drugset / Trial / NCT06843590

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

NCT06843590 ↗

Phase 2 Recruiting 126 enrolled Alkermes, Inc.
RandomizedParallel-groupDouble-blindTreatment

Summary

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

Timeline

Start
2025-05-22
Primary completion
2026-11
Completion
2026-11

Drugs

EvaluationDrugModalityDoseRoute
Subject ALKS 2680 Unknown 10 mg Oral
Subject ALKS 2680 Unknown 14 mg Oral
Subject ALKS 2680 Unknown 18 mg Oral