The global cancer
gene therapy market is expected to attain lucrative growth in the
forecast period mainly due to rise in funding for R&D activities for cancer
gene therapy, increasing prevalence of cancer, and rapid technological
advancements being witnessed in the market. Gene therapy is used for the
treatment of cancer, where a functional gene is inserted into the cells of a
patient to correct a genetic abnormality and provide new function to the cells.
Gene transfer therapies holds
the largest share in the global market and the category is also expected to
witness fastest growth in demand during the forecast period. The key end users in
the cancer gene therapy market include hospitals, oncology institutes,
biotechnological companies and clinical research laboratories.
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According to the American
Cancer Society (ACS), around 1,688,780 new cancer cases are expected to be
diagnosed, in the U.S., in 2017. Almost, 600,920 Americans are expected to die
of cancer in 2017, indicating that around 1,650 cancer patients are dying per
day, due to the disease. In 2013, the World Health Organization (WHO) launched
the Global Action Plan for the Prevention and Control of Noncommunicable
Diseases 2013-2020, that aimed at reducing the rate of premature mortality from
cancer, cardiovascular diseases, diabetes, and chronic respiratory diseases by
25%, by 2025.
North America is expected to
lead the global cancer gene therapy market throughout the forecast period
(2018–2023) followed by the Europe. This is mainly due to strong healthcare
infrastructure and high expenditure in R&D in North America.
Additionally, emerging
countries, such as India, and Korea, are characterized by a huge patient pool,
which can be attributed to the increasing burden of non-communicable diseases
and rising geriatric population in these countries. According to the WHO,
chronic diseases are estimated to increase by 57% by 2020, globally.
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The players in the global
market have been receiving approvals for the cancer gene therapy treatments to
provide better treatment to cancer patients, thus increasing their market
share. For instance, in December 2017, Celgene Corporation and bluebird bio,
Inc. announced the updated results from the ongoing CRB-401 Phase 1 clinical
study of bb2121, an investigational anti-B-cell maturation antigen (BCMA) CAR T
cell therapy, in 21 patients suffering with late-stage relapsed/refractory
multiple myeloma.
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