Sleep Medicine Research
Harmony Study
This study is currently closed to enrollment.
A Double-Blind, Placebo-Controlled, Randomized Withdrawal Study to Evaluate the Safety and Efficacy of Pitolisant in Adult Patients with Idiopathic Hypersomnia
AGE: +18 years old
GENDER: All
HEALTHY PARTICIPANTS: Yes
GENDER: All
HEALTHY PARTICIPANTS: Yes
TYPE: Interventional Study
CONDITION: Idiopathic Hypersomnia
CONDITION: Idiopathic Hypersomnia
LOCATION: UH Cleveland Medical Center
Purpose of Study
The purpose of this study is to learn about the safety and effectiveness of a study drug called pitolisant when compared with placebo (a tablet that does not contain any study drug) in treating some of the symptoms of Idiopathic Hypersomnia.