Study to Assess Change in Disease Activity and Adverse Events of RINVOQ in Adult Participants With Ankylosing Spondylitis in the Real-World Japan
← catalyst calendarSponsored by AbbVie (industry) · ABBV — their whole pipeline →.
Phase
—
Status
Completed
Study type
Observational
Enrollment
69actual
Sites
61
Country
Japan
Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →
Source: ClinicalTrials.gov, retrieved 2026-08-19
Dates
each axis at the precision it was filed, with the registry's own basis| Date | Filed | Basis | What it is |
|---|---|---|---|
| Start | 2022-07-06 | actual | When the study began enrolling |
| Primary completion | 2025-12-11 | actual | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | 2026-01-29 | actual | The whole study's end, after follow-up |
| First posted | 2022-11-08 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2026-02-17 | actual | The sponsor's own last edit to this record — every projection above is as current as this date |
What it studies
Condition
- Ankylosing Spondylitis
Primary outcome
what the primary-completion date above is the date OFIncidence Percentage of Serious Infection as Adverse Drug Reactions ( ADR)
measured Up to 52 Weeks
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