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Onychomycosis, a common pathology of the toenails, is even more prevalent among diabetic subjects. Nearly 26 million Americans suffer from diabetes, and approximately one-third of subjects with diabetes have toenail onychomycosis. Numerous studies have addressed the efficacy and safety of both topical and oral antifungal treatment options for onychomycosis in diabetic subjects. However, no study to date has specifically addressed the efficacy and safety of efinaconazole among diabetic subjects.
The objective of this noncomparative, uncontrolled study is to determine the efficacy of topical efinaconazole 10% for toenail onychomycosis among subjects with diabetes mellitus. Specific indicators to measure efficacy of treatment will be the mycological cure rate, complete cure rate, and treatment success. Furthermore, an additional goal of the study is to gain knowledge of safety in the setting of a cohort of diabetic subjects
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Intervention Group, receiving medication | Experimental | Enrolled subjects with confirmed onychomycosis will be dispensed topical medication for treatment. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Efinaconazole Topical | Drug | Enrolled subjects will be dispensed medical for topical application, and followed for a period of 50 weeks. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Primary Endpoint - Efficacy | The primary efficacy end point is the proportion of subjects achieving complete cure at week 50. Complete cure is to be defined as a combination of 0% clinical involvement and mycological cure (mycological cure defined as negative KOH examination and negative fungal culture of the target toenail sample). | 50 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Secondary Endpoint - Efficacy | The first secondary efficacy end point is mycological cure, defined as negative KOH examination and negative fungal culture of the target toenail sample. | 50 weeks |
| Secondary Endpoint - Efficacy |
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Inclusion Criteria:
Exclusion Criteria:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Western University of Health Sciences | Pomona | California | 91711 | United States |
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| ID | Title | Description |
|---|---|---|
| FG000 | Intervention Group, Receiving Medication | Enrolled subjects with confirmed onychomycosis will be dispensed topical medication for treatment. Efinaconazole Topical: Enrolled subjects will be dispensed medical for topical application, and followed for a period of 50 weeks. |
| Title | Milestones | Reasons Not Completed | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Overall Study |
|
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| ID | Title | Description |
|---|---|---|
| BG000 | Intervention Group, Receiving Medication | Enrolled subjects with confirmed onychomycosis will be dispensed topical medication for treatment. Efinaconazole Topical: Enrolled subjects will be dispensed medical for topical application, and followed for a period of 50 weeks. |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age, Continuous | Mean |
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | Primary Endpoint - Efficacy | The primary efficacy end point is the proportion of subjects achieving complete cure at week 50. Complete cure is to be defined as a combination of 0% clinical involvement and mycological cure (mycological cure defined as negative KOH examination and negative fungal culture of the target toenail sample). | Posted | Count of Participants | Participants | 50 weeks |
|
|
1 year
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | Intervention Group, Receiving Medication | Enrolled subjects with confirmed onychomycosis will be dispensed topical medication for treatment. Efinaconazole Topical: Enrolled subjects will be dispensed medical for topical application, and followed for a period of 50 weeks. |
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| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Application site vesicles, local | Skin and subcutaneous tissue disorders | Systematic Assessment |
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| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| David Shofler | Western University of Health Sciences | 9097063898 | dshofler@westernu.edu |
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| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| Prot_SAP | Yes | Yes | No | Study Protocol and Statistical Analysis Plan | May 23, 2017 | Sep 30, 2019 | Prot_SAP_000.pdf |
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| ID | Term |
|---|---|
| D014009 | Onychomycosis |
| ID | Term |
|---|---|
| D014005 | Tinea |
| D003881 | Dermatomycoses |
| D009181 | Mycoses |
| D001423 | Bacterial Infections and Mycoses |
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| ID | Term |
|---|---|
| C431707 | efinaconazole |
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The second secondary efficacy end point is clinical cure, defined as 0% clinical involvement of the target toenail.
| 50 weeks |
| Secondary Endpoint - Safety (Occurrence of Adverse Events: Type and Frequency) | The secondary safety endpoint is the occurrence of adverse events (type and frequency). | 50 weeks |
| years |
|
| Sex: Female, Male | Count of Participants | Participants |
|
| Race/Ethnicity, Customized | Count of Participants | Participants |
|
| Region of Enrollment | Number | participants |
|
| Counts |
|---|
| Participants |
|
|
| Secondary | Secondary Endpoint - Efficacy | The first secondary efficacy end point is mycological cure, defined as negative KOH examination and negative fungal culture of the target toenail sample. | Posted | Count of Participants | Participants | 50 weeks |
|
|
|
| Secondary | Secondary Endpoint - Efficacy | The second secondary efficacy end point is clinical cure, defined as 0% clinical involvement of the target toenail. | Posted | Count of Participants | Participants | 50 weeks |
|
|
|
| Secondary | Secondary Endpoint - Safety (Occurrence of Adverse Events: Type and Frequency) | The secondary safety endpoint is the occurrence of adverse events (type and frequency). | Posted | Count of Participants | Participants | 50 weeks |
|
|
|
| 0 |
| 40 |
| 0 |
| 40 |
| 2 |
| 40 |
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| D007239 |
| Infections |
| D012874 | Skin Diseases, Infectious |
| D009260 | Nail Diseases |
| D012871 | Skin Diseases |
| D017437 | Skin and Connective Tissue Diseases |