CompletedPhase 2NCT05668754

Placebo-Controlled, Double-Blind, Study to Determine the Safety and Efficacy of SDX in Patients With IH

Studying Idiopathic hypersomnia

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Key facts

Sponsor
Zevra Therapeutics
Principal Investigator
Christopher Drake, PhD
Investigator
Intervention
Serdexmethylphenidate(drug)
Enrollment
50 target
Eligibility
18 years · All sexes
Timeline
20222024

Study locations (30)

Collaborators

Rho, Inc.

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 NCT05668754 on ClinicalTrials.gov

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