Interdigital Tinea PedisPhase 2NCT01696799
Comparative PK Study of Econazole Nitrate Foam and Econazole Nitrate Cream in Subjects With Interdigital Tinea Pedis Aged 12 Years to Less Than 18 Years
A Phase 2 study testing Econazole Nitrate in people with Interdigital Tinea Pedis, run by AmDerma at 1 site in United States.
Trial summary
To compare the pharmacokinetics of Econazole Nitrate Foam with Econazole Nitrate Cream in subjects with interdigital tinea pedis aged 12 years to less than 18 years. Read more about this study
- Who is it for?
- Ages 12 to 18 years
- Conditions the study is for
- Interdigital Tinea Pedis
- What is being tested?
- Econazole Nitrate
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 42 participants
- Where
- 1 siteUnited States
- Study dates
- Sep 2011to Aug 2012
- Phase
- Phase 2
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 12 to 18 years
- All sexes
- No healthy volunteers
- Child, Adult
Who may be able to join
- Be between 12 years and less than 18 years of age and of either sex.
- Have a clinical diagnosis of interdigital tinea pedis
- Parent/guardian has provided written informed consent and the subject has provided written assent.
- Be willing and able to use the assigned study medication as directed and to commit to all follow-up visits for the duration of the study.
- Have microscopic evidence (positive KOH) of the presence of fungi and a positive fungal culture.
- Be in good health and free of any disease or physical condition which might, in the Investigator's opinion, expose the subject to an unacceptable risk by study participation.
- Females must be non-pregnant, non-lactating and not intending to become pregnant during the course of the study.
Who cannot join
- Is pregnant, nursing or planning a pregnancy during the study
- Has used topical antifungals or topical corticosteroids on the feet within 14 days prior to the start of the study.
- Has received systemic antifungal therapy within 12 weeks prior to the start of the study medication.
- Has used systemic antibacterials or systemic corticosteroids within 14 days prior to the start of the study.
- Has a history of uncontrolled diabetes mellitus or is immunocompromised (due to disease, e.g., HIV, or medications).
- Has concurrent moccasin-type tinea pedis (in the opinion of the Investigator).
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- Has any other skin disease which might interfere with the evaluation of tinea pedis.
- Is currently enrolled in an investigational drug or device study.
- Has received an investigational drug or treatment with an investigational device within 30 days prior to entering this study.
- Is unreliable, including subjects with a history of drug or alcohol abuse.
- Has known hypersensitivity to any of the components of the study medications.
Trial locations and contacts
1 site in 1 country.
About this study
Official title: A Multi-Center, Randomized Comparative Study of the Pharmacokinetics of Econazole Nitrate 1% Foam and Econazole Nitrate 1% Cream in Subjects With Interdigital Tinea Pedis Aged 12 Years to Less Than 18 Years
To compare the pharmacokinetics of Econazole Nitrate Foam with Econazole Nitrate Cream in subjects with interdigital tinea pedis aged 12 years to less than 18 years.
Read the detailed description
Based on the results of a previous clinical study evaluating the pharmacokinetics, safety and efficacy of EN Foam versus the reference listed econazole nitrate cream and the foam vehicle in adults, the current clinical study is being conducted to provide additional pharmacokinetic data for EN in the foam formulation in subjects ages 12 to less than 18 years with interdigital tinea pedis to support a clinical bridge for systemic safety to the RLD in this pediatric population. The study also includes clinical and safety endpoints.
- Conditions
- Interdigital Tinea Pedis
- Being tested
- Econazole Nitrate, placebo
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Econazole NitrateDrug
placeboDrug
| Study group | Role | What they receive |
|---|---|---|
| Econazole Nitrate Foam | Experimental | Investigational Drug Product Receives: Drug: Econazole Nitrate |
| Vehicle Foam | Placebo comparator | Vehicle Foam Comparator Receives: Drug: placebo |
| Econazole Nitrate Cream | Active comparator | Active comparator cream product Receives: Drug: Econazole Nitrate |
What is being measured
The primary outcome is the main question the study is designed to answer.
Plasma Levels of Econazole Nitrate
Blood will be taken at Baseline (Day 1) prior to the application of medication, and at the end of treatment (Day 28), just prior to the last dose of medication, and at 7 (±1 hr) hours post-drug application and a third blood draw 4 (±1 hr) hours after the second PK blood draw.
Measured: 28 Days
Investigator Assessment of Response to Treatment
At the end of treatment (Day 28), the Investigator will assess the subject's response to treatment using a 5-point scale (1 = excellent, 2 = very good, 3 = good, 4 = fair, and 5 = poor).
Measured: 28 Days
Secondary outcomes (1)
Dosing Compliance
Measures of study medication compliance will include the total number of applications, duration of treatment, and the total amount of study medication used. The amount of study medication used will be determined post-study following thereturn of all clinical supplies.
Measured: 28 Days
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted1 Oct 2012 (estimated)
- Study startSep 2011
- Primary completionApr 2012
- Study completionAug 2012
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Interdigital Tinea PedisStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 2
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind
- Who is masked
- Investigator
- Enrolment
- 42 participants (actual)
Sponsor and investigators
- Lead sponsor
- AmDerma
- Sponsor type
- Industry (pharma, biotech, devices)
- Collaborators
- AmDerma Pharmaceuticals, LLC
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT01696799
- Sponsor's protocol ID
- 079-2951-109
- Status last verified
- Sep 2012
- First submitted
- 27 Sep 2012
- Last updated
- 1 Oct 2012
- Results posted
- No
- Data monitoring committee
- No
Study at a glance
From the registry record, last updated by the sponsor on 1 Oct 2012. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Multi-Center, Randomized Comparative Study of the Pharmacokinetics of Econazole Nitrate 1% Foam and Econazole Nitrate 1% Cream in Subjects With Interdigital Tinea Pedis Aged 12 Years to Less Than 18 Years
- ClinicalTrials.gov ID
- NCT01696799
- Acronym / sponsor ID
- 079-2951-109
- Conditions
- Interdigital Tinea Pedis
- Phase
- Phase 2
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 42 participants (actual)
- Lead sponsor
- AmDermaIndustry (pharma, biotech, devices)
- Collaborators
- AmDerma Pharmaceuticals, LLC
- Study start
- Sep 2011
- Primary completion
- Apr 2012 (actual)
- Study completion
- Aug 2012 (actual)
- First posted
- 1 Oct 2012 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
To compare the pharmacokinetics of Econazole Nitrate Foam with Econazole Nitrate Cream in subjects with interdigital tinea pedis aged 12 years to less than 18 years.
Detailed description
Based on the results of a previous clinical study evaluating the pharmacokinetics, safety and efficacy of EN Foam versus the reference listed econazole nitrate cream and the foam vehicle in adults, the current clinical study is being conducted to provide additional pharmacokinetic data for EN in the foam formulation in subjects ages 12 to less than 18 years with interdigital tinea pedis to support a clinical bridge for systemic safety to the RLD in this pediatric population. The study also includes clinical and safety endpoints.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (investigator)
- Number of arms
- 3
| Arm | Type | Receives |
|---|---|---|
| Econazole Nitrate Foam | Experimental | Drug: Econazole NitrateInvestigational Drug Product |
| Vehicle Foam | Placebo comparator | Drug: placeboVehicle Foam Comparator |
| Econazole Nitrate Cream | Active comparator | Drug: Econazole NitrateActive comparator cream product |
Who may qualify
- Ages
- 12 to 18 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult
Key inclusion criteria (7 listed)
- Be between 12 years and less than 18 years of age and of either sex.
- Have a clinical diagnosis of interdigital tinea pedis
- Parent/guardian has provided written informed consent and the subject has provided written assent.
- Be willing and able to use the assigned study medication as directed and to commit to all follow-up visits for the duration of the study.
- Have microscopic evidence (positive KOH) of the presence of fungi and a positive fungal culture.
Key exclusion criteria (11 listed)
- Is pregnant, nursing or planning a pregnancy during the study
- Has used topical antifungals or topical corticosteroids on the feet within 14 days prior to the start of the study.
- Has received systemic antifungal therapy within 12 weeks prior to the start of the study medication.
- Has used systemic antibacterials or systemic corticosteroids within 14 days prior to the start of the study.
- Has a history of uncontrolled diabetes mellitus or is immunocompromised (due to disease, e.g., HIV, or medications).
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Econazole Nitrate | Drug | Econazole Nitrate Cream, Econazole Nitrate Foam |
| placebo | Drug | Vehicle Foam |
Primary outcome
Plasma Levels of Econazole Nitrate
Time frame: 28 Days
Blood will be taken at Baseline (Day 1) prior to the application of medication, and at the end of treatment (Day 28), just prior to the last dose of medication, and at 7 (±1 hr) hours post-drug application and a third blood draw 4 (±1 hr) hours after the second PK blood draw.
Investigator Assessment of Response to Treatment
Time frame: 28 Days
At the end of treatment (Day 28), the Investigator will assess the subject's response to treatment using a 5-point scale (1 = excellent, 2 = very good, 3 = good, 4 = fair, and 5 = poor).
1 secondary outcome
Dosing Compliance
Time frame: 28 Days
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 1 Oct 2012.
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 2 study testing Econazole Nitrate in people with Interdigital Tinea Pedis, run by AmDerma at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 7 inclusion and 11 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 1 Oct 2012. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Plasma Levels of Econazole Nitrate (time frame: 28 Days). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 1 Oct 2012.