Study of the Human Anti-TNF Monoclonal Antibody in Patients With Active Rheumatoid Arthritis
Study Identifier
M02-574
CT.gov Identifier
EudraCT Identifier
Not available
EUCTIS ID
Not available
For general inquiries, please contact
Results Available
Scientific Result Summary
Available Language(s): English
Study Details
Medical Condition
Study Drug
Phase
CSR.ORG
Sex
Female & Male
Age
18+ years
Protocol Summary
The primary objective of this study is to assess the safety (by collecting adverse events and
serious adverse events) of adalimumab administered every other week to patients with
moderately to severly active rheumatoid arthritis who have failed prior disease-modifying
anti-rheumatic drugs (DMARDs).
Study Locations
No locations found.