The primary objective of this study is to evaluate the efficacy of brodalumab, compared to placebo, in subjects with psoriatic arthritis. The key secondary objective is to evaluate the efficacy of brodalumab compared to placebo at week 16. The safety objective of this study is to evaluate the safety profile of brodalumab in subjects with psoriatic arthritis.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
484
210 mg brodalumab administered via subcutaneous injection.
140 mg brodalumab administered via subcutaneous injection.
Placebo administered via subcutaneous injection until week 24.
ACR20 (American College of Rheumatology 20% Improvement) Response Rate Through Week 16
ACR20 is used as a measurement of the proportion of subjects who are reaching a 20% improvement of tender an swollen joint counts. The higher percent of subjects reaching a higher improvement percentage shows greater success.
Time frame: Baseline and 16 Weeks
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Research Site
Peoria, Arizona, United States
Research Site
Little Rock, Arkansas, United States
Research Site
Cypress, California, United States
Research Site
Hemet, California, United States
Research Site
Huntington Beach, California, United States
Research Site
La Jolla, California, United States
Research Site
Palm Desert, California, United States
Research Site
Palo Alto, California, United States
Research Site
Victorville, California, United States
Research Site
Sarasota, Florida, United States
...and 93 more locations