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Completed Phase 3 Interventional

Safety of a Topical Antifungal Treatment for Tinea Cruris, Tinea Pedis and Tinea Corporis

ClinicalTrials.gov ID: NCT01349998

Public ClinicalTrials.gov record NCT01349998. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 18, 2026, 2:56 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

An Open-Label Study to Evaluate the Safety of Long-Term Administration of Product 33525 in Subjects With Tinea Pedis, Tinea Corporis, or Tinea Cruris

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to examine the long-term safety of treating recurrent episodes of tinea pedis for 14 days for each recurrence and recurrent episodes of tinea corporis or tinea cruris for 7 days for each recurrence with Product 33525.

Study identification

NCT ID
NCT01349998
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Tinea Pharmaceuticals
Industry
Enrollment
604 participants

Conditions and interventions

Eligibility (public fields only)

Age range
12 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 2011 (Type not available)
Primary completion
Sep 2012 (Actual)
Completion
Sep 2012 (Actual)
Last update posted
Jan 23, 2013

2011 – 2012

United States locations

U.S. sites
20
U.S. states
13
U.S. cities
20
Facility City State ZIP Site status
Not listed Fremont California — —
Not listed Los Angeles California — —
Not listed Miami Florida — —
Not listed Miramar Florida — —
Not listed St. Petersburg Florida — —
Not listed Augusta Georgia — —
Not listed Evansville Indiana — —
Not listed Warren Michigan — —
Not listed Omaha Nebraska — —
Not listed Paramus New Jersey — —
Not listed Albuquerque New Mexico — —
Not listed Cincinnati Ohio — —
Not listed Hershey Pennsylvania — —
Not listed Philadelphia Pennsylvania — —
Not listed Goodletsville Tennessee — —
Not listed Austin Texas — —
Not listed College Station Texas — —
Not listed Plano Texas — —
Not listed San Antonio Texas — —
Not listed Lynchburg Virginia — —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 4 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01349998, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jan 23, 2013 · Synced Oct 18, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01349998 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →