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SGS742 in Patients With Mild to Moderate Alzheimer's Disease (AD)

This study has been completed.

Sponsored by: Saegis Pharmaceuticals
Information provided by: National Institute on Aging (NIA)
ClinicalTrials.gov Identifier: NCT00093951
  Purpose

The purpose of this trial is to determine the effect of a new drug, SGS742, on memory and cognition in patients with mild to moderate Alzheimer's disease.


Condition Intervention Phase
Alzheimer's Disease
Drug: SGS742
Phase II

Genetics Home Reference related topics:   Alzheimer disease   

MedlinePlus related topics:   Alzheimer's Disease    Memory   

ChemIDplus related topics:   (3-aminopropyl)(n-butyl)phosphinic acid   

U.S. FDA Resources

Study Type:   Interventional
Study Design:   Treatment, Randomized, Double-Blind, Placebo Control, Safety/Efficacy Study
Official Title:   A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Phase II Study of the Efficacy and Safety of SGS742 in Subjects With Mild to Moderate Alzheimer's Disease

Further study details as provided by National Institute on Aging (NIA):

Estimated Enrollment:   280
Study Start Date:   April 2004
Estimated Study Completion Date:   December 2004

Detailed Description:

SGS742 is a GABA(B) receptor antagonist. It is an orally active drug and possesses neurochemical and psychopharmacologic features that suggest it could improve memory and cognition in humans. The primary objective of the SGS742 clinical trial will be to determine the effect of SGS742 on memory and cognition in individuals diagnosed with mild to moderate Alzheimer's disease. The duration of the study is 3 months with 5 clinic visits.

  Eligibility
Ages Eligible for Study:   55 Years to 90 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No

Criteria

Inclusion Criteria:

  • 55 to 90 years of age
  • Diagnosed with mild to moderate Alzheimer's disease
  • Willing caregiver
  • In general good health

Exclusion Criteria:

  • Call 1-877-MY-MEMORY and ask to be referred to a study center located near you for entry criteria information.

Prohibited Meds:

  • Alzheimer's medications (Aricept, Exelon, Remydl, Nemenda)
  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00093951

Show 59 study locations  Show 59 Study Locations

Sponsors and Collaborators
Saegis Pharmaceuticals
  More Information


Saegis Pharmaceuticals, Inc.  This link exits the ClinicalTrials.gov site
 

Publications:

Study ID Numbers:   IA0061
First Received:   October 7, 2004
Last Updated:   September 18, 2007
ClinicalTrials.gov Identifier:   NCT00093951
Health Authority:   United States: Food and Drug Administration

Keywords provided by National Institute on Aging (NIA):
Alzheimer disease  
memory  
cognition  
GABA(B)receptor antagonist  

Study placed in the following topic categories:
Delirium, Dementia, Amnestic, Cognitive Disorders
(3-aminopropyl)(n-butyl)phosphinic acid
Mental Disorders
Alzheimer Disease
Central Nervous System Diseases
Neurodegenerative Diseases
Brain Diseases
Dementia
Cognition Disorders
Delirium

Additional relevant MeSH terms:
GABA Antagonists
Neurotransmitter Agents
Molecular Mechanisms of Pharmacological Action
Therapeutic Uses
Physiological Effects of Drugs
Nervous System Diseases
GABA Agents
Tauopathies
Central Nervous System Agents
Protective Agents
Neuroprotective Agents
Pharmacologic Actions

ClinicalTrials.gov processed this record on October 09, 2008




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