Axial spondyloarthritis (axSpA), which encompasses radiographic axSpA (r-axSpA, also known as ankylosing spondylitis \[AS\]) is an immune-mediated inflammatory disease primarily affecting the axial skeleton. This study will assess how effective Rinvoq is in treating axSpA. Rinvoq is an approved drug for treating axSpA. Approximately 100 adult participants who are prescribed Rinvoq by their physician in accordance with local label will be enrolled in Japan. Participants will receive Rinvoq as prescribed by their physician according to their routine clinical practice and local label. Participants will be followed for up to 52 weeks. There is expected to be no additional burden for participants in this trial. Participants will attend regular visits during the study at a hospital or clinic according to their routine clinical practice.
Study Type
OBSERVATIONAL
Enrollment
69
Kurotsuchi Orthopaedic Clinic /ID# 251076
Kasugashi, Aichi-ken, Japan
Japan Organization of Occupational Health and Safety Chubu Rosai Hospital /ID# 258201
Nagoya, Aichi-ken, Japan
Nagoya University Hospital /ID# 254435
Nagoya, Aichi-ken, Japan
Fujita Health University Hospital /ID# 258204
Toyoake, Aichi-ken, Japan
Tomita Clinic /ID# 251075
Kashiwa-shi, Chiba, Japan
Noda Hospital /ID# 254429
Noda, Chiba, Japan
Yamada Rheumatology Clinic /ID# 264182
Matsuyama, Ehime, Japan
Matsuyama Red Cross Hospital /ID# 261974
Matsuyama, Ehime, Japan
Yagi Hospital - Fukuoka /ID# 251078
Fukuoka, Fukuoka, Japan
Kunou Orthopedic Clinic /ID# 252168
Kitakyushu-shi, Fukuoka, Japan
...and 51 more locations
Incidence Percentage of Serious Infection as Adverse Drug Reactions ( ADR)
Incidence of serious drug related adverse reactions will be assessed.
Time frame: Up to 52 Weeks
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