Iontophoretic Application of Terbinafine Gel to the Large Toe Nail

March 10, 2009 updated by: Transport Pharmaceuticals

A Study of Skin/Nail Sensation and the Pharmacokinetics of the Uptake of Terbinafine in the Great Toe Nail and Systemically Following Treatment With the Electrokinetic Transungual System (ETS)-Terbinafine Gel in Healthy Normal Voluneteers

Terbinafine is recognized as one of the most effective drugs for the treatment of toe nail fungus (onychomycosis). This trial will be the first test of a new device to improve the delivery of terbinafine directly to the toe nail. The device uses a low level of electric current, iontophoresis, to "push" the terbinafine into the nail.

The study will involve a single application of terbinafine, in a gel form, with the iontophoretic device. The treatment will be applied to the surface of both large toenails of healthy subjects. Subjects will be asked to report any sensations in the nail or surrounding skin experienced during or after treatment. Samples from the edge of the treated toe nail will be taken at 2-4 week intervals to measure how much terbinafine was delivered to the nails, and blood samples will be taken for the first 24 hours after treatment to determine how much, if any, terbinafine was absorbed into the subjects's body. Observations will also be made of the treated toes to look for any irritation of the surrounding skin due to the treatment.

Study Overview

Study Type

Interventional

Enrollment (Anticipated)

40

Phase

  • Phase 1

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

    • North Dakota
      • Fargo, North Dakota, United States, 58104
        • Cetero Research

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

Ages Eligible for Study

18 years to 75 years (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Male and female volunteers between 18 and 75 years of age, inclusive.

Exclusion Criteria:

  • Subjects with pacemakers or automatic implantable cardioverter/defibrillator
  • Subjects with an implantable electronic device.
  • Subjects with a history of diabetes.
  • Subjects with a history of onychomycosis or an abnormal appearing nail on the great toe
  • Subject using systemic antifungal medications within 6 months prior to study enrollment.
  • Subject using prescription topical antifungal medications for toenail fungus within 3 months or other commercially available medications for toenail fungus applied directly to the toenail within 1 week prior to study enrollment.
  • Subject with a history of allergic or adverse response to terbinafine or any related anti-fungal drug
  • Participation in a previous clinical trial involving an investigational drug or device within 30 days prior to study enrollment.
  • Subject requires chronic use of analgesics, pain medication, or non-steroidal anti-inflammatory agents (NSAIDS).
  • In females of childbearing potential, a positive urine pregnancy test at screening and just prior to dosing.
  • Nursing mothers.
  • Subject with a history of alcoholism or drug abuse within the preceding 12 months.

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: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: 1
Iontophoretic Dose Level 1

Iontophoresis in conjunction with a terbinafine gel

Drug Dose: ETS drug cartridge loaded with approximately 20 mg - 35 mg of terbinafine in the gel formulation, with the load depending on the size of the toenail to be treated.

Two different drug applicators to be tested on each subject

Single treatment on each toenail; one treatment with one drug applicator design, the second treatment with the alternative drug applicator design

Iontophoretic Dose: 3 mA-min as 0.3 mA for 10 min

Active Comparator: 2
Iontophoretic Dose Level 2

Iontophoresis in conjunction with a terbinafine gel

Drug Dose: ETS drug cartridge loaded with approximately 20 mg - 35 mg of terbinafine in the gel formulation, with the load depending on the size of the toenail to be treated.

Two different drug applicators to be tested on each subject

Single treatment on each toenail; one treatment with one drug applicator design, the second treatment with the alternative drug applicator design

Iontophoretic Dose: 6 mA-min as 0.5 mA for 12 min

Iontophoresis in conjunction with a terbinafine gel

Drug Dose: ETS drug cartridge loaded with approximately 20 mg - 35 mg of terbinafine in the gel formulation, with the load depending on the size of the toenail to be treated.

Two different drug applicators to be tested on each subject

Single treatment on each toenail; one treatment with one drug applicator design, the second treatment with the alternative drug applicator design

Iontophoretic Dose: 6 mA-min as 0.3 mA for 20 min

Iontophoresis in conjunction with a terbinafine gel

Drug Dose: ETS drug cartridge loaded with approximately 20 mg - 35 mg of terbinafine in the gel formulation, with the load depending on the size of the toenail to be treated.

Two different drug applicators to be tested on each subject

Single treatment on each toenail; one treatment with one drug applicator design, the second treatment with the alternative drug applicator design

Iontophoretic Dose: 10 mA-min as 0.5 mA for 20 min

Iontophoresis in conjunction with a terbinafine gel

Drug Dose: ETS drug cartridge loaded with approximately 20 mg - 35 mg of terbinafine in the gel formulation, with the load depending on the size of the toenail to be treated.

Two different drug applicators to be tested on each subject

Single treatment on each toenail; one treatment with one drug applicator design, the second treatment with the alternative drug applicator design

Iontophoretic Dose: 15 mA-min as 0.5 mA for 30 min

Active Comparator: 3
Iontophoretic Dose Level 3

Iontophoresis in conjunction with a terbinafine gel

Drug Dose: ETS drug cartridge loaded with approximately 20 mg - 35 mg of terbinafine in the gel formulation, with the load depending on the size of the toenail to be treated.

Two different drug applicators to be tested on each subject

Single treatment on each toenail; one treatment with one drug applicator design, the second treatment with the alternative drug applicator design

Iontophoretic Dose: 6 mA-min as 0.5 mA for 12 min

Iontophoresis in conjunction with a terbinafine gel

Drug Dose: ETS drug cartridge loaded with approximately 20 mg - 35 mg of terbinafine in the gel formulation, with the load depending on the size of the toenail to be treated.

Two different drug applicators to be tested on each subject

Single treatment on each toenail; one treatment with one drug applicator design, the second treatment with the alternative drug applicator design

Iontophoretic Dose: 6 mA-min as 0.3 mA for 20 min

Iontophoresis in conjunction with a terbinafine gel

Drug Dose: ETS drug cartridge loaded with approximately 20 mg - 35 mg of terbinafine in the gel formulation, with the load depending on the size of the toenail to be treated.

Two different drug applicators to be tested on each subject

Single treatment on each toenail; one treatment with one drug applicator design, the second treatment with the alternative drug applicator design

Iontophoretic Dose: 10 mA-min as 0.5 mA for 20 min

Iontophoresis in conjunction with a terbinafine gel

Drug Dose: ETS drug cartridge loaded with approximately 20 mg - 35 mg of terbinafine in the gel formulation, with the load depending on the size of the toenail to be treated.

Two different drug applicators to be tested on each subject

Single treatment on each toenail; one treatment with one drug applicator design, the second treatment with the alternative drug applicator design

Iontophoretic Dose: 15 mA-min as 0.5 mA for 30 min

Active Comparator: 4
Iontophoretic Dose Level 4

Iontophoresis in conjunction with a terbinafine gel

Drug Dose: ETS drug cartridge loaded with approximately 20 mg - 35 mg of terbinafine in the gel formulation, with the load depending on the size of the toenail to be treated.

Two different drug applicators to be tested on each subject

Single treatment on each toenail; one treatment with one drug applicator design, the second treatment with the alternative drug applicator design

Iontophoretic Dose: 6 mA-min as 0.5 mA for 12 min

Iontophoresis in conjunction with a terbinafine gel

Drug Dose: ETS drug cartridge loaded with approximately 20 mg - 35 mg of terbinafine in the gel formulation, with the load depending on the size of the toenail to be treated.

Two different drug applicators to be tested on each subject

Single treatment on each toenail; one treatment with one drug applicator design, the second treatment with the alternative drug applicator design

Iontophoretic Dose: 6 mA-min as 0.3 mA for 20 min

Iontophoresis in conjunction with a terbinafine gel

Drug Dose: ETS drug cartridge loaded with approximately 20 mg - 35 mg of terbinafine in the gel formulation, with the load depending on the size of the toenail to be treated.

Two different drug applicators to be tested on each subject

Single treatment on each toenail; one treatment with one drug applicator design, the second treatment with the alternative drug applicator design

Iontophoretic Dose: 10 mA-min as 0.5 mA for 20 min

Iontophoresis in conjunction with a terbinafine gel

Drug Dose: ETS drug cartridge loaded with approximately 20 mg - 35 mg of terbinafine in the gel formulation, with the load depending on the size of the toenail to be treated.

Two different drug applicators to be tested on each subject

Single treatment on each toenail; one treatment with one drug applicator design, the second treatment with the alternative drug applicator design

Iontophoretic Dose: 15 mA-min as 0.5 mA for 30 min

Active Comparator: 5
Iontophoretic Dose Level 5

Iontophoresis in conjunction with a terbinafine gel

Drug Dose: ETS drug cartridge loaded with approximately 20 mg - 35 mg of terbinafine in the gel formulation, with the load depending on the size of the toenail to be treated.

Two different drug applicators to be tested on each subject

Single treatment on each toenail; one treatment with one drug applicator design, the second treatment with the alternative drug applicator design

Iontophoretic Dose: 6 mA-min as 0.5 mA for 12 min

Iontophoresis in conjunction with a terbinafine gel

Drug Dose: ETS drug cartridge loaded with approximately 20 mg - 35 mg of terbinafine in the gel formulation, with the load depending on the size of the toenail to be treated.

Two different drug applicators to be tested on each subject

Single treatment on each toenail; one treatment with one drug applicator design, the second treatment with the alternative drug applicator design

Iontophoretic Dose: 6 mA-min as 0.3 mA for 20 min

Iontophoresis in conjunction with a terbinafine gel

Drug Dose: ETS drug cartridge loaded with approximately 20 mg - 35 mg of terbinafine in the gel formulation, with the load depending on the size of the toenail to be treated.

Two different drug applicators to be tested on each subject

Single treatment on each toenail; one treatment with one drug applicator design, the second treatment with the alternative drug applicator design

Iontophoretic Dose: 10 mA-min as 0.5 mA for 20 min

Iontophoresis in conjunction with a terbinafine gel

Drug Dose: ETS drug cartridge loaded with approximately 20 mg - 35 mg of terbinafine in the gel formulation, with the load depending on the size of the toenail to be treated.

Two different drug applicators to be tested on each subject

Single treatment on each toenail; one treatment with one drug applicator design, the second treatment with the alternative drug applicator design

Iontophoretic Dose: 15 mA-min as 0.5 mA for 30 min

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Evaluate the skin/nail sensation noted by subjects during and following iontophoretic application of terbinafine gel to the great toenail
Time Frame: 12 weeks
12 weeks

Secondary Outcome Measures

Outcome Measure
Time Frame
Evaluate the uptake into the nail of the great toe and the systemic uptake and pharmacokinetics of terbinafine following a single iontophoretic application of terbinafine gel
Time Frame: 12 weeks and 24 hours, respectively
12 weeks and 24 hours, respectively

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Craig Sprenger, MD, Cetero Research, San Antonio
  • Study Director: Eric M Morrel, PhD, Transport Pharmaceuticals, Inc.
  • Study Director: Philip M Friden, PhD, Transport Pharmaceuticals, Inc.

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

October 1, 2008

Primary Completion (Actual)

January 1, 2009

Study Completion (Actual)

March 1, 2009

Study Registration Dates

First Submitted

October 6, 2008

First Submitted That Met QC Criteria

October 6, 2008

First Posted (Estimate)

October 8, 2008

Study Record Updates

Last Update Posted (Estimate)

March 12, 2009

Last Update Submitted That Met QC Criteria

March 10, 2009

Last Verified

March 1, 2009

More Information

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.

Clinical Trials on Onychomycosis

3
Subscribe