{"id":457490,"date":"2021-03-15T08:08:08","date_gmt":"2021-03-15T12:08:08","guid":{"rendered":"http:\/\/www.marketnewsdesk.com\/?p=457490"},"modified":"2021-03-15T08:08:08","modified_gmt":"2021-03-15T12:08:08","slug":"maravai-lifesciences-offers-end-to-end-mrna-production-with-the-launch-of-trilink-biotechnologies-plasmid-dna-manufacturing-services","status":"publish","type":"post","link":"https:\/\/www.marketnewsdesk.com\/index.php\/maravai-lifesciences-offers-end-to-end-mrna-production-with-the-launch-of-trilink-biotechnologies-plasmid-dna-manufacturing-services\/","title":{"rendered":"Maravai LifeSciences Offers End-to-End mRNA Production with the Launch of TriLink BioTechnologies’ Plasmid DNA Manufacturing Services"},"content":{"rendered":"

\nNew integrated offering will help to meet expected increases in global demand by simplifying and accelerating production of GMP-grade mRNA product for downstream vaccine and therapeutic manufacturing
\n<\/h2>\n
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SAN DIEGO, March 15, 2021 (GLOBE NEWSWIRE) — Maravai LifeSciences<\/a> (NASDAQ: MRVI), a global provider of life science reagents and services to researchers and biotech innovators, has expanded its contract development and manufacturing organization (CDMO) capabilities at TriLink BioTechnologies<\/a> (\u201cTriLink\u201d) with the launch of its plasmid DNA (pDNA) manufacturing services<\/a>. TriLink\u2019s new plasmid services empower customers with the ease of an end-to-end messenger RNA (mRNA) solution from a single partner \u2013 with Current Good Manufacturing Practice (cGMP) capabilities from plasmid production through final release testing.<\/p>\n

\u201cThe ability to work with an expert, end-to-end manufacturing partner such as TriLink comes at a critical time for the pharmaceutical industry, when global demand for mRNA is expected to exceed the availability of GMP-quality plasmid DNA,\u201d said Carl Hull, CEO of Maravai LifeSciences. \u201cBy integrating pDNA production with our pioneering mRNA services, we believe TriLink will dramatically reduce production timelines and overcome tech transfer bottlenecks by reducing or eliminating plasmid sourcing wait-times that could otherwise last months.\u201d<\/p>\n

Plasmid is a critical raw material for a wide variety of therapeutic needs, such as novel gene editing and cell therapy applications, including CAR-T therapies<\/a>, as well as for mRNA vaccine technologies, like those enabling several in-market and emerging Covid-19 vaccines.<\/p>\n

By also enabling customers with its revolutionary CleanCap\u00ae<\/sup><\/a> mRNA capping technology and more than two decades of specialist experience manufacturing modified nucleotides, TriLink seeks to further optimize mRNA production and help accelerate customers\u2019 project timelines.<\/p>\n

\u201cLeveraging our deep mRNA knowledge and expertise, we seek to help our customers to manage the complexities, minimize the risks, and streamline the design process to and through clinical trials,\u201d added Brian Neel, Chief Operating Officer of TriLink BioTechnologies.<\/p>\n

TriLink\u2019s pDNA capabilities offer manufacturing for GMP-grade plasmid, and can be customized with our flexible GMPLink\u2122 grade to meet customer specific clinical needs. Its 118,000 square foot, state-of-the-art manufacturing facility includes 7 custom designed GMP suites dedicated to plasmid development and production, which enables TriLink to support customer programs from milligram through multigram scales.<\/p>\n

In addition, TriLink\u2019s plasmid manufacturing suites utilize leading automation and control platforms, including automated ultrafiltration and diafiltration processes. Analytical testing and mRNA production capabilities are also conveniently available onsite.<\/p>\n

\u201cWe\u2019re meeting growing customer needs for a one-stop shop for plasmid and mRNA development and manufacturing services,\u201d adds COO Brian Neel. \u201cCustomers have been very positive about our end-to-end offering thus far, and we look forward to doing even more to support our customers going forward.\u201d<\/p>\n

To learn more about Maravai LifeSciences, visit\u00a0www.maravai.com<\/strong><\/a>. To learn more about TriLink BioTechnologies and the new plasmid manufacturing services offering, visit\u00a0https:\/\/www.trilinkbiotech.com\/plasmid-manufacturing<\/strong><\/a>.<\/p>\n

\n About Maravai<\/strong>\n <\/p>\n

Maravai is a leading life sciences company providing critical products to enable the development of drug therapies, diagnostics, novel vaccines and support research on human diseases. Maravai\u2019s companies are leaders in providing products and services in the fields of nucleic acid synthesis, bioprocess impurity detection and analysis, and protein labeling and detection to many of the world’s leading biopharmaceutical, vaccine, diagnostics, and cell and gene therapy companies.<\/p>\n

For more information about Maravai LifeSciences, visit www.maravai.com<\/a>.\u00a0<\/p>\n

\n About TriLink BioTechnologies<\/strong>\n <\/p>\n

TriLink BioTechnologies, part of Maravai LifeSciences, is a CDMO helping life science leaders and innovators overcome challenges in the synthesis and scale-up of nucleic acids, NTPs and mRNA capping analogs with scale-up expertise and unique mRNA production capabilities, including its proprietary CleanCap\u00ae<\/sup>\u00a0mRNA capping technology. TriLink continues to expand its cGMP and general manufacturing capacity at its new global headquarters to support mRNA, oligonucleotide & plasmid therapeutic, vaccine and diagnostic customers.\u00a0www.trilinkbiotech.com<\/strong><\/a><\/p>\n

\n Forward-looking Statements <\/strong>\n <\/p>\n

This press release contains \u201cforward-looking statements\u201d within the meaning of the safe harbor provisions of the U.S. Private Securities Litigation Reform Act of 1995. Investors are cautioned that statements in this press release which are not strictly historical statements constitute forward-looking statements, including, without limitation, statements regarding the advantages of an end-to-end mRNA solution from a single supplier, demand for mRNA, demand for GMP-quality plasmid DNA, and advantages of CleanCap mRNA technology constitute forward-looking statements and are identified by words like \u201cbelieve,\u201d \u201cexpect,\u201d \u201cmay,\u201d \u201cwill,\u201d \u201cshould,\u201d \u201cseek,\u201d \u201canticipate,\u201d or \u201ccould\u201d and similar expressions. Such forward-looking statements are subject to a number of risks and uncertainties that could cause actual results to differ materially from those anticipated, including, without limitation and uncertainties related to the level of demand for our products and services, continued validation of the safety and effectiveness of our technology, new scientific developments and competition from other products. These and other risks and uncertainties are described in greater detail in the section entitled \u201cRisk Factors\u201d in Maravai\u2019s Prospectus dated November 19, 2020 on file with the U.S. Securities and Exchange Commission. Actual results may differ materially from those contemplated by these forward-looking statements, and therefore you should not rely upon them. These forward-looking statements reflect our current views and we do not undertake to update any of these forward-looking statements to reflect a change in its views or events or circumstances that occur after the date hereof except as required by law.<\/p>\n

\n Contact Information:<\/strong>
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\u00a0<\/p>\n


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Media Contact: Sara Michelmore\r\nMacDougall\r\n+1 781-235-3060\r\nmaravai@macbiocom.com\r\n\r\nInvestor Contact: Deb Hart\r\nMaravai LifeSciences\r\n+ 1 858-988-5917\r\nir@maravai.com<\/pre>\n<\/p><\/div>\n","protected":false},"excerpt":{"rendered":"
New integrated offering will help to meet expected increases in global demand by simplifying and accelerating production of GMP-grade mRNA product for downstream vaccine and therapeutic manufacturing SAN DIEGO, March 15, 2021 (GLOBE NEWSWIRE) — Maravai LifeSciences (NASDAQ: MRVI), a global provider of life science reagents and services to researchers and biotech innovators, has expanded its contract development and manufacturing organization (CDMO) capabilities at TriLink BioTechnologies (\u201cTriLink\u201d) with the launch of its plasmid DNA (pDNA) manufacturing services. TriLink\u2019s new plasmid services empower customers with the ease of an end-to-end messenger RNA (mRNA) solution from a single partner \u2013 with Current Good Manufacturing Practice (cGMP) capabilities from plasmid production through final release testing. \u201cThe ability to work with an expert, end-to-end … <\/p>\n
Continue reading “Maravai LifeSciences Offers End-to-End mRNA Production with the Launch of TriLink BioTechnologies’ Plasmid DNA Manufacturing Services”<\/span><\/a><\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[],"tags":[],"class_list":["post-457490","post","type-post","status-publish","format-standard","hentry"],"yoast_head":"\nMaravai LifeSciences Offers End-to-End mRNA Production with the Launch of TriLink BioTechnologies' Plasmid DNA Manufacturing Services - Market Newsdesk<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.marketnewsdesk.com\/index.php\/maravai-lifesciences-offers-end-to-end-mrna-production-with-the-launch-of-trilink-biotechnologies-plasmid-dna-manufacturing-services\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Maravai LifeSciences Offers End-to-End mRNA Production with the Launch of TriLink BioTechnologies' Plasmid DNA Manufacturing Services - Market Newsdesk\" \/>\n<meta property=\"og:description\" content=\"New integrated offering will help to meet expected increases in global demand by simplifying and accelerating production of GMP-grade mRNA product for downstream vaccine and therapeutic manufacturing SAN DIEGO, March 15, 2021 (GLOBE NEWSWIRE) — Maravai LifeSciences (NASDAQ: MRVI), a global provider of life science reagents and services to researchers and biotech innovators, has expanded its contract development and manufacturing organization (CDMO) capabilities at TriLink BioTechnologies (\u201cTriLink\u201d) with the launch of its plasmid DNA (pDNA) manufacturing services. 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