drugset / Trial / NCT04276883

Dexmedetomidine in the Treatment of Agitation Associated With Bipolar Disorder

NCT04276883 ↗

RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a definitive study to support the safety and efficacy evaluation of BXCL501 for the acute treatment of agitation in bipolar disorder. The BXCL501-302 study is designed to characterize the efficacy, safety and tolerability of BXCL501 (sublingual film formulation of DEX, HCl) in agitation associated with bipolar disorder.

Timeline

Start
2020-02-24
Primary completion
2020-05-21
Completion
2020-05-21

Outcome

Met primary endpoint

paper treatment with a sublingual film formulation of dexmedetomidine 120 μg or 180 μg, compared with placebo, resulted in significantly greater reduction in the agitation score at 2 hours. PMID 35191924 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Dexmedetomidine Other / unclassified 120 ug Other
Subject Dexmedetomidine Other / unclassified 180 ug Other

Indications