment-start, end and early-termination notifications submitted per Member State

Country Trial startTrial end Recruitment startRecruitment end Early termination
Belgium 2024-10-28 2025-07-17 2024-11-04 2025-07-06

Application history

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

#TypeCodeSubmittedReference MSConclusionDecision date
1 INITIAL IN 2024-09-10 Belgium Acceptable
2024-10-15
2024-10-15
2 SUBSTANTIAL MODIFICATION SM-1 2024-11-19 Belgium Acceptable
2024-12-18
2024-12-18
3 SUBSTANTIAL MODIFICATION SM-2 2025-03-26 Belgium Acceptable
2025-04-24
2025-04-24