Welcome to our dedicated page for Qiagen news (Ticker: QGEN), a resource for investors and traders seeking the latest updates and insights on Qiagen stock.
News about QIAGEN N.V. (QGEN) centers on its role as a Netherlands-based Sample to Insight company serving life sciences and molecular diagnostics customers worldwide. This news feed aggregates corporate announcements, product updates, regulatory milestones and financial communications directly related to QGEN.
Readers can follow updates on QIAGEN’s five growth pillars: Sample technologies, QIAstat-Dx syndromic testing, QIAcuity digital PCR, QIAGEN Digital Insights (QDI) bioinformatics and QuantiFERON latent tuberculosis testing. Company news often highlights launches and enhancements of automation systems such as QIAcube Connect, QIAsymphony Connect, QIAsprint, QIAmini and EZ2 Connect Fx, as well as new kits like the EZ2 DNA Investigator Sep&Prep Kit for forensic applications.
Regulatory and clinical diagnostics news includes items such as CE-IVDR certification for QIAstat-Dx panels in Europe, U.S. FDA clearance for QIAstat-Dx Rise, and expansions of test menus for respiratory, gastrointestinal and central nervous system infections. These announcements show how QIAGEN positions its platforms in infectious disease and syndromic testing.
Investors and analysts can also track financial and capital markets developments, including quarterly earnings releases furnished on Form 6-K, outlook updates, and capital return actions such as synthetic share repurchase plans that combine direct capital repayments with reverse stock splits. Strategic moves, for example the agreement to acquire Parse Biosciences to expand into single-cell analysis, are another recurring theme in QGEN news.
For users interested in precision oncology, bioinformatics and AI-enabled solutions, QIAGEN’s news includes information on partnerships, new software capabilities within QDI, and integrated Sample to Insight workflows. Bookmark this page to access an organized stream of QGEN-related announcements spanning products, diagnostics, automation, bioinformatics and investor communications.
QIAGEN N.V. has launched the QuantiFERON SARS-CoV-2 RUO solution, designed to detect T-cell responses to COVID-19. This innovative technology enables researchers to assess immunity levels and disease progression more effectively, as studies show T-cell responses decline slower than antibody responses. With the ability to indicate disease severity and long-term immunity, this tool enhances QIAGEN's COVID-19 portfolio, which includes sample-preparation technology and PCR testing.
QIAGEN N.V. has entered a strategic collaboration with BioNTech SE to develop a tissue-based companion diagnostic for identifying patients with head and neck squamous cell carcinoma (SCCHN) linked to human papilloma virus (HPV) infections. Utilizing QIAGEN’s RGQ MDx platform, the assay aims to expand its applications across various HPV-related cancers. With over 650,000 new SCCHN cases annually, and projections indicating doubled numbers by 2035, this collaboration positions QIAGEN to enhance its HPV diagnostic offerings, building on its established market leadership.
QIAGEN N.V. (NYSE: QGEN) has launched the NeuMoDx™ Flu A-B/RSV/SARS-CoV-2 Vantage Test in Europe, addressing the need for rapid diagnosis during flu season. This multiplex PCR test can differentiate between influenza A and B, RSV, and SARS-CoV-2 in just 80 minutes, aiding healthcare professionals in treatment decisions amidst similar respiratory symptoms. Following CE-IVD registration, the test has also received a request for Emergency Use Authorization from the FDA. The company has additionally expanded the use of saliva samples in its existing SARS-CoV-2 test.
QIAGEN has launched the QIAreach™ SARS-CoV-2 Antigen Test in the U.S., enabling rapid detection of SARS-CoV-2 antigens in 2-15 minutes for active infections. Developed with Ellume, the test can process over 30 samples per hour and offers digital results without subjective interpretation. An EUA application for symptomatic patients has been submitted, with plans for a POC claim later this year. The test addresses the need for scalable and accurate antigen testing as part of COVID-19 strategies, complementing PCR testing for higher throughput.
QIAGEN N.V. (NYSE: QGEN) announced a conference call set for October 28 to discuss third-quarter results for 2020, following the release of their financial report on October 27. The call will be at 14:00 Frankfurt time/13:00 London time/9:00 New York time, hosted by CEO Thierry Bernard and CFO Roland Sackers. Interested participants can join via phone or by accessing the webcast. QIAGEN specializes in Sample to Insight solutions, serving over 500,000 customers globally in Molecular Diagnostics and Life Sciences as of September 30, 2020.
QIAGEN N.V. (NYSE: QGEN) reported robust Q3 2020 results, with sales escalating by 26% to $483.8 million compared to $382.7 million in Q3 2019. Adjusted EPS soared 61% to $0.58. Encouraged by this performance, the company raised its 2020 outlook, forecasting 20% sales growth and adjusted EPS of $2.07-2.09. The significant sales increase is attributed to high demand for COVID-19 related products, alongside other portfolio areas. QIAGEN also expanded its COVID-19 testing capabilities and solidified its position in automated molecular testing through a recent acquisition.
QIAGEN N.V. (NYSE: QGEN) reported strong preliminary results for Q3 2020, with net sales rising 26% year-over-year to $481.3 million, surpassing prior growth forecasts. This growth is attributed to heightened demand for COVID-19 testing solutions, along with improved trends in non-COVID product sales. Adjusted EPS reached approximately $0.58, marking a 61% increase from $0.36 in Q3 2019. QIAGEN anticipates minimal currency impact on its results. Full Q3 results will be published on November 4, 2020, with a conference call scheduled for November 5.
QIAGEN (NYSE: QGEN) has announced a new approach to viral RNA epidemiology with its QIAprep Viral RNA UM Kit. This innovative kit simplifies PCR analysis for SARS-CoV-2 and other RNA viruses, allowing sample preparation in just two minutes. The streamlined process delivers results in under one hour, significantly faster than traditional methods that take about three hours. The kit can manage up to 2,600 samples in an eight-hour shift and minimizes plastic use while reducing reagent and labor costs. Initial studies show detection levels comparable to standard protocols.