Artesunate is under clinical development by Frantz Viral Therapeutics and currently in Phase II for Human Papillomavirus Infections. According to GlobalData, Phase II drugs for Human Papillomavirus Infections have a 19% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how Artesunate’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.

Artesunate overview

Artesunate is under development for the treatment of human papillomavirus (HPV) associated cervical intraepithelial neoplasia (CIN), vulvar high-grade squamous intraepithelial lesions (Vulvar HSIL) and anal intraepithelial neoplasia (AIN). It is administered as a suppository and topical route.

For a complete picture of Artesunate’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.