Life sciences · Phase 1 Trial
ClinicalTrials.gov · September 24, 2026
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Phase 1 Trial.
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Registry record from ClinicalTrials.gov (NCT07780383). This is a study registration, not published results. Lead sponsor: Bristol-Myers Squibb. Recruitment status: RECRUITING. Phase: PHASE1. Study type: INTERVENTIONAL. Enrollment: 84 participants (ESTIMATED). Conditions: Alzheimer's Disease, Healthy Participants. Interventions: DRUG: BMS-986446. Primary outcome measures: Absolute bioavailability estimated from geometric mean ratio (GMR) of area under the concentration-time curve from time zero extrapolated to infinite time (AUC(INF)) of BMS-986446 after subcutaneous (SC) infusion , Up to approximately 5 months; Absolute bioavailability estimated from GMR of AUC(INF) of BMS-986446 after intravenous (IV) infusion , Up to approximately 5 months; Maximum observed concentration (Cmax) , Up to approximately 5 months; Time of maximum observed concentration (Tmax) , Up to approximately 5 months; Area under the concentration-time curve from time zero to time of last quantifiable concentration (AUC(0-T)) , Up to approximately 5 months; Area under the serum concentration-time curve from time zero to 672 hours (AUC(0-672)) , Up to approximately 5 months; AUC(INF) , Up to approximately 5 months; Half-life (T-HALF) , Up to approximately 5 months; Apparent total body clearance in SC administration (CLT/F) , Up to approximately 5 months; Total body clearance in IV infusion (CLT) , Up to approximately 5 months; Apparent volume of distribution of terminal phase in SC administration (Vz/F) , Up to approximately 5 months; Volume of distribution of terminal phase (VZ) , Up to approximately 5 months. Brief 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