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Completed Phase 2 Interventional

A Study to Test the Efficacy, Safety, and Tolerability of Bepranemab (UCB0107) in Patients With Mild Cognitive Impairment or Mild Alzheimer's Disease (AD)

ClinicalTrials.gov ID: NCT04867616

Public ClinicalTrials.gov record NCT04867616. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 26, 2026, 4:06 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Patient- and Investigator-Blind, Placebo-Controlled Study to Evaluate the Efficacy, Safety, and Tolerability of Bepranemab (UCB0107) in Study Participants With Prodromal to Mild Alzheimer's Disease (AD), Followed by an Open-Label Extension Period

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of the study is to investigate the effect of bepranemab versus (vs) placebo on the Clinical Dementia Rating Scale Sum of Boxes (CDR-SB) up to Week 80 in study participants with prodromal or mild Alzheimer's Disease (AD).

Study identification

NCT ID
NCT04867616
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
UCB Biopharma SRL
Industry
Enrollment
466 participants

Conditions and interventions

Interventions

Other · Biological

Eligibility (public fields only)

Age range
50 Years to 80 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 9, 2021 (Actual)
Primary completion
May 24, 2024 (Actual)
Completion
Aug 1, 2025 (Actual)
Last update posted
Jul 24, 2026

2021 – 2025

United States locations

U.S. sites
40
U.S. states
13
U.S. cities
37
Facility City State ZIP Site status
Ah0003 50428 Fresno California 93710 —
Ah0003 50431 Fullerton California 92835 —
Ah0003 50442 Irvine California 92614 —
Ah0003 50458 Long Beach California 90807 —
Ah0003 50450 Palo Alto California 94303 —
Ah0003 50452 Pasadena California 91106 —
Ah0003 50447 San Diego California 92123 —
Ah0003 50434 Santa Ana California 92705 —
Ah0003 50422 New Haven Connecticut 06510 —
Ah0003 50467 New Haven Connecticut 06510 —
Ah0003 50421 Stamford Connecticut 06905 —
Ah0003 50465 Atlantis Florida 33462 —
Ah0003 50449 Aventura Florida 33180 —
Ah0003 50435 Boca Raton Florida 33487 —
Ah0003 50430 Delray Beach Florida 33445 —
Ah0003 50429 Fort Myers Florida 33912 —
Ah0003 50436 Hialeah Florida 33016 —
Ah0003 50426 Maitland Florida 32751 —
Ah0003 50427 Miami Florida 33125 —
Ah0003 50478 Naples Florida 34105 —
Ah0003 50464 Ocoee Florida 34761 —
Ah0003 50438 Pensacola Florida 32502 —
Ah0003 50623 Pensacola Florida 32503 —
Ah0003 50457 Port Orange Florida 32127 —
Ah0003 50454 Tampa Florida 33613 —
Ah0003 50444 West Palm Beach Florida 33407 —
Ah0003 50476 West Palm Beach Florida 33409 —
Ah0003 50446 Westchester Florida 33155 —
Ah0003 50479 Decatur Georgia 30033 —
Ah0003 50445 Braintree Massachusetts 02184 —
Ah0003 50453 Newton Massachusetts 02459 —
Ah0003 50448 Saint Paul Minnesota 55130 —
Ah0003 50420 Neptune City New Jersey 07753 —
Ah0003 50451 Cincinnati Ohio 45219 —
Ah0003 50423 East Providence Rhode Island 02914 —
Ah0003 50455 Cordova Tennessee 38018 —
Ah0003 50380 Houston Texas 77054 —
Ah0003 50424 Fairfax Virginia 22031 —
Ah0003 50432 Norfolk Virginia 23507 —
Ah0003 50440 Bellevue Washington 98007 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 63 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04867616, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 24, 2026 · Synced Oct 26, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04867616 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →