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    <title>Obesity</title>
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    <item>
      <title>Lilly’s triple-G retatrutide ‘best-in-class’ as BLA filing nears  </title>
      <description>Scoring high marks on two more phase III obesity trials, this time involving serious type 2 diabetes and cardiovascular complications, Eli Lilly and Co. has cleared the path for a BLA filing for its triple-G candidate retatrutide, which many expect will eventually surpass the top two marketed drugs in the space.</description>
      <content:encoded>
        <![CDATA[Scoring high marks on two more phase III obesity trials, this time involving serious type 2 diabetes and cardiovascular complications, Eli Lilly and Co. has cleared the path for a BLA filing for its triple-G candidate retatrutide, which many expect will eventually surpass the top two marketed drugs in the space.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732852</guid>
      <pubDate>Thu, 23 Jul 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732852-lillys-triple-g-retatrutide-best-in-class-as-bla-filing-nears</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Obesity/Male-feet-on-scale.webp?t=1699653457" type="image/jpeg" medium="image" fileSize="357330">
        <media:title type="plain">Feet on scale</media:title>
      </media:content>
    </item>
    <item>
      <title>China’s Mindrank raises $52M series B to advance oral GLP-1 </title>
      <description>Mindrank AI Ltd. completed a $52 million series B round to advance MDR-001, its AI-discovered oral small-molecule GLP-1 receptor agonist, which is in phase III trials for obesity in China.</description>
      <content:encoded>
        <![CDATA[Mindrank AI Ltd. completed a $52 million series B round to advance MDR-001, its AI-discovered oral small-molecule GLP-1 receptor agonist, which is in phase III trials for obesity in China.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732667</guid>
      <pubDate>Tue, 14 Jul 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732667-chinas-mindrank-raises-52m-series-b-to-advance-oral-glp-1</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Money/Blue-digital-dollar-sign.webp?t=1775054521" type="image/jpeg" medium="image" fileSize="639573">
        <media:title type="plain">Blue digital dollar sign</media:title>
      </media:content>
    </item>
    <item>
      <title>China’s Mindrank raises $52M series B to advance oral GLP-1 </title>
      <description>Mindrank AI Ltd. completed a $52 million series B round to advance MDR-001, its AI-discovered oral small-molecule GLP-1 receptor agonist, which is in phase III trials for obesity in China.</description>
      <content:encoded>
        <![CDATA[Mindrank AI Ltd. completed a $52 million series B round to advance MDR-001, its AI-discovered oral small-molecule GLP-1 receptor agonist, which is in phase III trials for obesity in China.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732583</guid>
      <pubDate>Mon, 13 Jul 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732583-chinas-mindrank-raises-52m-series-b-to-advance-oral-glp-1</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Money/Blue-digital-dollar-sign.webp?t=1775054521" type="image/jpeg" medium="image" fileSize="639573">
        <media:title type="plain">Blue digital dollar sign</media:title>
      </media:content>
    </item>
    <item>
      <title>Corxel-Vincentage’s oral GLP-1 meets phase II obesity endpoints</title>
      <description>Corxel Pharmaceuticals Ltd.’s oral small-molecule GLP-1 receptor agonist, CX-11, met the primary endpoints in a phase II trial evaluating the candidate in obese and overweight patients in the U.S., according to top-line results.</description>
      <content:encoded>
        <![CDATA[Corxel Pharmaceuticals Ltd.’s oral small-molecule GLP-1 receptor agonist, CX-11, met the primary endpoints in a phase II trial evaluating the candidate in obese and overweight patients in the U.S., according to top-line results.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732349</guid>
      <pubDate>Tue, 30 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732349-corxel-vincentages-oral-glp-1-meets-phase-ii-obesity-endpoints</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Drugs/Glass-of-water-and-tablets.webp?t=1764799994" type="image/jpeg" medium="image" fileSize="854423">
        <media:title type="plain">Glass of water and tablets</media:title>
      </media:content>
    </item>
    <item>
      <title>Corxel-Vincentage’s oral GLP-1 meets phase II obesity endpoints</title>
      <description>Corxel Pharmaceuticals Ltd.’s oral small-molecule GLP-1 receptor agonist, CX-11, met the primary endpoints in a phase II trial evaluating the candidate in obese and overweight patients in the U.S., according to top-line results.</description>
      <content:encoded>
        <![CDATA[Corxel Pharmaceuticals Ltd.’s oral small-molecule GLP-1 receptor agonist, CX-11, met the primary endpoints in a phase II trial evaluating the candidate in obese and overweight patients in the U.S., according to top-line results.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732050</guid>
      <pubDate>Wed, 24 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732050-corxel-vincentages-oral-glp-1-meets-phase-ii-obesity-endpoints</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Drugs/Glass-of-water-and-tablets.webp?t=1764799994" type="image/jpeg" medium="image" fileSize="854423">
        <media:title type="plain">Glass of water and tablets</media:title>
      </media:content>
    </item>
    <item>
      <title>China’s Micot targets HK$1.2B IPO to advance metabolic portfolio</title>
      <description>Chinese peptide therapeutics developer Shaanxi Micot Pharmaceutical Technology Co. Ltd. is seeking up to HK$1.22 billion (US$155 million) in a Hong Kong IPO to advance its lead phase III chronic kidney disease candidate, MT-1013, and next-generation obesity therapies.</description>
      <content:encoded>
        <![CDATA[Chinese peptide therapeutics developer Shaanxi Micot Pharmaceutical Technology Co. Ltd. is seeking up to HK$1.22 billion (US$155 million) in a Hong Kong IPO to advance its lead phase III chronic kidney disease candidate, MT-1013, and next-generation obesity therapies.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732154</guid>
      <pubDate>Tue, 23 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732154-chinas-micot-targets-hk12b-ipo-to-advance-metabolic-portfolio</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Money/Financing-IPO-up-arrow-stock.webp?t=1588707556" type="image/png" medium="image" fileSize="334505">
        <media:title type="plain">IPO, coins, upward arrow</media:title>
      </media:content>
    </item>
    <item>
      <title>China’s Micot targets HK$1.2B IPO to advance metabolic portfolio</title>
      <description>Chinese peptide therapeutics developer Shaanxi Micot Pharmaceutical Technology Co. Ltd. is seeking up to HK$1.22 billion (US$155 million) in a Hong Kong IPO to advance its lead phase III chronic kidney disease candidate, MT-1013, and next-generation obesity therapies.</description>
      <content:encoded>
        <![CDATA[Chinese peptide therapeutics developer Shaanxi Micot Pharmaceutical Technology Co. Ltd. is seeking up to HK$1.22 billion (US$155 million) in a Hong Kong IPO to advance its lead phase III chronic kidney disease candidate, MT-1013, and next-generation obesity therapies.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731909</guid>
      <pubDate>Wed, 17 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731909-chinas-micot-targets-hk12b-ipo-to-advance-metabolic-portfolio</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Money/Financing-IPO-up-arrow-stock.webp?t=1588707556" type="image/png" medium="image" fileSize="334505">
        <media:title type="plain">IPO, coins, upward arrow</media:title>
      </media:content>
    </item>
    <item>
      <title>GLP-1s need technologies for long-term use</title>
      <description>For the long-term impact of GLP-1 therapies in obesity to be realized, they must be paired with data and digital tools. While the drugs are effective, challenges are well known, such as loss of muscle mass loss, compliance and accessibility. With more treatments moving through the pipeline, innovation and technology will be key to supporting long-term use, delegates heard at the HLTH Europe conference in Amsterdam on June 17.</description>
      <content:encoded>
        <![CDATA[For the long-term impact of GLP-1 therapies in obesity to be realized, they must be paired with data and digital tools. While the drugs are effective, challenges are well known, such as loss of muscle mass loss, compliance and accessibility. With more treatments moving through the pipeline, innovation and technology will be key to supporting long-term use, delegates heard at the HLTH Europe conference in Amsterdam on June 17.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731908</guid>
      <pubDate>Wed, 17 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731908-glp-1s-need-technologies-for-long-term-use</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Obesity/Wireframe-of-feet-and-scale.webp?t=1781729006" type="image/jpeg" medium="image" fileSize="214769">
        <media:title type="plain">Wireframe of feet and scale</media:title>
      </media:content>
    </item>
    <item>
      <title>Chinese challenger Gan &amp; Lee gains momentum in metabolic disease </title>
      <description>Chinese diabetes specialist Gan &amp; Lee Pharmaceuticals is strengthening its position in metabolic disease after reporting positive phase III data for both once-weekly basal insulin candidate Ludefen and obesity therapy bofanglutide.</description>
      <content:encoded>
        <![CDATA[Chinese diabetes specialist Gan & Lee Pharmaceuticals is strengthening its position in metabolic disease after reporting positive phase III data for both once-weekly basal insulin candidate Ludefen and obesity therapy bofanglutide.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731983</guid>
      <pubDate>Tue, 16 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731983-chinese-challenger-gan-and-lee-gains-momentum-in-metabolic-disease</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Diabetes/Diabetes-illustration.webp?t=1724186440" type="image/png" medium="image" fileSize="300125">
        <media:title type="plain">Blood glucose chart and monitor, stethoscope, injector pen</media:title>
      </media:content>
    </item>
    <item>
      <title>Chinese challenger Gan &amp; Lee gains momentum in metabolic disease </title>
      <description>Chinese diabetes specialist Gan &amp; Lee Pharmaceuticals is strengthening its position in metabolic disease after reporting positive phase III data for both once-weekly basal insulin candidate Ludefen and obesity therapy bofanglutide.</description>
      <content:encoded>
        <![CDATA[Chinese diabetes specialist Gan & Lee Pharmaceuticals is strengthening its position in metabolic disease after reporting positive phase III data for both once-weekly basal insulin candidate Ludefen and obesity therapy bofanglutide.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731876</guid>
      <pubDate>Mon, 15 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731876-chinese-challenger-gan-and-lee-gains-momentum-in-metabolic-disease</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Diabetes/Diabetes-illustration.webp?t=1724186440" type="image/png" medium="image" fileSize="300125">
        <media:title type="plain">Blood glucose chart and monitor, stethoscope, injector pen</media:title>
      </media:content>
    </item>
    <item>
      <title>GLP-1s and more weigh in at ADA</title>
      <description>GLP-1 receptor agonists remained center stage at the 2026 Scientific Sessions of the American Diabetes Association with Boehringer Ingelheim GmbH and Astrazeneca plc, joining the leaders, Eli Lilly and Co. and Novo Nordisk A/S, in presenting data for their respective GLP-1 drugs.</description>
      <content:encoded>
        <![CDATA[GLP-1 receptor agonists remained center stage at the 2026 Scientific Sessions of the American Diabetes Association with Boehringer Ingelheim GmbH and Astrazeneca plc, joining the leaders, Eli Lilly and Co. and Novo Nordisk A/S, in presenting data for their respective GLP-1 drugs.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731706</guid>
      <pubDate>Tue, 09 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731706-glp-1s-and-more-weigh-in-at-ada</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Obesity/Close-up-of-injector-pen-in-hands.webp?t=1736374814" type="image/jpeg" medium="image" fileSize="117912">
        <media:title type="plain">Close-up of injector pen in hands</media:title>
      </media:content>
    </item>
    <item>
      <title>Another Triumph: Lilly’s triple G agonist scores in obesity </title>
      <description>Posting another win for its triple G agonist, Eli Lilly and Co. rolled out top-line phase III data from Triumph-1 showing that all doses of retatrutide met primary and key secondary endpoints for obesity, with participants losing on average between 19% and 28.3% of body weight and significantly improving their cardiovascular risk factors.</description>
      <content:encoded>
        <![CDATA[Posting another win for its triple G agonist, Eli Lilly and Co. rolled out top-line phase III data from Triumph-1 showing that all doses of retatrutide met primary and key secondary endpoints for obesity, with participants losing on average between 19% and 28.3% of body weight and significantly improving their cardiovascular risk factors.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731371</guid>
      <pubDate>Thu, 21 May 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731371-another-triumph-lillys-triple-g-agonist-scores-in-obesity</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Obesity/Feet-on-scale-and-measuring-tape.webp?t=1709071824" type="image/jpeg" medium="image" fileSize="141907">
        <media:title type="plain">Feet on scale and measuring tape</media:title>
      </media:content>
    </item>
    <item>
      <title>Vincentage’s oral GLP-1 meets phase III obesity endpoints   </title>
      <description>Vincentage Pharma Co. Ltd.’s once-daily oral small-molecule GLP-1 receptor agonist, VCT-220, met the primary endpoints in a pivotal phase III trial in overweight or obese patients in China. Based on the top-line data, the Chengdu, China-based company plans to submit an NDA for chronic weight management to China’s National Medical Products Administration.</description>
      <content:encoded>
        <![CDATA[Vincentage Pharma Co. Ltd.’s once-daily oral small-molecule GLP-1 receptor agonist, VCT-220, met the primary endpoints in a pivotal phase III trial in overweight or obese patients in China. Based on the top-line data, the Chengdu, China-based company plans to submit an NDA for chronic weight management to China’s National Medical Products Administration.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731330</guid>
      <pubDate>Tue, 19 May 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731330-vincentages-oral-glp-1-meets-phase-iii-obesity-endpoints</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Drugs/Oral-medication.webp?t=1652383335" type="image/png" medium="image" fileSize="350602">
        <media:title type="plain">Oral medication</media:title>
      </media:content>
    </item>
    <item>
      <title>In the mix post-Ventyx, more NLRP3s to seize?  </title>
      <description>Eli Lilly and Co.’s buyout of Ventyx Biosciences Inc. for $1.2 billion at the start of the year brought to the forefront NLR family pyrin domain containing 3 (NLRP3) inhibitors on which a handful of developers have been working, and research in the space continues to roll out, as with the paper published March 26 in Nature that delved into mechanisms that rev up the NLRP3 inflammasome.</description>
      <content:encoded>
        <![CDATA[Eli Lilly and Co.’s buyout of Ventyx Biosciences Inc. for $1.2 billion at the start of the year brought to the forefront NLR family pyrin domain containing 3 (NLRP3) inhibitors on which a handful of developers have been working, and research in the space continues to roll out, as with the paper published March 26 in <em>Nature</em> that delved into mechanisms that rev up the NLRP3 inflammasome.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731061</guid>
      <pubDate>Wed, 13 May 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731061-in-the-mix-post-ventyx-more-nlrp3s-to-seize</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/NLRP3-inflammasome.webp?t=1687271826" type="image/jpeg" medium="image" fileSize="295477">
        <media:title type="plain">NLRP3 inflammasome</media:title>
      </media:content>
    </item>
    <item>
      <title>GSK licenses siRNA asset in $1B deal for Siranbio</title>
      <description>In a deal that could be worth up to $1 billion for Suzhou Siran Biotechnology Co. Ltd. (Siranbio), GSK plc licensed exclusive worldwide rights to the siRNA oligonucleotide SA-030, which has recently entered phase I trials for cardiometabolic disease.</description>
      <content:encoded>
        <![CDATA[In a deal that could be worth up to $1 billion for Suzhou Siran Biotechnology Co. Ltd. (Siranbio), GSK plc licensed exclusive worldwide rights to the siRNA oligonucleotide SA-030, which has recently entered phase I trials for cardiometabolic disease.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731226</guid>
      <pubDate>Tue, 12 May 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731226-gsk-licenses-sirna-asset-in-1b-deal-for-siranbio</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/siRNA-structure-model.webp?t=1732119622" type="image/jpeg" medium="image" fileSize="568771">
        <media:title type="plain">Illustration of siRNA structure</media:title>
      </media:content>
    </item>
    <item>
      <title>MBX highlights early data for monthly obesity drug MBX-4291</title>
      <description>Shares of MBX Biosciences Inc. hit a 52-week high on preliminary phase I data for its MBX-4291, a GLP-1/GIP co-agonist prodrug for obesity. Though early and still blinded, findings from the trial showed promising efficacy, along with good tolerability and the potential for once-monthly dosing, factors that will likely be critical for MBX to compete in the crowded obesity space.</description>
      <content:encoded>
        <![CDATA[Shares of MBX Biosciences Inc. hit a 52-week high on preliminary phase I data for its MBX-4291, a GLP-1/GIP co-agonist prodrug for obesity. Though early and still blinded, findings from the trial showed promising efficacy, along with good tolerability and the potential for once-monthly dosing, factors that will likely be critical for MBX to compete in the crowded obesity space.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731031</guid>
      <pubDate>Mon, 11 May 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731031-mbx-highlights-early-data-for-monthly-obesity-drug-mbx-4291</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Obesity/Injector-pen-and-measuring-tape.webp?t=1767118584" type="image/jpeg" medium="image" fileSize="323464">
        <media:title type="plain">Injector pen and spiraling measuring tape</media:title>
      </media:content>
    </item>
    <item>
      <title>GSK licenses siRNA asset in $1B deal for Siranbio</title>
      <description>In a deal that could be worth up to $1 billion for Suzhou Siran Biotechnology Co. Ltd. (Siranbio), GSK plc licensed exclusive worldwide rights to the siRNA oligonucleotide SA-030, which has recently entered phase I trials for cardiometabolic disease.</description>
      <content:encoded>
        <![CDATA[In a deal that could be worth up to $1 billion for Suzhou Siran Biotechnology Co. Ltd. (Siranbio), GSK plc licensed exclusive worldwide rights to the siRNA oligonucleotide SA-030, which has recently entered phase I trials for cardiometabolic disease.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/730864</guid>
      <pubDate>Wed, 06 May 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/730864-gsk-licenses-sirna-asset-in-1b-deal-for-siranbio</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/siRNA-structure-model.webp?t=1732119622" type="image/jpeg" medium="image" fileSize="568771">
        <media:title type="plain">Illustration of siRNA structure</media:title>
      </media:content>
    </item>
    <item>
      <title>CMS to Bridge coverage for obesity drugs as BALANCE teeters</title>
      <description>When the U.S. CMS didn’t get takers for its voluntary Better Approaches to Lifestyle and Nutrition for Comprehensive Health (BALANCE) model to cover obesity drugs under Medicare Part D, the agency punted. It announced late April 21 that it will indefinitely delay the BALANCE model in Medicare but extend its temporary Medicare GLP-1 Bridge demonstration model through the end of 2027. (The Medicaid BALANCE model will still kick in this year in states that choose to participate in it.)</description>
      <content:encoded>
        <![CDATA[When the U.S. CMS didn’t get takers for its voluntary Better Approaches to Lifestyle and Nutrition for Comprehensive Health (BALANCE) model to cover obesity drugs under Medicare Part D, the agency punted. It announced late April 21 that it will indefinitely delay the BALANCE model in Medicare but extend its temporary Medicare GLP-1 Bridge demonstration model through the end of 2027. (The Medicaid BALANCE model will still kick in this year in states that choose to participate in it.)]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/730497</guid>
      <pubDate>Wed, 22 Apr 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/730497-cms-to-bridge-coverage-for-obesity-drugs-as-balance-teeters</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Drugs/Generic-injection-pens.webp?t=1725043126" type="image/jpeg" medium="image" fileSize="126406">
        <media:title type="plain">Generic injection pens</media:title>
      </media:content>
    </item>
    <item>
      <title>Obesity-focused Kailera goes for US biopharma record with $625M IPO</title>
      <description>Kailera Therapeutics Inc.’s “obesity-first” approach continues to resonate with investors, with the company pricing an upsized IPO, offering 39 million shares at $16 apiece for gross proceeds of $625 million. Full exercise of the underwriters’ option could add another $93.8 million, bringing the total to nearly $719 million, easily topping Sana Biotechnology Inc.’s $675.6 million 2021 IPO and setting a new record for U.S. biopharma IPOs, according to BioWorld data.</description>
      <content:encoded>
        <![CDATA[Kailera Therapeutics Inc.’s “obesity-first” approach continues to resonate with investors, with the company pricing an upsized IPO, offering 39 million shares at $16 apiece for gross proceeds of $625 million. Full exercise of the underwriters’ option could add another $93.8 million, bringing the total to nearly $719 million, easily topping Sana Biotechnology Inc.’s $675.6 million 2021 IPO and setting a new record for U.S. biopharma IPOs, according to <em>BioWorld</em> data.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/730403</guid>
      <pubDate>Fri, 17 Apr 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/730403-obesity-focused-kailera-goes-for-us-biopharma-record-with-625m-ipo</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Money/Gold-IPO-with-chart.webp?t=1776456932" type="image/jpeg" medium="image" fileSize="507410">
        <media:title type="plain">Gold IPO with chart</media:title>
      </media:content>
    </item>
    <item>
      <title>Lilly’s GLP-1 Foundayo aces MACE in DILI of a phase III </title>
      <description>Wall Street met with satisfaction but not surprise Eli Lilly and Co.’s undeniably positive top-line results from the phase III Achieve-4 study testing the efficacy and safety of Foundayo (orforglipron) compared to insulin glargine in adults with type 2 diabetes and obesity or overweight at increased cardiovascular risk.</description>
      <content:encoded>
        <![CDATA[Wall Street met with satisfaction but not surprise Eli Lilly and Co.’s undeniably positive top-line results from the phase III Achieve-4 study testing the efficacy and safety of Foundayo (orforglipron) compared to insulin glargine in adults with type 2 diabetes and obesity or overweight at increased cardiovascular risk.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/730389</guid>
      <pubDate>Thu, 16 Apr 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/730389-lillys-glp-1-foundayo-aces-mace-in-dili-of-a-phase-iii</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Drugs/Foundayo.webp?t=1776371156" type="image/jpeg" medium="image" fileSize="145217">
        <media:title type="plain">Foundayo</media:title>
        <media:description type="plain">Credit: Eli Lilly and Co.</media:description>
      </media:content>
    </item>
    <item>
      <title>In the mix post-Ventyx, more NLRP3s to seize?  </title>
      <description>Eli Lilly and Co.’s buyout of Ventyx Biosciences Inc. for $1.2 billion at the start of the year brought to the forefront NLR family pyrin domain containing 3 (NLRP3) inhibitors, on which a handful of developers have been working – and research in the space continues to roll out, as with the paper published March 26 in Nature that delved into mechanisms that rev up the NLRP3 inflammasome.</description>
      <content:encoded>
        <![CDATA[Eli Lilly and Co.’s buyout of Ventyx Biosciences Inc. for $1.2 billion at the start of the year brought to the forefront NLR family pyrin domain containing 3 (NLRP3) inhibitors, on which a handful of developers have been working – and research in the space continues to roll out, as with the paper published March 26 in <em>Nature</em> that delved into mechanisms that rev up the NLRP3 inflammasome.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/730313</guid>
      <pubDate>Wed, 15 Apr 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/730313-in-the-mix-post-ventyx-more-nlrp3s-to-seize</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/NLRP3-inflammasome.webp?t=1687271826" type="image/jpeg" medium="image" fileSize="295477">
        <media:title type="plain">NLRP3 inflammasome</media:title>
      </media:content>
    </item>
    <item>
      <title>Biologics in development outnumber small molecules for the first time</title>
      <description>More than four decades on from the approval of the first biologic drug, the industry has reached a tipping point, and biotech drugs now outnumber small molecules in the global R&amp;D pipeline.</description>
      <content:encoded>
        <![CDATA[More than four decades on from the approval of the first biologic drug, the industry has reached a tipping point, and biotech drugs now outnumber small molecules in the global R&D pipeline.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/730418</guid>
      <pubDate>Tue, 14 Apr 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/730418-biologics-in-development-outnumber-small-molecules-for-the-first-time</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Research-and-science/Drug-research-illustration1.webp?t=1600982220" type="image/png" medium="image" fileSize="443224">
        <media:title type="plain">Drug research illustration</media:title>
      </media:content>
    </item>
    <item>
      <title>Fit and fat: Study shows no such thing as metabolically healthy obesity</title>
      <description>There are new data to chew over in the ongoing controversy about obesity being diagnosed as a disease from a study tracking 157,159 participants in the UK Biobank over 13 years. This shows that even in the absence of any metabolic disturbance such as elevated lipids, high blood pressure or diabetes, there is an increased risk of heart attack, stroke, peripheral arterial disease, heart failure and liver disease in people with a body mass index over 30.</description>
      <content:encoded>
        <![CDATA[There are new data to chew over in the ongoing controversy about obesity being diagnosed as a disease from a study tracking 157,159 participants in the UK Biobank over 13 years. This shows that even in the absence of any metabolic disturbance such as elevated lipids, high blood pressure or diabetes, there is an increased risk of heart attack, stroke, peripheral arterial disease, heart failure and liver disease in people with a body mass index over 30.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/730369</guid>
      <pubDate>Mon, 13 Apr 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/730369-fit-and-fat-study-shows-no-such-thing-as-metabolically-healthy-obesity</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Obesity/Woman-exercising-with-hand-weights.webp?t=1775851436" type="image/jpeg" medium="image" fileSize="559918">
        <media:title type="plain">Woman exercising with hand weights</media:title>
      </media:content>
    </item>
    <item>
      <title>Fit and fat: Study shows no such thing as metabolically healthy obesity</title>
      <description>There are new data to chew over in the ongoing controversy about obesity being diagnosed as a disease from a study tracking 157,159 participants in the UK Biobank over 13 years. This shows that even in the absence of any metabolic disturbance such as elevated lipids, high blood pressure or diabetes, there is an increased risk of heart attack, stroke, peripheral arterial disease, heart failure and liver disease in people with a body mass index over 30.</description>
      <content:encoded>
        <![CDATA[There are new data to chew over in the ongoing controversy about obesity being diagnosed as a disease from a study tracking 157,159 participants in the UK Biobank over 13 years. This shows that even in the absence of any metabolic disturbance such as elevated lipids, high blood pressure or diabetes, there is an increased risk of heart attack, stroke, peripheral arterial disease, heart failure and liver disease in people with a body mass index over 30.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/730222</guid>
      <pubDate>Fri, 10 Apr 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/730222-fit-and-fat-study-shows-no-such-thing-as-metabolically-healthy-obesity</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Obesity/Woman-exercising-with-hand-weights.webp?t=1775851436" type="image/jpeg" medium="image" fileSize="559918">
        <media:title type="plain">Woman exercising with hand weights</media:title>
      </media:content>
    </item>
    <item>
      <title>Biologics in development outnumber small molecules for the first time</title>
      <description>More than four decades on from the approval of the first biologic drug, the industry has reached a tipping point, and biotech drugs now outnumber small molecules in the global R&amp;D pipeline. At the start of the biotech industry, progress was slow. Between 1983 and 1995, the U.S. FDA approved an average of two biologics each year. Now, biologics have taken the lead by the smallest of margins, accounting for 50.1% of drugs in development at the start of 2026, according to the Pharma Annual Review 2026, published by Pharmaprojects, a firm that tracks global pharma R&amp;D.</description>
      <content:encoded>
        <![CDATA[More than four decades on from the approval of the first biologic drug, the industry has reached a tipping point, and biotech drugs now outnumber small molecules in the global R&D pipeline. At the start of the biotech industry, progress was slow. Between 1983 and 1995, the U.S. FDA approved an average of two biologics each year. Now, biologics have taken the lead by the smallest of margins, accounting for 50.1% of drugs in development at the start of 2026, according to the <em>Pharma Annual Review 2026</em>, published by Pharmaprojects, a firm that tracks global pharma R&D.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/730343</guid>
      <pubDate>Fri, 10 Apr 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/730343-biologics-in-development-outnumber-small-molecules-for-the-first-time</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Research-and-science/Drug-research-illustration1.webp?t=1600982220" type="image/png" medium="image" fileSize="443224">
        <media:title type="plain">Drug research illustration</media:title>
      </media:content>
    </item>
    <item>
      <title>Biologics in development outnumber small molecules for the first time</title>
      <description>More than four decades on from the approval of the first biologic drug, the industry has reached a tipping point, and biotech drugs now outnumber small molecules in the global R&amp;D pipeline.</description>
      <content:encoded>
        <![CDATA[More than four decades on from the approval of the first biologic drug, the industry has reached a tipping point, and biotech drugs now outnumber small molecules in the global R&D pipeline.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/730211</guid>
      <pubDate>Thu, 09 Apr 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/730211-biologics-in-development-outnumber-small-molecules-for-the-first-time</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Research-and-science/Drug-research-illustration1.webp?t=1600982220" type="image/png" medium="image" fileSize="443224">
        <media:title type="plain">Drug research illustration</media:title>
      </media:content>
    </item>
    <item>
      <title>Ambrosia slurps up a $100M series B for its oral obesity drug pipeline</title>
      <description>Ambrosia Biosciences Inc., named after the drink of the Greek gods, secured a $100 million series B to advance its preclinical pipeline of oral obesity drugs. The startup formed after Pfizer Inc. shuttered its Boulder, Colo.-based research facility that the pharma gained through its 2019 acquisition of Array Biopharma Inc.</description>
      <content:encoded>
        <![CDATA[Ambrosia Biosciences Inc., named after the drink of the Greek gods, secured a $100 million series B to advance its preclinical pipeline of oral obesity drugs. The startup formed after Pfizer Inc. shuttered its Boulder, Colo.-based research facility that the pharma gained through its 2019 acquisition of Array Biopharma Inc.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/730076</guid>
      <pubDate>Thu, 02 Apr 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/730076-ambrosia-slurps-up-a-100m-series-b-for-its-oral-obesity-drug-pipeline</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Obesity/Pills-bottle-scale-and-measuring-tape.webp?t=1704492123" type="image/jpeg" medium="image" fileSize="266968">
        <media:title type="plain">Pills, bottle, scale and-measuring tape</media:title>
      </media:content>
    </item>
    <item>
      <title>Lilly’s Foundayo enters oral GLP-1 obesity market with speedy FDA nod</title>
      <description>Eli Lilly and Co. anticipates shipping newly approved Foundayo (orforglipron) within the next week, as the drug becomes the second oral weight-loss glucagon-like peptide-1 (GLP-1) receptor agonist to enter the U.S. market following December’s approval of Novo Nordisk A/S’ Wegovy (semaglutide) pill.</description>
      <content:encoded>
        <![CDATA[Eli Lilly and Co. anticipates shipping newly approved Foundayo (orforglipron) within the next week, as the drug becomes the second oral weight-loss glucagon-like peptide-1 (GLP-1) receptor agonist to enter the U.S. market following December’s approval of Novo Nordisk A/S’ Wegovy (semaglutide) pill.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/729976</guid>
      <pubDate>Wed, 01 Apr 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/729976-lillys-foundayo-enters-oral-glp-1-obesity-market-with-speedy-fda-nod</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Misc/Eli-Lilly-signage.webp?t=1767910760" type="image/jpeg" medium="image" fileSize="673005">
        <media:title type="plain">Eli Lilly logo atop Lilly Biotechnology Center campus in San Diego, Calif.</media:title>
        <media:description type="plain">Credit: MichaelVi - stock.adobe.com</media:description>
      </media:content>
    </item>
    <item>
      <title>China-developed triple incretin enters global diabetes race</title>
      <description>A next-generation triple incretin therapy jointly developed by Novo Nordisk A/S and China’s United Biotechnology outperformed semaglutide in a phase II trial, signaling intensifying competition in the GLP-1 obesity and diabetes market.</description>
      <content:encoded>
        <![CDATA[A next-generation triple incretin therapy jointly developed by Novo Nordisk A/S and China’s United Biotechnology outperformed semaglutide in a phase II trial, signaling intensifying competition in the GLP-1 obesity and diabetes market.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/730088</guid>
      <pubDate>Tue, 31 Mar 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/730088-china-developed-triple-incretin-enters-global-diabetes-race</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/Endocrine-Metabolic-glucose-bloodstream.webp?t=1674056639" type="image/png" medium="image" fileSize="1313266">
        <media:title type="plain">Illustration of glucose molecules in a bloodstream</media:title>
      </media:content>
    </item>
    <item>
      <title>US FDA pondering next steps for CNPV</title>
      <description>Introduced last year as a pilot program, the U.S. FDA Commissioner’s National Priority Voucher (CNPV) could be here to stay – at least for the duration of Marty Makary’s tenure as FDA commissioner. Since the FDA unveiled the CNPV last June, it has welcomed 18 products from 16 companies into the “game-changer” program for patients, as Makary described it. The goal is to provide an “ultrafast review pathway,” one to two months instead of the standard 10 to 12 months, for drugs and biologics of strategic national importance while maintaining the FDA’s scientific and regulatory standards, according to the agency.</description>
      <content:encoded>
        <![CDATA[Introduced last year as a pilot program, the U.S. FDA Commissioner’s National Priority Voucher (CNPV) could be here to stay – at least for the duration of Marty Makary’s tenure as FDA commissioner. Since the FDA unveiled the CNPV last June, it has welcomed 18 products from 16 companies into the “game-changer” program for patients, as Makary described it. The goal is to provide an “ultrafast review pathway,” one to two months instead of the standard 10 to 12 months, for drugs and biologics of strategic national importance while maintaining the FDA’s scientific and regulatory standards, according to the agency.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/729950</guid>
      <pubDate>Mon, 30 Mar 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/729950-us-fda-pondering-next-steps-for-cnpv</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Misc/Paper-airplanes.webp?t=1774904935" type="image/jpeg" medium="image" fileSize="152900">
        <media:title type="plain">Paper airplanes with red leading</media:title>
      </media:content>
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