drugset / Trial / NCT05466422

A Study of MK-2214 in Adults With Mild Cognitive Impairment or Mild-to-Moderate Alzheimer's Disease (MK-2214-002)

NCT05466422 ↗

Phase 1 Completed 34 enrolled Merck Sharp & Dohme LLC
RandomizedSequentialDouble-blindTreatment

Summary

The purpose of this study is to assess the safety, tolerability, pharmacokinetics (PK) and pharmacodynamics of MK-2214 in adults with mild cognitive impairment (MCI) or mild-to-moderate Alzheimer's Disease (AD). The primary hypothesis (Part 1) is that at a generally well tolerated dose level, the true geometric mean concentration at Day 85 of MK-2214 in cerebrospinal fluid is \>0.3 nanomolar (nM).

Timeline

Start
2022-09-20
Primary completion
2025-07-03
Completion
2025-07-03

Drugs

EvaluationDrugModalityDoseRoute
Subject MK-2214 Unknown — Intravenous

Indications