Condition: Psoriatic Arthritis · Sponsor: AbbVie
This is a Phase 3 multicenter study that included two periods. Period 1 was designed to compare the safety, tolerability, and efficacy of upadacitinib 15 mg once daily (QD) and 30 mg QD versus placebo in participants with moderately to severely active Psoriatic Arthritis (PsA) who had an inadequate response to Biological Disease Modifying Anti-Rheumatic Drug (bDMARDs). Period 2 evaluated the safety, tolerability and efficacy of upadacitinib 15 mg QD and 30 mg QD in subjects with PsA who completed Period 1.
This description comes directly from the study's public registry record.
No contact information is available for this study as per the public registry record.
Always discuss trial participation with your own doctor first.
| Alabama Medical Group, PC /ID# 159836 | Mobile, Alabama, United States | — |
| Arizona Arthritis & Rheumatology Research, PLLC /ID# 160047 | Mesa, Arizona, United States | — |
| Sun Valley Arthritis Center Ltd. /ID# 161203 | Peoria, Arizona, United States | — |
| Duplicate_AZ Arthritis and Rheumotology Research, PLLC /ID# 160006 | Phoenix, Arizona, United States | — |
| Osteoporosis Medical Center /ID# 161411 | Beverly Hills, California, United States | — |
| Covina Arthritis Clinic /ID# 159919 | Covina, California, United States | — |
| Triwest Research Associates /ID# 159915 | El Cajon, California, United States | — |
| Duplicate_Providence Medical Foundation /ID# 160005 | Fullerton, California, United States | — |
| C.V. Mehta MD, Med Corporation /ID# 161192 | Hemet, California, United States | — |
| Care Access Research, Huntington Beach /ID# 160049 | Huntington Beach, California, United States | — |
| Purushotham & Akther Kotha MD, Inc /ID# 159834 | La Mesa, California, United States | — |
| Stanford University School of Med /ID# 161402 | Stanford, California, United States | — |
+ 153 more locations — full list on the registry record.
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