drugset / Trial / NCT06555783

A Study to Evaluate the Safety and Effectiveness of ALKS 2680 in Subjects With Narcolepsy Type 2

NCT06555783 ↗

Phase 2 Completed 93 enrolled Alkermes, Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to measure the safety and decrease in sleepiness in subjects with narcolepsy type 2 (NT2) when taking ALKS 2680 tablets compared to placebo tablets.

Timeline

Start
2024-07-26
Primary completion
2025-11-11
Completion
2025-11-21

Outcome

Met primary endpoint

release “In Vibrance-2, once-daily alixorexton met the dual primary endpoints” alkermes.com ↗

Drugs

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