A Study of Ixekizumab in Participants With Active Psoriatic Arthritis
Status: | Completed |
---|---|
Conditions: | Arthritis, Psoriasis |
Therapuetic Areas: | Dermatology / Plastic Surgery, Rheumatology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 1/10/2019 |
Start Date: | December 2012 |
End Date: | September 2017 |
A Multicenter, Randomized, Double-Blind, Active and Placebo-Controlled 24-Week Study Followed by Long Term Evaluation of Efficacy and Safety of Ixekizumab (LY2439821) in Biologic Disease-Modifying Antirheumatic Drug-Naive Patients With Active Psoriatic Arthritis
This study will assess the safety and efficacy of ixekizumab (LY2439821) compared to placebo
in participants with active psoriatic arthritis.
in participants with active psoriatic arthritis.
Inclusion Criteria:
- Presents with established diagnosis of active psoriatic arthritis for at least 6
months, and currently meets Classification for Psoriatic Arthritis (CASPAR) criteria
- Active psoriatic arthritis (PsA) defined as the presence of at least 3 tender and at
least 3 swollen joints
- Presence of active psoriatic skin lesion or a personal history of plaque psoriasis
(Ps)
- Men must agree to use a reliable method of birth control or remain abstinent during
the study
- Women must agree to use reliable birth control or remain abstinent during the study
and for at least 12 weeks after stopping treatment
Exclusion Criteria:
- Current or prior use of biologic agents for treatment of Ps or PsA
- Inadequate response to greater than or equal to 4 conventional disease-modifying
antirheumatic drugs (DMARDs)
- Current use of more than one conventional DMARD
- Evidence of active inflammatory arthritic syndromes or spondyloarthropathies other
than PsA
- Have participated in any study with interleukin 17 (IL-17) antagonists, including
ixekizumab
- Serious disorder or illness other than psoriatic arthritis
- Serious infection within the last 3 months
- Breastfeeding or nursing (lactating) women
We found this trial at
38
sites
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