Study of Lumateperone in the Treatment of Patients With Bipolar Mania

Last updated: July 26, 2024
Sponsor: Intra-Cellular Therapies, Inc.
Overall Status: Active - Recruiting

Phase

3

Condition

Bipolar Disorder

Mood Disorders

Treatment

Lumateperone

Placebo

Clinical Study ID

NCT06462612
ITI-007-452
  • Ages 18-75
  • All Genders

Study Summary

This is a multicenter, randomized, double-blind, placebo-controlled, study in the acute treatment of patients with a diagnosis of bipolar I disorder with manic episodes or manic episodes with mixed features (bipolar mania), with or without psychotic symptoms, according to criteria of the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM 5).

Eligibility Criteria

Inclusion

Inclusion Criteria:

  1. Able to provide written informed consent before the initiation of any study specificprocedures;

  2. Male or female inpatient, between the ages of 18 and 75 years, inclusive;

  3. Meets the Diagnostic and Statistical Manual of Mental Disorders, 5th Edition (DSM 5)criteria for bipolar I disorder with a current episode of mania or mania with mixedfeatures with or without psychotic symptoms, as confirmed by a trained andSponsor-approved rater using the modified Structured Clinical Interview for DSM-5,Clinical Trials Version (SCID-5-CT);

  4. YMRS total score ≥ 20 and a score of at least 4 on two of the following YMRS items:irritability, speech, content, and disruptive/aggressive behavior at Screening andBaseline;

  5. Hospitalized voluntarily before Screening or admitted to inpatient unit at Visit 1with a primary diagnosis of mania but not > 14 days before Screening. Hospitaladmission must be a result of the current manic episode.

Exclusion

Exclusion Criteria:

  1. Has a current primary DSM 5 psychiatric diagnosis other than bipolar disorder. Theseinclude:

  2. Schizophrenia, schizoaffective disorder, or other psychotic disorders;

  3. Dementia or other cognitive disorders;

  4. Intellectual disability;

  5. Moderate or severe substance use disorder (excluding for nicotine);

  6. Experiencing first manic episode;

  7. In the opinion of the Investigator, the patient has a significant risk for suicidalbehavior during the course of his/her participation in the study or

  8. At Screening, the patient scores "yes" on Items 4 or 5 in the Suicidal Ideationsection of the Columbia-Suicide Severity Rating Scale (C-SSRS) within 6 monthsprior to Screening; or

  9. At Screening, the patient has had 1 or more suicidal attempts within 2 yearsprior to Screening; or

  10. At Baseline, the patient scores "yes" on Items 4 or 5 in the Suicidal Ideationsection of the C-SSRS since the Screening Visit; or

  11. At Screening or Baseline, scores ≥ 4 on Item 10 (suicidal thoughts) on therater administered Montgomery-Åsberg Depression Rating Scale (MADRS); or

  12. Considered to be an imminent danger to himself/herself or others.

Study Design

Total Participants: 350
Treatment Group(s): 2
Primary Treatment: Lumateperone
Phase: 3
Study Start date:
July 17, 2024
Estimated Completion Date:
June 30, 2026

Study Description

The study will be conducted in 3 phases:

  • Screening Period (up to 1 week) during which patient eligibility will be assessed.

  • Double-blind Treatment Period (3 weeks) during which all eligible patients will be randomized to receive lumateperone 42 mg or placebo in 1:1 ratio.

  • Safety Follow-up Period (1 week) during which all patients will return to the clinic for a safety follow-up visit

Connect with a study center

  • Clinical Site

    Bentonville, Arkansas 72712
    United States

    Site Not Available

  • Clinical Site

    Little Rock, Arkansas 72211
    United States

    Site Not Available

  • Clinical Site

    Anaheim, California 92805
    United States

    Site Not Available

  • Clinical Site

    Cerritos, California 90703
    United States

    Site Not Available

  • Clinical Site

    Orange, California 92868
    United States

    Site Not Available

  • Clinical Site

    Torrance, California 90504
    United States

    Site Not Available

  • Clinical Site

    Hialeah, Florida 33012
    United States

    Active - Recruiting

  • Clinical Site

    Miami, Florida 33145
    United States

    Site Not Available

  • Clinical Site

    Miami Lakes, Florida 33016
    United States

    Site Not Available

  • Clinical Site

    Tampa, Florida 33629
    United States

    Site Not Available

  • Clinical Site

    West Palm Beach, Florida 33407
    United States

    Site Not Available

  • Clinical Site

    Atlanta, Georgia 30331
    United States

    Active - Recruiting

  • Clinical Site

    Stockbridge, Georgia 30281
    United States

    Site Not Available

  • Clinical Site

    Chicago, Illinois 60641
    United States

    Site Not Available

  • Clinical Site

    Glen Oaks, New York 11004
    United States

    Site Not Available

  • Clinical Site

    Cincinnati, Ohio 45219
    United States

    Site Not Available

  • Clinical Site

    Richardson, Texas 75080
    United States

    Active - Recruiting

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