ERC-1671 is under clinical development by ERC Belgium and currently in Phase II for Gliosarcoma. According to GlobalData, Phase II drugs for Gliosarcoma does not have sufficient historical data to build an indication benchmark PTSR for Phase II. GlobalData uses proprietary data and analytics to create drugs-specific PTSR and LoA in the ERC-1671 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.
ERC-1671 overview
ERC-1671 (Gliovac) vaccine is under development for the prevention of recurrent glioblastoma multiforme and gliosarcoma. It is administered through intradermal route. Vaccine candidate is composed of a combination of autologous and allogeneic glioblastoma (GBM) tumor cells derived from GBM cancer patients.
ERC Belgium overview
ERC Belgium is a clinical stage biopharmaceutical company that research for generic cell therapy treatments. The company’s pipeline product include Gliovac-ERC1671, a therapeutic anti-glioblastoma vaccine that contains allogeneic and autologous tumor cells that is used for the treatment of glioblastoma multiforme. ERC Belgium products is used to treats patients diagnosed with grade IV glioma (glioblastoma multiforme and gliosarcoma), when other traditional treatments have failed. The company markets its products throughout Belgium, the Netherlands, the US, Canada and Australia. ERC Belgium is headquartered in Namur, Belgium.
For a complete picture of ERC-1671’s drug-specific PTSR and LoA scores, buy the report here.
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