MK-4830 is a Monoclonal Antibody owned by Merck & Co, and is involved in 13 clinical trials, of which 12 are ongoing, and 1 is planned.

MK-4830 elicits antineoplastic property by targeting immunoglobulin-like transcript 4. Checkpoints are employed by the body to prevent a deadly immune response and these checkpoint mechanisms can also be used by cancer cells as a defence against immune attack. An antibody binds to these checkpoint molecules to help immune cells overcome the checkpoint defences of cancer cells.

The revenue for MK-4830 is expected to reach a total of $201m through 2038. This change impacts the valuation of this asset and is an important factor to understand the current value of the drug in a clinical process. View the complete picture with the MK-4830 NPV Report.

MK-4830 was originated by Celexion and is currently owned by Merck & Co.

MK-4830 Overview

MK-4830 is under development for the treatment of solid tumors such as metastatic pancreatic adenocarcinoma, colorectal cancer, glioblastoma multiforme, metastatic renal cell carcinoma (RCC), recurrent or metastatic head and neck squamous cell cancer (HNSCC) of the oral cavity, oropharynx, hypopharynx, and/or larynx, mesothelioma, metastatic breast cancer, triple-negative breast cancer, high-grade epithelial ovarian, fallopian tube or primary peritoneal carcinoma, metastatic pancreatic adenocarcinoma, metastatic non-small-cell lung cancer, metastatic non-squamous non-small-cell lung cancer, small cell lung cancer, renal cell cancer and recurrent and/or metastatic gastric or gastroesophageal junction adenocarcinoma. The drug candidate comprises of human IgG4 monoclonal antibody and is developed based on retrocyte display technology and secant yeast display technology.  The drug candidate acts by targeting immunoglobulin like transcript 4.

Merck & Co Overview

Merck & Co (Merck) is a biopharmaceutical company focused on the discovery, development, manufacturing and marketing of prescription medicines, biologic therapies, vaccines and animal health products. It offers prescription products for therapy areas related to cardiovascular, cancer, immune disorders, infectious, respiratory and women’s diseases, and diabetes. 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 known as MSD outside the US and Canada and is headquartered in Kenilworth, New Jersey, the US.

The company reported revenues of (US Dollars) US$48,704 million for the fiscal year ended December 2021 (FY2021), an increase of 17.3% over FY2020. In FY2021, the company’s operating margin was 25.7%, compared to an operating margin of 12% in FY2020. In FY2021, the company recorded a net margin of 26.8%, compared to a net margin of 17% in FY2020. The company reported revenues of US$14,959 million for the third quarter ended September 2022, an increase of 2.5% over the previous quarter.

Quick View – MK-4830

Report Segments
  • Innovator
Drug Name
  • MK-4830
Administration Pathway
Therapeutic Areas
  • Oncology
Key Companies
  • Sponsor Company: Merck & Co
  • Originator: Celexion
Highest Development Stage
  • Phase II

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, potential applicable patients, drug margins, company expenses, and pricing estimates. 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 rNPV, 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.