Fosravuconazole is under clinical development by Eisai and currently in Phase II for Tinea Pedis (Athlete Foot). According to GlobalData, Phase II drugs for Tinea Pedis (Athlete Foot) have a 42% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how Fosravuconazole’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. Buy the report here.

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.

Fosravuconazole overview

Fosravuconazole (E-1224/ Nailin) is a triazole derivative, acts as an anti-fungal agent. It is formulated as hard gelatin capsules for oral route of administration. Fosravuconazole is indicated for the treatment of onychomycosis.

Fosravuconazole is under development for the treatment of fungal infections like nail tinea, nail candidiasis, eumycetoma and tinea pedis (athlete foot). E-1224 is a pro-drug of ravuconazole, administered orally as a tablet. It acts by targeting lanosterol 14 alpha demethylase. It was under development for the treatment of Chagas disease.

For a complete picture of Fosravuconazole’s drug-specific PTSR and LoA scores, buy the report here.

This content was updated on 10 June 2024

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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.