Fosciclopirox is under clinical development by CicloMed and currently in Phase I for Transitional Cell Carcinoma (Urothelial Cell Carcinoma). According to GlobalData, Phase I drugs for Transitional Cell Carcinoma (Urothelial Cell Carcinoma) have an 83% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how Fosciclopirox’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.

Fosciclopirox overview

CPX-POM (Ciclopirox prodrug) is under development for the treatment of advanced solid tumors, muscle invasive bladder cancer, transitional cell carcinoma (urothelial cell carcinoma) and non muscle invasive bladder cancer as third line therapy. The drug candidate is administered through intravenous route. It is being developed based on Predictive Precision Medicines Platform.
It was under development for relapsed/refractory acute myeloid leukemia (AML).

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

This content was updated on 22 April 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.