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Completed Phase 2 Interventional

Efficacy and Safety of 26-Week Treatment of AR1001 in Patients With Mild to Moderate Alzheimer's Disease

ClinicalTrials.gov ID: NCT03625622

Public ClinicalTrials.gov record NCT03625622. 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 27, 2026, 1:29 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 Double-Blind, Randomized, Placebo-Controlled Study to Evaluate Efficacy and Safety of 26-Week Treatment of AR1001 in Patients With Mild to Moderate Alzheimer's Disease

Brief summary

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

A double-blinded, randomized, placebo-controlled study will be performed to evaluate the efficacy and safety of treating AR1001 in patients with mild to moderate Alzheimer's disease for 26 weeks.

Study identification

NCT ID
NCT03625622
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
AriBio Co., Ltd.
Industry
Enrollment
210 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
55 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
Mar 31, 2019
Primary completion
Dec 21, 2020
Completion
Jun 27, 2021
Last update posted
Jul 20, 2021

2019 – 2021

United States locations

U.S. sites
21
U.S. states
11
U.S. cities
21
Facility City State ZIP Site status
Advanced Clinical Research, Inc. Banning California 92220 —
Northern California Research Sacramento California 95821 —
Syrentis Clinical Research Santa Ana California 92705 —
Meridien Research Lakeland Florida 33805 —
Meridien - Maitland Maitland Florida 32751 —
The Neurology Research Group Miami Florida 33176 —
Accelerated Enrollment Solutions (AES) Orlando Florida 32806 —
IMIC, Inc Palmetto Bay Florida 33157 —
Meridien Research - Spring Hill Spring Hill Florida 34609 —
Meridien Research - St Petersburg St. Petersburg Florida 33709 —
Meridien Research - Tampa Tampa Florida 33634 —
NeuroStudies, LLC Decatur Georgia 30033 —
Advanced Clinical Research Meridian Idaho 83642 —
Wake Research - CRCNV Las Vegas Nevada 89106 —
Rapid Medical Research Beachwood Ohio 44122 —
Lynn Health Science Institute Oklahoma City Oklahoma 73112 —
Palmetto Clinical Research Summerville South Carolina 29485 —
Advanced Clinical Research - Cedar Park Cedar Park Texas 78613 —
FMC Science Lampasas Texas 76550 —
Advanced Clinical Research, Inc. West Jordan Utah 84088 —
Kingfisher Cooperative, LLC Spokane Washington 99202 —

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 NCT03625622, 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 20, 2021 · Synced Sep 27, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03625622 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →