A 20 week study to assess the safety and efficacy of etanercept(Enbrel®)for the treatment of Discoid Lupus Erythematosus
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
20
etanercept(Enbrel®) 50mgs subcutaneous (SC) injections twice weekly for 20 weeks
Florida Academic Dermatology Centers
Miami, Florida, United States
RECRUITINGProportion of patients responding to study treatment using the Cutaneous Lupus Erythematous Disease Area Severity Index(CLASI)defined as a decrease of 50% form baseline.
Time frame: 20 weeks
Change from baseline to week 20 in Dermatology Life Quality Index and Pysician's Global Assessment of disease measurements
Time frame: 20 weeks
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