Long Term Extension Study Evaluating Safety, Tolerability and Immunogenicity Of ACC-001 In Subjects With Mild To Moderate Alzheimer's Disease

PHASE2CompletedINTERVENTIONAL
Enrollment

160

Participants

Timeline

Start Date

November 5, 2009

Primary Completion Date

December 17, 2013

Study Completion Date

December 17, 2013

Conditions
Alzheimer Disease
Interventions
BIOLOGICAL

ACC-001(3µg) + QS21

Vanutide Cridificar (ACC-001) 3µg + QS-21 (50µg), IM on Day 1, Month 6, Month 12 and Month 18

BIOLOGICAL

ACC-001(10µg) + QS21

Vanutide Cridificar (ACC-001) 10µg + QS-21 (50µg), IM on Day 1, Month 6, Month 12 and Month 18

BIOLOGICAL

ACC-001(30µg) + QS21

Vanutide Cridificar (ACC-001) 30 µg + QS-21 (50µg), IM on Day 1, Month 6, Month 12 and Month 18

Trial Locations (17)

13385

CHU La Timone, Marseille

14050

Klinik fuer Psychiatrie und Psychotherapie, Charite Universitaetsmedizin Berlin, Berlin

31059

Hôpital La Grave, Toulouse

33076

CMRR Bordeaux CHU Pellegrin, Bordeaux

37075

Klinik fuer Psychiatrie und Psychotherapie, Göttingen

48129

Universitatsklinikum und Poliklinik der Uni Bonn, Bonn

59037

Hopital Roger Salengro, Lille

Hôpital Roger Salengro, Lille

68072

Zentralinstitut fuer Seelische Gesundheit Mannheim, Mannheim

75013

Groupe Hospitalier Broca-La Rochefoucauld, Paris

75651

Hôpital Pitié-Salpétrière, Paris

79106

Klinikum der Albert-Ludwigs-Universitaet Freiburg, Freiburg im Breisgau

81675

Technische Universität München, Munich

75651 Cedex 13

Groupe Hospitalier Pitie-Salpetriere, Paris

08003

Hospital del Mar, Barcelona

08025

Hospital de la Santa Creu i Sant Pau, Barcelona

08036

Hospital Clinico y Provincial, Barcelona

Sponsors

Lead Sponsor

All Listed Sponsors
collaborator

JANSSEN Alzheimer Immunotherapy Research & Development, LLC

INDUSTRY

lead

Pfizer

INDUSTRY

NCT00955409 - Long Term Extension Study Evaluating Safety, Tolerability and Immunogenicity Of ACC-001 In Subjects With Mild To Moderate Alzheimer's Disease | Biotech Hunter | Biotech Hunter