Efficacy and Safety of Adalimumab in Adult Chinese Subjects With Active Ankylosing Spondylitis

PHASE3CompletedINTERVENTIONAL
Enrollment

344

Participants

Timeline

Start Date

January 31, 2010

Primary Completion Date

September 30, 2010

Study Completion Date

February 28, 2011

Conditions
Ankylosing Spondylitis
Interventions
BIOLOGICAL

adalimumab

Prefilled syringe, 40 mg/0.8 mL administered subcutaneously every other week

OTHER

placebo

Prefilled syringe, matching placebo administered subcutaneously every other week

Trial Locations (9)

100029

Site Reference ID/Investigator# 25522, Beijing

100032

Site Reference ID/Investigator# 24055, Beijing

100853

Site Reference ID/Investigator# 24052, Beijing

200001

Site Reference ID/Investigator# 24053, Shanghai

200003

Site Reference ID/Investigator# 24058, Shanghai

230022

Site Reference ID/Investigator# 24054, Hefei

310009

Site Reference ID/Investigator# 24243, Hangzhou

510630

Site Reference ID/Investigator# 24056, Guangzhou

710032

Site Reference ID/Investigator# 24057, Xi'an

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Abbott

INDUSTRY