LONDON--(BUSINESS WIRE)--Technavio has announced their latest pipeline analysis report for malignant pleural mesothelioma. The report comprises an in-depth analysis of the pipeline molecules under investigation within the defined data collection period to treat malignant pleural mesothelioma.
This report by Technavio presents a detailed analysis of the market, including regulatory framework, drug development strategies, recruitment strategies, and key companies that are expected to play an essential role in the growth of the market in the coming years.
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Malignant pleural mesothelioma: Market overview
Malignant pleural mesothelioma (MPM) is a rare and aggressive cancer that develops in a thin layer of tissue surrounding the lungs known as the pleura. As per a research, MPM is the most common form of malignant mesothelioma, accounting for 90%. The primary cause of MPM is the inhalation of microscopic asbestos fibers. Once the person inhales asbestos dust, the body struggles to eliminate the needle-like fibers of asbestos from lungs.
According to a senior analyst at Technavio for research on oncology, “The symptoms of MPM include dyspnea, persistent dry or raspy cough, chest pain, difficulty swallowing also known as dysphagia, and coughing up blood also known as hemoptysis. The incidence of MPM has been increasing since the middle of the 20th century. There are marked variations in the incidence of MPM within and between nations.”
Malignant pleural mesothelioma: Segmentation analysis
This market research report segments the malignant pleural mesothelioma market based on therapies employed (monotherapy and combination therapy), RoA (IV, oral, intrapleural, intratumoral, subcutaneous, intratumoral/ subcutaneous, and undisclosed), therapeutic modality (monoclonal antibody, small molecule, biological, cell therapy, oncolytic virus, recombinant fusion protein, and gene therapy), targets for drugs under development (PD-1, tubulin, tyrosine kinase, PD-1/CTLA-4 inhibitor, arginine deaminase, stemness of CSC, CD13 receptor isoform, CD26 antigen, CD8+T-cell, FAK, FGFs, interferon beta, megakaryocytic potentiating factor, mesothelin, N2 position of guanine in DNA, TEA domain, WT1, thymidine kinase, and undisclosed), MoA (PD-1 inhibitor, immunostimulant, thymidine kinase expression stimulants, tubulin polymerization inhibitor, tyrosine kinase inhibitor, WT1 inhibitor, PD-1/CTLA-4 inhibitor, alkylating agent, arginine deaminase replacement, stemness of CSC inhibitor, capillary permeability modulator, CD26 antigen inhibitor, FGF inhibitor, FAK inhibitor, interferon beat stimulant, megakaryocytic potentiating factor inhibitor, mesothelin inhibitor, YAP-TEAD inhibitor), and recruitment status (recruiting, active not recruiting, completed, active, enrolling by invitation, and undisclosed).
Monotherapy includes the use of a single drug to treat a disorder or a disease. In the current pipeline, 15 molecules that are under investigation are monotherapy.
IV delivers drugs directly into a vein. In the current pipeline, 16 molecules are administered by IV route.
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Some of the key topics covered in the report include:
Scope of the Report
Drug Development Landscape
- Drugs under development
- Indications coverage
Drug Development Strategies
- Therapies employed
- Therapeutic modality
- Geographical coverage
- Recruitment status
- Recruitment volume
- Type of players
- Company Overview
Discontinued or Dormant Molecules
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