Erlotinib for Treatment of Psoriasis
Part of paid clinical trials in Chicago, Illinois.
- Sponsor
- Northwestern University
- Study ID
- NCT01006096
- Phase
- PHASE2
- Status
- Withdrawn
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- erlotinib — DRUG100mg tablet, once daily for 16 weeks
- placebo tablet — OTHERplacebo tablet (lactose), once daily for 16 weeks
Study Details
The purpose of this study is to determine whether erlotinib is effective in the treatment of psoriasis.
Key Dates
- First listed
- Nov 2, 2009
- Status verified
- Nov 2014
Study Design
- Enrollment
- 0 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Erlotinib
- Placebo Comparator: Placebo tablets
Primary Outcome Measure
To determine efficacy of erlotinib in treatment of moderate to severe psoriasis measured by the Psoriasis Area and Severity Index (PASI) and the Physician's Global Assessment (PGA). [ Time Frame: week 4, 8, 12, 16, and 24 ]
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Northwestern University Feinberg School of Medicine Department of Dermatology | Chicago | Illinois | 60611 | - |
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