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Syros Pharmaceuticals, Inc. (SYRS)

NasdaqGS - NasdaqGS Real-time price. Currency in USD
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5.15+0.07 (+1.38%)
At close: 04:00PM EDT
5.15 0.00 (0.00%)
After hours: 04:06PM EDT
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Trade prices are not sourced from all markets
Previous close5.08
Open5.06
Bid5.09 x 100
Ask5.18 x 100
Day's range5.06 - 5.32
52-week range2.09 - 8.17
Volume105,556
Avg. volume202,188
Market cap137.651M
Beta (5Y monthly)1.78
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

    Syros to Participate in Upcoming Investor Conferences

    CAMBRIDGE, Mass., May 07, 2024--Syros Pharmaceuticals (NASDAQ:SYRS), a biopharmaceutical company committed to advancing new standards of care for the frontline treatment of hematologic malignancies, today announced that company management will participate in a fireside chat at two upcoming investor conferences. Details are as follows:

  • Business Wire

    Syros to Report First Quarter 2024 Financial Results on Tuesday, May 14, 2024

    CAMBRIDGE, Mass., May 07, 2024--Syros Pharmaceuticals (NASDAQ:SYRS), a biopharmaceutical company committed to advancing new standards of care for the frontline treatment of hematologic malignancies, today announced that it will host a live conference call and webcast at 8:30 a.m. ET on Tuesday, May 14, 2024 to report its first quarter 2024 financial results and provide a corporate update.

  • Business Wire

    Syros Receives Fast Track Designation from the FDA for Tamibarotene for the Treatment of Newly Diagnosed Unfit AML with RARA gene overexpression

    CAMBRIDGE, Mass., April 09, 2024--Syros Pharmaceuticals (NASDAQ:SYRS), a biopharmaceutical company committed to advancing new standards of care for the frontline treatment of hematologic malignancies, today announced that the United States Food and Drug Administration (FDA) has granted Fast Track Designation to tamibarotene in combination with azacitidine and venetoclax for the treatment of newly diagnosed acute myeloid leukemia (AML) with RARA overexpression as detected by an FDA approved test