A Study to Evaluate the Safety and Effectiveness of ALKS 2680 in Subjects With Idiopathic Hypersomnia (Vibrance-3)

June 22, 2026 updated by: Alkermes, Inc.

A Phase 2, Randomized, Parallel-Group, Double-Blind, Dose-Range-Finding Study to Evaluate the Safety and Efficacy of ALKS 2680 in Subjects With Idiopathic Hypersomnia (Vibrance-3)

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

Study Overview

Status

Status

Indicates the current recruitment status or the expanded access status.
Recruiting

Conditions

Conditions

The disease, disorder, syndrome, illness, or injury that is being studied. On ClinicalTrials.gov, conditions may also include other health-related issues, such as lifespan, quality of life, and health risks.

Intervention / Treatment

Intervention / Treatment

A process or action that is the focus of a clinical study. Interventions include drugs, medical devices, procedures, vaccines, and other products that are either investigational or already available. Interventions can also include noninvasive approaches, such as education or modifying diet and exercise.

Study Type

Study Type

Describes the nature of a clinical study. Study types include interventional studies (also called clinical trials), observational studies (including patient registries), and expanded access.
Interventional

Enrollment (Estimated)

Enrollment

The number of participants in a clinical study. The "anticipated" enrollment is the target number of participants that the researchers need for the study.
126

Phase

Phase

The stage of a clinical trial studying a drug or biological product, based on definitions developed by the U.S. Food and Drug Administration (FDA). The phase is based on the study's objective, the number of participants, and other characteristics. There are five phases: Early Phase 1 (formerly listed as Phase 0), Phase 1, Phase 2, Phase 3, and Phase 4. Not Applicable is used to describe trials without FDA-defined phases, including trials of devices or behavioral interventions.
  • Phase 2

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact

The name and contact information for the person who can answer enrollment questions for a clinical study. Each location where the study is being conducted may also have a specific contact, who may be better able to answer those questions.

Study Contact Backup

Study Locations

  • Australia
    • New South Wales
      • Sydney, New South Wales, Australia, 2113
        • Recruiting
        • Alkermes Investigator Site
    • South Australia
      • Bedford Park, South Australia, Australia, 5042
        • Recruiting
        • Alkermes Investigator Site
    • Victoria
      • Clayton, Victoria, Australia, 3168
        • Recruiting
        • Alkermes Investigator Site
  • Belgium
      • Alken, Belgium, 3570
        • Recruiting
        • Alkermes Investigator Site
      • Namur, Belgium, 5101
        • Recruiting
        • Alkermes Investigator Site
  • Czechia
      • Prague, Czechia, 128 21
        • Recruiting
        • Alkermes Investigator Site
  • France
    • Gironde
      • Bordeaux, Gironde, France, 33000
        • Recruiting
        • Alkermes Investigator Site
    • Herault
      • Montpellier, Herault, France, 34295
        • Recruiting
        • Alkermes Investigator Site
    • Isere
      • Grenoble, Isere, France, 38043
        • Recruiting
        • Alkermes Investigator Site
  • Italy
      • Bologna, Italy, 40139
        • Recruiting
        • Alkermes Investigator Site
      • Milan, Italy, 20127
        • Recruiting
        • Alkermes Investigator Site
      • Verona, Italy, 37134
        • Recruiting
        • Alkermes Investigator Site
  • Netherlands
      • Zwolle, Netherlands, 8025 BV
        • Recruiting
        • Alkermes Investigator Site
  • Spain
      • Barcelona, Spain, 8036
        • Recruiting
        • Alkermes Investigator Site
      • Madrid, Spain, 28036
        • Recruiting
        • Alkermes Investigator Site
      • Madrid, Spain, 28043
        • Recruiting
        • Alkermes Investigator Site
  • United States
    • Alabama
      • Cullman, Alabama, United States, 35055
        • Recruiting
        • Alkermes Investigator Site
    • Arizona
      • Phoenix, Arizona, United States, 85054
        • Recruiting
        • Alkermes Investigator Site
    • Arkansas
      • Little Rock, Arkansas, United States, 72211
        • Recruiting
        • Alkermes Investigator Site
    • California
      • Los Angeles, California, United States, 90025
        • Recruiting
        • Alkermes Investigator Site
      • Redwood City, California, United States, 94063
        • Recruiting
        • Alkermes Investigator Site
      • San Francisco, California, United States, 94143
        • Recruiting
        • Alkermes Investigator Site
    • Colorado
      • Boulder, Colorado, United States, 80301
        • Recruiting
        • Alkermes Investigational Site
      • Colorado Springs, Colorado, United States, 80918
        • Recruiting
        • Alkermes Investigator Site
    • Florida
      • Brandon, Florida, United States, 33511
        • Recruiting
        • Alkermes Investigator Site
      • Miami, Florida, United States, 33176
        • Recruiting
        • Alkermes Investigator Site
      • Winter Park, Florida, United States, 32789
        • Recruiting
        • Alkermes Investigator Site
    • Georgia
      • Atlanta, Georgia, United States, 30328
        • Recruiting
        • Alkermes Investigator Site
      • Macon, Georgia, United States, 31210
        • Recruiting
        • Alkermes Investigator Site
      • Stockbridge, Georgia, United States, 30281
        • Recruiting
        • Alkermes Investigator Site
    • Illinois
      • Peoria, Illinois, United States, 61637
        • Recruiting
        • Alkermes Investigator Site
    • Kansas
      • Kansas City, Kansas, United States, 66160
        • Recruiting
        • Alkermes Investigator Site
    • Massachusetts
      • Boston, Massachusetts, United States, 02215
        • Recruiting
        • Alkermes Investigational Site
    • Michigan
      • Lansing, Michigan, United States, 48911
        • Recruiting
        • Alkermes Investigator Site
    • Nebraska
      • Lincoln, Nebraska, United States, 68506
        • Recruiting
        • Alkermes Investigator Site
    • New Jersey
      • Middletown, New Jersey, United States, 07748
        • Recruiting
        • Alkermes Investigator Site
    • North Carolina
      • Denver, North Carolina, United States, 28037
        • Recruiting
        • Alkermes Investigator Site
      • Huntersville, North Carolina, United States, 28078
        • Recruiting
        • Alkermes Investigator Site
    • Ohio
      • Canton, Ohio, United States, 44718
        • Recruiting
        • Alkermes Investigator Site
      • Cincinnati, Ohio, United States, 45245
        • Recruiting
        • Alkermes Investigator Site
      • Cleveland, Ohio, United States, 44195
        • Recruiting
        • Alkermes Investigator Site
    • Pennsylvania
      • Danville, Pennsylvania, United States, 17822
        • Recruiting
        • Alkermes Investigator Site
      • Philadelphia, Pennsylvania, United States, 19107
        • Recruiting
        • Alkermes Investigator Site
      • Wyomissing, Pennsylvania, United States, 19610
        • Recruiting
        • Alkermes Investigator Site
    • South Carolina
      • Columbia, South Carolina, United States, 29201
        • Recruiting
        • Alkermes Investigator Site
    • Texas
      • Austin, Texas, United States, 78731
        • Recruiting
        • Alkermes Investigator Site
      • San Antonio, Texas, United States, 78229
        • Recruiting
        • Alkermes Investigator Site
      • Sugar Land, Texas, United States, 77478
        • Recruiting
        • Alkermes Investigator Site
      • Sugarland, Texas, United States, 77478
        • Recruiting
        • Alkermes Investigator Site
    • Wisconsin
      • Madison, Wisconsin, United States, 53792
        • Recruiting
        • Alkermes Investigator Site

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Eligibility Criteria

The key requirements that people who want to participate in a clinical study must meet or the characteristics they must have. Eligibility criteria consist of both inclusion criteria (which are required for a person to participate in the study) and exclusion criteria (which prevent a person from participating). Types of eligibility criteria include whether a study accepts healthy volunteers, has age or age group requirements, or is limited by sex.

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Is willing and able, in the opinion of the Investigator, to understand and comply with protocol requirements, including: lifestyle considerations and restrictions, adherence to contraception guidance, adherence to actigraphy and diary requirements, if receiving treatment for OSA, adherence to primary OSA therapy over the 30 days prior to Visit 1, and throughout the study, including during overnight visits.
  • Meets the diagnostic criteria of Idiopathic Hypersomnia according to ICSD-3-TR guidelines, confirmed by the diagnostic evaluations (PSG/MSLT/actigraphy) within the previous 10 years

Exclusion Criteria:

  • Has another comorbid sleep disorder or condition that may influence the sleep-wake cycle
  • Has a history or presence at Visit 1 of other clinically significant (treated or untreated) illness, disease, abnormality, or surgical procedure that, in the opinion of the Investigator, might compromise subject safety, interfere with any study assessment, or affect the subject's ability to complete the study
  • Is currently enrolled in another clinical study or used any investigational drug or device within 30 days prior to Visit 1
  • Is currently pregnant, breastfeeding, or is planning to become pregnant during the study

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm

Participant Group / Arm

A group or subgroup of participants in a clinical trial that receives a specific intervention/treatment, or no intervention, according to the trial's protocol.
Intervention / Treatment

Intervention / Treatment

A process or action that is the focus of a clinical study. Interventions include drugs, medical devices, procedures, vaccines, and other products that are either investigational or already available. Interventions can also include noninvasive approaches, such as education or modifying diet and exercise.
Experimental: ALKS 2680, 10 mg- Part A
Oral tablet containing 10 mg of ALKS 2680 for once daily administration
Drug: ALKS 2680
Oral tablet containing ALKS 2680 for daily, oral administration
Experimental: ALKS 2680, 14 mg -Part A
Oral tablet containing 14 mg of ALKS 2680 for once daily administration
Drug: ALKS 2680
Oral tablet containing ALKS 2680 for daily, oral administration
Experimental: ALKS 2680, 18 mg- Part A
Oral tablet containing 18 mg of ALKS 2680 for once daily administration
Drug: ALKS 2680
Oral tablet containing ALKS 2680 for daily, oral administration
Placebo Comparator: Placebo- Part A
Oral placebo tablet for once daily administration
Drug: Placebo
Oral placebo tablet for daily administration
Experimental: ALKS 2680 Dose 1- Part B
Oral tablets of ALKS 2680 taken, orally, daily
Drug: ALKS 2680
Oral tablet containing ALKS 2680 for daily, oral administration
Placebo Comparator: Placebo - Part B
Oral tablets of placebo taken, orally, daily
Drug: Placebo
Oral placebo tablet for daily administration

What is the study measuring?

Primary Outcome Measures

Primary Outcome Measures

In a clinical study's protocol, the planned outcome measure that is the most important for evaluating the effect of an intervention/treatment. Most clinical studies have one primary outcome measure, but some have more than one.
Outcome Measure
Time Frame
Change in Epworth Sleepiness Scale (ESS) from baseline to Week 8 by dose level
Time Frame: Up to 8 weeks
Up to 8 weeks

Secondary Outcome Measures

Secondary Outcome Measures

In a clinical study's protocol, a planned outcome measure that is not as important as the primary outcome measure for evaluating the effect of an intervention but is still of interest. Most clinical studies have more than one secondary outcome measure.
Outcome Measure
Time Frame
Change in Idiopathic Hypersomnia Severity Scale (IHSS) from baseline to Week 8 by dose level
Time Frame: Up to 8 weeks
Up to 8 weeks
Incidence of treatment emergent adverse events
Time Frame: Up to 10 weeks
Up to 10 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Sponsor

The organization or person who initiates the study and who has authority and control over the study.
Alkermes, Inc.

Investigators

Investigators

A researcher involved in a clinical study. Related terms include site principal investigator, site sub-investigator, study chair, study director, and study principal investigator.
  • Study Director: Medical Director, Alkermes, Inc.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Helpful Links

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

Study Start

The actual date on which the first participant was enrolled in a clinical study. The "anticipated" study start date is the date that the researchers think will be the study start date.
May 22, 2025

Primary Completion (Estimated)

Primary Completion

The date on which the last participant in a clinical study was examined or received an intervention to collect final data for the primary outcome measure. Whether the clinical study ended according to the protocol or was terminated does not affect this date. For clinical studies with more than one primary outcome measure with different completion dates, this term refers to the date on which data collection is completed for all the primary outcome measures. The "anticipated" primary completion date is the date that the researchers think will be the primary completion date for the study.
November 1, 2026

Study Completion (Estimated)

Study Completion

The date on which the last participant in a clinical study was examined or received an intervention/treatment to collect final data for the primary outcome measures, secondary outcome measures, and adverse events (that is, the last participant's last visit). The "anticipated" study completion date is the date that the researchers think will be the study completion date.
November 1, 2026

Study Registration Dates

First Submitted

First Submitted

The date on which the study sponsor or investigator first submitted a study record to ClinicalTrials.gov. There is typically a delay of a few days between the first submitted date and the record's availability on ClinicalTrials.gov (the first posted date).
February 21, 2025

First Submitted That Met QC Criteria

First Submitted That Met QC Criteria

The date on which the study sponsor or investigator first submits a study record that is consistent with National Library of Medicine (NLM) quality control (QC) review criteria. The sponsor or investigator may need to revise and submit a study record one or more times before NLM's QC review criteria are met. It is the responsibility of the sponsor or investigator to ensure that the study record is consistent with the NLM QC review criteria.
February 21, 2025

First Posted (Actual)

First Posted

The date on which the study record was first available on ClinicalTrials.gov after National Library of Medicine (NLM) quality control (QC) review has concluded. There is typically a delay of a few days between the date the study sponsor or investigator submitted the study record and the first posted date.
February 25, 2025

Study Record Updates

Last Update Posted (Actual)

Last Update Posted

The most recent date on which changes to a study record were made available on ClinicalTrials.gov. There may be a delay between when the changes were submitted to ClinicalTrials.gov by the study's sponsor or investigator (the last update submitted date) and the last update posted date.
June 24, 2026

Last Update Submitted That Met QC Criteria

Last Update Submitted That Met QC Criteria

The most recent date on which the study sponsor or investigator submitted changes to a study record that are consistent with National Library of Medicine (NLM) quality control (QC) review criteria. It is the responsibility of the sponsor or investigator to ensure that the study record is consistent with the NLM QC review criteria.
June 22, 2026

Last Verified

Last Verified

The most recent date on which the study sponsor or investigator confirmed the information about a clinical study on ClinicalTrials.gov as accurate and current. If a study with a recruitment status of recruiting; not yet recruiting; or active, not recruiting has not been confirmed within the past 2 years, the study's recruitment status is shown as unknown.
June 1, 2026

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

Other Study ID Numbers

Identifiers or ID numbers other than the NCT number that are assigned to a clinical study by the study's sponsor, funders, or others. These numbers may include unique identifiers from other trial registries and National Institutes of Health grant numbers.
  • ALKS 2680-203

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

Yes

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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