INB-400 is a gene-modified cell therapy commercialized by IN8bio, with a leading Phase II program in Recurrent Glioblastoma Multiforme (GBM). According to Globaldata, it is involved in 1 clinical trial, which is ongoing. GlobalData uses proprietary data and analytics to provide a complete picture of INB-400’s valuation in its risk-adjusted NPV model (rNPV). Buy the model here.
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The revenue for INB-400 is expected to reach an annual total of $100 mn by 2040 globally based off GlobalData’s Expiry Model. The drug’s revenue forecasts along with estimated costs are used to measure the value of an investment opportunity in that drug, otherwise known as net present value (NPV). Applying the drug’s phase transition success rate to remaining R&D costs and likelihood of approval (LoA) to sales related costs provides a risk-adjusted NPV model (rNPV). The rNPV model is a more conservative valuation measure that accounts for the risk of a drug in clinical development failing to progress.
INB-400 Overview
INB-400 is under development for the treatment of newly diagnosed recurrent glioblastoma multiforme and solid tumor such as ovarian cancer. The therapeutic candidate is developed based on DeltEx platform and drug resistant immunotherapy (DRI) platform technology and consists of genetically modified gamma delta T cells administered along with chemotherapy. The drug candidate acts by targeting PARP for solid tumors.
IN8bio Overview
IN8bio is a clinical-stage biopharmaceutical company that focused on discovery, and development of gamma-delta T cell product candidates for solid and liquid tumors. The company is headquartered in New York City, New York, the US.
The operating loss of the company was US$28.5 million in FY2022, compared to an operating loss of US$14.7 million in FY2021. The net loss of the company was US$28.5 million in FY2022, compared to a net loss of US$14.7 million in FY2021.
For a complete picture of INB-400’s valuation, buy the drug’s risk-adjusted NPV model (rNPV) here.
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To create this model, GlobalData takes into account factors including patent law, known and projected regulatory approval processes, cash flows, drug margins and company expenses. Combining these data points with GlobalData’s world class analysis creates high value models that companies can use to help in evaluation processes for each drug or company.
The rNPV method integrates the probability of a drug reaching a clinical stage into the cash flow at that time, which provides a more accurate valuation, as it considers the probability that the drug never makes it through the clinical pathway to commercialization. GlobalData’s rNPV model uses proprietary likelihood of approval (LoA) and phase transition success rate (PTSR) data for the indication in the highest development stage, which can be found on GlobalData’s Pharmaceutical Intelligence Center.
