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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/en/stock/Praxis-Precision-Medicines-Inc-US74006W1080">Praxis Precision Medicines Inc</a></div>
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        <div class="me-2 text-gray">4 months ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.globenewswire.com/news-release/2026/06/29/3319308/0/en/Praxis-Precision-Medicines-Announces-Extension-Period-for-Relutrigine-for-Treatment-of-SCN2A-and-SCN8A-Developmental-and-Epileptic-Encephalopathies.html">Praxis Precision Medicines Announces Extension Period for Relutrigine for Treatment of SCN2A and SCN8A Developmental and Epileptic Encephalopathies</a>
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        FDA sets updated PDUFA date of December 27, 2026 BOSTON, June 29, 2026 (GLOBE NEWSWIRE) -- Praxis Precision Medicines , Inc. (NASDAQ: PRAX), a fully integrated, leading central nervous system (CNS) precision neuroscience biopharmaceutical company, today announced that the U.S. Food and Drug Administration (FDA) notified Praxis that it has extended by three months the review period for its New D...
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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/en/stock/Praxis-Precision-Medicines-Inc-US74006W1080">Praxis Precision Medicines Inc</a></div>
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        <div class="me-2 text-gray">5 months ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.globenewswire.com/news-release/2026/06/22/3315249/0/en/praxis-precision-medicines-receives-fda-breakthrough-therapy-designation-for-elsunersen-for-the-treatment-of-seizures-associated-with-scn2a-developmental-and-epileptic-encephalopat.html">Praxis Precision Medicines Receives FDA Breakthrough Therapy Designation for Elsunersen for the Treatment of Seizures Associated with SCN2A Developmental and Epileptic Encephalopathy Caused by Gain of Function Variants</a>
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        The Breakthrough Therapy Designation (BTD) was granted based on the positive results from the EMBRAVE Part A trial of elsunersen Elsunersen demonstrated a 77% sham-adjusted reduction in monthly seizures (p=0.015), with benefit sustained in the open-label extension for up to one year The pivotal EMBRAVE3 study is enrolling under a streamlined, single-arm registrational pathway aligned with the F...
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        <div class="me-2 text-gray">5 months ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.globenewswire.com/news-release/2026/06/02/3305570/0/en/Praxis-Precision-Medicines-Inc-Announces-Inducement-Grants-Under-Nasdaq-Listing-Rule-5635-c-4.html">Praxis Precision Medicines, Inc. Announces Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)</a>
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        BOSTON, June 02, 2026 (GLOBE NEWSWIRE) -- Praxis Precision Medicines, Inc. (Nasdaq: PRAX), a fully integrated, leading central nervous system (CNS) precision neuroscience biopharmaceutical company, today announced that on June 1, 2026, the Compensation Committee of Praxis&#39; Board of Directors granted restricted stock unit awards covering an aggregate of 2,754 shares of its common stock to thirte...
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        <div class="me-2 text-gray">5 months ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.investors.com/news/technology/praxis-stock-praxis-precision-medicines-seizure-treatment/">The Shocking Twist That Sent This Seizure-Focused Biotech Into A Dive</a>
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        Praxis Precision Medicines unexpectedly halted enrollment in a late-stage study of its seizure drug. Praxis stock tumbled.
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        <div class="me-2 text-gray">5 months ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.reuters.com/legal/litigation/praxis-precisions-epilepsy-drug-misses-main-goal-mid-to-late-stage-study-2026-06-01/">Praxis Precision&#39;s epilepsy drug misses main goal of mid-to-late stage study</a>
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        Praxis Precision Medicines said on Monday its experimental epilepsy drug failed to meet the ​main goal of a mid- to late-stage ‌study, prompting it to pause enrollment in another ongoing study while it reassesses the program.
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      <a target="_blank" rel="nofollow" href="https://www.globenewswire.com/news-release/2026/06/01/3304714/0/en/Praxis-Precision-Medicines-Provides-Vormatrigine-Program-Update.html">Praxis Precision Medicines Provides Vormatrigine Program Update</a>
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        POWER1 Study in highly refractory patients with focal onset seizures did not meet its primary success measure Secondary measure, the 50% response rate, was met and seizure reduction during the second half of the study on higher dose (30 mg) was more pronounced Vormatrigine was generally well-tolerated; adverse event-related discontinuations were less than 10% Approximately 90% of patients from ...
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        <div class="me-2 text-gray">6 months ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.marketbeat.com/instant-alerts/praxis-precision-medicines-q1-earnings-call-highlights-2026-05-08/?utm_source=snapi">Praxis Precision Medicines Q1 Earnings Call Highlights</a>
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        Praxis Precision Medicines NASDAQ: PRAX said it is preparing for two potential U.S. product launches while advancing several late-stage clinical programs, as management outlined first-quarter 2026 results and pipeline updates on the company&#39;s earnings call.
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        <div class="me-2 text-gray">6 months ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.globenewswire.com/news-release/2026/05/07/3289917/0/en/Praxis-Precision-Medicines-Provides-Corporate-Update-and-Reports-First-Quarter-2026-Financial-Results.html">Praxis Precision Medicines Provides Corporate Update and Reports First Quarter 2026 Financial Results</a>
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        FDA accepted the new drug application (NDA) for ulixacaltamide in Essential Tremor with a PDUFA target action date of January 29, 2027, and the NDA for relutrigine, with priority review, in SCN2A and SCN8A developmental and epileptic encephalopathies (DEEs) with a PDUFA target action date of September 27, 2026
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