Infliximab biosimilar is under clinical development by Xentria and currently in Phase II for Pulmonary Sarcoidosis. According to GlobalData, Phase II drugs for Pulmonary Sarcoidosis 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 Infliximab biosimilar 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.

Infliximab biosimilar overview

Infliximab biosimilar (XTMAB-16) is under development for the treatment of pulmonary sarcoidosis. The drug candidate is a human recombinant monoclonal antibody. It is administered through intravenous route. It acts by targeting TNF alpha.

Xentria overview

Xentria is an integrated R&D, manufacturing, and commercial company. It is headquartered in Chicago, Illinois, the US.

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

This content was updated on 10 June 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.