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CompletedNCT05658510

Dexmedetomidine for agitation in bipolarity and schizophrenia

About this title

Dexmedetomidine in the Treatment of Agitation Associated With Schizophrenia and Bipolar Disorder (SERENITY III)

Read the official source — NCT05658510
Medication studyAges 18–75United States
The study in practice

Understand this study

Who was this study for?

Listed age limits: 18 years to 75 years.

Listed locations
Bellflower and 23 more locationsSee all locations and recruitment
Study phase
Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.

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Study clarity

Study information

Study start dateStarted: November 21, 2022
Recruitment status
Completed
Enrollment listed in the registry
452
Sponsor
BioXcel Therapeutics Inc
Sponsor type
Biotech company
Study type
Drug
Intervention type
Drug
Study phase
Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.
Locations
United States
Age range
From 18 Years to 75 Years
Official registry ID
NCT05658510
Official title
Show the full official title

Efficacy And Safety of BXCL501 Evaluated For At-Home Use In A Multisite Double-Blind Placebo-Controlled Trial For Agitation Associated With Schizophrenia And Bipolar Disorder

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Recruitment & locations

Completed

Bellflower · Cerritos · Culver City

19 more locations
  • Garden Grove
  • Lemon Grove
  • Los Angeles
  • Oceanside
  • Orange
  • Rancho Cucamonga
  • Riverside
  • Denver
  • Miami
  • Elgin
  • Gaithersburg
  • Las Vegas
  • Berlin
  • Beachwood
  • Austin
  • DeSoto
  • Irving
  • Plano
  • Everett

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FAQ

Questions about this study

Who is behind this study?

The study sponsor is BioXcel Therapeutics Inc.

Did this study involve medication?

Yes. The study involved medication, including BXCL501 and Matching Placebo.

Who was this study for?

Listed age limits: 18 years to 75 years.

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