This study in individuals with mild to moderate Alzheimer's Disease is designed to assess:(1) safety and tolerability (2) the capacity of subcutaneous bapineuzumab to reduce brain amyloid load as measured by positron emission tomography (PET) scans.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
146
Bapineuzumab 2 mg, Bapineuzumab 7 mg, Bapineuzumab 20 mg, Placebo
To evaluate the effect of bapineuzumab administered subcutaneously (SC) at monthly intervals compared to placebo on cerebral amyloid burden in subjects with mild to moderate AD.
Time frame: 24 months
To assess the safety of bapineuzumab administered SC at monthly intervals compared to placebo in subjects with mild to moderate AD
Time frame: 24 months
To assess the effect of bapineuzumab administered SC at monthly intervals compared to placebo on cognitive and functional endpoints.
Time frame: 24 months
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Janssen AI Investigational Site
Tucson, Arizona, United States
Janssen AI Investigational Site
Tucson, Arizona, United States
Janssen AI Investigational Site
La Habra, California, United States
Janssen AI Investigational Site
Lomita, California, United States
Janssen AI Investigational Site
Long Beach, California, United States
Janssen AI Investigational Site
Oceanside, California, United States
Janssen AI Investigational Site
Pasadena, California, United States
Janssen AI Investigational Site
Santa Monica, California, United States
Janssen AI Investigational Site
Sherman Oaks, California, United States
Janssen AI Investigational Site
Deerfield Beach, Florida, United States
...and 18 more locations