Giant Cell Arteritis (Temporal Arteritis/Cranial Arteritis/Horton Disease) is an indication for drug development with over 8 pipeline drugs currently active. According to GlobalData, preregistered drugs for Giant Cell Arteritis (Temporal Arteritis/Cranial Arteritis/Horton Disease) have a 100% likelihood of approval (LoA) indication benchmark. GlobalData’s report assesses how phase transition success rate (PTSR) and likelihood of approval (LoA) scores for pipeline drugs in Giant Cell Arteritis (Temporal Arteritis/Cranial Arteritis/Horton Disease) compared to historical 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.
Giant Cell Arteritis (Temporal Arteritis/Cranial Arteritis/Horton Disease) overview
Giant cell arteritis (GCA) is a form of vasculitis, a group of disorders that cause inflammation of blood vessels that affects the arteries of the head (especially the temporal arteries, located on each side of the head). It is also called as temporal arteritis (TA) or cranial arteritis or Horton’s syndrome.
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For a complete picture of PTSR and LoA scores for drugs in Giant Cell Arteritis (Temporal Arteritis/Cranial Arteritis/Horton Disease), buy the report here.
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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.
