A Clinical Study of Ulonivirine (MK-8507) With Atorvastatin and Metformin in Healthy Adults (MK-8507-018)

June 11, 2026 updated by: Merck Sharp & Dohme LLC

A Phase 1, Open-Label, Two-Period Fixed Sequence Study to Evaluate the Effects of a Single Oral Dose of Ulonivirine (MK-8507) on the Single-Dose Pharmacokinetics of Atorvastatin and Metformin in Healthy Adult Participants

Researchers want to learn about ulonivirine when given with atorvastatin and metformin in healthy people. The goal of this study is to compare the amount of atorvastatin and metformin in a person's body over time when given with and without ulonivirine.

Study Overview

Status

Status

Indicates the current recruitment status or the expanded access status.
Completed

Conditions

Conditions

The disease, disorder, syndrome, illness, or injury that is being studied. On ClinicalTrials.gov, conditions may also include other health-related issues, such as lifespan, quality of life, and health risks.

Intervention / Treatment

Intervention / Treatment

A process or action that is the focus of a clinical study. Interventions include drugs, medical devices, procedures, vaccines, and other products that are either investigational or already available. Interventions can also include noninvasive approaches, such as education or modifying diet and exercise.

Study Type

Study Type

Describes the nature of a clinical study. Study types include interventional studies (also called clinical trials), observational studies (including patient registries), and expanded access.
Interventional

Enrollment (Actual)

Enrollment

The number of participants in a clinical study. The "anticipated" enrollment is the target number of participants that the researchers need for the study.
12

Phase

Phase

The stage of a clinical trial studying a drug or biological product, based on definitions developed by the U.S. Food and Drug Administration (FDA). The phase is based on the study's objective, the number of participants, and other characteristics. There are five phases: Early Phase 1 (formerly listed as Phase 0), Phase 1, Phase 2, Phase 3, and Phase 4. Not Applicable is used to describe trials without FDA-defined phases, including trials of devices or behavioral interventions.
  • Phase 1

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact

The name and contact information for the person who can answer enrollment questions for a clinical study. Each location where the study is being conducted may also have a specific contact, who may be better able to answer those questions.

Study Locations

  • United States
    • Arizona
      • Tempe, Arizona, United States, 85283
        • Celerion ( Site 0001)

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Eligibility Criteria

The key requirements that people who want to participate in a clinical study must meet or the characteristics they must have. Eligibility criteria consist of both inclusion criteria (which are required for a person to participate in the study) and exclusion criteria (which prevent a person from participating). Types of eligibility criteria include whether a study accepts healthy volunteers, has age or age group requirements, or is limited by sex.

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Has body mass index (BMI) 18.0 and ≤ 32.0 kg/m^2
  • Is medically healthy with no clinically significant medical history, physical examination, clinical laboratory profiles, vital signs, and electrocardiogram (ECG)

Exclusion Criteria:

  • Has history of cancer (malignancy)
  • Positive results for human immunodeficiency virus (HIV), hepatitis B surface antigen (HBsAg), or hepatitis C virus (HCV)

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Basic Science
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm

Participant Group / Arm

A group or subgroup of participants in a clinical trial that receives a specific intervention/treatment, or no intervention, according to the trial's protocol.
Intervention / Treatment

Intervention / Treatment

A process or action that is the focus of a clinical study. Interventions include drugs, medical devices, procedures, vaccines, and other products that are either investigational or already available. Interventions can also include noninvasive approaches, such as education or modifying diet and exercise.
Experimental: Atorvastatin + metformin + ulonivirine
In Period 1, participants will receive atorvastatin and metformin. In Period 2, participants will receive atorvastatin, metformin, and ulonivirine.
Drug: Metformin
Oral tablet
Drug: Ulonivirine
Oral tablet
Other Names:
  • MK-8507
Drug: Atorvastatin
Oral tablet

What is the study measuring?

Primary Outcome Measures

Primary Outcome Measures

In a clinical study's protocol, the planned outcome measure that is the most important for evaluating the effect of an intervention/treatment. Most clinical studies have one primary outcome measure, but some have more than one.
Outcome Measure
Measure Description
Time Frame
AUC0-inf of Metformin
Time Frame: Day 1: Predose and at designated timepoints up to 72 hours post-dose
Blood samples will be collected at multiple time points to determine the AUC0-inf of metformin
Day 1: Predose and at designated timepoints up to 72 hours post-dose
Area Under the Concentration-Time Curve From Time 0 to Infinity (AUC0-inf) of Atorvastatin
Time Frame: Day 1: Predose and at designated timepoints up to 72 hours post-dose
Blood samples will be collected at multiple time points to determine the AUC0-inf of atorvastatin
Day 1: Predose and at designated timepoints up to 72 hours post-dose

Secondary Outcome Measures

Secondary Outcome Measures

In a clinical study's protocol, a planned outcome measure that is not as important as the primary outcome measure for evaluating the effect of an intervention but is still of interest. Most clinical studies have more than one secondary outcome measure.
Outcome Measure
Measure Description
Time Frame
Area Under the Curve From Time 0 to Last Quantifiable Sample (AUC0-last) of Atorvastatin
Time Frame: Day 1: Predose and at designated timepoints up to 72 hours post-dose
Blood samples will be collected at multiple time points to determine the AUC0-last of atorvastatin
Day 1: Predose and at designated timepoints up to 72 hours post-dose
Maximum Plasma Concentration (Cmax) of Atorvastatin
Time Frame: Day 1: Predose and at designated timepoints up to 72 hours post-dose
Blood samples will be collected at multiple time points to determine the Cmax of atorvastatin
Day 1: Predose and at designated timepoints up to 72 hours post-dose
Plasma Concentration at 24 Hours (C24) of Atorvastatin
Time Frame: 24 hours post-dose
Blood samples will be collected to estimate the C24 of atorvastatin
24 hours post-dose
Time to Maximum Plasma Concentration (Tmax) of Atorvastatin
Time Frame: Day 1: Predose and at designated timepoints up to 72 hours post-dose
Blood samples will be collected at multiple time points to estimate the Tmax of atorvastatin
Day 1: Predose and at designated timepoints up to 72 hours post-dose
Apparent Terminal Half-life (t1/2) of Atorvastatin
Time Frame: Day 1: Predose and at designated timepoints up to 72 hours post-dose
Blood samples will be collected at multiple time points to estimate the t1/2 of atorvastatin
Day 1: Predose and at designated timepoints up to 72 hours post-dose
AUC0-last of Atorvastatin Metabolite (2-OH Atorvastatin)
Time Frame: Day 1: Predose and at designated timepoints up to 72 hours post-dose
Blood samples will be collected at multiple time points to determine the AUC0-last of 2-OH atorvastatin
Day 1: Predose and at designated timepoints up to 72 hours post-dose
AUC0-inf of 2-OH Atorvastatin
Time Frame: Day 1: Predose and at designated timepoints up to 72 hours post-dose
Blood samples will be collected at multiple time points to determine the AUC0-inf of 2-OH atorvastatin
Day 1: Predose and at designated timepoints up to 72 hours post-dose
Cmax of 2-OH Atorvastatin
Time Frame: Day 1: Predose and at designated timepoints up to 72 hours post-dose
Blood samples will be collected at multiple time points to determine the Cmax of 2-OH atorvastatin
Day 1: Predose and at designated timepoints up to 72 hours post-dose
C24 of 2-OH Atorvastatin
Time Frame: 24 hours post-dose
Blood samples will be collected to estimate the C24 of 2-OH atorvastatin
24 hours post-dose
Tmax of 2-OH Atorvastatin
Time Frame: Day 1: Predose and at designated timepoints up to 72 hours post-dose
Blood samples will be collected at multiple time points to estimate the Tmax of 2-OH atorvastatin
Day 1: Predose and at designated timepoints up to 72 hours post-dose
t1/2 of 2-OH Atorvastatin
Time Frame: Day 1: Predose and at designated timepoints up to 72 hours post-dose
Blood samples will be collected at multiple time points to estimate the t1/2 of 2-OH atorvastatin
Day 1: Predose and at designated timepoints up to 72 hours post-dose
AUC0-last of Atorvastatin Metabolite (4-OH Atorvastatin)
Time Frame: Day 1: Predose and at designated timepoints up to 72 hours post-dose
Blood samples will be collected at multiple time points to determine the AUC0-last of 4-OH atorvastatin
Day 1: Predose and at designated timepoints up to 72 hours post-dose
AUC0-inf of 4-OH Atorvastatin
Time Frame: Day 1: Predose and at designated timepoints up to 72 hours post-dose
Blood samples will be collected at multiple time points to determine the AUC0-inf of 4-OH atorvastatin
Day 1: Predose and at designated timepoints up to 72 hours post-dose
Cmax of 4-OH Atorvastatin
Time Frame: Day 1: Predose and at designated timepoints up to 72 hours post-dose
Blood samples will be collected at multiple time points to determine the Cmax of 4-OH atorvastatin
Day 1: Predose and at designated timepoints up to 72 hours post-dose
C24 of 4-OH Atorvastatin
Time Frame: 24 hours post-dose
Blood samples will be collected to estimate the C24 of 4-OH atorvastatin
24 hours post-dose
Tmax of 4-OH Atorvastatin
Time Frame: Day 1: Predose and at designated timepoints up to 72 hours post-dose
Blood samples will be collected at multiple time points to estimate the Tmax of 4-OH atorvastatin
Day 1: Predose and at designated timepoints up to 72 hours post-dose
t1/2 of 4-OH Atorvastatin
Time Frame: Day 1: Predose and at designated timepoints up to 72 hours post-dose
Blood samples will be collected at multiple time points to estimate the t1/2 of 4-OH atorvastatin
Day 1: Predose and at designated timepoints up to 72 hours post-dose
AUC0-last of Metformin
Time Frame: Day 1: Predose and at designated timepoints up to 72 hours post-dose
Blood samples will be collected at multiple time points to determine the AUC0-last of metformin
Day 1: Predose and at designated timepoints up to 72 hours post-dose
Cmax of Metformin
Time Frame: Day 1: Predose and at designated timepoints up to 72 hours post-dose
Blood samples will be collected at multiple time points to determine the Cmax of metformin
Day 1: Predose and at designated timepoints up to 72 hours post-dose
C24 of Metformin
Time Frame: 24 hours post-dose
Blood samples will be collected to estimate the C24 of metformin
24 hours post-dose
Tmax of Metformin
Time Frame: Day 1: Predose and at designated timepoints up to 72 hours post-dose
Blood samples will be collected at multiple time points to estimate the Tmax of metformin
Day 1: Predose and at designated timepoints up to 72 hours post-dose
t1/2 of Metformin
Time Frame: Day 1: Predose and at designated timepoints up to 72 hours post-dose
Blood samples will be collected at multiple time points to estimate the t1/2 of metformin
Day 1: Predose and at designated timepoints up to 72 hours post-dose
Number of Participants Who Experience One or More Adverse Events (AEs)
Time Frame: Up to approximately 21 days after first dose
An AE is any untoward or unfavorable medical occurrence in a participant, including any abnormal sign (for example, abnormal physical exam or laboratory finding), symptom, or disease, temporally associated with the participant's participation in the research, whether or not considered related to the participant's participation in the research. The number of participants who experience an AE will be reported.
Up to approximately 21 days after first dose
Number of Participants Who Discontinue Study Intervention Due to an AE
Time Frame: Up to approximately 7 days after first dose
An AE is any untoward or unfavorable medical occurrence in a participant, including any abnormal sign (for example, abnormal physical exam or laboratory finding), symptom, or disease, temporally associated with the participant's participation in the research, whether or not considered related to the participant's participation in the research. The number of participants who discontinue study treatment due to an AE will be reported.
Up to approximately 7 days after first dose

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Sponsor

The organization or person who initiates the study and who has authority and control over the study.
Merck Sharp & Dohme LLC

Investigators

Investigators

A researcher involved in a clinical study. Related terms include site principal investigator, site sub-investigator, study chair, study director, and study principal investigator.
  • Study Director: Medical Director, Merck Sharp & Dohme LLC

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Helpful Links

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

Study Start

The actual date on which the first participant was enrolled in a clinical study. The "anticipated" study start date is the date that the researchers think will be the study start date.
April 29, 2026

Primary Completion (Actual)

Primary Completion

The date on which the last participant in a clinical study was examined or received an intervention to collect final data for the primary outcome measure. Whether the clinical study ended according to the protocol or was terminated does not affect this date. For clinical studies with more than one primary outcome measure with different completion dates, this term refers to the date on which data collection is completed for all the primary outcome measures. The "anticipated" primary completion date is the date that the researchers think will be the primary completion date for the study.
May 23, 2026

Study Completion (Actual)

Study Completion

The date on which the last participant in a clinical study was examined or received an intervention/treatment to collect final data for the primary outcome measures, secondary outcome measures, and adverse events (that is, the last participant's last visit). The "anticipated" study completion date is the date that the researchers think will be the study completion date.
June 3, 2026

Study Registration Dates

First Submitted

First Submitted

The date on which the study sponsor or investigator first submitted a study record to ClinicalTrials.gov. There is typically a delay of a few days between the first submitted date and the record's availability on ClinicalTrials.gov (the first posted date).
April 7, 2026

First Submitted That Met QC Criteria

First Submitted That Met QC Criteria

The date on which the study sponsor or investigator first submits a study record that is consistent with National Library of Medicine (NLM) quality control (QC) review criteria. The sponsor or investigator may need to revise and submit a study record one or more times before NLM's QC review criteria are met. It is the responsibility of the sponsor or investigator to ensure that the study record is consistent with the NLM QC review criteria.
April 7, 2026

First Posted (Actual)

First Posted

The date on which the study record was first available on ClinicalTrials.gov after National Library of Medicine (NLM) quality control (QC) review has concluded. There is typically a delay of a few days between the date the study sponsor or investigator submitted the study record and the first posted date.
April 15, 2026

Study Record Updates

Last Update Posted (Actual)

Last Update Posted

The most recent date on which changes to a study record were made available on ClinicalTrials.gov. There may be a delay between when the changes were submitted to ClinicalTrials.gov by the study's sponsor or investigator (the last update submitted date) and the last update posted date.
June 15, 2026

Last Update Submitted That Met QC Criteria

Last Update Submitted That Met QC Criteria

The most recent date on which the study sponsor or investigator submitted changes to a study record that are consistent with National Library of Medicine (NLM) quality control (QC) review criteria. It is the responsibility of the sponsor or investigator to ensure that the study record is consistent with the NLM QC review criteria.
June 11, 2026

Last Verified

Last Verified

The most recent date on which the study sponsor or investigator confirmed the information about a clinical study on ClinicalTrials.gov as accurate and current. If a study with a recruitment status of recruiting; not yet recruiting; or active, not recruiting has not been confirmed within the past 2 years, the study's recruitment status is shown as unknown.
June 1, 2026

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

Other Study ID Numbers

Identifiers or ID numbers other than the NCT number that are assigned to a clinical study by the study's sponsor, funders, or others. These numbers may include unique identifiers from other trial registries and National Institutes of Health grant numbers.
  • 8507-018
  • MK-8507-018 (Other Identifier: MSD)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

https://trialstransparency.msdclinicaltrials.com/pdf/ProcedureAccessClinicalTrialData.pdf

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

Yes

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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