WebFeb 10, 2024 · The study comprised of 260 women who were experiencing RVVC, which is defined as 3 or more per year. All patients were given a 3-day regimen of open-label … WebOct 21, 2024 · In June 2024, ibrexafungerp (BREXAFEMME ®) was approved as the first and only non-azole treatment for VVC, thereby providing a new, oral, 1-day treatment option for acute VVC that is well …
The Antifungal Pipeline: Fosmanogepix, Ibrexafungerp, Olorofim ...
WebMay 11, 2024 · In the study, ibrexafungerp was generally safe and well-tolerated with findings consistent with the existing Brexafemme (ibrexafungerp tablets) label. Earlier … WebOct 9, 2024 · Interim results of the ongoing phase III study show that oral ibrexafungerp was generally well tolerated, with the most common drug-related AEs being mild-to-moderate diarrhea, nausea, ... (CANDLE, NCT04029116). Future Role . Ibrexafungerp was approved by the FDA for the treatment of VVC on 1 June, 2024, with other approvals … the original anchor bar buffalo ny
Full article: Oral Ibrexafungerp: an investigational agent …
WebPhase 3 Study of Oral Ibrexafungerp (SCY-078) Vs. Placebo in Subjects With Recurrent Vulvovaginal Candidiasis (VVC) (CANDLE) Official Title: A Phase 3, Multicenter, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of Oral Ibrexafungerp (SCY-078) Compared to Placebo in Subjects With Recurrent … WebAug 4, 2024 · The CANDLE study met its primary endpoint, with 65.4% of patients with recurrent vulvovaginal candidiasis (RVCC) who received monthly single-day … WebMay 11, 2024 · In the study, ibrexafungerp was generally safe and well-tolerated with findings consistent with the existing Brexafemme (ibrexafungerp tablets) label. Earlier this year, Scynexis also announced positive results from its global Phase III CANDLE study investigating the safety and efficacy of oral ibrexafungerp for prevention of recurrent ... the original arizona jean co