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The placebo gel developed by Veloce BioPharma LLC is an inert topical formulation used as a control in clinical trials, specifically the Phase 2 study (NCT04253912) for verruca vulgaris (common warts). It is designed to be physically identical to VBP-245, a 2% povidone-iodine gel, but lacks the active antiseptic ingredient. The gel is applied topically to warts on the trunk or extremities. Veloce BioPharma uses this comparator to evaluate the efficacy and safety of their povidone-iodine platform in treating viral skin infections, including common warts and molluscum contagiosum.
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