A Study to Evaluate the Safety and Effectiveness of ALKS 2680 in Subjects With Idiopathic Hypersomnia
Part of paid clinical trials in Cullman, Alabama.
- Sponsor
- Alkermes, Inc.
- Study ID
- NCT06843590
- Phase
- PHASE2
- Status
- Recruiting
Conditions
- Idiopathic Hypersomnia
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 70 Years
- Healthy Volunteers
- Not accepted
Interventions
- ALKS 2680 — DRUGOral tablet containing ALKS 2680 for once daily administration
- Placebo — DRUGOral placebo tablet for once daily administration
Study Details
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
Key Dates
- Start date
- May 22, 2025
- Status verified
- Feb 2026
- Primary completion
- Jun 30, 2026
- Completion
- Jun 30, 2026
Study Design
- Enrollment
- 96 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: ALKS 2680, 10 mgOral tablet containing 10 mg of ALKS 2680 for once daily administration
- Experimental: ALKS 2680, 14 mgOral tablet containing 14 mg of ALKS 2680 for once daily administration
- Experimental: ALKS 2680, 18 mgOral tablet containing 18 mg of ALKS 2680 for once daily administration
- Placebo Comparator: PlaceboOral placebo tablet for once daily administration
Primary Outcome Measure
Change in Epworth Sleepiness Scale (ESS) from baseline to Week 8 by dose level [ Time Frame: Up to 8 weeks ]
Central Contacts
- Director, Global Clinical Services888-235-8008 (US Only)
- Director, Global Clinical Services571-599-2702 (Global)
Locations (32)
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