A clinical study of MK-1403 in healthy people (MK-1403-002)

2023-507239-39-00 Protocol MK-1403-002 Human pharmacology (Phase I) - Other Ended

Start 25 Apr 2025 · End 10 Sep 2025 · Status Ended · 1 EU/EEA countries · 1 sites · Protocol MK-1403-002

Overview

Sponsor-declared trial summary

Phase Human pharmacology (Phase I) - Other
Status Ended
Participants planned 56
Countries 1
Sites 1

Atherosclerosis

Key facts

Sponsor
Merck Sharp & Dohme LLC
Participant type
Healthy volunteers
Age range
18-64 years
Gender
Male and Female
Therapeutic area
Diseases [C] - Cardiovascular Diseases [C14]
Trial duration
25 Apr 2025 → 10 Sep 2025
Decision date (initial)
2025-04-17
Transition trial
No
Low-intervention
No
Rare-disease indication
No
Vulnerable population
No

External identifiers

EU CT number
2023-507239-39-00
WHO UTN
U1111-1317-5140

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
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 56 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 2025-04-25 2025-09-09 2025-05-02 2025-08-24

Application history

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

#TypeCodeSubmittedReference MSConclusionDecision date
1 INITIAL IN 2025-03-11 Belgium Acceptable
2025-04-14
2025-04-17
2 SUBSTANTIAL MODIFICATION SM-1 2025-07-09 Belgium Acceptable
2025-07-22
2025-07-22
3 NON SUBSTANTIAL MODIFICATION NSM-1 2025-08-28 Belgium Acceptable
2025-07-22
2025-08-28
4 NON SUBSTANTIAL MODIFICATION NSM-2 2025-09-02 Belgium Acceptable
2025-07-22
2025-09-02