Pitolisant for People with Prader-Willi Syndrome & Excessive Daytime Sleepiness  - the TEMPO Study
fpwr.org
Pitolisant for People with Prader-Willi Syndrome & Excessive Daytime Sleepiness  - the TEMPO Study
A Phase 2 Study to Evaluate the Safety and Efficacy of Pitolisant in People With Prader-Willi Syndrome, ages 6 to 65.
Feb 20, 2020
Pitolisant Reviews
Pitolisant was recently FDA approved for the treatment of narcolepsy in adults. Because people with PWS often struggle with wakefulness, Harmony plans to open a PWS clinical trial investigating Pitolisant for the treatment of excessive daytime sleepiness (EDS) in early 2020. Learn more about this potential treatment in this short video taken from our 2019 Clinical Trials Panel. | The Foundation for Prader-Willi Research
17:44
Pitolisant was recently FDA approved for the treatment of narcolepsy in adults. Because people with PWS often struggle with wakefulness, Harmony plans to open a PWS clinical trial investigating Pitolisant for the treatment of excessive daytime sleepiness (EDS) in early 2020. Learn more about this potential treatment in this short video taken from our 2019 Clinical Trials Panel. | The Foundation for Prader-Willi Research
FacebookThe Foundation for Prader
1.3K viewsOct 30, 2019
Pitolisant and the Role of Histamine in Narcolepsy | Psychiatric Times
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Harmony Receives RTF Letter for Pitolisant, FDA Accepts Vatiquinone NDA, Gene Therapy SGT-003 Performs Well in Phase 1/2 Trial | NeurologyLive - Clinical Neurology News and Neurology Expert Insights
Harmony Receives RTF Letter for Pitolisant, FDA Accepts Vatiquinone NDA, Gene Therapy SGT-003 Performs Well in Phase 1/2 Trial | NeurologyLive - Clinical Neurology News and Neurology Expert Insights
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