Plaque Psoriasis Clinical Trial
Official title:
The Effect of Enstilar Versus Vehicle on Target Lesions in Moderate Plaque Type Psoriasis Patients
This study seeks to show whether there is a benefit of prescribing Enstilar in the treatment of patients with moderate plaque type psoriasis. Subjects will receive study treatment of Enstilar foam.
Approximately 20 subjects from 3 sites will be enrolled in this open-label study. Subjects
will receive Enstilar foam and all adverse events and concomitant medications will be
recorded.
Subjects will attend a screening visit/baseline visit and those with plaque-type psoriasis
and bilateral symmetric psoriatic plaques will have a target lesion identified on knees or
elbows and subjects will receive study treatment as outlined above.
Enstilar will be initiated daily for the entire study period of four weeks. Study visits will
occur as follows: screening/baseline, week 2, week 4. Study assessments at each visit will be
Body Surface Area (BSA,) Physicians Global Assessment (PGA,) Target lesion size, Total Lesion
Severity Score (TLSS) and standard medical assessments. There will be standard
medication/treatment and washout periods.
NOTE: The original study protocol dated december 20, 2017, was designed to compare the effect
of Enstilar versus vehicle for the treatment of plaque psoriasis at a 1:1 ratio. A protocol
amendment on March 20, 2018 eliminated the chance of placebo and made this an open-label
study of the effects of Enstilar for the treatment of plaque psoriasis.
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