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A Phase 3, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of Oteseconazole (VT-1161) Oral Capsules in the Treatment of Subjects With Recurrent Vulvovaginal Candidiasis
Recurrent vulvovaginal candidiasis (RVVC), also known as recurrent yeast infections, is defined as at least 3 episodes of acute VVC in the past 12 months. Several properties of oteseconazole (VT-1161) suggest that it might be a safer and more effective treatment for RVVC than other oral antifungal medicines. This study will evaluate the effectiveness and safety of oteseconazole (VT-1161) for the treatment of RVVC and consists of 2 parts. The first part of the study is a 2-week period for the treatment of the patient's current VVC episode with 3 150mg doses of fluconazole. The 2nd part consists of 12 weeks, when the patient will take either oteseconazole (VT-1161) 150 mg or a placebo (according to a random assignment), and then a 36-week follow-up period. In addition, at participating sites, an amendment to the study allows US patients who complete the initial 48 weeks without experiencing a confirmed RVVC episode to continue in a 48-week observational extension period designed to evaluate the continued effectiveness of oteseconazole (VT-1161). This study is identical to VMT-VT-1161-CL-011.
Age
12 - No limit years
Sex
FEMALE
Healthy Volunteers
No
31215
Phoenix, Arizona, United States
31227
Little Rock, Arkansas, United States
31217
Los Angeles, California, United States
31240
Hartford, Connecticut, United States
31204
Homestead, Florida, United States
31233
North Bay Village, Florida, United States
31255
Wichita, Kansas, United States
31245
Hagerstown, Maryland, United States
31223
Winston-Salem, North Carolina, United States
31244
Columbus, Ohio, United States
Start Date
August 23, 2018
Primary Completion Date
October 13, 2020
Completion Date
August 3, 2021
Last Updated
February 17, 2026
425
ACTUAL participants
Oteseconazole (VT-1161)
DRUG
Placebo
DRUG
Lead Sponsor
Mycovia Pharmaceuticals Inc.
NCT06190509
NCT04699240
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT01067131