WMA-1 is under clinical development by WellMarker Bio and currently in Phase I for Non-Small Cell Lung Cancer. According to GlobalData, Phase I drugs for Non-Small Cell Lung Cancer have an 80% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how WMA-1’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.
WMA-1 overview
WMA-1 is under development for the treatment of solid tumor and non-small cell lung cancer. It acts by targeting IGSF1 (Immunoglobulin superfamily member 1). It is administered by intravenous route.
It was also under development for the treatment of liver cancer and gastric cancer.
WellMarker Bio overview
Wellmarker Bio, is manufactures and distributes drugs that produces biomarker-based cancer drugs and other related products. The company is headquartered in Republic of Korea (South Korea).
For a complete picture of WMA-1’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.
