DF-003 is under clinical development by Drug Farm and currently in Phase I for Unspecified Ophthalmological Disorders. According to GlobalData, Phase I drugs for Unspecified Ophthalmological 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 DF-003 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.
DF-003 overview
DF-003 is under development for the treatment of rare blindness (ROSAH syndrome) and cardio-renal disease, chronic kidney disease (chronic renal failure) and unspecified indication. It is administered through oral route in the form of capsules. It acts by targeting alpha-protein kinase 1 (ALPK1) and is being developed based on IDInVivo technology.
Drug Farm overview
Drug Farm developing innovative treatments targeting the innate immunity for hepatitis B, cancer, and autoimmune diseases. It is headquartered in Shanghai, China.
For a complete picture of DF-003’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.
