A Dose-Ranging Study Evaluating the Safety and Efficacy of IDP-108 in Patients With Onychomycosis

PHASE2CompletedINTERVENTIONAL
Enrollment

135

Participants

Timeline

Start Date

October 31, 2007

Primary Completion Date

April 30, 2009

Study Completion Date

April 30, 2009

Conditions
Onychomycosis
Interventions
DRUG

Low Strength IDP-108

Topical application once a day for 9 months

DRUG

High Strength IDP-108

Topical application once a day for 9 months

DRUG

High Strength IDP-108 under occlusion

Topical application once a day for 9 months

DRUG

Vehicle

Topical application once a day for 9 months

Trial Locations (10)

CP31205

Unidad de Investigación en Salud, Chihuahua City

CP54055

Clinical Research Institute, Mexico City

Unknown

Hospital Central Militar, Mexico City

CP 06726

Hospital General de México, México

CP45190

"Instituto Dermatólogico de Jalisco Dr. Jose Barba Rubio", Guadalajara

CP45200

Hospital Dr. Ángel Leaño, Zapopan

CP64000

MIRC/OCA Hospital, Monterrey

CP64460

Centro de Dermatología de Monterrey, Monterrey

"Hospital Universitario José E. González", Monterrey

CP 78240

Hospital Ignacio Morones Prieto SLP, San Luis Potosí City

Sponsors
All Listed Sponsors
lead

Dow Pharmaceutical Sciences

INDUSTRY