IMA-950 is under clinical development by Immatics and currently in Phase I for Low-Grade Glioma. According to GlobalData, Phase I drugs for Low-Grade Glioma have a 96% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how IMA-950’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.
IMA-950 overview
IMA-950 is under development for the treatment of relapsing glioblastoma, glioma including astrocytoma, oligoastrocytoma or oligodendroglioma and low grade glioma. The vaccine candidate is administered intradermally, and subcutaneously. It is a multi-peptide cancer vaccine containing 11 tumor-associated peptides. It consists of different synthetic tumor-associated peptides (TUMAPs). TUMAPs are dissolved in water and administered together with an adjuvant. These TUMAPs are derived from antigens overexpressed on tumor cells. The therapeutic candidate is developed using XPRESIDENT technology. It was also under development for the intradermal treatment of glioblastoma multiforme (GBM).
Immatics overview
Immatics is a biopharmaceutical company focused on the development of T cell immunotherapies to fight against cancer. The company is headquartered in Tubingen, Baden-Wurttemberg, Germany.
For a complete picture of IMA-950’s drug-specific PTSR and LoA scores, buy the report here.
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