GLPwatch

A Pilot Clinical Trial of Exendin-4 in Alzheimer's Disease

NCT01255163 · Terminated

Last updated 2026-05-28

This clinical trial is testing whether the drug Exendin-4 causes nausea in people with Alzheimer's disease or mild cognitive impairment.

Status Terminated Stopped early and will not restart.
Phase Phase 2 Tests whether it works and watches safety in a moderate group.
Type Interventional (clinical trial)
Design Randomized, quadruple-blind treatment study
Participants 57 people
Who can join Ages 60+ · all sexes
Timeline Started 2010-11 · est. completion 2016-11
Where 1 site · United States

What this study is testing ClinicalTrials.gov NCT01255163 ↗

Description as written by the study sponsor.

Background: Exendin-4 (or Exenatide) is a medication currently used to treat diabetes that has shown promising results in animal and cellular models of Alzheimer's disease. It is possible that Exendin-4 may be a treatment for Alzheimer's disease, which involves the gradual deterioration and death of neurons. Researchers are interested in studying the safety and comparing the effects of Exendin-4 with placebo on cognitive performance, clinical progression of dementia, various chemicals measured in blood and cerebrospinal fluid, and brain MRI, in individuals with early-stage Alzheimer's disease or mild cognitive impairment. Objectives: To determine the safety and tolerability of twice daily administration of Exendin-4, as well as to acquire preliminary evidence for effects on cognitive performance, clinical progression of dementia, various chemicals measured in blood and cerebrospinal fluid, and brain MRI, in individuals with early-stage Alzheimer's disease or mild cognitive impairment. Eligibility: Individuals at least 60 years of age who have objective evidence of early-stage Alzheimer's disease or mild cognitive impairment in screening testing. Design: * Participants will be screened. * Following the telephone screening, two in-person screening visits to determine eligibility. * The screening visit will involve a medical history and neurological examination, tests of memory and cognition, a lumbar puncture, collection of blood and saliva samples, and brain Magnetic Resonance Imagine (MRI) studies. Participants will be required to appoint a Durable Power of Attorney for research and medical care during this protocol. * Eligible participants will be divided into two groups (double-blind randomization). One group will receive Exendin-4 SC twice daily, and the other will receive a placebo. Participants will keep a medication diary and will be scheduled for additional study visits 1 and 2 weeks after the start of the treatment. * Participants will have regular followup visits with blood tests, cognitive tests, imaging studies, and other examinations 6, 12, and 18 months after the start of the treatment. Another lumbar puncture may be performed optionally at the 18-month followup visit.

Treatments tested

Main thing measuredNumber of Participants With Incidence of Nausea
SponsorNational Institute on Aging (NIA)
Conditions studiedAlzheimer's Disease, Mild Cognitive Impairment
GLP-1 drugs

Full protocol, eligibility, and contacts on ClinicalTrials.gov NCT01255163 ↗