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

PHASE2TerminatedINTERVENTIONAL
Enrollment

53

Participants

Timeline

Start Date

December 31, 2010

Primary Completion Date

December 31, 2013

Study Completion Date

December 31, 2013

Conditions
Alzheimer's Disease
Interventions
BIOLOGICAL

ACC-001

IM injection, dose of 3 micrograms, at Day 1, month 6, 12 and 18

BIOLOGICAL

ACC-001

IM injection, dose of 10 micrograms, at Day 1, month 6, 12 and 18

BIOLOGICAL

ACC-001

IM injection, dose of 30 micrograms, at Day 1, month 6, 12 and 18

Trial Locations (11)

451-8511

Meitetsu Hospital, Nagoya

309-1793

Ibaraki Prefectural Central Hospital, Kasama

243-8551

Shonan Atsugi Hospital, Atsugi

252-0380

Kitasato University East Hospital, Sagamihara-shi

392-8510

Suwa Red Cross Hospital, Suwa

530-8480

Tazuke Kofukai Medical Research Institute Kitano Hospital, Osaka

569-8686

Osaka Medical College Hospital, Takatsuki

113-8431

Juntendo University Hospital, Bunkyo-ku

136-0075

Juntendo Tokyo Koto Geriatric Medical Center, Koto-ku

105-8471

The Tokyo Jikei University School of Medicine, Minato-ku

158-8531

Kanto Central Hospital of the Mutual Aid Association of Public School Teachers, Setagaya-ku

Sponsors

Lead Sponsor

All Listed Sponsors
collaborator

JANSSEN Alzheimer Immunotherapy Research & Development, LLC

INDUSTRY

lead

Pfizer

INDUSTRY