MB-108 is under clinical development by Mustang Bio and currently in Phase I for Recurrent Malignant Glioma. According to GlobalData, Phase I drugs for Recurrent Malignant Glioma 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 MB-108 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.
MB-108 overview
MB-108 is under investigation for the treatment of recurrent glioblastoma multiform, malignant glioma, anaplastic astrocytoma and gliosarcoma. The therapeutic candidate is a next-generation HCMV/HSV-1 chimeric recombinant virus comprising delta-gamma(1)34.5 HSV viral vector with HCMV IRS1 or TRS1 gene. It is administered intratumorally.
Mustang Bio overview
Mustang Bio is an US based developer of cell and gene therapies for the treatment of AML and brain cancer.
For a complete picture of MB-108’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.
