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Terminated Phase 2 Interventional

A Randomized Study to Evaluate FK962 in Subjects With Mild to Moderate Alzheimer's Disease

ClinicalTrials.gov ID: NCT00087724

Public ClinicalTrials.gov record NCT00087724. 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 28, 2026, 5:03 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 Randomized, Double-Blind, Placebo-Controlled, Parallel Group, Phase 2 Study to Evaluate the Safety and Efficacy of FK962 in Subjects With Mild to Moderate Alzheimer's Disease

Brief summary

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

The purpose of this study is to evaluate the safety and efficacy of five fixed dosage levels of FK962 or placebo for 24 weeks in subjects with mild to moderate Alzheimer's disease. Patient visits are every six weeks with limited efficacy measurements at week 6 and 18.

Study identification

NCT ID
NCT00087724
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Astellas Pharma Inc
Industry
Enrollment
510 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
50 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 30, 2004
Primary completion
Not listed
Completion
Aug 31, 2006
Last update posted
Jun 6, 2012

2004 – 2006

United States locations

U.S. sites
72
U.S. states
31
U.S. cities
66
Facility City State ZIP Site status
Investigational Site Phoenix Arizona 85013 —
Investigational Site Phoenix Arizona 85032 —
Not listed Sun City Arizona 85351 —
Investigational Site Tucson Arizona 85724 —
Investigational Site Little Rock Arkansas 72205 —
Investigational Site Little Rock Arkansas 72211 —
Investigational Site Fresno California 93720 —
Investigational Site Irvine California 92618 —
Investigational Site Orange California 92656 —
Investigational Site San Francisco California 94115 —
Investigational Site Sherman Oaks California 91403 —
Investigational Site Torrance California 90505 —
Investigative Site Denver Colorado 80249 —
Investigational Site Denver Colorado 80262 —
Investigational Site Darien Connecticut 06820 —
Investigational Site Hamden Connecticut 06518 —
Not listed Hamden Connecticut 06518 —
Investigational Site Stamford Connecticut 06902 —
Investigational Site Fort Myers Florida 33912 —
Investigational Site Hialeah Florida 33016 —
Investigational Site Hollywood Florida 33021 —
Investigational Site Miami Florida 33176 —
Investigational Site North Miami Florida 33161 —
Investigational Site Ocala Florida 34471 —
Investigational Site Port Charlotte Florida 33952 —
Investigational Site Sarasota Florida 34243 —
Investigational Site Sebring Florida 33872 —
Investigational Site Tampa Florida 33613 —
Not listed West Palm Beach Florida 33407 —
Investigational Site Snellville Georgia 30078 —
Not listed Snellville Georgia 30078 —
Investigational Site Elk Grove Illinois 60007 —
Investigational Site Wichita Kansas 67207 —
Investigational Site New Orleans Louisiana 70112 —
Not listed Baltimore Maryland 21208 —
Investigational Site Newton Massachusetts 02459 —
Not listed Livonia Michigan 48152 —
Not listed Hattiesburg Mississippi 32401 —
Investigational Site St Louis Missouri 63128 —
Investigational Site Las Vegas Nevada 89102 —
Investigational Site Long Branch New Jersey 07740 —
Investigational Site Paterson New Jersey 08759 —
Investigational Site Piscataway New Jersey 08855 —
Investigational Site Albuquerque New Mexico 87102 —
Investigational Site Albany New York 12208 —
Investigational Site Buffalo New York 14221 —
Investigational Site Lawrence New York 11559 —
Investigational Site New York New York 10021 —
Investigational Site White Plains New York 10605 —
Not listed Charlotte North Carolina 28204 —
Investigational Site Centerville Ohio 45459 —
Investigational Site Columbus Ohio 43210 —
Not listed Dayton Ohio 45408 —
Investigational Site Dayton Ohio 45415 —
Investigational Site Toledo Ohio 43623 —
Investigational Site Oklahoma City Oklahoma 73112 —
Investigational Site Tulsa Oklahoma 74104 —
Investigational Site Eugene Oregon 97401 —
Investigational Site Medford Oregon 97504 —
Investigational Site Bala-Cynwyd Pennsylvania 19004 —
Investigational Site Jenkintown Pennsylvania 19046 —
Investigational Site Pawtucket Rhode Island 02860 —
Investigational Site Johnson City Tennessee 37601 —
Investigational Site Nashville Tennessee 37203 —
Investigational Site Houston Texas 77063 —
Investigational Site San Antonio Texas 78229 —
Investigational Site Wichita Falls Texas 76309 —
Investigational Site Salt Lake City Utah 84121 —
Investigational Site Bennington Vermont 05201 —
Not listed Burlington Vermont 05401 —
Investigational Site Norfolk Virginia 23507 —
Investigational Site Milwaukee Wisconsin 53227 —

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 12 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00087724, 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 Jun 6, 2012 · Synced Sep 28, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00087724 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →