drugset / Trial / NCT05025605

Determining Efficacy and Safety of BXCL501 in Agitation Associated With Pediatric Schizophrenia and Bipolar Disorder

NCT05025605

Phase 1 Recruiting 140 enrolled BioXcel Therapeutics Inc ProPharma Group · collab
RandomizedParallel-groupDouble-blindTreatment

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.

Timeline

Start
2021-08-27
Primary completion
2027-07-31
Completion
2027-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Dexmedetomidine Other / unclassified 60 ug Other
Subject Dexmedetomidine Other / unclassified 80 ug Other
Subject Dexmedetomidine Other / unclassified 120 ug Other