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The global lentiviral vectors market size was valued at USD 202.81 million in 2023, driven by the increasing prevalence of diabetes and increasing research and development activities across the globe. The market size is anticipated to grow at a CAGR of 15.1% during the forecast period of 2024-2032 to achieve a value of USD 719.05 million by 2032.
Lentiviral vectors are specialized instruments used in gene therapy and genetic engineering. They originated from a retrovirus family member called lentivirus, a particular class of virus. Given that lentiviruses may infect both proliferating and non-dividing cells, they are beneficial for transferring genetic material into a variety of cell types, including challenging-to-transfect cells like stem cells and neurons.
Lentiviral vectors are lentiviruses that have been modified for the goal of controlled and safe gene delivery. For a variety of purposes, including gene therapy, genetic research, and experimental studies, they can be used to introduce genes or genetic material into target cells.
The global market for lentiviral vectors is witnessing significant growth in the market and is anticipated to keep growing in the coming years as well. Factors such as the increasing research and development activities by key players and a significant shift towards patient centric healthcare are directly driving the lentiviral vectors market growth. Key players across the globe are now taking initiative towards collaborating with each other to produce more effective treatments of genetic disorders caused by single-gene mutations, such as severe combined immunodeficiency (SCID), hemophilia, muscular dystrophy, and certain types of blindness. The success of recent clinical trials using lentiviral vectors for certain genetic disorders, as it provides reliable techniques to deliver therapeutic genes into cells, has further fueled the demand for lentiviral vectors in the global market.
In response to the growing demand for starting materials for use in cell therapy, a leading cell therapy company based in the United States is creating allogeneic genetically modified CAR-NK cells using umbilical cord blood and has announced a collaboration agreement with California-based regenerative therapeutics company StemCyte. This collaboration is expected to further propel market growth as it is expected to cater as a catalyst for advancements and growth in the market.
Market Breakup by Components
Market Breakup by Indications
Market Breakup by Applications
Market Breakup by Region
The increasing geriatric population worldwide is a major factor driving the market growth. The increasing prevalence of chronic diseases, such as diabetes, are also contributing to the market growth due to the need for gene therapy improving glycemic control and reducing the need for insulin therapy.
According to WHO, diabetes was the cause of death of over 1.5 million people aged below 70 years of age in 2020. Lentiviral vectors are used to cure a wide range of disorders that are genetically influenced, such as cancer immunotherapy, neurodegenerative disease, hematopoietic disorders, inherited metabolic disorders, HIV/AIDS research, vaccine development, and rare diseases.
Lentiviral vectors act as prominent tools to study gene function, expression, and regulation. The increased demand for such tools with increasing awareness about the potential of lentiviral vectors is directly contributing to the rising global lentiviral vectors market share.
Additionally, due to the strong ability of lentiviral vectors in used in developing personalized treatments for patients by targeting specific genetic mutations accounting for diseases is also driving the market growth. The continuous ongoing research and development activities on lentiviral vectors are being explored for innovative therapeutic approaches, including cancer immunotherapy, neurodegenerative disease treatment, and regenerative medicine which is further propelling the market growth.
The key features of the market report include patent analysis, grants analysis, clinical trials analysis, funding and investment analysis, partnerships, and collaborations analysis by the leading key players. The major companies in the market are as follows:
REPORT FEATURES | DETAILS |
Base Year | 2023 |
Historical Period | 2017-2023 |
Forecast Period | 2024-2032 |
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*While we strive to always give you current and accurate information, the numbers depicted on the website are indicative and may differ from the actual numbers in the main report. At Expert Market Research, we aim to bring you the latest insights and trends in the market. Using our analyses and forecasts, stakeholders can understand the market dynamics, navigate challenges, and capitalize on opportunities to make data-driven strategic decisions.*
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The market attained a value of about USD 202.81 million in 2023, driven by the increasing demand for precision and personalized treatment across the globe.
The market is anticipated to grow at a CAGR of 15.1% during the forecast period of 2024-2032, likely to reach a market value of USD 719.05 million by 2032.
The increasing prevalence of chronic disease, such as diabetes, is among the major factors driving the market growth. The significant shift towards personalized and precision medicine are also among the major factors driving the market growth.
The increasing number of research and development activities by key players is the major trend influencing the market growth.
The major regions of the market include North America, Europe, Asia Pacific, Latin America, Middle East and Africa. North America is currently leading the global market.
The components include lentiviral promoter, lentiviral fusion tags, and lentivirus packaging systems.
Indications include cancer, genetic disorders, infectious diseases, and veterinary disease, among others.
They find wide applications in gene therapy and vaccinology.
Key players involved in the market are Cobra Biologics Limited, Sirion-Biotech GmbH, Merck KGaA, FinVector Oy, Oxford Biomedica, OriGene Technologies, Inc., Sino Biological Inc., Cell Biolabs, Inc., Batavia Biosciences B.V., and Lonza.
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