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
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Results Available

Scientific Result Summary
Available Language(s): English

Study Details

Medical Condition
  • Rheumatoid Arthritis
  • Study Drug
  • adalimumab
  • 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.