NCT07780383PHASE1RecruitingAccepts Healthy Volunteers
A Study to Evaluate the Drug Levels, Absolute Bioavailability, Safety, Tolerability, and Immunogenicity of Single-Dose of BMS-986446 in Healthy Adults After Single-dose Administration, and Participants With Early Alzheimer's Disease After Multiple Dose Administration
Bristol-Myers Squibb
Start Date
8/21/2026
Completion Date
6/17/2027
Summary
The purpose of this study is to evaluate the drug levels, absolute bioavailability, safety, tolerability, and immunogenicity of single-Dose of BMS-986446 in healthy adults after single-dose administration, and participants with early Alzheimer's Disease after multiple dose administration
Eligibility Criteria
Age Range: 18 years to 80 years
Inclusion Criteria
* Participants must have a BMI of 18.0 to 35.0 kg/m2.
* For Parts A and B: Participants must be healthy as determined by medical history, Physical Examination (PE), neurological examination, vital signs, 12-lead ECG, Columbia Suicide-Severity Rating Scale (C-SSRS), and clinical laboratory evaluations.
* For Part C: Participants must meet diagnostic criteria for MCI or mild AD dementia, consistent with the National Institute on Aging and the Alzheimer's Association (NIA-AA) diagnostic criteria.
* For Part C: Participants must have an Mini Mental State Examination (MMSE) score of ≥ 20 to 28 (inclusive).
* For Part C: Participants must have evidence of positive plasma pTau217.
Exclusion Criteria
* For Parts A and B: Participants must not have a general history of any clinically significant gastrointestinal, renal, hepatic, broncho-pulmonary, neurological, psychiatric, cardiovascular, endocrinological, immune-mediated disorder, hematological, ongoing allergic disorder requiring treatment, metabolic disorder, cancer, or cirrhosis.
* For Parts A and B: Participants must not have donated or lost 500 mL blood or more within 60 days prior to study intervention administration.
* For Part C: Participants must not have a neurological condition that in the opinion of the investigator may be contributing to cognitive impairment aside from the AD diagnosis, including but not limited to: Parkinson's disease, vascular dementia, dementia with Lewy bodies, frontotemporal dementia, Huntington's disease, normal pressure hydrocephalus, brain tumor, progressive supranuclear palsy, seizure disorder, subdural hematoma, multiple sclerosis, long COVID, or baseline intellectual disability.
* For Part C: Participants must not have any current primary psychiatric diagnosis (eg, major depression, schizoaffective disorder or bipolar disorder) other than AD or symptoms (eg, hallucination or delusions).
* Other protocol-defined Inclusion/Exclusion criteria apply.
Interventions
DRUG
BMS-986446
Conditions
Alzheimer's DiseaseHealthy Participants
Locations
CenExel ACT (Formerly Anaheim Clinical Trials; LLC)
Anaheim, California 92801
United States
Local Institution - 0003
Bradenton, Florida 34205
United States
Local Institution - 0005
Daytona Beach, Florida 32117
United States
Local Institution - 0007
Naples, Florida 34105
United States
Local Institution - 0006
The Villages, Florida 32162
United States
Local Institution - 0004
Decatur, Georgia 30030
United States