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Clinical trialNCT04931459CompletedPhase 1Interventional

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

SponsorAcumen PharmaceuticalsEnrollment65Alzheimer Disease
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

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).

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

17 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

United States
  • Clinical Endpoints

    Scottsdale, Arizona, United States

  • Orange County Research Institute

    Anaheim, California, United States

  • Hoag Hospital Newport Beach

    Newport Beach, California, United States

  • Velocity Clinical Research

    Hallandale, Florida, United States

  • Charter Research

    Lady Lake, Florida, United States

  • Columbus Clinical Services

    Miami, Florida, United States

  • Combined Research Orlando Phase I-Iv

    Orlando, Florida, United States

  • Progressive Medical Research

    Port Orange, Florida, United States

  • Santos Research Center

    Tampa, Florida, United States

  • Atlanta Center for Medical Research

    Atlanta, Georgia, United States

  • Iresearch Atlanta

    Decatur, Georgia, United States

  • Advanced Memory Research Institute of Nj

    Toms River, New Jersey, United States

  • Columbia University

    New York, New York, United States

  • Amc Research

    Matthews, North Carolina, United States

  • Abington Neurological Associates

    Abington, Pennsylvania, United States

  • Kerwin Medical Center

    Dallas, Texas, United States

  • Clinical Trials Network

    Houston, Texas, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

The drug and biological interventions registered on this study, normalized to their RxNorm ingredient where possible.

ACU193Placebo
Linked drugs open the directory filtered to KOLs working with them.clinicaltrials.gov ↗

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
21 Jun 2021
Primary completion
12 Jun 2023
Completion
12 Jun 2023
Last update posted
19 Jul 2023
Registered enrollment
65
Registry id
NCT04931459

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.