KEYTRUDA Drug Insight and Market Forecast - 2032

This “KEYTRUDA Drug Insight and Market Forecast - 2032” report provides comprehensive insights about KEYTRUDA for malignant pleural mesothelioma (MPM) in the seven major markets. A detailed picture of the KEYTRUDA for MPM in the 7MM, i.e., the United States, EU4 (Germany, France, Italy, and Spain) and the United Kingdom, and Japan for the study period 2019 -2032 is provided in this report along with a detailed description of the KEYTRUDA for MPM. The report provides insights about mechanism of action, dosage and administration, as well as research and development including regulatory milestones, along with other developmental activities. Further, it also consists of future market assessments inclusive of the KEYTRUDA market forecast analysis for MPM in the 7MM, SWOT, analysts' views, comprehensive overview of market competitors, and brief about other emerging therapies in MPM.

Drug Summary

KEYTRUDA (pembrolizumab) is an anti-PD-1 immunotherapy and it works with your immune system to help fight certain cancers. KEYTRUDA is a humanized monoclonal antibody that blocks the interaction between PD-1 and its ligands, PD-L1 and PD-L2, thereby activating T lymphocytes which may affect both tumor cells and healthy cells. Merck has the industry's largest immuno-oncology clinical research program. There are currently more than 1,200 trials studying KEYTRUDA across a wide variety of cancers and treatment settings (Merck Sharp & Dohme Corp, 2020). This drug has been approved by the US FDA and by the European Medicines Agency (EMA) to treat several types of cancer.

The immunotherapy drug pembrolizumab (KEYTRUDA) has shown effectiveness in mesothelioma patients through clinical trials and the Merck Access Program. In June 2020, the US Food and Drug Administration approved its use as a second-line treatment for cancer patients with high tumor mutation burden, or TMB-H, including late-stage mesothelioma patients. The FDA concluded that late-stage mesothelioma patients whose disease has progressed following prior treatment and who have no viable alternative options are eligible to receive KEYTRUDA.

Scope of the Report

The report provides insights into:

• A comprehensive product overview including the KEYTRUDA description, mechanism of action, dosage and administration, research and development activities in malignant pleural mesothelioma (MPM).
• Elaborated details on KEYTRUDA regulatory milestones and other development activities have been provided in this report.
• The report also highlights the KEYTRUDA research and development activities in MPM across the United States, Europe and Japan.
• The report also covers the patents information with expiry timeline around KEYTRUDA.
• The report contains forecasted sales of KEYTRUDA for MPM till 2032.
• Comprehensive coverage of the late-stage emerging therapies for MPM.
• The report also features the SWOT analysis with analyst views for KEYTRUDA in MPM.

Methodology

The report is built using data and information sourced primarily from internal databases, primary and secondary research and in-house analysis by the team of industry experts. Information and data from the secondary sources have been obtained from various printable and nonprintable sources like search engines, news websites, global regulatory authorities websites, trade journals, white papers, magazines, books, trade associations, industry associations, industry portals and access to available databases.

KEYTRUDA Analytical Perspective

In-depth KEYTRUDA Market Assessment

This report provides a detailed market assessment of KEYTRUDA for malignant pleural mesothelioma (MPM) in the seven major markets, i.e., the United States, EU4 (Germany, France, Italy, and Spain) and the United Kingdom, and Japan. This segment of the report provides forecasted sales data from 2023 to 2032.

KEYTRUDA Clinical Assessment

The report provides the clinical trials information of KEYTRUDA for MPM covering trial interventions, trial conditions, trial status, start and completion dates.

Report Highlights

• In the coming years, the market scenario for malignant pleural mesothelioma (MPM) is set to change due to the extensive research and incremental healthcare spending across the world; which would expand the size of the market to enable the drug manufacturers to penetrate more into the market.
• The companies are developing therapies that focus on novel approaches to treat/improve the disease condition, assess challenges, and seek opportunities that could influence KEYTRUDA dominance.
• Other emerging products for MPM are expected to give tough market competition to KEYTRUDA and launch of late-stage emerging therapies in the near future will significantly impact the market.
• A detailed description of regulatory milestones, and developmental activities, provide the current development scenario of KEYTRUDA in MPM.
• This in-depth analysis of the forecasted sales data of KEYTRUDA from 2023 to 2032 will support the clients in the decision-making process regarding their therapeutic portfolio by identifying the overall scenario of the KEYTRUDA in MPM.

Key Questions

• What is the product type, route of administration and mechanism of action of KEYTRUDA?
• What is the clinical trial status of the study related to KEYTRUDA in malignant pleural mesothelioma (MPM) and study completion date?
• What are the key collaborations, mergers and acquisitions, licensing and other activities related to the KEYTRUDA development?
• What are the key designations that have been granted to KEYTRUDA for MPM?
• What is the forecasted market scenario of KEYTRUDA for MPM?
• What are the forecasted sales of KEYTRUDA in the seven major countries, including the United States, Europe (Germany, France, Italy, Spain, and the United Kingdom), and Japan?
• What are the other emerging products available and how are these giving competition to KEYTRUDA for MPM?
• Which are the late-stage emerging therapies under development for the treatment of MPM?

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