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    <title>Endocrine/metabolic</title>
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    <item>
      <title>Street canvu MBX phase II HP data more than one way</title>
      <description>With full phase II results in hand, MBX Biosciences Inc. backers are stacking the odds of parathyroid hormone (PTH) peptide prodrug canvuparatide (canvu) against Yorvipath (palopegteriparatide} from Ascendis Pharma A/S, a PTH analog cleared by the U.S. FDA in August 2024 for hypoparathyroidism (HP).</description>
      <content:encoded>
        <![CDATA[With full phase II results in hand, MBX Biosciences Inc. backers are stacking the odds of parathyroid hormone (PTH) peptide prodrug canvuparatide (canvu) against Yorvipath (palopegteriparatide} from Ascendis Pharma A/S, a PTH analog cleared by the U.S. FDA in August 2024 for hypoparathyroidism (HP).]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731813</guid>
      <pubDate>Fri, 12 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731813-street-canvu-mbx-phase-ii-hp-data-more-than-one-way</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Endocrine/Endocrine-thyroid-parathyroid-glands.webp?t=1689173409" type="image/jpeg" medium="image" fileSize="95954">
        <media:title type="plain">3D illustration of thyroid in human body with parathyroid glands highlighted</media:title>
      </media:content>
    </item>
    <item>
      <title>Antag’s GIPR antagonist shows promise in obesity and cardiometabolic disease</title>
      <description>Glucose-dependent insulinotropic polypeptide receptor (GIPR) signaling regulates key metabolic processes, including postprandial insulin secretion, appetite control, lipid storage and overall energy balance. Researchers from Antag Therapeutics Aps presented preclinical efficacy data on the combination of AT-7687, a GIPR antagonist, and cagrilintide in obese insulin-resistant monkeys.</description>
      <content:encoded>
        <![CDATA[Glucose-dependent insulinotropic polypeptide receptor (GIPR) signaling regulates key metabolic processes, including postprandial insulin secretion, appetite control, lipid storage and overall energy balance. Researchers from Antag Therapeutics Aps presented preclinical efficacy data on the combination of AT-7687, a GIPR antagonist, and cagrilintide in obese insulin-resistant monkeys.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731855</guid>
      <pubDate>Fri, 12 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731855-antags-gipr-antagonist-shows-promise-in-obesity-and-cardiometabolic-disease</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/Endocrine-Metabolic-glucose-bloodstream.webp?t=1674056639" type="image/png" medium="image" fileSize="1313266">
        <media:title type="plain">Illustration of glucose molecules in a bloodstream</media:title>
      </media:content>
    </item>
    <item>
      <title>Another FDA no for Camurus’ monthly acromegaly drug Oclaiz</title>
      <description>In a repeat move, the U.S. FDA issued yet again a complete response letter (CRL) to Camurus AB for its subcutaneous extended-release injection drug CAM-2029 (octreotide) to treat the rare chronic growth disorder acromegaly. The drug, which expects to be branded Oclaiz in the U.S. upon approval, is called Oczyesa in the EU and the U.K., where it received marketing authorization in 2025.</description>
      <content:encoded>
        <![CDATA[In a repeat move, the U.S. FDA issued yet again a complete response letter (CRL) to Camurus AB for its subcutaneous extended-release injection drug CAM-2029 (octreotide) to treat the rare chronic growth disorder acromegaly. The drug, which expects to be branded Oclaiz in the U.S. upon approval, is called Oczyesa in the EU and the U.K., where it received marketing authorization in 2025.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731805</guid>
      <pubDate>Thu, 11 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731805-another-fda-no-for-camurus-monthly-acromegaly-drug-oclaiz</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Regulatory/FDA-icons-and-doctor.webp?t=1666903713" type="image/png" medium="image" fileSize="238204">
        <media:title type="plain">FDA icons and doctor</media:title>
      </media:content>
    </item>
    <item>
      <title>Laekna licenses LAE-118 ex-China to Vasque in $527M deal </title>
      <description>Laekna Inc. is handing ex-China rights to internally discovered PI3Kα pan-mutant selective inhibitor LAE-118 to U.S.-based Vasque Bio Inc. in a deal worth up to $527 million, marking another asset-monetization move by the Shanghai company as it looks to fund and accelerate development across its oncology and metabolic disease pipeline.</description>
      <content:encoded>
        <![CDATA[Laekna Inc. is handing ex-China rights to internally discovered PI3Kα pan-mutant selective inhibitor LAE-118 to U.S.-based Vasque Bio Inc. in a deal worth up to $527 million, marking another asset-monetization move by the Shanghai company as it looks to fund and accelerate development across its oncology and metabolic disease pipeline.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731802</guid>
      <pubDate>Thu, 11 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731802-laekna-licenses-lae-118-ex-china-to-vasque-in-527m-deal</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Deals-and-MAs/Deal-handshake-graphic-overlay.webp?t=1588276536" type="image/png" medium="image" fileSize="406049">
        <media:title type="plain">Deal handshake with graphic overlay</media:title>
      </media:content>
    </item>
    <item>
      <title>Researchers hit back after colleagues removed from ADA meeting</title>
      <description>Former principal officers of the American Diabetes Association (ADA) have hit back at the association’s board and CEO after it prohibited the distribution of an editorial published in its flagship journal Diabetes Care at the ADA’s meeting in New Orleans last Friday.</description>
      <content:encoded>
        <![CDATA[Former principal officers of the American Diabetes Association (ADA) have hit back at the association’s board and CEO after it prohibited the distribution of an editorial published in its flagship journal <em>Diabetes Care</em> at the ADA’s meeting in New Orleans last Friday.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731872</guid>
      <pubDate>Thu, 11 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731872-researchers-hit-back-after-colleagues-removed-from-ada-meeting</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Misc/Hands-holding-paper.webp?t=1781120310" type="image/jpeg" medium="image" fileSize="147197">
        <media:title type="plain">Hands holding paper</media:title>
      </media:content>
    </item>
    <item>
      <title>MTRX-31 restores mitochondrial metabolism in obesity</title>
      <description>Glucagon-like peptide 1 receptor agonist (GLP-1RA) compounds have become game changers in the treatment of obesity, but they have limitations due to long-term efficacy, lean mass preservation and tolerability in certain populations. Mitorx Therapeutics Ltd. has presented data for MTRX-31 (Myo-004), a mitochondrial-targeted compound that provides an alternative mode of action for treating obesity.</description>
      <content:encoded>
        <![CDATA[Glucagon-like peptide 1 receptor agonist (GLP-1RA) compounds have become game changers in the treatment of obesity, but they have limitations due to long-term efficacy, lean mass preservation and tolerability in certain populations. Mitorx Therapeutics Ltd. has presented data for MTRX-31 (Myo-004), a mitochondrial-targeted compound that provides an alternative mode of action for treating obesity.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731840</guid>
      <pubDate>Thu, 11 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731840-mtrx-31-restores-mitochondrial-metabolism-in-obesity</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Diabetes/human-body-metabolism.webp?t=1726239536" type="image/jpeg" medium="image" fileSize="320060">
        <media:title type="plain">Art concept for metabolism</media:title>
      </media:content>
    </item>
    <item>
      <title>VRB-103 shows potent and selective amylin receptor activity</title>
      <description>Researchers from Verdiva Bio Ltd. and collaborators recently presented preclinical data on VRB-103, an oral amylin analogue, comparing its profile with those of cagrilintide and eloralintide, two subcutaneously administered analogues currently in clinical development.</description>
      <content:encoded>
        <![CDATA[Researchers from Verdiva Bio Ltd. and collaborators recently presented preclinical data on VRB-103, an oral amylin analogue, comparing its profile with those of cagrilintide and eloralintide, two subcutaneously administered analogues currently in clinical development.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731839</guid>
      <pubDate>Thu, 11 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731839-vrb-103-shows-potent-and-selective-amylin-receptor-activity</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Research-and-science/Beta-cells.webp?t=1778592394" type="image/png" medium="image" fileSize="224899">
        <media:title type="plain">Beta cells</media:title>
        <media:description type="plain">β cell. Credit: Melton laboratory, Harvard University</media:description>
      </media:content>
    </item>
    <item>
      <title>Ractigen’s saRNA therapy delivers sustained fat loss while preserving muscle</title>
      <description>Researchers from Ractigen Therapeutics Co. Ltd. presented preclinical data on LiCO-saUcp1, a small activating RNA (saRNA) therapeutic designed to upregulate UCP1 expression in adipose tissue.</description>
      <content:encoded>
        <![CDATA[Researchers from Ractigen Therapeutics Co. Ltd. presented preclinical data on LiCO-saUcp1, a small activating RNA (saRNA) therapeutic designed to upregulate UCP1 expression in adipose tissue. ]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731837</guid>
      <pubDate>Thu, 11 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731837-ractigens-sarna-therapy-delivers-sustained-fat-loss-while-preserving-muscle</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/Obesity-adipose-tissue-fat-weight-loss.webp?t=1752245901" type="image/jpeg" medium="image" fileSize="742216">
        <media:title type="plain">Illustration of adipose tissue under the skin</media:title>
      </media:content>
    </item>
    <item>
      <title>Ethyreal Bio launches with focus on thyroid diseases</title>
      <description>Ethyreal Bio Inc. has launched with $101 million in financing and a focus on developing precision therapies for thyroid diseases with high unmet need.</description>
      <content:encoded>
        <![CDATA[Ethyreal Bio Inc. has launched with $101 million in financing and a focus on developing precision therapies for thyroid diseases with high unmet need.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731836</guid>
      <pubDate>Thu, 11 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731836-ethyreal-bio-launches-with-focus-on-thyroid-diseases</link>
    </item>
    <item>
      <title>Microbiota modulates the antidepressant effects of GLP-1 analogues</title>
      <description>Liraglutide, a glucagon-like peptide 1 (GLP-1) receptor agonist used in diabetes and obesity, could alleviate depression through a pathway that does not depend on the GLP-1 receptor but instead on the gut microbiota, since the treatment increases the presence of the bacterium Lactobacillus delbrueckii. This symbiotic microorganism produces a lipid that modulates neuronal activity, normalizing the hyperactivation of brain regions in mice involved in emotional processing, which ultimately reduces depressive behaviors.</description>
      <content:encoded>
        <![CDATA[Liraglutide, a glucagon-like peptide 1 (GLP-1) receptor agonist used in diabetes and obesity, could alleviate depression through a pathway that does not depend on the GLP-1 receptor but instead on the gut microbiota, since the treatment increases the presence of the bacterium <em>Lactobacillus delbrueckii</em>. This symbiotic microorganism produces a lipid that modulates neuronal activity, normalizing the hyperactivation of brain regions in mice involved in emotional processing, which ultimately reduces depressive behaviors.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731833</guid>
      <pubDate>Thu, 11 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731833-microbiota-modulates-the-antidepressant-effects-of-glp-1-analogues</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/Lactobacillus-gram-positive-rod-shaped-lactic-acid-bacteria.webp?t=1781188632" type="image/jpeg" medium="image" fileSize="1095139">
        <media:title type="plain">Illustration of Lactobacillus</media:title>
        <media:description type="plain">Lactobacillus</media:description>
      </media:content>
    </item>
    <item>
      <title>Researchers hit back after colleagues removed from ADA meeting</title>
      <description>Former principal officers of the American Diabetes Association (ADA) have hit back at the association’s board and CEO after it prohibited the distribution of an editorial published in its flagship journal Diabetes Care at the ADA’s meeting in New Orleans last Friday.</description>
      <content:encoded>
        <![CDATA[Former principal officers of the American Diabetes Association (ADA) have hit back at the association’s board and CEO after it prohibited the distribution of an editorial published in its flagship journal <em>Diabetes Care</em> at the ADA’s meeting in New Orleans last Friday.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731723</guid>
      <pubDate>Wed, 10 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731723-researchers-hit-back-after-colleagues-removed-from-ada-meeting</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Misc/Hands-holding-paper.webp?t=1781120310" type="image/jpeg" medium="image" fileSize="147197">
        <media:title type="plain">Hands holding paper</media:title>
      </media:content>
    </item>
    <item>
      <title>Columbia researchers use base editing to modify human embryo genome</title>
      <description>Scientists at Columbia University have used base editing to make precise changes in the genomes of human embryos, avoiding the damage to chromosomes that occurs following two-stranded DNA cuts with conventional CRISPR/Cas9 editing.</description>
      <content:encoded>
        <![CDATA[Scientists at Columbia University have used base editing to make precise changes in the genomes of human embryos, avoiding the damage to chromosomes that occurs following two-stranded DNA cuts with conventional CRISPR/Cas9 editing.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731851</guid>
      <pubDate>Wed, 10 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731851-columbia-researchers-use-base-editing-to-modify-human-embryo-genome</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/DNA-gene-edit-genomics.webp?t=1747837759" type="image/jpeg" medium="image" fileSize="1061729">
        <media:title type="plain">DNA double helix under a magnifying glass</media:title>
      </media:content>
    </item>
    <item>
      <title>Shanghai Curegene Pharmaceutical divulges new THR-β agonists</title>
      <description>Shanghai Curegene Pharmaceutical Co. Ltd. has identified thyroid hormone receptor β (THR-β) agonists that are potentially useful for the treatment of metabolic dysfunction-associated steatotic liver disease (MASLD; NAFLD), diabetes and obesity.</description>
      <content:encoded>
        <![CDATA[Shanghai Curegene Pharmaceutical Co. Ltd. has identified thyroid hormone receptor β (THR-β) agonists that are potentially useful for the treatment of metabolic dysfunction-associated steatotic liver disease (MASLD; NAFLD), diabetes and obesity.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731788</guid>
      <pubDate>Wed, 10 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731788-shanghai-curegene-pharmaceutical-divulges-new-thr-agonists</link>
    </item>
    <item>
      <title>Syntax Bio and Mayo Clinic partner in type 1 diabetes</title>
      <description>Syntax Bio Inc. has established a research and development collaboration with Mayo Clinic focused on advancing stem cell-derived pancreatic cell therapies for type 1 diabetes.</description>
      <content:encoded>
        <![CDATA[Syntax Bio Inc. has established a research and development collaboration with Mayo Clinic focused on advancing stem cell-derived pancreatic cell therapies for type 1 diabetes. ]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731779</guid>
      <pubDate>Wed, 10 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731779-syntax-bio-and-mayo-clinic-partner-in-type-1-diabetes</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Diabetes/pancreas-insulin-diabetic.webp?t=1588881992" type="image/png" medium="image" fileSize="410518">
        <media:title type="plain">Pancreas illustration</media:title>
      </media:content>
    </item>
    <item>
      <title>Pumps, patches and fixes at the ADA</title>
      <description>Dexcom Inc. and Insulet Corp. reported new clinical trial data on their diabetes technologies at the 2026 Scientific Sessions of the American Diabetes Association in New Orleans, offering insights that could aid in clinical adoption. Abbott Laboratories, meanwhile, highlighted the risks of diabetic ketoacidosis (DKA) and presented data showing the growing challenge of identifying DKA as it can develop quickly and mimic common illnesses.</description>
      <content:encoded>
        <![CDATA[Dexcom Inc. and Insulet Corp. reported new clinical trial data on their diabetes technologies at the 2026 Scientific Sessions of the American Diabetes Association in New Orleans, offering insights that could aid in clinical adoption. Abbott Laboratories, meanwhile, highlighted the risks of diabetic ketoacidosis (DKA) and presented data showing the growing challenge of identifying DKA as it can develop quickly and mimic common illnesses.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731707</guid>
      <pubDate>Tue, 09 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731707-pumps-patches-and-fixes-at-the-ada</link>
      <media:content url="https://www.bioworld.com/ext/resources/BMT-source/2022/12-8-Dexcom_G7_CGM.webp?t=1781033282" type="image/png" medium="image" fileSize="246353">
        <media:title type="plain">Dexcom G7 CGM</media:title>
        <media:description type="plain">Dexcom Inc.’s G7 continuous glucose monitoring system.</media:description>
      </media:content>
    </item>
    <item>
      <title>Engitix seals GSK deal for targets to reverse liver fibrosis</title>
      <description>Extracellular matrix specialist Engitix Ltd. is teaming up with GSK plc to delve into the mechanisms underlying regression of fibrosis after treatment for chronic liver disease, and identify and validate new drug targets involved in this process.</description>
      <content:encoded>
        <![CDATA[Extracellular matrix specialist Engitix Ltd. is teaming up with GSK plc to delve into the mechanisms underlying regression of fibrosis after treatment for chronic liver disease, and identify and validate new drug targets involved in this process.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731798</guid>
      <pubDate>Tue, 09 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731798-engitix-seals-gsk-deal-for-targets-to-reverse-liver-fibrosis</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>Eli Lilly identifies new GCGR agonists</title>
      <description>Eli Lilly and Co. has synthesized glucagon receptor (GCGR) agonists found to be potentially useful for the treatment of type 2 diabetes and obesity.</description>
      <content:encoded>
        <![CDATA[Eli Lilly and Co. has synthesized glucagon receptor (GCGR) agonists found to be potentially useful for the treatment of type 2 diabetes and obesity.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731770</guid>
      <pubDate>Tue, 09 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731770-eli-lilly-identifies-new-gcgr-agonists</link>
    </item>
    <item>
      <title>CNTY-813 enables durable glucose control without immunosuppression need</title>
      <description>At the recent American Diabetes Association meeting, researchers from Century Therapeutics Inc. presented preclinical efficacy data on CNTY-813, an induced pluripotent stem cell (iPSC)-derived cell therapy engineered using the company’s proprietary Allo-Evasion 5.0 platform.</description>
      <content:encoded>
        <![CDATA[At the recent American Diabetes Association meeting, researchers from Century Therapeutics Inc. presented preclinical efficacy data on CNTY-813, an induced pluripotent stem cell (iPSC)-derived cell therapy engineered using the company’s proprietary Allo-Evasion 5.0 platform.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731758</guid>
      <pubDate>Tue, 09 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731758-cnty-813-enables-durable-glucose-control-without-immunosuppression-need</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/Diabetes-pancreas-islets.webp?t=1681310705" type="image/png" medium="image" fileSize="713568">
        <media:title type="plain">Illustration of pancreas, close up of islet</media:title>
      </media:content>
    </item>
    <item>
      <title>Engitix seals GSK deal for targets to reverse liver fibrosis</title>
      <description>Extracellular matrix specialist Engitix Ltd. is teaming up with GSK plc to delve into the mechanisms underlying regression of fibrosis after treatment for chronic liver disease, and identify and validate new drug targets involved in this process.</description>
      <content:encoded>
        <![CDATA[Extracellular matrix specialist Engitix Ltd. is teaming up with GSK plc to delve into the mechanisms underlying regression of fibrosis after treatment for chronic liver disease, and identify and validate new drug targets involved in this process.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731693</guid>
      <pubDate>Mon, 08 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731693-engitix-seals-gsk-deal-for-targets-to-reverse-liver-fibrosis</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>Dual PPARδ/α agonists reported in Shenzhen Hightide Biotechnology patent</title>
      <description>Shenzhen Hightide Biopharmaceutical Ltd. has identified new peroxisome proliferator-activated receptor δ (PPARδ) and PPARα dual agonists potentially useful for the treatment of obesity, aging, cardiovascular disorders, heart failure, inflammatory disorders, metabolic dysfunction-associated steatotic liver disease (MASLD; NAFLD), metabolic syndrome and renal failure.</description>
      <content:encoded>
        <![CDATA[Shenzhen Hightide Biopharmaceutical Ltd. has identified new peroxisome proliferator-activated receptor δ (PPARδ) and PPARα dual agonists potentially useful for the treatment of obesity, aging, cardiovascular disorders, heart failure, inflammatory disorders, metabolic dysfunction-associated steatotic liver disease (MASLD; NAFLD), metabolic syndrome and renal failure.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731667</guid>
      <pubDate>Thu, 04 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731667-dual-ppar-agonists-reported-in-shenzhen-hightide-biotechnology-patent</link>
    </item>
    <item>
      <title>FB-7033 demonstrates efficacy in MASH management</title>
      <description>17-β-Hydroxysteroid dehydrogenase 13 (HSD17B13) and lipid transferase CIDEB are known to contribute to metabolic dysfunction-associated steatohepatitis (MASH) progression, where HSD17B13 exacerbates hepatic lipid metabolism, while CIDEB mainly mediates lipid droplet dynamics and storage. In this context, Frontier Biotechnologies Inc. has presented data on FB-7033, a bispecific siRNA approach targeting both HSD17B13 and CIDEB for the management of MASH.</description>
      <content:encoded>
        <![CDATA[17-β-Hydroxysteroid dehydrogenase 13 (HSD17B13) and lipid transferase CIDEB are known to contribute to metabolic dysfunction-associated steatohepatitis (MASH) progression, where HSD17B13 exacerbates hepatic lipid metabolism, while CIDEB mainly mediates lipid droplet dynamics and storage. In this context, Frontier Biotechnologies Inc. has presented data on FB-7033, a bispecific siRNA approach targeting both HSD17B13 and CIDEB for the management of MASH.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731658</guid>
      <pubDate>Thu, 04 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731658-fb-7033-demonstrates-efficacy-in-mash-management</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>TAK1 emerges as a therapeutic target in MASLD</title>
      <description>Transforming growth factor-β-activated kinase 1 (TAK1) is a crucial central signaling molecule of hepatic cell death, inflammation and fibrogenesis through NF-κB and MAPK in metabolic dysfunction-associated steatotic liver disease (MASLD). Its pharmacological inhibition using the TAK1 inhibitor HS-276 was tested in vivo in a murine model of diet-induced MASLD.</description>
      <content:encoded>
        <![CDATA[Transforming growth factor-β-activated kinase 1 (TAK1) is a crucial central signaling molecule of hepatic cell death, inflammation and fibrogenesis through NF-κB and MAPK in metabolic dysfunction-associated steatotic liver disease (MASLD). Its pharmacological inhibition using the TAK1 inhibitor HS-276 was tested in vivo in a murine model of diet-induced MASLD.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731600</guid>
      <pubDate>Wed, 03 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731600-tak1-emerges-as-a-therapeutic-target-in-masld</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/Liver-research-investigation-microscope.webp?t=1780498148" type="image/jpeg" medium="image" fileSize="237511">
        <media:title type="plain">Illustration of doctors examining a liver with magnifier and microscope</media:title>
      </media:content>
    </item>
    <item>
      <title>GPR119 activation ameliorates alcohol-related liver disease</title>
      <description>There is a growing consensus that alcohol-related liver disease (ALD) should be considered a metabolic disorder under the influence of the gut-liver axis. Metabolome data have highlighted fatty acid-activated G protein-coupled receptors (GPCRs) as the main affected pathways, where the relationship of G-protein-coupled receptor 119 (GPR119) with ALD remains unexplored.</description>
      <content:encoded>
        <![CDATA[There is a growing consensus that alcohol-related liver disease (ALD) should be considered a metabolic disorder under the influence of the gut-liver axis. Metabolome data have highlighted fatty acid-activated G protein-coupled receptors (GPCRs) as the main affected pathways, where the relationship of G-protein-coupled receptor 119 (GPR119) with ALD remains unexplored.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731599</guid>
      <pubDate>Wed, 03 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731599-gpr119-activation-ameliorates-alcohol-related-liver-disease</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>D&amp;D’s zabopegdutide shows more upbeat top-line phase II MASH data </title>
      <description>D&amp;D Pharmatech Inc. announced May 27 positive top-line tissue biopsy results of zabopegdutide (DD-01) from a 48-week phase II study of metabolic dysfunction-associated steatohepatitis (MASH), pushing company shares up 30% on the day.</description>
      <content:encoded>
        <![CDATA[D&D Pharmatech Inc. announced May 27 positive top-line tissue biopsy results of zabopegdutide (DD-01) from a 48-week phase II study of metabolic dysfunction-associated steatohepatitis (MASH), pushing company shares up 30% on the day.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731650</guid>
      <pubDate>Tue, 02 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731650-d-and-ds-zabopegdutide-shows-more-upbeat-top-line-phase-ii-mash-data</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Gastrointestinal/Liver-damage-fibrosis-cirrhosis.webp?t=1769528466" type="image/jpeg" medium="image" fileSize="677639">
        <media:title type="plain">Art concept for liver damage, such as fatty liver, fibrosis or cirrhosis</media:title>
      </media:content>
    </item>
    <item>
      <title>Hanmi, Haisco win billion-dollar partnerships with Eli Lilly</title>
      <description>Hanmi Pharmaceutical Co. Ltd. secured a $1.26 billion deal with Eli Lilly and Co. to out-license ex-Korea rights to sonefpeglutide (HM-15912), a Lapscovery-based glucagon-like peptide-2 analog in development for multiple indications, including an ongoing phase II study of short bowel syndrome. It was one of two billion-dollar Asian company deals signed by Lilly on June 1, with the second transaction involving Haisco Pharmaceutical Group Co. Ltd., of Beijing.</description>
      <content:encoded>
        <![CDATA[Hanmi Pharmaceutical Co. Ltd. secured a $1.26 billion deal with Eli Lilly and Co. to out-license ex-Korea rights to sonefpeglutide (HM-15912), a Lapscovery-based glucagon-like peptide-2 analog in development for multiple indications, including an ongoing phase II study of short bowel syndrome. It was one of two billion-dollar Asian company deals signed by Lilly on June 1, with the second transaction involving Haisco Pharmaceutical Group Co. Ltd., of Beijing.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731645</guid>
      <pubDate>Tue, 02 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731645-hanmi-haisco-win-billion-dollar-partnerships-with-eli-lilly</link>
      <media:content url="https://www.bioworld.com/ext/resources/BW-source/2026/Hanmi-signage-6-1.webp?t=1780342948" type="image/jpeg" medium="image" fileSize="195343">
        <media:title type="plain">Hanmi signage</media:title>
        <media:description type="plain">Credit: Hanmi Pharmaceutical Co. Ltd.</media:description>
      </media:content>
    </item>
    <item>
      <title>AX-2911 shows in vivo activity by correcting PNPLA3 in MASH</title>
      <description>Alterations in PNPLA3, particularly the I148M variant, impair lipid metabolism in hepatocytes, leading to lipid accumulation and driving progression from steatosis to fibrosis and cirrhosis. Targeting this genetic driver may offer a strategy to reduce steatosis and limit disease progression.</description>
      <content:encoded>
        <![CDATA[Alterations in PNPLA3, particularly the I148M variant, impair lipid metabolism in hepatocytes, leading to lipid accumulation and driving progression from steatosis to fibrosis and cirrhosis. Targeting this genetic driver may offer a strategy to reduce steatosis and limit disease progression.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731582</guid>
      <pubDate>Tue, 02 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731582-ax-2911-shows-in-vivo-activity-by-correcting-pnpla3-in-mash</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>PRD-001 shows synergy with Rezdiffra for treating MASH</title>
      <description>Metabolic dysfunction-associated steatohepatitis (MASH) is characterized by lipid accumulation in the liver and inflammation. Sterol O-acyltransferase 2 (SOAT2) is a key enzyme in intestinal absorption and hepatic secretion of cholesterol. PRD Therapeutics Inc. has developed PRD-001, a selective SOAT2 inhibitor currently in phase I trials for MASH.</description>
      <content:encoded>
        <![CDATA[Metabolic dysfunction-associated steatohepatitis (MASH) is characterized by lipid accumulation in the liver and inflammation. Sterol O-acyltransferase 2 (SOAT2) is a key enzyme in intestinal absorption and hepatic secretion of cholesterol. PRD Therapeutics Inc. has developed PRD-001, a selective SOAT2 inhibitor currently in phase I trials for MASH.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731581</guid>
      <pubDate>Tue, 02 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731581-prd-001-shows-synergy-with-rezdiffra-for-treating-mash</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>Hanmi, Haisco win billion-dollar partnerships with Eli Lilly</title>
      <description>Hanmi Pharmaceutical Co. Ltd. secured a $1.26 billion deal with Eli Lilly and Co. to out-license ex-Korea rights to sonefpeglutide (HM-15912), a Lapscovery-based glucagon-like peptide-2 analog in development for multiple indications, including an ongoing phase II study of short bowel syndrome. It was one of two billion-dollar Asian company deals signed by Lilly on June 1, with the second transaction involving Haisco Pharmaceutical Group Co. Ltd., of Beijing.</description>
      <content:encoded>
        <![CDATA[Hanmi Pharmaceutical Co. Ltd. secured a $1.26 billion deal with Eli Lilly and Co. to out-license ex-Korea rights to sonefpeglutide (HM-15912), a Lapscovery-based glucagon-like peptide-2 analog in development for multiple indications, including an ongoing phase II study of short bowel syndrome. It was one of two billion-dollar Asian company deals signed by Lilly on June 1, with the second transaction involving Haisco Pharmaceutical Group Co. Ltd., of Beijing.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731459</guid>
      <pubDate>Mon, 01 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731459-hanmi-haisco-win-billion-dollar-partnerships-with-eli-lilly</link>
      <media:content url="https://www.bioworld.com/ext/resources/BW-source/2026/Hanmi-signage-6-1.webp?t=1780342948" type="image/jpeg" medium="image" fileSize="195343">
        <media:title type="plain">Hanmi signage</media:title>
        <media:description type="plain">Credit: Hanmi Pharmaceutical Co. Ltd.</media:description>
      </media:content>
    </item>
    <item>
      <title>Muna Therapeutics discloses TREM2 agonists</title>
      <description>Muna Therapeutics Aps has patented new dihydropyrrolopyrimidinone compounds acting as triggering receptor expressed on myeloid cells 2 (TREM2) agonists potentially useful for the treatment of osteoporosis, rheumatoid arthritis, systemic lupus erythematosus, type 2 diabetes, obesity, metabolic dysfunction-associated steatotic liver disease (MASLD; NAFLD), neurodegeneration and inflammatory bowel disease, among others.</description>
      <content:encoded>
        <![CDATA[Muna Therapeutics Aps has patented new dihydropyrrolopyrimidinone compounds acting as triggering receptor expressed on myeloid cells 2 (TREM2) agonists potentially useful for the treatment of osteoporosis, rheumatoid arthritis, systemic lupus erythematosus, type 2 diabetes, obesity, metabolic dysfunction-associated steatotic liver disease (MASLD; NAFLD), neurodegeneration and inflammatory bowel disease, among others.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731569</guid>
      <pubDate>Mon, 01 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731569-muna-therapeutics-discloses-trem2-agonists</link>
    </item>
    <item>
      <title>Deep Apple Therapeutics synthesizes GIPR antagonists</title>
      <description>Deep Apple Therapeutics Inc. has divulged new alkylphenyl substituted compounds acting as gastric inhibitory polypeptide receptor (GIPR) antagonists potentially useful for the treatment of obesity and type 2 diabetes.</description>
      <content:encoded>
        <![CDATA[Deep Apple Therapeutics Inc. has divulged new alkylphenyl substituted compounds acting as gastric inhibitory polypeptide receptor (GIPR) antagonists potentially useful for the treatment of obesity and type 2 diabetes.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731567</guid>
      <pubDate>Mon, 01 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731567-deep-apple-therapeutics-synthesizes-gipr-antagonists</link>
    </item>
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