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Terminated Phase 3 Interventional

Safety and Efficacy of NAB001 in the Treatment of Mild to Moderate Onychomycosis of the Toenails

ClinicalTrials.gov ID: NCT01208129

Public ClinicalTrials.gov record NCT01208129. 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 Jul 21, 2026, 6:04 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

A Randomized, Double-Blind, Vehicle-Controlled, Multicenter, Parallel Group Study of the Safety and Efficacy of NAB001 in the Treatment of Mild to Moderate Distal Subungual Onychomycosis of the Toenails for 52 Weeks

Study identification

NCT ID
NCT01208129
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Promius Pharma, LLC
Industry
Enrollment
458 participants

Conditions and interventions

Conditions

Interventions

  • NAB001 Drug
  • Placebo control Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 70 Years
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
Aug 31, 2010
Primary completion
Jun 30, 2012
Completion
Jun 30, 2012
Last update posted
Jul 10, 2013

2010 – 2012

United States locations

U.S. sites
25
U.S. states
15
U.S. cities
25
Facility City State ZIP Site status
Radiant Research, Inc. Tucson Arizona 85710
Associated Foot & Ankle Specialists, LLC Phoenix Arkansas 85015
Family Foot Health Center Rogers Arkansas 72758
Center for Dermatology Clinical Research, Inc. Fremont California 94538
UCSF Dermatology Research San Francisco California 94115
Avail Clinical Research DeLand Florida 32720
North Florida Dermatology Association Jacksonville Florida 32204
Altus Research Lake Worth Florida 33461
Lake Washington Foot and Ankle Center Melbourne Florida 32935
Park Avenue Dermatology Orange Park Florida 32073
Radiant Research, Inc. Pinellas Park Florida 33781
Deaconess Clinic Downtown Evansville Indiana 47713
Michigan Center for Skin Care Research Clinton Township Michigan 48038
Department of Veteran's Affairs Minneapolis Minnesota 55417
Pinkas Lebovits New York New York 10019
Skin Search of Rochester, Inc. Rochester New York 14623
Care Plus Podiatry, PC Wading River New York 11792
Oregon Medical Research Center, PC Portland Oregon 97223
Radiant Research, Inc. Greer South Carolina 29651
The Skin Wellness Center, PC Knoxville Tennessee 37922
Research Across America Plano Texas 75093
Endeavor Clinical Trials San Antonio Texas 78229
Dermatology Research Center Salt Lake City Utah 84124
Coastal Podiatry, Inc. Virginia Beach Virginia 23464
Madison Skin and Research, Inc. Madison Wisconsin 53719

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01208129, 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 Jul 10, 2013 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01208129 live on ClinicalTrials.gov.

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