ARTHEx-01 by ARTHEx Biotech for Myotonic Dystrophy: Likelihood of Approval

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 route.

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, buy the report here.

This content was updated on 12 April 2024

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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.