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Qiagen N.V.

QGENFDA catalysts, PDUFA dates & pipeline intelligence
$45.38
▲ +0.85 · +1.91%

Financials

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Operating CF
Total Assets
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Quarterly Cash
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52W LOW $32.5352W HIGH $57.81
Volume
1.26 M
Value Traded
130.50 M
Short % Float
3.74%
-0.9%Week
+7.71%1 Month
+9.51%3 Month
+8.28%6 Month
-35.02%5 Year
+1,504.93%All Time

Cash Data

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  • Monthly Burn
  • Burn Trend
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  • SEC Filing

Key Stats

Market Cap
9.35 B
EPS (TTM)
1.95
P/E Ratio
23.27
Ent. Value
8.25 B
Total Shares
206.01 M
Float Shares
204.83 M
Insiders
0.60%
Institutions
77.98%

Upcoming Catalysts

FDA decisions, readouts and PDUFA dates · scored by probability of approval

Catalyst Drug / Treatment Stage Prob. of Approval Description Drug Type Therapeutic Area Source
PDUFA
2026
Example Drug
Treatment for example condition requiring FDA review
Phase 3Small MoleculeOncology-
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Every FDA decision, readout and PDUFA date, with drug type, therapeutic area and a PoA score you can trade on.
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PoA blends historical approval base rates, trial design score and FDA review track record.

QGEN Catalyst Timeline

Dated clinical, regulatory and corporate events for Qiagen N.V.

Catalyst Timeline

Dated clinical, regulatory & corporate events for Qiagen N.V.

399Total events
10Upcoming
104Tier-1 (high impact)
2005 to 2028Coverage

Upcoming catalysts 2

T3Corporate Approval
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T3Corporate Approval
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Event history 50

▲FDA ApprovalFDA Decision
FDA clearance of QIAstat-Dx BCID GN Plus AMR Panel for gram-negative bloodstream infections
bloodstream infections (gram-negative bacteria and antibiotic resistance markers)source ↗
▲Product LaunchQIAminiPost-Market
QIAGEN launches QIAmini compact automated sample preparation system
●Management ChangeCorporate
Thierry Bernard stepped down as Chief Executive Officer and Managing Board member
▲Product LaunchPost-Market
Commercial launch of QIAsymphony Connect
▲Other Regulator MilestoneEx-US Regulatory
FDA listing completed for QIAsymphony Connect
▲Quarterly UpdateCorporate
Initial customer orders received for QIAsymphony Connect
▲FDA ApprovalFDA Decision
FDA cleared QIAstat-Dx BCID GPF Plus AMR Panel
bloodstream infectionssource ↗
●Quarterly UpdateCorporate
Q2 2026 conference call scheduled
▲Quarterly UpdateCorporate
Q2 2026 net sales and EPS exceed outlook
▲Product LaunchPost-Market
Launch of CE-IVDR-certified QIAstat-Dx BCID GN Plus AMR Panel in Europe
bloodstream infectionsource ↗
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Every PDUFA date, readout, approval and corporate move, tiered by market impact and updated daily.
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Past FDA Catalysts and PDUFA Decisions

How QGEN actually traded into and out of each decision

Date Drug Catalyst Stage Reaction Event Move % Best Trade %
-Example Drug Phase 3 data readout Phase 3
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Reaction: 30 trading days around the event · Event Move: close to close on decision day · Best Trade: peak run-up from entry 10 days before the decision

Drug Pipeline Intelligence

No drug pipeline

Qiagen N.V. is a services and tools company (CRO, lab tools or healthcare services). The clinical trials it takes part in test other companies' drugs, so it has no drug pipeline of its own to score.

Clinical Trial Results

Readouts, endpoints and source filings for every QGEN program

Drug Name Indication Phase Date Trial Results SummaryTitleSource
Example Drug Example indication for clinical evaluationPhase 32025-12-01The study met its primary endpoint demonstrating statistically significant improvement.Read MorePhase 3 Study Results AnnouncementRead More
Scroll for more · summaries link to the source press release
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Inside Trades

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Monthly insider buys and sells against the stock price, with the insider sentiment reading.
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InsiderSideSharesPriceValueDate
John SmithCEOBuy 50,000 150,000 held$45.50 01/10/2026
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Hedge Fund 13F Activity

Fund % of Portfolio Current MV Shares Owned Activity
PARKMAN HEALTHCARE PARTNERS LLC 2.1 % 20.02 M 500.00 K 1.14% ( 5.65 K)
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Every 13F position with quarter over quarter share flow and average entry price.
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Shares held by hedge funds each quarter, and who bought or sold.

QGEN Institutional Ownership Trends

Options Data

Option Volume

Open Interest
Call OI
Put OI
Put-Call Ratio
OI 30-day avg
Today vs avg
Option Volume
Call Vol
Put Vol
Put-Call Ratio
Vol 30-day avg
Today vs avg

Option Chain Statistics

ExpiryCall VolPut VolVol P/CCall OIPut OIOI P/CIV CallIV Call OI-WtdIV Call Vol-WtdIV PutIV Put OI-WtdIV Put Vol-Wtd
2026-12-18
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Per-expiry call and put volume, open interest, put-call ratios and implied volatility.
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Real-Time Option Chain

CallsStrikePuts
LastVolOILastVolOI
No data available
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Live calls and puts by strike: last price, volume and open interest for every expiry.
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Calls vs Puts by Expiry

CallsPutsLog scale
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Competitive positioning

How QGEN ranks across every disease it competes in

Competitive Position is a premium feature
See how QGEN ranks against every competitor across each disease it develops in: phase, best drug, trials and likelihood of approval.
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QGEN News

QGEN
Oct 6, 2026
QGENGeneral
▲ +1.9%today

QIAGEN Expands AI-Powered Bioinformatics for Research and Drug Discovery

QIAGEN N.V. has announced the expansion of its artificial intelligence capabilities aimed at enhancing the analysis of complex biological and genomic data. The new tools include IPA Investigator, which serves as an AI research companion for the QIAGEN Ingenuity Pathway Analysis, and the QIAGEN Discovery Platform, designed to extend these advanced capabilities further.

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QGEN
Sep 28, 2026
QGENFDA Updates

QIAGEN Completes U.S. QIAstat-Dx Bloodstream Infection Portfolio With FDA Clearance of New Bacteria Detection Panel

QIAGEN N.V. has announced the FDA clearance of a new bacteria detection panel for its QIAstat-Dx bloodstream infection portfolio. This new panel allows U.S. laboratories to detect gram-negative bacteria and antibiotic resistance markers in approximately one hour. It complements an earlier FDA-cleared panel for gram-positive bacteria and fungi, enhancing the company's diagnostic capabilities.

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QGEN
Sep 24, 2026
QGENGeneral

QIAGEN Launches QIAmini to Automate Small-Batch Sample Preparation

QIAGEN N.V. has launched QIAmini, an automated sample preparation system aimed at research laboratories. This compact system provides a time-saving and cost-effective solution for processing small sample batches, primarily targeting academic institutions. The introduction of QIAmini is expected to enhance efficiency in laboratories that do not require larger automation systems.

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QGEN
Sep 18, 2026
QGENGeneral

QIAGEN Calls Extraordinary General Meeting for Appointment of Jonathan M. Pratt to Managing Board

QIAGEN N.V. has scheduled an Extraordinary General Meeting for November 6, 2026, to vote on the appointment of Jonathan M. Pratt to its Managing Board. Pratt, who joined as CEO on September 1, 2026, will potentially join CFO Roland Sackers on the board. This meeting highlights QIAGEN's commitment to shareholder involvement.

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QGEN
Aug 27, 2026
QGENGeneral

QIAGEN Launches QIAsymphony Connect for Automated Clinical Nucleic Acid Extraction

QIAGEN has launched QIAsymphony Connect, an IVD-compliant platform designed for automated clinical nucleic acid extraction. This new platform aims to standardize extraction processes across various assay workflows in clinical laboratories. Leveraging the success of the existing QIAsymphony platform, it promises to enhance efficiency and reliability in nucleic acid extraction.

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QGEN
Aug 24, 2026
QGENGeneral

QIAGEN Appoints Jonathan M. Pratt as Chief Executive Officer

QIAGEN N.V. has appointed Jonathan M. Pratt as the new Chief Executive Officer, effective September 1, 2026. Pratt brings over 25 years of international experience in life sciences, laboratory technologies, and healthcare. His previous role was as President and CEO of Filtration Group, where he successfully led the company through a significant sale.

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QGEN
Aug 24, 2026
QGENGeneral

QIAGEN ernennt Jonathan M. Pratt zum Vorstandsvorsitzenden

QIAGEN N.V. has appointed Jonathan M. Pratt as the new CEO, effective September 1, 2026. Pratt has over 25 years of international leadership experience in life sciences, laboratory technologies, and healthcare. His previous role was as President and CEO of the Filtration Group, where he successfully led the company.

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QGEN
Aug 10, 2026
QGENFDA Updates

QIAGEN Receives U.S. FDA Clearance for First QIAstat-Dx Bloodstream Infection Panel

QIAGEN has received FDA clearance for its QIAstat-Dx BCID GPF Plus AMR Panel, marking the first panel designed for bloodstream infections. This approval broadens QIAGEN's offerings in the syndromic testing market, now covering four major infectious disease areas. The panel aims to enhance diagnostic capabilities in critical infection management.

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QGEN
Aug 5, 2026
QGENGeneral

QIAGEN Exceeds Q2 2026 Outlook as Pillars Deliver Solid Sales Growth; Reaffirms Full-Year Outlook

QIAGEN N.V. reported its Q2 2026 results, showcasing net sales of $535 million, which surpassed expectations. The company maintained profitability and achieved a 5% growth in its key growth pillars. Despite a forecasted decline, QIAGEN's performance remained stable, leading to a reaffirmation of its full-year outlook.

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QGEN
Jul 15, 2026
QGENGeneral

QIAGEN Highlights Molecular Testing Solutions Supporting Response to Growing U.S. Cyclospora Outbreak

QIAGEN N.V. has emphasized its molecular testing solutions that aid in the public health response to the rising cases of cyclosporiasis in the U.S. Since May, over 1,600 confirmed cases have been reported, with an additional 7,000 potential cases under investigation. The company is collaborating with health authorities to tackle the outbreaks effectively.

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QGEN
Jul 15, 2026
QGENConferences/Events

QIAGEN N.V. to Release Results for Q2 2026 and Hold Webcast

QIAGEN N.V. has announced the release of its second quarter 2026 financial results, scheduled for August 5, 2026. A conference call will follow on August 6, allowing stakeholders to discuss the results. This event highlights QIAGEN's commitment to transparency and investor relations.

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QGEN
Jul 14, 2026
QGENGeneral

QIAGEN Expands QIAstat-Dx Bloodstream Infection Testing Menu in Europe

QIAGEN N.V. has launched the CE-IVDR-certified QIAstat-Dx BCID GN Plus AMR Panel in Europe, enhancing its bloodstream infection testing capabilities. This new panel can detect 13 gram-negative bacterial pathogens and 18 antimicrobial resistance markers from positive blood cultures within approximately one hour. This expansion aims to improve diagnostic efficiency in clinical settings.

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QGEN
Jul 14, 2026
QGENGeneral

QIAGEN erweitert QIAstat-Dx-Testmenü für die Diagnostik von Blutstrominfektionen in Europa

QIAGEN has launched the CE-IVDR certified QIAstat-Dx BCID GN Plus AMR Panel in Europe. This new diagnostic tool enhances the QIAstat-Dx platform's capabilities for detecting bloodstream infections. It targets 13 gram-negative bacterial pathogens and includes 18 antimicrobial resistance markers, providing comprehensive diagnostic options for healthcare providers.

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QGEN
Jun 15, 2026
QGENGeneral

QIAGEN erweitert sein QIAcuity-Portfolio für Genexpressionsanalysen und treibt so den Einsatz der digitalen PCR in Forschung und Biopharma weiter voran

QIAGEN is expanding its QIAcuity portfolio for gene expression analysis, enhancing the application of digital PCR in research and biopharma. This move indicates a strategic effort to advance technological capabilities in the field. The expansion aims to meet growing demands in gene expression studies.

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QGEN
Jun 15, 2026
QGENGeneral

QIAGEN Expands QIAcuity Gene Expression Portfolio to Accelerate Digital PCR Adoption Across Research and Biopharma

QIAGEN has announced an expansion of its QIAcuity gene expression portfolio. This initiative is designed to enhance the adoption of digital PCR technologies within the research and biopharma industries. The company's efforts reflect a commitment to advancing molecular diagnostics and supporting scientific innovation.

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QGEN
May 28, 2026
QGENGeneral

QIAGEN Supports Infectious Disease Research and Surveillance Efforts for Bundibugyo Ebolavirus Outbreak

QIAGEN is involved in supporting research and surveillance efforts related to the Bundibugyo Ebolavirus outbreak. The company's contributions aim to enhance the understanding and management of this infectious disease. Further details on specific initiatives or collaborations were not provided in the article.

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QGEN
May 20, 2026
QGENGeneral

QIAGEN launches QIA Agent, connecting AI-driven scientific guidance across Sample to Insight workflows

QIAGEN has launched the QIA Agent, an innovative tool designed to provide AI-driven scientific guidance throughout its Sample to Insight workflows. This new product aims to enhance the efficiency and effectiveness of scientific research by integrating advanced AI capabilities. The launch reflects QIAGEN's commitment to leveraging technology for improved scientific outcomes.

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QGEN
May 19, 2026
QGENGeneral

QIAGEN to advance AI-driven drug discovery with graph-based AI and curated bioinformatics knowledge with NVIDIA

QIAGEN is set to enhance its drug discovery efforts by utilizing AI-driven technologies, particularly graph-based AI and curated bioinformatics knowledge in collaboration with NVIDIA. This initiative aims to streamline and improve the efficiency of drug discovery processes. The partnership is expected to leverage advanced computational methods to analyze biological data effectively.

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QGEN
May 12, 2026
QGENGeneral

QIAGEN to Appoint Dr. Metin Colpan as Honorary Chairman of the Supervisory Board, Continue Governance Renewal and Propose Increased Returns at 2026 Annual General Meeting

QIAGEN has announced the appointment of Dr. Metin Colpan as the Honorary Chairman of the Supervisory Board. This decision is part of the company's ongoing governance renewal efforts. Additionally, QIAGEN plans to propose increased returns at the upcoming 2026 Annual General Meeting.

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QGEN
May 7, 2026
QGENGeneral

QIAGEN plant Einführung eines neuen, vollautomatisierten Sample-to-Insight-Workflows und eines KI-gestützten Tools zur Risikostratifizierung als Weiterentwicklung seines QuantiFERON-Tests zum Nachweis latenter Tuberkulose

QIAGEN announced plans to enhance its QuantiFERON test for latent tuberculosis (TB) with a new automated Sample-to-Insight workflow and an AI-based risk stratification tool. These innovations aim to support high-throughput laboratories in meeting the increasing demand for latent TB screenings. The automated workflow is set to launch by the end of 2027, targeting users of Diasorin's LIAISON systems.

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About Qiagen N.V.

5,500 employees qiagen.com
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