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The 'Global and Southeast Asia Gefitinib Tablet Industry, 2013-2023 Market Research Report' is a professional and in-depth study on the current state of the global Gefitinib Tablet industry with a focus on the Southeast Asia market.
The report provides key statistics on the market status of the Gefitinib Tablet manufacturers and is a valuable source of guidance and direction for companies and individuals interested in the industry.Firstly, the report provides a basic overview of the industry including its definition, applications and manufacturing technology.
Then, the report explores the international and Southeast Asia major industry players in detail.
In this part, the report presents the company profile, product specifications, capacity, production value, and 2013-2018 market shares for each company.
Through the statistical analysis, the report depicts the global and Southeast Asia total market of Gefitinib Tablet industry including capacity, production, production value, cost/profit, supply/demand and Southeast Asia import/export.
The total market is further divided by company, by country, and by application/type for the competitive landscape analysis.
Non-small Cell Lung Cancer (NSCLC) is the most common type of lung cancer.
Gefitinib (Brand Iressa by AstraZeneca) a targeted therapy (called kinase inhibitor) works by blocking the EGFR protein that helps cancer cell growth.Early clinical trials for gefitinib were designed prior to the discovery of the EGFR mutation.With the long-term use of gefitinib, few of the patients suffering from NSCLC responded well with a low rate of toxicity.
For the above conclusion, 191 patients (enrolled in US Iressa Clinical Access Program) with advanced NSCLC were taken into consideration, and their results have been assessed and analysed by researchers in order to come up with the above conclusion.Gefitinib / Iressa medication cost information Among the 191 patients, 79 underwent a retrospective chart review that depicted survival, safety, and demographic data.
The median duration of the study was 11 years 1 months and 6 days, with a survival rate of 86% at 10 years and 59% at 15 years.Some serious adverse events were observed in 64 patients in the study; the majority of which were comorbidities and underlying disease and only 3 patients had treatment-related adverse events.The US FDA had approved gefitinib (Brand Iressa by AstraZeneca) for the treatment of Non-Small Cell Lung Cancer (NSCLC) in 2003.
But now the US FDA has approved a test for the gene mutations in NSCLC which contains a specific mutation in the EGFR gene.The approval was given on the basis of a study conducted with the help of 106 people who are suffering from non-small cell lung cancer with EGFR-mutated gene and they haven’t received any prior treatment related to it before.
After the completion of the study, it was founded that half of the patients in the study have their tumours reduced/shrink or disappear, just by using gefitinib (Brand Iressa by AstraZeneca).
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