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

Completed · Phase 3

Conditions studied: Tinea Pedis, Tinea Cruris, Tinea Corporis

In brief

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.

Key facts

Study ID

NCT01349998

Run by

Tinea Pharmaceuticals

People needed

604

Starts

2011-05-01

Expected to finish

2012-09-01

Last updated by the study team

2013-01-23

Who can join

Age: 12 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Evidence of tinea cruris, tinea pedis, or tinea corporis. Additional criteria listed in protocol

You may not qualify if…

• Pregnancy and allergies. Additional criteria listed in protocol

Where it is running

• Study site — Fremont, California, United States
• Study site — Los Angeles, California, United States
• Study site — Miami, Florida, United States
• Study site — Miramar, Florida, United States
• Study site — St. Petersburg, Florida, United States
• Study site — Augusta, Georgia, United States
• Study site — Evansville, Indiana, United States
• Study site — Warren, Michigan, United States
• Study site — Omaha, Nebraska, United States
• Study site — Paramus, New Jersey, United States
• Study site — Albuquerque, New Mexico, United States
• Study site — Cincinnati, Ohio, United States
• Study site — Hershey, Pennsylvania, United States
• Study site — Philadelphia, Pennsylvania, United States
• Study site — Goodletsville, Tennessee, United States
• Study site — Austin, Texas, United States
• Study site — College Station, Texas, United States
• Study site — Plano, Texas, United States
• Study site — San Antonio, Texas, United States
• Study site — Lynchburg, Virginia, United States
• Study site — Belize City, Belize District, Belize
• Study site — San Salvador, El Salvador
• Study site — San Pedro, Sula, Honduras
• Study site — Cidra, Puerto Rico

Full record on ClinicalTrials.gov

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