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NCT06690398RecruitingPhase 3

Multicenter Study of Lumateperone for the Treatment of Irritability Associated With Autism Spectrum Disorder 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
13 Nov 2024
Start date
22 Nov 2024
Primary completion date
21 Jun 2027
Lead sponsor
Intra-Cellular Therapies, Inc.
Diseases
Autism
NCT number
NCT06690398

What you commit to

  • Study type: Interventional · Phase 3
  • Planned participants: 160
  • From 22 Nov 2024 to the primary completion date, 21 Jun 2027
  • 39 sites in 2 countries
  • 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 (C-SSRS) 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 (39)

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

SiteCityCountrySite status
Clinic of Neurology and Psychiatry for Children and Youth
Coordinator of this site? Confirm its status
BelgradeSerbiaRecruiting
Institute of Mental Health Serbia 1
Coordinator of this site? Confirm its status
BelgradeSerbiaRecruiting
Institute of Mental Health Serbia
Coordinator of this site? Confirm its status
BelgradeSerbiaRecruiting
University Clinical Center NIS
Coordinator of this site? Confirm its status
NišSerbiaRecruiting
Advanced Research Center, Inc.
Coordinator of this site? Confirm its status
AnaheimUnited StatesRecruiting
REX Clinical Trials LLC
Coordinator of this site? Confirm its status
BeaumontUnited StatesRecruiting
Northwest Clinical Research Center
Coordinator of this site? Confirm its status
BellevueUnited StatesRecruiting
Massachusetts General Hospital
Coordinator of this site? Confirm its status
BostonUnited StatesCompleted
MCB Clinical Research Centers LLC
Coordinator of this site? Confirm its status
Colorado SpringsUnited StatesCompleted
Harmonex Neuroscience Research
Coordinator of this site? Confirm its status
DothanUnited StatesRecruiting
Revive Research Institute
Coordinator of this site? Confirm its status
ElginUnited StatesRecruiting
North Pointe Psychiatry
Coordinator of this site? Confirm its status
Flower MoundUnited StatesCompleted
Royal Palm Clinical Research
Coordinator of this site? Confirm its status
Fort MyersUnited StatesSuspended
Sarkis Clinical Trials
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GainesvilleUnited StatesRecruiting
Charak Center for Health and Wellness
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GarfieldUnited StatesRecruiting
Kaleidoscope Clinical Research
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HoustonUnited StatesRecruiting
Green Leaf Clinical Trials
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JacksonvilleUnited StatesRecruiting
Vector Clinical Trials
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Las VegasUnited StatesRecruiting
Columbus Clinical Services LLC
Coordinator of this site? Confirm its status
MiamiUnited StatesRecruiting
Anchor Medical Research LLC
Coordinator of this site? Confirm its status
MiamiUnited StatesRecruiting
South Florida Research Phase I-IV
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MiamiUnited StatesRecruiting
Diverse Clinical Research LLC
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MiamiUnited StatesRecruiting
Links Clinical Trials
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MiamiUnited StatesRecruiting
The Angel Medical Research Corporation
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Miami GardensUnited StatesRecruiting
Access Clinical Trials
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NashvilleUnited StatesRecruiting
Excell Research, Inc.
Coordinator of this site? Confirm its status
OceansideUnited StatesRecruiting
Clinical Research Partners, LLC
Coordinator of this site? Confirm its status
PetersburgUnited StatesRecruiting
Southwest Autism Research and Resource Center
Coordinator of this site? Confirm its status
PhoenixUnited StatesRecruiting
AIM Trials
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PlanoUnited StatesRecruiting
Inland Psychiatric Medical Group, Inc.
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RedlandsUnited StatesRecruiting
Perceptive Pharma Research
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RichmondUnited StatesRecruiting
Midwest Research Group
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Saint CharlesUnited StatesRecruiting
CenExeli Research LLC
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SavannahUnited StatesRecruiting
Southern Illinois University School of Medicine
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SpringfieldUnited StatesSuspended
Buena Park Research
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UplandUnited StatesCompleted
Next Level Clinical Trials, LLC
Coordinator of this site? Confirm its status
West CovinaUnited StatesRecruiting
Westlake Brain Health
Coordinator of this site? Confirm its status
WestlakeUnited StatesCompleted
Health Synergy Clinical Research
Coordinator of this site? Confirm its status
West Palm BeachUnited StatesRecruiting
UMass Memorial Healthcare
Coordinator of this site? Confirm its status
WorcesterUnited StatesRecruiting

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