Peptide to Inhibit CD200 for Oncology is under clinical development by OX2 Therapeutics and currently in Phase I for High-Grade Glioma. According to GlobalData, Phase I drugs for High-Grade Glioma 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 Peptide to Inhibit CD200 for Oncology 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.
Peptide to Inhibit CD200 for Oncology overview
Peptide is under development for the treatment of high-grade glioma, diffuse midline glioma/diffuse intrinsic pontine glioma and recurrent glioblastoma. It acts by targeting CD200. It is administered through parenteral route. It was also under development for the treatment of breast cancer.
OX2 Therapeutics overview
OX2 Therapeutics is developing inhibitors for the treatment of central nervous system tumors. The company is headquartered in Mound, Minnesota, the US.
For a complete picture of Peptide to Inhibit CD200 for Oncology’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.
