Scynexis announces submission of new drug application to the U.S. FDA for oral ibrexafungerp for the treatment of vaginal yeast infection

Scynexis

15 October 2020 - NDA submission is supported by positive data from two Phase 3 studies (VANISH Program) in women with vulvovaginal candidiasis.

Scynexis today announced the submission of a new drug application to the U.S. FDA for oral ibrexafungerp for the treatment of vulvovaginal candidiasis, also known as vaginal yeast infection.

As a qualified infectious disease product, ibrexafungerp is expected to receive a 6 month priority review following new drug application acceptance.

Read Scynexis press release

Michael Wonder

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Michael Wonder

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Medicine , US , Dossier