drugset / Trial / NCT07455383

A Study to Evaluate the Efficacy and Safety of ALKS 2680 in Adults With Narcolepsy Type 1

NCT07455383 ↗

Phase 3 Recruiting 150 enrolled Alkermes, Inc.
RandomizedParallel-groupTriple-blindTreatment

Summary

The purpose of this study is to measure decreases in daytime sleepiness, cataplexy (sudden loss of muscle tone), and disease symptoms in participants with NT1 when taking ALKS 2680 tablets compared with placebo tablets.

Timeline

Start
2026-04-06
Primary completion
2027-05
Completion
2027-06

Drugs

EvaluationDrugModalityDoseRoute
Subject ALKS 2680 Unknown — Oral

Indications