ZMA-001 is under clinical development by Zymedi and currently in Phase I for Pulmonary Arterial Hypertension. According to GlobalData, Phase I drugs for Pulmonary Arterial Hypertension have an 85% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how ZMA-001’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.
ZMA-001 overview
ZMA-001 is under development for the treatment of pulmonary arterial hypertension. It acts by targeting lysyl-tRNA synthetase 1 (KARS1). It is administered through intravenous route.
Zymedi overview
Zymedi focuses on novel therapeutics which tries to improve the quality of life of people suffering from diseases like minoacyl-tRNA synthetases, pulmonary arterial hypertension, and liver fibrosis. The company is headquartered in Incheon, South Korea.
For a complete picture of ZMA-001’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.
