TNT-119 is under clinical development by Eliem Therapeutics and currently in Phase I for Membranous Glomerulonephritis. According to GlobalData, Phase I drugs for Membranous Glomerulonephritis 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 TNT-119 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.

TNT-119 overview

TNT-119 is under development for the treatment of membranous nephropathy, systemic lupus erythematosus and immune thrombocytopenia. The therapeutic candidate is a monoclonal antibody (mAb) which acts by targeting B lymphocyte antigen CD19.

Eliem Therapeutics overview

Eliem Therapeutics is a biotechnology company that develops and markets novel therapies for the treatment of chronic pain, psychiatry, epilepsy and other peripheral and central nervous system disorders. The company is headquartered in Redmond, Washington, the US.

For a complete picture of TNT-119’s drug-specific PTSR and LoA scores, buy the report here.

This content was updated on 20 May 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.