RecruitingPhase 3NCT07500090

A Phase 3 Efficacy and Safety Study of HBS-301 in Participants With Idiopathic Hypersomnia (IH)

Studying Idiopathic hypersomnia

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Key facts

Sponsor
Harmony Biosciences Management, Inc.
Principal Investigator
David Seiden, MD
Harmony Biosciences Management, Inc.
Intervention
HBS-301 tablet(drug)
Enrollment
248 target
Eligibility
18 years · All sexes
Timeline
20262028

Study locations (12)

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT07500090 on ClinicalTrials.gov

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