Long Term Open Label Continuation Study

Study Identifier
DE020
CT.gov Identifier
NCT00195650
EudraCT Identifier
Not available
EUCTIS ID
Not available
For general inquiries, please contact

844-663-3742 or [email protected]

Study Complete

Results Available

Scientific Result Summary
Available Language(s): English
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Study Details

Medical Condition
  • Rheumatoid Arthritis
    • Study Drug
  • Adalimumab
    • Phase
    Phase 3
    Sex
    Female & Male
    Age
    18+ years
    Inclusion and Exclusion Criteria
    Inclusion Criteria:
    Inclusion Criteria - Participant was in a prior D2E7 (adalimumab) study - Participant was age 18 or older and in good health (Investigator discretion) with a recent stable medical history. Exclusion Criteria - Participant was considered by the investigator, for any reason, to be an unsuitable candidate for the study - Participant was a female subject who is pregnant or breast-feeding or considering becoming pregnant - Participant had any ongoing chronic or active infection

    Protocol Summary

    The purpose of the study was to assess the long-term safety and clinical efficacy following

    repeated administration of adalimumab in patients with rheumatoid arthritis.

    Study Locations

    Location
    Status
    Location
    Site Reference ID/Investigator# 538
    Birmingham, Alabama, United States, 35205
    Status
    Not applicable
    Location
    Site Reference ID/Investigator# 4111
    Birmingham, Alabama, United States, 35294-7201
    Status
    Not applicable
    Location
    Site Reference ID/Investigator# 4113
    Mobile, Alabama, United States, 36608
    Status
    Not applicable
    Location
    Site Reference ID/Investigator# 408
    Anchorage, Alaska, United States, 99508
    Status
    Not applicable
    Location
    Site Reference ID/Investigator# 537
    Tucson, Arizona, United States, 85710
    Status
    Not applicable
    Location
    Site Reference ID/Investigator# 66822
    Anaheim, California, United States, 92801
    Status
    Not applicable
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