Vulvovaginal Candidiasis (VVC) Clinical Trial
Official title:
A Phase IIa Randomized, Active-controlled, Double-blind, Dose-escalation Study in Patients With Vulvovaginal Candidiasis to Evaluate Dose Response Relationship of Clinical Efficacy, Safety and Tolerability of Topically Administered ProF-001
This is a multi-center, randomized, prospective, active-controlled, double-blind,
dose-escalation study comparing dose response of clinical efficacy, safety, local
tolerability of three different doses of ProF-001/Candiplus® (Candiplus® 0.2%, Candiplus®
with 0.3%, Candiplus® with 0.4%) to 1% clotrimazole vaginal cream.
Patients with acute episode of vulvovaginal candidiasis (VVC) will be randomized to receive a
daily dose of either 5 ml (intravaginal) of Candiplus® at three different doses for the first
3 days and 2.5 ml for the remaining 3 days or 5 ml (intravaginal) application of 1%
clotrimazole cream over the first 3 days and 2.5 ml for the remaining 3 days according to the
following scheme (with each application 2 cm of cream will be applied to the vulvar region):
Cohort 1: Candiplus® 0.2% versus clotrimazole mono Cohort 2: Candiplus® 0.3% versus
clotrimazole mono Cohort 3: Candiplus® 0.4% versus clotrimazole mono Randomization into the
cohorts will occur consecutively from the lowest dose to the highest dose, i.e. patients will
be randomized first in cohort 1 and finally in cohort 3.
The proposed study is - after a pilot study to assess critical pharmacokinetic data - the
second study within a clinical trial program with the objective to develop a new combination
therapy for the treatment of vulvovaginal candidiasis.
The new combination consists of two registered drug substances.
n/a