AHEAD 3-45 Study: A Placebo-Controlled, Double-Blind, Parallel-TreatmentArm, 216 Week Study to Evaluate Efficacy and Safety of Treatment With BAN2401 in Subjects With Preclinical Alzheimers Disease and Elevated Amyloid (A45 Trial) and in Subjects With Early Preclinical Alzheimers Disease and Intermediate Amyloid (A3 Trial)
Study of BAN2401 in Subjects with Preclinical Alzheimer's Disease
Sponsor: Eisai Inc.
Enrolling: Male and Female Patients
Study Length: 4 Years
IRB Number: AAAT3026
U.S. Govt. ID: NCT04468659
Contact: Chrismary De La Cruz: 212-305-7661 / cd3097@cumc.columbia.edu
Additional Study Information: We are seeking men & women, ages 55 to 80, who have preclinical Alzheimer's disease for a 216-week treatment, multi-center, double-blind, placebo-controlled, parallel-treatment arm study to determine whether the BAN2401 study drug will reduce the risk of developing Alzheimer's disease. The study participant will receive MRI, and PET scans and will receive intravenous study drug or placebo every 2 weeks.
Investigator
Karen Bell, MD
Do You Qualify?
Have you been diagnosed with Alzheimer's disease? Yes No
Are you between 55-80 years old? Yes No
Submit
Cancel
You may be eligible for this study

Place Holder




For more information, please contact:
Chrismary De La Cruz
cd3097@cumc.columbia.edu
212-305-7661