Safety, Tolerability, And Immunogenicity Study Of ACC-001 In Japanese Subjects With Mild To Moderate Alzheimer's Disease

PHASE2CompletedINTERVENTIONAL
Enrollment

32

Participants

Timeline

Start Date

August 31, 2009

Primary Completion Date

January 31, 2013

Study Completion Date

January 31, 2013

Conditions
Alzheimer's Disease
Interventions
BIOLOGICAL

ACC-001

IM injection, dose of 3, 10 and 30 micrograms, at Day 1, month 1, 3, 6 and 12

OTHER

QS-21

IM injection, dose of 50 micrograms, at Day 1, month 1, 3, 6 and 12

OTHER

QS-21

IM injection, dose 50 micrograms, at Day 1, month 1, 3, 6 and 12

Trial Locations (9)

530-8480

Tazuke Kofukai Medical Research Institute Kitano Hospital, Osaka

451-8511

Meitetsu Hospital, Aichi

309-1793

Ibaraki Prefectural Central Hospital, Ibaraki

243-8551

Shonan Atsugi Hospital, Kanagawa

252-0380

Kitasato University East Hospital, Kanagawa

105-8471

The Jikei University School of medicine, Tokyo

113-8431

Juntendo University Hospital, Tokyo

136-0075

Juntendo Tokyo Koto Geriatric Medical Center, Tokyo

158-8531

Kanto Ctrl Hp of the Mutual Aid Asso of Public school Teache, Tokyo

Sponsors

Lead Sponsor

All Listed Sponsors
collaborator

JANSSEN Alzheimer Immunotherapy Research & Development, LLC

INDUSTRY

lead

Pfizer

INDUSTRY