QuTEM's Breakthrough in Gene Therapy Analysis
QuTEM has achieved a significant milestone in enhancing gene therapy quality.

Sammanfattning
QuTEM's innovative electron microscopy technology is now a reliable standard for gene therapy analysis, marking a pivotal moment in the sector.
Stockholm-based QuTEM has reached a critical milestone in its mission to improve the quality and safety of next-generation medicines. A new peer-reviewed study, published in Molecular Therapy: Methods & Clinical Development, highlights QuTEM’s innovative electron microscopy technology and image analysis as a reliable and precise standard for analyzing the building blocks of gene therapy.
This breakthrough originates from QuTEM’s proprietary technology. In collaboration with Viralgen SL, a leader in the manufacturing of gene therapy vectors, Viralgen applied complementary analytical methods that further confirmed QuTEM’s breakthrough. The study demonstrated that QuTEM’s method is more reliable than several established techniques, underscoring its potential as a new benchmark for quality control in gene therapy.
Peter Almberg, Chairman of Katalysen Ventures, expressed his enthusiasm: 'QuTEM is a real success story in our portfolio. We have observed how QuTEM has evolved from an imaging company to, today, being an analytics company with its own proprietary software developed in-house, Gridsee, and immense amounts of unique data collected over 15+ years. As investors, we see that from such a position QuTEM is uniquely placed to extract increasing value from its analytical capabilities and insights. An undeniable prerequisite is first to achieve gold-standard status in the industry.'
Josefina Nilsson, CEO of QuTEM, added, 'This recognition confirms QuTEM’s role as a potential golden standard for quality control in gene therapy. The fact that Viralgen, a leader in AAV manufacturing, together with other major pharmaceutical companies, have decided to outsource an essential part of their quality control to us demonstrates that QuTEM’s innovative approach is already embraced by the industry’s most respected players.'
For investors, this milestone highlights QuTEM’s growing relevance in a rapidly expanding global market. The gene therapy sector is forecast to see strong growth in the coming decade, and demand for reliable quality control tools is set to rise sharply. With confirmation from both the scientific community and leading players in gene therapy manufacturing, QuTEM is well positioned to play a central role in ensuring the safety, consistency, and success of future therapies.
Peter Almberg concludes, 'QuTEM's long-term trajectory is extremely exciting for investors. It is one of our core investments, and our holding is approximately 15% of the company. The fact that the company is now profitable, while at the same time adding a new sales model that significantly increases global scalability, makes QuTEM’s outlook all the more compelling.'
Given QuTEM's advancements and strategic positioning, investors should consider holding their current investments as the company continues to establish itself as a leader in gene therapy quality control.
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Sammanfattning
Stockholmsbaserade QuTEM har nått ett viktigt steg i sitt uppdrag att förbättra kvaliteten och säkerheten hos nästa generations läkemedel. En ny studie i Molecular Therapy: Methods & Clinical Development visar att QuTEM:s innovativa elektronmikroskopiteknologi och bildanalys är en tillförlitlig och precis standard för att analysera byggstenarna i genterapi. I samarbete med Viralgen SL, en ledare inom tillverkning av genterapivektorer, har QuTEM:s metod visat sig vara mer tillförlitlig än flera etablerade tekniker, vilket pekar på dess potential som en ny standard för kvalitetskontroll inom genterapi. Josefina Nilsson, VD för QuTEM, noterar att erkännandet bekräftar QuTEM:s roll som en potentiell guldstandard för kvalitetskontroll inom genterapi, och att stora läkemedelsföretag har börjat outsourca en viktig del av sin kvalitetskontroll till QuTEM. Detta framhäver företagets växande relevans på en snabbt växande global marknad för genterapi, där efterfrågan på tillförlitliga kvalitetskontrollverktyg förväntas öka kraftigt. QuTEM:s metod erbjuder ett mer exakt sätt att skilja mellan fulla, delvis fyllda och tomma AAV-partiklar, och har utvecklats enligt internationella kvalitetsriktlinjer och opererar under ett GMP-certifikat från den svenska Läkemedelsverket. Deras metod är redan integrerad som en viktig kvalitetskontrollmätning och frigivningstest för genterapiprodukter, vilket stöder både bioteknikinnovatörer och stora läkemedelsföretag.