Clinical Trial Comparing BL123 Versus Ketoconazole in Patients With Tinea Pedis

Tinea Pedis Clinical Trial

Official title:

Non-inferiority Phase II Trial Comparing BL123 (Biolab Sanus Farmacêutica Ltda.) Versus Ketoconazole (Nizoral® Janssen-Cilag) in Patients With Tinea Pedis

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02824926
• Other study ID #: GDN 083/13
• Status: Completed
• Phase: Phase 2
• First received: June 30, 2016
• Last updated: July 3, 2016
• Start date: July 2014
• Est. completion date: January 2015

Study information

• Verified date: July 2016
• Source: Galeno Desenvolvimento de Pesquisas Clínicas
• Contact: n/a
• Is FDA regulated: No
• Health authority: Brazil: Comitê de Ética em Pesquisa da Universidade Estadual de Campinas
• Study type: Interventional

Clinical Trial Summary

This is a non-inferiority, Phase II, open-label, randomized, parallel trial to evaluate efficacy and safety of the new intervention (Dapaconazole cream 2%) versus the active control (Ketoconazole cream 2%) in patients with Tinea Pedis. Study schedule comprises enrollment, treatment and follow-up visits. Treatment period is 14 days.

Description:

The study sample consists of male and female subjects aged between 18 and 60 years-old, either with single or multiple Tinea Pedis lesion(s). Sixty (60) patients will be enrolled, but each foot with lesion(s) will be considered as one (1) sample. Therefore, if a patient has bilateral lesions, one foot will be allocated to investigational product (Dapaconazole) and the other foot will be allocated to active control (Ketoconazole). Randomization will determine which foot (right or left) will be treated with Dapaconazole or Ketoconazole.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 60
• Est. completion date: January 2015
• Est. primary completion date: December 2014
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 60 Years

Eligibility

Inclusion Criteria:

• Male or female subjects, aged between 18 and 60 years-old;

• Presence of skin lesion(s) characteristic of Tinea Pedis, with diagnosis confirmed by direct mycological exam;

• Absence of previous antifungic treatment for the current lesion(s) under study;

• Absence of other significant diseases which, at physician's discretion, could have an impact on subject's participation in the trial, according to protocol requirements and study evaluations: medical history, blood pressure and heart rate, physical examination and screening laboratory tests;

• Ability to understand the nature and objectives of the trial, including its risks and adverse events; willingness to cooperate with the researcher and proceed according to all study requirements, which shall be confirmed by Informed Consent Form signature.

Exclusion Criteria:

• Known hypersensitivity to ketoconazole or chemically related compounds; history of serious adverse reactions;

• Current evidence of clinically significant diseases which, at physician's discretion, prevent subject's participation in the trial and/or expose the subject to risks other than what is normally expected;

• Use of medications that, at principal investigator's discretion, might expose the subject to risks other than what is normally expected;

• Screening laboratory tests results showing clinically relevant deviations that, due to potential risks, prevent participation in the trial, at the researcher's discretion;

• Drugs addiction, including alcohol;

• Use of any previous treatment to the lesion(s) under study that, according to principal investigator's discretion, might interfere with the study objectives;

• Treatment, within 3 months before this trial, with any drugs known to have a well-established toxic potential to major organs;

• Participation in any other experimental research or administration of any experimental drug within 6 months before this trial;

• Positive pregnancy test, labor or miscarriage within 12 weeks before study treatment;

• Any conditions, according to investigator's discretion, that prevent subjects to participate in the trial.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Tinea
• Tinea Pedis

Intervention

Drug:
• Dapaconazole

• Ketoconazole

Locations

Country	Name	City	State
n/a

Sponsors (2)

Lead Sponsor	Collaborator
Gilberto De Nucci	Biolab Sanus Farmaceutica

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Incidence of Treatment-Emergent Adverse Events (Safety and Tolerability)	Number of adverse events	45 days	Yes
Other	Incidence of Treatment-Emergent Adverse Events (Safety and Tolerability)	Changes of laboratory parameters that are out of normal values/ranges and/or considered as clinically significant by the investigator.	45 days	Yes
Primary	Clinical cure of the lesion(s)	Assessment of presence or absence of lesion(s) by clinical examination	14 days	No
Primary	Mycological cure of the lesion(s)	Laboratory test for presence or absence of Tinea Pedis	14 days	No
Secondary	Time (days) to clinical diagnosis of lesion(s) cure		14 days	No
Secondary	Time (days) to absence of itching at lesion(s) site		14 days	No