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Touchlight and GSK sign license agreement for use of enzymatic dbDNA production technology for mRNA manufacturing

An agreement enables GSK access to enzymatic production technology for rapid GMP production of DNA template for mRNA vaccine manufacturing.
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Original story from Biotech Newswire.


HAMPTON, UK, July 23, 2024 / Biotech Newswire / -- Touchlight, an innovation-driven CDMO pioneering enzymatic DNA production to enable the genetic medicine revolution, today announced a license agreement with GSK, a global leader in biopharmaceutical innovation. This agreement grants GSK non-exclusive rights to use Touchlight’s proprietary enzymatic dbDNA™ (doggybone DNA™) technology for the development and production of mRNA-based products.

The license will enable GSK to access the leading technology for rapid and scalable GMP production of DNA, with the potential to accelerate substantially the production of multivalent mRNA vaccines, including for use against seasonal epidemics and pandemic threats. While financial terms of the agreement are undisclosed, the deal includes an upfront payment, ongoing technology access fees, clinical and regulatory milestone payments and royalties on GSK’s mRNA products manufactured with Touchlight’s enzymatic dbDNA.

Touchlight’s dbDNA technology can produce high-purity GMP DNA using an enzymatic process, offering a faster, more scalable alternative to traditional plasmid DNA production. dbDNA is particularly well suited for mRNA vaccine development, as it enables rapid and efficient production of the DNA templates required for mRNA synthesis.

In 2023 Touchlight brought online its state-of-the-art multi-kg production facility, and now has numerous client products that have implemented dbDNA for clinical development, including three with accepted IND/CTAs. In addition to being deployed as both a critical starting material for mRNA production and within AAV products, dbDNA will enter clinical development later in 2024 as an Active Pharmaceutical Ingredient for a therapeutic cancer vaccine, alongside multiple other anticipated INDs across various modalities.

Jonny Ohlson, Executive Chair and Founder of Touchlight, commented on the partnership: “GSK is a global leader in vaccination, and we are delighted they have licensed our proprietary enzymatic dbDNA™ technology for the development and production of their mRNA-based products. The adoption of Touchlight’s enzymatic DNA is gathering pace and becoming an important part of the advanced therapy supply chain. Our technology delivers the speed, scalability and high-quality DNA products that are essential for the next generation of mRNA therapeutics”.

About Touchlight
Touchlight is a privately-owned innovation-driven CDMO based in London, U.K., focused on the provision of DNA services and manufacture of enzymatically produced dbDNA™ (doggybone DNA) to enable the development of genetic medicines. Touchlight provide rapid, enzymatic DNA development and manufacturing for all advanced therapy production, including mRNA, viral and non-viral gene therapy and DNA API. dbDNA is a minimal, linear, covalently closed structure, which eliminates bacterial sequences. Touchlight’s revolutionary enzymatic production platform enables unprecedented speed, scale, and the ability to target genes with a size and complexity that is impossible with current technologies. Clients can be supported from pre-clinical through development and supply, to licencing and tech transfer for use in-house.

About GSK
GSK is a global biopharma company with a purpose to unite science, technology, and talent to get ahead of disease together. Find out more at gsk.com.




This article has been republished from the following materials. Note: material may have been edited for length and content. For further information, please contact the cited source. Our press release republishing policy can be accessed here.

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