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NCT06706674RecruitingPhase 3

Multicenter Study of Lumateperone for the Treatment of Irritability Associated With Autism Spectrum Disorder (ASD) in Pediatric Patients

A Randomized, Double-blind, Placebo-controlled, Multicenter Study to Assess the Efficacy and Safety of Lumateperone in the Treatment of Irritability Associated With Autism Spectrum Disorder in Pediatric Patients 5 to 17 Years of Age

Source: ClinicalTrials.gov · Last updated 3 Nov 2026

Brief summary (registry, in English)

This is a multicenter, randomized, double-blind, placebo-controlled study in pediatric patients aged 5 to 17 years with a primary diagnosis of irritability associated with Autism Spectrum Disorder (ASD) based on Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition Text Revision (DSM-5-TR) and confirmed by the Kiddie Schedule for Affective Disorders and Schizophrenia Present and Lifetime Version (K-SADS-PL).

Status (registry)
Recruiting
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
160 (estimated)
First submitted
22 Nov 2024
Start date
6 Dec 2024
Primary completion date
21 Jun 2027
Lead sponsor
Intra-Cellular Therapies, Inc.
Diseases
Autism
NCT number
NCT06706674

What you commit to

  • Study type: Interventional · Phase 3
  • Planned participants: 160
  • From 6 Dec 2024 to the primary completion date, 21 Jun 2027
  • 41 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Has a primary psychiatric diagnosis other than ASD. Exceptions include:
    • Attention Deficit Hyperactivity Disorder (ADHD). If a patient is taking medication(s) for ADHD, they must be on a stable treatment regimen of these medication(s) for 30 days prior to screening and the treatment regimen is expected to remain stable throughout the study. This must be confirmed by the Investigator and noted in the source records.
    • Mild and moderate intellectual disability based on Investigator judgment and DSM-5 criteria (severe and profound intellectual disability are excluded).
  • In the opinion of the Investigator, the patient has a significant risk for suicidal behavior during their participation in the study or
    • At Screening, the patient scores "yes" on Suicidal Ideation Items 3, 4, or 5 of the Columbia-Suicide Severity Rating Scale (CSSRS) within 6 months prior to Screening or, at Baseline, the patient scores "yes" on Suicidal Ideation Items 3, 4, or 5 since the Screening Visit;
    • At Screening, the patient has had 1 or more suicidal attempts within the 2 years prior to Screening; or
    • The patient is considered to be an imminent danger to themselves or others.

Other illness

  • History or current diagnosis of Rett syndrome or Fragile X syndrome;

Who the study is looking for

  • All patients must have a legally authorized representative LAR (eg, parent or legal guardian) who is willing and able to be responsible for the safety and well-being of the patient, provide information about the patient's condition, and accompany the patient to study visits.
  • Able to provide consent as follows:
    • The patient's LAR must provide written, informed consent.
    • When developmentally appropriate based on Investigator judgment, the patient should provide written assent.
  • Male or female patients 5 to 17 years of age. Currently, only patients aged 13 to 17 years will be eligible for enrollment.
  • Meet Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition Text Revision (DSM-5-TR) primary diagnosis of ASD as confirmed by the Kiddie Schedule for Affective Disorders and Schizophrenia for School-Age Children-Present and Lifetime Version (K-SADS-PL);
  • ABC-I subscale score of \>18 at Screening and Baseline;
  • CGI-S score \> 4 with respect to irritability associated with ASD at Screening and Baseline.

Age in the registry: 5 years to 17 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (41)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Advanced Discovery Research
Coordinator of this site? Confirm its status
AtlantaUnited StatesCompleted
BioBehavioral Research of Austin PC
Coordinator of this site? Confirm its status
AustinUnited StatesCompleted
Quest Therapeutics of Avon Lake
Coordinator of this site? Confirm its status
Avon LakeUnited StatesCompleted
NeuroBehavioral Medicine Group
Coordinator of this site? Confirm its status
Bloomfield HillsUnited StatesRecruiting
Medical University of South Carolina
Coordinator of this site? Confirm its status
CharlestonUnited StatesRecruiting
EmVenio Research at Chicago
Coordinator of this site? Confirm its status
ChicagoUnited StatesRecruiting
Texas Research Group
Coordinator of this site? Confirm its status
CoppellUnited StatesRecruiting
Future Search Trials of Dallas
Coordinator of this site? Confirm its status
DallasUnited StatesCompleted
Core Clinical Research
Coordinator of this site? Confirm its status
EverettUnited StatesRecruiting
North Texas Clinical Trials
Coordinator of this site? Confirm its status
Fort WorthUnited StatesRecruiting
United Research Institute
Coordinator of this site? Confirm its status
HialeahUnited StatesRecruiting
Advanced Research Institute of Miami
Coordinator of this site? Confirm its status
HomesteadUnited StatesSuspended
Red Oak Psychiatry Associates
Coordinator of this site? Confirm its status
HoustonUnited StatesCompleted
Riley Hospital for Children at Indiana University Health
Coordinator of this site? Confirm its status
IndianapolisUnited StatesCompleted
Salveo Integrative Health Inc
Coordinator of this site? Confirm its status
LawrencevilleUnited StatesCompleted
Alivation Research, LLC
Coordinator of this site? Confirm its status
LincolnUnited StatesRecruiting
Pillar Clinical Research, LLC
Coordinator of this site? Confirm its status
Little RockUnited StatesRecruiting
Blue Medical Research
Coordinator of this site? Confirm its status
MiamiUnited StatesRecruiting
Vital Care Research
Coordinator of this site? Confirm its status
MiamiUnited StatesSuspended
AP Medical Research
Coordinator of this site? Confirm its status
MiamiUnited StatesRecruiting
Care Research Center Inc
Coordinator of this site? Confirm its status
MiamiUnited StatesRecruiting
GTL Medical and Research Group
Coordinator of this site? Confirm its status
MiamiUnited StatesCompleted
New Med Research Inc
Coordinator of this site? Confirm its status
Miami GardensUnited StatesRecruiting
Riveldi Biomedical Research
Coordinator of this site? Confirm its status
Miami LakesUnited StatesSuspended
Baber Research Group
Coordinator of this site? Confirm its status
NapervilleUnited StatesRecruiting
Yale University School Of Medicine
Coordinator of this site? Confirm its status
New HavenUnited StatesRecruiting
NYU Child Study Center
Coordinator of this site? Confirm its status
New YorkUnited StatesSuspended
Sooner Clinical Research
Coordinator of this site? Confirm its status
NormanUnited StatesRecruiting
SP Research, PLLC (dba Rivus Wellness & Research Institute)
Coordinator of this site? Confirm its status
Oklahoma CityUnited StatesRecruiting
Nathan Kline Institute
Coordinator of this site? Confirm its status
OrangeburgUnited StatesRecruiting
APG Research, LLC
Coordinator of this site? Confirm its status
OrlandoUnited StatesRecruiting
Orlando Psychiatric Associates
Coordinator of this site? Confirm its status
OrlandoUnited StatesCompleted
Clinical Research Center of Florida
Coordinator of this site? Confirm its status
Pompano BeachUnited StatesRecruiting
Virginia Commonwealth University
Coordinator of this site? Confirm its status
RichmondUnited StatesRecruiting
University of California - Davis
Coordinator of this site? Confirm its status
SacramentoUnited StatesRecruiting
California Neuroscience Research
Coordinator of this site? Confirm its status
Sherman OaksUnited StatesRecruiting
Louisiana State University Health Sciences Center Shreveport
Coordinator of this site? Confirm its status
ShreveportUnited StatesRecruiting
Richmond Behavioral Associates
Coordinator of this site? Confirm its status
Staten IslandUnited StatesRecruiting
University of South Florida Rothman Center of Neuropsychiatry
Coordinator of this site? Confirm its status
St. PetersburgUnited StatesRecruiting
Albert Einstein College of Medicine
Coordinator of this site? Confirm its status
The BronxUnited StatesRecruiting
Advantage Clinical Trials
Coordinator of this site? Confirm its status
The BronxUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.