A Clinical Study of MK-2214 in People With Early Alzheimer's Disease (MK-2214-004)
Sponsored by Merck Sharp & Dohme LLC
About this study
Researchers want to know if the study treatment called MK-2214 works to slow certain changes in the brains of people with Alzheimer's disease (AD). AD is a type of dementia that can cause loss of memory, communication (such as speech), and decision-making skills. It can limit a person's ability to do daily tasks. MK-2214 is a study treatment designed to slow down AD. The goals of the study are to learn: * If MK-2214 slows the spread of tau in the brain compared to placebo. Tau is a protein that accumulates in AD \& damages brain cells. A placebo looks like the study treatment but has no study treatment in it. Using a placebo helps researchers better understand the effects of a study treatment. * About the safety of MK-2214 and if people tolerate it
Where this study is enrolling (36)
- Call 949-753-1663
Irvine Clinical Research ( Site 1041)
Irvine, California
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- Call 415-353-3585
UCSF Memory and Aging Center ( Site 1031)
San Francisco, California
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- Call 909-792-9007
Anderson Clinical Research ( Site 1024)
Redlands, California
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- Call 714-542-3008
Syrentis Clinical Research ( Site 1001)
Santa Ana, California
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- Call 562-606-5999
Healthy Brain Clinic ( Site 1005)
Long Beach, California
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Show all 36 locations
- Call 949-265-1612
Inglewood Clinical ( Site 1062)
Los Angeles, California
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- Call 203-764-8100
Yale University, Alzheimer's Disease Research Unit ( Site 1059)
New Haven, Connecticut
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- Call 727-849-4131
Suncoast Clinical Research ( Site 1007)
New Port Richey, Florida
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- Call 352-629-5800
Renstar Medical Research ( Site 1012)
Ocala, Florida
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- Call 352-775-1000
Charter Research - Lady Lake ( Site 1019)
The Villages, Florida
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- Call 407-337-3000
Charter Research - Orlando ( Site 1051)
Orlando, Florida
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- Call 407-680-0534
ClinCloud LLC ( Site 1039)
Melbourne, Florida
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- Call 239-939-7777
Neuropsychiatric Research Center of Southwest Florida ( Site 1003)
Fort Myers, Florida
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- Call 407-916-0060
Conquest Research LLC ( Site 1053)
Winter Park, Florida
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- Call 407-500-5252
K2 Medical Research ( Site 1047)
Maitland, Florida
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- Call 813-353-9613
Axiom Brain Health ( Site 1029)
Tampa, Florida
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- Call 561-968-2933
JEM Research Institute ( Site 1046)
Atlantis, Florida
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- Call 813-800-5252
K2 Medical Research ( Site 1020)
Tampa, Florida
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- Call 305-825-6588
Indago Research and Health Center Inc ( Site 1044)
Miami Lakes, Florida
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- Call 239-529-6780
Aqualane Clinical Research ( Site 1035)
Naples, Florida
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- Call 404-537-1281
CenExel iResearch, LLC ( Site 1015)
Decatur, Georgia
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- Call 847-593-8553
Alexian Brothers Medical Center-Neurosciences ( Site 1017)
Elk Grove Village, Illinois
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- Call 617-699-6927
Boston Center for Memory ( Site 1008)
Newton, Massachusetts
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- Call 636-220-1200
Clinical Research Professionals ( Site 1004)
Chesterfield, Missouri
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- Call 732-341-9500
CenExel- AMRI ( Site 1018)
Toms River, New Jersey
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- Call 201-850-4622
The Cognitive and Research Center of New Jersey - Ridgewood ( Site 1064)
Ridgewood, New Jersey
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- Call 973-850-4622
The Cognitive and Research Center of NJ ( Site 1057)
Springfield, New Jersey
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- Call 518-426-0575
Alzheimer Disease Research Center (ADRC) ( Site 1000)
Albany, New York
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- Call 845-674-9398
Mid Hudson Medical Research ( Site 1050)
New Windsor, New York
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- Call 917-672-3275
Basil Clinical ( Site 1065)
Queens, New York
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- Call 704-364-4000
AMC Research, LLC ( Site 1006)
Matthews, North Carolina
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- Call 216-245-6556
Insight Clinical Trials ( Site 1011)
Independence, Ohio
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- Call 330-493-1118
Neuro-Behavioral Clinical Research ( Site 1028)
North Canton, Ohio
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- Call 610-277-8073
Flourish Research ( Site 1048)
Plymouth Meeting, Pennsylvania
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- Call 409-331-6040
Gadolin Research ( Site 1032)
Beaumont, Texas
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- Call 949-491-0710
Horizon Clinical Research Center - Houston ( Site 1026)
Cypress, Texas
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Who can participate
Inclusion criteria
- ✓The main inclusion criteria include but are not limited to the following:
- ✓Has mild cognitive impairment (MCI) or mild dementia due to Alzheimer's Disease (AD)
- ✓Has a designated study partner who can fulfill the requirements of this study
- ✓If on an approved AD therapy for symptomatic AD, the dosing regimen must have been stable for 3 months prior to screening
Exclusion criteria
- ✕The main exclusion criteria include but are not limited to the following:
- ✕Has a known history of stroke or cerebrovascular disease
- ✕Has diagnosis of a clinically relevant central nervous system disease other than AD or other condition that negatively impacts cognition or cognitive status chronically
- ✕Has structural brain disease
- ✕Has a history of seizures or epilepsy within 5 years before screening
- ✕Has any other major central nervous system trauma, or infections that affect brain function
- ✕Has major medical illness or unstable medical condition within 3 months before screening
- ✕Has a severe, acute, or chronic medical or psychiatric condition or laboratory abnormality
- ✕Has any immunological disease, which is not adequately controlled, or which requires treatment with biologics and/or immunosuppressants during the study
- ✕Has a bleeding disorder that is not under adequate control
- ✕Has a history of malignancy occurring within 5 years of screening
- ✕Has a risk factor for corrected QT interval (QTc) prolongation
- ✕Has liver disease
- ✕Is unwilling or unable to undergo computed tomography (CT), positron emission tomography (PET), or magnetic resonance imaging (MRI) scan
- ✕Resides in a nursing home or assisted care facility with need for direct continuous medical care and nursing supervision
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.