Lumateperone for the Prevention of Relapse in Patients With Schizophrenia

Last updated: November 6, 2024
Sponsor: Intra-Cellular Therapies, Inc.
Overall Status: Completed

Phase

3

Condition

Tourette's Syndrome

Schizotypal Personality Disorder (Spd)

Mood Disorders

Treatment

Lumateperone 42 mg

Placebo

Clinical Study ID

NCT04959032
ITI-007-304
  • Ages 18-60
  • All Genders

Study Summary

This is a multicenter, randomized, double-blind, placebo-controlled, parallel-group, fixed-dose study in adult patients with a primary diagnosis of schizophrenia according to criteria of the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition, (DSM-5).

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Male or female, 18 to 60 years of age, inclusive.

  • Current diagnosis of schizophrenia according to DSM-5 criteria as determined by themodified Structured Clinical Interview for DSM-5 (modified SCID-5).

  • Diagnosis of schizophrenia for a minimum of 1 year before Visit 1.

  • Current psychotic episode < 4 weeks duration at Visit 1.

  • PANSS total score ≥ 70 and ≤ 120 at Visit 1 and Visit 2.

  • Rating of at least 4 (moderate) on at least two of the following four PANSS positivesymptoms: delusions (P1), hallucinatory behavior (P3), conceptual disorganization (P2), suspiciousness/persecution (P6) at Visit 1 and Visit 2.

  • Patient must identify a caregiver who provides consents to participate in the study.

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

Exclusion

Exclusion Criteria:

  • Currently meeting DSM-5 criteria for any of the following:

Schizoaffective disorder, schizophreniform disorder, and other psychotic disorders; Bipolar I or Bipolar II Disorder; Intellectual developmental disorder, delirium, dementia, amnestic and other cognitive disorders; Known or suspected borderline or antisocial personality disorder or other DSM 5 personality disorder of sufficient severity to interfere with participation in this study; Substance use disorder (other than nicotine) within the 3 months prior to Visit 1 of this study.

  • Patients in their first episode of psychosis.

  • Treatment-resistant schizophrenia over the last 2 years, defined as little or nosymptomatic response to at least 2 courses of antipsychotic treatment of an adequateduration (at least 6 weeks) and at a therapeutic dose (according to the packageinsert for the antipsychotic treatment).

Study Design

Total Participants: 228
Treatment Group(s): 2
Primary Treatment: Lumateperone 42 mg
Phase: 3
Study Start date:
July 08, 2021
Estimated Completion Date:
August 07, 2024

Study Description

The study will be conducted in the following 5 phases:

  • A no-drug Screening Phase up to 7 days in duration during which patient eligibility will be assessed;

  • A 6-week, open-label Run-in Phase (RIP) during which all patients will receive oral lumateperone 42 mg/day;

  • A 12-week, open-label Stabilization Phase (SP) during which all patients will receive oral lumateperone 42 mg/day;

  • A Double-blind Treatment Phase (DBTP) 26 weeks in duration during which patients receive either lumateperone 42 mg or placebo (1:1 ratio);

  • A 2-week Safety Follow-up (SFU) Phase.

Connect with a study center

  • Clinical Site

    Burgas, 8000
    Bulgaria

    Site Not Available

  • Clinical Site

    Kardzhali, 6600
    Bulgaria

    Site Not Available

  • Clinical Site

    Kazanlak, 6100
    Bulgaria

    Site Not Available

  • Clinical Site

    Lovech, 5500
    Bulgaria

    Site Not Available

  • Clinical Site

    Novi Iskar, 1282
    Bulgaria

    Site Not Available

  • Clinical Site

    Pleven, 5800
    Bulgaria

    Site Not Available

  • Clinical Site

    Plovdiv, 4002
    Bulgaria

    Site Not Available

  • Clinical Site

    Russe, 7003
    Bulgaria

    Site Not Available

  • Clinical Site

    Sofia, 1377
    Bulgaria

    Site Not Available

  • Clinical Site

    Targovishte, 7700
    Bulgaria

    Site Not Available

  • Clinical Site

    Tsarev Brod, 9747
    Bulgaria

    Site Not Available

  • Clinical Site

    Tserova Koria, 5047
    Bulgaria

    Site Not Available

  • Clinical Site

    Veliko Tarnovo, 5000
    Bulgaria

    Site Not Available

  • Clinical Site

    Vratsa, 3000
    Bulgaria

    Site Not Available

  • Clinical Site

    Gdańsk, 80-282
    Poland

    Site Not Available

  • Clinical Site

    Gorlice, 3-8300
    Poland

    Site Not Available

  • Clinical Site

    Tuszyn, 95080
    Poland

    Site Not Available

  • Clinical site

    Belgrade, 11000
    Serbia

    Site Not Available

  • Clinical Site

    Kovin, 26220
    Serbia

    Site Not Available

  • Clinical Site

    Kragujevac, 34000
    Serbia

    Site Not Available

  • Clinical Site

    Novi Kneževac, 23330
    Serbia

    Site Not Available

  • Clinical Site

    Novi Sad, 21000
    Serbia

    Site Not Available

  • Clinical Site

    Little Rock, Arkansas 72211
    United States

    Site Not Available

  • Clinical Site

    Bellflower, California 907006
    United States

    Site Not Available

  • Clinical Site

    Cerritos, California 90703
    United States

    Site Not Available

  • Clinical Site

    Culver City, California 90230
    United States

    Site Not Available

  • Clinical Site

    Garden Grove, California 92845
    United States

    Site Not Available

  • Clinical Site

    Lemon Grove, California 91945
    United States

    Site Not Available

  • Clinical Site

    Montclair, California 91763
    United States

    Site Not Available

  • Clinical Site

    Orange, California 92869
    United States

    Site Not Available

  • Clinical Site

    Hollywood, Florida 33021
    United States

    Site Not Available

  • Clinical Site

    Lauderhill, Florida 33319
    United States

    Site Not Available

  • Clinical Site

    Miami Lakes, Florida 33016
    United States

    Site Not Available

  • Clinical Site

    Oakland Park, Florida 33334
    United States

    Site Not Available

  • Clinical Site

    Atlanta, Georgia 30331
    United States

    Site Not Available

  • Clinical Site

    Chicago, Illinois 60640
    United States

    Site Not Available

  • Clinical Site

    Boston, Massachusetts 02114
    United States

    Site Not Available

  • Clinical Site

    Saint Louis, Missouri 63141
    United States

    Site Not Available

  • Clinical Site

    Las Vegas, Nevada 89102
    United States

    Site Not Available

  • Clinical Site

    Berlin, New Jersey 08009
    United States

    Site Not Available

  • Clinical Site

    North Canton, Ohio 44720
    United States

    Site Not Available

  • Clinical Site

    Austin, Texas 78754
    United States

    Site Not Available

  • Clinical Site

    DeSoto, Texas 75115
    United States

    Site Not Available

  • Clinical Site

    Houston, Texas 77074
    United States

    Site Not Available

  • Clinical Site

    Richardson, Texas 75080
    United States

    Site Not Available

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