A Clinical Trial of MK-6916 in Participants With Moderate and Severe Kidney Disease Compared to Healthy Controls (MK-6916-013)
NCT07922174, Phase 1, Not yet recruiting, Merck Sharp & Dohme LLC
Trial 10
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
| Field | Value | Source |
|---|---|---|
| Title | A Clinical Trial of MK-6916 in Participants With Moderate and Severe Kidney Disease Compared to Healthy Controls (MK-6916-013) | ClinicalTrials.gov |
| NCT number | NCT07922174 | ClinicalTrials.gov |
| Status | Not yet recruiting | ClinicalTrials.gov |
| Phases | Phase 1 | ClinicalTrials.gov |
| Enrollment | 32 participants, estimated | ClinicalTrials.gov |
| Lead sponsor | Merck Sharp & Dohme LLC | ClinicalTrials.gov |
| Conditions | Healthy, Renal Impairment | ClinicalTrials.gov |
| Interventions | MK-6916 | ClinicalTrials.gov |
| First posted | 2026-11-06 | ClinicalTrials.gov |
| Last updated | 2026-11-06 | ClinicalTrials.gov |
Registered outcomes 40
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description | Source |
|---|---|---|---|---|
| Primary | Area Under the Concentration-Time Curve from Time 0 to 12 Hours (AUC0-12) of MK-6916 on Day 16 | Day 16: Predose and at designated timepoints (up to approximately 12 hours postdose) | Blood samples will be collected to determine the AUC0-12 of MK-6916. | ClinicalTrials.gov |
| Secondary | AUC0-12 of MK-6916 on Day 1 | Day 1: Predose and at designated timepoints (up to approximately 12 hours postdose) | Blood samples will be collected to determine the AUC0-12 of MK-6916. | ClinicalTrials.gov |
| Secondary | Maximum Plasma Concentration (Cmax) of MK-6916 on Day 1 | Day 1: Predose and at designated timepoints (up to approximately 336 hours postdose) | Blood samples will be collected to determine the Cmax of MK-6916. | ClinicalTrials.gov |
| Secondary | Cmax of MK-6916 on Day 16 | Day 16: Predose and at designated timepoints (up to approximately 336 hours postdose) | Blood samples will be collected to determine the Cmax of MK-6916. | ClinicalTrials.gov |
| Secondary | Plasma Concentration at 12 Hours (C12) of MK-6916 on Day 1 | Day 1: Predose and at designated timepoints (up to approximately 12 hours postdose) | Blood samples will be collected to determine the C12 of MK-6916. | ClinicalTrials.gov |
| Secondary | C12 of MK-6916 on Day 16 | Day 16: Predose and at designated timepoints(up to approximately 12 hours postdose) | Blood samples will be collected to determine the C12 of MK-6916. | ClinicalTrials.gov |
| Secondary | Time to Maximum Plasma Concentration (Tmax) of MK-6916 on Day 1 | Day 1: Predose and at designated timepoints (up to approximately 336 hours postdose) | Blood samples will be collected to determine the Tmax of MK-6916. | ClinicalTrials.gov |
| Secondary | Tmax of MK-6916 on Day 16 | Day 16: Predose and at designated timepoints (up to approximately 336 hours postdose) | Blood samples will be collected to determine the Tmax of MK-6916. | ClinicalTrials.gov |
| Secondary | Apparent Terminal Half-life (t1/2) of MK-6916 on Day 16 | Day 16: Predose and at designated timepoints (up to approximately 336 hours postdose) | Blood samples will be collected to determine the t1/2 of MK-6916. | ClinicalTrials.gov |
| Secondary | Clearance at Steady State (CL,ss/F) of MK-6916 on Day 16 | Day 16: Predose and at designated timepoints (up to approximately 336 hours postdose) | Blood samples will be collected to determine the CL,ss/F of MK-6916. | ClinicalTrials.gov |
| Secondary | Apparent Volume of Distribution at Steady State (Vz,ss/F) of MK-6916 on Day 16 | Day 16: Predose and at designated timepoints (up to approximately 336 hours postdose) | Blood samples will be collected to determine the Vz,ss/F of MK-6916 | ClinicalTrials.gov |
| Secondary | AUC0-12 of MK-6916 Metabolite M5 on Day 1 | Day 1: Predose and at designated timepoints (up to approximately 12 hours postdose) | Blood samples will be collected to determine the AUC0-12 of MK-6916 M5. | ClinicalTrials.gov |
| Secondary | AUC0-12 of MK-6916 Metabolite M9 on Day 1 | Day 1: Predose and at designated timepoints (up to approximately 12 hours postdose) | Blood samples will be collected to determine the AUC0-12 of MK-6916 M9. | ClinicalTrials.gov |
| Secondary | AUC0-12 of MK-6916 Metabolite M10 on Day 1 | Day 1: Predose and at designated timepoints (up to approximately 12 hours postdose) | Blood samples will be collected to determine the AUC0-12 of MK-6916 M10. | ClinicalTrials.gov |
| Secondary | AUC0-12 of MK-6916 Metabolite M5 on Day 16 | Day 16: Predose and at designated timepoints (up to approximately 12 hours postdose) | Blood samples will be collected to determine the AUC0-12 of MK-6916 M5. | ClinicalTrials.gov |
| Secondary | AUC0-12 of MK-6916 Metabolite M9 on Day 16 | Day 16: Predose and at designated timepoints (up to approximately 12 hours postdose) | Blood samples will be collected to determine the AUC0-12 of MK-6916 M9. | ClinicalTrials.gov |
| Secondary | AUC0-12 of MK-6916 Metabolite M10 on Day 16 | Day 16: Predose and at designated timepoints (up to approximately 12 hours postdose) | Blood samples will be collected to determine the AUC0-12 of MK-6916 M10. | ClinicalTrials.gov |
| Secondary | Cmax of MK-6916 Metabolite M5 on Day 1 | Day 1: Predose and at designated timepoints (up to approximately 336 hours postdose) | Blood samples will be collected to determine the Cmax of MK-6916 M5. | ClinicalTrials.gov |
| Secondary | Cmax of MK-6916 Metabolite M5 on Day 16 | Day 16: Predose and at designated timepoints (up to approximately 336 hours postdose) | Blood samples will be collected to determine the Cmax of MK-6916 M5. | ClinicalTrials.gov |
| Secondary | Cmax of MK-6916 Metabolite M9 on Day 1 | Day 1: Predose and at designated timepoints (up to approximately 336 hours postdose) | Blood samples will be collected to determine the Cmax of MK-6916 M9. | ClinicalTrials.gov |
Outcomes 0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as | Source |
|---|
Results by group 0
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units | Source |
|---|
Participant flow 0
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted | Source |
|---|
Adverse events 0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
| Type | Event | Organ system | Group | Affected | At risk | Events | Source |
|---|
Adverse event totals 0
The totals the trial posted for each group.
| Total | Group | Affected | At risk | Source |
|---|
Papers 0
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as | Source |
|---|
Grants 0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
| Project | Title | Principal investigators | Organization | Funder | Fiscal years | Source |
|---|
Trial comparisons 0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
| Comparison | Source |
|---|
Tests 0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
| Test | Named as | Source |
|---|
Source 5
| Field | Value | Source |
|---|---|---|
| Release | trials-2026-11-12-0.4.0 | ClinicalTrials.gov |
| Release manifest SHA-256 | 0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4 | ClinicalTrials.gov |
| Registry capture | 2026-11-12 | ClinicalTrials.gov |
| Results copy, AACT | 2026-03-23 | ClinicalTrials.gov |
| NIH clinical studies file | 2026-11-13 | ClinicalTrials.gov |
Release trials-2026-11-12-0.4.0
ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299 ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
NIH RePORTER's clinical studies and project files: Public domain (NIH RePORTER)