Skip to content
Trial Eligibility
Menu

Topical Tolnaftate Stick for Tinea Pedis: An Open-Label Interventional Study

NCT07245667

This study is recruiting at 2 US sites in 1 state, according to its ClinicalTrials.gov record last updated .

Summary

This study is designed to evaluate the safety and effectiveness of multiple 1% tolnaftate formulations delivered through novel stick-based vehicles in individuals with tinea pedis (athlete's foot).

Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov

Conditions studied

  • Tinea Pedis

Eligibility basics and study details

Study type
Interventional
Phase
Phase 2
Ages
16 years and older
Sex
All
Healthy volunteers
Accepted
Sponsor
Propedix, Inc.
Last updated on ClinicalTrials.gov
November 28, 2025

These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.

US recruiting sites

Massachusetts · 2

  • Kuchnir Dermatology and Dermatological Surgery · Framingham, MA
  • Kuchnir Dermatology and Dermatological Surgery · Milford, MA

Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.