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    <title>Inflammatory</title>
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    <item>
      <title>Beijing Double-Crane Runchuang identifies new TLR7/8 antagonists</title>
      <description>Beijing Double-Crane Runchuang Technology Co. Ltd. has discovered new Toll-like receptor 7 (TLR7) and/or TLR8 antagonists potentially useful for the treatment of rheumatoid arthritis, systemic lupus erythematosus, cutaneous lupus erythematosus, dermatomyositis, hidradenitis suppurativa, polymyositis, psoriasis and Sjogren’s syndrome, among others.</description>
      <content:encoded>
        <![CDATA[Beijing Double-Crane Runchuang Technology Co. Ltd. has discovered new Toll-like receptor 7 (TLR7) and/or TLR8 antagonists potentially useful for the treatment of rheumatoid arthritis, systemic lupus erythematosus, cutaneous lupus erythematosus, dermatomyositis, hidradenitis suppurativa, polymyositis, psoriasis and Sjogren’s syndrome, among others.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732410</guid>
      <pubDate>Mon, 06 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732410-beijing-double-crane-runchuang-identifies-new-tlr7-8-antagonists</link>
    </item>
    <item>
      <title>NLRP3 inflammasome inhibitors disclosed in MSD patent</title>
      <description>Merck Sharp &amp; Dohme LLC (MSD) has synthesized new benzimidazole derivatives acting as NLRP3 inflammasome inhibitors. As such, they are potentially useful for the treatment of atherosclerosis, metabolic dysfunction-associated steatohepatitis (MASH), neuroinflammation, inflammatory skin, inflammatory joint and autoimmune disease, Alzheimer’s and Parkinson’s disease, among others.</description>
      <content:encoded>
        <![CDATA[Merck Sharp & Dohme LLC (MSD) has synthesized new benzimidazole derivatives acting as NLRP3 inflammasome inhibitors. As such, they are potentially useful for the treatment of atherosclerosis, metabolic dysfunction-associated steatohepatitis (MASH), neuroinflammation, inflammatory skin, inflammatory joint and autoimmune disease, Alzheimer’s and Parkinson’s disease, among others.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732386</guid>
      <pubDate>Fri, 03 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732386-nlrp3-inflammasome-inhibitors-disclosed-in-msd-patent</link>
    </item>
    <item>
      <title>CINP 2026: Prenatal and adolescent stress shape brain vulnerability </title>
      <description>Human biology is extraordinarily complex, and that sophistication emerges from the very beginning. During embryonic and fetal development, the organism’s architecture is shaped through the organization of tissues, the establishment of molecular pathways, and the coordination of signals that will later sustain the body as an integrated system. It is likely the most delicate stage of life, where any disturbance in that foundational process can have lasting consequences on health.</description>
      <content:encoded>
        <![CDATA[ Human biology is extraordinarily complex, and that sophistication emerges from the very beginning. During embryonic and fetal development, the organism’s architecture is shaped through the organization of tissues, the establishment of molecular pathways, and the coordination of signals that will later sustain the body as an integrated system. It is likely the most delicate stage of life, where any disturbance in that foundational process can have lasting consequences on health.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732374</guid>
      <pubDate>Fri, 03 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732374-cinp-2026-prenatal-and-adolescent-stress-shape-brain-vulnerability</link>
    </item>
    <item>
      <title>Nuvectis shares continue to rally after $1.46B Haisco deal</title>
      <description>Nuvectis Pharma Inc.’s shares climbed further after the oncology-focused biotech nabbed select rights to a late-stage complement factor B inhibitor (HSK-39297/NXP-100) and a phase I BRAF inhibitor (HSK-42360/NXP-200) from Haisco Pharmaceutical Group Co. Ltd. for $40 million up front.</description>
      <content:encoded>
        <![CDATA[Nuvectis Pharma Inc.’s shares climbed further after the oncology-focused biotech nabbed select rights to a late-stage complement factor B inhibitor (HSK-39297/NXP-100) and a phase I BRAF inhibitor (HSK-42360/NXP-200) from Haisco Pharmaceutical Group Co. Ltd. for $40 million up front.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732348</guid>
      <pubDate>Tue, 30 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732348-nuvectis-shares-continue-to-rally-after-146b-haisco-deal</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Money/Dollar-symbol-with-arrow-graph-moving-up.webp?t=1701900511" type="image/jpeg" medium="image" fileSize="197116">
        <media:title type="plain">Dollar symbol with arrow graph</media:title>
      </media:content>
    </item>
    <item>
      <title>Hexapharmatec identifies new TFEB inducers</title>
      <description>Hexapharmatec Co. Ltd. has discovered new transcription factor EB (TFEB) inducers described as potentially useful for the treatment of colitis, kidney and hepatic fibrosis.</description>
      <content:encoded>
        <![CDATA[Hexapharmatec Co. Ltd. has discovered new transcription factor EB (TFEB) inducers described as potentially useful for the treatment of colitis, kidney and hepatic fibrosis.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732324</guid>
      <pubDate>Tue, 30 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732324-hexapharmatec-identifies-new-tfeb-inducers</link>
    </item>
    <item>
      <title>Changchun Genescience Pharmaceuticals discloses new VAV1 degradation inducers</title>
      <description>Changchun Genescience Pharmaceuticals Co. Ltd. has synthesized new molecular glue degraders comprising E3 ubiquitin-protein ligase-binding agents acting as proto-oncogene Vav (VAV1) degradation inducers. They are described as potentially useful for the treatment of ulcerative colitis, Crohn’s disease, rheumatoid arthritis, multiple sclerosis, systemic lupus erythematosus and myasthenia gravis.</description>
      <content:encoded>
        <![CDATA[Changchun Genescience Pharmaceuticals Co. Ltd. has synthesized new molecular glue degraders comprising E3 ubiquitin-protein ligase-binding agents acting as proto-oncogene Vav (VAV1) degradation inducers. They are described as potentially useful for the treatment of ulcerative colitis, Crohn’s disease, rheumatoid arthritis, multiple sclerosis, systemic lupus erythematosus and myasthenia gravis.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732216</guid>
      <pubDate>Mon, 29 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732216-changchun-genescience-pharmaceuticals-discloses-new-vav1-degradation-inducers</link>
    </item>
    <item>
      <title>IRAK4-targeting PROTAC degrader suppresses inflammatory signaling in vitro</title>
      <description>Chronic activation or upregulation of interleukin-1 receptor-associated kinase 4 (IRAK4) has been linked to several diseases, including systemic lupus erythematosus, rheumatoid arthritis, atopic dermatitis, Alzheimer’s disease and atherosclerosis. Researchers from the Ocean University of China aimed to address the limitations of traditional small-molecule inhibitors by designing novel proteolysis targeting chimeras (PROTACs) for IRAK4 degradation.</description>
      <content:encoded>
        <![CDATA[Chronic activation or upregulation of interleukin-1 receptor-associated kinase 4 (IRAK4) has been linked to several diseases, including systemic lupus erythematosus, rheumatoid arthritis, atopic dermatitis, Alzheimer’s disease and atherosclerosis. Researchers from the Ocean University of China aimed to address the limitations of traditional small-molecule inhibitors by designing novel proteolysis targeting chimeras (PROTACs) for IRAK4 degradation.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732208</guid>
      <pubDate>Mon, 29 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732208-irak4-targeting-protac-degrader-suppresses-inflammatory-signaling-in-vitro</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/IRAK4-protein-kinase-structure.webp?t=1782744590" type="image/jpeg" medium="image" fileSize="474262">
        <media:title type="plain">3D rendering of interleukin-1 receptor-associated kinase 4</media:title>
        <media:description type="plain">IRAK4, a protein kinase involved in signaling innate immune responses from Toll-like receptors.</media:description>
      </media:content>
    </item>
    <item>
      <title>EMA to pull Amgen’s Tavneos over ‘incorrect and misleading’ data</title>
      <description>The EMA is recommending withdrawing Amgen Inc.’s complement inhibitor Tavneos (avacopan) from the market in Europe, saying data provided at the time it assessed the MAA “were found to be incorrect and misleading and could no longer be relied upon for demonstrating Tavneos’ effectiveness.”</description>
      <content:encoded>
        <![CDATA[The EMA is recommending withdrawing Amgen Inc.’s complement inhibitor Tavneos (avacopan) from the market in Europe, saying data provided at the time it assessed the MAA “were found to be incorrect and misleading and could no longer be relied upon for demonstrating Tavneos’ effectiveness.”]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732171</guid>
      <pubDate>Fri, 26 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732171-ema-to-pull-amgens-tavneos-over-incorrect-and-misleading-data</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Drugs/Tavneos.webp?t=1782503657" type="image/jpeg" medium="image" fileSize="49212">
        <media:title type="plain">Tavneos</media:title>
        <media:description type="plain">Credit: Amgen Inc.</media:description>
      </media:content>
    </item>
    <item>
      <title>New RIPK1 inhibitor protects from hepatic fibrosis</title>
      <description>Receptor-interacting protein kinase 1 (RIPK1) acts as a central signaling node regulating apoptosis, necroptosis and inflammatory pathways. Researchers from China Pharmaceutical University reported the discovery and preclinical characterization of LT-1339-553, a novel RIPK1 inhibitor, in models of schistosomiasis-induced hepatic fibrosis.</description>
      <content:encoded>
        <![CDATA[Receptor-interacting protein kinase 1 (RIPK1) acts as a central signaling node regulating apoptosis, necroptosis and inflammatory pathways. Researchers from China Pharmaceutical University reported the discovery and preclinical characterization of LT-1339-553, a novel RIPK1 inhibitor, in models of schistosomiasis-induced hepatic fibrosis.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732192</guid>
      <pubDate>Fri, 26 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732192-new-ripk1-inhibitor-protects-from-hepatic-fibrosis</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/RIPK1-molecular-model.webp?t=1782483869" type="image/png" medium="image" fileSize="1086452">
        <media:title type="plain">3D molecular model illustration of RIPK1</media:title>
        <media:description type="plain">RIPK1</media:description>
      </media:content>
    </item>
    <item>
      <title>Nuvectis shares continue to rally after $1.46B Haisco deal</title>
      <description>Nuvectis Pharma Inc.’s shares climbed further after the oncology-focused biotech nabbed select rights to a late-stage complement factor B inhibitor (HSK-39297/NXP-100) and a phase I BRAF inhibitor (HSK-42360/NXP-200) from Haisco Pharmaceutical Group Co. Ltd. for $40 million up front.</description>
      <content:encoded>
        <![CDATA[Nuvectis Pharma Inc.’s shares climbed further after the oncology-focused biotech nabbed select rights to a late-stage complement factor B inhibitor (HSK-39297/NXP-100) and a phase I BRAF inhibitor (HSK-42360/NXP-200) from Haisco Pharmaceutical Group Co. Ltd. for $40 million up front.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732081</guid>
      <pubDate>Wed, 24 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732081-nuvectis-shares-continue-to-rally-after-146b-haisco-deal</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Money/Dollar-symbol-with-arrow-graph-moving-up.webp?t=1701900511" type="image/jpeg" medium="image" fileSize="197116">
        <media:title type="plain">Dollar symbol with arrow graph</media:title>
      </media:content>
    </item>
    <item>
      <title>Pulmonary inflammation unveils three severe pneumonia subtypes</title>
      <description>Molecular subtyping of disease is typically associated with cancer. Now, researchers at the University of Cambridge are applying it to infections.</description>
      <content:encoded>
        <![CDATA[Molecular subtyping of disease is typically associated with cancer. Now, researchers at the University of Cambridge are applying it to infections. ]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732184</guid>
      <pubDate>Wed, 24 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732184-pulmonary-inflammation-unveils-three-severe-pneumonia-subtypes</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Respiratory/Lungs-anatomy.webp?t=1691698481" type="image/jpeg" medium="image" fileSize="421630">
        <media:title type="plain">Lungs anatomy</media:title>
      </media:content>
    </item>
    <item>
      <title>J-Pharma drives first cancer LAT1 to phase III study with FDA nod </title>
      <description>J-Pharma Co. Ltd. is progressing the most clinically advanced L-type amino acid transport 1 (LAT1) inhibitor, nanvuranlat (JPH‑203), in a global phase III Beacon-BTC study of biliary tract cancer following U.S. FDA alignment.</description>
      <content:encoded>
        <![CDATA[J-Pharma Co. Ltd. is progressing the most clinically advanced L-type amino acid transport 1 (LAT1) inhibitor, nanvuranlat (JPH‑203), in a global phase III Beacon-BTC study of biliary tract cancer following U.S. FDA alignment.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732153</guid>
      <pubDate>Tue, 23 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732153-j-pharma-drives-first-cancer-lat1-to-phase-iii-study-with-fda-nod</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/Cholangiocarcinoma-Bile-Duct-Cancer.webp?t=1674573514" type="image/png" medium="image" fileSize="810777">
        <media:title type="plain">Illustration of cancer in the bile ducts</media:title>
      </media:content>
    </item>
    <item>
      <title>hPLA2-G5 inhibition exerts analgesic and anti-inflammatory effects</title>
      <description>Researchers from Bayer AG reported the discovery and preclinical characterization of BAY-439, a potent and selective hPLA2-G5 inhibitor, in models of pain.</description>
      <content:encoded>
        <![CDATA[Researchers from Bayer AG reported the discovery and preclinical characterization of BAY-439, a potent and selective hPLA2-G5 inhibitor, in models of pain.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732114</guid>
      <pubDate>Tue, 23 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732114-hpla2-g5-inhibition-exerts-analgesic-and-anti-inflammatory-effects</link>
    </item>
    <item>
      <title>Pulmonary inflammation unveils three severe pneumonia subtypes</title>
      <description>Molecular subtyping of disease is typically associated with cancer. Now, researchers at the University of Cambridge are applying it to infections. Some patients with severe pneumonia progress in different ways. Predicting their trajectories could help tailor treatments and prevent fatal outcomes. To do this, the scientists analyzed bronchoalveolar fluid from several patient cohorts and identified three biological pneumotypes based on which cells are present, which genes are active, and which inflammatory proteins are produced.</description>
      <content:encoded>
        <![CDATA[Molecular subtyping of disease is typically associated with cancer. Now, researchers at the University of Cambridge are applying it to infections. Some patients with severe pneumonia progress in different ways. Predicting their trajectories could help tailor treatments and prevent fatal outcomes. To do this, the scientists analyzed bronchoalveolar fluid from several patient cohorts and identified three biological pneumotypes based on which cells are present, which genes are active, and which inflammatory proteins are produced.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732108</guid>
      <pubDate>Tue, 23 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732108-pulmonary-inflammation-unveils-three-severe-pneumonia-subtypes</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Respiratory/Lungs-anatomy.webp?t=1691698481" type="image/jpeg" medium="image" fileSize="421630">
        <media:title type="plain">Lungs anatomy</media:title>
      </media:content>
    </item>
    <item>
      <title>Asahi Kasei Therapeutics reports new TNFR1 antagonists</title>
      <description>Asahi Kasei Therapeutics Corp. has identified new tumor necrosis factor receptor superfamily member 1A (TNFRSF1A; TNFR1; p55; CD120a) antagonists potentially useful for the treatment of rheumatoid arthritis, psoriasis, ankylosing spondylitis, hidradenitis suppurativa, ulcerative colitis and Crohn's disease.</description>
      <content:encoded>
        <![CDATA[Asahi Kasei Therapeutics Corp. has identified new tumor necrosis factor receptor superfamily member 1A (TNFRSF1A; TNFR1; p55; CD120a) antagonists potentially useful for the treatment of rheumatoid arthritis, psoriasis, ankylosing spondylitis, hidradenitis suppurativa, ulcerative colitis and Crohn's disease.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732105</guid>
      <pubDate>Mon, 22 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732105-asahi-kasei-therapeutics-reports-new-tnfr1-antagonists</link>
    </item>
    <item>
      <title>New VAV1 degradation inducers reported in Haisco Pharmaceutical Group patents</title>
      <description>Haisco Pharmaceutical Group Co. Ltd. has divulged molecular glue degraders comprising cereblon (CRBN)-binding agents acting as proto-oncogene Vav (VAV1) degradation inducers. They are reported to be useful for the treatment of rheumatoid arthritis, multiple sclerosis and gastroenteritis.</description>
      <content:encoded>
        <![CDATA[Haisco Pharmaceutical Group Co. Ltd. has divulged molecular glue degraders comprising cereblon (CRBN)-binding agents acting as proto-oncogene Vav (VAV1) degradation inducers. They are reported to be useful for the treatment of rheumatoid arthritis, multiple sclerosis and gastroenteritis.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732040</guid>
      <pubDate>Fri, 19 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732040-new-vav1-degradation-inducers-reported-in-haisco-pharmaceutical-group-patents</link>
    </item>
    <item>
      <title>J-Pharma drives first cancer LAT1 to phase III study with FDA nod </title>
      <description>J-Pharma Co. Ltd. is progressing the most clinically advanced L-type amino acid transport 1 (LAT1) inhibitor, nanvuranlat (JPH‑203), in a global phase III Beacon-BTC study of biliary tract cancer following U.S. FDA alignment.</description>
      <content:encoded>
        <![CDATA[J-Pharma Co. Ltd. is progressing the most clinically advanced L-type amino acid transport 1 (LAT1) inhibitor, nanvuranlat (JPH‑203), in a global phase III Beacon-BTC study of biliary tract cancer following U.S. FDA alignment.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731921</guid>
      <pubDate>Thu, 18 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731921-j-pharma-drives-first-cancer-lat1-to-phase-iii-study-with-fda-nod</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/Cholangiocarcinoma-Bile-Duct-Cancer.webp?t=1674573514" type="image/png" medium="image" fileSize="810777">
        <media:title type="plain">Illustration of cancer in the bile ducts</media:title>
      </media:content>
    </item>
    <item>
      <title>Shanghai Pharmaceuticals discovers new IL-17A inhibitors</title>
      <description>Shanghai Pharmaceuticals Holding Co. Ltd. has reported interleukin-17A (IL-17A) inhibitors that are potentially useful for the treatment of psoriasis, rheumatoid arthritis, spondyloarthritis, hidradenitis suppurativa, psoriatic arthritis and uveitis.</description>
      <content:encoded>
        <![CDATA[Shanghai Pharmaceuticals Holding Co. Ltd. has reported interleukin-17A (IL-17A) inhibitors that are potentially useful for the treatment of psoriasis, rheumatoid arthritis, spondyloarthritis, hidradenitis suppurativa, psoriatic arthritis and uveitis.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732020</guid>
      <pubDate>Thu, 18 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732020-shanghai-pharmaceuticals-discovers-new-il-17a-inhibitors</link>
    </item>
    <item>
      <title>Spyre’s Skyline-UC double win lifts hopes for IBD antibody combos</title>
      <description>Spyre Therapeutics Inc.’s striking “two for two” data on ulcerative colitis (UC) candidates, SPY-001 and SPY-002, drew applause from multiple analysts, putting eyes on the Boston biotech’s upcoming top-line data of anti-IL-23 antibody SPY-003 – the third biologic module in a six-strong inflammatory bowel disease (IBD) lineup.</description>
      <content:encoded>
        <![CDATA[Spyre Therapeutics Inc.’s striking “two for two” data on ulcerative colitis (UC) candidates, SPY-001 and SPY-002, drew applause from multiple analysts, putting eyes on the Boston biotech’s upcoming top-line data of anti-IL-23 antibody SPY-003 – the third biologic module in a six-strong inflammatory bowel disease (IBD) lineup.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731905</guid>
      <pubDate>Wed, 17 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731905-spyres-skyline-uc-double-win-lifts-hopes-for-ibd-antibody-combos</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Gastrointestinal/Gastrointestinal-system-illustration.webp?t=1769098607" type="image/jpeg" medium="image" fileSize="679694">
        <media:title type="plain">Gastrointestinal system</media:title>
      </media:content>
    </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/731984</guid>
      <pubDate>Tue, 16 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731984-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>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>
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