DKB-19002 is under clinical development by DongKoo Bio & Pharma and currently in Phase I for Type 2 Diabetes. According to GlobalData, Phase I drugs for Type 2 Diabetes have a 65% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how DKB-19002’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.
DKB-19002 overview
DKB-19002 is under development for the treatment of type 2 diabetes. It is a modified new drug.
DongKoo Bio & Pharma overview
DongKoo Bio & Pharma (DongKoo) develops, manufactures, and exports generic drugs and provides contract manufacturing services. The company’s product portfolio includes prescribed medicines, including digestants; antiplatelet agents, allergics; nonsteroidal anti-inflammatory drugs decongestants and nasal preparation products; and oral hypoglycemic agents, non-medical products, CMO products, medical apparatus such as smart X, a stem-cell extraction kit, and cosmetics. It offers products in various forms, such as soft gelatin capsules, hard capsules, tablets, powders or granules, externals and liquids. The company has a presence across Vietnam, New Zealand, Thailand, Hong Kong, and Singapore. DongKoo is headquartered in Seoul, South Korea.
For a complete picture of DKB-19002’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.
