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Donepezil for Alzheimer's Disease (DDI Trial)

Phase 1
Waitlist Available
Research Sponsored by Merck Sharp & Dohme Corp.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up day 21 (morning dose only): predose and 0.5, 1, 2, 3, 4, 6, and 12 hours postdose

Summary

This trial is testing a new drug, MK-1942, together with an existing Alzheimer's medication, donepezil. It focuses on patients with mild-to-moderate Alzheimer's who are already taking donepezil. The study aims to see if this combination is safe and if it causes any new or more severe side effects. Researchers will also check how the body processes both drugs when taken together. Donepezil is a well-established treatment for Alzheimer's disease, used to improve cognition and global function in patients with mild to severe stages of the disease.

Eligible Conditions
  • Alzheimer's Disease

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~days 1, 7, 14, and 21 (morning dose only): predose and 0.5, 1, 2, 3, 4, 6, and 12 hours postdose
This trial's timeline: 3 weeks for screening, Varies for treatment, and days 1, 7, 14, and 21 (morning dose only): predose and 0.5, 1, 2, 3, 4, 6, and 12 hours postdose for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Change From Baseline in Heart Rate (HR)
Change From Baseline in Systolic Blood Pressure (SBP)
Mean Change From Baseline in Diastolic Blood Pressure (DBP)
+8 more
Secondary study objectives
AUC From Dosing to 24 Hours Postdose (AUC0-24) of MK-1942
AUC0-24 of Donepezil
Apparent Clearance at Steady-state (CLss/F) of MK-1942
+9 more

Trial Design

2Treatment groups
Experimental Treatment
Placebo Group
Group I: DonepezilExperimental Treatment2 Interventions
Participants receive Dose Level 1: 8-mg MK-1942 twice daily (BID) x 7 days (7D), Day 1 to Day 7; Dose Level 2: 15-mg MK-1942 BID x 7D, Day 8 to Day 14; Dose Level 3: 30-mg MK-1942 BID x 7D, Day 15 to Day 21; Dose Level 4: ≤50-mg MK-1942 BID x 7D (Provisional Dose Level), Day 22 to Day 28 All participants to receive Donepezil once daily.
Group II: PlaceboPlacebo Group2 Interventions
Placebo to MK-1942 BID x 21 \[28\] D All participants to receive Donepezil once daily.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
MK-1942
2021
Completed Phase 1
~30
Donepezil
2011
Completed Phase 4
~2070

Find a Location

Who is running the clinical trial?

Merck Sharp & Dohme Corp.Lead Sponsor
2,286 Previous Clinical Trials
4,582,469 Total Patients Enrolled
Merck Sharp & Dohme LLCLead Sponsor
4,000 Previous Clinical Trials
5,181,805 Total Patients Enrolled
Medical DirectorStudy DirectorMerck Sharp & Dohme LLC
2,880 Previous Clinical Trials
8,085,093 Total Patients Enrolled
~6 spots leftby Nov 2025