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BEN-2001 in Parkinson Disease Patients With Excessive Daytime Sleepiness — CASPAR  

Parkinson Disease Clinical Trial

Official title:
Dose Finding Phase IIb Study of Bavisant to Evaluate Its Safety and effiCacy in treAtment of exceSsive Daytime sleePiness (EDS) in PARkinson's Disease (PD).

Clinical Trial Summary

This phase 2b study is designed as multicentre, multinational, randomized, double blind, parallel group and placebo controlled with three doses of Bavisant (0.5, 1, and 3 mg/d) in subjects with excessive daytime sleepiness with Parkinson's disease.

Clinical Trial Description

Phase 2b study will be conducted with the aim of investigating the efficacy and safety of three fixed doses of Bavisant (0.5, 1 and 3 mg/d) compared to placebo for the treatment of excessive daytime sleepiness (EDS) in subjects with Parkinson's disease. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03194217
Study type Interventional
Source BenevolentAI Bio
Contact
Status Completed
Phase Phase 2
Start date November 10, 2017
Completion date May 28, 2019
View Details
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