Lacutamab is a monoclonal antibody commercialized by Innate Pharma, with a leading Phase II program in Cutaneous T-Cell Lymphoma;Transformed Mycosis Fungoides. According to Globaldata, it is involved in 4 clinical trials, of which 2 were completed, and 2 are ongoing. GlobalData uses proprietary data and analytics to provide a complete picture of Lacutamab’s valuation in its risk-adjusted NPV model (rNPV). Buy the model here.

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The revenue for Lacutamab is expected to reach an annual total of $68 mn by 2036 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.

Lacutamab Overview

Lacutamab (IPH-4102) is under development for the treatment of relapsed and refractory sezary syndrome (SS),cutaneous T-cell lymphomas such as transformed mycosis fungoides (TMF),and relapsed and refractory including angioimmunoblastic T-cell lymphoma (AITL), anaplastic large cell lymphoma (ALCL), follicular T-cell lymphoma, nodal peripheral T-cell lymphoma with TFH phenotype, adult T-cell leukemia/lymphoma (ATL), hepatosplenic T-cell lymphoma (HSTL), enteropathy-associated T-cell lymphoma (EATL), monomorphic epitheliotropic intestinal T cell lymphoma (MEITL), NK-T cell lymphoma (NKT) and aggressive NK-cell leukemia (ANKL). It was administered intravenously. The drug candidate is a cytotoxic antibody against KIR3DL2-expressing cancers.

Innate Pharma Overview

Innate Pharma is a clinical-stage biotechnology company that develops immunotherapies for cancer patients. Its pipeline products include lacutamab which treats cutaneous t cell lymphoma and peripheral t cell lymphoma; monalizumab treats unresectable stage III non-small cell lung cancer; IPH5201 for neoadjuvant non-small cell lung cancer; IPH5301 which treats cancer (solid tumors); IPH6101 for acute myeloid leukemia, b-cell acute lymphoblastic leukemia, high risk-myelodysplasia; IPH6401 treats multiple myeloma; IPH62, IPH67, IPH6501 which treats cancer and pre clinical products comprise IPH45, IPH43. The company uses ANKET (Antibody-based NK cell Engager Therapeutics) a proprietary platform to develop multi-specific NK cell engagers to treat certain types of cancer. It collaborates with biopharmaceutical companies and research institutions to develop its products. Innate Pharma is headquartered in Marseille, France.
The company reported revenues of (Euro) EUR51.9 million for the fiscal year ended December 2023 (FY2023), an increase of 4.7% over FY2022. The operating loss of the company was EUR12.7 million in FY2023, compared to an operating loss of EUR57.4 million in FY2022. The net loss of the company was EUR7.6 million in FY2023, compared to a net loss of EUR58.1 million in FY2022.

For a complete picture of Lacutamab’s valuation, buy the drug’s risk-adjusted NPV model (rNPV) here.

This content was updated on 11 March 2024

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GlobalData, the leading provider of industry intelligence, provided the underlying data, research, and analysis used to produce this article.

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.