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Terminated Phase 3 Interventional

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

ClinicalTrials.gov ID: NCT01208168

Public ClinicalTrials.gov record NCT01208168. 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, 10:15 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 Wks

Study identification

NCT ID
NCT01208168
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Promius Pharma, LLC
Industry
Enrollment
468 participants

Conditions and interventions

Conditions

Interventions

  • NAB001 Drug
  • Vehicle alone 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
22
U.S. states
15
U.S. cities
22
Facility City State ZIP Site status
Not listed Phoenix Arkansas 85032
T. Joseph Raoof, MD, Inc. Encino California 91436
Skin Surgery Medical Group, Inc. San Diego California 92117
Longmont Medical Research Network Longmont Colorado 80501
Jacksonville Center for Clinical Research Jacksonville Florida 32216
Internaional Dermatology Research, Inc. Miami Florida 33144
MedaPhase, Inc. Newnan Georgia 30263
Clinical Research Atlanta Stockbridge Georgia 30281
Northwest Clinical Trials Boise Idaho 83704
Minnesota Clinical Study Center Fridley Minnesota 55432
Gerard Furst, DPM, PLLC East Setauket New York 11733
Dermatology Consulting Services High Point North Carolina 27262
Wake Research Associates Raleigh North Carolina 27612
Mazur Foot and Ankle Salisbury North Carolina 28144
Radiant Research Cincinnati Ohio 45249
Oregon Dermatology & Research Network Portland Oregon 97210
Temple University - School of Podiatric Medicine Philadelphia Pennsylvania 19107
Carolina Dermatology of Greenville, PA Greenville South Carolina 29681
Coastal Carolina Research Center Mt. Pleasant South Carolina 29464
Tennessee Clinical Research Center Nashville Tennessee 37215
Ashton Podiatry Associates, PA Dallas Texas 75243
Progressive Clinical Research San Antonio Texas 78229

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 2 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01208168, 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 NCT01208168 live on ClinicalTrials.gov.

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