Sacituzumab tirumotecan is a monoclonal antibody conjugated commercialized by Merck, with a leading Phase III program in Adenocarcinoma Of The Gastroesophageal Junction. According to Globaldata, it is involved in 20 clinical trials, of which 14 are ongoing, and 6 are planned. GlobalData uses proprietary data and analytics to provide a complete picture of Sacituzumab tirumotecan’s valuation in its risk-adjusted NPV model (rNPV). Buy the model here.

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The revenue for Sacituzumab tirumotecan is expected to reach an annual total of $238 mn by 2039 in the US 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.

Sacituzumab tirumotecan Overview

sacituzumab tirumotecan (SKB-264) is under development for the treatment of ovarian epithelial cancer, gastric adenocarcinoma, triple negative breast cancer, endometrial carcinoma, HER2 negative breast cancer, metastatic pancreatic ductal adenocarcinoma, colorectal cancer, bile duct cancer, head and neck cancer squamous cell carcinoma, adenocarcinoma of the gastroesophageal junction, squamous and non-squamous non-small cell lung cancer, small cell lung cancer, nasopharyngeal carcinoma, metastatic cervical cancer, metastatic castration-resistant prostate cancer, esophageal squamous cell carcinoma and Urothelial cancers. It is a third-generation antibody-drug conjugate that acts by targeting cells expressing (trophoblast antigen) TROP2. It is administered through intravenous route in the form of powder. The drug candidate is being developed based on the ADC conjugation technology.

It was under development for the treatment of pancreatic ductal adenocarcinoma, colorectal cancer and bladder cancer.

Merck Overview

Merck is a biopharmaceutical company with focus on the discovery, development, manufacturing and marketing of prescription medicines, biologic therapies, vaccines, and animal health products. It offers prescription products for the treatment of cardiovascular conditions, cancer, immune disorders, infectious and respiratory diseases, and diabetes, among others. The company provides animal health products such as vaccines, poultry products, livestock products and aquaculture products. Merck sells medicines to drug wholesalers, retailers, hospitals, government agencies and managed health care providers; and animal health products to veterinarians, distributors, and animal producers. The company and its subsidiaries operate in the Americas, Europe, the Middle East, Africa, Asia Pacific, and Latin America. Merck is headquartered in Rahway, New Jersey, the US.
The company reported revenues of (US Dollars) US$60,115 million for the fiscal year ended December 2023 (FY2023), an increase of 1.4% over FY2022. In FY2023, the company’s operating margin was 3%, compared to an operating margin of 30.3% in FY2022. In FY2023, the company recorded a net margin of 0.6%, compared to a net margin of 24.5% in FY2022. The company reported revenues of US$15,775 million for the first quarter ended March 2024, an increase of 7.8% over the previous quarter.

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

This content was updated on 10 June 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.