Rheumatoid Arthritis
Conditions
Interventions
- Upadacitinib+Adalimumab matching Placebo
Description: Participants will receive upadacitinib once a day along with matching placebo for adalimumab at eow (every other week) in Period 1. Eligible participants will continue to receive same stu
Description: Participants will receive adalimumab at eow (every other week) along with matching placebo for upadacitinib once a day in Period 1. Eligible participants will continue to receive same stu
Sponsors
Otani Tetsuya
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: - Diagnosis of Rheumatoid Arthritis (RA) for >= 3 months based on the 2010 American College of Rheumatology/European Alliance of Associations for Rheumatology (ACR/EULAR) classification criteria for RA. - Treated for >= 3 consecutive months prior to screening with 1 tumor necrosis factor inhibitor (TNFi) (only 1 of originator or biosimilar certolizumab pegol, etanercept, golimumab or infliximab) for RA, but continue to exhibit active RA, or had to discontinue due to intolerability or toxicity, irrespective of treatment duration. Up to 15% of participants who were intolerant to 1 TNFi will be allowed to enroll. Prior administration of different biosimilar versions for the same originator TNFi or switching between originator and biosimilar version of the same originator TNFi are acceptable. Cycling between biosimilars of different originator TNF inhibitors is not acceptable. - On oral or parenteral methotrexate (MTX) therapy >= 3 consecutive months and on a stable prescription of 15 to 25 mg/week (or >= 10 mg/week in participants intolerant of MTX at doses >= 15 mg/week) for >= 4 weeks prior to the first dose of study drug. In addition, all participants should take a dietary supplement of folic acid or folinic acid throughout the study participation. -- For a Chinese, Japanese, Korean, or Taiwanese participant, a stable dose of MTX >= 7.5 mg/week is acceptable. -- Additional local requirements for MTX may apply. - Meets both of the following disease activity criteria: -- >= 6 swollen joint (based on 66 joint counts) and >= 6 tender joints (based on 68 joint counts) at screening and baseline;(central lab, upper limit of normal [ULN] 2.87 mg/L) at screening. -- High-sensitivity C-reactive protein (hsCRP) >= 3 mg/L
Exclusion criteria
Exclusion criteria: - History of any arthritis with onset prior to age 17 years or current diagnosis of inflammatory joint disease other than Rheumatoid Arthritis (RA). - Prior exposure to any janus kinase (JAK) inhibitor. - Prior exposure to adalimumab (original or biosimilar) or to any approved or investigational TNFi other than infliximab, etanercept, certolizumab pegol and golimumab. - Prior exposure to an approved or investigational non-TNFi biologic disease modifying anti-rheumatic drug (bDMARD) or targeted synthetic disease modifying antirheumatic drug (tsDMARD).
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Percentage of Participants Achieving Disease Activity Score 28 C-reactive Protein (DAS28-CRP) <=3.2 | — |
Secondary
| Measure | Time frame |
|---|---|
| - Percentage of Participants Achieving American College of Rheumatology 50 % (ACR50) Response - Percentage of Participants Achieving Disease Activity Score 28 C-reactive Protein [DAS28-CRP]) < 2.6 - Change from Baseline in Disease Activity Score 28 C-reactive Protein [DAS28-CRP]) - Change from Baseline in Participants Assessment of Pain - Change from Baseline in Health Assessment Questionnaire - Disability Index (HAQ-DI) Score | — |
Countries
Argentina, Belgium, Brazil, Bulgaria, Canada, Chile, China, Colombia, Croatia, France, Germany, Greece, Hungary, Italy, Japan, Mexico, Portugal, Puerto Rico, Republic of Korea, Romania, Serbia, South Africa, Spain, United Kingdom, United States
Contacts
Public ContactContact for Patients and HCP
AbbVie. G.K.
Outcome results
None listed