{"id":988623,"date":"2026-08-03T11:01:15","date_gmt":"2026-08-03T15:01:15","guid":{"rendered":"https:\/\/www.marketnewsdesk.com\/index.php\/zevra-therapeutics-zvra-securities-investigation-notice-levi-korsinsky\/"},"modified":"2026-08-03T11:01:15","modified_gmt":"2026-08-03T15:01:15","slug":"zevra-therapeutics-zvra-securities-investigation-notice-levi-korsinsky","status":"publish","type":"post","link":"https:\/\/www.marketnewsdesk.com\/index.php\/zevra-therapeutics-zvra-securities-investigation-notice-levi-korsinsky\/","title":{"rendered":"Zevra Therapeutics (ZVRA) Securities Investigation Notice &#8211; Levi &amp; Korsinsky"},"content":{"rendered":"<div class=\"xn-newslines\">\n<p class=\"xn-distributor\">PR Newswire<\/p>\n<\/p><\/div>\n<div class=\"xn-content\">\n<p>\n        <i> Zevra investors who relied on public statements about arimoclomol&#8217;s approval status faced losses after the July 24, 2026 negative opinion issued by the\u00a0<\/i>European Medicines Agency&#8217;s Committee for Medicinal Products for Human Use (&#8220;CHMP&#8221;).<\/p>\n<p>\n        <span class=\"legendSpanClass\">NEW YORK<\/span>, <span class=\"legendSpanClass\">Aug. 3, 2026<\/span> \/PRNewswire\/ &#8212; On July 24, 2026, Zevra Therapeutics (NASDAQ: ZVRA) shares fell approximately 24% after the European Medicines Agency&#8217;s CHMP issued a negative opinion on the Marketing Authorization Application for arimoclomol, branded Meplyffa, for Niemann-Pick disease type C. Investors who lost money on ZVRA are encouraged to act now as Levi &amp; Korsinsky reviews potential securities law claims. <a href=\"https:\/\/edge.prnewswire.com\/c\/link\/?t=0&amp;l=en&amp;o=4743568-2&amp;h=2081314568&amp;u=https%3A%2F%2Fzlk.com%2Fcases%2Fzevra-therapeutics-inc-class-action-lawsuit-zvra-2%3Fprid%3D196413%26wire%3D4&amp;a=+Report+your+Zevra+losses+today\" target=\"_blank\" rel=\"nofollow\"> Report your Zevra losses today<\/a>\u00a0or call (212) 363-7500.<\/p>\n<div class=\"PRN_ImbeddedAssetReference\" id=\"DivAssetPlaceHolder1\">\n<p>\n          <img decoding=\"async\" src=\"https:\/\/mmx.prnewswire.com\/media\/MS650751\/Levi-and-Korsinsky-Logo.jpg?id=OA2820215\" title=\"Levi &amp; Korsinsky, LLP\" alt=\"Levi &amp; Korsinsky, LLP\" \/>\n        <\/p>\n<\/p><\/div>\n<p>The July 24 decline followed the CHMP decision announced before regular market hours. Financial media characterized the resulting decline as the stock&#8217;s worst single-day percentage loss in more than five years, causing shareholders who held ZVRA into the announcement to experience the market reaction.<\/p>\n<p>Levi &amp; Korsinsky&#8217;s investigation is focused on investor impact tied to Zevra&#8217;s public statements about arimoclomol. On May 8, 2024, during Zevra&#8217;s Q1 2024 earnings call, President &amp; CEO Neil McFarlane stated that arimoclomol would &#8220;most likely be the only approved foundational therapy for patients with NPC.&#8221;<\/p>\n<p>If your Zevra investment declined after the July 24, 2026 CHMP news, <a href=\"https:\/\/edge.prnewswire.com\/c\/link\/?t=0&amp;l=en&amp;o=4743568-2&amp;h=2121301486&amp;u=https%3A%2F%2Fzlk.com%2Fcases%2Fzevra-therapeutics-inc-class-action-lawsuit-zvra-2%3Fprid%3D196413%26wire%3D4&amp;a=+submit+your+ZVRA+loss+details+\" target=\"_blank\" rel=\"nofollow\"> submit your ZVRA loss details <\/a> or call (212) 363-7500.<\/p>\n<p>\n        <b> Levi &amp; Korsinsky, LLP\u00a0<\/b>&#8212; Top 50 securities litigation firm (ISS, seven consecutive years). Over 70 professionals. Hundreds of millions recovered.<\/p>\n<p>Frequently Asked Questions About the ZVRA Investigation<\/p>\n<p>\n        <b> Q: What is the ZVRA investigation about?\u00a0<\/b>A: A securities investigation is pending concerning Zevra Therapeutics (NASDAQ: ZVRA) regarding potential misstatements about arimoclomol. Shares fell approximately 24% on July 24, 2026 after CHMP issued a negative opinion on the Marketing Authorization Application for arimoclomol, causing losses for shareholders.<\/p>\n<p>\n        <b> Q: Who is eligible to participate in the ZVRA investigation?\u00a0<\/b>A: Investors who purchased ZVRA stock or securities and suffered financial losses may be eligible. Eligibility is based on purchase date and documented losses &#8212; not on whether you still hold the shares.<\/p>\n<p>\n        <b> Q: Which statements are being investigated as potentially misleading?<\/b>\u00a0A: The investigation concerns public statements about arimoclomol, including the May 8, 2024 earnings-call statement by President &amp; CEO Neil McFarlane that arimoclomol would &#8220;most likely be the only approved foundational therapy for patients with NPC.&#8221;<\/p>\n<p>\n        <b> Q: What do ZVRA investors need to do right now?\u00a0<\/b>A: Investors may gather brokerage records showing purchase dates, share quantities, and prices paid. Investors may request a free, no-obligation evaluation from Levi &amp; Korsinsky.<\/p>\n<p>\n        <b> Q: What documents do I need to participate?<\/b>\u00a0A: Brokerage statements or trade confirmations showing purchase dates, share quantities, prices paid, and any subsequent sale dates and prices.<\/p>\n<p>\n        <b> Q: What if I already sold my ZVRA shares &#8212; can I still recover losses?\u00a0<\/b>A: Yes. Eligibility is based on when you purchased, not whether you still hold the shares. Investors who bought ZVRA and sold at a loss may still participate in the investigation.<\/p>\n<p>\n        <b> Q: What if my ZVRA losses are small &#8212; is it still worth contacting a lawyer?\u00a0<\/b>A: Yes. There is no minimum loss amount required to participate in the investigation.<\/p>\n<p>\n        <b>Q: What does it cost me to participate?\u00a0<\/b>A: There is no upfront cost to participate. Securities investigations and any later investor recovery efforts are generally handled on a contingency basis. No upfront fees, no retainer, and no out-of-pocket costs.<\/p>\n<p>CONTACT:\\<\/p>\n<p>Levi &amp; Korsinsky, LLP\\<\/p>\n<p>Joseph E. Levi, Esq.\\<\/p>\n<p>Ed Korsinsky, Esq.\\<\/p>\n<p>33 Whitehall Street, 27th Floor\\<\/p>\n<p>New York, NY 10004\\<\/p>\n<p>\n        <a href=\"mailto:jlevi@levikorsinsky.com\" target=\"_blank\" rel=\"nofollow\"> jlevi@levikorsinsky.com<\/a>\\<\/p>\n<p>Tel: (212) 363-7500\\<\/p>\n<p>Fax: (212) 363-7171<\/p>\n<p>Attorney Advertising. Prior results do not guarantee similar outcomes.<\/p>\n<p id=\"PURL\">\n        <img loading=\"lazy\" decoding=\"async\" title=\"Cision\" width=\"12\" height=\"12\" alt=\"Cision\" src=\"https:\/\/edge.prnewswire.com\/c\/img\/favicon.png?sn=NY17018&amp;sd=2026-08-03\" \/> View original content to download multimedia:<a id=\"PRNURL\" rel=\"nofollow\" href=\"https:\/\/www.prnewswire.com\/news-releases\/zevra-therapeutics-zvra-securities-investigation-notice---levi--korsinsky-302840726.html\" target=\"_blank\">https:\/\/www.prnewswire.com\/news-releases\/zevra-therapeutics-zvra-securities-investigation-notice&#8212;levi&#8211;korsinsky-302840726.html<\/a><\/p>\n<p>SOURCE Levi &amp; Korsinsky, LLP<\/p>\n<\/p><\/div>\n<p>    <img decoding=\"async\" alt=\"\" src=\"https:\/\/rt.prnewswire.com\/rt.gif?NewsItemId=NY17018&amp;Transmission_Id=202608031007PR_NEWS_USPR_____NY17018&amp;DateId=20260803\" style=\"border:0px;width:1px;height:1px\" \/><\/p>\n","protected":false},"excerpt":{"rendered":"<p>PR Newswire Zevra investors who relied on public statements about arimoclomol&#8217;s approval status faced losses after the July 24, 2026 negative opinion issued by the\u00a0European Medicines Agency&#8217;s Committee for Medicinal Products for Human Use (&#8220;CHMP&#8221;). NEW YORK, Aug. 3, 2026 \/PRNewswire\/ &#8212; On July 24, 2026, Zevra Therapeutics (NASDAQ: ZVRA) shares fell approximately 24% after the European Medicines Agency&#8217;s CHMP issued a negative opinion on the Marketing Authorization Application for arimoclomol, branded Meplyffa, for Niemann-Pick disease type C. Investors who lost money on ZVRA are encouraged to act now as Levi &amp; Korsinsky reviews potential securities law claims. Report your Zevra losses today\u00a0or call (212) 363-7500. The July 24 decline followed the CHMP decision announced before regular market hours. Financial &hellip; <\/p>\n<p class=\"link-more\"><a href=\"https:\/\/www.marketnewsdesk.com\/index.php\/zevra-therapeutics-zvra-securities-investigation-notice-levi-korsinsky\/\" class=\"more-link\">Continue reading<span class=\"screen-reader-text\"> &#8220;Zevra Therapeutics (ZVRA) Securities Investigation Notice &#8211; Levi &amp; Korsinsky&#8221;<\/span><\/a><\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[],"tags":[],"class_list":["post-988623","post","type-post","status-publish","format-standard","hentry"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v28.1 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Zevra Therapeutics (ZVRA) Securities Investigation Notice - Levi &amp; Korsinsky - Market Newsdesk<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.marketnewsdesk.com\/index.php\/zevra-therapeutics-zvra-securities-investigation-notice-levi-korsinsky\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Zevra Therapeutics (ZVRA) Securities Investigation Notice - Levi &amp; Korsinsky - Market Newsdesk\" \/>\n<meta property=\"og:description\" content=\"PR Newswire Zevra investors who relied on public statements about arimoclomol&#8217;s approval status faced losses after the July 24, 2026 negative opinion issued by the\u00a0European Medicines Agency&#8217;s Committee for Medicinal Products for Human Use (&#8220;CHMP&#8221;). NEW YORK, Aug. 3, 2026 \/PRNewswire\/ &#8212; On July 24, 2026, Zevra Therapeutics (NASDAQ: ZVRA) shares fell approximately 24% after the European Medicines Agency&#8217;s CHMP issued a negative opinion on the Marketing Authorization Application for arimoclomol, branded Meplyffa, for Niemann-Pick disease type C. Investors who lost money on ZVRA are encouraged to act now as Levi &amp; Korsinsky reviews potential securities law claims. Report your Zevra losses today\u00a0or call (212) 363-7500. The July 24 decline followed the CHMP decision announced before regular market hours. 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NEW YORK, Aug. 3, 2026 \/PRNewswire\/ &#8212; On July 24, 2026, Zevra Therapeutics (NASDAQ: ZVRA) shares fell approximately 24% after the European Medicines Agency&#8217;s CHMP issued a negative opinion on the Marketing Authorization Application for arimoclomol, branded Meplyffa, for Niemann-Pick disease type C. Investors who lost money on ZVRA are encouraged to act now as Levi &amp; Korsinsky reviews potential securities law claims. Report your Zevra losses today\u00a0or call (212) 363-7500. The July 24 decline followed the CHMP decision announced before regular market hours. Financial &hellip; Continue reading \"Zevra Therapeutics (ZVRA) Securities Investigation Notice &#8211; Levi &amp; Korsinsky\"","og_url":"https:\/\/www.marketnewsdesk.com\/index.php\/zevra-therapeutics-zvra-securities-investigation-notice-levi-korsinsky\/","og_site_name":"Market Newsdesk","article_published_time":"2026-08-03T15:01:15+00:00","og_image":[{"url":"https:\/\/mmx.prnewswire.com\/media\/MS650751\/Levi-and-Korsinsky-Logo.jpg?id=OA2820215","type":"","width":"","height":""}],"author":"Newsdesk","twitter_card":"summary_large_image","twitter_misc":{"Written by":"Newsdesk","Est. reading time":"3 minutes"},"schema":{"@context":"https:\/\/schema.org","@graph":[{"@type":"Article","@id":"https:\/\/www.marketnewsdesk.com\/index.php\/zevra-therapeutics-zvra-securities-investigation-notice-levi-korsinsky\/#article","isPartOf":{"@id":"https:\/\/www.marketnewsdesk.com\/index.php\/zevra-therapeutics-zvra-securities-investigation-notice-levi-korsinsky\/"},"author":{"name":"Newsdesk","@id":"https:\/\/www.marketnewsdesk.com\/#\/schema\/person\/482f27a394d4fda80ecb5499e519d979"},"headline":"Zevra Therapeutics (ZVRA) Securities Investigation Notice &#8211; 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