Can an antibody slow Alzheimer's? a new trial seeks answers
NCT ID NCT04867616
First seen Jul 24, 2026 · Last updated Jul 24, 2026
Summary
This phase 2 trial is testing whether an experimental antibody called bepranemab can slow the progression of Alzheimer's disease in people with early-stage symptoms. Participants receive either bepranemab or a placebo by intravenous infusion over 80 weeks. The study measures changes in memory, thinking, and daily function to see if the drug can preserve cognitive abilities.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- an experimental antibody called bepranemab
- What this could lead to
- If it works, this could point toward a treatment that slows memory loss and cognitive decline in early Alzheimer's disease.
- What could go wrong
- This is a mid-stage trial, so the drug may not prove effective or could cause side effects. Alzheimer's is complex, and many experimental treatments have failed before.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
-
466 people
The number who actually took part.
- Started
-
Jun 2021
- Finished
-
Aug 2025
- Lead sponsor
-
A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
50 to 80 years
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * 50 to 80 years of age * Diagnosis of prodromal/mild cognitive impairment (MCI) due to Alzheimer's Disease (AD) or mild AD according to National Institute of Aging-Alzheimer's Association (NIA-AA) * A global Clinical Dementia Rating (CDR) score of 0.5 to 1.0 and CDR-Memory Box (CDRMB) score ≥0.5 at Screening and Baseline * Score of ≤85 for the delayed recall domain of the Repeatable Battery for the Assessment of Neuropsychological Status (RBANS) at Screening * Mini-Mental State Examination (MMSE) score ≥20 at Screening * Participant has an identified informant that has and will maintain sufficient contact (minimum of 5 hours per week) with the participant to be able to provide accurate information on the participant's cognitive, functional, and emotional states and of the participant's personal care * At least 6 years of formal education after the age of 5 or work experience to exclude mental deficits other than prodromal or mild AD dementia * Evidence of cerebral Aβ accumulation by either positive amyloid assessment by either positron emission tomography (PET) scan or cerebrospinal fluid pTau181/Aβ1-42 ratio assessment Exclusion Criteria: * Any evidence of a condition that may affect cognition other than AD * Contraindications to PET imaging * Inability to tolerate or contraindication to magnetic resonance imaging * Any serious medical condition or abnormality that in the opinion of the investigator would preclude safe participation in and completion of the study or interfere with study assessments and/or study interpretation * Alcohol or drug abuse within 2 years of screening * Use of any experimental therapy within the past 6 months (or 5 half lives) prior to screening * Previous treatment with medication intended to treat a neurodegenerative disorder (other than AD) within 1 year of screening * Chronic daily treatment with atypical antipsychotics, opiates or opioids, benzodiazepines, barbiturates, hypnotics, or any medication with clinically significant centrally acting antihistamine or anticholinergic activitiy * Received treatment with monoclonal antibodies (mAbs), cytokines, immunoglobulins, or other blood products within 3 months or 5 half-lives (whichever is longer) prior to first dosing
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Ah0003 40002
Leuven, Belgium
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Ah0003 40028
Berlin, Germany
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Ah0003 40049
Seville, Spain
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Ah0003 40105
Córdoba, Spain
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Ah0003 40123
Brussels, Belgium
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Ah0003 40129
Bordeaux, France
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Ah0003 40159
Barcelona, Spain
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Ah0003 40160
Barcelona, Spain
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Ah0003 40201
Rennes, France
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Ah0003 40230
Valencia, Spain
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Ah0003 40267
Barcelona, Spain
-
Ah0003 40280
Sant Cugat del Vallès, Spain
-
Ah0003 40352
Pamplona, Spain
-
Ah0003 40371
Monza, Italy
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Ah0003 40430
Munich, Germany
-
Ah0003 40438
Roma, Italy
-
Ah0003 40449
's-Hertogenbosch, Netherlands
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Ah0003 40450
Amsterdam, Netherlands
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Ah0003 40453
Terrassa, Spain
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Ah0003 40493
Marseille, France
-
Ah0003 40540
Madrid, Spain
-
Ah0003 40575
Brussels, Belgium
-
Ah0003 40576
Kortrijk, Belgium
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Ah0003 40578
Paris, France
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Ah0003 40579
Villeurbanne, France
-
Ah0003 40580
Bron, France
-
Ah0003 40581
Toulouse, France
-
Ah0003 40596
Rome, Italy
-
Ah0003 40597
Pavia, Italy
-
Ah0003 40598
Rome, Italy
-
Ah0003 40600
Parma, Italy
-
Ah0003 40601
Zwolle, Netherlands
-
Ah0003 40602
Warsaw, Poland
-
Ah0003 40603
Bialystok, Poland
-
Ah0003 40604
Warsaw, Poland
-
Ah0003 40605
Katowice, Poland
-
Ah0003 40606
Bydgoszcz, Poland
-
Ah0003 40607
Warsaw, Poland
-
Ah0003 40608
Szczecin, Poland
-
Ah0003 40609
Katowice, Poland
-
Ah0003 40611
Wroclaw, Poland
-
Ah0003 40612
Barcelona, Spain
-
Ah0003 40613
Valencia, Spain
-
Ah0003 40614
Donostia / San Sebastian, Spain
-
Ah0003 40615
Madrid, Spain
-
Ah0003 40616
Zaragoza, Spain
-
Ah0003 40618
London, United Kingdom
-
Ah0003 40619
Bristol, United Kingdom
-
Ah0003 40621
London, United Kingdom
-
Ah0003 40622
Guildford, United Kingdom
-
Ah0003 40623
Plymouth, United Kingdom
-
Ah0003 40635
Nantes, France
-
Ah0003 40638
Ścinawa, Poland
-
Ah0003 40662
Birmingham, United Kingdom
-
Ah0003 40691
Winchester, United Kingdom
-
Ah0003 40774
Katowice, Poland
-
Ah0003 50045
Toronto, Canada
-
Ah0003 50291
Toronto, Canada
-
Ah0003 50380
Houston, Texas, 77054, United States
-
Ah0003 50420
Neptune City, New Jersey, 07753, United States
-
Ah0003 50421
Stamford, Connecticut, 06905, United States
-
Ah0003 50422
New Haven, Connecticut, 06510, United States
-
Ah0003 50423
East Providence, Rhode Island, 02914, United States
-
Ah0003 50424
Fairfax, Virginia, 22031, United States
-
Ah0003 50426
Maitland, Florida, 32751, United States
-
Ah0003 50427
Miami, Florida, 33125, United States
-
Ah0003 50428
Fresno, California, 93710, United States
-
Ah0003 50429
Fort Myers, Florida, 33912, United States
-
Ah0003 50430
Delray Beach, Florida, 33445, United States
-
Ah0003 50431
Fullerton, California, 92835, United States
-
Ah0003 50432
Norfolk, Virginia, 23507, United States
-
Ah0003 50434
Santa Ana, California, 92705, United States
-
Ah0003 50435
Boca Raton, Florida, 33487, United States
-
Ah0003 50436
Hialeah, Florida, 33016, United States
-
Ah0003 50438
Pensacola, Florida, 32502, United States
-
Ah0003 50440
Bellevue, Washington, 98007, United States
-
Ah0003 50442
Irvine, California, 92614, United States
-
Ah0003 50444
West Palm Beach, Florida, 33407, United States
-
Ah0003 50445
Braintree, Massachusetts, 02184, United States
-
Ah0003 50446
Westchester, Florida, 33155, United States
-
Ah0003 50447
San Diego, California, 92123, United States
-
Ah0003 50448
Saint Paul, Minnesota, 55130, United States
-
Ah0003 50449
Aventura, Florida, 33180, United States
-
Ah0003 50450
Palo Alto, California, 94303, United States
-
Ah0003 50451
Cincinnati, Ohio, 45219, United States
-
Ah0003 50452
Pasadena, California, 91106, United States
-
Ah0003 50453
Newton, Massachusetts, 02459, United States
-
Ah0003 50454
Tampa, Florida, 33613, United States
-
Ah0003 50455
Cordova, Tennessee, 38018, United States
-
Ah0003 50457
Port Orange, Florida, 32127, United States
-
Ah0003 50458
Long Beach, California, 90807, United States
-
Ah0003 50461
Ottawa, Canada
-
Ah0003 50462
Toronto, Canada
-
Ah0003 50463
Kelowna, Canada
-
Ah0003 50464
Ocoee, Florida, 34761, United States
-
Ah0003 50465
Atlantis, Florida, 33462, United States
-
Ah0003 50467
New Haven, Connecticut, 06510, United States
-
Ah0003 50476
West Palm Beach, Florida, 33409, United States
-
Ah0003 50478
Naples, Florida, 34105, United States
-
Ah0003 50479
Decatur, Georgia, 30033, United States
-
Ah0003 50520
Québec, Canada
-
Ah0003 50522
West Vancouver, Canada
-
Ah0003 50623
Pensacola, Florida, 32503, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Randomized, delayed start, double blind, parallel group, placebo controlled, multicenter study of piromelatine 20 mg in participants with mild dementia due to Alzheimer's disease
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