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ARTHEx-01 is under clinical development by ARTHEx Biotech and currently in Phase II for Myotonic Dystrophy. According to GlobalData, Phase II drugs for Myotonic Dystrophy does not have sufficient historical data to build an indication benchmark PTSR for Phase II. 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. ARTHEx-01 overview ARTHEx-01 is under development for the treatment of myotonic dystrophy type 1 (DM1), myotonic dystrophy type 2 (DM2) and congenital DM1. It acts by targeting microRNA 23b (miR-23b) which is associated with regulating the expression of MBNL protein. It is administered through intravenous ARTHEx Biotech overview ARTHEx Biotech, is a spin-off company of the University of Valencia that is developing advanced RNA treatments against genetic diseases. The company is headquartered in Spain. For a complete picture of ARTHEx-01’s drug-specific PTSR and LoA scores, This content was updated on 12 April 2024 From Blending expert knowledge with cutting-edge technology, GlobalData’s unrivalled proprietary data will enable you to decode what’s happening in your market. You can make better informed decisions and gain a future-proof advantage over your competitors. , 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 .US sanctions founder of Georgia’s ruling political party
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