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Qiagen N.V.. (1/23/18). "Press Release: Qiagen Receives FDA Clearance for First-ever JAK2 Test for Use in Diagnosis of Additional Myeloproliferative Neoplasms". Hilden & Germantown, MD.

Region Region United States (USA)
Organisations Organisation Qiagen GmbH
  Group Qiagen (Group)
  Organisation 2 FDA (US Food and Drug Administration)
  Group United States (govt)
Products Product Ipsogen® JAK2 RGQ PCR Kit
  Product 2 cancer test, classfication
Person Person Bernard, Thierry (Qiagen 201502– SVP Molecular Dx business area before bioMérieux Corp VP Commcercial Operations)

Expanded use of ipsogen test provides diagnostic testing needs for all myeloproliferative neoplasms in line with the latest WHO guidelines

QIAGEN (NYSE: QGEN; Frankfurt Prime Standard: QIA) announced today that it has received clearance for its ipsogen JAK2 RGQ PCR Kit (ipsogen JAK2 assay) from the U.S. Food and Drug Administration (FDA) for additional use in the diagnosis of all myeloproliferative neoplasms (MPNs), which are a group of cancers in which immature blood cells in the bone marrow do not mature and become healthy blood cells.

This U.S. 510k clearance comes after the FDA cleared the use of the ipsogen JAK2 assay as a qualitative in vitro diagnostic test for the detection of the JAK2 V617F/G1849T allele in genomic DNA extracted from EDTA whole blood*. This mutation is found in nearly all patients with polycythemia vera (PV), one of three types of MPNs that affect about 300,000 patients in the U.S.

The FDA clearance now covers two additional types of MPN: essential thrombocythemia (ET) and primary myelofibrosis (PMF).

The analysis of JAK2 is a major criterion for the diagnosis of all MPNs in the WHO (World Health Organization) 2016 guidelines for the classification of MPNs. MPNs are relatively rare with about 20,000 new cases per year, but about 5 suspected patients are tested for JAK2 to diagnose one case of MPN, which makes JAK2 among the most frequently performed molecular oncology tests.

“We are eager to expand the use of our ipsogen JAK2 assay, which is already available in Europe and other markets, for use in a wider range of patients in the U.S. Our JAK2 assay makes it easier for hematologists and oncologists to follow recommended diagnostic testing algorithms and international guidelines for their patients suspected of having MPNs,” said Thierry Bernard, Senior Vice President and Head of QIAGEN’s Molecular Diagnostics Business Area.

QIAGEN is at the forefront of developing oncology tests to diagnose, guide the selection of therapies and monitor the treatment of cancer patients. QIAGEN offers a range of personalized healthcare assays for use around the world under the ipsogen (blood cancers) and therascreen (solid tumors) brands, covering about 30 biomarkers and spanning a range of automation platforms and tumor sample types.

QIAGEN is the exclusive worldwide licensee of intellectual property rights that cover the detection of the V617F JAK2 mutation for diagnostic purposes, and offers the only FDA-cleared JAK2 test. QIAGEN recently reached a settlement with a molecular diagnostics industry supplier in Europe, which agreed to stop selling its own JAK2 V617F kit, after a court-appointed expert issued a positive opinion in favor of QIAGEN in regard to the validity and infringement of the licensed intellectual property. QIAGEN has a strong position for JAK2 intellectual property, and intends to assert its rights to protect this technology.

The ipsogen JAK2 assay is the latest addition to QIAGEN’s ipsogen market-leading portfolio of assays for common and rare leukemia types. In Europe, QIAGEN offers the CE-IVD marked ipsogen CALR RGQ PCR Kit for identification and detection of various mutations of the calreticulin (CALR) gene in patients with suspected MPNs. QIAGEN is also the exclusive licensee of intellectual property rights covering detection CALR mutations for diagnostic purposes. The ipsogen JAK2 and CALR test kits are highly synergistic, and can be processed on the QIAsymphony platform from a single patient sample. These genes are also included in the myeloid NGS panel which QIAGEN is currently developing for its GeneReader NGS platform and which is expected to launch later in the year for clinical research.

The ipsogen JAK2 assay is processed on QIAGEN’s Rotor-Gene Q MDx instrument, which is a member of the modular QIAsymphony family of automation solutions that offers a full Sample to Insight workflow. It also marks the sixth FDA clearance or approval of a QIAGEN oncology-related test for personalized healthcare. QIAGEN continues to expand its pipeline of Sample to Insight technologies for personalized healthcare applications and intends to submit more tests for regulatory clearance or approval. More than 20 master collaboration agreements have been reached with leading pharmaceutical and biotech companies to co-develop and market companion diagnostics assays.

*The ipsogen JAK2 RGQ PCR Kit is a qualitative in vitro diagnostic test for the detection of the JAK2 V617F/G1849T allele in genomic DNA extracted from EDTA whole blood. The ipsogen JAK2 RGQ PCR Kit is a real time PCR test performed on the QIAGEN Rotor-Gene Q MDx instrument. The test is intended for use as an adjunct to evaluation of suspected myeloproliferative neoplasms, in conjunction with other clinicopathological factors. This test does not detect less common JAK2 mutations associated with myeloproliferative neoplasms including mutations in exon 12 and is not intended for standalone diagnosis of myeloproliferative neoplasms.


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), Applied Testing (forensics, veterinary testing and food safety), Pharma (pharma and biotech companies) and Academia (life sciences research). As of September 30, 2017, QIAGEN employed approximately 4,600 people in over 35 locations worldwide. Further information can be found at

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, 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. 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 (SEC).

Record changed: 2021-07-18


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