Cellular Immunotherapy to Target CD3 and EGFR for Oncology is under clinical development by Transtarget and currently in Phase I for Gliosarcoma. According to GlobalData, Phase I drugs for Gliosarcoma 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 Cellular Immunotherapy to Target CD3 and EGFR for Oncology LoA Report. 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.
Cellular Immunotherapy to Target CD3 and EGFR for Oncology overview
Cellular immunotherapy is under development for the treatment of metastatic colorectal cancer, glioblastoma, gliosarcoma and pancreatic adenocarcinoma. It is administered through intrathecal and intravenous infusion route. The therapeutic candidate constitutes autologous T cells armed with bi-specific antibody produced by hetero conjugation of anti-CD3 and anti-EGFR monoclonal antibodies. It was also under development for non-small cell lung cancer, recurrent or refractory glioblastoma multiforme.
For a complete picture of Cellular Immunotherapy to Target CD3 and EGFR 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.
