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Clinical Trials in Canada / NCT07284745
Starting soon Phase 3

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

NCT07284745 · tracked via the Priya Life Science Canada tracker
Phase
Phase 3
Started
2026-09-11
Last updated
2026-08-24

Condition(s) studied

Irritability Associated With Autism Spectrum Disorder

Investigational drug(s) / intervention(s)

KarXT →KarX-EC →KarXT + KarX-EC Matching Placebo

KarXT: Specified dose on specified days

KarX-EC: Specified dose on specified days

KarXT + KarX-EC Matching Placebo: Specified dose on specified days

Study summary

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

Eligibility

Sex
ALL
Min age
5 Years
Max age
17 Years
Healthy volunteers
No
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.

Primary outcome measure(s)

Trial sites (39)

FacilityCityRegionStatus
Local Institution - 0036 Dothan Alabama
Local Institution - 0236 Phoenix Arizona
Local Institution - 0031 Anaheim California
Local Institution - 0257 Glendale California
Local Institution - 0233 Redlands California
Local Institution - 0181 San Rafael California
Local Institution - 0252 Colorado Springs Colorado
Local Institution - 0264 Boca Raton Florida
Local Institution - 0099 Gainesville Florida
Local Institution - 0278 Gainesville Florida
Local Institution - 0155 Peachtree Corners Georgia
Local Institution - 0266 Chicago Illinois
Local Institution - 0242 Louisville Kentucky
Local Institution - 0160 Bloomfield Hills Michigan
Local Institution - 0220 Detroit Michigan
Local Institution - 0110 Las Vegas Nevada
Local Institution - 0246 Staten Island New York
Local Institution - 0263 The Bronx New York
Local Institution - 0122 Cincinnati Ohio
Local Institution - 0247 West Chester Ohio
Local Institution - 0269 Danville Pennsylvania
Local Institution - 0041 Dallas Texas
Local Institution - 0034 Houston Texas
Local Institution - 0273 Plano Texas
Local Institution - 0291 San Antonio Texas
Local Institution - 0185 Spring Texas
Local Institution - 0074 Bountiful Utah
Local Institution - 0271 Provo Utah
Local Institution - 0260 Richmond Virginia
Local Institution - 0010 Westmead New South Wales
Local Institution - 0007 Brisbane Queensland
Local Institution - 0045 Melbourne Victoria
Local Institution - 0286 Melbourne Victoria
Local Institution - 0289 Airdrie Alberta
Local Institution - 0136 Edmonton Alberta
Local Institution - 0135 Kingston Ontario
Local Institution - 0205 Toronto Ontario
Local Institution - 0187 Montreal Quebec
Local Institution - 0234 San Juan Puerto Rico

More Bristol-Myers Squibb trials in Canada

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07284745 on ClinicalTrials.gov ↗ ← All trials in Canada