Vulvovaginal Candidiasis is an indication for drug development with over 10 pipeline drugs currently active. According to GlobalData, preregistered drugs for Vulvovaginal Candidiasis have a 100% likelihood of approval (LoA) indication benchmark. GlobalData’s report assesses how phase transition success rate (PTSR) and likelihood of approval (LoA) scores for pipeline drugs in Vulvovaginal Candidiasis compared to historical benchmarks. Buy the report here.

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GlobalData tracks drug-specific phase transition and likelihood of approval scores, in addition to indication benchmarks based off 18 years of historical drug development data. Attributes of the drug, company and its clinical trials play a fundamental role in drug-specific PTSR and likelihood of approval.

Vulvovaginal Candidiasis overview

An excessive growth of yeast in the vagina that results in irritation, a local fungal infection caused by the Candida genus. It is most commonly seen in females in high estrogen states, pregnancy, oral contraceptive use, obesity, diabetes mellitus. It is not considered an STI although it can be transmitted by sexual intercourse.

For a complete picture of PTSR and LoA scores for drugs in Vulvovaginal Candidiasis, buy the report here.

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GlobalData, the leading provider of industry intelligence, provided the underlying data, research, and analysis used to produce this article. 

GlobalData’s Likelihood of Approval analytics tool dynamically assesses and predicts how likely a drug will move to the next stage in clinical development (PTSR), as well as how likely the drug will be approved (LoA). This is based on a combination of machine learning and a proprietary algorithm to process data points from various databases found on GlobalData’s Pharmaceutical Intelligence Center.