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Xenon Pharmaceuticals to Present at the BofA Securities Health Care Conference 2023
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Xenon Pharmaceuticals Inc. to present at BofA Securities Health Care Conference 2023
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Xenon Pharmaceuticals Inc. will present at the BofA Securities Health Care Conference 2023 on May 10, 2023 at 4:20 pm Pacific Time. The presentation will be available via live webcast on the company's website.
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VANCOUVER, British Columbia, May 03, 2023 (GLOBE NEWSWIRE) -- Xenon Pharmaceuticals Inc. (Nasdaq:XENE), a neurology-focused biopharmaceutical company, today announced that the company will present at the BofA Securities Health Care Conference 2023 taking place May 9-11, 2023.
Company Fireside Chat Presentation Details:
Date:
Wednesday, May 10, 2023
Time:
4:20 pm Pacific Time (7:20 pm Eastern Time)
Presenters:
Ian Mortimer, President and CEO Sherry Aulin, CFO
A live webcast of the company presentation will be available on the “Investors” section of Xenon's website and posted for replay following the event. The above listed dates and times are subject to change.
About Xenon Pharmaceuticals Inc.
Xenon Pharmaceuticals (NASDAQ:XENE) is a clinical stage biopharmaceutical company committed to developing innovative therapeutics to improve the lives of patients with neurological disorders. We are advancing a novel product pipeline of neurology therapies to address areas of high unmet medical need, with a focus on epilepsy. For more information, please visit www.xenon-pharma.com.
“Xenon” and the Xenon logo are registered trademarks or trademarks of Xenon Pharmaceuticals Inc. in various jurisdictions. All other trademarks belong to their respective owner.
xenon® (nasdaq: xene) is a biopharmaceutical company focused on the development of novel medicines through the application of our proprietary discovery platform, which we refer to as extreme genetics. our product candidates are based on genetic insights derived from our research of families where individuals exhibit severe traits, or phenotypes. we apply our expertise to predict which phenotypes are caused by single-gene defects. by identifying and characterizing the single-gene defects responsible for such severe phenotypes, we gain valuable insights into their function in human biology and their potential as drug targets. given that these targets are often involved in diseases beyond the rare genetic disorders in which they are first identified, we are developing proprietary product candidates to treat both orphan as well as more prevalent diseases.
