An Evaluation of the Safety and Pharmacokinetics of Tavaborole Topical Solution for the Treatment of Fungal Disease of the Toenail in Children and Adolescents

NCT ID: NCT03405818

Last Updated: 2018-04-17

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE4
• Total Enrollment: 55 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2015-10-22
• Study Completion Date: 2017-07-27

Brief Summary

This was an open-label study to evaluate the safety and pharmacokinetics of tavaborole 5% topical solution in treating distal subungual onychomycosis (a fungal infection) of the toenail in children and adolescents (ages 6 to 16 years).

Following confirmation of eligibility, including laboratory evidence of a fungal organism in the toenail, tavaborole topical solution was applied once daily to all affected toenails for a 48-week treatment period.

Clinical assessment of the extent of infection and safety assessments were performed periodically throughout the 48-week treatment period, and again at 52 weeks (4 weeks after stopping the treatment).

A subgroup of enrolled subjects applied the topical solution to all 10 toenails and a small area of surrounding skin during the first 28 days. These subjects had blood samples analyzed to evaluate the pharmacokinetics (how the drug moves in the body) of tavaborole topical solution in children and adolescents.

Detailed Description

This was an open-label study to evaluate the safety, tolerability, and pharmacokinetics of tavaborole 5% topical solution in treating distal subungual onychomycosis (DSO) of the toenail in pediatric subjects aged 6 to 16 years and 11 months. An eligible subject had a target great toenail (TGT) with at least 20% involvement, with a positive potassium hydroxide (KOH) wet mount and positive fungal culture for T. rubrum or T. mentagrophytes.

Eligible subjects applied tavaborole 5% topical solution, once daily to all affected toenails (the TGT as well as all other toenails having the clinical characteristics of onychomycosis) throughout the 48 week treatment period.

Subjects were evaluated at Screening, Baseline (Day 1), and at Weeks 2, 4, 8, 16, 24, 32, 40, 48, and 52. Each evaluation included a clinical assessment of the AEs and local tolerability evaluation.

Additional procedures were performed as follows:

• Mycology sampling at Screening, Week 24, and Week 52/early termination (ET);
• Clinical disease severity of the TGT at Screening, Week 24, and Week 52/ET;
• Safety laboratory testing at Baseline, Week 24, and Week 52/ET;

In this study, there was a PK subgroup of evaluable subjects aged 12 to 16 years and 11 months studied under maximal use conditions. Subjects in this maximal use subgroup applied the study drug on all 10 toenails, including up to 2 mm of the surrounding skin, for 28 days. On Day 15, a predose PK sample was collected to assess steady state trough level. On Day 29, the study drug application was done at the study site, and PK samples were collected prior to dosing, as well as 4, 6, 8, and 24 hours postdose on Days 29 to 30.

Conditions

Onychomycosis; Tinea Unguium

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Tavaborole 5% Topical Solution

All study participants apply study drug

Group Type: EXPERIMENTAL

Tavaborole 5% Topical Solution

Intervention Type: DRUG

topical solution for application to toenails

Interventions

Tavaborole 5% Topical Solution

topical solution for application to toenails

Intervention Type: DRUG

Other Intervention Names

Kerydin

Eligibility Criteria

Inclusion Criteria

• males or females, ages >/= 6 years and </= 16 years and 11 months
• clinical diagnosis of distal subungual onychomycosis affecting at least 20% of one of the great toenails (target nail); and with positive KOH and positive culture for T. rubrum or T. mentagrophytes from either great toenail

Exclusion Criteria

• the target toenail has proximal subungual onychomycosis, onychomycosis involving the nail lunula, superficial white onychomycosis, dermatophytoma, exclusively lateral disease, or yellow or brown spikes, or has co-infection with certain fungi or molds
• anatomic abnormalities of the toes or toenail
• current or past history of chronic moccasin-type tinea pedis
• current or past history of psoriasis or lichen planus
• history of significant chronic fungal disease (other than onychomycosis)
• diabetes
• immunodeficiency

• Minimum Eligible Age: 72 Months
• Maximum Eligible Age: 203 Months
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Pfizer

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Pfizer CT.gov Call Center

Role: STUDY_DIRECTOR

Pfizer

Locations

Madera Family Medical Group

Madera, California, United States

Stanford University School of Medicine

Palo Alto, California, United States

MedStar Health Research Institute - MedStar Georgetown University Hospital

Washington D.C., District of Columbia, United States

Doctors Research Network

South Miami, Florida, United States

University Hospital, SUNY Downstate Medical Center

Brooklyn, New York, United States

Skin Specialty Dermatology

New York, New York, United States

Cyn3rgy Research

Gresham, Oregon, United States

Oregon Dermatology & Research Center

Portland, Oregon, United States

West Houston Clinical Research Services LLC

Houston, Texas, United States

Texas Dermatology and Laser Specialists

San Antonio, Texas, United States

Jordan Valley Dermatology Center

West Jordan, Utah, United States

PI Coor Clinical Research, LLC

Burke, Virginia, United States

Countries

United States

References

Rich P, Spellman M, Purohit V, Zang C, Crook TJ. Tavaborole 5% Topical Solution for the Treatment of Toenail Onychomycosis in Pediatric Patients: Results from a Phase 4 Open-Label Study. J Drugs Dermatol. 2019 Feb 1;18(2):190-195.

Reference Type: DERIVED

PMID: 30811142 (View on PubMed)

Provided Documents

Document Type: Study Protocol

View Document

Document Type: Statistical Analysis Plan

View Document

Other Identifiers

C3371003

Identifier Type: OTHER

Identifier Source: secondary_id

TAV-ONYC-401

Identifier Type: -

Identifier Source: org_study_id