Tavo-103 is under clinical development by Tavotek Biotherapeutics and currently in Phase I for Chronic Inflammation. According to GlobalData, Phase I drugs for Chronic Inflammation 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 Tavo-103 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.

Tavo-103 overview

Tavo-103 is under development for the treatment of chronic inflammation. It is being developed based on TavoPrecise antibody platform. It is administered by intravenous route.

Tavotek Biotherapeutics overview

Tavotek Biotherapeutics (Tavotek) is a biopharmaceutical company focused on discovering, acquiring, developing, and commercializing therapeutic medicines for oncology, autoimmune and inflammatory diseases. The company’s proprietary TavoMIP Platform uses small molecule and antibody drugs for Binding and targeting intracellular tumors; TavoSelect provides human antibody sequences that can be utilized in different formats using computational analysis and machine learning; and TavoPrecise, a fit-for-purpose monoclonal antibody, and multi-specific to identify unique epitopes. It has an operational presence in China. The company works in collaboration with Yisheng Biopharma Co Ltd, to discover, develop and commercialize biotherapeutics for cancer and infectious disease using its novel PIKA immunomodulating technology. Tavotek is headquartered in Lower Gwynedd, Pennsylvania, the US.

For a complete picture of Tavo-103’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.