Phase
Condition
Bipolar Disorder
Mood Disorders
Treatment
Lumateperone
Placebo
Clinical Study ID
Ages 18-75 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Able to provide written informed consent before the initiation of any study specificprocedures;
Male or female inpatient, between the ages of 18 and 75 years, inclusive;
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);
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;
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:
Has a current primary DSM 5 psychiatric diagnosis other than bipolar disorder. Theseinclude:
Schizophrenia, schizoaffective disorder, or other psychotic disorders;
Dementia or other cognitive disorders;
Intellectual disability;
Moderate or severe substance use disorder (excluding for nicotine);
Experiencing first manic episode;
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
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
At Screening, the patient has had 1 or more suicidal attempts within 2 yearsprior to Screening; or
At Baseline, the patient scores "yes" on Items 4 or 5 in the Suicidal Ideationsection of the C-SSRS since the Screening Visit; or
At Screening or Baseline, scores ≥ 4 on Item 10 (suicidal thoughts) on therater administered Montgomery-Åsberg Depression Rating Scale (MADRS); or
Considered to be an imminent danger to himself/herself or others.
Study Design
Study Description
Connect with a study center
Clinical Site
Rogers, Arkansas 72758
United StatesSite Not Available
Clinical Site
Bellflower, California 90706
United StatesSite Not Available
Clinical Site
Culver City, California 90230
United StatesSite Not Available
Clinical Site
Garden Grove, California 92845
United StatesSite Not Available
Clinical Site
Lemon Grove, California 91945
United StatesActive - Recruiting
Clinical Site
Montclair, California 91763
United StatesSite Not Available
Clinical Site
Hallandale Beach, Florida 33009
United StatesSite Not Available
Clinical Site
Hialeah, Florida 33016
United StatesActive - Recruiting
Clinical Site
Miami, Florida 33184
United StatesSite Not Available
Clinical Site
Miami Gardens, Florida 33056
United StatesSite Not Available
Clinical Site
Miami Lakes, Florida 33016
United StatesActive - Recruiting
Clinical Site
Miami Springs, Florida 33166
United StatesActive - Recruiting
Clinical Site
Orlando, Florida 32807
United StatesSite Not Available
Clinical Site
Atlanta, Georgia 30324
United StatesActive - Recruiting
Clinical Site
Decatur, Georgia 30030
United StatesActive - Recruiting
Clinical Site
Savannah, Georgia 31405
United StatesSite Not Available
Clinical Site
Shreveport, Louisiana 71101
United StatesActive - Recruiting
Clinical Site
Marlton, New Jersey 08053
United StatesSite Not Available
Clinical Site
North Canton, Ohio 44720
United StatesSite Not Available
Clinical Site
Austin, Texas 78754
United StatesSite Not Available
Clinical Site
DeSoto, Texas 75115
United StatesActive - Recruiting
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