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“"IMFINZI Emerging Drug Insight and Market Forecast - 2032" report provides comprehensive insights about IMFINZI for malignant pleural mesothelioma (MPM) in the seven major markets. A detailed picture of the IMFINZI 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 IMFINZI 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 IMFINZI market forecast analysis for MPM in the 7MM, SWOT, analysts' views, comprehensive overview of market competitors, and brief about other emerging therapies in MPM.
IMFINZI (durvalumab; MEDI4736)-a product of AstraZeneca, is a human immunoglobulin G1 kappa (IgG1¥ê) monoclonal antibody. IMFINZI is a prescription medicine used to treat adults with a type of lung cancer called non-small cell lung cancer (NSCLC), extensive-stage small cell lung cancer (ES-SCLC), and for people with previously treated, locally advanced or metastatic urothelial carcinoma (bladder cancer). IMFINZI is administered intravenously and works by blocking the interaction of PD-L1 with PD-1 and CD80. This blockade of PD-L1/PD-1 and PD-L1/CD80 interactions releases the inhibition of immune responses without inducing antibody-dependent cell-mediated cytotoxicity (ADCC).
PrECOG, a cancer research group, formed as a not-for-profit limited liability company in 2006 by the ECOG Research and Education Foundation, with funding from AstraZeneca, has initiated clinical trials investigating IMFINZI in the first-line treatment in advanced pleural mesothelioma patients. Currently, two clinical trials are ongoing, which are NCT02899195 (PrE0505) and NCT04334759 (DREAM3R).
PrE0505 is a single-arm, open-label Phase II study in which durvalumab is under investigation in combination with standard chemotherapy. Pemetrexed and cisplatin will be given for up to six 3-week cycles with the addition of concurrent durvalumab dosed every 3 weeks. This study is being conducted in the United States and met its primary endpoint. In addition, DREAM3R is an international, open-label, multicenter, Phase III study where patients will be randomized 2:1 to receive durvalumab with standard chemotherapy or to receive standard chemotherapy alone.
The report provides insights into:
The report is built using data and information sourced primarily from internal databases, primary and secondary research and in-house analysis by DelveInsight's 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.
IMFINZI Analytical Perspective by DelveInsight
This report provides a detailed market assessment of IMFINZI 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 2026 to 2032.
The report provides the clinical trials information of IMFINZI for MPM covering trial interventions, trial conditions, trial status, start and completion dates.
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