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    <title>American Association for the Study of Liver Diseases</title>
    <description></description>
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    <item>
      <title>Opko’s OPK-88006 shows hepatoprotection in MASH</title>
      <description>Opko Health Inc. has recently presented data for their GLP-1/glucagon receptor dual agonist OPK-88006, which is in preclinical development for the treatment of metabolic disease, including metabolic dysfunction-associated steatohepatitis (MASH) and obesity.</description>
      <content:encoded>
        <![CDATA[Opko Health Inc. has recently presented data for their GLP-1/glucagon receptor dual agonist OPK-88006, which is in preclinical development for the treatment of metabolic disease, including metabolic dysfunction-associated steatohepatitis (MASH) and obesity.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/726542</guid>
      <pubDate>Tue, 25 Nov 2025 08:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/726542-opkos-opk-88006-shows-hepatoprotection-in-mash</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Gastrointestinal/NASH-liver-disease.webp?t=1745258690" type="image/jpeg" medium="image" fileSize="287464">
        <media:title type="plain">Liver disease</media:title>
      </media:content>
    </item>
    <item>
      <title>AASLD: AZ-505 exerts antitumoral activity in HCC</title>
      <description>Though immune checkpoint inhibitors have improved the outcomes of patients with hepatocellular carcinoma (HCC), the response rates remain limited. At the annual meeting of the American Association for the Study of Liver Diseases, researchers highlighted N-lysine methyltransferase SMYD2 as an oncogenic protein overexpressed in several tumor types.</description>
      <content:encoded>
        <![CDATA[Though immune checkpoint inhibitors have improved the outcomes of patients with hepatocellular carcinoma (HCC), the response rates remain limited. At the annual meeting of the American Association for the Study of Liver Diseases, researchers highlighted N-lysine methyltransferase SMYD2 as an oncogenic protein overexpressed in several tumor types.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/726523</guid>
      <pubDate>Mon, 24 Nov 2025 08:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/726523-aasld-az-505-exerts-antitumoral-activity-in-hcc</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Cancer/HCC-hepatocellular-carcinoma-liver-cancer.webp?t=1722888982" type="image/jpeg" medium="image" fileSize="265067">
        <media:title type="plain">Illustration of tumor in the liver</media:title>
      </media:content>
    </item>
    <item>
      <title>Synergistic antiviral efficacy of HEC-191834 with siRNA in HBV models</title>
      <description>In preclinical studies at Sunshine Lake Pharma Co. Ltd., researchers investigated the antiviral and immune-modulatory potential of HEC-191834, a novel and highly selective human Toll-like receptor 8 (TLR8) agonist, in chronic hepatitis B virus (HBV) models, as well as its activity when combined with siRNA.</description>
      <content:encoded>
        <![CDATA[In preclinical studies at Sunshine Lake Pharma Co. Ltd., researchers investigated the antiviral and immune-modulatory potential of HEC-191834, a novel and highly selective human Toll-like receptor 8 (TLR8) agonist, in chronic hepatitis B virus (HBV) models, as well as its activity when combined with siRNA.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/726280</guid>
      <pubDate>Tue, 18 Nov 2025 08:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/726280-synergistic-antiviral-efficacy-of-hec-191834-with-sirna-in-hbv-models</link>
    </item>
    <item>
      <title>Bluejay way: Positive phase II data for treating hepatitis D</title>
      <description>Bluejay Therapeutics Inc.’s lead compound, the fully human monoclonal antibody brelovitug (BJT-778), produced positive virologic response data in the company’s phase II study of chronic hepatitis D virus, a condition with no approved treatment in the U.S.</description>
      <content:encoded>
        <![CDATA[Bluejay Therapeutics Inc.’s lead compound, the fully human monoclonal antibody brelovitug (BJT-778), produced positive virologic response data in the company’s phase II study of chronic hepatitis D virus, a condition with no approved treatment in the U.S.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/726111</guid>
      <pubDate>Tue, 11 Nov 2025 12:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/726111-bluejay-way-positive-phase-ii-data-for-treating-hepatitis-d</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Gastrointestinal/Liver-anatomy-with-virus.webp?t=1717618903" type="image/jpeg" medium="image" fileSize="305581">
        <media:title type="plain">Liver anatomy with virus</media:title>
      </media:content>
    </item>
    <item>
      <title>MASH prospects from Rivus, Metavia show promise in phase II</title>
      <description>Phase II data being presented at the American Association for the Study of Liver Diseases annual meeting indicate drug development in the field of metabolic dysfunction-associated steatohepatitis (MASH) is making steady progress.</description>
      <content:encoded>
        <![CDATA[Phase II data being presented at the American Association for the Study of Liver Diseases annual meeting indicate drug development in the field of metabolic dysfunction-associated steatohepatitis (MASH) is making steady progress.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/725887</guid>
      <pubDate>Fri, 07 Nov 2025 12:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/725887-mash-prospects-from-rivus-metavia-show-promise-in-phase-ii</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Gastrointestinal/Liver-on-digital-lens.webp?t=1709588066" type="image/jpeg" medium="image" fileSize="175206">
        <media:title type="plain">Liver over digital lens background</media:title>
      </media:content>
    </item>
    <item>
      <title> Ausperbio bags $73M series B for hep B-targeting RNA therapy</title>
      <description>Ausperbio Therapeutics Inc. raised $110 million from two financing rounds in 2024 to advance its lead antisense oligonucleotide candidate as a functional cure for chronic hepatitis B.</description>
      <content:encoded>
        <![CDATA[Ausperbio Therapeutics Inc. raised $110 million from two financing rounds in 2024 to advance its lead antisense oligonucleotide candidate as a functional cure for chronic hepatitis B.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/715880</guid>
      <pubDate>Tue, 31 Dec 2024 12:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/715880-ausperbio-bags-73m-series-b-for-hep-b-targeting-rna-therapy</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/Hepatitis-B-virus-CC-by-2-0.webp?t=1780407811" type="image/jpeg" medium="image" fileSize="351561">
        <media:title type="plain">Hepatitis B virus rendering</media:title>
        <media:description type="plain">Hepatitis B virus. Credit: NIAID, CC BY 2.0.</media:description>
      </media:content>
    </item>
    <item>
      <title>Ausperbio bags $73M series B for hep B-targeting RNA therapy</title>
      <description>Ausperbio Therapeutics Inc. raised $110 million from two financing rounds in 2024 to advance its lead antisense oligonucleotide candidate as a functional cure for chronic hepatitis B.</description>
      <content:encoded>
        <![CDATA[Ausperbio Therapeutics Inc. raised $110 million from two financing rounds in 2024 to advance its lead antisense oligonucleotide candidate as a functional cure for chronic hepatitis B.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/715774</guid>
      <pubDate>Mon, 30 Dec 2024 12:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/715774-ausperbio-bags-73m-series-b-for-hep-b-targeting-rna-therapy</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/Hepatitis-B-virus-CC-by-2-0.webp?t=1780407811" type="image/jpeg" medium="image" fileSize="351561">
        <media:title type="plain">Hepatitis B virus rendering</media:title>
        <media:description type="plain">Hepatitis B virus. Credit: NIAID, CC BY 2.0.</media:description>
      </media:content>
    </item>
    <item>
      <title>New siRNA therapy candidate, ETX-312, shows efficacy in MASH mouse model</title>
      <description>Researchers from E-Therapeutics plc presented preclinical data for ETX-312, a GalNAc-conjugated short interfering RNA (siRNA), produced using the Galomic platform and being developed for the treatment of metabolic dysfunction-associated steatohepatitis (MASH).</description>
      <content:encoded>
        <![CDATA[Researchers from E-Therapeutics plc presented preclinical data for ETX-312, a GalNAc-conjugated short interfering RNA (siRNA), produced using the Galomic platform and being developed for the treatment of metabolic dysfunction-associated steatohepatitis (MASH).]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/715062</guid>
      <pubDate>Thu, 05 Dec 2024 09:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/715062-new-sirna-therapy-candidate-etx-312-shows-efficacy-in-mash-mouse-model</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Gastrointestinal/Liver-and-DNA.webp?t=1602177503" type="image/png" medium="image" fileSize="311397">
        <media:title type="plain">Liver and DNA</media:title>
      </media:content>
    </item>
    <item>
      <title>SA-1211, a dual-target siRNA with promising antiviral activity in AAV-HBV mice</title>
      <description>Researchers from Suzhou Siran Biotech Co. Ltd. presented the discovery and preclinical characterization of SA-1211, an N-acetylgalactosamine (GalNAc)-conjugated siRNA dimer targeting both hepatitis B virus (HBV) and PD-L1 gene expression, being developed as a potential new therapeutic candidate for the treatment of chronic hepatitis B (CHB).</description>
      <content:encoded>
        <![CDATA[Researchers from Suzhou Siran Biotech Co. Ltd. presented the discovery and preclinical characterization of SA-1211, an <em>N</em>-acetylgalactosamine (GalNAc)-conjugated siRNA dimer targeting both hepatitis B virus (HBV) and PD-L1 gene expression, being developed as a potential new therapeutic candidate for the treatment of chronic hepatitis B (CHB).]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/715090</guid>
      <pubDate>Wed, 04 Dec 2024 09:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/715090-sa-1211-a-dual-target-sirna-with-promising-antiviral-activity-in-aav-hbv-mice</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Infectious/Hepatitis-B-virus.webp?t=1589308217" type="image/png" medium="image" fileSize="338579">
        <media:title type="plain">Hepatitis B virus </media:title>
      </media:content>
    </item>
    <item>
      <title>Preclinical characterization of Tune-401, a first-in-class LNP-encapsulated epigenetic silencer therapy for hepatitis B</title>
      <description>Tune Therapeutics Inc. is evaluating Tune-401.</description>
      <content:encoded>
        <![CDATA[Tune Therapeutics Inc. is evaluating Tune-401.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/715028</guid>
      <pubDate>Wed, 04 Dec 2024 09:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/715028-preclinical-characterization-of-tune-401-a-first-in-class-lnp-encapsulated-epigenetic-silencer-therapy-for-hepatitis-b</link>
    </item>
    <item>
      <title>EA-3571, a dual inhibitor of enteropeptidase and trypsin with efficacy in mouse model of MASH</title>
      <description>Recently presented preclinical data show that EA Pharma Co. Ltd.'s EA-3571 is a highly potent dual inhibitor of enteropeptidase and trypsin with luminal action, resulting in potential anti-insulin resistance and fat-burning properties.</description>
      <content:encoded>
        <![CDATA[Recently presented preclinical data show that EA Pharma Co. Ltd.'s EA-3571 is a highly potent dual inhibitor of enteropeptidase and trypsin with luminal action, resulting in potential anti-insulin resistance and fat-burning properties.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/715050</guid>
      <pubDate>Tue, 03 Dec 2024 09:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/715050-ea-3571-a-dual-inhibitor-of-enteropeptidase-and-trypsin-with-efficacy-in-mouse-model-of-mash</link>
    </item>
    <item>
      <title>SRT-015 prevents acute liver injury in preclinical tests</title>
      <description>Genfit SA and its collaborators have described the preclinical efficacy of SRT-015, a liver-selective ASK1 inhibitor in models of liver failure.</description>
      <content:encoded>
        <![CDATA[Genfit SA and its collaborators have described the preclinical efficacy of SRT-015, a liver-selective ASK1 inhibitor in models of liver failure.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/715007</guid>
      <pubDate>Tue, 03 Dec 2024 09:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/715007-srt-015-prevents-acute-liver-injury-in-preclinical-tests</link>
    </item>
    <item>
      <title>Therapeutic hepatitis B vaccine generates robust HBc-specific T-cell responses in preclinical tests</title>
      <description>Researchers from presented preclinical data for AVX-70371, a novel therapeutic vaccine being developed for the treatment of chronic hepatitis B virus (HBV) infection.</description>
      <content:encoded>
        <![CDATA[Researchers from presented preclinical data for AVX-70371, a novel therapeutic vaccine being developed for the treatment of chronic hepatitis B virus (HBV) infection.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/714961</guid>
      <pubDate>Mon, 02 Dec 2024 09:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/714961-therapeutic-hepatitis-b-vaccine-generates-robust-hbc-specific-t-cell-responses-in-preclinical-tests</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/NIH-NIAID-Hepatitis-B-virus-particles.webp?t=1672411746" type="image/png" medium="image" fileSize="2361724">
        <media:title type="plain">Transmission electron micrograph of hepatitis B virus particles</media:title>
        <media:description type="plain">Hepatitis B virus particles. Credit: NIAID/NIH and CDC</media:description>
      </media:content>
    </item>
    <item>
      <title>EA-3571, a dual inhibitor of enteropeptidase and trypsin with efficacy in mouse model of MASH</title>
      <description>Recently presented preclinical data show that EA Pharma Co. Ltd.'s EA-3571 is a highly potent dual inhibitor of enteropeptidase and trypsin with luminal action, resulting in potential anti-insulin resistance and fat-burning properties.</description>
      <content:encoded>
        <![CDATA[Recently presented preclinical data show that EA Pharma Co. Ltd.'s EA-3571 is a highly potent dual inhibitor of enteropeptidase and trypsin with luminal action, resulting in potential anti-insulin resistance and fat-burning properties.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/714957</guid>
      <pubDate>Mon, 02 Dec 2024 09:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/714957-ea-3571-a-dual-inhibitor-of-enteropeptidase-and-trypsin-with-efficacy-in-mouse-model-of-mash</link>
    </item>
    <item>
      <title>Orsobio ACMSD inhibitor reverses liver injury in preclinical models </title>
      <description>The enzyme aminocarboxymuconate semialdehyde decarboxylase (ACMSD) is a regulator of de novo NAD+ synthesis and is reduced in patients with advanced liver disease.</description>
      <content:encoded>
        <![CDATA[The enzyme aminocarboxymuconate semialdehyde decarboxylase (ACMSD) is a regulator of de novo NAD+ synthesis and is reduced in patients with advanced liver disease.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/714929</guid>
      <pubDate>Fri, 29 Nov 2024 09:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/714929-orsobio-acmsd-inhibitor-reverses-liver-injury-in-preclinical-models</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/NIH-NCI-Liver-Tissue-with-NAFLD.webp?t=1724338589" type="image/png" medium="image" fileSize="851944">
        <media:title type="plain">A microscopic image of liver tissue affected by metabolic dysfunction-associated steatotic liver disease.</media:title>
        <media:description type="plain">Liver tissue affected by metabolic dysfunction-associated steatotic liver disease (previously known as nonalcoholic fatty liver disease). The large and small white spots are excess fat droplets filling liver cells (hepatocytes). Credit: David Kleiner, National Cancer Institute, NIH
</media:description>
      </media:content>
    </item>
    <item>
      <title>Dual-targeted approach for hepatobiliary diseases presented </title>
      <description>Rectify Pharmaceuticals Inc. has conducted preclinical testing on RTY-694, an oral dual-targeted positive functional modulator for use in the treatment of hepatobiliary disorders.</description>
      <content:encoded>
        <![CDATA[Rectify Pharmaceuticals Inc. has conducted preclinical testing on RTY-694, an oral dual-targeted positive functional modulator for use in the treatment of hepatobiliary disorders.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/714913</guid>
      <pubDate>Thu, 28 Nov 2024 09:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/714913-dual-targeted-approach-for-hepatobiliary-diseases-presented</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Gastrointestinal/Liver-7-7.webp?t=1657229334" type="image/png" medium="image" fileSize="759348">
        <media:title type="plain">Liver </media:title>
      </media:content>
    </item>
    <item>
      <title>CLM-022, an NLRP3 inflammasome inhibitor, reverses chronic and acute liver inflammation</title>
      <description>NLRP3 inflammasome activation, pro-inflammatory cytokine production and pyroptosis are key features of inflammation that contribute to liver fibrosis progression, cirrhosis and end-stage liver failure. Pyroptosis, a lytic form of inflammatory-regulated cell death, is regulated by multiprotein complexes expressed in both parenchymal and nonparenchymal hepatic cells. Researchers from Genfit SA presented preclinical efficacy data on CLM-022, a synthetic pentacyclic triterpenoid derivative designed to target the NLRP3 complex.</description>
      <content:encoded>
        <![CDATA[NLRP3 inflammasome activation, pro-inflammatory cytokine production and pyroptosis are key features of inflammation that contribute to liver fibrosis progression, cirrhosis and end-stage liver failure. Pyroptosis, a lytic form of inflammatory-regulated cell death, is regulated by multiprotein complexes expressed in both parenchymal and nonparenchymal hepatic cells. Researchers from Genfit SA presented preclinical efficacy data on CLM-022, a synthetic pentacyclic triterpenoid derivative designed to target the NLRP3 complex.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/714862</guid>
      <pubDate>Wed, 27 Nov 2024 00:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/714862-clm-022-an-nlrp3-inflammasome-inhibitor-reverses-chronic-and-acute-liver-inflammation</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Gastrointestinal/Liver-collage.webp?t=1663106040" type="image/png" medium="image" fileSize="360588">
        <media:title type="plain">Liver illustration</media:title>
      </media:content>
    </item>
    <item>
      <title>EDP-514 demonstrates favorable preclinical PK profile, excellent target tissue penetration</title>
      <description>Enanta Pharmaceuticals Inc. has released preclinical pharmacokinetics (PK) data for EDP-514, a potent and selective class II core assembly modulator in phase I development for the oral treatment of hepatitis B.</description>
      <content:encoded>
        <![CDATA[Enanta Pharmaceuticals Inc. has released preclinical pharmacokinetics (PK) data for EDP-514, a potent and selective class II core assembly modulator in phase I development for the oral treatment of hepatitis B.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/714727</guid>
      <pubDate>Fri, 22 Nov 2024 09:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/714727-edp-514-demonstrates-favorable-preclinical-pk-profile-excellent-target-tissue-penetration</link>
    </item>
    <item>
      <title>New preclinical data on CVI-2742 for treating MASH</title>
      <description>The efficacy and capabilities of CVI Pharmaceuticals Inc.'s CVI-2742, a THR-β agonist, were tested in nonhuman primates.</description>
      <content:encoded>
        <![CDATA[The efficacy and capabilities of CVI Pharmaceuticals Inc.'s CVI-2742, a THR-β agonist, were tested in nonhuman primates.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/714695</guid>
      <pubDate>Thu, 21 Nov 2024 09:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/714695-new-preclinical-data-on-cvi-2742-for-treating-mash</link>
    </item>
    <item>
      <title>RTX-001, an engineered macrophage therapy with hepatic regenerative effects </title>
      <description>As a consequence of chronic liver disease progression, severe cirrhosis, decompensation and fibrosis culminates in end-stage liver disease (ESLD). There are no treatment options approved for ESLD, but, among others, regenerative therapies with autologous, nonengineered, pro-regenerative macrophages have shown good tolerability and improved transplant-free survival in the clinical setting.</description>
      <content:encoded>
        <![CDATA[As a consequence of chronic liver disease progression, severe cirrhosis, decompensation and fibrosis culminates in end-stage liver disease (ESLD). There are no treatment options approved for ESLD, but, among others, regenerative therapies with autologous, nonengineered, pro-regenerative macrophages have shown good tolerability and improved transplant-free survival in the clinical setting.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/714684</guid>
      <pubDate>Thu, 21 Nov 2024 09:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/714684-rtx-001-an-engineered-macrophage-therapy-with-hepatic-regenerative-effects</link>
    </item>
    <item>
      <title>FAP inhibitor AZD-2389 improves liver fibrosis and MASH</title>
      <description>Astrazeneca plc has developed a potent oral fibroblast activation protein (FAP) inhibitor, AZD-2389, that avoids the cleavage of FGF21 and α2-AP. AZD-2389 was tested in cynomolgus monkeys with diet-induced MASH.</description>
      <content:encoded>
        <![CDATA[Astrazeneca plc has developed a potent oral fibroblast activation protein (FAP) inhibitor, AZD-2389, that avoids the cleavage of FGF21 and α2-AP. AZD-2389 was tested in cynomolgus monkeys with diet-induced MASH.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/714598</guid>
      <pubDate>Wed, 20 Nov 2024 09:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/714598-fap-inhibitor-azd-2389-improves-liver-fibrosis-and-mash</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/liver-cirrhosis-fibrosis.webp?t=1712672928" type="image/jpeg" medium="image" fileSize="823791">
        <media:title type="plain">Photomicrograph of liver biopsy in a patient with cirrhosis. </media:title>
        <media:description type="plain">Photomicrograph of liver biopsy in a patient with cirrhosis, showing bridging septal fibrosis and regenerative nodules. Stained with trichrome to highlight fibrosis (blue).</media:description>
      </media:content>
    </item>
    <item>
      <title>Bifunctional molecule capsid modulator and cGAS agonist achieves complete cure in AAV-HBV mice</title>
      <description>LW-231, under development by Shanghai Longwood Biopharmaceuticals Co. Ltd., is a novel bifunctional molecule designed to simultaneously modulate hepatitis B virus (HBV) capsid assembly and activate cGAS-STING pathway. Preclinical data were recently presented.</description>
      <content:encoded>
        <![CDATA[LW-231, under development by Shanghai Longwood Biopharmaceuticals Co. Ltd., is a novel bifunctional molecule designed to simultaneously modulate hepatitis B virus (HBV) capsid assembly and activate cGAS-STING pathway. Preclinical data were recently presented.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/703299</guid>
      <pubDate>Thu, 30 Nov 2023 09:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/703299-bifunctional-molecule-capsid-modulator-and-cgas-agonist-achieves-complete-cure-in-aav-hbv-mice</link>
    </item>
    <item>
      <title>Lerna Biopharma presents first-in-class GalNAc-siRNA therapeutic for treatment of liver diseases</title>
      <description>Researchers from Lerna Biopharma Pte. Ltd. (formerly Cargene Therapeutics Pte. Ltd.) recently presented the discovery and preclinical evaluation of a first-in-class GalNAc-siRNA therapeutic, CG-LR1, being developed for the treatment of liver diseases.</description>
      <content:encoded>
        <![CDATA[Researchers from Lerna Biopharma Pte. Ltd. (formerly Cargene Therapeutics Pte. Ltd.) recently presented the discovery and preclinical evaluation of a first-in-class GalNAc-siRNA therapeutic, CG-LR1, being developed for the treatment of liver diseases.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/703075</guid>
      <pubDate>Thu, 23 Nov 2023 09:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/703075-lerna-biopharma-presents-first-in-class-galnac-sirna-therapeutic-for-treatment-of-liver-diseases</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/Liver-gallbladder-stomach-pancreas.webp?t=1674573513" type="image/png" medium="image" fileSize="1379557">
        <media:title type="plain">Illustration of the liver, gallbladder, stomach, and pancreas</media:title>
      </media:content>
    </item>
    <item>
      <title>A-7387 inhibits bile acid transporter and blocks hepatitis infection</title>
      <description>Researchers from Ipsen Ltd. and affiliated organizations presented the discovery and preclinical characterization of a novel NTCP inhibitor, A-7387, being developed for the treatment of HBV and HDV infections.</description>
      <content:encoded>
        <![CDATA[Researchers from Ipsen Ltd. and affiliated organizations presented the discovery and preclinical characterization of a novel NTCP inhibitor, A-7387, being developed for the treatment of HBV and HDV infections.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/703032</guid>
      <pubDate>Tue, 21 Nov 2023 09:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/703032-a-7387-inhibits-bile-acid-transporter-and-blocks-hepatitis-infection</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/NIH-NIAID-Hepatitis-B-virus-particles.webp?t=1672411746" type="image/png" medium="image" fileSize="2361724">
        <media:title type="plain">Transmission electron micrograph of hepatitis B virus particles</media:title>
        <media:description type="plain">Hepatitis B virus particles. Credit: NIAID/NIH and CDC</media:description>
      </media:content>
    </item>
    <item>
      <title>HNF4A upregulation confers protection in liver fibrosis</title>
      <description>Omega Therapeutics Inc. has presented preclinical data on hepatocyte nuclear factor 4-alpha (HNF4A) modulation in fibrotic liver disease models to enhance its key role and suggest it as a potent therapeutic target.</description>
      <content:encoded>
        <![CDATA[Omega Therapeutics Inc. has presented preclinical data on hepatocyte nuclear factor 4-alpha (HNF4A) modulation in fibrotic liver disease models to enhance its key role and suggest it as a potent therapeutic target.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/703025</guid>
      <pubDate>Tue, 21 Nov 2023 09:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/703025-hnf4a-upregulation-confers-protection-in-liver-fibrosis</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Gastrointestinal/fatty-liver-disease.webp?t=1589217291" type="image/png" medium="image" fileSize="932342">
        <media:title type="plain">Liver disease</media:title>
      </media:content>
    </item>
    <item>
      <title>ALG-001075 demonstrates promising preclinical resistance profile</title>
      <description>Researchers from Aligos Therapeutics Inc. presented preclinical data for ALG-001075, a novel capsid assembly modulator leading to the formation of empty capsids (CAM-E), being developed for the treatment of hepatitis B.</description>
      <content:encoded>
        <![CDATA[Researchers from Aligos Therapeutics Inc. presented preclinical data for ALG-001075, a novel capsid assembly modulator leading to the formation of empty capsids (CAM-E), being developed for the treatment of hepatitis B.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/703011</guid>
      <pubDate>Mon, 20 Nov 2023 09:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/703011-alg-001075-demonstrates-promising-preclinical-resistance-profile</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/NIAID-3D-print-Hepatitis-B.webp?t=1700497695" type="image/jpeg" medium="image" fileSize="286993">
        <media:title type="plain">3D print imagery of hepatitis B virus</media:title>
        <media:description type="plain">Hepatitis B virus illustration. Credit: NIAID, NHS.</media:description>
      </media:content>
    </item>
    <item>
      <title>ALG-094103 is liver-targeted, orally available PD-L1 inhibitor</title>
      <description>Researchers from Aligos Therapeutics Inc. have presented the discovery and preclinical evaluation of a novel next-generation liver targeted PD-L1 small molecule inhibitor, ALG-094103, which is being developed for the treatment of chronic hepatitis B and liver cancer.</description>
      <content:encoded>
        <![CDATA[Researchers from Aligos Therapeutics Inc. have presented the discovery and preclinical evaluation of a novel next-generation liver targeted PD-L1 small molecule inhibitor, ALG-094103, which is being developed for the treatment of chronic hepatitis B and liver cancer.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/702928</guid>
      <pubDate>Wed, 15 Nov 2023 09:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/702928-alg-094103-is-liver-targeted-orally-available-pd-l1-inhibitor</link>
    </item>
    <item>
      <title>IFNα-like small molecules successfully inhibit HBV replication</title>
      <description>It’s known that interferon-alpha (IFNα) activates interferon-stimulated genes (ISGs) and disrupts the hepatitis B virus (HBV) replication cycle. Pegylated (PEG)-IFNα has been widely used for its immunomodulatory and antiviral properties but it is not always well tolerated and thus its use is limited.</description>
      <content:encoded>
        <![CDATA[It’s known that interferon-alpha (IFNα) activates interferon-stimulated genes (ISGs) and disrupts the hepatitis B virus (HBV) replication cycle. Pegylated (PEG)-IFNα has been widely used for its immunomodulatory and antiviral properties but it is not always well tolerated and thus its use is limited.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/702867</guid>
      <pubDate>Wed, 15 Nov 2023 09:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/702867-ifn-like-small-molecules-successfully-inhibit-hbv-replication</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/immun-interferon-alpha-IFN.webp?t=1700063288" type="image/jpeg" medium="image" fileSize="336282">
        <media:title type="plain">3D illustration of interferon-alpha molecular structure</media:title>
      </media:content>
    </item>
    <item>
      <title>At AASLD 2022, polygenic risk score subtypes NAFLD</title>
      <description>Modern molecular techniques have progressed to the point where sequencing can seem almost quaint. At the Basic Science Symposium of The Liver Meeting 2022, new techniques were on full display, with sessions devoted to epigenetics, microbiome analysis and spatial transcriptomics. But the first session was still on genetic variants in all their forms – rare variants, common variants and non-germline mutations.</description>
      <content:encoded>
        <![CDATA[Modern molecular techniques have progressed to the point where sequencing can seem almost quaint. At the Basic Science Symposium of The Liver Meeting 2022, new techniques were on full display, with sessions devoted to epigenetics, microbiome analysis and spatial transcriptomics. But the first session was still on genetic variants in all their forms – rare variants, common variants and non-germline mutations.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/691345</guid>
      <pubDate>Mon, 07 Nov 2022 12:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/691345-at-aasld-2022-polygenic-risk-score-subtypes-nafld</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Gastrointestinal/Liver-illustration.webp?t=1613674462" type="image/png" medium="image" fileSize="432664">
        <media:title type="plain">Liver illustration</media:title>
        <media:description type="plain">Credit: Georgia State University</media:description>
      </media:content>
    </item>
    <item>
      <title>AASLD meeting: Cholangiocytes can induce liver regeneration</title>
      <description>In contrast to most adult mammalian tissues, the liver can regenerate itself to an impressive degree. That regeneration is critical to survival – as a key digestive organ, the liver deals with all sorts of toxins, from rotten-ish food in the wild to alcohol in more cultured settings.</description>
      <content:encoded>
        <![CDATA[In contrast to most adult mammalian tissues, the liver can regenerate itself to an impressive degree. That regeneration is critical to survival – as a key digestive organ, the liver deals with all sorts of toxins, from rotten-ish food in the wild to alcohol in more cultured settings.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/513404</guid>
      <pubDate>Tue, 16 Nov 2021 09:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/513404-aasld-meeting-cholangiocytes-can-induce-liver-regeneration</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Gastrointestinal/Liver-illustration.webp?t=1613674462" type="image/png" medium="image" fileSize="432664">
        <media:title type="plain">Liver illustration</media:title>
        <media:description type="plain">Credit: Georgia State University</media:description>
      </media:content>
    </item>
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