Clin2
NCT07521137Likely a fitRecruiting

Biweekly occidiofungin for recurring yeast infections

Candidiasis, Vulvovaginal

Part of Infections, Women’s health & pregnancy clinical trials.

This study tests occidiofungin, a new antifungal medication inserted into the vagina twice a week to prevent recurring yeast infections (vulvovaginal candidiasis). The goal is to see if this treatment can stop yeast infections from coming back.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 2
Enrollment
36 people
Ages
18 years to 65 years
Study type
Interventional

Who can take part

  • You are a woman between 18 and 65 years old
  • You have a confirmed yeast infection with symptoms and visible signs of moderate severity (itching, burning, irritation, redness, or swelling)
  • Your vaginal yeast infection has been confirmed with a lab test showing yeast cells
  • You weigh between 99 and 242 pounds and have a healthy body mass index (BMI between 18-35)
  • You are able to avoid sexual contact from day 1 through day 10 and on days you receive the medication
  • You are not pregnant, breastfeeding, or planning to become pregnant during the study

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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