drugset / Trial / NCT03316898

A FDG-PET Study of AGN-242071 Added to Standard-of-Care (Donepezil ± Memantine) for the Treatment of Participants With Mild to Moderate Alzheimer's Disease

NCT03316898

Phase 1 Withdrawn Allergan
RandomizedParallel-groupTriple-blindTreatment

Summary

This is a study to evaluate the brain metabolic response using Fluorodeoxyglucose Positron Emission Tomography (FDG-PET), safety, tolerability and pharmacokinetics of AGN-242071 in patients with mild to moderate Alzheimer's Disease on a stable dose of 10 mg donepezil with or without memantine standard of care.

Timeline

Start
2018-09-30
Primary completion
2018-11-04
Completion
2018-11-04

Drugs

EvaluationDrugModalityDoseRoute
Subject AGN-242071 Unknown 5 mg
Subject AGN-242071 Unknown 15 mg
Subject AGN-242071 Unknown 25 mg
Background Donepezil Small molecule 10 mg
Background Memantine Unknown

Indications