Open Label Extension Study Evaluating Safety and Tolerability of AAB-003 (PF-05236812) in Subject With Mild to Moderate Alzheimer's Disease



Status:Completed
Conditions:Alzheimer Disease
Therapuetic Areas:Neurology
Healthy:No
Age Range:50 - 90
Updated:11/23/2013
Start Date:July 2011
End Date:October 2014
Contact:Pfizer CT.gov Call Center
Phone:1-800-718-1021

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A Multicenter, Open-label Extension, Multiple-dose, Parallel Group Study to Investigate the Long-term Safety and Tolerability of AAB-003 (PF-05236812) Administered Intravenously in Subjects With Mild to Moderate Alzheimer's Disease Previously Treated With AAB-003 or Placebo in Protocol B2601001


This is a study to evaluate the safety and tolerability of multiple doses of AAB-003
(PF-05236812) in patients with mild to moderate Alzheimer's Disease. Patients who complete
study B2601001 may participate in this trial and receive AAB-003 (PF-05236812). Each
patient's participation will last approximately 52 weeks.


Inclusion Criteria:

- Successful completion of study B2601001

- MMSE 12 or greater

Exclusion Criteria:

- Study B2601001 Week 32 MRI with clinically important exclusionary findings.

- Experienced SAE, vasogenic edema and/or intracranial hemorrhage in study B2601001
We found this trial at
7
sites
235 East 42nd Street
Clifton, New Jersey 07013
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Atlanta, Georgia 30309
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Atlantis, Florida 33462
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Baltimore, Maryland 21234
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Biloxi, Mississippi 39531
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Cape Girardeau, Missouri 63703
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Detroit, Michigan 48202
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Detroit, MI
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