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    <title>Inflammatory</title>
    <description></description>
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    <language>en-us</language>
    <item>
      <title>CCR6 antagonists disclosed in Wuhan Createrna patent</title>
      <description>Wuhan Createrna Science and Technology Co. Ltd. has synthesized new cyclobutenedione compounds acting as C-C chemokine receptor type 6 (CCR6) antagonists potentially useful for the treatment of inflammatory bowel disease, allergy, dry eye, psoriasis, rheumatoid arthritis and multiple sclerosis.</description>
      <content:encoded>
        <![CDATA[Wuhan Createrna Science and Technology Co. Ltd. has synthesized new cyclobutenedione compounds acting as C-C chemokine receptor type 6 (CCR6) antagonists potentially useful for the treatment of inflammatory bowel disease, allergy, dry eye, psoriasis, rheumatoid arthritis and multiple sclerosis.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731970</guid>
      <pubDate>Tue, 16 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731970-ccr6-antagonists-disclosed-in-wuhan-createrna-patent</link>
    </item>
    <item>
      <title> Elixiron’s enrupatinib shows upbeat interim phase II AD results </title>
      <description>Elixiron Immunotherapeutics Inc. announced positive interim open-label phase II Alzheimer’s disease (AD) study findings of enrupatinib, an oral brain-penetrant colony-stimulating factor 1 receptor inhibitor, with plans to move the asset into a biomarker-based and placebo-controlled study.</description>
      <content:encoded>
        <![CDATA[Elixiron Immunotherapeutics Inc. announced positive interim open-label phase II Alzheimer’s disease (AD) study findings of enrupatinib, an oral brain-penetrant colony-stimulating factor 1 receptor inhibitor, with plans to move the asset into a biomarker-based and placebo-controlled study.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731877</guid>
      <pubDate>Mon, 15 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731877-elixirons-enrupatinib-shows-upbeat-interim-phase-ii-ad-results</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Neurology/amyloid-alzheimers-nerve-cells.webp?t=1712242653" type="image/jpeg" medium="image" fileSize="182461">
        <media:title type="plain">Illustration of amyloid plaques in Alzheimer's disease</media:title>
      </media:content>
    </item>
    <item>
      <title>Anti-C5aR1 antibodies linked to outcomes in giant cell arteritis</title>
      <description>More effective glucocorticoid-sparing therapies are needed for the treatment of giant cell arteritis (GCA). Studies found that complement signaling pathways involving complement factor 5 and its receptor (C5aR1) were overexpressed, and that a C5aR1 antagonist, avacopan, reduced the need for glucocorticoids and improved renal recovery. This led researchers to investigate the association of anti-C5aR1 antibodies with GCA and its outcomes.</description>
      <content:encoded>
        <![CDATA[More effective glucocorticoid-sparing therapies are needed for the treatment of giant cell arteritis (GCA). Studies found that complement signaling pathways involving complement factor 5 and its receptor (C5aR1) were overexpressed, and that a C5aR1 antagonist, avacopan, reduced the need for glucocorticoids and improved renal recovery. This led researchers to investigate the association of anti-C5aR1 antibodies with GCA and its outcomes.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731857</guid>
      <pubDate>Fri, 12 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731857-anti-c5ar1-antibodies-linked-to-outcomes-in-giant-cell-arteritis</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Cardiovascular/artery-cross-section-parts.webp?t=1715180484" type="image/jpeg" medium="image" fileSize="142511">
        <media:title type="plain">Medical illustration showing layers of a blood vessel</media:title>
      </media:content>
    </item>
    <item>
      <title>CD45RC identified as therapeutic target in Sjögren disease</title>
      <description>CD45RC is an isoform of protein tyrosine phosphatase receptor type C, a protein that plays a key role in regulating antigen receptor signaling in T and B cells. While it is expressed on most circulating B cells, it is only highly expressed on Th1 precursors, Th1 cells and T effector memory CD45RA+ cells (TEMRA).</description>
      <content:encoded>
        <![CDATA[CD45RC is an isoform of protein tyrosine phosphatase receptor type C, a protein that plays a key role in regulating antigen receptor signaling in T and B cells. While it is expressed on most circulating B cells, it is only highly expressed on Th1 precursors, Th1 cells and T effector memory CD45RA+ cells (TEMRA).]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731838</guid>
      <pubDate>Thu, 11 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731838-cd45rc-identified-as-therapeutic-target-in-sjogren-disease</link>
    </item>
    <item>
      <title>Sanofi phase III CIDP quit dents Dianthus; C1 mismatch?</title>
      <description>Investors in Dianthus Therapeutics Inc. apparently chose to ignore subtleties in the difference between efforts with that firm’s claseprubart vs. those by competitor Sanofi SA, which said that the phase III Mobilize study testing riliprubart in chronic inflammatory demyelinating polyneuropathy (CIDP) will be stopped for futility.</description>
      <content:encoded>
        <![CDATA[Investors in Dianthus Therapeutics Inc. apparently chose to ignore subtleties in the difference between efforts with that firm’s claseprubart vs. those by competitor Sanofi SA, which said that the phase III Mobilize study testing riliprubart in chronic inflammatory demyelinating polyneuropathy (CIDP) will be stopped for futility.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731720</guid>
      <pubDate>Wed, 10 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731720-sanofi-phase-iii-cidp-quit-dents-dianthus-c1-mismatch</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Neurology/Neurology-nerve-cell-pain.webp?t=1682600134" type="image/jpeg" medium="image" fileSize="413083">
        <media:title type="plain">3D illustration of a nerve cell</media:title>
      </media:content>
    </item>
    <item>
      <title>‘Disciplined’ $665M deal moves Oscotec’s cevidoplenib to Agios  </title>
      <description>Agios Pharmaceuticals Inc.’s potential $665 million deal for Oscotec Inc.’s cevidoplenib, a phase III-ready oral SYK inhibitor to treat immune thrombocytopenia, marks a new chapter of development focused on cancer therapy resistance for Oscotec, CEO Yoon Tae-young said.</description>
      <content:encoded>
        <![CDATA[Agios Pharmaceuticals Inc.’s potential $665 million deal for Oscotec Inc.’s cevidoplenib, a phase III-ready oral SYK inhibitor to treat immune thrombocytopenia, marks a new chapter of development focused on cancer therapy resistance for Oscotec, CEO Yoon Tae-young said.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731828</guid>
      <pubDate>Tue, 09 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731828-disciplined-665m-deal-moves-oscotecs-cevidoplenib-to-agios</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Deals-and-MAs/Deal-handshake-with-coin-chart-background.webp?t=1704408549" type="image/jpeg" medium="image" fileSize="317806">
        <media:title type="plain">Deal handshake with coin, chart background</media:title>
      </media:content>
    </item>
    <item>
      <title>CD39 mRNA-loaded nanoliposomes attenuate local acute inflammation</title>
      <description>CD39, also known as ectonucleoside triphosphate diphosphohydrolase-1 (ENTPD1), is a cell surface ectonucleotidase with key roles in modulating inflammation and localized immune regulation. Researchers from the Baker Heart and Diabetes Institute and collaborators recently proposed leveraging mRNA technologies to provide sustained, localized CD39 expression without genomic integration.</description>
      <content:encoded>
        <![CDATA[CD39, also known as ectonucleoside triphosphate diphosphohydrolase-1 (ENTPD1), is a cell surface ectonucleotidase with key roles in modulating inflammation and localized immune regulation. Researchers from the Baker Heart and Diabetes Institute and collaborators recently proposed leveraging mRNA technologies to provide sustained, localized CD39 expression without genomic integration.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731738</guid>
      <pubDate>Mon, 08 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731738-cd39-mrna-loaded-nanoliposomes-attenuate-local-acute-inflammation</link>
    </item>
    <item>
      <title>‘Disciplined’ $665M deal moves Oscotec’s cevidoplenib to Agios  </title>
      <description>Agios Pharmaceuticals Inc.’s potential $665 million deal for Oscotec Inc.’s cevidoplenib, a phase III-ready oral SYK inhibitor to treat immune thrombocytopenia, marks a new chapter of development focused on cancer therapy resistance for Oscotec, CEO Yoon Tae-young said.</description>
      <content:encoded>
        <![CDATA[Agios Pharmaceuticals Inc.’s potential $665 million deal for Oscotec Inc.’s cevidoplenib, a phase III-ready oral SYK inhibitor to treat immune thrombocytopenia, marks a new chapter of development focused on cancer therapy resistance for Oscotec, CEO Yoon Tae-young said.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731632</guid>
      <pubDate>Fri, 05 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731632-disciplined-665m-deal-moves-oscotecs-cevidoplenib-to-agios</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Deals-and-MAs/Deal-handshake-with-coin-chart-background.webp?t=1704408549" type="image/jpeg" medium="image" fileSize="317806">
        <media:title type="plain">Deal handshake with coin, chart background</media:title>
      </media:content>
    </item>
    <item>
      <title>Technique links non-coding mutations to disease genes they regulate</title>
      <description>Genome-wide association studies (GWAS) have identified multiple loci associated with complex diseases, but these are mostly on regulatory genes in the non-coding part of the genome and it has proved difficult to identify the effector genes that they control. Now, researchers in the U.K. have shown how single cell sequencing at scale can be used to precisely link non-coding GWAS loci to specific protein coding genes and cell types.</description>
      <content:encoded>
        <![CDATA[Genome-wide association studies (GWAS) have identified multiple loci associated with complex diseases, but these are mostly on regulatory genes in the non-coding part of the genome and it has proved difficult to identify the effector genes that they control. Now, researchers in the U.K. have shown how single cell sequencing at scale can be used to precisely link non-coding GWAS loci to specific protein coding genes and cell types.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731755</guid>
      <pubDate>Fri, 05 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731755-technique-links-non-coding-mutations-to-disease-genes-they-regulate</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Gastrointestinal/GI-system-with-DNA-scientific-background.webp?t=1774388477" type="image/jpeg" medium="image" fileSize="500606">
        <media:title type="plain">Gastrointestinal system with DNA, scientific background</media:title>
      </media:content>
    </item>
    <item>
      <title>Technique links non-coding mutations to disease genes they regulate</title>
      <description>Genome-wide association studies (GWAS) have identified multiple loci associated with complex diseases, but these are mostly on regulatory genes in the non-coding part of the genome and it has proved difficult to identify the effector genes that they control. Now, researchers in the U.K. have shown how single cell sequencing at scale can be used to precisely link non-coding GWAS loci to specific protein coding genes and cell types.</description>
      <content:encoded>
        <![CDATA[Genome-wide association studies (GWAS) have identified multiple loci associated with complex diseases, but these are mostly on regulatory genes in the non-coding part of the genome and it has proved difficult to identify the effector genes that they control. Now, researchers in the U.K. have shown how single cell sequencing at scale can be used to precisely link non-coding GWAS loci to specific protein coding genes and cell types.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731544</guid>
      <pubDate>Wed, 03 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731544-technique-links-non-coding-mutations-to-disease-genes-they-regulate</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Gastrointestinal/GI-system-with-DNA-scientific-background.webp?t=1774388477" type="image/jpeg" medium="image" fileSize="500606">
        <media:title type="plain">Gastrointestinal system with DNA, scientific background</media:title>
      </media:content>
    </item>
    <item>
      <title>ATGL inhibition reshapes immunometabolism in liver fibrosis</title>
      <description>Adipose triglyceride lipase (ATGL), a central mediator of triglyceride hydrolysis and fatty acid mobilization, modulates hepatic lipid homeostasis and metabolic signaling pathways that contribute to the activation of fibrogenic responses.</description>
      <content:encoded>
        <![CDATA[Adipose triglyceride lipase (ATGL), a central mediator of triglyceride hydrolysis and fatty acid mobilization, modulates hepatic lipid homeostasis and metabolic signaling pathways that contribute to the activation of fibrogenic responses.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731598</guid>
      <pubDate>Wed, 03 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731598-atgl-inhibition-reshapes-immunometabolism-in-liver-fibrosis</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Gastrointestinal/Liver-doctor.webp?t=1589217270" type="image/png" medium="image" fileSize="244160">
        <media:title type="plain">Doctor pointing at liver</media:title>
      </media:content>
    </item>
    <item>
      <title>China Pharmaceutical University discloses new asiaticoside saponin compounds</title>
      <description>China Pharmaceutical University and the Chongqing Innovation Institute, China Pharmaceutical University have synthesized new asiaticoside saponin compounds reported to be useful for the treatment of inflammation, cancer and ulcerative colitis.</description>
      <content:encoded>
        <![CDATA[China Pharmaceutical University and the Chongqing Innovation Institute, China Pharmaceutical University have synthesized new asiaticoside saponin compounds reported to be useful for the treatment of inflammation, cancer and ulcerative colitis.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731590</guid>
      <pubDate>Tue, 02 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731590-china-pharmaceutical-university-discloses-new-asiaticoside-saponin-compounds</link>
    </item>
    <item>
      <title>Army Medical University reports new cGAS/STING pathway inhibitors</title>
      <description>Army Medical University has identified new cyclic GMP-AMP synthase (MB21D1; cGAS)/STING pathway inhibitors potentially useful for the treatment of inflammatory disorders.</description>
      <content:encoded>
        <![CDATA[Army Medical University has identified new cyclic GMP-AMP synthase (MB21D1; cGAS)/STING pathway inhibitors potentially useful for the treatment of inflammatory disorders.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731570</guid>
      <pubDate>Mon, 01 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731570-army-medical-university-reports-new-cgas-sting-pathway-inhibitors</link>
    </item>
    <item>
      <title>New evidence links autoimmunity to long COVID symptoms</title>
      <description>Recent findings are reshaping current understanding of the post-infection landscape of SARS-CoV-2. Although previous studies had already suggested that autoimmunity might underlie the persistent neurological symptoms seen in long COVID, researchers at Yale University and Mount Sinai now reinforce this hypothesis. SARS-CoV-2 infection appears to trigger an autoimmune mechanism that drives chronic pain, fatigue and cognitive impairment in some patients.</description>
      <content:encoded>
        <![CDATA[Recent findings are reshaping current understanding of the post-infection landscape of SARS-CoV-2. Although previous studies had already suggested that autoimmunity might underlie the persistent neurological symptoms seen in long COVID, researchers at Yale University and Mount Sinai now reinforce this hypothesis. SARS-CoV-2 infection appears to trigger an autoimmune mechanism that drives chronic pain, fatigue and cognitive impairment in some patients.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731473</guid>
      <pubDate>Thu, 28 May 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731473-new-evidence-links-autoimmunity-to-long-covid-symptoms</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Infectious/Immune-antibodies-attacking-virus.webp?t=1769615802" type="image/jpeg" medium="image" fileSize="939811">
        <media:title type="plain">Illustration of antibodies and viral infection</media:title>
      </media:content>
    </item>
    <item>
      <title>Recludix presents STAT1/3 inhibitors for dermatological diseases</title>
      <description>Recludix Pharma Inc. recently presented data on their new STAT1/3 inhibitors REX-6553 and REX-6547 for treating dermatological inflammatory skin diseases.</description>
      <content:encoded>
        <![CDATA[Recludix Pharma Inc. recently presented data on their new STAT1/3 inhibitors REX-6553 and REX-6547 for treating dermatological inflammatory skin diseases.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731235</guid>
      <pubDate>Thu, 21 May 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731235-recludix-presents-stat1-3-inhibitors-for-dermatological-diseases</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Dermatologic/Dermatologic-atopic-dermatitis2.webp?t=1588881560" type="image/png" medium="image" fileSize="357317">
        <media:title type="plain">Skin irritation on hands</media:title>
      </media:content>
    </item>
    <item>
      <title>Beijing Tide Pharmaceutical synthesizes new angiotensin AT2 antagonists</title>
      <description>Beijing Tide Pharmaceutical Co. Ltd. has divulged new salts of known angiotensin AT2 recpetor antagonists potentially useful for the treatment of allergy, autoimmune and demyelinating diseases, cerebrovascular, respiratory, cognitive, gastrointestinal and inflammatory disorders, among others.</description>
      <content:encoded>
        <![CDATA[Beijing Tide Pharmaceutical Co. Ltd. has divulged new salts of known angiotensin AT2 recpetor antagonists potentially useful for the treatment of allergy, autoimmune and demyelinating diseases, cerebrovascular, respiratory, cognitive, gastrointestinal and inflammatory disorders, among others.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731189</guid>
      <pubDate>Wed, 20 May 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731189-beijing-tide-pharmaceutical-synthesizes-new-angiotensin-at2-antagonists</link>
    </item>
    <item>
      <title>Neurolambda Therapeutics patents new TYK2 inhibitors</title>
      <description>Neurolambda Therapeutics Inc. has disclosed new non-receptor tyrosine-protein kinase TYK2 inhibitors potentially useful for the treatment of cancer, systemic lupus erythematosus, rheumatoid arthritis and psoriatic arthritis.</description>
      <content:encoded>
        <![CDATA[Neurolambda Therapeutics Inc. has disclosed new non-receptor tyrosine-protein kinase TYK2 inhibitors potentially useful for the treatment of cancer, systemic lupus erythematosus, rheumatoid arthritis and psoriatic arthritis.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731149</guid>
      <pubDate>Mon, 18 May 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731149-neurolambda-therapeutics-patents-new-tyk2-inhibitors</link>
    </item>
    <item>
      <title>AAV-encoded dimeric PICK1 inhibitors reduce inflammatory, neuropathic pain in mice</title>
      <description>Researchers from the University of Copenhagen and collaborating institutions aimed to develop a therapy for chronic neuropathic pain based on gene therapy delivered with adeno-associated viral (AAV) vectors.</description>
      <content:encoded>
        <![CDATA[Researchers from the University of Copenhagen and collaborating institutions aimed to develop a therapy for chronic neuropathic pain based on gene therapy delivered with adeno-associated viral (AAV) vectors.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731138</guid>
      <pubDate>Mon, 18 May 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731138-aav-encoded-dimeric-pick1-inhibitors-reduce-inflammatory-neuropathic-pain-in-mice</link>
    </item>
    <item>
      <title>KSI-028 suppresses STING-driven inflammation </title>
      <description>Korean researchers reported the discovery and preclinical characterization of KSI-028, a novel tetrahydroquinoline-based STING inhibitor with activity across multiple models of STING activation.</description>
      <content:encoded>
        <![CDATA[Korean researchers reported the discovery and preclinical characterization of KSI-028, a novel tetrahydroquinoline-based STING inhibitor with activity across multiple models of STING activation.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731120</guid>
      <pubDate>Fri, 15 May 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731120-ksi-028-suppresses-sting-driven-inflammation</link>
    </item>
    <item>
      <title>Aeovian Pharmaceuticals synthesizes new CD38 inhibitors</title>
      <description>Aeovian Pharmaceuticals Inc. has divulged new ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 1 (CD38) inhibitors potentially useful for the treatment of neurodegeneration, inflammation, fibrosis, systemic scleroderma, vascular disorders, Duchenne muscular dystrophy, liver and metabolic diseases, among others.</description>
      <content:encoded>
        <![CDATA[Aeovian Pharmaceuticals Inc. has divulged new ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 1 (CD38) inhibitors potentially useful for the treatment of neurodegeneration, inflammation, fibrosis, systemic scleroderma, vascular disorders, Duchenne muscular dystrophy, liver and metabolic diseases, among others.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731086</guid>
      <pubDate>Wed, 13 May 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731086-aeovian-pharmaceuticals-synthesizes-new-cd38-inhibitors</link>
    </item>
    <item>
      <title>Boehringer Ingelheim licenses Immunitas antibody program</title>
      <description>Boehringer Ingelheim Pharma GmbH &amp; Co. KG and Immunitas Therapeutics Inc. have signed a global licensing agreement for a preclinical antibody program being developed for chronic inflammatory and autoimmune diseases.</description>
      <content:encoded>
        <![CDATA[Boehringer Ingelheim Pharma GmbH & Co. KG and Immunitas Therapeutics Inc. have signed a global licensing agreement for a preclinical antibody program being developed for chronic inflammatory and autoimmune diseases.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731077</guid>
      <pubDate>Wed, 13 May 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731077-boehringer-ingelheim-licenses-immunitas-antibody-program</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Immune/Antibody-detail-blue-orange.webp?t=1778683956" type="image/jpeg" medium="image" fileSize="608014">
        <media:title type="plain">3D illustration antibody</media:title>
      </media:content>
    </item>
    <item>
      <title>AOP Health and VRG Therapeutics partner on immunology program</title>
      <description>AOP Orphan Pharmaceuticals GmbH (AOP Health) has established a strategic partnership with VRG Therapeutics Zrt to advance a novel Kv1.3 potassium channel inhibitor for use in inflammation and immunology indications.</description>
      <content:encoded>
        <![CDATA[AOP Orphan Pharmaceuticals GmbH (AOP Health) has established a strategic partnership with VRG Therapeutics Zrt to advance a novel Kv1.3 potassium channel inhibitor for use in inflammation and immunology indications.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731074</guid>
      <pubDate>Wed, 13 May 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731074-aop-health-and-vrg-therapeutics-partner-on-immunology-program</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Research-and-science/Scientist-microscope-dropper.webp?t=1682529627" type="image/png" medium="image" fileSize="550680">
        <media:title type="plain">Scientist, microscope and dropper</media:title>
      </media:content>
    </item>
    <item>
      <title>Odyssey’s IPO, placement brings $304M to lead drugs in IBD, lupus</title>
      <description>Raising $279 million in an IPO and another $25 million in a concurrent private placement, Odyssey Therapeutics Inc. is advancing its lead phase II asset, OD-001, in ulcerative colitis, with plans to bring its SLC15A4 program into the clinic for lupus.</description>
      <content:encoded>
        <![CDATA[Raising $279 million in an IPO and another $25 million in a concurrent private placement, Odyssey Therapeutics Inc. is advancing its lead phase II asset, OD-001, in ulcerative colitis, with plans to bring its SLC15A4 program into the clinic for lupus.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/730980</guid>
      <pubDate>Fri, 08 May 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/730980-odysseys-ipo-placement-brings-304m-to-lead-drugs-in-ibd-lupus</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Money/IPO-coins.webp?t=1588705630" type="image/png" medium="image" fileSize="384858">
        <media:title type="plain">IPO, coins, financial chart</media:title>
      </media:content>
    </item>
    <item>
      <title>Abdakibart phase II graded, puts Avalo in HS upper class </title>
      <description>Avalo Therapeutics Inc. may have designed in lead asset abdakibart, a drug for hidradenitis suppurativa (HS) that offers a novel mechanism of action, wide dosing interval, and more-than-satisfying outcomes on the Hidradenitis Suppurativa Clinical Response 75 endpoint, just what the doctor – and Wall Street – ordered.</description>
      <content:encoded>
        <![CDATA[Avalo Therapeutics Inc. may have designed in lead asset abdakibart, a drug for hidradenitis suppurativa (HS) that offers a novel mechanism of action, wide dosing interval, and more-than-satisfying outcomes on the Hidradenitis Suppurativa Clinical Response 75 endpoint, just what the doctor – and Wall Street – ordered.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/730861</guid>
      <pubDate>Wed, 06 May 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/730861-abdakibart-phase-ii-graded-puts-avalo-in-hs-upper-class</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Dermatologic/Armpit.webp?t=1778102194" type="image/jpeg" medium="image" fileSize="161790">
        <media:title type="plain">Hand held near armpit</media:title>
      </media:content>
    </item>
    <item>
      <title>Korea Research Institute of Chemical Technology reports new JAK1 inhibitors</title>
      <description>A team at the Korea Research Institute of Chemical Technology has synthesized tetrahydroisoquinoline- or isoindoline-substituted [1,2,4]triazolo[1,5-a]pyridine derivatives acting as tyrosine-protein kinase JAK1 inhibitors.</description>
      <content:encoded>
        <![CDATA[A team at the Korea Research Institute of Chemical Technology has synthesized tetrahydroisoquinoline- or isoindoline-substituted [1,2,4]triazolo[1,5-<em>a</em>]pyridine derivatives acting as tyrosine-protein kinase JAK1 inhibitors.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/730915</guid>
      <pubDate>Wed, 06 May 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/730915-korea-research-institute-of-chemical-technology-reports-new-jak1-inhibitors</link>
    </item>
    <item>
      <title>Eyes are first prize for newco Link Biologics</title>
      <description>The classic origin story for a biotech startup is that of a scientist who nurtures his work out of a university and to commercial success. For Link Biologics Ltd. and its TSG6-based pipeline, the story is the other way around; it began with now-CEO Reuben Dawkins meeting University of Manchester scientists Tony Day and Caroline Milner while he was on the lookout for “great science that needs help to make it to patients.” The three are now co-founders of Link, which spun out of the University of Manchester in 2021 and has four programs in three indications, all based on TSG-6 biology.</description>
      <content:encoded>
        <![CDATA[The classic origin story for a biotech startup is that of a scientist who nurtures his work out of a university and to commercial success. For Link Biologics Ltd. and its TSG6-based pipeline, the story is the other way around; it began with now-CEO Reuben Dawkins meeting University of Manchester scientists Tony Day and Caroline Milner while he was on the lookout for “great science that needs help to make it to patients.” The three are now co-founders of Link, which spun out of the University of Manchester in 2021 and has four programs in three indications, all based on TSG-6 biology.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/730902</guid>
      <pubDate>Wed, 06 May 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/730902-eyes-are-first-prize-for-newco-link-biologics</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Ocular/Ocular-digital-eye.webp?t=1589292031" type="image/png" medium="image" fileSize="615294">
        <media:title type="plain">Rays of light beaming from eye</media:title>
      </media:content>
    </item>
    <item>
      <title>Evotec and Almirall derm alliance yields development candidate</title>
      <description>Evotec SE has announced the nomination of a small-molecule preclinical development candidate from its multi-target drug discovery alliance in medical dermatology with Almirall SA. The program is aimed at developing novel treatments for immune-mediated inflammatory skin diseases with high unmet medical need. The collaboration, established in 2022, leverages Evotec’s fully integrated, AI/machine learning enhanced discovery and preclinical development platforms.</description>
      <content:encoded>
        <![CDATA[Evotec SE has announced the nomination of a small-molecule preclinical development candidate from its multi-target drug discovery alliance in medical dermatology with Almirall SA. The program is aimed at developing novel treatments for immune-mediated inflammatory skin diseases with high unmet medical need. The collaboration, established in 2022, leverages Evotec’s fully integrated, AI/machine learning enhanced discovery and preclinical development platforms.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/730882</guid>
      <pubDate>Tue, 05 May 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/730882-evotec-and-almirall-derm-alliance-yields-development-candidate</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Dermatologic/Dermatologic-skin-layer-molecules-drug.webp?t=1777994425" type="image/jpeg" medium="image" fileSize="407682">
        <media:title type="plain">Illustration showing skin anatomy</media:title>
      </media:content>
    </item>
    <item>
      <title>TMEM175 activators reported in Ono Pharmaceutical patent</title>
      <description>Ono Pharmaceutical Co. Ltd. has synthesized bridged bicyclic compounds acting as endosomal/lysosomal proton channel TMEM175 activators. As such, they are described as potentially useful for the treatment of inflammatory disorders, lysosomal storage diseases, autoimmune disease and Parkinson’s disease.</description>
      <content:encoded>
        <![CDATA[Ono Pharmaceutical Co. Ltd. has synthesized bridged bicyclic compounds acting as endosomal/lysosomal proton channel TMEM175 activators. As such, they are described as potentially useful for the treatment of inflammatory disorders, lysosomal storage diseases, autoimmune disease and Parkinson’s disease.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/730805</guid>
      <pubDate>Thu, 30 Apr 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/730805-tmem175-activators-reported-in-ono-pharmaceutical-patent</link>
    </item>
    <item>
      <title>EQ-504 is AhR agonist for ulcerative colitis, related disorders</title>
      <description>Activating the aryl hydrocarbon receptor (AhR) in immune cells enhances anti-inflammatory pathways and limits pathogenic immune responses. Equillium Inc. has recently presented data for their AhR agonist EQ-504 for the potential treatment of immune-related diseases.</description>
      <content:encoded>
        <![CDATA[Activating the aryl hydrocarbon receptor (AhR) in immune cells enhances anti-inflammatory pathways and limits pathogenic immune responses. Equillium Inc. has recently presented data for their AhR agonist EQ-504 for the potential treatment of immune-related diseases.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/730794</guid>
      <pubDate>Thu, 30 Apr 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/730794-eq-504-is-ahr-agonist-for-ulcerative-colitis-related-disorders</link>
    </item>
    <item>
      <title>Quintuple GLP-1-GIP-PPAR agonist for obesity and diabetes control</title>
      <description>A new molecule combines the action of two incretins, GLP-1 and GIP, hormones that regulate glucose and appetite, with lanifibranor, a triple agonist of peroxisome proliferator activated receptors (PPAR α/γ/δ). GLP-1-GIP-Lani enables targeted delivery of the PPAR agonist to cells that express incretin receptors, enhancing weight loss, improving glucose control and reducing inflammation in obese mice. In these models, it surpassed the effects of GLP-1 receptor agonists such as semaglutide and GLP-1-GIP co-agonists such as tirzepatide in reducing body weight, improving glycemic control and enhancing metabolic outcomes during active treatment.</description>
      <content:encoded>
        <![CDATA[A new molecule combines the action of two incretins, GLP-1 and GIP, hormones that regulate glucose and appetite, with lanifibranor, a triple agonist of peroxisome proliferator activated receptors (PPAR α/γ/δ). GLP-1-GIP-Lani enables targeted delivery of the PPAR agonist to cells that express incretin receptors, enhancing weight loss, improving glucose control and reducing inflammation in obese mice. In these models, it surpassed the effects of GLP-1 receptor agonists such as semaglutide and GLP-1-GIP co-agonists such as tirzepatide in reducing body weight, improving glycemic control and enhancing metabolic outcomes during active treatment.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/730790</guid>
      <pubDate>Thu, 30 Apr 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/730790-quintuple-glp-1gipppar-agonist-for-obesity-and-diabetes-control</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/Glucagon-like-peptide-1-receptor-GLP-1R-binding-site-small-molecule-agonist.webp?t=1777564710" type="image/jpeg" medium="image" fileSize="637678">
        <media:title type="plain">Glucagon-like peptide-1 receptor (GLP-1R) complex</media:title>
        <media:description type="plain">Glucagon-like peptide-1 receptor (GLP-1R) complex, representing the molecular target for GLP-1 agonists. Detailed view of the binding site with small-molecule agonist.</media:description>
      </media:content>
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