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Recruiting Phase 3 2024-519994-20-00

CN012-0025: A Phase 3, Open-label Extension Study to Evaluate the Long-term Safety and Tolerability of KarXT + KarX-EC for the Treatment of Agitation Associated with Alzheimer’s Disease (ADAGIO-3)

Phase 3 – large-scale trial before approval
Conditions: Agitation Associated with Alzheimer’s Disease

Sponsor: Bristol-Myers Squibb Services Unlimited Company

trial.available_in: БГ
Overview
Trial status: Authorised Reported adverse events (AEs), TEAEs, serious AEs, and TEAEs leading to study withdrawal and deaths, AEs of special interest, Assessment of abnormal involuntary movements or restlessness, Body weight, Blood pressure and heart rate, Laboratory evaluations, Suicidal ideation, Assessment of cognition, Assessment of urinary retention. Incidence of any Treatment-Emergent Adverse Events (TEAEs).
Description
Reported adverse events (AEs), TEAEs, serious AEs, and TEAEs leading to study withdrawal and deaths, AEs of special interest, Assessment of abnormal involuntary movements or restlessness, Body weight, Blood pressure and heart rate, Laboratory evaluations, Suicidal ideation, Assessment of cognition, Assessment of urinary retention.
Who can participate
Age group: 65+ years, 18-64 years Gender: Female, Male Target enrollment: 193 participants
Interventions
KarX-EC
Drug
KarXT
Drug
KarX-EC
Drug
KarX-EC
Drug
KarXT
Drug
KarX-EC
Drug
KarXT
Drug
KarXT
Drug
Locations 11
Bulgaria (1)
Croatia (1)
Czech Republic (1)
France (1)
Greece (1)
Hungary (1)
Italy (1)
Poland (1)
Portugal (1)
Romania (1)
Spain (1)
Technical details
Status
Recruiting
Phase
Phase 3
Study type
INTERVENTIONAL
Sex
Male and female
Minimum age
18 Years
Healthy volunteers
No
Start date
21.10.2025
Registry ID
2024-519994-20-00
Source
euclinicaltrials.eu
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