Cellular Immunotherapy to Target CD3 and EGFR for Oncology is under clinical development by Transtarget and currently in Phase I for Glioblastoma Multiforme (GBM). According to GlobalData, Phase I drugs for Glioblastoma Multiforme (GBM) have an 82% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how Cellular Immunotherapy to Target CD3 and EGFR for Oncology’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.
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.
Data Insights
From
The gold standard of business intelligence.
Blending expert knowledge with cutting-edge technology, GlobalData’s unrivalled proprietary data will enable you to decode what’s happening in your market. You can make better informed decisions and gain a future-proof advantage over your competitors.