A Study of Donanemab (LY3002813) in Participants Who Completed Study AACM (TRAILBLAZER-ALZ 3-EXT).
Sponsored by Eli Lilly and Company
About this study
The main purpose of this study is to determine if participants who previously took donanemab get clinical benefit when they receive annual doses. For each participant, the study will last up to 2.5 years and will include 6 visits.
Where this study is enrolling (48)
- Call 602-839-6900
Banner Alzheimer's Institute
Phoenix, Arizona
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- Call 562-606-5999
Healthy Brain Clinic
Long Beach, California
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- Call 714-542-3008
Syrentis Clinical Research
Santa Ana, California
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- Call 916-434-8230
Clinical Trials Research
Sacramento, California
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- Call 951-374-1190
Artemis Institute for Clinical Research
Riverside, California
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Show all 48 locations
- Call 714-378-2440
Care Access - Huntington Beach
Huntington Beach, California
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- Call 707-521-3830
Providence Medical Foundation
Santa Rosa, California
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- Call 949-753-1663
Irvine Clinical Research
Irvine, California
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- Call 858-278-3647
Artemis Institute for Clinical Research
San Diego, California
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- Call 925-947-2334
Infectious Disease Doctors Medical Group, APC
Walnut Creek, California
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- Call 786-655-8010
VIN-Andrew Lerman
Miami, Florida
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- Call 941-708-0005
Bradenton Research Center, Inc.
Bradenton, Florida
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- Call 877-791-0656
Care Access - Tampa
Tampa, Florida
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- Call 407-337-3000
Charter Research - Orlando
Orlando, Florida
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- Call 352-441-2000
Charter Research - The Villages
The Villages, Florida
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- Call 407-916-0060
Conquest Research
Winter Park, Florida
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- Call 850-438-1136
Emerald Coast Neurology - Airport Boulevard
Pensacola, Florida
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- Call 561-766-2181
Finlay Medical Research
Greenacres City, Florida
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- Call 407-705-3471
Headlands Research Orlando
Orlando, Florida
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- Call 305-825-6588
Indago Research & Health Center, Inc
Miami Lakes, Florida
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- Call 904-730-0101
Jacksonville Center for Clinical Research
Jacksonville, Florida
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- Call 407-500-5252
K2 Medical Research ORLANDO
Maitland, Florida
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- Call 813-800-5252
K2 Medical Research - Tampa
Tampa, Florida
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- Call 386-304-7070
Progressive Medical Research
Port Orange, Florida
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- Call 727-849-4131
Suncoast Clinical Research, Inc.
New Port Richey, Florida
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- Call 305-933-5993
VIN - Aventura
Aventura, Florida
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- Call 352-383-8222
Adult Medicine of Lake County, Inc.
Mt. Dora, Florida
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- Call 678-494-5735
North Georgia Clinical Research
Woodstock, Georgia
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- Call 770-534-5154
Center for Advanced Research & Education
Gainesville, Georgia
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- Call 208-685-0600
Northwest Clinical Trials
Boise, Idaho
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- I'm interested
Great Lakes Clinical Trials - Andersonville
Chicago, Illinois
- Call 317-537-6099
Josephson Wallack Munshower Neurology, PC
Indianapolis, Indiana
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- Call 877-791-0656
Care Access - South Indianapolis
Indianapolis, Indiana
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- Call 319-272-2112
Covenant Medical Center
Waterloo, Iowa
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- Call 337-602-6642
Care Access - Lake Charles (Bayou Pines)
Lake Charles, Louisiana
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- Call 617-744-1310
MedVadis Research Corporation
Waltham, Massachusetts
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- Call 617-699-6927
Boston Center for Memory
Newton, Massachusetts
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- Call 586-276-7453
Revival Research Institute, LLC
Southfield, Michigan
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- Call 417-328-7781
Citizens Memorial Hospital District
Bolivar, Missouri
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- Call 702-750-000
Vector Clinical Trials
Las Vegas, Nevada
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- Call 704-283-7359
Monroe Biomedical Research
Monroe, North Carolina
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- Call 877-791-0656
Care Access - Lima
Lima, Ohio
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- Call 937-224-8200
NDx Clinical Research, Inc.
Dayton, Ohio
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- Call 409-331-6040
Gadolin Research
Beaumont, Texas
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- Call 210-545-4900
Consano Clinical Research, LLC
Shavano Park, Texas
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- Call 512-407-8628
Senior Adults Specialty Research
Austin, Texas
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- Call 713-486-0536
The University of Texas Health Science Center at Houston
Houston, Texas
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- Call 253-882-1070
Universal Research Group
Tacoma, Washington
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Who can participate
Inclusion criteria
- ✓Have completed study AACM Addendum 7.
- ✓Have a reliable study partner and backup study partner familiar with overall function and behavior, such as day-to-day activities and cognitive abilities.
- ✓Are individuals assigned female at birth who are not of childbearing potential, or are individuals assigned male at birth.
- ✓Contraceptive use by participants should be consistent with local regulations regarding the methods of contraception for those participating in clinical studies.
Exclusion criteria
- ✕Current serious or unstable illnesses that, in the investigator's opinion, could interfere with participation in this study.
- ✕Have any contraindications for magnetic resonance imaging (MRI), including claustrophobia or the presence of contraindicated metal (ferromagnetic) implants/cardiac pacemaker.
- ✕Have any intracranial abnormality or lesion, including but not limited to macrohemorrhage, inflammation, or structural findings that, in the opinion of the investigator, may pose an unacceptable safety risk to the participant. Screening MRI finding of amyloid-related imaging abnormalities with edema (ARIA-E) may be monitored for resolution.
- ✕Contraindication to florbetapir F 18 PET.
- ✕Have had history of amyloid-targeting therapy treatment outside donanemab trials.
- ✕Have participated, within the last 30 days, in a clinical trial involving a study intervention judged not to be scientifically or medically compatible with this study.
Only the research team can confirm whether you qualify. The intake questionnaire is the best way to find out.
Completing a questionnaire on Clinably does not enroll you in a clinical trial or confirm your eligibility. Only the research team can determine whether you qualify to participate. These results are based on the information you provide and are intended to help you start a conversation with the research team.
Trial data sourced from ClinicalTrials.gov.