This is a multi-center, randomized, double-blind, placebo-controlled phase 2 study in subjects 8 years of age and older who present with verruca vulgaris (common warts) and desire treatment. Subjects may have up to a total of 6 common warts located on their trunk or extremities that will be treated with study medication and followed throughout the study protocol therapy. All warts will be treated two times per day (BID) for12 weeks. Approximately 90 subjects will be enrolled in this study.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
90
2% Povidone-Iodine Gel
Placebo Gel (no Povidone-Iodine)
Veloce BioPharma Clinical Trial Site
Hunt Valley, Maryland, United States
Veloce BioPharma Clinical Trial Site
Plymouth Meeting, Pennsylvania, United States
Veloce BioPharma Clinical Trial Site
Sugarloaf, Pennsylvania, United States
Veloce BioPharma Clinical Trial Site
Upper Saint Clair, Pennsylvania, United States
Decrease in wart diameter (mm)
Time frame: 12 weeks
Resolution of wart
Wart diameter = 0 mm
Time frame: 12 weeks
Application Site Reaction Adverse Events
Time frame: 12 weeks
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Veloce BioPharma Clinical Trial Site
Fort Mill, South Carolina, United States
Veloce BioPharma Clinical Trial Site
Arlington, Virginia, United States
Veloce BioPharma Clinical Trial Site
Lynchburg, Virginia, United States