Amikacin is under clinical development by PureIMS and currently in Phase I for Tuberculosis. According to GlobalData, Phase I drugs for Tuberculosis have an 88% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how Amikacin’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.
Amikacin overview
Amikacin is under the development for the treatment of tuberculosis and non tuberculosis mycobacterial infection. It is administered through inhalational route with a pre-filled dry powder inhaler, Cyclops.
PureIMS overview
PureIMS is a developer of disposable dry powder inhaler devices & drugs for multiple diseases. PureIMS is headquartered in Roden, the Netherlands.
For a complete picture of Amikacin’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.
