ClinicalTrials.gg
CompletedNCT00509275Updated May 30, 2017

A Study to Evaluate Efficacy and Safety of Three W0027 Regimens in the Treatment of Moccasin Type Tinea Pedis (MTTP)

A Phase 1 interventional study of W0027 and Placebo in Tinea Pedis, sponsored by Stiefel, a GSK Company. Completed at 9 sites in 2 countries. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2017-05-30.

Sponsored by Stiefel, a GSK Company (part of GlaxoSmithKline) · Phase 1, Interventional, and Treatment

Phase
Phase 1
Study type
Interventional
Enrollment
120
Allocation
Randomized
Ages
18 Years to 65 Years
Sex
All
01

Study summary

In this phase Ib, multi-centre, randomized, double-blind, placebo-controlled parallel group study, 120 subjects with moccasin type tinea pedis (MTTP) will be enrolled at approximately 11 centres in the USA, Canada and Australia.

The primary objective of the study is to assess the patient response to three W0027 regimens in subjects with MTTP. Secondary objectives include assessment of the safety, tolerability and skin and nail pharmacokinetics to the three Albaconazole regimens.

02

Conditions studied

  • Tinea Pedis

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03

In context

Tinea Pedis

73 studies on the registry are indexed under Tinea Pedis; 8 are open to participants now.

This study's enrollment of 120 is close to the median of 128 across 66 interventional studies indexed under Tinea Pedis.

Browse Tinea Pedis studies →

Lead sponsor

Stiefel, a GSK Company is the lead sponsor of 56 studies on the registry; none are open to participants now.

First submitted before Stiefel became part of GlaxoSmithKline.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Subjects aged 18-65 years, who have been diagnosed with moccasin type tinea pedis (by positive dermatophyte culture, positive potassium hydroxide/calcofluor white preparation, and a Total Signs and Symptoms Score of at least 4).
  • Females of must use methods .

Exclusion criteria

Exclusion Criteria:

  • Subjects who are receiving any substrates with potential for ;
  • have used systemic antifungal drugs within 30 days of first dose; or topical antifungals within 2 weeks of first dose.
  • Also excluded are those who have a medical condition.
Terms in these criteria, in plain language(5)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Childbearing potential

Able to become pregnant: from the first period until menopause, unless permanently unable to through surgery (removal of the womb, or of both ovaries or both fallopian tubes).

Criteria for people of childbearing potential usually ask for a negative pregnancy test and for contraception during the study and for a time after it.

Contraception

Ways of preventing pregnancy. “Highly effective” methods fail less than 1% of the time a year when used correctly — for example an IUD or an implant.

Criteria usually say which methods count and how long to keep using them after the last dose, sometimes for male participants too. Some studies accept a partner’s vasectomy if it was confirmed successful and that person is the participant’s only sexual partner.

CYP3A (CYP3A4) inhibitors and inducers

CYP3A is a group of enzymes, mainly CYP3A4, in the liver and gut that break down many medicines. Some medicines, supplements and foods (grapefruit, St John’s wort) slow them down or speed them up, which changes how much of a study drug stays in the body.

Studies list them so they can be avoided or switched; bring a list of everything you take, including supplements.

QT and QTc

On an ECG, the QT interval is the time the heart’s lower chambers take to activate electrically and recover in each beat. QTc is that time adjusted for heart rate (QTcF by Fridericia’s formula, QTcB by Bazett’s). Some medicines lengthen it, and a long QTc can raise the risk of a dangerous heart rhythm.

The study may name a correction formula and a limit in milliseconds, often around 450–480.

Clinically significant

Judged by the study doctor to matter for your health or for the study. It is a doctor’s decision, so ask the study team if you are unsure whether something counts.

05

Study design

Phase
Phase 1
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Investigator)
Enrollment
120 participants (actual)

Study arms

  • Experimental
    1

    W0027

    Drug: W0027

  • Experimental
    2

    W0027

    Drug: W0027

  • Experimental
    3

    W0027

    Drug: W0027

  • Placebo comparator
    4

    Placebo

    Drug: Placebo

Interventions

  • DrugW0027

    capsule

  • DrugPlacebo

    Placebo

06

What researchers measure

Primary outcomes

  1. The primary objective of this study is to assess the subject response to three W0027 regimens in subjects with MTTP.

    Time frame: Week 8

Secondary outcomes

  1. The secondary objectives of this study are: To assess the safety and tolerability of three W0027 regimens in subjects with MTTP; To assess skin and nail pharmacokinetics of three Albaconazole doses in subjects with MTTP.

    Time frame: Skin and Plasma samples Week 0 (Visit 2) through to Week 8 (Visit 9), Nail samples Week 0 (Visit 2) Week 4(Visit 7) and Week 8(Visit 9)

07

Study locations

9 sites
  • Dermatology Specialists
    Louisville, Kentucky 40202, United States
  • Warren, Michigan 48088, United States
  • Albuquerque, New Mexico 87106, United States
  • University Dermatology Consultants, Inc.
    Cincinnati, Ohio 45219, United States
  • St George Dermatology and Skin Cancer Centre
    Kogarah, New South Wales NSW 2217, Australia
  • The Skin Centre
    Benowa, Queensland QLD 4217, Australia
  • South East Dermatology
    Carina, Queensland QLD 4152, Australia
  • Dermatology on Ward
    North Adelaide, South Australia SA 5006, Australia
  • Skin and Cancer Foundation
    Carlton, Victoria VIC 3053, Australia
08

Timeline

Tracking since Sep 25, 2026
Not marked actual or estimatedDates not marked actual or estimated

The record gives a start of Jul 2007, a primary completion of Aug 2008 and a completion of Aug 2008. It does not say whether these dates are actual or estimated.

How these figures are worked out, and which studies are left out of them.

Registered
Jul 30, 2007
First posted
Jul 31, 2007
Start
Jul 2007
Primary completionActual
Aug 2008
CompletionActual
Aug 2008
Last update
May 30, 2017
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on May 30, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00509275
Collaborators
GlaxoSmithKline
Responsible party
Sponsor
First posted
Jul 31, 2007
Start date
Jul 2007
Primary completion
Aug 2008
Completion
Aug 2008
Last update
May 30, 2017

Study contacts

Lynda Spelman, MD
principal investigator · South East Dermatology, South East Dermatology, Carina QLD 4152, Australia
Michael Freeman, MD
principal investigator · The Skin Centre, Benowa QLD 4217, Australia
Peter Foley, MD
principal investigator · Skin and Cancer Foundation, Carlton VIC 3053 , Australia
Stephen Shumack, MD
principal investigator · St George Dermatology and Skin Cancer Centre, Kogarah NSW 2217, Australia
Warren Weightman, MD
principal investigator · Dermatology on Ward, North Adelaide SA 5006, Australia
Debra Breneman, MD
principal investigator · University Dermatology Consultants, Inc., Cincinnati, OH, 45219, US
Eduardo Tschen, MD
principal investigator · Albuquerque, NM 87106, US
Yves Poulin, MD
principal investigator · Centre de Dermatologie de Québec Métropolitain, Quebec, QC, G1V 4X7, Canada
David Gratton, MD
principal investigator · International Dermatology Research Inc., Montreal, QC, H3H 1V4, Canada
Wayne Gulliver Gulliver, MD
principal investigator · NewLab Clinical Research, St. John's, NF, A1B 3E1, Canada
Steven Grekin, MD
principal investigator · 13450 East 12 Mile Road, Warren, MI 48088, US
Joseph Fowler, MD
principal investigator · Dermatology Specialists, 501 South Second Street, Louisville, KY 40202, US

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in May 2017. You cannot join it, but the record below documents what was studied.

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Discussion

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Studies of the drug tested here: Albaconazole

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