Extension Study of Two Dosing Schedules of Adalimumab in Subjects With Moderate to Severe Chronic Plaque Psoriasis
- Registration Number
- NCT00645892
- Lead Sponsor
- Abbott
- Brief Summary
Extension Study of Two Dosing Schedules of Adalimumab in Subjects with Moderate to Severe Chronic Plaque Psoriasis
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 32
Inclusion Criteria
- Subject participated and relapsed in prior PS study
Exclusion Criteria
- Subject has other active skin diseases
- Multiple concomitant therapy restrictions and/or washouts (topicals, UV, other systemic PS therapies)
- Poorly controlled medical conditions
- History of neurologic symptoms suggestive of central nervous system (CNS) demyelinating disease.
- History of cancer or lymphoproliferative disease
- History of active TB or listeriosis, or persistent chronic or active infections
- Known to have immune deficiency or is immunocompromised
- Clinically significant abnormal laboratory test results
- Erythrodermic psoriasis or generalized pustular psoriasis
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description A adalimumab - B placebo for adalimumab -
- Primary Outcome Measures
Name Time Method Psoriasis Area and Severity Index Week 12 Adverse Events Throughout Study Participation
- Secondary Outcome Measures
Name Time Method Psoriasis Area and Severity Index Week 12, Week 24 Physician's Global Assessment Week 12, Week 24