Mycovia Pharmaceuticals Announces Positive Topline Results from its Third Phase 3 Clinical Trial (ultraVIOLET) of Oteseconazole for the Treatment of Recurrent Vulvovaginal Candidiasis
- ultraVIOLET Evaluated the Efficacy and Safety of Oteseconazole over 50 weeks
- Efficacy of Oteseconazole Compared to Fluconazole in Treating Acute VVC Infection in Women with RVVC
- NDA Submission Planned in First Half of 2021
Durham, N.C. – January 6, 2021 – Mycovia Pharmaceuticals, Inc. (“Mycovia”), an emerging biopharmaceutical company dedicated to recognizing and empowering those living with unmet medical needs by developing novel therapies, today announced positive topline results from its Phase 3 clinical trial for oteseconazole (ultraVIOLET), its drug candidate for treating patients with recurrent vulvovaginal candidiasis (RVVC). RVVC, commonly known as chronic yeast infection, is a debilitating infectious condition defined as three or more episodes per year. Oteseconazole is designed to be highly selective for its pathogenic target, with fewer side effects and improved efficacy over current treatment options, including the current standard of care for vulvovaginal candidiasis (VVC), fluconazole.