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.

CBG-002 overview

CBG-002 is under development for the treatment of relapsed/refractory multiple myeloma and unspecified indication. It is administered by intravenous route. The therapeutic candidate is a retroviral vector-transduced autologous T cells to express anti-BCMA CAR. it is being developed based on chimeric antigen receptor T cell therapy technology. It is administered through intravenous route.

For a complete picture of CBG-002’s drug-specific PTSR and LoA scores, buy the report here.

This content was updated on 2 September 2023

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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.