Overview

Dexmedetomidine in the Treatment of Agitation Associated With Dementia (TRANQUILITY III)

Status:
Recruiting
Trial end date:
2024-02-01
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 168 doses within a 12-week treatment period.
Phase:
Phase 3
Details
Lead Sponsor:
BioXcel Therapeutics Inc
Collaborator:
Cognitive Research Corporation
Treatments:
Dexmedetomidine