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
Sites (41)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Advanced Discovery Research Coordinator of this site? Confirm its status | Atlanta | United States | Completed |
| BioBehavioral Research of Austin PC Coordinator of this site? Confirm its status | Austin | United States | Completed |
| Quest Therapeutics of Avon Lake Coordinator of this site? Confirm its status | Avon Lake | United States | Completed |
| NeuroBehavioral Medicine Group Coordinator of this site? Confirm its status | Bloomfield Hills | United States | Recruiting |
| Medical University of South Carolina Coordinator of this site? Confirm its status | Charleston | United States | Recruiting |
| EmVenio Research at Chicago Coordinator of this site? Confirm its status | Chicago | United States | Recruiting |
| Texas Research Group Coordinator of this site? Confirm its status | Coppell | United States | Recruiting |
| Future Search Trials of Dallas Coordinator of this site? Confirm its status | Dallas | United States | Completed |
| Core Clinical Research Coordinator of this site? Confirm its status | Everett | United States | Recruiting |
| North Texas Clinical Trials Coordinator of this site? Confirm its status | Fort Worth | United States | Recruiting |
| United Research Institute Coordinator of this site? Confirm its status | Hialeah | United States | Recruiting |
| Advanced Research Institute of Miami Coordinator of this site? Confirm its status | Homestead | United States | Suspended |
| Red Oak Psychiatry Associates Coordinator of this site? Confirm its status | Houston | United States | Completed |
| Riley Hospital for Children at Indiana University Health Coordinator of this site? Confirm its status | Indianapolis | United States | Completed |
| Salveo Integrative Health Inc Coordinator of this site? Confirm its status | Lawrenceville | United States | Completed |
| Alivation Research, LLC Coordinator of this site? Confirm its status | Lincoln | United States | Recruiting |
| Pillar Clinical Research, LLC Coordinator of this site? Confirm its status | Little Rock | United States | Recruiting |
| Blue Medical Research Coordinator of this site? Confirm its status | Miami | United States | Recruiting |
| Vital Care Research Coordinator of this site? Confirm its status | Miami | United States | Suspended |
| AP Medical Research Coordinator of this site? Confirm its status | Miami | United States | Recruiting |
| Care Research Center Inc Coordinator of this site? Confirm its status | Miami | United States | Recruiting |
| GTL Medical and Research Group Coordinator of this site? Confirm its status | Miami | United States | Completed |
| New Med Research Inc Coordinator of this site? Confirm its status | Miami Gardens | United States | Recruiting |
| Riveldi Biomedical Research Coordinator of this site? Confirm its status | Miami Lakes | United States | Suspended |
| Baber Research Group Coordinator of this site? Confirm its status | Naperville | United States | Recruiting |
| Yale University School Of Medicine Coordinator of this site? Confirm its status | New Haven | United States | Recruiting |
| NYU Child Study Center Coordinator of this site? Confirm its status | New York | United States | Suspended |
| Sooner Clinical Research Coordinator of this site? Confirm its status | Norman | United States | Recruiting |
| SP Research, PLLC (dba Rivus Wellness & Research Institute) Coordinator of this site? Confirm its status | Oklahoma City | United States | Recruiting |
| Nathan Kline Institute Coordinator of this site? Confirm its status | Orangeburg | United States | Recruiting |
| APG Research, LLC Coordinator of this site? Confirm its status | Orlando | United States | Recruiting |
| Orlando Psychiatric Associates Coordinator of this site? Confirm its status | Orlando | United States | Completed |
| Clinical Research Center of Florida Coordinator of this site? Confirm its status | Pompano Beach | United States | Recruiting |
| Virginia Commonwealth University Coordinator of this site? Confirm its status | Richmond | United States | Recruiting |
| University of California - Davis Coordinator of this site? Confirm its status | Sacramento | United States | Recruiting |
| California Neuroscience Research Coordinator of this site? Confirm its status | Sherman Oaks | United States | Recruiting |
| Louisiana State University Health Sciences Center Shreveport Coordinator of this site? Confirm its status | Shreveport | United States | Recruiting |
| Richmond Behavioral Associates Coordinator of this site? Confirm its status | Staten Island | United States | Recruiting |
| University of South Florida Rothman Center of Neuropsychiatry Coordinator of this site? Confirm its status | St. Petersburg | United States | Recruiting |
| Albert Einstein College of Medicine Coordinator of this site? Confirm its status | The Bronx | United States | Recruiting |
| Advantage Clinical Trials Coordinator of this site? Confirm its status | The Bronx | United States | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.