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Completed Phase 1 Interventional Accepts healthy volunteers

A Study of MK-6552 in Sleep Deprived Healthy Participants (MK-6552-003)

ClinicalTrials.gov ID: NCT06619665

Public ClinicalTrials.gov record NCT06619665. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 8, 2026, 8:10 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Double-blind, 3-Period Crossover Study to Assess the Effects of MK-6552 on Sleep Latency in Sleep Deprived Healthy Participants With Modafinil as a Positive Control

Study identification

NCT ID
NCT06619665
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
Merck Sharp & Dohme LLC
Industry
Enrollment
18 participants

Conditions and interventions

Interventions

  • MK-6552 Drug
  • MK-6552 placebo Drug
  • Modafinil Drug
  • Modafinil placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 55 Years
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 18, 2024
Primary completion
Jul 15, 2024
Completion
Jul 15, 2024
Last update posted
Sep 30, 2024

2024

United States locations

U.S. sites
2
U.S. states
2
U.S. cities
2
Facility City State ZIP Site status
NeuroTrials Research Inc (Site 0001) Atlanta Georgia 30328
Clinilabs (Site 0003) Eatontown New Jersey 07724

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06619665, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 30, 2024 · Synced May 8, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06619665 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →