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RECRUITING Phase 2

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

NCT07245667 · View on ClinicalTrials.gov ↗

Study 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).

Conditions Studied

Interventions

  • DRUG 1% Tolnaftate Stick Formula A
  • DRUG 1% Tolnaftate Stick Formula B
  • DRUG 1% Tolnaftate Stick Formula C

Study Locations (2)

Massachusetts

  • Kuchnir Dermatology and Dermatological Surgery — Framingham
  • Kuchnir Dermatology and Dermatological Surgery — Milford

Trial Details

FieldValue
Enrollment Target 150 participants
Start Date 2024-12-30
Est. Completion 2026-02
Phase Phase 2

Sponsor

Propedix

1 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT07245667

The ClinicalTrials.gov registry entry for NCT07245667 describes a study currently listed as recruiting. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 150 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Propedix, which has 1 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Tinea Pedis appearing as the primary indexed condition, and to 3 interventions — of which 1% Tolnaftate Stick Formula A is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT07245667 reports 2 study locations spanning 1 distinct geographic area — top geographies include Massachusetts. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT07245667 about?

NCT07245667 is a clinical study titled "Topical Tolnaftate Stick for Tinea Pedis: An Open-Label Interventional Study". 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).

What is the current status of trial NCT07245667?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 150 participants. The study started on 2024-12-30. Estimated completion is 2026-02.

What conditions does trial NCT07245667 study?

This clinical trial studies the following conditions: Tinea Pedis. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT07245667?

The interventions under investigation include: 1% Tolnaftate Stick Formula A (DRUG), 1% Tolnaftate Stick Formula B (DRUG), 1% Tolnaftate Stick Formula C (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT07245667?

This trial is sponsored by Propedix, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT07245667 being conducted?

This trial has 2 study locations across Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial