Tadekinig alfa is under clinical development by AB2 Bio and currently in Phase III for Lymphoproliferative Disorders. According to GlobalData, Phase III drugs for Lymphoproliferative Disorders does not have sufficient historical data to build an indication benchmark PTSR for Phase III. GlobalData uses proprietary data and analytics to create drugs-specific PTSR and LoA in the Tadekinig alfa 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.

Tadekinig alfa overview

Tadekinig alfa is under development for the treatment of hemophagocytic lymphohistiocytosis (XIAP deficiency), NLRC4-macrophage activation syndrome (lymphoproliferative disorders) in children and adults, unspecified cancer and COVID-19 cytokine release syndrome. The drug candidate is administered through subcutaneous route in the form of solution. It acts by targeting the cytokine interleukin-18.

The drug candidate was under development for the treatment of chronic obstructive pulmonary disorder, dry eye disease, adult onset Still's disease (AOSD) and systemic onset juvenile idiopathic arthritis (Still Disease).

AB2 Bio overview

AB2 Bio is a drug discovery and development company focused on developing innovative therapies for the treatment of inflammatory diseases with large unmet medical needs. It is headquartered in Lausanne, Waadt, Switzerland.

For a complete picture of Tadekinig alfa’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.