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    <title>American Academy of Neurology</title>
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    <item>
      <title>Neuro deals aplenty: UCB’s $1B+ takeover of Neurona the latest </title>
      <description>A flurry of deals focused on the neurological disease space in 2026 suggest large biopharma companies are searching for the next best therapeutics for everything from epilepsy and narcolepsy to post-traumatic stress disorder and hyperphagia.</description>
      <content:encoded>
        <![CDATA[A flurry of deals focused on the neurological disease space in 2026 suggest large biopharma companies are searching for the next best therapeutics for everything from epilepsy and narcolepsy to post-traumatic stress disorder and hyperphagia.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/730616</guid>
      <pubDate>Fri, 24 Apr 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/730616-neuro-deals-aplenty-ucbs-1b-takeover-of-neurona-the-latest</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Neurology/Epileptic-brain.webp?t=1648507237" type="image/png" medium="image" fileSize="319894">
        <media:title type="plain">Epileptic brain and abnormal EEG wave discharges</media:title>
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    </item>
    <item>
      <title>KHN-702 as a potent nonopioid analgesic</title>
      <description>Chengdu Kanghong Pharmaceutical Group Co. Ltd. is developing a nonopioid Nav1.8 inhibitor, KHN-702. The effects of KHN-702 were evaluated both in vitro and in vivo, in a plantar incision pain model, and results were presented at the recent American Academy of Neurology meeting in Chicago.</description>
      <content:encoded>
        <![CDATA[Chengdu Kanghong Pharmaceutical Group Co. Ltd. is developing a nonopioid Nav1.8 inhibitor, KHN-702. The effects of KHN-702 were evaluated both in vitro and in vivo, in a plantar incision pain model, and results were presented at the recent American Academy of Neurology meeting in Chicago.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/730637</guid>
      <pubDate>Fri, 24 Apr 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/730637-khn-702-as-a-potent-nonopioid-analgesic</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Neurology/Pain-illustration.webp?t=1598381807" type="image/png" medium="image" fileSize="413040">
        <media:title type="plain">Pain illustration</media:title>
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    </item>
    <item>
      <title>Synendos’ first-in-class SERI effective in models of anxiety</title>
      <description>At the recently concluded meeting of the American Academy of Neurology, Synendos Therapeutics AG reported preclinical data from the pharmacological characterization of SYT-510, which is the first selective endocannabinoid reuptake inhibitor (SERI) to enter the clinic for the potential treatment of disorders affecting the CNS, such as anxiety or movement disorders. A new class of endocannabinoid system (ECS) modulators, SERIs potently and selectively inhibit endocannabinoid reuptake to help the ECS restore normal brain function under disease conditions.</description>
      <content:encoded>
        <![CDATA[At the recently concluded meeting of the American Academy of Neurology, Synendos Therapeutics AG reported preclinical data from the pharmacological characterization of SYT-510, which is the first selective endocannabinoid reuptake inhibitor (SERI) to enter the clinic for the potential treatment of disorders affecting the CNS, such as anxiety or movement disorders. A new class of endocannabinoid system (ECS) modulators, SERIs potently and selectively inhibit endocannabinoid reuptake to help the ECS restore normal brain function under disease conditions.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/730585</guid>
      <pubDate>Thu, 23 Apr 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/730585-synendos-first-in-class-seri-effective-in-models-of-anxiety</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Neurology/Silhouette-of-head-and-brainwith-fractal-art.webp?t=1776955680" type="image/jpeg" medium="image" fileSize="995438">
        <media:title type="plain">Silhouette of head and brainwith fractal art</media:title>
      </media:content>
    </item>
    <item>
      <title>Walking the talk, Kyverna phase II stiffens miv-cel CAR T case</title>
      <description>Optimism rose for what could be the first CAR T therapy in autoimmune disease as Kyverna Therapeutics Inc. made public a positive primary analysis from its registrational trial, KYSA-8, of mivocabtagene autoleucel (miv-cel, KYV-101) in stiff-person syndrome. Kyverna plans to submit a BLA to the U.S. FDA in the first half of this year.</description>
      <content:encoded>
        <![CDATA[Optimism rose for what could be the first CAR T therapy in autoimmune disease as Kyverna Therapeutics Inc. made public a positive primary analysis from its registrational trial, KYSA-8, of mivocabtagene autoleucel (miv-cel, KYV-101) in stiff-person syndrome. Kyverna plans to submit a BLA to the U.S. FDA in the first half of this year.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/730495</guid>
      <pubDate>Wed, 22 Apr 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/730495-walking-the-talk-kyverna-phase-ii-stiffens-miv-cel-car-t-case</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Musculoskeletal/Woman-stretching-her-arms-and-hands.webp?t=1776888974" type="image/jpeg" medium="image" fileSize="445659">
        <media:title type="plain">Woman stretching her arms and hands</media:title>
      </media:content>
    </item>
    <item>
      <title>XPC-837 restores network dysfunction in Dravet syndrome models</title>
      <description>Researchers from Xenon Pharmaceuticals Inc. described the preclinical efficacy of XPC-837 in models of Dravet syndrome, a severe developmental and epileptic encephalopathy most commonly caused by de novo loss of function mutations in the SCN1A gene.</description>
      <content:encoded>
        <![CDATA[Researchers from Xenon Pharmaceuticals Inc. described the preclinical efficacy of XPC-837 in models of Dravet syndrome, a severe developmental and epileptic encephalopathy most commonly caused by de novo loss of function mutations in the <em>SCN1A</em> gene.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/730539</guid>
      <pubDate>Tue, 21 Apr 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/730539-xpc-837-restores-network-dysfunction-in-dravet-syndrome-models</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Neurology/Brain-and-DNA.webp?t=1616096016" type="image/png" medium="image" fileSize="453052">
        <media:title type="plain">Brain and DNA</media:title>
      </media:content>
    </item>
    <item>
      <title>ASO targeting SNCA p.A53T shows promise in Parkinson’s</title>
      <description>Vanda Pharmaceuticals Inc. presented data this week at the annual American Academy of Neurology conference regarding allele-specific antisense oligonucleotides (ASOs) that specifically target the mutant p.A53T allele from the SNCA gene while preserving the expression of the wild-type allele. The mutant allele is associated with increased risk of early-onset Parkinson’s disease (PD) and current ASOs target SNCA regardless of its mutation status.</description>
      <content:encoded>
        <![CDATA[Vanda Pharmaceuticals Inc. presented data this week at the annual American Academy of Neurology conference regarding allele-specific antisense oligonucleotides (ASOs) that specifically target the mutant p.A53T allele from the <em>SNCA</em> gene while preserving the expression of the wild-type allele. The mutant allele is associated with increased risk of early-onset Parkinson’s disease (PD) and current ASOs target SNCA regardless of its mutation status.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/730537</guid>
      <pubDate>Tue, 21 Apr 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/730537-aso-targeting-snca-pa53t-shows-promise-in-parkinsons</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Neurology/Parkinsons-disease.webp?t=1589296424" type="image/png" medium="image" fileSize="449161">
        <media:title type="plain">Steadying hand while reaching for glass</media:title>
      </media:content>
    </item>
    <item>
      <title>‘Complement’-ary approaches? FcRn holds ground in myasthenia gravis</title>
      <description>Watchers of the percolating myasthenia gravis space are waiting eagerly for data from Dianthus Therapeutics Inc.’s phase II Magic study testing DNTH-103, an active C1s inhibitor, compared to placebo in patients with anti-AChR-positive generalized disease.</description>
      <content:encoded>
        <![CDATA[Watchers of the percolating myasthenia gravis space are waiting eagerly for data from Dianthus Therapeutics Inc.’s phase II Magic study testing DNTH-103, an active C1s inhibitor, compared to placebo in patients with anti-AChR-positive generalized disease.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/719349</guid>
      <pubDate>Mon, 21 Apr 2025 11:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/719349-complement-ary-approaches-fcrn-holds-ground-in-myasthenia-gravis</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/Motor-neuron-muscle.webp?t=1675957121" type="image/png" medium="image" fileSize="1756485">
        <media:title type="plain">Illustration of motor neuron connecting to muscle fiber</media:title>
      </media:content>
    </item>
    <item>
      <title>Remegen’s lupus drug surfaces with phase III myasthenia gravis data</title>
      <description>Remegen Co. Ltd. emerged as a surprise challenger in the generalized myasthenia gravis space, unveiling positive phase III data of its China-approved lupus drug, telitacicept (RCT-18; Tai’ai), in the rare autoimmune neuromuscular disorder at the 2025 American Academy of Neurology conference.</description>
      <content:encoded>
        <![CDATA[Remegen Co. Ltd. emerged as a surprise challenger in the generalized myasthenia gravis space, unveiling positive phase III data of its China-approved lupus drug, telitacicept (RCT-18; Tai’ai), in the rare autoimmune neuromuscular disorder at the 2025 American Academy of Neurology conference.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/719310</guid>
      <pubDate>Tue, 15 Apr 2025 11:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/719310-remegens-lupus-drug-surfaces-with-phase-iii-myasthenia-gravis-data</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Drugs/Telitacicept-packaging.webp?t=1744227540" type="image/jpeg" medium="image" fileSize="82685">
        <media:title type="plain">Telitacicept packaging</media:title>
        <media:description type="plain">Credit: Remegen Co. Ltd.</media:description>
      </media:content>
    </item>
    <item>
      <title>Neurosense phase II combo to hail new Paradigm in ALS?</title>
      <description>As developers continue to search for better amyotrophic lateral sclerosis (ALS) therapies, Neurosense Therapeutics Ltd. turned up some hopeful findings from its phase IIb Paradigm trial with PrimeC. The drug, a combination therapy (ciprofloxacin and celecoxib) designed to target multiple ALS pathways, is having salutary effects on microRNA modulation (miRNA), Neurosense said, with the study showing a “profound and consistent” downregulation of 161 mature miRNAs across all time points in the double-blind period of the experiment.</description>
      <content:encoded>
        <![CDATA[As developers continue to search for better amyotrophic lateral sclerosis (ALS) therapies, Neurosense Therapeutics Ltd. turned up some hopeful findings from its phase IIb Paradigm trial with PrimeC. The drug, a combination therapy (ciprofloxacin and celecoxib) designed to target multiple ALS pathways, is having salutary effects on microRNA modulation (miRNA), Neurosense said, with the study showing a “profound and consistent” downregulation of 161 mature miRNAs across all time points in the double-blind period of the experiment.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/718993</guid>
      <pubDate>Wed, 09 Apr 2025 11:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/718993-neurosense-phase-ii-combo-to-hail-new-paradigm-in-als</link>
    </item>
    <item>
      <title>Remegen’s lupus drug surfaces with phase III myasthenia gravis data</title>
      <description>Remegen Co. Ltd. emerged as a surprise challenger in the generalized myasthenia gravis space, unveiling positive phase III data of its China-approved lupus drug, telitacicept (RCT-18; Tai’ai), in the rare autoimmune neuromuscular disorder at the 2025 American Academy of Neurology conference.</description>
      <content:encoded>
        <![CDATA[Remegen Co. Ltd. emerged as a surprise challenger in the generalized myasthenia gravis space, unveiling positive phase III data of its China-approved lupus drug, telitacicept (RCT-18; Tai’ai), in the rare autoimmune neuromuscular disorder at the 2025 American Academy of Neurology conference.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/718992</guid>
      <pubDate>Wed, 09 Apr 2025 11:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/718992-remegens-lupus-drug-surfaces-with-phase-iii-myasthenia-gravis-data</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Drugs/Telitacicept-packaging.webp?t=1744227540" type="image/jpeg" medium="image" fileSize="82685">
        <media:title type="plain">Telitacicept packaging</media:title>
        <media:description type="plain">Credit: Remegen Co. Ltd.</media:description>
      </media:content>
    </item>
    <item>
      <title>FHND-1002 regenerates neuron damage in Parkinson’s disease model</title>
      <description>Jiangsu Chia Tai Fenghai Pharmaceutical Co. Ltd. has developed a new small-molecule oral compound for the treatment of Parkinson’s disease, FHND-1002, which demonstrated neuronal protection in models of neurodegenerative diseases and neuron trauma.</description>
      <content:encoded>
        <![CDATA[Jiangsu Chia Tai Fenghai Pharmaceutical Co. Ltd. has developed a new small-molecule oral compound for the treatment of Parkinson’s disease, FHND-1002, which demonstrated neuronal protection in models of neurodegenerative diseases and neuron trauma.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/707958</guid>
      <pubDate>Fri, 26 Apr 2024 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/707958-fhnd-1002-regenerates-neuron-damage-in-parkinsons-disease-model</link>
    </item>
    <item>
      <title>AAV-CaV1.3-shRNA ameliorates parkinsonian symptoms in aged macaques</title>
      <description>Proof-of-concept findings had shown that mRNA silencing of striatal Cav1.3 channels prevented and reversed established levodopa-induced dyskinesia in parkinsonian rats, with these effects being maintained in aged rats.</description>
      <content:encoded>
        <![CDATA[Proof-of-concept findings had shown that mRNA silencing of striatal Cav1.3 channels prevented and reversed established levodopa-induced dyskinesia in parkinsonian rats, with these effects being maintained in aged rats.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/707804</guid>
      <pubDate>Tue, 23 Apr 2024 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/707804-aav-cav13-shrna-ameliorates-parkinsonian-symptoms-in-aged-macaques</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Neurology/Parkinsons-disease.webp?t=1589296424" type="image/png" medium="image" fileSize="449161">
        <media:title type="plain">Steadying hand while reaching for glass</media:title>
      </media:content>
    </item>
    <item>
      <title>Pan-IgG protease S-1117 reduces IgG levels and ameliorates nephritis in murine model</title>
      <description>The generation of pathogenic autoantibodies is a crucial event in the development of inflammation and complement activation, leading to immune cell responses.</description>
      <content:encoded>
        <![CDATA[The generation of pathogenic autoantibodies is a crucial event in the development of inflammation and complement activation, leading to immune cell responses. ]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/707778</guid>
      <pubDate>Mon, 22 Apr 2024 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/707778-pan-igg-protease-s-1117-reduces-igg-levels-and-ameliorates-nephritis-in-murine-model</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Nephrology/kidney-nephrology.webp?t=1589217921" type="image/png" medium="image" fileSize="520589">
        <media:title type="plain">Kidneys</media:title>
      </media:content>
    </item>
    <item>
      <title>eIF2B activator ABBV-CLS-7262 shows promise in vanishing white matter disease</title>
      <description>Vanishing white matter disease (VWM) is a rare and progressive leukoencephalopathy caused by loss-of-function mutations, in a recessive pattern of inheritance, in any of the genes encoding eIF2B, a guanine nucleotide exchange factor for eIF2 and an effector of the integrated stress response (ISR). At last week’s American Academy of Neurology meeting, Calico Life Sciences LLC and Abbvie Inc. presented preclinical results for their brain-penetrant compound ABBV-CLS-7262 (fosigotifator sodium tromethamine) in VWM.</description>
      <content:encoded>
        <![CDATA[Vanishing white matter disease (VWM) is a rare and progressive leukoencephalopathy caused by loss-of-function mutations, in a recessive pattern of inheritance, in any of the genes encoding eIF2B, a guanine nucleotide exchange factor for eIF2 and an effector of the integrated stress response (ISR). At last week’s American Academy of Neurology meeting, Calico Life Sciences LLC and Abbvie Inc. presented preclinical results for their brain-penetrant compound ABBV-CLS-7262 (fosigotifator sodium tromethamine) in VWM.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/707776</guid>
      <pubDate>Mon, 22 Apr 2024 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/707776-eif2b-activator-abbv-cls-7262-shows-promise-in-vanishing-white-matter-disease</link>
    </item>
    <item>
      <title>Head of the class? Vaxxinity could ease migraine ache with new CGRP approach</title>
      <description>The U.S. FDA’s green light April 17 for Abbvie Inc. to expand the label of Qulipta (atogepant) – the first and only oral calcitonin gene-related peptide (CGRP) receptor antagonist for migraine, with language that includes prevention of such headaches chronically in adults – provided a welcome addition to the arsenal, but sufferers are still waiting for an improved remedy. Vaxxinity Inc. just might have it. And with a vaccine, no less.</description>
      <content:encoded>
        <![CDATA[The U.S. FDA’s green light April 17 for Abbvie Inc. to expand the label of Qulipta (atogepant) – the first and only oral calcitonin gene-related peptide (CGRP) receptor antagonist for migraine, with language that includes prevention of such headaches chronically in adults – provided a welcome addition to the arsenal, but sufferers are still waiting for an improved remedy. Vaxxinity Inc. just might have it. And with a vaccine, no less.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/696325</guid>
      <pubDate>Fri, 21 Apr 2023 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/696325-head-of-the-class-vaxxinity-could-ease-migraine-ache-with-new-cgrp-approach</link>
    </item>
    <item>
      <title>Conference data for June 28, 2022: EAN</title>
      <description>New and updated preclinical and clinical data presented by biopharma firms at the European Academy of Neurology Congress, including: Bristol Myers Squibb, Horizon, Teva.</description>
      <content:encoded>
        <![CDATA[New and updated preclinical and clinical data presented by biopharma firms at the European Academy of Neurology Congress, including: Bristol Myers Squibb, Horizon, Teva.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/520124</guid>
      <pubDate>Tue, 28 Jun 2022 11:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/520124-conference-data-for-june-28-2022-ean</link>
    </item>
    <item>
      <title>Conference data for April 4, 2022: AAN</title>
      <description>New and updated preclinical and clinical data presented by biopharma firms at the American Academy of Neurology annual meeting, including: Clene, Emalex, Genentech, H. Lundbeck, Horizon, Mitsubishi, Neurelis, Neurocrine, Neuroderm, TG.</description>
      <content:encoded>
        <![CDATA[New and updated preclinical and clinical data presented by biopharma firms at the American Academy of Neurology annual meeting, including: Clene, Emalex, Genentech, H. Lundbeck, Horizon, Mitsubishi, Neurelis, Neurocrine, Neuroderm, TG.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/517574</guid>
      <pubDate>Mon, 04 Apr 2022 11:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/517574-conference-data-for-april-4-2022-aan</link>
    </item>
    <item>
      <title>Conference data for April 19, 2021: AAN</title>
      <description>New and updated preclinical and clinical data presented by biopharma firms at the American Academy of Neurology Annual Meeting, including: Autobahn, Avadel, Lundbeck, Prothena, Teva.</description>
      <content:encoded>
        <![CDATA[New and updated preclinical and clinical data presented by biopharma firms at the American Academy of Neurology Annual Meeting, including: Autobahn, Avadel, Lundbeck, Prothena, Teva.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/506082</guid>
      <pubDate>Mon, 19 Apr 2021 11:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/506082-conference-data-for-april-19-2021-aan</link>
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