Efficacy Study of LIQUICURE™ to Treat Toe Nail Fungus

Completed · Not applicable

Conditions studied: Onychomycosis

In brief

There is a major clinical need for an inexpensive topically-applied product that can inhibit the growth of the dermatophytes that cause nail fungus. Chesson Labs has developed LIQUICURE with a longer drying/curing time that will allow better nail penetration or adsorption. Though the product may have inherent antimicrobial activity, the product does not contain a drug or antimicrobial agent. Consistent use of LIQUICURE as described will clear fungal nail infection. Clearing of nail fungal infection is defined by negative dermatophyte culture and visual improvement in nail characteristics within six months, with few, if any product-related adverse events.

Key facts

Study ID

NCT00960089

Run by

Chesson Laboratory Associates, Inc

People needed

63

Starts

2008-07-01

Expected to finish

2010-10-01

Last updated by the study team

2016-01-27

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Nail fungal infection of at least one great toe [per visual assessment, positive KOH preparation, and positive dermatophyte culture]
• Subjects who have target toenail showing 20-65% involvement as judged by the clinical investigator
• 2 mm of clear nail proximally on great toenail / no lunula involvement
• Subject must be physically able to reach toes to clean them and apply product
• Subject is willing to discontinue use of other nail fungus treatment products and nail cosmetic products for duration of this study
• Subject is willing and available to return for study follow up
• Ability of the subject or legal representative to understand and provide signed consent for participating in the study
• Negative urine pregnancy test for women of child bearing age
• Females must be post menopausal or must agree to use approved contraceptives (actions, devices or medications to prevent or reduce the likelihood of pregnancy) throughout the study (Note: abstinence is NOT an accepted form of contraception)

You may not qualify if…

• Known hypersensitivity or allergy to the product materials
• Negative KOH preparation or dermatophyte culture
• Thickness of nail greater than 3 mm
• Enrollment in another investigational drug or product protocol that would interfere with this study
• Continuation or use of other topical or pharmaceutical treatments for the condition; a wash-out period of at least four weeks after discontinuation of a topical product or 180 days after discontinuation of an oral product for treatment of nail fungus is required
• Chronic disease, including: diabetes, psoriasis, immune deficiency, severe foot injury, chronic vascular disease or any other condition that would decrease circulation to the extremities at the discretion of the investigator Pregnant or nursing females
• Investigators, Chesson personnel, or Chesson Scientific Advisory Board members or their immediate family

Where it is running

• Triangle Medical Research Associates — Cary, North Carolina, United States
• Central Dermatology Center — Chapel Hill, North Carolina, United States
• Wake Research Associates — Raleigh, North Carolina, United States
• Crescent Medical Research — Salisbury, North Carolina, United States

Full record on ClinicalTrials.gov

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