RECRUITING

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

Description

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).

Study Overview

Study Details

Study overview

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).

A Randomized, Double-blind, Placebo-controlled, Multicenter Study to Evaluate the Efficacy and Safety of Lumateperone for the Treatment of Major Depressive Episodes (MDEs) Associated With Bipolar I or Bipolar II Disorder (Bipolar Depression) in Pediatric Patients Aged 10 to 17 Years

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

Condition
Bipolar Depression
Intervention / Treatment

-

Contacts and Locations

Anaheim

Clinical Site, Anaheim, California, United States, 92805

Sacramento

Clinical Site, Sacramento, California, United States, 95817

San Diego

Clinical Site, San Diego, California, United States, 92103

Colorado Springs

Clinical Site, Colorado Springs, Colorado, United States, 80910

Gainesville

Clinical Site, Gainesville, Florida, United States, 32607

Hialeah

Clinical Site, Hialeah, Florida, United States, 33012

Miami Lakes

Clinical Site, Miami Lakes, Florida, United States, 33014

Miami Lakes

Clinical Site, Miami Lakes, Florida, United States, 33016

Miami Springs

Clinical Site, Miami Springs, Florida, United States, 33166

Orlando

Clinical Site, Orlando, Florida, United States, 32803

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • 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;
  • 7. Young Mania Rating Scale (YMRS) score ≤ 15 (with YMRS Item 1 \[elevated mood\] score ≤ 2) at Screening and Baseline.
  • 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
  • 3. At Screening or Baseline, scores \> 3 on Item 13 (suicidal ideation) on the CDRS-R; or
  • 4. The patient is considered to be an imminent danger to him/herself or others.

Ages Eligible for Study

10 Years to 17 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Intra-Cellular Therapies, Inc.,

Study Record Dates

2027-05