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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05557409
Other study ID # AXS-05-AD-304
Secondary ID
Status Recruiting
Phase Phase 3
First received
Last updated
Start date September 6, 2022
Est. completion date June 2025

Study information

Verified date April 2024
Source Axsome Therapeutics, Inc.
Contact Study Director
Phone 212-332-5061
Email ADVANCE-2@axsome.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This trial is a multi-center, double-blind, placebo-controlled, randomized study to evaluate the efficacy and safety of AXS-05 compared to placebo for the treatment of agitation associated with Alzheimer's disease.


Description:

Eligible subjects will be randomized in a 1:1 ratio for up to 5 weeks to be treated with AXS-05 or placebo.


Recruitment information / eligibility

Status Recruiting
Enrollment 350
Est. completion date June 2025
Est. primary completion date June 2025
Accepts healthy volunteers No
Gender All
Age group 65 Years to 90 Years
Eligibility Inclusion Criteria: - Diagnosis of probable Alzheimer's disease (AD) based on the 2011 National Institute on Aging-Alzheimer Association (NIA-AA) criteria. - Diagnosis of clinically significant agitation resulting from probable AD according to the International Psychogeriatric Association (IPA) provisional definition of agitation. Exclusion Criteria: - Patient has dementia predominantly of non-Alzheimer's type. - Unable to comply with study procedures. - Medically inappropriate for study participation in the opinion of the investigator.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
AXS-05
AXS-05 tablets, taken twice daily
Placebo
Placebo tablets, taken twice daily

Locations

Country Name City State
Puerto Rico Clinical Research Site Bayamon
Puerto Rico Clinical Research Site San Juan
United States Clinical Research Site Arlington Virginia
United States Clinical Research Site Augusta Georgia
United States Clinical Research Site Austin Texas
United States Clinical Research Site Berlin New Jersey
United States Clinical Research Site Braintree Massachusetts
United States Clinical Research Site Brandon Florida
United States Clinical Research Site Bronx New York
United States Clinical Research Site Brooklyn New York
United States Clinical Research Site Canoga Park California
United States Clinical Research Site Charlotte North Carolina
United States Clinical Research Site Chesterfield Missouri
United States Clinical Research Site Cincinnati Ohio
United States Clinical Research Site Columbus Georgia
United States Clinical Research Site Cypress Texas
United States Clinical Research Site Flint Michigan
United States Clinical Research Site Greenacres City Florida
United States Clinical Research Site Hialeah Florida
United States Clinical Research Site Hickory North Carolina
United States Clinical Research Site Hollywood Florida
United States Clinical Research Site Kissimmee Florida
United States Clinical Research Site Lafayette California
United States Clinical Research Site Long Beach California
United States Clinical Research Site Los Alamitos California
United States Clinical Research Site Marrero Louisiana
United States Clinical Research Site Mesquite Texas
United States Clinical Research Site Methuen Massachusetts
United States Clinical Research Site Miami Florida
United States Clinical Research Site Miami Florida
United States Clinical Research Site Miami Florida
United States Clinical Research Site Miami Florida
United States Clinical Research Site Miami Florida
United States Clinical Research Site Miami Florida
United States Clinical Research Site Miami Florida
United States Clinical Research Site Miami Gardens Florida
United States Clinical Research Site Miami Lakes Florida
United States Clinical Research Site Middleburg Heights Ohio
United States Clinical Research Site New Windsor New York
United States Clinical Research Site Orlando Florida
United States Clinical Research Site Pembroke Pines Florida
United States Clinical Research Site Peoria Arizona
United States Clinical Research Site Rochester Hills Michigan
United States Clinical Research Site San Antonio Texas
United States Clinical Research Site San Marcos California
United States Clinical Research Site Staten Island New York
United States Clinical Research Site Sugar Land Texas
United States Clinical Research Site Tempe Arizona
United States Clinical Research Site Toms River New Jersey
United States Clinical Research Site Tucson Arizona
United States Clinical Research Site West Covina California
United States Clinical Research Site Wichita Kansas
United States Clinical Research Site Woodmere New York

Sponsors (1)

Lead Sponsor Collaborator
Axsome Therapeutics, Inc.

Countries where clinical trial is conducted

United States,  Puerto Rico, 

Outcome

Type Measure Description Time frame Safety issue
Primary Cohen-Mansfield Agitation Inventory (CMAI) Up to 5 weeks
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