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Completed

NCT Number: NCT03141840

Clinical Trial of Topical ABL01 Treatment of Onychomycosis

This clinical trial seeks to investigate if an experimental medical device, ABL01, can be used to treat onychomycosis. In a 1-year trial the effectiveness of ABL01 will be tested against placebo in 70 study subjects with onychomycosis of the big toe nail. The endpoint of the trial is clinical improvement and cure at the 6 and 12 month time-point.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Fotcompaniet Stockholm

Stockholm, 113 52, Sweden

About this study

The purpose of this clinical trial is to determine the safety and effectiveness of the medical device ABL01. The intended use of ABL01 is to reduce and treat onychomycosis, fungal nail infection. ABL01 is a solution intended to be topically administered weekly to infected nails. The trial is designed as a double blinded randomized placebo controlled clinical trial. The trial involves 70 study subjects, half of which will receive ABL01 and the other half placebo. The inclusion criteria for study subjects are adult men and women that present with distal lateral subungual onychomycosis (DSU) on the big toe nails. Furthermore, the extent of DSU should not involve more than half of the area of the nail.

The study subjects will themselves apply the study solution weekly to the treated nail. The trial will run for 6 months with a possible extension to maximum 12 months. There will be a total of 4 study visits at baseline, 3, 6 and 12 months to follow up the progress of the trial. The primary objective of the trial is to determine if ABL01 treatment are able to reduce and treat onychomycosis. Secondary objectives are to collect safety data, determine if the ABL01 are perceived as easy to use and assess long term effects of the treatment. The endpoint of the trial is reduction in clinical signs or complete cure of onychomycosis at the 6- or 12-month time-point.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Provision of written informed consent
  • Men and women above age 18 weighing over 40 kg
  • Present with distal lateral subungual onychomycosis of any of the big toe nails
  • The onychomycosis should involve less than 50 % of the nail bed and may not have reached the cuticle

Exclusion criteria

  • Unable to come for study visits
  • Known allergy to any of the components in ABL01
  • Not willing to participate in the trial or not able to understand the content of the trial
  • Present with proximal subungual onychomycosis or superficial onychomycosis.
  • Present with distal lateral subungual onychomycosis of other nails than the big toe.
  • More than 50 % of the nailbed affected by onychomycosis or the cuticles infected
  • Known conditions (like psoriasis) that cause abnormal nail appearance
  • Nail damage caused by trauma, pressure or other mechanical reasons
  • Currently on immunosuppressive therapy
  • Showing signs of poor peripheral blood circulation
  • Used another topical antifungal treatment within 1 month of screening
  • Used a systemic antifungal treatment within 3 months of screening
  • Participated in any other clinical onychomycosis trial in the previous 3 months

Treatment and study plan

ABL01

Device

Experimental medical device

PLACEBO

Device

ABL01 lacking active component

Primary outcomes

  1. Number of study subjects with a reduction in infected nail area at 6 months.

    Time frame: 6 months

    Clinical improvement of the condition is assessed by analyzing changes in infected nail area (in relation to total nail area) due to ABL01 or placebo treatment. Clinical improvement is considered to be a 40% reduction in infected area at the 6 month time period.

Secondary outcomes

  1. Questionnaire regarding subjects opinion of the treatment, nail improvement.

    Time frame: 12 months

    Subjects score (1-5) the perceived improvement of their nail condition.

  2. Questionnaire regarding subjects opinion of the treatment, ease of use.

    Time frame: 12 months

    Subjects score (1-5) the perceived ease of using ABL01.

  3. Number of study subjects with treatment-related adverse events

    Time frame: 12 months

    Subject reported safety data in combination with reported adverse events and adverse device effects related to the topical administration of ABL01.

  4. Number of study subjects with a reduction in infected area of the nail

    Time frame: 12 months

    Clinical improvement of the condition is assessed by analyzing changes in infected nail area (in relation to total nail area) due to ABL01 or placebo treatment. Clinical improvement is considered to be a 80% reduction in infected area at the 12 month time period.

  5. Number of study subjects with clinical cure

    Time frame: 12 months

    Clinical cure is established with a negative test for dermatophytes as assessed by DNA-analysis.

Sponsors and collaborators

Lead sponsor

Abbell AB

Industry

Registry information

Official study title

Clinical Trial of Safety and Efficacy of Topical ABL01 Treatment of Onychomycosis

Important dates

Study start
2017
Primary completion
2019
Study completion
2019
First posted
May 5, 2017
Registry last updated
Feb 20, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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