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    <title>Asia-Pacific</title>
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    <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>Rx tariff just around the corner </title>
      <description>In a little more than a month, 17 big biopharma companies will be subject to U.S. President Donald Trump’s long-promised section 232 global biopharma sector tariff. But instead of paying the 100% duty on imported patented drugs and their key ingredients, most of those companies, if not all, will pay much reduced rates or no tariff at all, based on where the imports are coming from, what type of drug is being imported, and whether the companies have signed onshoring and most-favored-nation pricing agreements with the administration.</description>
      <content:encoded>
        <![CDATA[In a little more than a month, 17 big biopharma companies will be subject to U.S. President Donald Trump’s long-promised section 232 global biopharma sector tariff. But instead of paying the 100% duty on imported patented drugs and their key ingredients, most of those companies, if not all, will pay much reduced rates or no tariff at all, based on where the imports are coming from, what type of drug is being imported, and whether the companies have signed onshoring and most-favored-nation pricing agreements with the administration.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731904</guid>
      <pubDate>Wed, 17 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731904-rx-tariff-just-around-the-corner</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Money/Prescription-bottle-with-dollar-sign-shadow.webp?t=1758913403" type="image/jpeg" medium="image" fileSize="81696">
        <media:title type="plain">Prescription bottle with dollar sign shadow</media:title>
      </media:content>
    </item>
    <item>
      <title>Laekna licenses LAE-118 ex-China to Vasque in $527M deal </title>
      <description>Laekna Inc. is handing ex-China rights to internally discovered PI3Kα pan-mutant selective inhibitor LAE-118 to U.S.-based Vasque Bio Inc. in a deal worth up to $527 million, marking another asset-monetization move by the Shanghai company as it looks to fund and accelerate development across its oncology and metabolic disease pipeline.</description>
      <content:encoded>
        <![CDATA[Laekna Inc. is handing ex-China rights to internally discovered PI3Kα pan-mutant selective inhibitor LAE-118 to U.S.-based Vasque Bio Inc. in a deal worth up to $527 million, marking another asset-monetization move by the Shanghai company as it looks to fund and accelerate development across its oncology and metabolic disease pipeline.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731987</guid>
      <pubDate>Tue, 16 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731987-laekna-licenses-lae-118-ex-china-to-vasque-in-527m-deal</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Deals-and-MAs/Deal-handshake-graphic-overlay.webp?t=1588276536" type="image/png" medium="image" fileSize="406049">
        <media:title type="plain">Deal handshake with graphic overlay</media:title>
      </media:content>
    </item>
    <item>
      <title>Oricell brings first pivotal-stage CAR T in liver cancer </title>
      <description>Oricell Therapeutics Holdings Ltd.’s glypican-3 (GPC3)-targeted autologous CAR T therapy, Ori-C101, is heading into a confirmatory registration phase II trial in patients with GPC3-positive advanced hepatocellular carcinoma, positioning it as the first GPC3-directed immune cell therapy – and the first CAR T therapy for liver cancer – to reach that stage of development.</description>
      <content:encoded>
        <![CDATA[Oricell Therapeutics Holdings Ltd.’s glypican-3 (GPC3)-targeted autologous CAR T therapy, Ori-C101, is heading into a confirmatory registration phase II trial in patients with GPC3-positive advanced hepatocellular carcinoma, positioning it as the first GPC3-directed immune cell therapy – and the first CAR T therapy for liver cancer – to reach that stage of development.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731986</guid>
      <pubDate>Tue, 16 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731986-oricell-brings-first-pivotal-stage-car-t-in-liver-cancer</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Gastrointestinal/Liver-anatomy.webp?t=1781289684" type="image/jpeg" medium="image" fileSize="171891">
        <media:title type="plain">Liver anatomy</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>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>Three deals in six days: Everest builds late-stage APAC portfolio </title>
      <description>Fresh off a deal with Travere Therapeutics Inc. for civorebrutinib worth more than $1.14 billion, Everest Medicines Ltd. went on a shopping spree, striking three deals in six days to expand its pipeline and geographic reach across Asia Pacific.</description>
      <content:encoded>
        <![CDATA[Fresh off a deal with Travere Therapeutics Inc. for civorebrutinib worth more than $1.14 billion, Everest Medicines Ltd. went on a shopping spree, striking three deals in six days to expand its pipeline and geographic reach across Asia Pacific.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731982</guid>
      <pubDate>Tue, 16 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731982-three-deals-in-six-days-everest-builds-late-stage-apac-portfolio</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Deals-and-MAs/Hands-and-gears.webp?t=1590606316" type="image/png" medium="image" fileSize="377385">
        <media:title type="plain">Hands holding gears</media:title>
      </media:content>
    </item>
    <item>
      <title>Takeda’s zasocitinib bests Sotyktu in phase III psoriasis trial</title>
      <description>Takeda Pharmaceutical Co. Ltd.’s oral TYK2 inhibitor zasocitinib (TAK-279) demonstrated statistical superiority over Bristol Myers Squibb Co.’s first-in-class Sotyktu (deucravacitinib) in a top-line phase III Latitude Atlas readout of moderate to severe plaque psoriasis.</description>
      <content:encoded>
        <![CDATA[Takeda Pharmaceutical Co. Ltd.’s oral TYK2 inhibitor zasocitinib (TAK-279) demonstrated statistical superiority over Bristol Myers Squibb Co.’s first-in-class Sotyktu (deucravacitinib) in a top-line phase III Latitude Atlas readout of moderate to severe plaque psoriasis.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731981</guid>
      <pubDate>Tue, 16 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731981-takedas-zasocitinib-bests-sotyktu-in-phase-iii-psoriasis-trial</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Dermatologic/Dermatology-exam.webp?t=1781289685" type="image/jpeg" medium="image" fileSize="153337">
        <media:title type="plain">Dermatology exam</media:title>
      </media:content>
    </item>
    <item>
      <title>Longbio’s LP-003 meets phase III allergy endpoints</title>
      <description>After raising HK$1.255 billion (US$160 million) in its IPO on the Hong Kong Stock Exchange earlier this month, Longbio Pharma Co. Ltd.’s lead candidate, LP-003, met the primary endpoint of total nasal symptom scores during peak pollen season in moderate to severe seasonal allergic rhinitis.</description>
      <content:encoded>
        <![CDATA[After raising HK$1.255 billion (US$160 million) in its IPO on the Hong Kong Stock Exchange earlier this month, Longbio Pharma Co. Ltd.’s lead candidate, LP-003, met the primary endpoint of total nasal symptom scores during peak pollen season in moderate to severe seasonal allergic rhinitis.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731980</guid>
      <pubDate>Tue, 16 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731980-longbios-lp-003-meets-phase-iii-allergy-endpoints</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Respiratory/Pollen-seasonal-allergy-illustration.webp?t=1781555706" type="image/jpeg" medium="image" fileSize="124611">
        <media:title type="plain">Woman holding tissue to nose with plants, pollen</media:title>
      </media:content>
    </item>
    <item>
      <title>China clears Alphamab’s HER2 bispecific antibody in gastric cancer</title>
      <description>China’s National Medical Products Administration has approved Suzhou Alphamab Co. Ltd.’s HER2 bispecific antibody, anbenitamab (KN-026), through priority review for adults with locally advanced or metastatic HER2-positive gastric or gastroesophageal junction adenocarcinoma who have received at least one trastuzumab-containing regimen.</description>
      <content:encoded>
        <![CDATA[China’s National Medical Products Administration has approved Suzhou Alphamab Co. Ltd.’s HER2 bispecific antibody, anbenitamab (KN-026), through priority review for adults with locally advanced or metastatic HER2-positive gastric or gastroesophageal junction adenocarcinoma who have received at least one trastuzumab-containing regimen.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731979</guid>
      <pubDate>Tue, 16 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731979-china-clears-alphamabs-her2-bispecific-antibody-in-gastric-cancer</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Gastrointestinal/Stomach-cross-section.webp?t=1762813318" type="image/jpeg" medium="image" fileSize="384614">
        <media:title type="plain">Stomach cross-section on scientific background</media:title>
      </media:content>
    </item>
    <item>
      <title>Dimerix out-licenses DMX-200 to Everest in AU$481M deal</title>
      <description>Dimerix Ltd. has signed an exclusive licensing deal with Everest Medicines Ltd. to commercialize its phase III kidney disease candidate DMX-200 in a transaction worth up to AU$481 million (US$340 million), plus sales royalties.</description>
      <content:encoded>
        <![CDATA[Dimerix Ltd. has signed an exclusive licensing deal with Everest Medicines Ltd. to commercialize its phase III kidney disease candidate DMX-200 in a transaction worth up to AU$481 million (US$340 million), plus sales royalties.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731893</guid>
      <pubDate>Tue, 16 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731893-dimerix-out-licenses-dmx-200-to-everest-in-au481m-deal</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Nephrology/Kidneys.webp?t=1585681893" type="image/png" medium="image" fileSize="393213">
        <media:title type="plain">Kidneys</media:title>
      </media:content>
    </item>
    <item>
      <title>Longbio’s LP-003 meets phase III allergy endpoints</title>
      <description>After raising HK$1.255 billion (US$160 million) in its IPO on the Hong Kong Stock Exchange earlier this month, Longbio Pharma Co. Ltd.’s lead candidate, LP-003, met the primary endpoint of total nasal symptom scores during peak pollen season in moderate to severe seasonal allergic rhinitis.</description>
      <content:encoded>
        <![CDATA[After raising HK$1.255 billion (US$160 million) in its IPO on the Hong Kong Stock Exchange earlier this month, Longbio Pharma Co. Ltd.’s lead candidate, LP-003, met the primary endpoint of total nasal symptom scores during peak pollen season in moderate to severe seasonal allergic rhinitis.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731878</guid>
      <pubDate>Mon, 15 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731878-longbios-lp-003-meets-phase-iii-allergy-endpoints</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Respiratory/Pollen-seasonal-allergy-illustration.webp?t=1781555706" type="image/jpeg" medium="image" fileSize="124611">
        <media:title type="plain">Woman holding tissue to nose with plants, pollen</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/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>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>Oricell brings first pivotal-stage CAR T in liver cancer </title>
      <description>Oricell Therapeutics Holdings Ltd.’s glypican-3 (GPC3)-targeted autologous CAR T therapy, Ori-C101, is heading into a confirmatory registration phase II trial in patients with GPC3-positive advanced hepatocellular carcinoma, positioning it as the first GPC3-directed immune cell therapy – and the first CAR T therapy for liver cancer – to reach that stage of development.</description>
      <content:encoded>
        <![CDATA[Oricell Therapeutics Holdings Ltd.’s glypican-3 (GPC3)-targeted autologous CAR T therapy, Ori-C101, is heading into a confirmatory registration phase II trial in patients with GPC3-positive advanced hepatocellular carcinoma, positioning it as the first GPC3-directed immune cell therapy – and the first CAR T therapy for liver cancer – to reach that stage of development.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731817</guid>
      <pubDate>Fri, 12 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731817-oricell-brings-first-pivotal-stage-car-t-in-liver-cancer</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Gastrointestinal/Liver-anatomy.webp?t=1781289684" type="image/jpeg" medium="image" fileSize="171891">
        <media:title type="plain">Liver anatomy</media:title>
      </media:content>
    </item>
    <item>
      <title>Takeda’s zasocitinib bests Sotyktu in phase III psoriasis trial</title>
      <description>Takeda Pharmaceutical Co. Ltd.’s oral TYK2 inhibitor zasocitinib (TAK-279) demonstrated statistical superiority over Bristol Myers Squibb Co.’s first-in-class Sotyktu (deucravacitinib) in a top-line phase III Latitude Atlas readout of moderate to severe plaque psoriasis.</description>
      <content:encoded>
        <![CDATA[Takeda Pharmaceutical Co. Ltd.’s oral TYK2 inhibitor zasocitinib (TAK-279) demonstrated statistical superiority over Bristol Myers Squibb Co.’s first-in-class Sotyktu (deucravacitinib) in a top-line phase III Latitude Atlas readout of moderate to severe plaque psoriasis.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731816</guid>
      <pubDate>Fri, 12 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731816-takedas-zasocitinib-bests-sotyktu-in-phase-iii-psoriasis-trial</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Dermatologic/Dermatology-exam.webp?t=1781289685" type="image/jpeg" medium="image" fileSize="153337">
        <media:title type="plain">Dermatology exam</media:title>
      </media:content>
    </item>
    <item>
      <title>Laekna licenses LAE-118 ex-China to Vasque in $527M deal </title>
      <description>Laekna Inc. is handing ex-China rights to internally discovered PI3Kα pan-mutant selective inhibitor LAE-118 to U.S.-based Vasque Bio Inc. in a deal worth up to $527 million, marking another asset-monetization move by the Shanghai company as it looks to fund and accelerate development across its oncology and metabolic disease pipeline.</description>
      <content:encoded>
        <![CDATA[Laekna Inc. is handing ex-China rights to internally discovered PI3Kα pan-mutant selective inhibitor LAE-118 to U.S.-based Vasque Bio Inc. in a deal worth up to $527 million, marking another asset-monetization move by the Shanghai company as it looks to fund and accelerate development across its oncology and metabolic disease pipeline.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731802</guid>
      <pubDate>Thu, 11 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731802-laekna-licenses-lae-118-ex-china-to-vasque-in-527m-deal</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Deals-and-MAs/Deal-handshake-graphic-overlay.webp?t=1588276536" type="image/png" medium="image" fileSize="406049">
        <media:title type="plain">Deal handshake with graphic overlay</media:title>
      </media:content>
    </item>
    <item>
      <title>China clears Alphamab’s HER2 bispecific antibody in gastric cancer</title>
      <description>China’s National Medical Products Administration has approved Suzhou Alphamab Co. Ltd.’s HER2 bispecific antibody, anbenitamab (KN-026), through priority review for adults with locally advanced or metastatic HER2-positive gastric or gastroesophageal junction adenocarcinoma who have received at least one trastuzumab-containing regimen.</description>
      <content:encoded>
        <![CDATA[China’s National Medical Products Administration has approved Suzhou Alphamab Co. Ltd.’s HER2 bispecific antibody, anbenitamab (KN-026), through priority review for adults with locally advanced or metastatic HER2-positive gastric or gastroesophageal junction adenocarcinoma who have received at least one trastuzumab-containing regimen.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731801</guid>
      <pubDate>Thu, 11 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731801-china-clears-alphamabs-her2-bispecific-antibody-in-gastric-cancer</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Gastrointestinal/Stomach-cross-section.webp?t=1762813318" type="image/jpeg" medium="image" fileSize="384614">
        <media:title type="plain">Stomach cross-section on scientific background</media:title>
      </media:content>
    </item>
    <item>
      <title>Three deals in six days: Everest builds late-stage APAC portfolio </title>
      <description>Fresh off a deal with Travere Therapeutics Inc. for civorebrutinib worth more than $1.14 billion, Everest Medicines Ltd. went on a shopping spree, striking three deals in six days to expand its pipeline and geographic reach across Asia Pacific.</description>
      <content:encoded>
        <![CDATA[Fresh off a deal with Travere Therapeutics Inc. for civorebrutinib worth more than $1.14 billion, Everest Medicines Ltd. went on a shopping spree, striking three deals in six days to expand its pipeline and geographic reach across Asia Pacific.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731721</guid>
      <pubDate>Wed, 10 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731721-three-deals-in-six-days-everest-builds-late-stage-apac-portfolio</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Deals-and-MAs/Hands-and-gears.webp?t=1590606316" type="image/png" medium="image" fileSize="377385">
        <media:title type="plain">Hands holding gears</media:title>
      </media:content>
    </item>
    <item>
      <title>Hemab soars 89% on debut as biopharma IPOs stay strong in May</title>
      <description>Total biopharma financing through the first five months of 2026 reached $49.46 billion, the third-highest total for the period in the dataset and more than doubling of 2025’s $21.4 billion over the same stretch.</description>
      <content:encoded>
        <![CDATA[Total biopharma financing through the first five months of 2026 reached $49.46 billion, the third-highest total for the period in the dataset and more than doubling of 2025’s $21.4 billion over the same stretch. ]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731832</guid>
      <pubDate>Tue, 09 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731832-hemab-soars-89-on-debut-as-biopharma-ipos-stay-strong-in-may</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Money/Gray-and-green-glass-dollar-symbols-with-arrow-pointing-up.webp?t=1731016850" type="image/jpeg" medium="image" fileSize="116588">
        <media:title type="plain">Gray and green glass dollar symbols with arrow pointing up</media:title>
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      <title>UK Biobank seeks to recall downloads after health data breach</title>
      <description>After a major breach of trust when its data were advertised for sale in China, the UK Biobank will now attempt to recall data previously downloaded by legitimate researchers and seek assurances information has been deleted from local servers.</description>
      <content:encoded>
        <![CDATA[After a major breach of trust when its data were advertised for sale in China, the UK Biobank will now attempt to recall data previously downloaded by legitimate researchers and seek assurances information has been deleted from local servers.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731831</guid>
      <pubDate>Tue, 09 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731831-uk-biobank-seeks-to-recall-downloads-after-health-data-breach</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Misc/Data-breach.webp?t=1780687893" type="image/jpeg" medium="image" fileSize="372921">
        <media:title type="plain">Data breach - red broken padlock</media:title>
      </media:content>
    </item>
    <item>
      <title>Innovent submits NDA for CLDN18.2 ADC for gastric cancer</title>
      <description>Innovent Biologics Co. Ltd.’s Claudin18.2-targeted antibody-drug conjugate (ADC), arcotatug tavatecan (IBI-343, TAK-921), met the primary endpoint in the international multicenter phase III G-Hope-001 trial in advanced gastric cancer, according to interim results.</description>
      <content:encoded>
        <![CDATA[Innovent Biologics Co. Ltd.’s Claudin18.2-targeted antibody-drug conjugate (ADC), arcotatug tavatecan (IBI-343, TAK-921), met the primary endpoint in the international multicenter phase III G-Hope-001 trial in advanced gastric cancer, according to interim results.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731830</guid>
      <pubDate>Tue, 09 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731830-innovent-submits-nda-for-cldn182-adc-for-gastric-cancer</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Cancer/Gastric-cancer-illustration.webp?t=1610744617" type="image/png" medium="image" fileSize="551352">
        <media:title type="plain">Gastric cancer</media:title>
      </media:content>
    </item>
    <item>
      <title>ASCO 2026: Chinese biopharma arrives at ASCO with pivotal wins </title>
      <description>If the 2026 American Society of Clinical Oncology (ASCO) annual meeting in Chicago from May 30 to June 3 demonstrated anything about the evolution of China’s biotechnology sector, it was that the industry’s center of gravity is shifting. While Chinese companies once relied heavily on PD-1 antibodies and licensing deals to gain international visibility, this year’s oral presentations showcased a broader innovation base.</description>
      <content:encoded>
        <![CDATA[If the 2026 American Society of Clinical Oncology (ASCO) annual meeting in Chicago from May 30 to June 3 demonstrated anything about the evolution of China’s biotechnology sector, it was that the industry’s center of gravity is shifting. While Chinese companies once relied heavily on PD-1 antibodies and licensing deals to gain international visibility, this year’s oral presentations showcased a broader innovation base.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731829</guid>
      <pubDate>Tue, 09 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731829-asco-2026-chinese-biopharma-arrives-at-asco-with-pivotal-wins</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Geographic-regions/Asia/China-compass.webp?t=1770672078" type="image/jpeg" medium="image" fileSize="512881">
        <media:title type="plain">China compass </media:title>
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    <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>
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    <item>
      <title>Competitive approach better than restricting deals with China?</title>
      <description>The recent introduction of the bipartisan Biotech Investment National Security Act in the U.S. House has industry and venture capitalists urging lawmakers to take a breath, step back, and consider a less invasive approach than restricting U.S. biopharma deals with Chinese innovators.</description>
      <content:encoded>
        <![CDATA[The recent introduction of the bipartisan Biotech Investment National Security Act in the U.S. House has industry and venture capitalists urging lawmakers to take a breath, step back, and consider a less invasive approach than restricting U.S. biopharma deals with Chinese innovators.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731827</guid>
      <pubDate>Tue, 09 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731827-competitive-approach-better-than-restricting-deals-with-china</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Geographic-regions/Asia/china-us-deal.webp?t=1591119558" type="image/png" medium="image" fileSize="1457539">
        <media:title type="plain">China U.S. handshake</media:title>
      </media:content>
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      <title>NMPA gives conditional nods to drugs by Lupeng, Vcare, Staidson</title>
      <description>China’s National Medical Products Administration (NMPA) on June 4 granted conditional approvals to two oncology drugs from Lupeng Pharmaceutical Co. Ltd. and Vcare Pharmatech Co. Ltd., as well as one hemophilia drug developed by Staidson Biopharmaceutical Co. Ltd.</description>
      <content:encoded>
        <![CDATA[China’s National Medical Products Administration (NMPA) on June 4 granted conditional approvals to two oncology drugs from Lupeng Pharmaceutical Co. Ltd. and Vcare Pharmatech Co. Ltd., as well as one hemophilia drug developed by Staidson Biopharmaceutical Co. Ltd.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731712</guid>
      <pubDate>Tue, 09 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731712-nmpa-gives-conditional-nods-to-drugs-by-lupeng-vcare-staidson</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Regulatory/Wood-approved-stamp-red.webp?t=1670969940" type="image/png" medium="image" fileSize="323015">
        <media:title type="plain">Red wooden approved stamp</media:title>
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    <item>
      <title>Japan backs Oncolys virus therapy for esophageal cancer</title>
      <description>Japan has granted marketing approval to Oncolys Biopharma Inc.’s oncolytic adenovirus product, Telomelysin (suratadenoturev, OBP-301), for treating esophageal cancer in patients who are not eligible for curative resection or chemoradiotherapy. The approval marks the first oncolytic adenovirus product approved for esophageal cancer.</description>
      <content:encoded>
        <![CDATA[Japan has granted marketing approval to Oncolys Biopharma Inc.’s oncolytic adenovirus product, Telomelysin (suratadenoturev, OBP-301), for treating esophageal cancer in patients who are not eligible for curative resection or chemoradiotherapy. The approval marks the first oncolytic adenovirus product approved for esophageal cancer.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731711</guid>
      <pubDate>Tue, 09 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731711-japan-backs-oncolys-virus-therapy-for-esophageal-cancer</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Cancer/esophageal-cancer-illustration.webp?t=1741727451" type="image/jpeg" medium="image" fileSize="514154">
        <media:title type="plain">Illustration of cancer on the esophagus</media:title>
      </media:content>
    </item>
    <item>
      <title>Wuxi Apptec insists it’s ‘not a Chinese military company’ </title>
      <description>Wuxi Apptec isn’t going down without a fight after the U.S. Department of Defense added it to the Section 1260H list June 8 as a designated “Chinese military company,” which makes it a “biotechnology company of concern” under the Biosecure Act. “Such designation is mistaken and baseless,” the global contract research, development and manufacturing organization said in an open letter to its life sciences partners. “We will pursue every available avenue to correct this mistake.” That includes appealing the designation.</description>
      <content:encoded>
        <![CDATA[Wuxi Apptec isn’t going down without a fight after the U.S. Department of Defense added it to the Section 1260H list June 8 as a designated “Chinese military company,” which makes it a “biotechnology company of concern” under the Biosecure Act. “Such designation is mistaken and baseless,” the global contract research, development and manufacturing organization said in an open letter to its life sciences partners. “We will pursue every available avenue to correct this mistake.” That includes appealing the designation.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731710</guid>
      <pubDate>Tue, 09 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731710-wuxi-apptec-insists-its-not-a-chinese-military-company</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Misc/Wuxi-Apptec-signage.webp?t=1781036355" type="image/jpeg" medium="image" fileSize="104349">
        <media:title type="plain">Wuxi Apptec signage </media:title>
        <media:description type="plain">Credit: Wuxi Apptec</media:description>
      </media:content>
    </item>
    <item>
      <title>Competitive approach better than restricting deals with China?</title>
      <description>The recent introduction of the bipartisan Biotech Investment National Security Act in the U.S. House has industry and venture capitalists urging lawmakers to take a breath, step back, and consider a less invasive approach than restricting U.S. biopharma deals with Chinese innovators.</description>
      <content:encoded>
        <![CDATA[The recent introduction of the bipartisan Biotech Investment National Security Act in the U.S. House has industry and venture capitalists urging lawmakers to take a breath, step back, and consider a less invasive approach than restricting U.S. biopharma deals with Chinese innovators.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731692</guid>
      <pubDate>Mon, 08 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731692-competitive-approach-better-than-restricting-deals-with-china</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Geographic-regions/Asia/china-us-deal.webp?t=1591119558" type="image/png" medium="image" fileSize="1457539">
        <media:title type="plain">China U.S. handshake</media:title>
      </media:content>
    </item>
    <item>
      <title>ASCO 2026: Chinese biopharma arrives at ASCO with pivotal wins </title>
      <description>If the 2026 American Society of Clinical Oncology (ASCO) annual meeting in Chicago from May 30 to June 3 demonstrated anything about the evolution of China’s biotechnology sector, it was that the industry’s center of gravity is shifting. While Chinese companies once relied heavily on PD-1 antibodies and licensing deals to gain international visibility, this year’s oral presentations showcased a broader innovation base.</description>
      <content:encoded>
        <![CDATA[If the 2026 American Society of Clinical Oncology (ASCO) annual meeting in Chicago from May 30 to June 3 demonstrated anything about the evolution of China’s biotechnology sector, it was that the industry’s center of gravity is shifting. While Chinese companies once relied heavily on PD-1 antibodies and licensing deals to gain international visibility, this year’s oral presentations showcased a broader innovation base.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731634</guid>
      <pubDate>Fri, 05 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731634-asco-2026-chinese-biopharma-arrives-at-asco-with-pivotal-wins</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Geographic-regions/Asia/China-compass.webp?t=1770672078" type="image/jpeg" medium="image" fileSize="512881">
        <media:title type="plain">China compass </media:title>
      </media:content>
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