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).
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).
Multicenter Study of Lumateperone for the Treatment of Bipolar Depression in Pediatric Patients
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Clinical Site, Anaheim, California, United States, 92805
Clinical Site, Sacramento, California, United States, 95817
Clinical Site, San Diego, California, United States, 92103
Clinical Site, Colorado Springs, Colorado, United States, 80910
Clinical Site, Gainesville, Florida, United States, 32607
Clinical Site, Hialeah, Florida, United States, 33012
Clinical Site, Miami Lakes, Florida, United States, 33014
Clinical Site, Miami Lakes, Florida, United States, 33016
Clinical Site, Miami Springs, Florida, United States, 33166
Clinical Site, Orlando, Florida, United States, 32803
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.
10 Years to 17 Years
ALL
No
Intra-Cellular Therapies, Inc.,
2027-05