RecruitingBipolar Depression

Multicenter Study of Lumateperone for the Treatment of Bipolar Depression in Pediatric Patients

Eligible age

10–17 yrs

Accepts

All genders

Locations

18 states

Healthy volunteers

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About this study

This is a multicenter, randomized, double-blind, placebo-controlled study in pediatric patients who are experiencing major depressive episodes (MDEs) associated with a primary diagnosis of bipolar I or bipolar II disorder as confirmed by Kiddie Schedule for Affective Disorders and Schizophrenia for School-Age Children-Present and Lifetime Version (K-SADS-PL), according to criteria of the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM 5).

Sponsor: Intra-Cellular Therapies, Inc.

You may qualify if…

✓ 1. Able to provide consent as follows:
✓ The Legally Authorized Representative (LAR) must provide written, informed consent.
✓ The patient must provide written assent;
✓ 2. Male or female patients 10 to 17 years of age, inclusive;
✓ 3. Have a Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition Text Revision (DSM-5-TR) primary diagnosis of bipolar I or bipolar II disorder with a current MDE without psychosis as confirmed by Kiddie Schedule for Affective Disorders and Schizophrenia for School-Age Children-Present and Lifetime Version (K-SADS-PL);
✓ 4. Subject has a lifetime history of at least one manic or hypomanic episode.
✓ 5. Subject's current major depressive episode is ≥ 4 weeks and less than 12 months in duration;
✓ 6. CDRS-R total score ≥ 45 with ≥ 5 on Item 11 (depressed feelings) at Screening and Baseline;

You may not qualify if…

✕ 1. Has a primary psychiatric diagnosis other than bipolar I or bipolar II disorder. Exception includes:
✕ Attention deficit hyperactivity disorder (ADHD). If a subject is taking medications for ADHD, they must have been 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.
✕ 2. Intellectual disability based on Investigator opinion and DSM-5 criteria
✕ 3. Patient has been hospitalized for a bipolar manic episode within the 30 days prior to randomization;
✕ 4. Demonstrates a ≥ 25% decrease (improvement) in the CDRS-R total score between Screening and Baseline visits, or the CDRS-R is below 45 at Baseline;
✕ 5. In the opinion of the Investigator, the patient has a significant risk for suicidal behavior during his/her participation in the study or
✕ 1. 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;
✕ 2. At Screening, the patient has had 1 or more suicidal attempts within the 2 years prior to Screening; or