Surveillance of Humira Injection in Korean Patients

Study Identifier
P10-053
CT.gov Identifier
EudraCT Identifier
Not available
EUCTIS ID
Not available
For general inquiries, please contact
Study Complete

Study Details

Medical Condition
  • Rheumatoid Arthritis
  • Psoriatic Arthritis (PsA)
  • Axial Spondyloarthritis (axSpA)
  • Crohn's Disease (CD)
  • Dermatology - Psoriasis (PsO)
  • Study Drug
    N/A
    Phase
    N/A
    Sex
    Female & Male
    Age
    19+ years

    Protocol Summary

    Patients who take Humira as prescribed by physicians as per Korean label will be enrolled and observed in normal medical practice setting for not less than 3 months following first dose of Humira. Information on demographics, diagnosis and medical history, results of tuberculosis skin test, results of chest X-ray, Humira treatment information, concomitant medication, physician's global assessment for effectiveness, disease activity assessment for rheumatoid arthritis, disease activity assessment for Crohn's Disease, disease activity assessment for Psoriasis and adverse events will be recorded on case report forms.

    Study Locations

    Location
    Status
    Location
    Site Reference ID/Investigator# 29724
    Ansan, Republic of Korea, 152-703
    Status
    Not applicable
    Location
    Site Reference ID/Investigator# 53586
    Ansan, Republic of Korea, 152-703
    Status
    Not applicable
    Location
    Site Reference ID/Investigator# 29729
    Bucheon-si, Republic of Korea, 420-767
    Status
    Not applicable
    Location
    Site Reference ID/Investigator# 29009
    Bucheon-si, Republic of Korea, 420-818
    Status
    Not applicable
    Location
    Site Reference ID/Investigator# 29726
    Busan, Republic of Korea, 602-715
    Status
    Not applicable
    Location
    Site Reference ID/Investigator# 29733
    Busan, Republic of Korea, 602-739
    Status
    Not applicable
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