FP-020 is under clinical development by Foresee Pharmaceuticals and currently in Phase I for Sarcoidosis. According to GlobalData, Phase I drugs for Sarcoidosis 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 FP-020 LoA Report. 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.
FP-020 overview
FP-020 is under development for the treatment of interstitial lung diseases, sarcoidosis, idiopathic pulmonary fibrosis, asthma, inflammatory bowel disease and COPD. The therapeutic candidate is administered orally. It acts by targeting matrix metalloproteinase 12 (MMP-12). The therapeutic candidate is a new chemical entity (NCE).
It was under development for the treatment of Alport syndrome, systemic sclerosis.
Foresee Pharmaceuticals overview
Foresee Pharmaceuticals (FP) is a clinical-stage pharmaceutical company. It focuses on developing drugs for unmet medical needs. The company’s product portfolio comprises FP-001, for prostate cancer, FP-025, for asthma and chronic obstructive pulmonary disease, FP-020, for Alport syndrome and FP-014, for prostate cancer among others. It harnesses the stabilized injectable formulation (SIF) platform technology to develop controlled release drug delivery systems for peptides, small molecules and proteins. The company works in collaboration with ScinoPharm and Pierre Fabre to research and develop its product portfolio. It has an operational presence in Taiwan and the US. FP is headquartered in Taipei, Taiwan.
For a complete picture of FP-020’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.
