MTX-463 is under clinical development by Mediar Therapeutics and currently in Phase I for Fibrosis. According to GlobalData, Phase I drugs for Fibrosis 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 MTX-463 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.

MTX-463 overview

MTX-463 is under development for the treatment of fibrosis and idiopathic pulmonary fibrosis. It acts by targeting WISP1.

Mediar Therapeutics overview

Mediar Therapeutics, is a biotechnology company that discovers and develops antibody-based therapeutics to halt fibrosis. The company is headquartered in United States.

For a complete picture of MTX-463’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.