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Completed Phase 1 Interventional

A Study to Evaluate the Safety, Tolerability, and Blood Levels of ACU193 in Participants With MCI or Mild AD

ClinicalTrials.gov ID: NCT04931459

Public ClinicalTrials.gov record NCT04931459. 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 25, 2026, 2:40 PM 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 1 Placebo-Controlled, Single- and Multiple-Dose Study of the Safety, Tolerability, and Pharmacokinetics of Intravenous ACU193 in Mild Cognitive Impairment or Mild Dementia Due to Alzheimer's Disease

Brief summary

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

This Phase 1 study is a single ascending dose (SAD) and multiple ascending dose (MAD), placebo-controlled study to evaluate the safety, tolerability, pharmacokinetics (PK), and pharmacodynamics (PD) of intravenous ACU193 when administered to participants diagnosed with Mild Cognitive Impairment (MCI) or Mild Dementia due to Alzheimer's disease (AD).

Study identification

NCT ID
NCT04931459
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
Acumen Pharmaceuticals
Industry
Enrollment
65 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
55 Years to 90 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 21, 2021 (Actual)
Primary completion
Jun 12, 2023 (Actual)
Completion
Jun 12, 2023 (Actual)
Last update posted
Jul 19, 2023

2021 – 2023

United States locations

U.S. sites
17
U.S. states
9
U.S. cities
17
Facility City State ZIP Site status
Clinical Endpoints Scottsdale Arizona 85258 —
Orange County Research Institute Anaheim California 92801 —
Hoag Hospital Newport Beach Newport Beach California 92663 —
Velocity Clinical Research Hallandale Florida 33009 —
Charter Research Lady Lake Florida 32159 —
Columbus Clinical Services Miami Florida 33125 —
Combined Research Orlando Phase I-IV Orlando Florida 32807 —
Progressive Medical Research Port Orange Florida 32321 —
Santos Research Center Tampa Florida 33615 —
Atlanta Center for Medical Research Atlanta Georgia 30331 —
iResearch Atlanta Decatur Georgia 30030 —
Advanced Memory Research Institute of NJ Toms River New Jersey 08755 —
Columbia University New York New York 10032 —
AMC Research Matthews North Carolina 28105 —
Abington Neurological Associates Abington Pennsylvania 19001 —
Kerwin Medical Center Dallas Texas 75231 —
Clinical Trials Network Houston Texas 77074 —

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04931459, 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 19, 2023 · Synced Oct 25, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04931459 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →