Adalimumab biosimilar is under clinical development by Aprogen and currently in Phase I for Autoimmune Disorders. According to GlobalData, Phase I drugs for Autoimmune Disorders have a 73% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how Adalimumab biosimilar’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.
Adalimumab biosimilar overview
Adalimumab biosimilar is under development for the treatment of unspecified autoimmune disease. The drug candidate is administered through subcutaneous route. It acts by targeting tumor necrosis factor (TNF)–alpha.
Aprogen overview
Aprogen is into the manufacture of equipment used in the steel, environmental, energy and chemical, and oil sand plant facilities. The company manufactures and supplies cokes, fired heaters, thermal sprays, wear plates and hard-facing products. It also offers thermal insulation works. The company operates in South Korea. Aprogen is head quartered in Seoul, South Korea.
For a complete picture of Adalimumab biosimilar’s drug-specific PTSR and LoA scores, 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.
