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
Sites (39)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Clinic of Neurology and Psychiatry for Children and Youth Coordinator of this site? Confirm its status | Belgrade | Serbia | Recruiting |
| Institute of Mental Health Serbia 1 Coordinator of this site? Confirm its status | Belgrade | Serbia | Recruiting |
| Institute of Mental Health Serbia Coordinator of this site? Confirm its status | Belgrade | Serbia | Recruiting |
| University Clinical Center NIS Coordinator of this site? Confirm its status | Niš | Serbia | Recruiting |
| Advanced Research Center, Inc. Coordinator of this site? Confirm its status | Anaheim | United States | Recruiting |
| REX Clinical Trials LLC Coordinator of this site? Confirm its status | Beaumont | United States | Recruiting |
| Northwest Clinical Research Center Coordinator of this site? Confirm its status | Bellevue | United States | Recruiting |
| Massachusetts General Hospital Coordinator of this site? Confirm its status | Boston | United States | Completed |
| MCB Clinical Research Centers LLC Coordinator of this site? Confirm its status | Colorado Springs | United States | Completed |
| Harmonex Neuroscience Research Coordinator of this site? Confirm its status | Dothan | United States | Recruiting |
| Revive Research Institute Coordinator of this site? Confirm its status | Elgin | United States | Recruiting |
| North Pointe Psychiatry Coordinator of this site? Confirm its status | Flower Mound | United States | Completed |
| Royal Palm Clinical Research Coordinator of this site? Confirm its status | Fort Myers | United States | Suspended |
| Sarkis Clinical Trials Coordinator of this site? Confirm its status | Gainesville | United States | Recruiting |
| Charak Center for Health and Wellness Coordinator of this site? Confirm its status | Garfield | United States | Recruiting |
| Kaleidoscope Clinical Research Coordinator of this site? Confirm its status | Houston | United States | Recruiting |
| Green Leaf Clinical Trials Coordinator of this site? Confirm its status | Jacksonville | United States | Recruiting |
| Vector Clinical Trials Coordinator of this site? Confirm its status | Las Vegas | United States | Recruiting |
| Columbus Clinical Services LLC Coordinator of this site? Confirm its status | Miami | United States | Recruiting |
| Anchor Medical Research LLC Coordinator of this site? Confirm its status | Miami | United States | Recruiting |
| South Florida Research Phase I-IV Coordinator of this site? Confirm its status | Miami | United States | Recruiting |
| Diverse Clinical Research LLC Coordinator of this site? Confirm its status | Miami | United States | Recruiting |
| Links Clinical Trials Coordinator of this site? Confirm its status | Miami | United States | Recruiting |
| The Angel Medical Research Corporation Coordinator of this site? Confirm its status | Miami Gardens | United States | Recruiting |
| Access Clinical Trials Coordinator of this site? Confirm its status | Nashville | United States | Recruiting |
| Excell Research, Inc. Coordinator of this site? Confirm its status | Oceanside | United States | Recruiting |
| Clinical Research Partners, LLC Coordinator of this site? Confirm its status | Petersburg | United States | Recruiting |
| Southwest Autism Research and Resource Center Coordinator of this site? Confirm its status | Phoenix | United States | Recruiting |
| AIM Trials Coordinator of this site? Confirm its status | Plano | United States | Recruiting |
| Inland Psychiatric Medical Group, Inc. Coordinator of this site? Confirm its status | Redlands | United States | Recruiting |
| Perceptive Pharma Research Coordinator of this site? Confirm its status | Richmond | United States | Recruiting |
| Midwest Research Group Coordinator of this site? Confirm its status | Saint Charles | United States | Recruiting |
| CenExeli Research LLC Coordinator of this site? Confirm its status | Savannah | United States | Recruiting |
| Southern Illinois University School of Medicine Coordinator of this site? Confirm its status | Springfield | United States | Suspended |
| Buena Park Research Coordinator of this site? Confirm its status | Upland | United States | Completed |
| Next Level Clinical Trials, LLC Coordinator of this site? Confirm its status | West Covina | United States | Recruiting |
| Westlake Brain Health Coordinator of this site? Confirm its status | Westlake | United States | Completed |
| Health Synergy Clinical Research Coordinator of this site? Confirm its status | West Palm Beach | United States | Recruiting |
| UMass Memorial Healthcare Coordinator of this site? Confirm its status | Worcester | United States | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.