RecruitingPhase 2NCT06843590
A Study to Evaluate the Safety and Effectiveness of ALKS 2680 in Subjects With Idiopathic Hypersomnia
Studying Idiopathic hypersomnia
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Alkermes, Inc.
- Principal Investigator
- Medical DirectorAlkermes, Inc.
- Intervention
- ALKS 2680(drug)
- Enrollment
- 96 target
- Eligibility
- 18-70 years · All sexes
- Timeline
- 2025 – 2026
Study locations (30)
- Alkermes Investigator Site, Cullman, Alabama, United States
- Alkermes Investigator Site, Phoenix, Arizona, United States
- Alkermes Investigator Site, Little Rock, Arkansas, United States
- Alkermes Investigator Site, Los Angeles, California, United States
- Alkermes Investigator Site, Redwood City, California, United States
- Alkermes Investigator Site, San Francisco, California, United States
- Alkermes Investigator Site, Colorado Springs, Colorado, United States
- Alkermes Investigator Site, Brandon, Florida, United States
- Alkermes Investigator Site, Miami, Florida, United States
- Alkermes Investigator Site, Winter Park, Florida, United States
- Alkermes Investigator Site, Atlanta, Georgia, United States
- Alkermes Investigator Site, Macon, Georgia, United States
- Alkermes Investigator Site, Stockbridge, Georgia, United States
- Alkermes Investigator Site, Peoria, Illinois, United States
- Alkermes Investigator Site, Kansas City, Kansas, United States
- +15 more locations on ClinicalTrials.gov
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 NCT06843590 on ClinicalTrials.govOther trials for Idiopathic hypersomnia
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