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Clinical Trial Summary

The purpose of this research study is to assess the safety and efficacy of ALKS 2680 compared to placebo, including whether participants taking ALKS 2680 experience a greater decrease in sleepiness and a decrease in cataplexy ("sudden loss of muscle control"), compared to participants taking placebo alone.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06358950
Study type Interventional
Source Alkermes, Inc.
Contact Global Clinical Services
Phone US: 888-235-8008
Email clinicaltrials@alkermes.com
Status Recruiting
Phase Phase 2
Start date March 28, 2024
Completion date July 2025

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