TeLE is under clinical development by Bodor Laboratories and currently in Phase I for Unspecified Dermatological Disorders. According to GlobalData, Phase I drugs for Unspecified Dermatological Disorders does not have sufficient historical data to build an indication benchmark PTSR for Phase I. GlobalData uses proprietary data and analytics to create drugs-specific PTSR and LoA in the TeLE LoA Report. 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.
TeLE overview
Tele is under development for the treatment of unspecified nasal, dermatological, ophthalmic, otic and respiratory disorders. The drug candidate is being developed based on retrometabolic drug design technology.
Bodor Laboratories overview
Bodor Laboratories is a Pharmaceuticals and Healthcare company that Design and manufactures Drug. The company is Headquartered in Miami, Florida, The U.S.
For a complete picture of TeLE’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.
