MT-303 is under clinical development by Myeloid Therapeutics and currently in Phase I for Metastatic Hepatocellular Carcinoma (HCC). According to GlobalData, Phase I drugs for Metastatic Hepatocellular Carcinoma (HCC) have an 80% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how MT-303’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. Buy the report here.
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.
MT-303 overview
MT-303 is under development for the treatment of metastatic hepatocellular carcinoma. The therapeutic candidate comprises of lipid-nanoparticles (LNP) encapsulating mRNA encoding a Fcalpha fusion receptor targeting GPC3. It is administered through intravenous route.
Myeloid Therapeutics overview
Myeloid Therapeutics, Inc., a US based company harnessing and reprogramming myeloid cells to treat cancers.
For a complete picture of MT-303’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.
