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Topical 2% Povidone-Iodine Gel in Verruca Vulgaris

Sponsored by Veloce BioPharma LLC

About this trial

Last updated 4 years ago

Study ID

VBP-245-WART2A

Status

Unknown status

Type

Interventional

Phase

Phase 2

Placebo

No

Accepting

18-75 Years
8+ Years
All
All

Not accepting

Not accepting
Healthy Volunteers

Trial Timing

Ended 4 years ago

What is this trial about?

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.

What are the participation requirements?

Yes

Inclusion Criteria

- Subject is able to comprehend and is willing to sign an informed consent/assent for participation in this study.

- Male or female ≥ 8 years old.

- Subject has a clinical diagnosis of verruca vulgaris (common warts).

- Subject has up to 6 warts located on the trunk or extremities

No

Exclusion Criteria

- Subject has clinically atypical warts on the trunk or extremities.

- Subject is immunocompromised (e.g., due to chemotherapy, systemic steroids, genetic immunodeficiency, transplant status, etc.)

- Subject has periungual, subungual, genital, anal, mosaic, plantar, flat, or filiform wart identified as a wart for study treatment.

Locations

Location

Status