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          Negative
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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">Investors Business Daily</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.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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          Negative
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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.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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        <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/2026/06/01/3304714/0/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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          Neutral
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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">MarketBeat</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.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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          Neutral
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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/2026/05/07/3289917/0/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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          Neutral
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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/2026/05/05/3288208/0/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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      <div class="me-0 me-md-5">
        BOSTON, May 05, 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 May 1, 2026, the Compensation Committee of Praxis&#39; Board of Directors granted restricted stock unit awards covering an aggregate of 5,420 shares of its common stock to twenty-o...
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          Neutral
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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 text-size-10">●</div>
        <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/2026/05/04/3287106/0/en/Praxis-Precision-Medicines-to-Report-First-Quarter-2026-Financial-Results-on-Thursday-May-7-2026-and-Participate-in-Upcoming-Investor-Conference.html">Praxis Precision Medicines to Report First Quarter 2026 Financial Results on Thursday, May 7, 2026, and Participate in Upcoming Investor Conference</a>
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      <div class="me-0 me-md-5">
        BOSTON, May 04, 2026 (GLOBE NEWSWIRE) -- Praxis Precision Medicines, Inc. (NASDAQ: PRAX), a fully integrated, leading central nervous system (CNS) precision neuroscience biopharmaceutical company, today announced it will report its financial results for the first quarter ended March 31, 2026, and provide a corporate update before the financial markets open on Thursday, May 7, 2026.
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          Positive
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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.investors.com/news/technology/biotech-stock-praxis-precision-medicines-essential-tremor-treatment/">Why Praxis, A Top 1% Biotech, Just Surged Into A Bullish Breakout</a>
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        Praxis, a top biotech stock, surged Tuesday after the FDA assigned a potential approval date for its essential tremor treatment.
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