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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

About this study

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.

Based on ClinicalTrials.gov records.

What participants do

  • 1.Placebo
  • 2.Take KarX-EC
  • 3.Take KarXT
PhasePhase 3
DrugKarXT
Primary goalChange from baseline in Alzheimer's Disease Assessment Scale-Cognitive Subscale 11 (ADAS-Cog11)

Participation effort

Estimated from trial records. Details can vary by site.

Time + visits
Low8%
Logistics
Moderate50%

Logistics difficulty varies by site location and availability.

Trial highlights

Treatment details

Auto-extracted from trial records to preview treatments and outcomes.

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