drugset / Trial / NCT01492374

Study to Evaluate the Safety, Tolerability and the Effect of BMS-241027 on Cerebrospinal Fluid Biomarkers in Subjects With Mild Alzheimer's Disease

NCT01492374 ↗

Phase 1 Completed 40 enrolled Bristol-Myers Squibb
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of the study is to evaluate safety and the pharmacodynamic effects of BMS-241027 on cerebrospinal fluid (CSF) Tau, connectivity magnetic resonance imaging (MRI), and computerized cognitive tests in mild Alzheimer's disease (AD) subjects, following 9 weekly intravenous (IV) infusions of BMS-241027

Timeline

Start
2012-02
Primary completion
2013-10
Completion
2013-10

Drugs

EvaluationDrugModalityDoseRoute
Subject BMS-241027 Unknown 0.003 mg/kg Intravenous
Subject BMS-241027 Unknown 0.01 mg/kg Intravenous
Subject BMS-241027 Unknown 0.03 mg/kg Intravenous

Indications