drugset / Trial / NCT02941822
Ambroxol in Disease Modification in Parkinson Disease
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Ambroxol | Small molecule | 420 mg | Oral |