The Viral Vectors and Plasmid DNA Manufacturing Market Overview and Analysis by Vector Type (Plasmid DNA, Viral Vector, Non-viral Vector), by Disease Type(Cancer, Genetic Disorder, and Infectious Disease), by Applications (Antisense RNAi Therapy,Gene Therapy,Cell Therapy, Vaccinology, and Research), by Workflow (Upstream Processing and Downstream Processing), by End User (Pharmaceutical and Biopharmaceutical Companies, and Research Institutes) and by Region (North America, Europe, Asia-Pacific, and Rest of the World) - Forecast till 2032

Viral Vectors and Plasmid DNA Manufacturing Market Size was valued at USD 0.3 billion in 2022 and is projected to grow from USD 0.35 Billion in 2023 to USD 1.1 billion by 2030, exhibiting a compound annual growth rate (CAGR) of 16.1% during the forecast period (2023 - 2032).

The global viral vector and plasmid DNA manufacturing market is driven by the rising demand for viral vector-based vaccines for infectious diseases and a shift in the treatment paradigm of several life-threatening diseases through advanced the rapies and technological advancements in viral vectors.

Severalkey players are dominating the global viral vector and plasmid DNA manufacturing market, contributing to a significant revenue share. The prominent players are involved in organic and inorganic strategies such asagreements, new product development launches, mergers acquisitions, joint ventures, collaborations, partnershipsand geographic expansions, to sustaintheir market positions.For instance,in  April 2021, Albumedix (UK) extended itsresearch collaboration with Cobra Biologics (US) for the upstream and downstream processing of AAV and lentiviral vector. The collaboration was intended for stability enhancement and process optimization by the company.

Regional Analysis

Based on region, North America is expected to dominate the global viral vector and plasmid DNA manufacturing market size in 2020. Factors such as the presence of a largenumber of centers and institutes engaged in the RD of advanced therapies and key players in this region involved in new product launches, expansion, acquisition,and strategic collaborations are driving the market growth. For instance, In March 2021, ABECMA (idecabtagenevicleucel), a lentivirus-based gene therapy, received the US FDA approvalto treat R/R multiple myeloma.

Europe is expected to hold the second-largest position in the global viral vector and plasmid DNA manufacturing market size in 2021. Key factors attributing to the market growth are the increasing RD spendings to enhance research activities in the healthcare industry. For instance, according to the data published in Eurostat in 2018, the EU spent approximately 348 USD million on Research Development. The RD expenditure as a percentage of GDP was 2.18% in 2018, compared to 1.87 % in 2008.

Asia-Pacific is anticipated to be the fastest-growing regional market over the assessment period due to the increasing prevalence of target disorders and healthcare needs. Furthermore, the growth of the market in the rest of the world is attributed to the rising penetration of advanced healthcare technologies in research organizations focused on viral vector and plasmid DNA manufacturing incountries such as Saudi Arabia and the UAE. Developing countries such as Argentina, Brazil, and Colombia, among others in Latin America, are also key contributors to the growth of the market.

Segmentation

The global viral vectors and plasmid manufacturing market has been segmented intovector type, workflow, disease type, application, and end user.

By vector type, the market is segmented into plasmid DNA, viral vector, non-viral vector. The viral vector segment represented the dominant share in 2020, owing to the rising prevalence of target diseases and disorders, the effectiveness of viral vectors in gene therapy delivery, and rising research activities focused on viral vector-based gene cell therapies.

Based on the workflow, the market is segmented into upstream processing, downstream processing. Downstream processing dominated the market for viral vectors and plasmid DNA manufacturing in 2020. Increasing adoption of downstream processing methods to help reduce contaminants originating from host cells or culture media is driving the market growth of this segment.

On the basis of disease type, the market has been segmented into genetic disorders, cancer, infectious diseases, and others. Cancer held the largest market share in 2020 due to the increasing prevalence of cancer cases globally. Furthermore, geneticdisordersare expected to be the fastest-growing segment.

Based on application, the market is segmented into antisense RNAi therapy, gene therapy, cell therapy, vaccinology, and research. The vaccinology segment dominated the market in 2020, owing tothe rising adoption of viral vectors in vaccine development.

By end user, pharmaceutical biopharmaceutical companies and research institutes. Research institutes held a major share in the global viral vectors and plasmid DNA manufacturing market. The increasing number of research centers in gene and cell therapy coupled with rising research activities for viral vectors and plasmid DNA is projected to increase the demand for viral vectors in the global market.

Key Players

Some of the key players in the global Viral Vector and Plasmid DNA Manufacturing market are Cognate BioServices, Inc. (US), Catalent Pharma Solutions (US), Fujifilm Holdings Corporation (Japan), Johnson Johnson (US), Sanofi Corporation (France), F. Hoffmann-LA Roche Ltd (Switzerland), 4D Molecular Therapeutics (US), Sirion Biotech GmbH (Germany), Voyager Therapeutics (US), Thermo Fisher Scientific, Inc. (US), Gene Therapy Catapult (UK), UniQure (Netherlands), MassBiologics (US), Renova Therapeutics (US) and Shenzhen SiBionoGeneTech Co., Ltd (China).

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