Vulvovaginal Candidiasis
Conditions
Brief summary
This is a randomized, multicenter, evaluator blinded study to evaluate the safety, tolerability, efficacy and pharmacokinetics of SCY-078 compared to Fluconazole in adult patients with moderate to severe Vulvovaginal Candidiasis (VVC) and a history of frequent episodes of VVC. Approximately 90 subjects, meeting the inclusion criteria will be enrolled and randomized in a 1:1:1 ratio to one of the 3 treatment arms: Oral SCY-078 in 2 dose regimens or oral Fluconazole. After enrollment, subjects will be evaluated on Day-5 (end of treatment visit), Day-24 (test of cure visit), Day-60, Day 90 and Day 120 (end of observation period visit) or at any time that a recurrence or clinical failure is suspected, up to the end of observation period.
Detailed description
This is a randomized, multicenter, evaluator blinded study to evaluate the safety, tolerability, efficacy and pharmacokinetics of SCY-078 compared to Fluconazole in adult patients, from 18 to 65 years of age, with moderate to severe Vulvovaginal Candidiasis (VVC) and a history of frequent episodes of VVC. Approximately 90 subjects, meeting the inclusion criteria will be enrolled and randomized in a 1:1:1 ratio to one of the 3 treatment arms: oral SCY-078 does regimen 1, or oral SCY-078 does regimen 2, or oral Fluconazole. After enrollment, subjects will be evaluated on Day-5 (end of treatment visit), Day-24 (test of cure visit), Day-60, Day 90 and Day 120 (end of observation period visit) or at any time that a recurrence or clinical failure is suspected, up to the end of observation period. Primary Objectives: \* To evaluate the safety and efficacy of 2 dosing regimens of Oral SCY-078 in subjects with moderate to severe Vulvovaginal Candidiasis (VVC) Secondary Objectives: \* To estimate the effect of Oral SCY-078 therapy in the rate and time to recurrence in subjects with a history of frequent episodes of VVC
Interventions
DRUGSCY-078
DRUGFluconazole
Sponsors
ethica Clinical Research Inc.
Scynexis, Inc.
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Investigator)
Eligibility
Sex/Gender
FEMALE
Age
18 Years to 65 Years
Healthy volunteers
No
Inclusion criteria
Subjects must fulfill all of the following criteria to be eligible for study admission: 1. Female subjects from 18 to 65 years of age in good general health 2. Diagnosis of symptomatic moderate to severe vulvovaginal candidiasis 3. The ability to understand and sign a written informed consent form (ICF), which must be obtained prior to treatment and any study-related procedures. 4. The ability to understand and sign a consent or authorization form which shall permit the use, disclosure and transfer of the subject's personal health information (e.g., in the U.S. HIPAA Authorization form). 5. The ability to understand and follow all study-related procedures including study drug administration. 6. Females of childbearing potential must agree to use a medically acceptable method of contraception while receiving protocol-assigned product.
Exclusion criteria
A subject will be excluded from participation in the study if she meets any of the following
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Proportion of subjects achieving therapeutic cure at the test of cure visit (Day 24 +/-3) | Day 24 +/- 3 | Therapeutic Cure defined as achieving both a Clinical Cure (resolution of signs and symptoms) and a Mycological Eradication (negative culture). |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Proportion of subjects with recurrence of VVC during the observation period | 4-month observation period | Recurrence defined as a symptomatic and culture-verified episode of VVC after achieving Therapeutic Cure. |
Countries
Dominican Republic
Outcome results
None listed