{"id":967175,"date":"2026-05-27T02:35:10","date_gmt":"2026-05-27T06:35:10","guid":{"rendered":"https:\/\/www.marketnewsdesk.com\/index.php\/aligos-therapeutics-presents-positive-data-at-the-easl-congress-2026\/"},"modified":"2026-05-27T02:35:10","modified_gmt":"2026-05-27T06:35:10","slug":"aligos-therapeutics-presents-positive-data-at-the-easl-congress-2026","status":"publish","type":"post","link":"https:\/\/www.marketnewsdesk.com\/index.php\/aligos-therapeutics-presents-positive-data-at-the-easl-congress-2026\/","title":{"rendered":"Aligos Therapeutics Presents Positive Data at the EASL Congress 2026"},"content":{"rendered":"<div class=\"mw_release\">\n<ul type=\"disc\">\n<li style=\"margin-bottom:6pt\">\n          <em>Long-term follow up data from the Phase 1 study of pevifoscorvir sodium continues to suggest a reduction in the cccDNA reservoir<\/em>\n        <\/li>\n<li style=\"margin-bottom:6pt\">\n          <em>Data on the preclinical characteristics of the Aligos\/Amoytop ASO program to be presented<\/em>\n        <\/li>\n<li style=\"margin-bottom:6pt\">\n          <em>40% of HBeAg+ participants with chronic HBV infection treated with pevifoscorvir sodium at week 48 had reductions in HBsAg that would potentially allow them to qualify for ASO treatment<\/em><br \/>\n          \n        <\/li>\n<\/ul>\n<p>SOUTH SAN FRANCISCO, Calif., May  27, 2026  (GLOBE NEWSWIRE) &#8212; Aligos Therapeutics, Inc. (Nasdaq: ALGS), a clinical stage biopharmaceutical company focused on improving patient outcomes through best-in-class therapies for liver and viral diseases, today announced positive data from ten presentations at the European Association for the Study of the Liver (EASL) Congress 2026, being held May 27 \u2013 30, 2026 in Barcelona, Spain.<\/p>\n<p>\u201cWe are pleased to present positive data, including an investigator led study of \u226524 week follow up in HBeAg+ participants with nucleos(t)ide analogs (NAs) after 96 weeks of pevifoscorvir sodium monotherapy, which further supports our belief that we are reducing the cccDNA reservoir by activating the secondary mechanism of CAM-Es. By accessing this mechanism, we are also reducing HBsAg to a level that may allow additional patients to be eligible for functional cure therapy, including the ASO ALG-170675, being developed by Aligos and partner Amoytop,\u201d stated Lawrence Blatt, Ph.D., M.B.A., Chairman, President, and Chief Executive Officer of Aligos Therapeutics. \u201cFurther, we will present data demonstrating that the combination of pevifoscorvir sodium and our antisense oligonucleotide ALG-170675 showed an additive to synergistic effects on reductions in HBV viral markers. Taken together, these data signal that pevifoscorvir sodium has the potential to not only replace NAs as the standard of care for chronic HBV infection but play a meaningful part in a functional cure regimen.\u201d<\/p>\n<p>\n        <em>Pevifoscorvir Sodium Post Treatment Data<\/em>\n      <\/p>\n<p>Newly presented data highlight outcomes for treatment-na\u00efve or currently not treated HBeAg+ subjects who completed 96 weeks of 300 mg pevifoscorvir sodium monotherapy, followed by \u226524 weeks of nucleos(t)ide analog (NA) monotherapy. Among HBeAg+ subjects, 9 of 10 subjects transitioned to NA monotherapy; of these, 4 (44%) maintained HBV DNA levels below the lower limit of quantification (LLOQ; 10 IU\/mL, target detected [TD] or target not detected [TND]) throughout the NA only \u226524 week follow-up period. Reductions in HBV antigens and HBV RNA were maintained during the NA only \u226524 week follow-up period. Notably, these viral biomarkers, such as HBV antigens and HBV RNA, are typically unaffected by NA therapy, suggesting that pevifoscorvir sodium may reduce the cccDNA reservoir through engagement of its secondary mechanism of action.<\/p>\n<p>In addition, newly presented data showed that among participants with a baseline HBsAg \u22653,000 IU\/mL, 40% (4\/10) achieved HBsAg &lt;3,000 IU\/mL at 48 weeks, suggesting eligibility for a functional cure regimen, which may include an antisense oligonucleotide (ASO) agent. In clinical trials conducted to date, certain ASO agents under development for chronic HBV infection have seen 20-30% functional cure rates in a patient population of HBsAg &lt;3,000 IU\/mL.<\/p>\n<p>Additionally, preclinical in vitro data demonstrated that long-term treatment with ALG-001075, the active parent moiety of pevifoscorvir sodium, resulted in profound suppression of HBeAg, HBsAg and intracellular HBV RNAs which was durable after treatment withdrawal in HBV-infected HepaRG cells, suggesting a potential reduction in cccDNA level and\/or transcriptional activity.<\/p>\n<p>\n        <em>Preclinical Data<\/em>\n      <\/p>\n<p>The preclinical posters showcased Aligos\u2019 and its collaborators\u2019 continued innovation and commitment to advancing next-generation therapies in the liver and viral spaces with presentations spanning novel approaches and mechanistic insights.<\/p>\n<p>In particular, an analog of ALG-170675, a potential best-in-class antisense oligonucleotide (ASO), demonstrated an additive to synergistic effect when combined in vitro and in vivo with ALG-001075, the active parent moiety of pevifoscorvir sodium.<\/p>\n<p>Additionally, in vitro data from the hepatitis delta virus (HDV) program demonstrates how the novel approach of targeting HDV replication could be a valuable addition to the current therapeutic arsenal.<\/p>\n<p>Details on the presentations are as follows:<\/p>\n<p>\n        <strong><br \/>\n          <u>Pevifoscorvir sodium: Potential first-\/best-in-class small molecule CAM-E for chronic hepatitis B<\/u><br \/>\n        <\/strong><br \/>\n        <u>\u00a0<\/u><br \/>\n        <strong><br \/>\n          <u>virus (HBV) infection<\/u><br \/>\n        <\/strong>\n      <\/p>\n<p>\n        <strong>Abstract #:<\/strong> 588<br \/><strong>Title: <\/strong><em>Sustained reduction of HBV antigen levels at \u22656 months follow-up in HBeAg-positive participants with chronic hepatitis B infection after 96 weeks of 300 mg pevifoscorvir sodium monotherapy<\/em><br \/><strong>Presenter:<\/strong> Professor Lung-Yi Mak, MBBS(HK), MD(HK), MRCP(UK), PDipID (HK), FHKCP, FHKAM (Medicine), FRCP (Glasg), FRCP (Edin), FRCP, Clinical Assistant Professor at The University of Hong Kong<br \/><strong>Date\/Time:<\/strong> May 27, 2026 at 8:30am \u2013 5:00pm CET<br \/><strong>Session: <\/strong>Poster Tour \u2013 Track 8 \u2013 Viral Hepatitis; Viral Hepatitis B and D: New therapies, unapproved therapies or strategies<\/p>\n<p>\n        <strong>Abstract #:<\/strong> 602<br \/><strong>Title: <\/strong><em>Pevifoscorvir sodium demonstrated profound antiviral activity in untreated HBeAg+ subjects, regardless of baseline ALT level<\/em><br \/><strong>Presenter:<\/strong> Professor Man-Fung Yuen, MBBS, MD, PhD, DSc, Chair and Chief of the Division of Gastroenterology and Hepatology, University of Hong Kong<br \/><strong>Date\/Time:<\/strong> May 27, 2026 at 8:30am \u2013 5:00pm CET<br \/><strong>Session: <\/strong>Poster Tour \u2013 Track 8 \u2013 Viral Hepatitis; Viral Hepatitis B and D: New therapies, unapproved therapies or strategies<\/p>\n<p>\n        <strong>Abstract #:<\/strong> 586<br \/><strong>Title: <\/strong><em>Population pharmacokinetics of pevifoscorvir sodium (ALG-000184) in healthy participants and participants with chronic hepatitis B in support of phase 2 dose selection<\/em><br \/><strong>Presenter:<\/strong> Kha Le, PhD<br \/><strong>Date\/Time:<\/strong> May 27, 2026 at 8:30am \u2013 5:00pm CET<br \/><strong>Session:<\/strong> Viral Hepatitis B and D: New therapies, unapproved therapies or strategies<\/p>\n<p>\n        <strong>Abstract #:<\/strong> 570<br \/><strong>Title: <\/strong><em>ALG-001075, the parent of pevifoscorvir sodium, exhibits potent in vitro antiviral properties compared to other HBV capsid assembly modulators in clinical development<\/em><br \/><strong>Presenter:<\/strong> Yannick Debing, PhD<br \/><strong>Date\/Time:<\/strong> May 28, 2026 at 8:30am \u2013 5:00pm CET<br \/><strong>Session: <\/strong>Viral Hepatitis: Experimental and pathophysiology<\/p>\n<p>\n        <strong>Abstract #:<\/strong> 634<br \/><strong>Title: <\/strong><em>Potent and durable off-treatment reduction of HBsAg levels and cccDNA-derived transcripts by the CAM-E ALG-001075 in cell-based experiments<\/em><br \/><strong>Presenter:<\/strong> Professor Barbara Testoni, PhD, HDR, DR2 INSERM &#8211; Team Leader &#8220;Hepatitis Viruses and Liver pathogenesis&#8221;. Universit\u00e9 Claude Bernand Lyon 1, Inserm UMR 1350 &#8211; PaThLiv<br \/><strong>Date\/Time:<\/strong> May 28, 2026 at 8:30am \u2013 5:00pm CET<br \/><strong>Session: <\/strong>Viral Hepatitis: Experimental and pathophysiology<\/p>\n<p>\n        <strong><br \/>\n          <u>ALG-170675: Potential best-in-class antisense oligonucleotide (ASO) for chronic hepatitis B virus (HBV) infection<\/u><br \/>\n        <\/strong>\n      <\/p>\n<p>\n        <strong>Abstract #:<\/strong> 587<br \/><strong>Title: <\/strong><em>The potentially best-in-class HBV ASO ALG-170674 demonstrates additive to synergistic antiviral activities when combined with other anti-HBV modalities<\/em><br \/><strong>Presenter:<\/strong> Jin Hong, PhD<br \/><strong>Date\/Time:<\/strong> May 28, 2026 at 8:30am \u2013 5:00pm CET<br \/><strong>Session: <\/strong>Viral Hepatitis: Experimental and pathophysiology<\/p>\n<p>\n        <strong><br \/>\n          <u>ALG-055009: Potential best-in-class small molecule THR-<\/u><br \/>\n        <\/strong><br \/>\n        <strong><br \/>\n          <u>\u03b2<\/u><br \/>\n        <\/strong><br \/>\n        <strong><br \/>\n          <u> Agonist for Metabolic Dysfunction-Associated Steatohepatitis (MASH)<\/u><br \/>\n        <\/strong>\n      <\/p>\n<p>\n        <strong>Abstract #: <\/strong>184<br \/><strong>Title: <\/strong><em>Synergistic fat mass loss in diet-induced obese mice when thyroid hormone receptor-\u03b2 agonist ALG-055009 was administered in combination with incretin receptor agonists<\/em><br \/><strong>Presenter:<\/strong> Xuan Luong, PhD<br \/><strong>Date\/Time: <\/strong>May 30, 2025 at 8:30am \u2013 4:00pm CET<br \/><strong>Session:<\/strong> Poster &#8211; MASLD: Experimental and pathophysiology<\/p>\n<p>\n        <strong><br \/>\n          <u>Preclinical<\/u><br \/>\n        <\/strong>\n      <\/p>\n<p>\n        <strong>Abstract #:<\/strong> 606<br \/><strong>Title: <\/strong><em>Antisense oligonucleotide-based strategy to target hepatitis delta virus infections<\/em><br \/><strong>Presenter:<\/strong> Julie Lucifora, PhD, HDR, Director of Research, INSERM, CIRI &#8211; Centre International de Recherche en Infectiologie <br \/><strong>Date\/Time:<\/strong> May 28, 2026 at 12:45 \u2013 1:45pm CET; May 28, 2026 at 8:30am \u2013 5:00pm CET<br \/><strong>Session:<\/strong> Poster Tour \u2013 Track 8 \u2013 Viral Hepatitis; Viral Hepatitis: Experimental and pathophysiology<\/p>\n<p>\n        <strong>Abstract #:<\/strong> 610<br \/><strong>Title: <\/strong><em>Discovery of novel HDV entry inhibitors with selectivity over bile acid inhibition<\/em><br \/><strong>Presenter:<\/strong> David McGowan, MS<br \/><strong>Date\/Time:<\/strong> May 28, 2026 at 8:30am \u2013 5:00pm CET<br \/><strong>Session: <\/strong>Viral Hepatitis: Experimental and pathophysiology<\/p>\n<p>\n        <strong>Abstract #:<\/strong> 620<br \/><strong>Title: <\/strong><em>Preclinical characterization of ALG-093940, a potent and orally bioavailable small molecule PD-1\/PD-L1 inhibitor for the treatment of chronic hepatitis B infection and liver cancer<\/em><br \/><strong>Presenter:<\/strong> Heleen Roose, PhD<br \/><strong>Date\/Time:<\/strong> May 28, 2026 at 8:30am \u2013 5:00pm CET<br \/><strong>Session: <\/strong>Viral Hepatitis: Experimental and pathophysiology<\/p>\n<p>The presentations can be found on the Posters &amp; Presentations section of the Aligos website (<a href=\"https:\/\/www.globenewswire.com\/Tracker?data=6kN9H4VPhPp8MpsNkBmrW2bPziEQ4F9xtpBx3AR_lq5mJ7VXHJMpX7mkcb2uu1ytiTNh5KtUJheI_ngFgGXaMA==\" rel=\"nofollow\" target=\"_blank\">www.aligos.com<\/a>) after the live event.<\/p>\n<p>\n        <strong>About Aligos<\/strong>\n      <\/p>\n<p>Aligos Therapeutics, Inc. (NASDAQ: ALGS) is a clinical stage biotechnology company founded with the mission to improve patient outcomes by developing best-in-class therapies for the treatment of liver and viral diseases. Aligos applies its science driven approach and deep R&amp;D expertise to advance its purpose-built pipeline of therapeutics for high unmet medical needs such as chronic hepatitis B virus infection, metabolic dysfunction-associated steatohepatitis (MASH), obesity, and coronaviruses.<\/p>\n<p>For more information, please visit <a href=\"https:\/\/www.globenewswire.com\/Tracker?data=6kN9H4VPhPp8MpsNkBmrW9JPZqDt3ht8gtVmVighPG_PBllxLnnBExNmx2OZmS783m1K0r4BcLW-Do3FGw6BXA==\" rel=\"nofollow\" target=\"_blank\">www.aligos.com<\/a> or follow us on LinkedIn or X.<\/p>\n<p>\n        <strong>Forward-Looking Statements <\/strong>\n      <\/p>\n<p>This press release contains forward-looking statements within the meaning of the U.S. Private Securities Litigation Reform Act of 1995. Any statements in this press release that are not historical facts may be considered \u201cforward-looking statements,\u201d including without limitation, statements regarding Aligos\u2019 financial results and performance as well as research and development activities, including regulatory status and the timing of announcements and updates relating to our regulatory filings and clinical trials; statements about the potential benefits of pevifoscorvir sodium including its potential to replace NAs as the standard of care for chronic HBV infection and be part of a functional cure regimen, and whether the B-SUPREME study will show superiority of pevifoscorvir sodium over NAs; statements about whether pevifoscorvir sodium will be shown to reduce the cccDNA reservoir; and statements about the potential benefits of combining pevifoscorvir sodium with an ASO agent. Such forward looking statements are subject to substantial risks and uncertainties that could cause our development programs, future results, performance, or achievements to differ materially from those anticipated in the forward-looking statements. Such risks and uncertainties include, without limitation, risks and uncertainties inherent in the drug development process, including Aligos\u2019 clinical-stage of development, the process of designing and conducting clinical trials, the regulatory approval processes, and other matters that could affect the sufficiency of Aligos\u2019 capital resources to fund operations. For a further description of the risks and uncertainties that could cause actual results to differ from those anticipated in these forward-looking statements, as well as risks relating to the business of Aligos in general, see Aligos\u2019 Quarterly Report on Form 10-Q filed with the Securities and Exchange Commission on May 7, 2026 and its future periodic reports to be filed or submitted with the Securities and Exchange Commission. Except as required by law, Aligos undertakes no obligation to update any forward-looking statements to reflect new information, events or circumstances, or to reflect the occurrence of unanticipated events. <\/p>\n<p>\n        <strong>Investor Contact<\/strong><br \/>\n        <br \/>Aligos Therapeutics, Inc.<br \/>Jordyn Tarazi<br \/>Vice President, Investor Relations &amp; Corporate Communications<br \/>+1 (650) 910-0427<br \/><a href=\"https:\/\/www.globenewswire.com\/Tracker?data=XMSNbAhbZw4YVdcUEmBoExAWPbEiCWxhnG-NgcZWTd2e9r1OFuTltji__NWSCVQcyW8GcXavLXy2ly7PaIT9o1jdoc7yMe_VmRpxA5A9s7c=\" rel=\"nofollow\" target=\"_blank\">jtarazi@aligos.com<\/a><\/p>\n<p>\n        <strong>Media Contact<\/strong><br \/>\n        <br \/>Inizio Evoke<br \/>Jake Robison<br \/>Vice President<br \/><a href=\"https:\/\/www.globenewswire.com\/Tracker?data=v8chmawbpwK-YP6PooH8VPPQapTtEiPNot0uW6-R_GgHQwDh2HYxCICEA3_YNxM0F5R9HbFRPYnNVoAwvGTyqElCz9A8kE2oB9YoH2E1NaeIlKWUyXwN2QRluDrNalE7\" rel=\"nofollow\" target=\"_blank\">Jake.Robison@inizioevoke.com<\/a><\/p>\n<p>      <img decoding=\"async\" alt=\"\" class=\"__GNW8366DE3E__IMG\" src=\"https:\/\/www.globenewswire.com\/newsroom\/ti?nf=OTcyNjY2NCM3NjIxMTM5IzIyMDM5MTY=\" \/><br \/>\n      <br \/>\n      <img decoding=\"async\" alt=\"\" src=\"https:\/\/ml.globenewswire.com\/media\/ZDVjMjU4MDgtYTQwYi00MjJkLTgxNTMtNGYwZWM2NWEyOGNkLTEyMTU0NjktMjAyNi0wNS0yNy1lbg==\/tiny\/Aligos-Therapeutics.png\" \/>\n    <\/div>\n<div class=\"mw_contactinfo\"><\/div>\n","protected":false},"excerpt":{"rendered":"<p>Long-term follow up data from the Phase 1 study of pevifoscorvir sodium continues to suggest a reduction in the cccDNA reservoir Data on the preclinical characteristics of the Aligos\/Amoytop ASO program to be presented 40% of HBeAg+ participants with chronic HBV infection treated with pevifoscorvir sodium at week 48 had reductions in HBsAg that would potentially allow them to qualify for ASO treatment SOUTH SAN FRANCISCO, Calif., May 27, 2026 (GLOBE NEWSWIRE) &#8212; Aligos Therapeutics, Inc. (Nasdaq: ALGS), a clinical stage biopharmaceutical company focused on improving patient outcomes through best-in-class therapies for liver and viral diseases, today announced positive data from ten presentations at the European Association for the Study of the Liver (EASL) Congress 2026, being held May 27 &hellip; <\/p>\n<p class=\"link-more\"><a href=\"https:\/\/www.marketnewsdesk.com\/index.php\/aligos-therapeutics-presents-positive-data-at-the-easl-congress-2026\/\" class=\"more-link\">Continue reading<span class=\"screen-reader-text\"> &#8220;Aligos Therapeutics Presents Positive Data at the EASL Congress 2026&#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-967175","post","type-post","status-publish","format-standard","hentry"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.6 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Aligos Therapeutics Presents Positive Data at the EASL Congress 2026 - 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\/aligos-therapeutics-presents-positive-data-at-the-easl-congress-2026\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Aligos Therapeutics Presents Positive Data at the EASL Congress 2026 - Market Newsdesk\" \/>\n<meta property=\"og:description\" content=\"Long-term follow up data from the Phase 1 study of pevifoscorvir sodium continues to suggest a reduction in the cccDNA reservoir Data on the preclinical characteristics of the Aligos\/Amoytop ASO program to be presented 40% of HBeAg+ participants with chronic HBV infection treated with pevifoscorvir sodium at week 48 had reductions in HBsAg that would potentially allow them to qualify for ASO treatment SOUTH SAN FRANCISCO, Calif., May 27, 2026 (GLOBE NEWSWIRE) &#8212; Aligos Therapeutics, Inc. (Nasdaq: ALGS), a clinical stage biopharmaceutical company focused on improving patient outcomes through best-in-class therapies for liver and viral diseases, today announced positive data from ten presentations at the European Association for the Study of the Liver (EASL) Congress 2026, being held May 27 &hellip; Continue reading &quot;Aligos Therapeutics Presents Positive Data at the EASL Congress 2026&quot;\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.marketnewsdesk.com\/index.php\/aligos-therapeutics-presents-positive-data-at-the-easl-congress-2026\/\" \/>\n<meta property=\"og:site_name\" content=\"Market Newsdesk\" \/>\n<meta property=\"article:published_time\" content=\"2026-05-27T06:35:10+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/www.globenewswire.com\/newsroom\/ti?nf=OTcyNjY2NCM3NjIxMTM5IzIyMDM5MTY=\" \/>\n<meta name=\"author\" content=\"Newsdesk\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Written by\" \/>\n\t<meta name=\"twitter:data1\" content=\"Newsdesk\" \/>\n\t<meta name=\"twitter:label2\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data2\" content=\"8 minutes\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\\\/\\\/schema.org\",\"@graph\":[{\"@type\":\"Article\",\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/aligos-therapeutics-presents-positive-data-at-the-easl-congress-2026\\\/#article\",\"isPartOf\":{\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/aligos-therapeutics-presents-positive-data-at-the-easl-congress-2026\\\/\"},\"author\":{\"name\":\"Newsdesk\",\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/#\\\/schema\\\/person\\\/482f27a394d4fda80ecb5499e519d979\"},\"headline\":\"Aligos Therapeutics Presents Positive Data at the EASL Congress 2026\",\"datePublished\":\"2026-05-27T06:35:10+00:00\",\"mainEntityOfPage\":{\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/aligos-therapeutics-presents-positive-data-at-the-easl-congress-2026\\\/\"},\"wordCount\":1623,\"image\":{\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/aligos-therapeutics-presents-positive-data-at-the-easl-congress-2026\\\/#primaryimage\"},\"thumbnailUrl\":\"https:\\\/\\\/www.globenewswire.com\\\/newsroom\\\/ti?nf=OTcyNjY2NCM3NjIxMTM5IzIyMDM5MTY=\",\"inLanguage\":\"en-US\"},{\"@type\":\"WebPage\",\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/aligos-therapeutics-presents-positive-data-at-the-easl-congress-2026\\\/\",\"url\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/aligos-therapeutics-presents-positive-data-at-the-easl-congress-2026\\\/\",\"name\":\"Aligos Therapeutics Presents Positive Data at the EASL Congress 2026 - 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