This study evaluates the safety profile and effectiveness of adalimumab in Korean intestinal Behcet's disease (BD) patients in routine clinical practice.
Study Type
OBSERVATIONAL
Enrollment
59
Kyungpook National Univ Hosp /ID# 147937
Daegu, Daegu Gwang Yeogsi, South Korea
Ajou University Hospital /ID# 147938
Suwon, Gyeonggido, South Korea
Pusan Nat Univ Yangsan Hosp /ID# 169243
Yangsan, Gyeongsangnam-do, South Korea
Number of participants with adverse events
All adverse events including serious and unexpected events will be assessed.
Time frame: From Day 1 to 70 days following 56 weeks from first dose of adalimumab or the last administration of adalimumab if the participant stopped receiving adalimumab before 56 weeks
Number of participants with adverse drug reactions
All adverse reactions including serious and unexpected reactions will be assessed.
Time frame: From Day 1 to 70 days following 56 weeks from first dose of adalimumab or the last administration of adalimumab if the participant stopped receiving adalimumab before 56 weeks
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Yonsei University Health System, Severance Hospital /ID# 147932
Seodaemun-gu, Seoul Teugbyeolsi, South Korea
Samsung Medical Center /ID# 147934
Seoul, Seoul Teugbyeolsi, South Korea
Cath Univ Seoul St Mary's Hosp /ID# 147936
Seoul, Seoul Teugbyeolsi, South Korea
Kosin University Gospel Hosp /ID# 169244
Busan, South Korea
The Catholic Univ. of Korea /ID# 169245
Gyeonggi-do, South Korea
Seoul National University Hospital /ID# 147933
Seoul, South Korea
Asan Medical Center /ID# 147935
Seoul, South Korea