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Poxel S.A. (0RA2.L)

LSE - LSE Delayed price. Currency in EUR
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5.64+0.34 (+6.48%)
As of 03:38PM GMT. Market open.
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Previous close5.30
Open5.64
Bid0.00 x 0
Ask0.00 x 0
Day's range5.64 - 5.64
52-week range5.64 - 5.64
Volume78,599
Avg. volumeN/A
Market cap139.325M
Beta (5Y monthly)1.33
PE ratio (TTM)N/A
EPS (TTM)-1.16
Earnings dateN/A
Forward dividend & yieldN/A (N/A)
Ex-dividend dateN/A
1y target estN/A
  • Business Wire

    Poxel to Report its 2022 Full Year Results by the End of March 2023

    LYON, France, March 22, 2023--Regulatory News: POXEL SA (Euronext: POXEL - FR0012432516), a clinical stage biopharmaceutical company developing innovative treatments for serious chronic diseases with metabolic pathophysiology, including non-alcoholic steatohepatitis (NASH) and rare metabolic disorders, announced today that it will report its 2022 full year results by the end of March 2023.

  • Business Wire

    Poxel Announces Upcoming Participation at Evercore ISI’s NASH Renaissance Event

    LYON, France, March 15, 2023--Regulatory News: POXEL SA (Paris:POXEL) (Euronext: POXEL - FR0012432516), a clinical stage biopharmaceutical company developing innovative treatments for serious chronic diseases with metabolic pathophysiology, including non-alcoholic steatohepatitis (NASH) and rare metabolic disorders, today announced its participation at the NASH Renaissance virtual event hosted by Evercore ISI on Thursday, March 30, 2023.

  • Business Wire

    Poxel Announces Publication of Positive Phase 2 Results from Phase 2 NASH Trial (DESTINY-1) for PXL065 in Journal of Hepatology

    LYON, France, March 07, 2023--Regulatory News: POXEL SA (Euronext : POXEL – FR0012432516), clinical stage biopharmaceutical company developing innovative treatments for chronic serious diseases with metabolic pathophysiology, including non-alcoholic steatohepatitis (NASH) and rare metabolic disorders, today announced publication in Journal of Hepatology of positive results for DESTINY-1 (Deuterium-stabilized R-pioglitazone [PXL065] Efficacy and Safety Trial In NASH), a 36-week dose-ranging Phase