Ftortiazinon is under clinical development by Gamaleya Federal Research Center of Epidemiology and Microbiology and currently in Phase II for Urinary Tract Infections. According to GlobalData, Phase II drugs for Urinary Tract Infections have a 73% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how Ftortiazinon’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication 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.
Ftortiazinon overview
Ftortiazinon is under investigation for the treatment of complicated urinary tract infections caused by Pseudomonas aeruginosa. It is formulated as a tablet for oral administration.
Gamaleya Federal Research Center of Epidemiology and Microbiology overview
Gamaleya Federal Research Center of Epidemiology and Microbiology (Gamaleya Research Center) is a research institution that utilizes adenoviral vectors to develop vaccines against influenza and middle east respiratory syndrome (MERS). Gamaleya Research Center is headquartered in Moscow, Russia.
For a complete picture of Ftortiazinon’s drug-specific PTSR and LoA scores, 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.
