SR-Exenatide (PT320) to Eveluate Efficacy and Safety in Patients With Early Parkinson's Disease
NCT04269642 · Unknown status
Last updated 2026-05-28This clinical trial is testing whether the drug SR-Exenatide (PT320) is safe and effective for people in the early stages of 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 99 people Planned (estimated).
Who can join Ages 40–75 · all sexes
Timeline Started 2020-03 · est. completion 2021-12
Where 5 sites · South Korea
What this study is testing ClinicalTrials.gov NCT04269642 ↗
Description as written by the study sponsor.
This study is to evaluate the safety and efficacy of sustained release (SR)-Exenatide (PT320, Q1W and Q2W) in the treatment of patients with early Parkinson's disease (PD).
Treatments tested
- PT320 2.0mg Placebo Drug
PT320 2.0mg Placebo
- PT320 2.0 mg Drug
Exenatide slowly released formulation
- PT320 2.5 mg Drug
Exenatide slowly released formulation
| Main thing measured | Change of MDS-UPDRS part 3 score |
|---|---|
| Sponsor | Peptron, Inc. |
| Conditions studied | Early Parkinson's Disease |
| GLP-1 drugs | exenatide |
Full protocol, eligibility, and contacts on ClinicalTrials.gov NCT04269642 ↗