drugset / Trial / NCT02914366

Summary

The present study will test the hypothesis that the medication Ambroxol is safe and well tolerated and will improve cognitive and motor symptoms of Parkinson's Disease Dementia (PDD). Ambroxol has been shown to raise the levels of the enzyme beta-glucocerebrosidase resulting in lower the levels of the protein alpha-synuclein, both of which have been shown to improve cognition in mouse models. This will be a 52 week trial of Ambroxol in 75 individuals with PDD. Participants will undergo clinical, neuropsychological and neuroimaging assessment throughout the study to assess changes.

Timeline

Start
2015-11
Primary completion
2025-12
Completion
2025-12

Outcome

Missed primary endpoint

paper There was no evidence to suggest differences between groups on primary or secondary outcomes. PMID 40587145 ↗

paper However, the effect of ambroxol on cognition was not confirmed. PMID 40587145 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Ambroxol Small molecule 525 mg —
Subject Ambroxol Small molecule 1050 mg —

Indications