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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT00087724
Other study ID # 03-0-189
Secondary ID
Status Terminated
Phase Phase 2
First received July 12, 2004
Last updated June 6, 2012
Start date July 2004
Est. completion date September 2006

Study information

Verified date June 2012
Source Astellas Pharma Inc
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Terminated
Enrollment 510
Est. completion date September 2006
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 50 Years to 90 Years
Eligibility Inclusion Criteria:

- Subject satisfies the criteria for the clinical diagnosis of probable AD

- Subject has a score =< 4 on the Modified Hachinski Ischemia Scale at the screening visit

Exclusion Criteria:

- Subject has history or evidence of significant neurologic disease other than AD

- Subject has a history of stroke

- Subject has been treated for schizophrenia or recurrent mood disorder within the previous three years

- Subject has a hematologic or solid malignancy diagnosed within five years prior to study entry

- Subject has medically unstable COPD or asthma

- Subject has end stage CHF (NYHA Class III or IV) or unstable angina

- Subject has evidence of significant renal insufficiency

- Subject has insulin-dependent diabetes mellitus or HbA1C>8.5% at screening

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
FK962


Locations

Country Name City State
Canada Investigational Site Barrie Ontario
Canada Investigational Site Kelowna British Columbia
Canada Investigational Site North York Ontario
Canada Investigational Site North York Ontario
Canada Investigational Site Ottawa Ontario
Canada Investigational Site Penticton British Columbia
Canada Investigational Site Regina Saskatchewan
Canada Investigational Site Sudbury Ontario
Canada Investigational Site Sydney Nova Scotia
Canada Investigational Site Toronto Ontario
Canada Investigational Site Victoria British Columbia
Canada Investigational Site Willowdale Ontario
United States Investigational Site Albany New York
United States Investigational Site Albuquerque New Mexico
United States Investigational Site Bala Cynwyd Pennsylvania
United States Investigational Site Bennington Vermont
United States Investigational Site Buffalo New York
United States Investigational Site Centerville Ohio
United States Investigational Site Columbus Ohio
United States Investigational Site Darien Connecticut
United States Investigational Site Dayton Ohio
United States Investigational Site Denver Colorado
United States Investigative Site Denver Colorado
United States Investigational Site Elk Grove Illinois
United States Investigational Site Eugene Oregon
United States Investigational Site Fort Myers Florida
United States Investigational Site Fresno California
United States Investigational Site Hamden Connecticut
United States Investigational Site Hialeah Florida
United States Investigational Site Hollywood Florida
United States Investigational Site Houston Texas
United States Investigational Site Irvine California
United States Investigational Site Jenkintown Pennsylvania
United States Investigational Site Johnson City Tennessee
United States Investigational Site Las Vegas Nevada
United States Investigational Site Lawrence New York
United States Investigational Site Little Rock Arkansas
United States Investigational Site Little Rock Arkansas
United States Investigational Site Long Branch New Jersey
United States Investigational Site Manchester New Jersey
United States Investigational Site Medford Oregon
United States Investigational Site Miami Florida
United States Investigational Site Milwaukee Wisconsin
United States Investigational Site Nashville Tennessee
United States Investigational Site New Orleans Louisiana
United States Investigational Site New York New York
United States Investigational Site Newton Massachusetts
United States Investigational Site Norfolk Virginia
United States Investigational Site North Miami Florida
United States Investigational Site Ocala Florida
United States Investigational Site Oklahoma City Oklahoma
United States Investigational Site Orange California
United States Investigational Site Pawtucket Rhode Island
United States Investigational Site Phoenix Arizona
United States Investigational Site Phoenix Arizona
United States Investigational Site Piscataway New Jersey
United States Investigational Site Port Charlotte Florida
United States Investigational Site Salt Lake City Utah
United States Investigational Site San Antonio Texas
United States Investigational Site San Francisco California
United States Investigational Site Sarasota Florida
United States Investigational Site Sebring Florida
United States Investigational Site Sherman Oaks California
United States Investigational Site Snellville Georgia
United States Investigational Site St. Louis Missouri
United States Investigational Site Stamford Connecticut
United States Investigational Site Tampa Florida
United States Investigational Site Toledo Ohio
United States Investigational Site Torrance California
United States Investigational Site Tucson Arizona
United States Investigational Site Tulsa Oklahoma
United States Investigational Site White Plains New York
United States Investigational Site Wichita Kansas
United States Investigational Site Wichita Falls Texas

Sponsors (2)

Lead Sponsor Collaborator
Astellas Pharma Inc Astellas Pharma US, Inc.

Countries where clinical trial is conducted

United States,  Canada, 

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