🔎 Trials Near Me

Home › Autism Spectrum Disorder › NCT07284745

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

RecruitingPhase 3

A Phase 3, Multicenter, Randomized, Double-blind, Placebo-controlled Study to Assess the Efficacy, Safety, Tolerability, and Pharmacokinetics 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 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 — NCT07284745

Locations in the U.S.

AlabamaLocal Institution - 0036, Dothan (Not yet recruiting)
ArizonaLocal Institution - 0236, Phoenix (Not yet recruiting)
CaliforniaLocal Institution - 0031, Anaheim (Not yet recruiting)
Cortica - Glendale, Glendale
Cortica - Marin, San Rafael
FloridaLocal Institution - 0264, Boca Raton (Not yet recruiting)
Local Institution - 0099, Gainesville (Not yet recruiting)
Local Institution - 0278, Gainesville (Not yet recruiting)
Local Institution - 0295, Virginia Gardens (Not yet recruiting)
GeorgiaLocal Institution - 0155, Peachtree Corners (Not yet recruiting)
IllinoisEmVenio Research - Chicago, Chicago
KentuckyLocal Institution - 0242, Louisville (Not yet recruiting)
MichiganLocal Institution - 0160, Bloomfield Hills (Not yet recruiting)
NevadaLocal Institution - 0110, Las Vegas (Not yet recruiting)
New YorkLocal Institution - 0290, New York (Not yet recruiting)
Local Institution - 0246, Staten Island (Not yet recruiting)
Local Institution - 0263, The Bronx (Not yet recruiting)
OhioLocal Institution - 0122, Cincinnati (Not yet recruiting)
PennsylvaniaLocal Institution - 0269, Danville (Not yet recruiting)
TennesseeLocal Institution - 0292, Nashville (Not yet recruiting)
TexasLocal Institution - 0041, Dallas (Not yet recruiting)
Local Institution - 0034, Houston (Not yet recruiting)
Local Institution - 0273, Plano (Not yet recruiting)
Local Institution - 0291, San Antonio (Not yet recruiting)
Local Institution - 0185, Spring (Not yet recruiting)
UtahLocal Institution - 0294, Orem (Not yet recruiting)
Local Institution - 0293, West Point (Not yet recruiting)
VirginiaLocal Institution - 0260, Richmond (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.