QIAGEN expands QIAcuity digital PCR offering with over new 100 assays via GeneGlobe platform
QIAGEN (NYSE: QGEN) has expanded its QIAcuity digital PCR platform with over 100 new assays for cancer research, genetic disorders, and infectious disease surveillance. The company has launched more than 130 new assays in 2024, surpassing its goal and bringing the total to over 2,300 validated assays.
Key developments include:
- New dPCR LNA Mutation and CNV Probe Assays for cancer-relevant mutations
- dPCR Microbial DNA Detection Assays for pathogens and antibiotic resistance
- Expanded portfolio for animal diseases and plant pathogens
QIAcuity has seen strong adoption with over 2,000 placements by end of 2023. An in-vitro diagnostic version is set for launch in fall 2024, targeting clinical applications. QIAGEN is also partnering with pharma companies to develop companion diagnostics on the platform.
QIAGEN (NYSE: QGEN) ha espanso la sua piattaforma di PCR digitale QIAcuity con oltre 100 nuovi test per la ricerca sul cancro, i disturbi genetici e il monitoraggio delle malattie infettive. L'azienda ha lanciato più di 130 nuovi test nel 2024, superando i suoi obiettivi e portando il totale a oltre 2.300 test validati.
I principali sviluppi includono:
- Nuovi test per dPCR LNA per mutazioni e CNV rilevanti per i tumori
- Test di rilevamento del DNA microbico dPCR per patogeni e resistenza agli antibiotici
- Portafoglio ampliato per malattie animali e patogeni vegetali
QIAcuity ha visto una forte adozione con oltre 2.000 collocamenti entro la fine del 2023. Una versione di diagnostica in vitro è prevista per il lancio nell'autunno del 2024, con l'obiettivo delle applicazioni cliniche. QIAGEN sta anche collaborando con aziende farmaceutiche per sviluppare diagnostica complementare sulla piattaforma.
QIAGEN (NYSE: QGEN) ha ampliado su plataforma de PCR digital QIAcuity con más de 100 nuevas pruebas para la investigación sobre el cáncer, trastornos genéticos y vigilancia de enfermedades infecciosas. La compañía ha lanzado más de 130 nuevas pruebas en 2024, superando su meta y llevando el total a más de 2.300 pruebas validadas.
Los desarrollos clave incluyen:
- Nuevas pruebas de dPCR para mutaciones LNA y CNV relacionadas con el cáncer
- Pruebas de detección de ADN microbiano dPCR para patógenos y resistencia a antibióticos
- Portafolio ampliado para enfermedades animales y patógenos de plantas
QIAcuity ha mostrado una fuerte adopción con más de 2.000 ubicaciones a finales de 2023. Una versión de diagnóstico in vitro está programada para lanzarse en otoño de 2024, enfocándose en aplicaciones clínicas. QIAGEN también está colaborando con empresas farmacéuticas para desarrollar diagnósticos complementarios en la plataforma.
QIAGEN (NYSE: QGEN)은 QIAcuity 디지털 PCR 플랫폼을 확장하였습니다 새롭게 100개 이상의 암 연구, 유전 질환 및 감염병 감시를 위한 신규 검사를 추가했습니다. 이 회사는 2024년에 130개 이상의 신규 검사를 출시했습니다, 목표를 초과 달성하여 총 2,300개 이상의 검증된 검사로 늘었습니다.
주요 개발 사항은 다음과 같습니다:
- 암 관련 변이를 위한 새로운 dPCR LNA 변이 및 CNV 탐지 검사
- 병원체 및 항생제 내성을 위한 dPCR 미생물 DNA 탐지 검사
- 동물 질병 및 식물 병원체를 위한 포트폴리오 확장
QIAcuity는 2023년 말까지 2,000건 이상의 설치로 강력한 채택을 보였습니다. 인비트로 진단 버전은 2024년 가을에 출시될 예정입니다, 임상 응용 프로그램을 목표로 하고 있습니다. QIAGEN은 또한 이 플랫폼에서 동반 진단을 개발하기 위해 제약 회사와 파트너십을 맺고 있습니다.
QIAGEN (NYSE: QGEN) a élargi sa plateforme de PCR numérique QIAcuity avec plus de 100 nouveaux tests pour la recherche sur le cancer, les troubles génétiques et la surveillance des maladies infectieuses. L'entreprise a lancé plus de 130 nouveaux tests en 2024, dépassant son objectif et portant le total à plus de 2 300 tests validés.
Les développements clés comprennent :
- Nouveaux tests LNA dPCR pour les mutations et CNV pertinentes pour le cancer
- Tests de détection d'ADN microbien dPCR pour les pathogènes et la résistance aux antibiotiques
- Portefeuille élargi pour les maladies animales et les pathogènes des plantes
QIAcuity a connu une forte adoption avec plus de 2 000 installations d'ici la fin 2023. Une version de diagnostic in vitro est prévue pour être lancée à l'automne 2024, visant des applications cliniques. QIAGEN s'associe également à des entreprises pharmaceutiques pour développer des diagnostics compagnons sur la plateforme.
QIAGEN (NYSE: QGEN) hat seine QIAcuity digitale PCR-Plattform erweitert und über 100 neue Tests für die Krebsforschung, genetische Störungen und die Überwachung von Infektionskrankheiten eingeführt. Das Unternehmen hat im Jahr 2024 mehr als 130 neue Tests eingeführt, damit seine Ziele übertroffen und die Gesamtzahl auf über 2.300 validierte Tests erhöht.
Wichtige Entwicklungen sind:
- Neue dPCR LNA Mutations- und CNV-Sondenassays für krebsrelevante Mutationen
- dPCR Mikrobielles DNA-Erkennungstests für Krankheitserreger und Antibiotikaresistenz
- Erweitertes Portfolio für Tierkrankheiten und Pflanzenpathogene
QIAcuity hat eine starke Akzeptanz mit über 2.000 Installationen bis Ende 2023 gesehen. Eine in-vitro Diagnoselösung soll im Herbst 2024 auf den Markt kommen, die klinische Anwendungen anvisiert. QIAGEN arbeitet auch mit Pharmaunternehmen zusammen, um Begleitdiagnosen auf der Plattform zu entwickeln.
- Launched over 100 new assays for QIAcuity digital PCR platform, expanding research capabilities
- Exceeded 2024 goal with more than 130 new assays launched this year
- Strong adoption of QIAcuity with over 2,000 cumulative placements by end of 2023
- QIAcuity cited in over 450 publications, indicating scientific relevance
- Planned launch of in-vitro diagnostic version of QIAcuity in fall 2024, expanding into clinical testing
- Partnerships with pharma companies for companion diagnostics development on QIAcuity
- None.
Insights
QIAGEN's expansion of 100+ new digital PCR assays for QIAcuity is a significant development in genetic research and diagnostics. This broadens the platform's utility across various fields, including cancer research, infectious disease surveillance and genetic disorder studies. The increased assay menu, now totaling over 2,300 validated assays, enhances QIAcuity's versatility and market appeal.
The new assays, particularly the dPCR LNA Mutation and CNV Probe Assays, offer improved capabilities in detecting cancer-related genetic alterations. This could accelerate cancer research and potentially lead to more precise diagnostics. The Microbial DNA Detection Assays expand QIAcuity's reach into infectious disease research, antibiotic resistance studies and agricultural pathogen detection, addressing critical areas in public health and food security.
With over 2,000 cumulative placements and citations in 450+ publications, QIAcuity is gaining traction in the scientific community. The planned launch of an in-vitro diagnostic version in fall 2024 could open new revenue streams in clinical diagnostics, particularly in cancer monitoring and infectious disease diagnosis.
QIAGEN's expansion of its QIAcuity digital PCR offering is a strategic move to capitalize on the growing dPCR market. The introduction of 100+ new assays not only enhances the platform's versatility but also strengthens QIAGEN's competitive position in the life sciences and diagnostics sectors.
The company's ability to exceed its 2024 goal for new assay launches demonstrates strong R&D execution and market responsiveness. This expansion could drive increased adoption of QIAcuity, potentially boosting instrument sales and recurring revenue from assay purchases.
The planned launch of an in-vitro diagnostic version of QIAcuity in fall 2024 represents a significant opportunity to tap into the clinical diagnostics market, which typically offers higher margins and more stable revenue streams. Partnerships with pharmaceutical companies for companion diagnostics development further diversify QIAGEN's revenue potential and align with the trend towards personalized medicine.
While specific financial figures are not provided, the growing installed base of over 2,000 QIAcuity systems suggests a solid foundation for future consumables sales. Investors should monitor the adoption rate of these new assays and the success of the IVD launch as indicators of QIAGEN's growth in the dPCR market.
QIAGEN adds over 100 new validated QIAcuity digital PCR assays for cancer research, inherited genetic disorders, infectious disease surveillance, and other applications // QIAcuity digital PCR enables accurate and sensitive detection of low-abundance pathogens, copy number alterations and identification of rare mutations // Portfolio expansion and partnerships support increased adoption of QIAcuity across multiple application areas
Venlo, the Netherlands, Sept. 18, 2024 (GLOBE NEWSWIRE) -- QIAGEN (NYSE: QGEN; Frankfurt Prime Standard: QIA) today announced an important milestone with the launch of 100 new assays for its digital PCR (dPCR) platform QIAcuity for use in the study of cancer, inherited genetic disorders, infectious disease surveillance, and food and environmental monitoring.
These new assays are available through QIAGEN’s comprehensive GeneGlobe platform which integrates pre-designed assays with a database of more than 10,000 biological entities including genes, miRNAs, and pathways.
QIAGEN has so far launched more than 130 new assays this year, exceeding the 2024 goal and adding to the existing total of more than 2,300 validated assays.
“This important expansion of the menu for QIAcuity digital PCR underscores how QIAGEN is addressing the urgent needs of our customers for new solutions to help use this powerful technology in research and applied testing applications,” said Nitin Sood, Senior Vice President, Head of the Life Sciences Business Area at QIAGEN. “QIAcuity is proving to be a valuable tool for a broad range of applications requiring accurate and sensitive detection of genetic targets, driving the development of new multiplexed assay capabilities. Our efforts won’t stop here as we look to further expand QIAcuity into clinical and biopharma applications as well as new areas of Life Sciences research.”
The newly launched assays include:
- dPCR LNA (locked nucleic acid) Mutation and dPCR CNV (copy number variation) Probe Assays are designed to investigate cancer-relevant mutations and CNVs, which means changes in the number of copies of certain DNA sequences, in genes, including mutations associated with colorectal cancer, malignant tumors of the connective and supporting tissue, so-called sarcoma, or thyroid cancer.
- dPCR Microbial DNA Detection Assays are designed to target critical pathogens responsible for various infectious and tropical diseases, sexually transmitted and urinary tract infections as well as genes associated with antibiotic resistance. The portfolio is also being expanded to detect animal diseases and plant pathogens affecting crops.
The adoption of QIAcuity digital PCR remains strong with more than 2,000 cumulative placements at the end of 2023 and citations in over 450 publications. Key customers include pharmaceutical and biotechnology companies, academic and research organizations, diagnostic centers and forensic laboratories.
QIAGEN's QIAcuity digital PCR platform utilizes nanoplates to disperse a sample into thousands of tiny partitions and then reads the reaction in each one simultaneously to quantify even the faintest signals from DNA and RNA. The platform integrates partitioning, thermocycling, and imaging into a streamlined multiplex workflow, reducing processing times from six hours to just two. Available in one-, four-, and eight-plate versions, the platform meets the needs of a wide range of laboratory sizes and throughput requirements.
Expanding QIAGEN’s successful dPCR portfolio into clinical testing, an in-vitro diagnostic version of QIAcuity is set for launch in the fall of 2024. The device will support applications such as diagnosing infectious diseases and monitoring cancer disease progression and treatment response with less invasive liquid biopsies. QIAGEN is also partnering with pharma companies to develop companion diagnostics on QIAcuity, making use of the platform’s sensitivity and accuracy for disease monitoring.
For more information about QIAGEN's digital PCR solutions and the new assays, please visit https://geneglobe.qiagen.com/applications/digital-pcr.
About QIAGEN
QIAGEN N.V., a Netherlands-based holding company, is the leading global provider of Sample to Insight solutions that enable customers to gain valuable molecular insights from samples containing the building blocks of life. Our sample technologies isolate and process DNA, RNA and proteins from blood, tissue and other materials. Assay technologies make these biomolecules visible and ready for analysis. Bioinformatics software and knowledge bases interpret data to report relevant, actionable insights. Automation solutions tie these together in seamless and cost-effective workflows. QIAGEN provides solutions to more than 500,000 customers around the world in Molecular Diagnostics (human healthcare) and Life Sciences (academia, pharma R&D and industrial applications, primarily forensics). As of June 30, 2024, QIAGEN employed more than 5,900 people in over 35 locations worldwide. Further information can be found at https://www.qiagen.com.
Forward-Looking Statement
Certain statements contained in this press release may be considered forward-looking statements within the meaning of Section 27A of the U.S. Securities Act of 1933, as amended, and Section 21E of the U.S. Securities Exchange Act of 1934, as amended. To the extent that any of the statements contained herein relating to QIAGEN's products, timing for launch and development, marketing and/or regulatory approvals, financial and operational outlook, growth and expansion, collaborations, markets, strategy or operating results, including without limitation its expected adjusted net sales and adjusted diluted earnings results, are forward-looking, such statements are based on current expectations and assumptions that involve a number of uncertainties and risks. Such uncertainties and risks include, but are not limited to, risks associated with management of growth and international operations (including the effects of currency fluctuations, regulatory processes and dependence on logistics), variability of operating results and allocations between customer classes, the commercial development of markets for our products to customers in academia, pharma, applied testing and molecular diagnostics; changing relationships with customers, suppliers and strategic partners; competition; rapid or unexpected changes in technologies; fluctuations in demand for QIAGEN's products (including fluctuations due to general economic conditions, the level and timing of customers' funding, budgets and other factors); our ability to obtain regulatory approval of our products; difficulties in successfully adapting QIAGEN's products to integrated solutions and producing such products; the ability of QIAGEN to identify and develop new products and to differentiate and protect our products from competitors' products; market acceptance of QIAGEN's new products and the integration of acquired technologies and businesses; actions of governments, global or regional economic developments, weather or transportation delays, natural disasters, political or public health crises, and its impact on the demand for our products and other aspects of our business, or other force majeure events; as well as the possibility that expected benefits related to recent or pending acquisitions may not materialize as expected; and the other factors discussed under the heading “Risk Factors in our most recent Annual Report on Form 20-F. For further information, please refer to the discussions in reports that QIAGEN has filed with, or furnished to, the U.S. Securities and Exchange Commission.
Source: QIAGEN N.V.
Category: Corporate
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