Canavan Disease |
ACY2 deficiency; Aminoacylase 2 deficiency; Asp deficiency; Aspa deficiency; Aspartoacylase deficiency; Leukodystrophy, spongiform; Spongy degeneration of central nervous system; Spongy degeneration of the brain; Spongy degeneration of white matter in infancy; Van Bogaert-Bertrand syndrome; Von Bogaert-Bertrand disease |
Clinical Trial: Evaluation of Alzhemed™ in Patients with Mild to Moderate Alzheimer's Disease
Evaluation of Alzhemed™ in Patients with Mild to Moderate Alzheimer’s Disease
This study is currently recruiting patients.
|
Purpose
The purpose of this Phase III study is to evaluate the efficacy and safety of Alzhemed™ compared to placebo (inactive substance pill) in patients with mild to moderate Alzheimer’s disease.
| Condition | Treatment or Intervention | Phase |
|---|---|---|
| Alzheimer Disease | Drug: Alzhemed™ | Phase III |
MedlinePlus related topics: Alzheimer's Caregivers; Alzheimer's Disease
Genetics Home Reference related topics: Alzheimer disease
Study Type: Interventional
Study Design: Educational/Counseling/Training, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Safety/Efficacy Study
Official Title: A Phase III Study of the Efficacy and Safety of Alzhemed™ in Patients with Mild to Moderate Alzheimer’s Disease
Study start: June 2004
Eligibility
Ages Eligible for Study: 50 Years and above, Genders Eligible for Study: Both
Criteria
Inclusion Criteria:
Patients may be included in this study if they meet all of the following criteria:
- Male or Female (age 50 years and older): Female must be of non-childbearing potential (i.e. surgically sterilized or at least 2 years post-menopausal).
- Diagnosis of probable Alzheimer’s disease based on the National Institute of Neurological and Communicative Disorders and Stroke/Alzheimer’s Disease and Related Disorders Association (NINCDS-ADRDA criteria).
- Severity of dementia of mild to moderate degree as assessed by the Mini Mental State Examination (MMSE) performed at the screening visit.
- Patient must be living in the community with a reliable caregiver. Participant living in an assisted living facility may be included if study medication intake is supervised and participant has a reliable caregiver.
- Potential participant must be treated with conventional Alzheimer’s disease therapies and must be on stable dose for at least 4 months prior to the screening visit and during the entire study period.
- Fluency in English, French or Spanish (oral and written).
- Signed informed consent from potential participant or legal representative and caregiver.
Exclusion Criteria:
Patients will not be eligible to participate in the study if they meet any of the following criteria:
- Potential participant with any other cause of dementia.
- Life expectancy less than 2 years.
- Potential participant with a clinically significant and/or uncontrolled condition or other significant medical disease.
- Use of an investigational drug within 30 days prior to the screening visit or during the entire study.
- Previous use of Alzhemed™.
Patient recruitment is done by participating centers.
Location and Contact Information
Other locations will be listed upon availability.
Arizona
Pivotal Research Centers, Peoria, Arizona, United States; Recruiting
21st Century Neurology, a division of Xenoscience, Phoenix, Arizona, United States; Recruiting
Arkansas
Central Arkansas Research, Hot Springs, Arkansas, United States; Recruiting
California
Margolin Brain Institute, Fresno, California, United States; No longer recruiting
Pacific Research Network, Inc., San Diego, California, United States; Recruiting
Senior Clinical Trials, Inc., Laguna Hills, California, United States; No longer recruiting
San Francisco Clinical Research Center, San Francisco, California, United States; Recruiting
Colorado
Radiant Research, Denver, Colorado, United States; Recruiting
Connecticut
Yale University, Alzheimer's Disesase Research Unit, New Haven, Connecticut, United States; Recruiting
Research Center for Clinical Studies, Inc., Darien, Connecticut, 06820, United States; Recruiting
Danilo de la Pena, MD 203-662-0070
New England Research Institute, Stamford, Connecticut, United States; No longer recruiting
District of Columbia
Georgetown University Medical Center, Washington, District of Columbia, United States; Recruiting
Florida
Berma Research Group, Hialeah, Florida, United States; Recruiting
Stedman Clinical Trials, Tampa, Florida, United States; Recruiting
Tukoi Institute for Clinical Research, Miami, Florida, United States; No longer recruiting
Palm Beach Neurological Center, Palm Beach Gardens, Florida, United States; Recruiting
Premiere Research Institute Palm Beach Neurology, West Palm Beach, Florida, United States; Recruiting
Axiom Clinical Research, Tampa, Florida, United States; Recruiting
Neuropsychiatric Research Center of SouthWest Florida, Fort Myers, Florida, United States; Recruiting
Byrd Alzheimer’s Center and Research Institute, Tampa, Florida, United States; Recruiting
Quantum Laboratories Inc at the Memory Disorders Clinic, North Broward Medical Center, Pompano Beach, Florida, United States; Recruiting
University of South Florida, Suncoast Gerontology Center, Tampa, Florida, United States; Recruiting
Georgia
Emory University, Atlanta, Georgia, United States; No longer recruiting
Comprehensive Neurology Specialists, PC, Atlanta, Georgia, United States; Recruiting
Illinois
Southern Illinois University (SIU) School of Medicine, Department of Neurology, Springfield, Illinois, United States; Recruiting
Massachusetts
Brigham & Women's Hospital, Boston, Massachusetts, United States; Recruiting
Michigan
Mood & Memory Clinic - Dr Aronson, Farmington Hills, Michigan, United States; Recruiting
New Jersey
Memory Enhancement Center, Long Branch, New Jersey, United States; Recruiting
New York
Neurological Associates of Albany, Albany, New York, United States; Recruiting
Lisa or Greg 518-426-0575
Global Research and Consulting, Olean, New York, United States; Recruiting
Eastside Comprehensive Medical Center, New York, New York, United States; Recruiting
NYU School of Medicine, New York, New York, United States; Recruiting
University of Rochester-Program in Neurobehavioral Therapeutics, Rochester, New York, United States; Recruiting
Nathan S. Kline Institute, Orangeburg, New York, United States; Recruiting
North Carolina
Richard H. Weisler, MD, PA and Associates, Raleigh, North Carolina, United States; No longer recruiting
Wake Forest University School of Medicine, Department of Psychiatry and Behavioral Medicine, Winston Salem, North Carolina, United States; Recruiting
Ohio
Neurology and Neuroscience Center of Ohio, Toledo, Ohio, United States; No longer recruiting
University Memory and Aging Center, Cleveland, Ohio, United States; Recruiting
Oklahoma
Clinical Pharmaceuticals Trials, Inc., Tulsa, Oklahoma, United States; Recruiting
Pennsylvania
CNS Research Institute, Philadelphia, Pennsylvania, United States; No longer recruiting
Farber Institute for Neurosciences, Philadelphia, Pennsylvania, United States; Recruiting
University of Pennsylvania, Philadelphia, Pennsylvania, United States; No longer recruiting
University of Pittsburgh ADRC, Pittsburgh, Pennsylvania, United States; Recruiting
Rhode Island
CNS Research, Inc., East Providence, Rhode Island, United States; Recruiting
Memory and Aging Program, Butler Hospital, Providence, Rhode Island, United States; Recruiting
South Carolina
MUSC - Alzheimer's Research and Clinical Programs, North Charleston, South Carolina, United States; Recruiting
Tennessee
Clinical Research Services at Tennessee Christian Medical Center, Madison, Tennessee, United States; Recruiting
Lauren Sade 615-860-6530
Texas
Air Force Villages-Freedom House Research (Study open to Air Force Village residents only), San Antonio, Texas, United States; Recruiting
University of Texas Mental Sciences Institute, Houston, Texas, United States; Recruiting
Vermont
The Memory Clinic, Bennington, Vermont, United States; Recruiting
Canada, Alberta
Calgary, Alberta, Canada; Recruiting
Canada, British Columbia
The Medical Arts Health Research Group, a Division of PCT Networks, Inc., Penticton, British Columbia, Canada; Recruiting
Canada, New Brunswick
St. Joseph's Hospital, Saint John, New Brunswick, Canada; No longer recruiting
Canada, Nova Scotia
Queen Elizabeth II Health Sciences Centre, Halifax, Nova Scotia, Canada; Recruiting
Canada, Ontario
Gerontion Research, Toronto, Ontario, Canada; Recruiting
Geriatric Clinical Trials Group, Parkwood Hospital, London, Ontario, Canada; Recruiting
Toronto Memory Program, Toronto, Ontario, Canada; Recruiting
Ottawa, Ontario, Canada; Recruiting
Sunnybrook and Women's College Health Science Centre, Toronto, Ontario, Canada; No longer recruiting
Queen's University, Kingston, Ontario, Canada; No longer recruiting
Canada, Quebec
Memory & Motor Skills Disorders Clinic, Ville de Québec, Quebec, Canada; Recruiting
Centre de recherche Novabyss, Sherbrooke, Quebec, Canada; Recruiting
Clinique Neuro Rive-Sud, Greenfield Park, Quebec, Canada; Recruiting
Hôpital Maisonneuve-Rosemont, Recherche Clinique de Neurologie, Montreal, Quebec, Canada; Recruiting
Jewish General Hospital- Memory Clinic, Montreal, Quebec, Canada; Recruiting
McGill Centre for Studies in Aging, Verdun (Montreal), Quebec, Canada; Recruiting
Hôpital de l'Enfant-Jésus, Ville de Quebec, Quebec, Canada; Recruiting
More Information
Record last reviewed: April 2005
Last Updated: April 4, 2005
Record first received: July 30, 2004
ClinicalTrials.gov Identifier: NCT00088673
Health Authority: United States: Food and Drug Administration
ClinicalTrials.gov processed this record on 2005-04-08
Source: ClinicalTrials.gov
Cache Date: April 9, 2005

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