WAKIX® (Pitolisant) Pregnancy Registry

Recruiting Observational Study
Pregnancy Related Narcolepsy
No Placebo Group Every participant receives an active treatment — no one gets a placebo. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Sex
Female
Study type
Observational
Participants needed
1,329 (estimated)
Sponsor
Harmony Biosciences Management, Inc. · Industry
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About This Trial

The WAKIX (pitolisant) Pregnancy Registry is a US-based, prospective, observational cohort study designed to evaluate the association between pitolisant exposure during pregnancy and subsequent maternal, fetal, and infant outcomes.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Pregnant woman of any age * Consent to participate * Authorization for her HCP(s) to provide data to the registry * For participants with a diagnosis of narcolepsy: exposure to at least one dose of pitolisant or one dose of a comparator product, or, unexposed to pitolisant or …
Contacts

WAKIX Pregnancy Registry Associate

1-877-302-2813

wakixpregnancyregistry@ppd.com

CONTACT