BITR-2101 is under clinical development by Boston Immune Technologies and Therapeutics and currently in Phase I for Mantle Cell Lymphoma. According to GlobalData, Phase I drugs for Mantle Cell Lymphoma have a 74% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how BITR-2101’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.
BITR-2101 overview
BITR-2101 IS under development for the treatment of infectious diseases and relapsed or refractory non-Hodgkin’s lymphoma subgroups including cutaneous T cell lymphoma (CTCL), primary cutaneous peripheral T cell lymphoma (PTCL), adult T cell leukemia/lymphoma (ATLL), diffuse large B cell lymphoma (DLBCL), mantle cell lymphoma (MCL), and marginal zone lymphoma (MZL). The drug candidates are composed of a highly enriched population of immunosuppressive regulatory T cells (Tregs) that act by targeting tumor necrosis factor receptor 2 (TNFR2). These are developed based on DOMab technology platform. It is administered through intravenous route.
Boston Immune Technologies and Therapeutics overview
Boston Immune Technologies and Therapeutics develops novel tumor necrosis factor superfamily receptor antagonist antibodies. It is headquartered in Boston, Massachusetts, the US.
For a complete picture of BITR-2101’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.
