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European Study of 3APS in Mild to Moderate Alzheimer's Disease Patients

Phase 3
Conditions
Alzheimer's Disease
Registration Number
NCT00217763
Lead Sponsor
Bellus Health Inc. - a GSK company
Brief Summary

The purpose of this Phase 3 study is to evaluate the efficacy and safety of 3APS as an add-on therapy to most standard medication for Alzheimer's disease compared to placebo (inactive substance pill) in patients with mild to moderate Alzheimer's disease.

Detailed Description

* Duration of treatment: 18 months

* 3 treatment arms:

Placebo and 2 different doses of active drug.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
930
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (48)

Middelheim Ziekenhuis Lindendreef

🇧🇪

Antwerp, Belgium

University Hospital Antwerp - Neurology - Prof. Dr. Patrick Cras, MD, PhD

🇧🇪

Edegem, Belgium

Memory Clinic University Hospital Gasthuisberg, Neurology Department

🇧🇪

Leuven, Belgium

Memory Centre, Polycliniques Brull, CHU de Liège

🇧🇪

Liege, Belgium

Hôpital Pellegrin CHU de Bordeaux

🇫🇷

Bordeaux, France

Centre Hospitalier Régional Universitaire de Lille

🇫🇷

Lille, France

Hôpital Sainte Marguerite Service de neuro-geriatrie

🇫🇷

Marseille, France

Hôpital Gui de Chauliac - Service de Neurologie du Pr J. Touchon

🇫🇷

Montpellier, France

Centre Mémoire de Ressources et de Recherche Hôpital Pasteur

🇫🇷

Nice, France

Hôpital BROCA

🇫🇷

Paris, France

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Middelheim Ziekenhuis Lindendreef
🇧🇪Antwerp, Belgium

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