Drug Use Investigation for Humira® - All Patient Investigation for Rheumatoid Arthritis

Study Identifier
P10-559
CT.gov Identifier
NCT01076959
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
    N/A
    Phase
    PMOS
    Sex
    Female & Male
    Age
    16+ years
    Inclusion and Exclusion Criteria
    Inclusion Criteria:
    - All patients prescribed and treated with Humira are included in this survey.
    Exclusion Criteria:
    - Contraindications according to the Package Insert: - Patients who have serious infections, - Patients who have tuberculosis, - Patients with a history of hypersensitivity to any ingredient of Humira, - Patients who have demyelinating disease or with a history of demyelinating disease, - Patients who have cardiac failure congestive.

    Protocol Summary

    To clarify the following matters:

    - Unknown adverse reactions (especially clinically significant adverse reactions)

    - Incidence and conditions of occurrence of adverse reactions in the clinical setting

    - Factors that may affect the safety and effectiveness of Humira

    Study Locations

    Location
    Status
    Location
    Site Reference ID/Investigator# 35904
    Aichi, Japan
    Status
    Not applicable
    Location
    Site Reference ID/Investigator# 35905
    Aichi, Japan
    Status
    Not applicable
    Location
    Site Reference ID/Investigator# 35906
    Aichi, Japan
    Status
    Not applicable
    Location
    Site Reference ID/Investigator# 35907
    Aichi, Japan
    Status
    Not applicable
    Location
    Site Reference ID/Investigator# 35908
    Aichi, Japan
    Status
    Not applicable
    Location
    Site Reference ID/Investigator# 35909
    Aichi, Japan
    Status
    Not applicable
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