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Completed Phase 2 Interventional

A Study to Evaluate the Safety and Effectiveness of ALKS 2680 in Subjects With Narcolepsy Type 1 (ALKS 2680-201)

ClinicalTrials.gov ID: NCT06358950

Public ClinicalTrials.gov record NCT06358950. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 21, 2026, 3:01 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2, Parallel-Group, Dose-Range-Finding Study With Randomized Double-Blind Treatment and Open-Label Periods to Evaluate the Safety and Efficacy of ALKS 2680 in Subjects With Narcolepsy Type 1

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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.

Study identification

NCT ID
NCT06358950
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Alkermes, Inc.
Industry
Enrollment
92 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 70 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 24, 2024 (Actual)
Primary completion
Jun 19, 2025 (Actual)
Completion
Jul 31, 2025 (Actual)
Last update posted
Jun 10, 2026

2024 – 2025

United States locations

U.S. sites
29
U.S. states
13
U.S. cities
27
Facility City State ZIP Site status
Alkermes Investigational Site Los Angeles California 90025 —
Alkermes Investigational Site Redwood City California 94063 —
Alkermes Investigator Site San Francisco California 94107 —
Alkermes Investigational Site Santa Ana California 92705 —
Alkermes Investigational Site Aurora Colorado 80045 —
Alkermes Investigational Site Colorado Springs Colorado 80918 —
Alkermes Investigational Site Brandon Florida 33511 —
Alkermes Investigator Site Brandon Florida 33511 —
Alkermes Investigational Site Miami Florida 33176 —
Alkermes Investigator Site Winter Park Florida 32789 —
Alkermes Investigational Site Atlanta Georgia 30328 —
Alkermes Investigational Site Macon Georgia 31210 —
Alkermes Investigational Site Stockbridge Georgia 30281 —
Alkermes Investigator Site Peoria Illinois 61637 —
Alkermes Investigator Site Lansing Michigan 48911 —
Alkermes Investigator Site Sterling Heights Michigan 48314 —
Alkermes Investigator Site Lincoln Nebraska 68506 —
Alkermes Investigational Site Middletown New Jersey 07748 —
Alkermes Investigational Site Denver North Carolina 28037 —
Alkermes Investigational Site Huntersville North Carolina 28708 —
Alkermes Investigator Site Canton Ohio 44718 —
Alkermes Investigational Site Cincinnati Ohio 45227 —
Alkermes Investigational Site Cincinnati Ohio 45245 —
Alkermes Investigational Site Dublin Ohio 43017 —
Alkermes Investigational Site Wyomissing Pennsylvania 19610 —
Alkermes Investigational Site Columbia South Carolina 29201 —
Alkermes Investigational Site Austin Texas 78731 —
Alkermes Investigational Site San Antonio Texas 78229 —
Alkermes Investigational Site The Woodlands Texas 77380 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 16 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06358950, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jun 10, 2026 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06358950 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →