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QIAGEN Launches QIAprep& Plasmodium Kit to Strengthen Malaria Research and Surveillance Efforts

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QIAGEN (NYSE: QGEN) has launched the QIAprep& Plasmodium Kit and two companion assays to enhance malaria research and surveillance. The new solution combines sample preparation and quantitative PCR into a single workflow for detecting malaria-causing parasites from blood samples.

The kit enables detection of all five Plasmodium species with high sensitivity (one parasite per microliter) and is compatible with both liquid and dried blood samples. The technology includes two key assays: the QIAGEN Pf/Non-Pf Detection Assay for screening Plasmodium falciparum, and the QIAGEN Pv/Pm/Po/Pk Detection Assay for distinguishing between P. vivax, P. malariae, P. ovale, and P. knowlesi.

This launch addresses a critical global health challenge, as malaria caused over 250 million cases worldwide in 2024, with more than 90% occurring in Africa. The solution aims to support mixed-infection tracking, vaccine impact assessment, and malaria control strategies, particularly in regions with healthcare infrastructure.

QIAGEN (NYSE: QGEN) ha lanciato il QIAprep& Plasmodium Kit e due test complementari per migliorare la ricerca e la sorveglianza della malaria. La nuova soluzione combina la preparazione del campione e la PCR quantitativa in un unico flusso di lavoro per rilevare i parassiti responsabili della malaria nei campioni di sangue.

Il kit consente di rilevare tutte e cinque le specie di Plasmodium con alta sensibilità (un parassita per microlitro) ed è compatibile sia con campioni di sangue liquido che essiccato. La tecnologia include due test chiave: il QIAGEN Pf/Non-Pf Detection Assay per lo screening di Plasmodium falciparum, e il QIAGEN Pv/Pm/Po/Pk Detection Assay per distinguere tra P. vivax, P. malariae, P. ovale e P. knowlesi.

Questo lancio affronta una sfida critica per la salute globale, poiché la malaria ha causato oltre 250 milioni di casi in tutto il mondo nel 2024, con oltre il 90% dei casi che si sono verificati in Africa. La soluzione mira a supportare il monitoraggio delle infezioni miste, la valutazione dell'impatto dei vaccini e le strategie di controllo della malaria, in particolare nelle regioni con infrastrutture sanitarie limitate.

QIAGEN (NYSE: QGEN) ha lanzado el QIAprep& Plasmodium Kit y dos ensayos complementarios para mejorar la investigación y vigilancia de la malaria. La nueva solución combina la preparación de muestras y la PCR cuantitativa en un único flujo de trabajo para detectar parásitos causantes de malaria en muestras de sangre.

El kit permite la detección de las cinco especies de Plasmodium con alta sensibilidad (un parásito por microlitro) y es compatible tanto con muestras de sangre líquida como seca. La tecnología incluye dos ensayos clave: el QIAGEN Pf/Non-Pf Detection Assay para el cribado de Plasmodium falciparum, y el QIAGEN Pv/Pm/Po/Pk Detection Assay para distinguir entre P. vivax, P. malariae, P. ovale y P. knowlesi.

Este lanzamiento aborda un desafío crítico de salud global, ya que la malaria causó más de 250 millones de casos en todo el mundo en 2024, con más del 90% de los casos ocurriendo en África. La solución tiene como objetivo apoyar el seguimiento de infecciones mixtas, la evaluación del impacto de las vacunas y las estrategias de control de la malaria, particularmente en regiones con infraestructura de salud limitada.

QIAGEN (NYSE: QGEN)은 말라리아 연구 및 감시를 강화하기 위해 QIAprep& Plasmodium Kit과 두 가지 보조 검사를 출시했습니다. 새로운 솔루션은 혈액 샘플에서 말라리아를 유발하는 기생충을 감지하기 위한 샘플 준비와 정량적 PCR을 단일 작업 흐름으로 결합합니다.

이 키트는 높은 민감도로 모든 다섯 개의 Plasmodium 종을 감지할 수 있으며 (1 마이크로리터당 1 기생충) 액체 및 건조 혈액 샘플 모두와 호환됩니다. 이 기술에는 두 가지 주요 검사법이 포함되어 있습니다: Plasmodium falciparum을 선별하기 위한 QIAGEN Pf/Non-Pf Detection Assay와 P. vivax, P. malariae, P. ovale 및 P. knowlesi를 구분하기 위한 QIAGEN Pv/Pm/Po/Pk Detection Assay입니다.

이번 출시는 2024년 전 세계에서 2억 5천만 건 이상의 말라리아 사례가 발생한 중대한 글로벌 건강 문제를 다루고 있으며, 이 중 90% 이상이 아프리카에서 발생했습니다. 이 솔루션은 혼합 감염 추적, 백신 영향 평가 및 말라리아 통제 전략을 지원하는 것을 목표로 하며, 특히 의료 인프라가 제한된 지역에서 그렇습니다.

QIAGEN (NYSE: QGEN) a lancé le QIAprep& Plasmodium Kit ainsi que deux tests complémentaires pour améliorer la recherche et la surveillance du paludisme. La nouvelle solution combine la préparation d'échantillons et la PCR quantitative dans un flux de travail unique pour détecter les parasites responsables du paludisme à partir d'échantillons de sang.

Le kit permet la détection des cinq espèces de Plasmodium avec une grande sensibilité (un parasite par microlitre) et est compatible avec des échantillons de sang liquides et séchés. La technologie comprend deux tests clés : le QIAGEN Pf/Non-Pf Detection Assay pour le dépistage de Plasmodium falciparum, et le QIAGEN Pv/Pm/Po/Pk Detection Assay pour distinguer P. vivax, P. malariae, P. ovale et P. knowlesi.

Ce lancement répond à un défi critique de santé mondiale, puisque le paludisme a causé plus de 250 millions de cas dans le monde en 2024, avec plus de 90 % des cas survenant en Afrique. La solution vise à soutenir le suivi des infections mixtes, l'évaluation de l'impact des vaccins et les stratégies de contrôle du paludisme, en particulier dans les régions disposant d'infrastructures de santé limitées.

QIAGEN (NYSE: QGEN) hat das QIAprep& Plasmodium Kit und zwei begleitende Tests zur Verbesserung der Malariaforschung und -überwachung auf den Markt gebracht. Die neue Lösung kombiniert die Probenvorbereitung und die quantitative PCR in einem einzigen Arbeitsablauf zur Erkennung von malariaerregenden Parasiten aus Blutproben.

Das Kit ermöglicht die Erkennung aller fünf Plasmodium-Arten mit hoher Sensitivität (ein Parasit pro Mikroliter) und ist sowohl mit flüssigen als auch mit getrockneten Blutproben kompatibel. Die Technologie umfasst zwei wichtige Tests: den QIAGEN Pf/Non-Pf Detection Assay zum Screening von Plasmodium falciparum und den QIAGEN Pv/Pm/Po/Pk Detection Assay zur Unterscheidung zwischen P. vivax, P. malariae, P. ovale und P. knowlesi.

Dieser Launch adressiert eine kritische globale Gesundheitsherausforderung, da Malaria im Jahr 2024 weltweit über 250 Millionen Fälle verursacht hat, wobei mehr als 90 % in Afrika auftraten. Die Lösung zielt darauf ab, das Tracking von Mischinfektionen, die Bewertung der Impfstoffauswirkungen und die Malariakontrollstrategien zu unterstützen, insbesondere in Regionen mit eingeschränkter Gesundheitsinfrastruktur.

Positive
  • Launch of innovative QIAprep& Plasmodium Kit combining sample preparation and qPCR in one workflow
  • High detection sensitivity of one parasite per microliter
  • Versatile compatibility with both liquid and dried blood samples
  • Expansion into the large malaria testing market (250M+ cases annually)
Negative
  • None.

Insights

QIAGEN's launch of the QIAprep& Plasmodium Kit represents a strategic expansion of their infectious disease portfolio, adapting their COVID-19 platform technology for another significant global health challenge. The product addresses the 250+ million malaria cases reported in 2024, with particular relevance to African markets where 90% of cases occur.

The technology offers several competitive advantages, including the ability to detect all five Plasmodium species and an impressive sensitivity threshold of one parasite per microliter. By integrating sample preparation and qPCR into a single workflow, QIAGEN is addressing efficiency needs in resource- settings where malaria is endemic.

From a business perspective, this launch leverages QIAGEN's existing molecular diagnostics infrastructure and creates synergies with their Rotor-Gene Q platform. While not likely to drive immediate significant revenue growth given the economics of target markets, it strengthens QIAGEN's position in infectious disease surveillance and establishes presence in regions experiencing increased healthcare investment.

The timing aligns with the recent integration of vaccines into anti-malaria programs, creating demand for monitoring tools to track vaccine effectiveness and parasite evolution. This positions QIAGEN to capture value from the broader ecosystem of malaria control initiatives beyond just diagnostic revenue.

  • Malaria remains a major global health threat, with more than 250 million cases and 600,000 deaths in 2024 – over 90% of them in Africa
  • QIAprep&amp Plasmodium Kit enables streamlined detection of five malaria-causing parasites for epidemiological research and surveillance
  • Novel QIAGEN assays support mixed-infection tracking, vaccine impact assessment and malaria control strategies in regions with limited healthcare infrastructure

VENLO, Netherlands--(BUSINESS WIRE)-- QIAGEN N.V. (NYSE: QGEN; Frankfurt Prime Standard: QIA) today announced the launch of the QIAprep&amp Plasmodium Kit and two companion assays to support malaria research and surveillance efforts.

This new solution combines sample preparation and quantitative PCR (qPCR) into a single workflow, providing a rapid and accessible tool for detecting malaria-causing parasites from blood samples.

Malaria remains one of the world’s most pressing public health challenges, particularly in tropical and subtropical regions. The disease is caused by five species of Plasmodium parasites, with Plasmodium falciparum responsible for the most severe cases. In 2024 alone, malaria accounted for more than 250 million cases worldwide, with over 90% occurring in Africa.

While the integration of vaccines into anti-malaria programs began in 2024, and mark a significant milestone, comprehensive monitoring of parasite prevalence and evolution is essential for disease control. The QIAprep&amp Plasmodium Kit simplifies malaria research by enabling the detection of all five Plasmodium species in human samples.

“Malaria research and surveillance remains critical in the fight against this potentially fatal disease, especially as control efforts evolve,” said Swathi Kumar, Head of Global PCR, Enzymes & Oligos at QIAGEN. “Our new QIAprep&amp Plasmodium Kit and assays allow researchers to monitor disease prevalence through high-frequency screening so they can better track the spread of this disease, study vaccine effectiveness and identify emerging dominant parasite strains that may impact treatment and containment strategies.”

QIAGEN’s QIAprep&amp technology – originally developed for COVID-19 research – integrates liquid-based sample preparation with qPCR into a streamlined and cost-efficient workflow. It offers high sensitivity, detecting as little as one parasite per microliter, and is compatible with both liquid and dried blood samples, including QIAcard FTA cards. It is also suitable for use on many qPCR platforms, including QIAGEN’s Rotor-Gene Q.

The accompanying assays further enhance malaria research detection and differentiation. The QIAGEN Pf/Non-Pf Detection Assay is a single-reaction screen for the most common cause of malaria in humans involving Plasmodium falciparum, while the QIAGEN Pv/Pm/Po/Pk Detection Assay helps distinguish between the remaining four common species that cause malaria – P. vivax, P. malariae, P. ovale, and P. knowlesi – allowing scientists to track mixed infections, study parasite evolution during vaccine rollouts and ensure that comprehensive epidemiological surveillance data is available when designing response measures.

For more information about the QIAprep&amp Plasmodium Kit and assays, visit: https://www.qiagen.com/de/products/discovery-and-translational-research/pcr-qpcr-dpcr/real-time-pcr-enzymes-and-kits/qiaprep-and-amp-plasmodium-kit

About QIAGEN

QIAGEN N.V., a Netherlands-based holding company, is the leading global provider of Sample to Insight solutions, enabling customers to extract and 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 prepare these biomolecules for analysis while bioinformatics software and knowledge bases can be used to interpret data to find actionable insights. Automation solutions bring these processes together into seamless and cost-effective workflows. QIAGEN serves over 500,000 customers globally in Life Sciences (academia, pharma R&D and industrial applications, primarily forensics) and Molecular Diagnostics for clinical healthcare. As of December 31, 2024, QIAGEN employed more than 5,700 people in over 35 locations worldwide. For more information, visit www.qiagen.com.

Forward-Looking Statement

Certain statements in this press release may constitute 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. These statements, including those regarding QIAGEN's products, development timelines, marketing and / or regulatory approvals, financial and operational outlook, growth strategies, collaborations and operating results - such as expected adjusted net sales and adjusted diluted earnings - are based on current expectations and assumptions. However, they involve uncertainties and risks. These risks include, but are not limited to, challenges in managing growth and international operations (including the effects of currency fluctuations, regulatory processes and logistical dependencies), variability in operating results and allocations between customer classes, commercial development for our products to customers in the Life Sciences and clinical healthcare, changes in relationships with customers, suppliers or strategic partners; competition and rapid technological advancements; fluctuating demand for QIAGEN's products due to factors such as economic conditions, customer budgets and funding cycles; obtaining and maintaining regulatory approvals for our products; difficulties in successfully adapting QIAGEN's products into integrated solutions and producing these products; and protecting product differentiation from competitors. Additional uncertainties may arise from market acceptance of new products, integration of acquisitions, governmental actions, global or regional economic developments, natural disasters, political or public health crises, and other "force majeure" events. There is also no guarantee that anticipated benefits from acquisitions will materialize as expected. For a comprehensive overview of risks, please refer to the “Risk Factors” contained in our most recent Annual Report on Form 20-F and other reports filed with or furnished to the U.S. Securities and Exchange Commission.

Source: QIAGEN N.V.

Category: Corporate

Contacts QIAGEN:

Investor Relations

John Gilardi +49 2103 29 11711

Domenica Martorana +49 2103 29 11244

e-mail: ir@QIAGEN.com

Public Relations

Thomas Theuringer +49 2103 29 11826

Lisa Specht +49 2103 29 14181

e-mail: pr@QIAGEN.com

Source: QIAGEN N.V.

FAQ

What is the detection sensitivity of QIAGEN's new QIAprep& Plasmodium Kit?

The kit can detect as little as one parasite per microliter of blood sample.

How many malaria cases were reported globally in 2024 according to QGEN's release?

Over 250 million malaria cases were reported worldwide in 2024, with more than 90% occurring in Africa.

What types of blood samples can be used with QGEN's new malaria detection kit?

The kit is compatible with both liquid blood samples and dried blood samples, including QIAcard FTA cards.

Which Plasmodium species can QIAGEN's new malaria detection assays identify?

The assays can detect all five species: P. falciparum through the Pf/Non-Pf assay, and P. vivax, P. malariae, P. ovale, and P. knowlesi through the Pv/Pm/Po/Pk assay.
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