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Study identifier: NCT06843590 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

A Study to Evaluate the Safety and Effectiveness of ALKS 2680 in Subjects With Idiopathic Hypersomnia

Condition: Idiopathic Hypersomnia  ·  Sponsor: Alkermes, Inc.

PhasePhase 2
Planned participants126
Who can joinAll sexes, 18 Years to 70 Years
Healthy volunteersNo

About this study

The purpose of this study is to measure the safety and decrease in daytime sleepiness in subjects with Idiopathic Hypersomnia when taking ALKS 2680 tablets compared with placebo tablets

This description comes directly from the study's public registry record.

Talk to the study team

Director, Global Clinical Services  ·  888-235-8008 (US Only)  ·  clinicaltrials@alkermes.com

Director, Global Clinical Services  ·  571-599-2702 (Global)  ·  clinicaltrials@alkermes.com

Always discuss trial participation with your own doctor first.

Locations (50)

Alkermes Investigator SiteCullman, Alabama, United StatesRecruiting
Alkermes Investigator SitePhoenix, Arizona, United StatesRecruiting
Alkermes Investigator SiteLittle Rock, Arkansas, United StatesRecruiting
Alkermes Investigator SiteLos Angeles, California, United StatesRecruiting
Alkermes Investigator SiteRedwood City, California, United StatesRecruiting
Alkermes Investigator SiteSan Francisco, California, United StatesRecruiting
Alkermes Investigational SiteBoulder, Colorado, United StatesRecruiting
Alkermes Investigator SiteColorado Springs, Colorado, United StatesRecruiting
Alkermes Investigator SiteBrandon, Florida, United StatesRecruiting
Alkermes Investigator SiteMiami, Florida, United StatesRecruiting
Alkermes Investigator SiteWinter Park, Florida, United StatesRecruiting
Alkermes Investigator SiteAtlanta, Georgia, United StatesRecruiting

+ 38 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT06843590