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Malignant pleural mesothelioma is a rare and aggressive cancer that develops in a thin layer of tissue surrounding the lungs known as pleura. MPM is caused by the inhalation of microscopic asbestos fibers. Once the person inhales asbestos dust, the human body struggles to eliminate the needle-like fibers of asbestos from lungs. According to the NIH, the incidences of MPM in Europe is about 20 per million inhabitants, and it is increasing globally. This will subsequently demand the need for the development of innovative treatments for malignant pleural mesothelioma, driving the market’s growth.
Furthermore, according to the CDC, the median survival of MPM patients is approximately one year from the time of diagnosis. Also, the global estimated incidences of MPM is around 2,000-3,000 cases annually, and the number is likely to increase owing to the exposure to asbestos, in turn, will influence the malignant pleural mesothelioma market growth in the forthcoming years.
According to this pipeline analysis report, most of the drug development molecules in the pipeline are being developed for the treatment of malignant pleural mesothelioma. Our market research analysts have also identified that most of these molecules are in the pre-clinical development stage and a considerable number of molecules have been discontinued from development.
This pipeline analysis report provides a detailed analysis of the companies that are involved in the drug development for malignant pleural mesothelioma. In addition to providing information on the various stages of molecules developed by companies for different indications, this pipeline analysis report also provides information about the drug development discontinued by companies.
Some of the companies covered in this pipeline analysis report are –
The IV route of administration (ROA) involves the application of the drug directly into a vein.
Malignant pleural mesothelioma industry analysis, all the molecules in the drug development for malignant pleural mesothelioma are being developed as monotherapy drugs and most of these molecules are in the pre-clinical stage of development.
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PART 01: EXECUTIVE SUMMARY
PART 02: SCOPE OF THE REPORT
PART 03: RESEARCH METHODOLOGY
PART 04: INTRODUCTION
PART 05: MAJOR REGULATORY AUTHORITIES
PART 06: PIPELINE LANDSCAPE
PART 07: COMPARATIVE ANALYSIS
PART 08: INDICATION ANALYSIS
PART 09: THERAPEUTIC ASSESSMENT (THERAPY BASED)
PART 10: THERAPEUTIC ASSESSMENT (ROA BASED)
PART 11: THERAPEUTIC ASSESSMENT BY TARGET
PART 12: KEY COMPANIES
PART 13: APPENDIX
Research Framework
Technavio presents a detailed picture of the market by way of study, synthesis, and summation of data from multiple sources. The analysts have presented the various facets of the market with a particular focus on identifying the key industry influencers. The data thus presented is comprehensive, reliable, and the result of extensive research, both primary and secondary.
INFORMATION SOURCES
Primary sources
Secondary sources
DATA ANALYSIS
Data Synthesis
Data Validation
REPORT WRITING
Qualitative
Quantitative
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