LP-005 is under clinical development by Tianchen Biopharmaceutical (Suzhou) and currently in Phase I for Paroxysmal Nocturnal Hemoglobinuria. According to GlobalData, Phase I drugs for Paroxysmal Nocturnal Hemoglobinuria have an 80% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how LP-005’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.
LP-005 overview
LP-005 (RX-001) is under development for the treatment of age-related macular degeneration, nephropathy, paroxysmal nocturnal hemoglobinuria (PNH) and unspecified immunological disorders. The drug candidate is a bi-specific monoclonal antibody. It is administered through intravenous route.
Tianchen Biopharmaceutical (Suzhou) overview
Tianchen Biopharmaceutical (Suzhou) (Tianchen Biomedicine) is an innovative drug research and development company focused on developing biological macromolecules. Tianchen Biomedicine is headquartered in Shanghai, China.
For a complete picture of LP-005’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.
