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Quanterix Corporation (QTRX)

NasdaqGM - NasdaqGM Real-time price. Currency in USD
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17.02+0.10 (+0.59%)
At close: 04:00PM EDT
17.02 0.00 (0.00%)
After hours: 04:04PM EDT
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Trade prices are not sourced from all markets
Previous close16.92
Open17.19
Bid16.91 x 100
Ask17.04 x 200
Day's range16.67 - 17.67
52-week range15.32 - 29.70
Volume360,546
Avg. volume372,746
Market cap650.966M
Beta (5Y monthly)1.33
PE ratio (TTM)N/A
EPS (TTM)N/A
Earnings dateN/A
Forward dividend & yieldN/A (N/A)
Ex-dividend dateN/A
1y target estN/A
  • Business Wire

    Quanterix To Report First Quarter 2024 Financial Results

    BILLERICA, Mass., April 29, 2024--Quanterix Corporation (NASDAQ: QTRX), a company fueling scientific discovery through ultrasensitive biomarker detection, today announced that it will host a conference call on Wednesday, May 8, 2024 at 8:30 a.m. E.T., to discuss its first quarter 2024 financial results.

  • Business Wire

    Quanterix Outlines Partner Path With Labs to Expedite Building Global Alzheimer’s Disease Testing Infrastructure

    BILLERICA, Mass., March 21, 2024--Quanterix Corporation (NASDAQ: QTRX), a leading provider of ultra-sensitive research products and high-definition diagnostics, today announced a specific partnership path for laboratories interested in offering Tau based research and diagnostic testing services. Quanterix has secured over thirty U.S. patents protecting our innovative ultra-sensitive research products and high-definition diagnostics, and we continue to secure additional patent protection, both in

  • Business Wire

    Quanterix Granted Breakthrough Device Designation from U.S. FDA for Blood-Based p-Tau 217 Test for Alzheimer’s Disease

    BILLERICA, Mass., March 04, 2024--Quanterix Corporation (NASDAQ: QTRX), a leading provider of ultra-sensitive research products and high-definition diagnostics, announced today that its Simoa® phospho-Tau 217 (p-Tau 217) blood test has been granted Breakthrough Device designation by the U.S. Food and Drug Administration (FDA) as an aid in diagnostic evaluation of Alzheimer’s Disease (AD). The FDA’s Breakthrough Device designation is granted to products that have the potential to offer more effec