AT-002 is under clinical development by Arctic Therapeutics ehf and currently in Phase I for Uveitis. According to GlobalData, Phase I drugs for Uveitis have an 86% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how AT-002’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. 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.

AT-002 overview

AT-002 is under development for the treatment of autoimmune uveitis and juvenile dermatomyositis. The therapeutic candidate acts by suppressing of cytokine signaling 1(SOCS1) and is being developed by AT's genetic drug discovery platform based on artificial intelligence (AI).

Arctic Therapeutics ehf overview

Arctic Therapeutics International (ATI) is a medication discovery and development business that focuses on figuring out the genetic causes of both common and unusual diseases in order to provide cutting-edge treatments. The company is headquartered in Iceland.

For a complete picture of AT-002’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.