176 Participants NeededMy employer runs this trial

ALKS 2680 for Narcolepsy

(Brilliance NT2 Trial)

Recruiting at 37 trial locations
DC
Overseen ByDirector Clinical Trial Manager
Age: 18+
Sex: Any
Trial Phase: Phase 3
Sponsor: Alkermes, Inc.
Pivotal Trial (Near Approval)This treatment is in the last trial phase before FDA approval
Prior Safety DataThis treatment has passed at least one previous human trial

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial tests a new tablet, ALKS 2680, to determine its effectiveness in reducing daytime sleepiness and other symptoms in people with Narcolepsy Type 2 (NT2), a condition that causes excessive sleepiness. Participants will receive one of three different doses of ALKS 2680 or a placebo (a pill with no active medicine) to compare the effects. Individuals diagnosed with NT2 who struggle with daily sleepiness might be suitable for this study. As a Phase 3 trial, this study represents the final step before FDA approval, offering participants a chance to contribute to a potentially groundbreaking treatment.

Do I have to stop taking my current medications for the trial?

The trial information does not specify whether you need to stop taking your current medications. It's best to discuss this with the study team or your doctor.

Is there any evidence suggesting that ALKS 2680 is likely to be safe for humans?

Research has shown that ALKS 2680 is generally safe for both healthy adults and those with narcolepsy. In earlier studies, participants taking ALKS 2680 reported few serious side effects. For instance, single doses up to 8 mg improved sleep without major issues. Other studies found that the treatment was well-tolerated at all doses tested and enhanced wakefulness compared to a placebo. These findings suggest that ALKS 2680 is safe to use, with minimal side effects reported in these studies.12345

Why do researchers think this study treatment might be promising for narcolepsy?

ALKS 2680 is unique because it offers a new approach to treating narcolepsy, a condition often managed by stimulants like modafinil or sodium oxybate. Unlike these standard treatments, ALKS 2680 is being tested in multiple doses, which could offer more personalized and optimized treatment options. Researchers are excited about its potential to provide a different mechanism of action, which might lead to improved wakefulness and reduced symptoms with potentially fewer side effects. This trial is particularly promising because it explores varied dosing, which could lead to more tailored and effective narcolepsy management.

What evidence suggests that ALKS 2680 might be an effective treatment for narcolepsy?

Research has shown that ALKS 2680 may help treat narcolepsy type 2. Studies have found that it significantly improves alertness and reduces daytime sleepiness. For individuals with narcolepsy type 1, ALKS 2680 also enhanced sleep and alertness. Participants generally tolerated the treatment well, and higher doses led to better outcomes. Early evidence suggests that ALKS 2680 could effectively manage symptoms of narcolepsy type 2.12367

Who Is on the Research Team?

SD

Study Director, MD

Principal Investigator

Alkermes, Inc.

Are You a Good Fit for This Trial?

This trial is for adults diagnosed with Narcolepsy Type 2 who can follow study instructions and, if they have sleep apnea, are consistently using their prescribed treatment. Participants must be able to comply with lifestyle rules and keep required diaries.

Inclusion Criteria

* Is willing and able, in the opinion of the Investigator, to understand and comply with protocol requirements, including the following: 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 NT2 according to ICSD-3-TR guidelines, confirmed by diagnostic evaluations (either PSG/MSLT).

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive ALKS 2680 or placebo tablets to measure decreases in daytime sleepiness and disease symptoms

12 weeks

Follow-up

Participants are monitored for safety and effectiveness after treatment

4 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • ALKS 2680

Trial Overview

The study tests different doses of a new tablet called ALKS 2680 against a placebo (inactive pill) to see if it reduces daytime sleepiness and other symptoms in people with Narcolepsy Type 2.

How Is the Trial Designed?

4

Treatment groups

Experimental Treatment

Placebo Group

Group I: ALKS 2680 Dose 3Experimental Treatment1 Intervention
Group II: ALKS 2680 Dose 2Experimental Treatment1 Intervention
Group III: ALKS 2680 Dose 1Experimental Treatment1 Intervention
Group IV: PlaceboPlacebo Group1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Alkermes, Inc.

Lead Sponsor

Trials
118
Recruited
27,200+

Richard Pops

Alkermes, Inc.

Chief Executive Officer since 1991

BA in Economics from Stanford University

Dr. Craig Hopkinson

Alkermes, Inc.

Chief Medical Officer since 2017

MD

Citations

Alixorexton (ALKS 2680) Narcolepsy Type 1 Phase 2 Data ...

The results demonstrated alixorexton's significant effect on wakefulness and other important measures and a generally well tolerated profile.

The Orexin 2 Receptor Agonist ALKS 2680 in Patients with ...

ALKS 2680 was generally well-tolerated. Single doses up to 8 mg led to statistically significant, clinically meaningful improvements in sleep ...

NCT07540897 | A Study to Evaluate the Efficacy, Safety ...

A Study to Evaluate the Efficacy, Safety and Tolerability of ALKS 2680 in Adults With Narcolepsy Type 1 (Brilliance NT1 - 304). ClinicalTrials.

Orexin Receptor Agent ALKS 2680 Meets End Points in ...

ALKS 2680 showed significant, dose-dependent improvements in sleep latency and wakefulness in NT1 patients, supporting phase 3 trials. The trial ...

Alkermes Presents Data From Phase 1b Study of ALKS 2680 ...

"Data from this phase 1b study provide evidence of a significant treatment effect of single doses of ALKS 2680 in patients with narcolepsy type ...

A Study To Evaluate The Safety And Effectiveness Of ALKS ...

The purpose of this research study is to assess the safety and efficacy of ALKS 2680 compared to placebo, including whether participants taking ...

O013 Preliminary Results from a Phase 1 Study of ALKS 2680 ...

Preliminary results suggest that the OX2R agonist ALKS 2680 is generally well-tolerated with a pharmacokinetic profile potentially suitable for once-daily oral ...