drugset / Trial / NCT02941822

Ambroxol in Disease Modification in Parkinson Disease

NCT02941822

NaSingle-groupOpen-labelPrevention

Summary

This study will evaluate the safety, tolerability and pharmacodynamics of ambroxol in participants with Parkinson Disease. Participants will administer ambroxol at five dose levels and will undergo clinical assessments, lumbar punctures, venepuncture, biomarker blood analysis and cognitive assessment throughout the course of the study.

Timeline

Start
2016-12
Primary completion
2018-04
Completion
2018-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Ambroxol Small molecule 420 mg Oral

Indications