DOC-1021 is under clinical development by Diakonos Oncology 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 DOC-1021’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. 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.
DOC-1021 overview
DOC-1021 is under development for the treatment of glioblastoma multiforme, pancreatic ductal adenocarcinoma, cutaneous angiosarcoma, prostate cancer. The therapeutic candidate comprises of dendritic cells.
It was also under development for the treatment of triple negative breast cancer (TNBC).
Diakonos Oncology overview
Diakonos Oncology is a clinical-stage biotechnology company focused on addressing the critical and unmet medical needs of late-stage and aggressive cancers. The company is headquartered in Dallas, Texas, the US.
For a complete picture of DOC-1021’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.
