Overview

Dexmedetomidine in the Treatment of Agitation Associated With Dementia

Status:
Not yet recruiting
Trial end date:
2022-12-01
Target enrollment:
Participant gender:
Summary
A study to determine the safety and efficacy of BXCL501 dosing for episodes of agitation associated with dementia when they occur (given as needed [PRN]), for a maximum of 28 doses within a 12-week treatment period.
Phase:
Phase 3
Details
Lead Sponsor:
BioXcel Therapeutics Inc
Treatments:
Dexmedetomidine