Bexotegrast is under clinical development by Pliant Therapeutics and currently in Phase II for Liver Fibrosis. According to GlobalData, Phase II drugs for Liver Fibrosis does not have sufficient historical data to build an indication benchmark PTSR for Phase II. GlobalData uses proprietary data and analytics to create drugs-specific PTSR and LoA in the Bexotegrast 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.

Bexotegrast overview

Bexotegrast (PLN-74809) is under development for the treatment of primary sclerosing cholangitis, idiopathic pulmonary fibrosis (IPF), liver fibrosis and COVID-19-related acute respiratory distress syndrome. The drug candidate acts by targeting integrin alpha 5 beta 6 and integrin alpha 5 beta 1.

Pliant Therapeutics overview

Pliant Therapeutics is a clinical-stage biopharmaceutical company that primarily focuses on the development of treatments for fibrotic diseases. The company’s pipeline products include PLN-74809, idiopathic pulmonary fibrosis (IPF); PLN-101095, primary sclerosing cholangitis (PSC); PLN-101325 and PLN-1474. Pliant Therapeutics‘ products are primarily targeted towards patients suffering from fibrotic diseases and related conditions. Its therapies are designed to inhibit integrin-mediated activation of transforming growth factor beta (TGF-ß), a key driver in fibrosis. Pliant Therapeutics is headquartered in South San Francisco, California, the US.

For a complete picture of Bexotegrast’s drug-specific PTSR and LoA scores, buy the report here.

This content was updated on 12 April 2024

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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.