Efficacy And Safety Of Tofacitinib In Psoriatic Arthritis: Comparator Study
| Status: | Completed |
|---|---|
| Conditions: | Arthritis, Psoriasis |
| Therapuetic Areas: | Dermatology / Plastic Surgery, Rheumatology |
| Healthy: | No |
| Age Range: | 18 - Any |
| Updated: | 4/21/2016 |
| Start Date: | January 2014 |
| End Date: | December 2015 |
A Phase 3, Randomized, Double-Blind, Placebo-Controlled Study Of The Efficacy And Safety Of 2 Doses Of Tofacitinib (CP-690,550) Or Adalimumab In Subjects With Active Psoriatic Arthritis
This is a 12 month study investigating the effectiveness and safety of tofactinib in
treating the signs and symptoms, improving physical function and preserving bone structure
in patients with active psoriatic arthritis and had inadequate response to a traditional,
non-biologic disease modifying anti-rheumatic drug. Adalimumab is use as a comparator.
treating the signs and symptoms, improving physical function and preserving bone structure
in patients with active psoriatic arthritis and had inadequate response to a traditional,
non-biologic disease modifying anti-rheumatic drug. Adalimumab is use as a comparator.
Inclusion Criteria:
- Males or females, aged >= 18 years at time of consent.
- Have a diagnosis of Psoriatic arthritis (PsA) of >= 6 months
- Meet the Classification Criteria of PsA (CASPAR) at time of screening
- Must not have been adequately treated with a a traditional non-biologic disease
modifying anti-rheumatic drug (DMARD).
- Concurrent treatment with methotrexate, leflunomide, or sulfasalazine allowed and
required
- Must not have taken a biologic Tumour Necrosis Factor Inhibitor
- Must have 3 or more swollen joints AND 3 or more tender joints
- Must have active psoriasis skin lesions
Exclusion Criteria:
- Have non-plaque forms of psoriasis, eg erythrodermic, guttate or pustular, with the
exception of nail psoriasis which is allowed
- Pregnant or breast feeding, females of child-bearing potential not using highly
effective contraception
- New York Heart Association Class III and IV congestive heart failure
- History of hypersensitivity or infusion reaction to biologic agents
- Infection with HIV, hepatitis B virus, hepatitis C virus, or other chronic infection
We found this trial at
25
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Salt Lake City, Utah 84112
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Swedish Medical Center Since 1910, Swedish has been the region's hallmark for excellence in health...
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