Safety and Efficacy of Topical IDP-108 Versus Vehicle in Patients With Onychomycosis

June 20, 2012 updated by: Dow Pharmaceutical Sciences
The purpose of this study is to evaluate the safety and efficacy of topical application of IDP-108 versus vehicle in treating patients with onychomycosis.

Study Overview

Status

Status

Indicates the current recruitment status or the expanded access status.
Completed

Conditions

Conditions

The disease, disorder, syndrome, illness, or injury that is being studied. On ClinicalTrials.gov, conditions may also include other health-related issues, such as lifespan, quality of life, and health risks.

Intervention / Treatment

Intervention / Treatment

A process or action that is the focus of a clinical study. Interventions include drugs, medical devices, procedures, vaccines, and other products that are either investigational or already available. Interventions can also include noninvasive approaches, such as education or modifying diet and exercise.

Study Type

Study Type

Describes the nature of a clinical study. Study types include interventional studies (also called clinical trials), observational studies (including patient registries), and expanded access.
Interventional

Enrollment (Actual)

Enrollment

The number of participants in a clinical study. The "anticipated" enrollment is the target number of participants that the researchers need for the study.
870

Phase

Phase

The stage of a clinical trial studying a drug or biological product, based on definitions developed by the U.S. Food and Drug Administration (FDA). The phase is based on the study's objective, the number of participants, and other characteristics. There are five phases: Early Phase 1 (formerly listed as Phase 0), Phase 1, Phase 2, Phase 3, and Phase 4. Not Applicable is used to describe trials without FDA-defined phases, including trials of devices or behavioral interventions.
  • Phase 3

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Canada
    • Alberta
      • Calgary, Alberta, Canada, T2S 3B3
        • Kirk Barber Research
      • Edmonton, Alberta, Canada, T5K 1X3
        • Stratica Medical
    • Ontario
      • Barrie, Ontario, Canada, L4M 6L2
        • Ultranova Skincare
      • New London, Ontario, Canada, N5X 2P1
        • Mediprobe Research
      • North Bay, Ontario, Canada, P1B 3Z7
        • North Bay Dermatology Centre
      • Windsor, Ontario, Canada, N8W 1E6
        • XLR8 Medical Research
    • Quebec
      • Québec, Quebec, Canada, G1V 4X7
        • Centre De Recherche Dermatologique Du Quebec Metropolitain
  • Japan
      • Fukuoka, Japan
        • Kaken Investigational Site - Chuo-ku #1
      • Fukuoka, Japan
        • Kaken Investigational Site - Chuo-ku #2
      • Fukuoka, Japan
        • Kaken Investigational Site - Higashi-ku
      • Fukuoka, Japan
        • Kaken Investigational Site - Minami-ku #1
      • Fukuoka, Japan
        • Kaken Investigational Site - Minami-ku #2
      • Nagasaki, Japan
        • Kaken Investigational Site
      • Okinawa, Japan
        • Kaken Investigational Site - Okinawa #1
      • Okinawa, Japan
        • Kaken Investigational Site - Okinawa #2
    • Fukuoka
      • Dazaifu, Fukuoka, Japan
        • Kaken Investigational Site
      • Itoshima, Fukuoka, Japan
        • Kaken Investigational Site
    • Hokkaido
      • Sapporo, Hokkaido, Japan
        • Kaken Investigational Site - Atsubetsu-ku #1
      • Sapporo, Hokkaido, Japan
        • Kaken Investigational Site - Atsubetsu-ku #2
      • Sapporo, Hokkaido, Japan
        • Kaken Investigational Site - Atsubetsu-ku #3
      • Sapporo, Hokkaido, Japan
        • Kaken Investigational Site - Chuo-ku
      • Sapporo, Hokkaido, Japan
        • Kaken Investigational Site - Kita-ku
      • Sapporo, Hokkaido, Japan
        • Kaken Investigational Site - Kiyota-ku
      • Sapporo, Hokkaido, Japan
        • Kaken Investigational Site - Nishi-ku
      • Sapporo, Hokkaido, Japan
        • Kaken Investigational Site - Shiroishi-ku
      • Sapporo, Hokkaido, Japan
        • Kaken Investigational Site - Teine-ku #1
      • Sapporo, Hokkaido, Japan
        • Kaken Investigational Site - Teine-ku #2
    • Kanagawa
      • Kawasaki, Kanagawa, Japan
        • Kaken Investigational Site
    • Okinawa
      • Ginowan, Okinawa, Japan
        • Kaken Investigational Site
      • Naha, Okinawa, Japan
        • Kaken Investigational Site
      • Nakagami, Okinawa, Japan
        • Kaken Investigational Site
      • Urasoe, Okinawa, Japan
        • Kaken Investigational Site
    • Saitama
      • Kawaguchi, Saitama, Japan
        • Kaken Investigational Site
    • Tokyo
      • Nakano-ku, Tokyo, Japan
        • Kaken Investigational Site - Nakano-ku #1
      • Nakano-ku, Tokyo, Japan
        • Kaken Investigational Site - Nakano-ku #2
      • Setagaya-ku, Tokyo, Japan
        • Kaken Investigational Site - Setagaya-ku #1
      • Setagaya-ku, Tokyo, Japan
        • Kaken Investigational Site - Setagaya-ku #2
      • Shinagawa-ku, Tokyo, Japan
        • Kaken Investigational Site - Shinagawa-ku #1
      • Shinagawa-ku, Tokyo, Japan
        • Kaken Investigational Site - Shinagawa-ku #2
  • United States
    • Alabama
      • Birmingham, Alabama, United States, 35233
        • University of Alabama, Birmingham
    • Arizona
      • Phoenix, Arizona, United States, 85050
        • Hope Research Institute
    • California
      • San Diego, California, United States, 92123
        • Therapeutics Clinical Research
      • San Diego, California, United States, 92123
        • University Clinical Trials, Inc
      • San Francisco, California, United States, 94115
        • University of California, San Francisco
    • Colorado
      • Longmont, Colorado, United States, 80501
        • Longmont Medical Research Network
    • Connecticut
      • New Haven, Connecticut, United States, 06511
        • The Savin Center, PC
    • Florida
      • Altamonte Springs, Florida, United States, 32701
        • Foot and Ankle Associates of Florida, Inc
      • Miami, Florida, United States, 33144
        • International Dermatology Research, Inc.
      • Ormond Beach, Florida, United States, 32174
        • Ameriderm Research
    • Georgia
      • Augusta, Georgia, United States, 30909
        • Augusta Centre for Dermatology and Skin Renewal, LLC
      • Snellville, Georgia, United States, 30078
        • Gwinnett Clinical Research Center, Inc.
    • Idaho
      • Boise, Idaho, United States, 83704
        • Northwest Clinical Trials
    • Indiana
      • Evansville, Indiana, United States, 47714
        • Hudson Dermatology
    • Kentucky
      • Louisville, Kentucky, United States, 40202
        • Dermatology Specialists
    • Michigan
      • Clinton Township, Michigan, United States, 48038
        • Michigan Center for Research Corp.
    • New Mexico
      • Albuquerque, New Mexico, United States, 87106
        • Academic Dermatology
    • New York
      • New Hyde Park, New York, United States, 11040
        • Impact Clinical Trials
    • Ohio
      • Cinncinati, Ohio, United States, 45249
        • Radiant Research
      • South Euclid, Ohio, United States, 44118
        • Haber Dermatology & Cosmetic Surgery
    • Oregon
      • Portland, Oregon, United States, 97219
        • Oregon Dermatology and Research Center
    • Pennsylvania
      • Hershey, Pennsylvania, United States, 17033
        • Penn State Milton S. Hershey Medical Center
      • Philadelphia, Pennsylvania, United States, 19107
        • Temple University School of Podiatric Medicine
    • South Carolina
      • Greenville, South Carolina, United States, 29607
        • Palmetto Clinical Trial Services, LLC
    • Tennessee
      • Goodlettsville, Tennessee, United States, 37072
        • Rivergate Dermatology
    • Texas
      • Austin, Texas, United States, 78705
        • Austin Dermatology Associates
      • College Station, Texas, United States, 77845
        • J & S Studies, Inc.
      • Dallas, Texas, United States, 75246
        • Baylor Research Institute
      • San Antonio, Texas, United States, 78229
        • Stephen Miller, MD, PA
    • Utah
      • Salt Lake City, Utah, United States, 84124
        • Dermatology Resarch Center
    • Virginia
      • Lynchburg, Virginia, United States, 24501
        • The Education and Research Foundation, Inc.
      • Norfolk, Virginia, United States, 23507
        • Virginia Clinical Research, Inc
    • Wisconsin
      • Milwaukee, Wisconsin, United States, 53209
        • Aurora Advanced Healthcare, Inc. - Clinical Research Center

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Eligibility Criteria

The key requirements that people who want to participate in a clinical study must meet or the characteristics they must have. Eligibility criteria consist of both inclusion criteria (which are required for a person to participate in the study) and exclusion criteria (which prevent a person from participating). Types of eligibility criteria include whether a study accepts healthy volunteers, has age or age group requirements, or is limited by sex.

Ages Eligible for Study

18 years to 70 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Clinically diagnosed onychomycosis of the target nail
  • Presence of mild to moderate onychomycosis, defined as 20 - 50% of the area of the target nail being clinically affected
  • Has a positive KOH examination from the target nail
  • Has a positive dermatophyte culture from the target nail

Exclusion Criteria:

  • Presence of any disease or condition that might cause nail abnormalities or may interfere with the evaluation of the study drug
  • Use of any systemic antifungal therapy within 4 weeks prior to the Screening visit or non-responsive to systemic antifungal therapy for onychomycosis
  • Use of any prescription or over-the-counter topical antifungal therapy for the toenails within 4 weeks prior to the Screening visit
  • Woman who is pregnant, nursing an infant, or planning a pregnancy during the study period

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm

Participant Group / Arm

A group or subgroup of participants in a clinical trial that receives a specific intervention/treatment, or no intervention, according to the trial's protocol.
Intervention / Treatment

Intervention / Treatment

A process or action that is the focus of a clinical study. Interventions include drugs, medical devices, procedures, vaccines, and other products that are either investigational or already available. Interventions can also include noninvasive approaches, such as education or modifying diet and exercise.
Placebo Comparator: Vehicle
Drug: Vehicle
Topical application once a day for 48 weeks
Experimental: IDP-108
Drug: IDP-108
Topical application once a day for 48 weeks

What is the study measuring?

Primary Outcome Measures

Primary Outcome Measures

In a clinical study's protocol, the planned outcome measure that is the most important for evaluating the effect of an intervention/treatment. Most clinical studies have one primary outcome measure, but some have more than one.
Outcome Measure
Time Frame
Percentage of patients who achieve clinical cure
Time Frame: 52 weeks
52 weeks

Secondary Outcome Measures

Secondary Outcome Measures

In a clinical study's protocol, a planned outcome measure that is not as important as the primary outcome measure for evaluating the effect of an intervention but is still of interest. Most clinical studies have more than one secondary outcome measure.
Outcome Measure
Time Frame
Percentage of patients who achieve clinical efficacy
Time Frame: 52 weeks
52 weeks
Percentage of patients who achieve mycologic cure
Time Frame: 52 weeks
52 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Sponsor

The organization or person who initiates the study and who has authority and control over the study.
Dow Pharmaceutical Sciences

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

Study Start

The actual date on which the first participant was enrolled in a clinical study. The "anticipated" study start date is the date that the researchers think will be the study start date.
November 1, 2009

Primary Completion (Actual)

Primary Completion

The date on which the last participant in a clinical study was examined or received an intervention to collect final data for the primary outcome measure. Whether the clinical study ended according to the protocol or was terminated does not affect this date. For clinical studies with more than one primary outcome measure with different completion dates, this term refers to the date on which data collection is completed for all the primary outcome measures. The "anticipated" primary completion date is the date that the researchers think will be the primary completion date for the study.
November 1, 2011

Study Completion (Actual)

Study Completion

The date on which the last participant in a clinical study was examined or received an intervention/treatment to collect final data for the primary outcome measures, secondary outcome measures, and adverse events (that is, the last participant's last visit). The "anticipated" study completion date is the date that the researchers think will be the study completion date.
December 1, 2011

Study Registration Dates

First Submitted

First Submitted

The date on which the study sponsor or investigator first submitted a study record to ClinicalTrials.gov. There is typically a delay of a few days between the first submitted date and the record's availability on ClinicalTrials.gov (the first posted date).
November 3, 2009

First Submitted That Met QC Criteria

First Submitted That Met QC Criteria

The date on which the study sponsor or investigator first submits a study record that is consistent with National Library of Medicine (NLM) quality control (QC) review criteria. The sponsor or investigator may need to revise and submit a study record one or more times before NLM's QC review criteria are met. It is the responsibility of the sponsor or investigator to ensure that the study record is consistent with the NLM QC review criteria.
November 3, 2009

First Posted (Estimate)

First Posted

The date on which the study record was first available on ClinicalTrials.gov after National Library of Medicine (NLM) quality control (QC) review has concluded. There is typically a delay of a few days between the date the study sponsor or investigator submitted the study record and the first posted date.
November 5, 2009

Study Record Updates

Last Update Posted (Estimate)

Last Update Posted

The most recent date on which changes to a study record were made available on ClinicalTrials.gov. There may be a delay between when the changes were submitted to ClinicalTrials.gov by the study's sponsor or investigator (the last update submitted date) and the last update posted date.
June 22, 2012

Last Update Submitted That Met QC Criteria

Last Update Submitted That Met QC Criteria

The most recent date on which the study sponsor or investigator submitted changes to a study record that are consistent with National Library of Medicine (NLM) quality control (QC) review criteria. It is the responsibility of the sponsor or investigator to ensure that the study record is consistent with the NLM QC review criteria.
June 20, 2012

Last Verified

Last Verified

The most recent date on which the study sponsor or investigator confirmed the information about a clinical study on ClinicalTrials.gov as accurate and current. If a study with a recruitment status of recruiting; not yet recruiting; or active, not recruiting has not been confirmed within the past 2 years, the study's recruitment status is shown as unknown.
June 1, 2012

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

Other Study ID Numbers

Identifiers or ID numbers other than the NCT number that are assigned to a clinical study by the study's sponsor, funders, or others. These numbers may include unique identifiers from other trial registries and National Institutes of Health grant numbers.
  • DPSI-IDP-108-P3-01

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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