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A Study to Evaluate Safety and Efficacy of ALKS 7290 Compared With Placebo in Adult Participants With Attention Deficit Hyperactivity Disorder (ALKS 7290-201)

RecruitingPhase 2

A Phase 2, Randomized, Parallel-Group, Double-Blind, Study to Evaluate the Safety and Efficacy of ALKS 7290 Compared to Placebo in Adult Participants With Attention Deficit Hyperactivity Disorder

Who can join

Ages 18 to 65 · All sexes

Full eligibility criteria
Inclusion Criteria:

* Meets the Diagnostic and Statistical Manual of Mental Disorders -5 criteria for ADHD, as confirmed by the Mini-International Neuropsychiatric Interview (MINI) for ADHD Studies 7.0.2.
* Is otherwise healthy as determined by medical evaluation, including medical history, physical examination, laboratory tests, and cardiac monitoring. Participants must be stable on permitted medication for 2 months prior to first visit, without anticipated changes to dose.
* AISRS total score of ≥26
* CGI-S score ≥ 4 (moderately ill or worse)
* Has a Body Mass Index within 18 to 35 kg/m2

Exclusion Criteria:

* Has a known history of intellectual developmental disorder or cognitive impairment that, in the opinion of the Investigator, would interfere with study participation.
* Has any of the following psychiatric conditions per the DSM-5 criteria, as assessed by the MINI. Conditions not assessable by the MINI should be assessed by clinical judgement; Diagnosis of schizophrenia, schizoaffective disorder, or bipolar I or II disorder, or current, unstable, MDD or GAD.
* Clinically significant cognitive difficulties including dementia, delirium or amnestic syndromes, or any other cognitive disorder present with the past 2 years that could interfere with participation in the study.
* Moderate to severe substance use disorder according to DSM-5 guidelines, including use of alcohol, nicotine, cannabis, narcotics, or any illicit substance.
* Any other psychiatric condition that could interfere with participation in the study.

About the study

The purpose of this study is to measure safety and the improvement in symptoms in subjects with ADHD when taking ALKS 7290 tablets compared with placebo tablets.

What is being tested

Sponsor: Alkermes, Inc. · Participants: 312 · Started: Aug 10, 2026

Contact the study team

Official record on ClinicalTrials.gov — NCT07755410

Locations in the U.S.

ArkansasAlkermes Investigational Site, Little Rock
CaliforniaAlkermes Investigational Site, Chino
Alkermes Investigator Site, Chino
FloridaAlkermes Investigational Site, Clermont
Alkermes Investigational Site, Jacksonville
Alkermes Investigational Site, Lakeland
Alkermes Investigational Site, Largo
Alkermes Investigational Site, Maitland
Alkermes Investigational Site, Maitland
Alkermes Investigator Site, Maitland
Alkermes Investigational Site, Orange City
Alkermes Investigational Site, Orlando
Alkermes Investigational Site, Tampa
GeorgiaAlkermes Investigational Site, Decatur
MassachusettsAlkermes Investigational Site, Foxborough
Alkermes Investigational Site, Watertown
MichiganAlkermes Investigational Site, Detroit
Alkermes Investigational Site, Memphis
NebraskaAlkermes Investigational Site, Lincoln
NevadaAlkermes Investigational Site, Las Vegas
Alkermes Investigational Site, Las Vegas
OhioAlkermes Investigational Site, North Canton
Rhode IslandAlkermes Investigational Site, East Providence
South CarolinaAlkermes Investigational Site, North Charleston
TexasAlkermes Investigational Site, Austin
Alkermes Investigational Site, Austin
Alkermes Investigational Site, The Woodlands
WashingtonAlkermes Investigational Site, Bellevue

Conditions

From ClinicalTrials.gov, data retrieved Nov 15, 2026. Each study sets its own eligibility; the study team decides who can join.