A Study of Diltiazem With a Single Dose of MK-6552 in Healthy Adult Participants (MK-6552-007)
NCT ID: NCT06662396
Last Updated: 2024-10-28
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE1
14 participants
INTERVENTIONAL
2024-06-13
2024-09-27
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
BASIC_SCIENCE
NONE
Study Groups
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MK-6552 + Diltiazem
Participants receive a single dose of MK-6552 on Period 1 Day 1. Participants receive a Diltiazem every day (QD) for 6 days (Period 2 Days 1-6). On Period 2 Day 2 participants receive a single dose of MK-6552.
MK-6552
Oral Gelatin Coated Capsule
Diltiazem
Oral Extended-Release Capsule
Interventions
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MK-6552
Oral Gelatin Coated Capsule
Diltiazem
Oral Extended-Release Capsule
Eligibility Criteria
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Inclusion Criteria
* Body Mass Index (BMI) between 18 and 32 kg/m\^2, inclusive
Exclusion Criteria
* History of cancer (malignancy)
18 Years
55 Years
ALL
Yes
Sponsors
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Merck Sharp & Dohme LLC
INDUSTRY
Responsible Party
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Principal Investigators
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Medical Director
Role: STUDY_DIRECTOR
Merck Sharp & Dohme LLC
Locations
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ICON (Site 0001)
Lenexa, Kansas, United States
Countries
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Related Links
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Merck Clinical Trials Information
Other Identifiers
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MK-6552-007
Identifier Type: OTHER
Identifier Source: secondary_id
6552-007
Identifier Type: -
Identifier Source: org_study_id
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