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Sponsored by: |
Saegis Pharmaceuticals |
Information provided by: | National Institute on Aging (NIA) |
ClinicalTrials.gov Identifier: | NCT00093951 |
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 |
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 |
Estimated Enrollment: | 280 |
Study Start Date: | April 2004 |
Estimated Study Completion Date: | December 2004 |
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.
Ages Eligible for Study: | 55 Years to 90 Years |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Prohibited Meds:
Show 59 Study Locations |
Saegis Pharmaceuticals |
Saegis Pharmaceuticals, Inc. 
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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 |
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