MT-302 is under clinical development by Myeloid Therapeutics and currently in Phase I for Pancreatic Ductal Adenocarcinoma. According to GlobalData, Phase I drugs for Pancreatic Ductal Adenocarcinoma does not have sufficient historical data to build an indication benchmark PTSR for Phase I. GlobalData uses proprietary data and analytics to create drugs-specific PTSR and LoA in the MT-302 LoA Report. 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.
MT-302 overview
MT-302 is under development for the treatment of metastatic colorectal cancer, non-small cell lung cancer, urothelial cancer, cervical cancer, epithelial ovarian cancer, HER2 negative breast cancer, pancreatic ductal adenocarcinoma, gastric adenocarcinoma, esophageal carcinoma, and triple negative breast cancer. The therapeutic candidate comprises mRNA delivered through lipid nanoparticles (LNPs), for modifying myeloid cells in vivo to express chimeric antigen receptors (CAR) targeting TROP2 expressing cancer cells. It is administered through intravenous route. It is being developed based on CRISPR-Enabled Autonomous Transposable Element (CREATE) platform.
Myeloid Therapeutics overview
Myeloid Therapeutics, Inc., a US based company harnessing and reprogramming myeloid cells to treat cancers.
For a complete picture of MT-302’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.
