Also known as chronic yeast infection, RVVC is a distinct condition from vulvovaginal candidiasis and is defined by the Centers for Disease Control and Prevention as three or more symptomatic episodes of yeast infection in 12 months.
Vivjoa is the first and only FDA-approved medication for RVVC indicated to reduce the incidence of RVVC in females with a history of RVVC who are NOT of reproductive potential.
The Vivjoa extension study followed the successful completion of Mycovia's two global, pivotal Phase 3 VIOLET studies to assess the long-term protective profile of Vivjoa given its pharmacokinetic profile and extended half-life beyond the original 48-week study duration.
US participants in the VIOLET studies treated with a 12-week course of Vivjoa who did not experience a VVC episode during the 48-week study were offered the opportunity to participate in an extension study, during which they were monitored for an additional 48 weeks (96 weeks total).
Of the 71 patients enrolled in the observational extension study, 85% completed 96 weeks without a recurrent VVC episode. The average time without recurrence was 92 weeks.
The authors concluded that Vivjoa may play an important role in providing long-term reduction in the incidence of disease recurrence for women with RVVC.
Recurrent Vulvovaginal Candidiasis is a debilitating, chronic infectious condition that affects 138m women worldwide each year.
RVVC, also known as chronic yeast infection, is a distinct condition from vulvovaginal candidiasis and defined as three or more symptomatic acute episodes of yeast infection in 12 months.
Primary symptoms include vaginal itching, burning, irritation and inflammation. Some women may experience abnormal vaginal discharge and painful sexual intercourse or urination, causing variable but often severe discomfort and pain.
Vivjoa (oteseconazole) capsules is an azole antifungal indicated to reduce the incidence of recurrent vulvovaginal candidiasis in females with a history of RVVC who are NOT of reproductive potential.
Vivjoa is the first and only FDA-approved medication that provides sustained efficacy demonstrated by significant long-term reduction of RVVC recurrence through 50 weeks versus comparators.
Oteseconazole is designed to inhibit fungal CYP51, which is required for fungal cell wall integrity, and this selective interaction is also toxic to fungi, resulting in the inhibition of fungal growth.
Due to its chemical structure, oteseconazole has a lower affinity for human CYP enzymes as compared to fungal CYP enzymes.
The FDA approved Vivjoa based upon the positive results from three Phase 3 clinical trials of oteseconazole two global, pivotal VIOLET studies and one US-focused ultraVIOLET study, including 875 patients at 232 sites across 11 countries.
Vivjoa (oteseconazole) capsules, the first FDA-approved product for Mycovia, is an azole antifungal indicated to reduce the incidence of recurrent vulvovaginal candidiasis in females with a history of RVVC who are NOT of reproductive potential.
Oteseconazole received FDA Qualified Infectious Disease Product and Fast-Track designations to become the first FDA-approved therapy for RVVC.
In 2019, Mycovia licensed oteseconazole to Jiangsu Hengrui Pharmaceuticals Co., Ltd., to develop and commercialize oteseconazole in China, including mainland China, Hong Kong, Macau and Taiwan, and Gedeon Richter plc., a Hungary-based pharmaceutical company, to commercialize and manufacture oteseconazole in Europe, Russia, the Commonwealth of Independent States, Latin America and Australia.
Mycovia also recognizes a tremendous potential for its oral fungal inhibitors and a growing need to treat a range of multi-drug resistant fungal pathogens.
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