RecruitingPhase 3NCT07502443

A Study to Evaluate the Efficacy and Safety of ALKS 2680 in Adults With Narcolepsy Type 2

Studying Narcolepsy

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Key facts

Sponsor
Alkermes, Inc.
Principal Investigator
Study Director, MD
Alkermes, Inc.
Intervention
ALKS 2680 Dose 1(drug)
Enrollment
176 enrolled
Eligibility
18-70 years · All sexes
Timeline
20262027

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 NCT07502443 on ClinicalTrials.gov

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