Determining Efficacy and Safety of BXCL501 in Agitation Associated With Pediatric Schizophrenia and Bipolar Disorder
Condition(s) studied
Investigational drug(s) / intervention(s)
BXCL501 80 Micrograms: Sublingual film containing 80 Micrograms BXCL501
Placebo Film: Matching Sublingual Placebo film
BXCL501 120 Micrograms: Sublingual film containing 120 Micrograms BXCL501
BXCL501 60 Micrograms: Sublingual film containing 60 Micrograms BXCL501 Europe Only
Study summary
This is a study of the efficacy and safety of BXCL501 in children and adolescents with acute agitation and either bipolar disorder or schizophrenia.
Eligibility
Primary outcome measure(s)
- Absolute change from baseline in the Positive and Negative Syndrome Scale - Excited Component (PEC) total score — 120 minutes - Group one only
The Positive and Negative Syndrome Scale - Excited Component (PEC) comprises 5 items associated with agitation: poor impulse control, tension, hostility, uncooperativeness, and excitement; each scored 1 (minimum) to 7 (maximum). The PEC, the sum of these 5 subscales, thus ranges from 5 (absence of agitation) to 35 (extremely severe)
Trial sites (5)
| Facility | City | Region | Status |
|---|---|---|---|
| BioXcel Clinical Research Site | Anaheim | California | Recruiting |
| Bioxcel Clinical Research Site | Hialeah | Florida | Recruiting |
| BioXcel Clinical Research Site | Atlanta | Georgia | Completed |
| Bioxcel Clinical Research Site | Decatur | Georgia | Recruiting |
| BioXcel Clinical Research Site | DeSoto | Texas | Recruiting |
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT05025605 on ClinicalTrials.gov ↗ ← All trials in the USA