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Study details
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A Study to Evaluate the Efficacy and Safety of KarXT + KarX-EC for Cognitive Impairment in Alzheimer's Disease

Bristol-Myers Squibb
NCT IDNCT06976216ClinicalTrials.gov data as of Apr 2026
Phase

Phase 3

Target enrollment

586

Study length

about 3.6 years

Ages

60–85

Locations

28 sites in CA, CO, DC +14

What this study is about

Researchers are testing whether KarXT plus KarX-EC, a treatment, improves cognitive function in people with Alzheimer's disease. The trial will last 1320 days and involve approximately 586 participants.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Placebo
  • 2.Take KarX-EC
  • 3.Take KarXT

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Standard

How treatment is administered

Treatment Assignment
Randomized & Blinded

You may get a placebo/standard care, and you won't know which.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Endpoints

Primary: Change from baseline in Alzheimer's Disease Assessment Scale-Cognitive Subscale 11 (ADAS-Cog11)

Secondary: Change from baseline in Alzheimer's Disease Cooperative Study-Activities of Daily Living scale (ADCS-ADL), Change from baseline in neuro psychiatric inventory (NPI) total score, Number of participants with AEs leading to death, Number of participants with AEs leading to study discontinuation, Number of participants with AEs leading to study intervention discontinuation, Number of participants with adverse event of special interest (AESIs), Number of participants with adverse events (AEs), Number of participants with serious adverse events (SAEs)

Body systems

Neurology