🔎 Trials Near Me

Home › Autism Spectrum Disorder › NCT07285798

A Study of KarXT + KarX-EC for Treatment of Irritability in Children and Adolescents With Autism Spectrum Disorder

RecruitingPhase 3

A Phase 3, Multicenter, Randomized, Double-blind, Placebo-controlled Study to Assess the Efficacy, Safety, and Tolerability of KarXT + KarX-EC in Children and Adolescents (5 to 17 Years of Age) With Irritability Associated With Autism Spectrum Disorder

Who can join

Ages 5 to 17 · All sexes

Full eligibility criteria
Inclusion Criteria

* Participants must have a confirmed diagnosis of ASD, as defined by the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition, Text Revision (DSM-5-TR) criteria, confirmed by the K-SADS-PL and must be experiencing symptoms of irritability.
* Participants must have an ABC-I ≥18 (Irritability subscale of the ABC) and CGIS specific to irritability ≥4, at screening and baseline (Day 1).

Exclusion Criteria

* Participants must not have a current primary DSM-5 diagnosis of bipolar disorder, including bipolar II disorder, schizophrenia, schizoaffective disorder, major depressive episode as determined by clinical instrument, or post-traumatic stress disorder (PTSD).
* Exception Include: Participants with comorbid ADHD, provided that attention deficit/hyperactivity disorder (ADHD) is not the primary disorder, the participant is adequately treated and based on the investigator judgment the disorder is clinically stable.
* Participants must not have history/presence of clinically significant disease or disorder that would jeopardize participant safety or validity of study results.
* Participants must not have a risk for suicidal behavior, and any clinically significant abnormal laboratory test.
* Other protocol-defined Inclusion/Exclusion criteria may apply.

About the study

The purpose of this study is to assess KarXT + KarX-EC for the treatment of irritability associated with autism in children and adolescents.

What is being tested

Sponsor: Bristol-Myers Squibb · Participants: 176 · Started: Oct 6, 2026

Contact the study team

Official record on ClinicalTrials.gov — NCT07285798

Locations in the U.S.

ArizonaLocal Institution - 0062, Phoenix (Not yet recruiting)
CaliforniaCortica - Glendale, Glendale
Local Institution - 0117, Los Angeles (Not yet recruiting)
Local Institution - 0126, Orange (Not yet recruiting)
Local Institution - 0132, San Diego (Not yet recruiting)
Local Institution - 0115, San Juan Capistrano (Not yet recruiting)
Cortica - Marin, San Rafael
ConnecticutLocal Institution - 0130, New Haven (Not yet recruiting)
FloridaLocal Institution - 0048, Gainesville (Not yet recruiting)
Local Institution - 0080, Orlando (Not yet recruiting)
GeorgiaLocal Institution - 0072, Decatur (Not yet recruiting)
IllinoisEmVenio Research - Chicago, Chicago
MassachusettsLocal Institution - 0051, Lexington (Not yet recruiting)
MichiganLocal Institution - 0140, Bloomfield Hills (Not yet recruiting)
MissouriLocal Institution - 0016, Columbia (Not yet recruiting)
Local Institution - 0036, Saint Charles (Not yet recruiting)
NebraskaLocal Institution - 0046, Lincoln (Not yet recruiting)
New JerseyLocal Institution - 0114, Neptune City (Not yet recruiting)
New YorkLocal Institution - 0038, Staten Island (Not yet recruiting)
OhioLocal Institution - 0052, Cincinnati (Not yet recruiting)
PennsylvaniaLocal Institution - 0003, Pittsburgh (Not yet recruiting)
TexasLocal Institution - 0125, Spring (Not yet recruiting)
UtahLocal Institution - 0009, Orem (Not yet recruiting)
WashingtonLocal Institution - 0019, Everett (Not yet recruiting)

Conditions

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