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Clinical Trials in the USA / NCT07661108
Active, not recruiting Phase 1

A Clinical Study of MK-8527 in Healthy Participants (MK-8527-021)

NCT07661108 · tracked via the Priya Life Science USA tracker
Sponsor
Merck Sharp & Dohme LLC
Phase
Phase 1
Started
2026-06-30
Last updated
2026-09-03

Condition(s) studied

Healthy

Investigational drug(s) / intervention(s)

MK-8527 →ProbenecidItraconazole →

MK-8527: Oral tablet

Probenecid: Oral tablet

Itraconazole: Oral solution

Study summary

Researchers are studying a medicine called MK-8527 to learn how it behaves in the body of healthy adults.

The goal of this study is to learn about the effect of MK-8527 when it is taken with food or with other medicines. Researchers also want to learn about the safety of MK-8527 and if people tolerate it. Tolerate means participants will receive treatment in the trial unless they need to stop it due to health problems.

Eligibility

Sex
ALL
Min age
18 Years
Max age
55 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Be in good health * Has a body mass index (BMI) between 18 and 32 kg/m\^2, inclusive Exclusion Criteria: * Has an estimated glomerular filtration rate (eGFR) ≤90 mL/min/1.73 m\^2 * Has a history of clinically significant endocrine, gastrointestinal (GI), cardiovascular, hematological, hepatic, immunological, renal, respiratory, genitourinary, or major neurological (including stroke and chronic seizures) abnormalities or diseases * Has a history of stomach or intestinal surgery or resection that would potentially alter absorption and/or excretion of orally administered drugs (uncomplicated appendectomy and hernia repair are allowed) * Has a history of cancer (malignancy) * Is taking any medication that contains emtricitabine (FTC) or lamivudine (3TC)

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Fortrea Clinical Research Unit Inc ( Site 0001) Daytona Beach Florida

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07661108 on ClinicalTrials.gov ↗ ← All trials in the USA