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Recruiting Phase 1Phase 2 Interventional

A Study to Assess the Effects of ACI-24.060 in Alzheimer's Disease and in Down Syndrome (ABATE Study)

ClinicalTrials.gov ID: NCT05462106

Public ClinicalTrials.gov record NCT05462106. 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 Sep 3, 2026, 12:40 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 Phase 1b/2, Multicenter, Adaptive, Double-blind, Randomized, Placebo-controlled Study to Assess the Safety, Tolerability, Immunogenicity, and Pharmacodynamic Effects of ACI-24.060 in Subjects With Prodromal Alzheimer's Disease and in Adults With Down Syndrome (ABATE)

Brief summary

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

The purpose of this study is to assess the safety, tolerability, immunogenicity and pharmacodynamic effects of ACI-24.060 in subjects with prodromal Alzheimer's disease and in non-demented adults with Down syndrome.

Study identification

NCT ID
NCT05462106
Recruitment status
Recruiting
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
AC Immune SA
Industry
Enrollment
304 participants

Conditions and interventions

Eligibility (public fields only)

Age range
35 Years to 85 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 20, 2022
Primary completion
Mar 31, 2029
Completion
Mar 31, 2029
Last update posted
Jul 9, 2026

2022 – 2029

United States locations

U.S. sites
13
U.S. states
9
U.S. cities
12
Facility City State ZIP Site status
Barrow Neurological Institute Phoenix Arizona 85013 Withdrawn
K2 Medical Research The Villages LLC Lady Lake Florida 32159 Recruiting
Charter Research, LLC Orlando Florida 32803 Recruiting
Headlands Horizons LLC Orlando Florida 32819 Not yet recruiting
Charter Research, LLC The Villages Florida 32162 Recruiting
Indiana University / IU Health Indianapolis Indiana 46202 Active, not recruiting
University of Kansas Medical Center Research Institute Fairway Kansas 66205-2513 Active, not recruiting
Massachusetts General Hospital Boston Massachusetts 02114 Active, not recruiting
The Washington University St Louis Missouri 63130 Active, not recruiting
Flourish Research Matthews North Carolina 28105 Not yet recruiting
Neurology Clinical, P.C. Cordova Tennessee 38018 Recruiting
Vanderbilt University Medical Center Nashville Tennessee 37232-2103 Active, not recruiting
UT Health San Antonio San Antonio Texas 78229 Withdrawn

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 13 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05462106, 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 9, 2026 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05462106 live on ClinicalTrials.gov.

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