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
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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