GLPwatch

Exenatide Treatment in Parkinson's Disease

NCT04305002 · Unknown status

Last updated 2026-05-28

This clinical trial tests whether the drug exenatide can affect brain activity in people with Parkinson's disease.

Status Unknown status The sponsor has not confirmed the status recently.
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 60 people
Who can join Ages 25–80 · all sexes
Timeline Started 2020-01 · est. completion 2023-10
Where 1 site · Sweden

What this study is testing ClinicalTrials.gov NCT04305002 ↗

Description as written by the study sponsor.

The development of a disease-modifying therapy that delays, reverses or stops the symptom progression remains the most important unmet goal in the treatment of Parkinson's disease (PD). Apart from its glucose lowering effect, glucagon-like peptide-1 (GLP-1) receptor stimulation has been investigated in animal models of PD and shown to increase neurogenesis, to arrest and possible reverse nigrostriatal damage, and to protect dopaminergic neurons from neurodegeneration. Exenatide is a synthetic analogue of human GLP-1, resistant to the metabolic processes that degrade it in its naturally occurring form. Results from a recent randomised, double-blind, placebo-controlled trial in PD showed that patients in active treatment for one year were improved compared to the placebo arm with regard to their performance in Movement Disorders Society - Unified Parkinson's Disease Rating Scale (MDS-UPDRS) motor subscale in the practically defined OFF medication state. The aim of this trial is to investigate the effect of Exenatide, 2 mg, subcutaneous injection, once weekly on disease progression represented by the change in longitudinal Positron emission tomography with 2-deoxy-2-\[fluorine-18\]fluoro- D-glucose (FDG-PET) in individual PD subjects, and to identify an Exenatide-related pattern in FDG-PET that will provide insight into the treatment-effect in the brain. The investigators chose the standard regimen prescribed in Type 2 Diabetes Mellitus (T2DM) and the regimen used in a recent trial in PD. The treatment period will be 18 months, and patients will be randomly assigned to either active treatment or placebo. Patients with PD diagnosis, stable on medication during the last year, and Hoehn and Yahr stage 2 or less will be evaluated for the inclusion.

Treatments tested

Main thing measuredFDG-PET network analysis
SponsorCenter for Neurology, Stockholm
Conditions studiedParkinson Disease
GLP-1 drugs exenatide

Full protocol, eligibility, and contacts on ClinicalTrials.gov NCT04305002 ↗