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    <title>Cancer</title>
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    <item>
      <title>Lilly taps Abbisko for $1.9B discovery deal </title>
      <description>Abbisko Therapeutics Co. Ltd. has entered a research collaboration and license agreement with Eli Lilly and Co. to discover and develop innovative medicines across multiple targets, with the aim of advancing novel drug candidates with global potential.</description>
      <content:encoded>
        <![CDATA[Abbisko Therapeutics Co. Ltd. has entered a research collaboration and license agreement with Eli Lilly and Co. to discover and develop innovative medicines across multiple targets, with the aim of advancing novel drug candidates with global potential.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732203</guid>
      <pubDate>Thu, 25 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732203-lilly-taps-abbisko-for-19b-discovery-deal</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Research-and-science/Microscope.webp?t=1588872688" type="image/png" medium="image" fileSize="408468">
        <media:title type="plain">Microscope</media:title>
      </media:content>
    </item>
    <item>
      <title>University of Melbourne patent divulges new radionuclide-drug conjugates</title>
      <description>The University of Melbourne has reported new radionuclide-drug conjugates (RDCs) comprising copper ion chelated to sarcophagine covalently bound to a peptide-targeting glutamate carboxypeptidase 2 (FOLH1; NAALAD1; PSMA) and another peptide targeting gastrin-releasing peptide receptor (GRPR).</description>
      <content:encoded>
        <![CDATA[The University of Melbourne has reported new radionuclide-drug conjugates (RDCs) comprising copper ion chelated to sarcophagine covalently bound to a peptide-targeting glutamate carboxypeptidase 2 (FOLH1; NAALAD1; PSMA) and another peptide targeting gastrin-releasing peptide receptor (GRPR).]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732141</guid>
      <pubDate>Thu, 25 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732141-university-of-melbourne-patent-divulges-new-radionuclide-drug-conjugates</link>
    </item>
    <item>
      <title>University North Carolina patents new SLC7A5 inhibitors</title>
      <description>The University of North Carolina at Chapel Hill has disclosed new large neutral amino acids transporter small subunit 1 (SLC7A5; LAT1) inhibitors reported to be useful for the diagnosis and treatment of cancer.</description>
      <content:encoded>
        <![CDATA[The University of North Carolina at Chapel Hill has disclosed new large neutral amino acids transporter small subunit 1 (SLC7A5; LAT1) inhibitors reported to be useful for the diagnosis and treatment of cancer.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732139</guid>
      <pubDate>Thu, 25 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732139-university-north-carolina-patents-new-slc7a5-inhibitors</link>
    </item>
    <item>
      <title>Combotope and Boehringer Ingelheim partner in cancer</title>
      <description>Combotope Therapeutics ApS has established a strategic research collaboration with Boehringer Ingelheim Pharma GmbH &amp; Co. KG that will leverage Combotope’s proprietary SMART-Phage platform to generate highly tumor-selective antibodies for next-generation cancer therapies.</description>
      <content:encoded>
        <![CDATA[Combotope Therapeutics ApS has established a strategic research collaboration with Boehringer Ingelheim Pharma GmbH & Co. KG that will leverage Combotope’s proprietary SMART-Phage platform to generate highly tumor-selective antibodies for next-generation cancer therapies.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732136</guid>
      <pubDate>Thu, 25 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732136-combotope-and-boehringer-ingelheim-partner-in-cancer</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Immune/antibodies-lab-research.webp?t=1717686528" type="image/jpeg" medium="image" fileSize="266442">
        <media:title type="plain">Lab glassware and antibodies art concept</media:title>
      </media:content>
    </item>
    <item>
      <title>GT-02897 exerts efficacy in preclinical multiple myeloma</title>
      <description>Investigators from the Karl Landsteiner University aimed to evaluate the therapeutic potential of a novel CDK9 inhibitor/degrader, GT-02897, for the potential treatment of multiple myeloma.</description>
      <content:encoded>
        <![CDATA[Investigators from the Karl Landsteiner University aimed to evaluate the therapeutic potential of a novel CDK9 inhibitor/degrader, GT-02897, for the potential treatment of multiple myeloma.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732134</guid>
      <pubDate>Thu, 25 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732134-gt-02897-exerts-efficacy-in-preclinical-multiple-myeloma</link>
    </item>
    <item>
      <title>Extracellular vesicle-based photoimmunotherapy for MDK+ solid tumors</title>
      <description>Midkine (MDK) is a multifunctional heparin-binding cytokine highly overexpressed and extracellularly enriched in the tumor microenvironment (TME) of several cancers.</description>
      <content:encoded>
        <![CDATA[Midkine (MDK) is a multifunctional heparin-binding cytokine highly overexpressed and extracellularly enriched in the tumor microenvironment (TME) of several cancers.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732133</guid>
      <pubDate>Thu, 25 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732133-extracellular-vesicle-based-photoimmunotherapy-for-mdk-solid-tumors</link>
    </item>
    <item>
      <title>BMS’s dual CAR T-cell therapy shows efficacy in multiple myeloma</title>
      <description>Researchers from Bristol Myers Squibb Co. (BMS) presented preclinical data on BMS-986453 (tunlucabtagene autoleucel), a dual-targeting BCMA×GPRC5D CAR T-cell therapy, in models of multiple myeloma.</description>
      <content:encoded>
        <![CDATA[Researchers from Bristol Myers Squibb Co. (BMS) presented preclinical data on BMS-986453 (tunlucabtagene autoleucel), a dual-targeting BCMA×GPRC5D CAR T-cell therapy, in models of multiple myeloma.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732132</guid>
      <pubDate>Thu, 25 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732132-bmss-dual-car-t-cell-therapy-shows-efficacy-in-multiple-myeloma</link>
    </item>
    <item>
      <title>Nuvectis shares continue to rally after $1.46B Haisco deal</title>
      <description>Nuvectis Pharma Inc.’s shares climbed further after the oncology-focused biotech nabbed select rights to a late-stage complement factor B inhibitor (HSK-39297/NXP-100) and a phase I BRAF inhibitor (HSK-42360/NXP-200) from Haisco Pharmaceutical Group Co. Ltd. for $40 million up front.</description>
      <content:encoded>
        <![CDATA[Nuvectis Pharma Inc.’s shares climbed further after the oncology-focused biotech nabbed select rights to a late-stage complement factor B inhibitor (HSK-39297/NXP-100) and a phase I BRAF inhibitor (HSK-42360/NXP-200) from Haisco Pharmaceutical Group Co. Ltd. for $40 million up front.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732081</guid>
      <pubDate>Wed, 24 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732081-nuvectis-shares-continue-to-rally-after-146b-haisco-deal</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Money/Dollar-symbol-with-arrow-graph-moving-up.webp?t=1701900511" type="image/jpeg" medium="image" fileSize="197116">
        <media:title type="plain">Dollar symbol with arrow graph</media:title>
      </media:content>
    </item>
    <item>
      <title>Antares, Novartis pursuing undruggable cancer targets in $1.9B deal</title>
      <description>Antares Therapeutics Inc. drew Novartis AG to the table for a potential $1.9 billion collaboration, including a $105 million up-front payment, to discover small-molecule programs against oncology targets considered to be undruggable. It’s Antares’ first partnership since spinning out of Scorpion Therapeutics Inc. about a year ago.</description>
      <content:encoded>
        <![CDATA[Antares Therapeutics Inc. drew Novartis AG to the table for a potential $1.9 billion collaboration, including a $105 million up-front payment, to discover small-molecule programs against oncology targets considered to be undruggable. It’s Antares’ first partnership since spinning out of Scorpion Therapeutics Inc. about a year ago.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732077</guid>
      <pubDate>Wed, 24 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732077-antares-novartis-pursuing-undruggable-cancer-targets-in-19b-deal</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/Targeted-cancer-cell.webp?t=1748961673" type="image/jpeg" medium="image" fileSize="966728">
        <media:title type="plain">Cancer cell in the cross-hairs</media:title>
      </media:content>
    </item>
    <item>
      <title>Lilly taps Abbisko for $1.9B discovery deal </title>
      <description>Abbisko Therapeutics Co. Ltd. has entered a research collaboration and license agreement with Eli Lilly and Co. to discover and develop innovative medicines across multiple targets, with the aim of advancing novel drug candidates with global potential.</description>
      <content:encoded>
        <![CDATA[Abbisko Therapeutics Co. Ltd. has entered a research collaboration and license agreement with Eli Lilly and Co. to discover and develop innovative medicines across multiple targets, with the aim of advancing novel drug candidates with global potential.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732075</guid>
      <pubDate>Wed, 24 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732075-lilly-taps-abbisko-for-19b-discovery-deal</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Research-and-science/Microscope.webp?t=1588872688" type="image/png" medium="image" fileSize="408468">
        <media:title type="plain">Microscope</media:title>
      </media:content>
    </item>
    <item>
      <title>J-Pharma drives first cancer LAT1 to phase III study with FDA nod </title>
      <description>J-Pharma Co. Ltd. is progressing the most clinically advanced L-type amino acid transport 1 (LAT1) inhibitor, nanvuranlat (JPH‑203), in a global phase III Beacon-BTC study of biliary tract cancer following U.S. FDA alignment.</description>
      <content:encoded>
        <![CDATA[J-Pharma Co. Ltd. is progressing the most clinically advanced L-type amino acid transport 1 (LAT1) inhibitor, nanvuranlat (JPH‑203), in a global phase III Beacon-BTC study of biliary tract cancer following U.S. FDA alignment.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732153</guid>
      <pubDate>Tue, 23 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732153-j-pharma-drives-first-cancer-lat1-to-phase-iii-study-with-fda-nod</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/Cholangiocarcinoma-Bile-Duct-Cancer.webp?t=1674573514" type="image/png" medium="image" fileSize="810777">
        <media:title type="plain">Illustration of cancer in the bile ducts</media:title>
      </media:content>
    </item>
    <item>
      <title>EFPIA report: Every €1 spent on new drugs returns €5.67 to Europe’s economy</title>
      <description>The industry is stepping up its campaign to persuade European governments to increase their drugs budgets, in what is described as a landmark report making the case that spending on patented drugs is not a cost to be contained, but an investment in health and the economy.</description>
      <content:encoded>
        <![CDATA[The industry is stepping up its campaign to persuade European governments to increase their drugs budgets, in what is described as a landmark report making the case that spending on patented drugs is not a cost to be contained, but an investment in health and the economy.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732066</guid>
      <pubDate>Tue, 23 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732066-efpia-report-every-1-spent-on-new-drugs-returns-567-to-europes-economy</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Money/Pill-with-an-euro-sign.webp?t=1762898652" type="image/jpeg" medium="image" fileSize="109856">
        <media:title type="plain">Pill with Euro currency symbol</media:title>
      </media:content>
    </item>
    <item>
      <title>China approves first CAR T for solid tumors </title>
      <description>China’s National Medical Products Administration approved Carsgen Therapeutics Holdings Ltd.’s NDA for satricabtagene autoleucel (satri-cel, CT-041), marking the first global approval of a CAR T therapy for solid tumors. The autologous Claudin18.2-targeted CAR T was approved for patients with Claudin18.2-positive, HER2-negative advanced gastric/gastroesophageal junction adenocarcinoma who have failed at least two prior lines of therapy.</description>
      <content:encoded>
        <![CDATA[China’s National Medical Products Administration approved Carsgen Therapeutics Holdings Ltd.’s NDA for satricabtagene autoleucel (satri-cel, CT-041), marking the first global approval of a CAR T therapy for solid tumors. The autologous Claudin18.2-targeted CAR T was approved for patients with Claudin18.2-positive, HER2-negative advanced gastric/gastroesophageal junction adenocarcinoma who have failed at least two prior lines of therapy.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732064</guid>
      <pubDate>Tue, 23 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732064-china-approves-first-car-t-for-solid-tumors</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/CAR-T-cells-illustration.webp?t=1751551786" type="image/jpeg" medium="image" fileSize="620563">
        <media:title type="plain">AI-generated illustration of CAR T cells</media:title>
      </media:content>
    </item>
    <item>
      <title>Pfizer ADC, from Seagen M&amp;A, fails in phase III NSCLC trial</title>
      <description>Missing statistical significance on the primary overall survival phase III endpoint with antibody-drug conjugate (ADC) sigvotatug vedotin compared with docetaxel in non-small-cell lung cancer (NSCLC), Pfizer Inc., which gained the candidate through its $43 billion buyout of Seagen Inc. in 2023, is forging ahead based on subgroup signals, phase I data and an ongoing phase III Keytruda combination effort currently underway.</description>
      <content:encoded>
        <![CDATA[Missing statistical significance on the primary overall survival phase III endpoint with antibody-drug conjugate (ADC) sigvotatug vedotin compared with docetaxel in non-small-cell lung cancer (NSCLC), Pfizer Inc., which gained the candidate through its $43 billion buyout of Seagen Inc. in 2023, is forging ahead based on subgroup signals, phase I data and an ongoing phase III Keytruda combination effort currently underway.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732060</guid>
      <pubDate>Tue, 23 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732060-pfizer-adc-from-seagen-m-and-a-fails-in-phase-iii-nsclc-trial</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Cancer/Lung-cancer-3d-illo.webp?t=1745257422" type="image/jpeg" medium="image" fileSize="363200">
        <media:title type="plain">Lung cancer illustration</media:title>
      </media:content>
    </item>
    <item>
      <title>K2 nabs two Antengene bispecific TCEs in $2B license, option deal</title>
      <description>MPM Bioimpact-spawned K2 Therapeutics Inc. inked a license deal plus option agreement, worth $980.5 million apiece, to gain ex-China rights to two of Antengene Corp. Ltd.’s preclinical anticancer bispecific T-cell engager (TCE) assets. The deal, announced June 21, will grant Singapore-based K2 exclusive rights to develop and commercialize Antengene’s ATG-106 outside of mainland China, Hong Kong, Macau and Taiwan.</description>
      <content:encoded>
        <![CDATA[MPM Bioimpact-spawned K2 Therapeutics Inc. inked a license deal plus option agreement, worth $980.5 million apiece, to gain ex-China rights to two of Antengene Corp. Ltd.’s preclinical anticancer bispecific T-cell engager (TCE) assets. The deal, announced June 21, will grant Singapore-based K2 exclusive rights to develop and commercialize Antengene’s ATG-106 outside of mainland China, Hong Kong, Macau and Taiwan.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732152</guid>
      <pubDate>Tue, 23 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732152-k2-nabs-two-antengene-bispecific-tces-in-2b-license-option-deal</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/Handshake-lab-research-purple.webp?t=1782139494" type="image/jpeg" medium="image" fileSize="961804">
        <media:title type="plain">Photo of two people shaking hands near lab equipment</media:title>
      </media:content>
    </item>
    <item>
      <title>Rin Institute discovers new insoluble fibrin-targeting ADCs</title>
      <description>Rin Institute Inc. has disclosed antibody-drug conjugates consisting of an antibody targeting insoluble fibrin conjugated to MMAE through a plasmin-cleavable linker reported to be useful for the treatment of cancer.</description>
      <content:encoded>
        <![CDATA[Rin Institute Inc. has disclosed antibody-drug conjugates consisting of an antibody targeting insoluble fibrin conjugated to MMAE through a plasmin-cleavable linker reported to be useful for the treatment of cancer.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732123</guid>
      <pubDate>Tue, 23 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732123-rin-institute-discovers-new-insoluble-fibrin-targeting-adcs</link>
    </item>
    <item>
      <title>EVmiR-885-5p limits TNBC spread in preclinical models</title>
      <description>Researchers at Theramir Ltd. presented preclinical proof-of-concept data for a new extracellular vesicle (EV) platform engineered to deliver miR-885-5p (EVmiR885-5p), targeting leukocyte-specific protein-1 (LCP-1)-mediated cytoskeletal remodeling in triple-negative breast cancer (TNBC) models.</description>
      <content:encoded>
        <![CDATA[Researchers at Theramir Ltd. presented preclinical proof-of-concept data for a new extracellular vesicle (EV) platform engineered to deliver miR-885-5p (EVmiR885-5p), targeting leukocyte-specific protein-1 (LCP-1)-mediated cytoskeletal remodeling in triple-negative breast cancer (TNBC) models.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732097</guid>
      <pubDate>Mon, 22 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732097-evmir-885-5p-limits-tnbc-spread-in-preclinical-models</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Cancer/Triple-negative-breast-cancer-TNBC-cell.webp?t=1770997255" type="image/jpeg" medium="image" fileSize="432025">
        <media:title type="plain">Illustration of triple-negative breast cancer cells</media:title>
      </media:content>
    </item>
    <item>
      <title>CATA-001 yields promising results for light chain multiple myeloma</title>
      <description>Light chain multiple myeloma (LCMM) is a cancer driven by malignant plasma cells that produce excessive pathogenic free light chains (FLCs) that may cause kidney dysfunction and form amyloid deposits in key organs, thus leading to poor outcomes. Ab Studio Inc.’s CATA-001 is a bispecific antibody targeting both CD38 and aggregated light chains (ALs) designed to deplete CD38+ plasma cells and clear both circulating and tissue-deposited pathogenic FLC aggregates for the treatment of LCMM and AL amyloidosis.</description>
      <content:encoded>
        <![CDATA[Light chain multiple myeloma (LCMM) is a cancer driven by malignant plasma cells that produce excessive pathogenic free light chains (FLCs) that may cause kidney dysfunction and form amyloid deposits in key organs, thus leading to poor outcomes. Ab Studio Inc.’s CATA-001 is a bispecific antibody targeting both CD38 and aggregated light chains (ALs) designed to deplete CD38+ plasma cells and clear both circulating and tissue-deposited pathogenic FLC aggregates for the treatment of LCMM and AL amyloidosis.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732095</guid>
      <pubDate>Mon, 22 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732095-cata-001-yields-promising-results-for-light-chain-multiple-myeloma</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Research-and-science/Red-and-blue-bispecific-antibodies.webp?t=1765991281" type="image/jpeg" medium="image" fileSize="372546">
        <media:title type="plain">Red and blue bispecific antibodies</media:title>
      </media:content>
    </item>
    <item>
      <title>K2 nabs two Antengene bispecific TCEs in $2B license, option deal</title>
      <description>MPM Bioimpact-spawned K2 Therapeutics Inc. inked a license deal plus option agreement, worth $980.5 million apiece, to gain ex-China rights to two of Antengene Corp. Ltd.’s preclinical anticancer bispecific T-cell engager (TCE) assets. The deal, announced June 21, will grant Singapore-based K2 exclusive rights to develop and commercialize Antengene’s ATG-106 outside of mainland China, Hong Kong, Macau and Taiwan.</description>
      <content:encoded>
        <![CDATA[MPM Bioimpact-spawned K2 Therapeutics Inc. inked a license deal plus option agreement, worth $980.5 million apiece, to gain ex-China rights to two of Antengene Corp. Ltd.’s preclinical anticancer bispecific T-cell engager (TCE) assets. The deal, announced June 21, will grant Singapore-based K2 exclusive rights to develop and commercialize Antengene’s ATG-106 outside of mainland China, Hong Kong, Macau and Taiwan.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732090</guid>
      <pubDate>Mon, 22 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732090-k2-nabs-two-antengene-bispecific-tces-in-2b-license-option-deal</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/Handshake-lab-research-purple.webp?t=1782139494" type="image/jpeg" medium="image" fileSize="961804">
        <media:title type="plain">Photo of two people shaking hands near lab equipment</media:title>
      </media:content>
    </item>
    <item>
      <title>Nankai University and Accendatech present new majusculamide D derivatives</title>
      <description>Scientists from Nankai University Tianjin and Accendatech Technology Co. Ltd. have identified a majusculamide D derivative found to be useful for the treatment of cancer.</description>
      <content:encoded>
        <![CDATA[Scientists from Nankai University Tianjin and Accendatech Technology Co. Ltd. have identified a majusculamide D derivative found to be useful for the treatment of cancer.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732041</guid>
      <pubDate>Fri, 19 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732041-nankai-university-and-accendatech-present-new-majusculamide-d-derivatives</link>
    </item>
    <item>
      <title>Chinese scientists identify new macrocyclic compounds as kinase inhibitors</title>
      <description>Henan Normal University and Henan Zhiwei Biological Engineering Co. Ltd. have discovered macrocyclic compounds acting as neurotrophic tyrosine kinase receptors (TRK) and/or proto-oncogene tyrosine-protein kinase ROS (ROS1; MCF3) and/or hepatocyte growth factor receptor (HGFR; MET) and/or macrophage colony-stimulating factor 1 receptor (CSF1R; CD115; c-Fms) and/or ALK tyrosine kinase receptor inhibitors found to be potentially useful for the treatment of cancer and pain.</description>
      <content:encoded>
        <![CDATA[Henan Normal University and Henan Zhiwei Biological Engineering Co. Ltd. have discovered macrocyclic compounds acting as neurotrophic tyrosine kinase receptors (TRK) and/or proto-oncogene tyrosine-protein kinase ROS (ROS1; MCF3) and/or hepatocyte growth factor receptor (HGFR; MET) and/or macrophage colony-stimulating factor 1 receptor (CSF1R; CD115; c-Fms) and/or ALK tyrosine kinase receptor inhibitors found to be potentially useful for the treatment of cancer and pain.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732039</guid>
      <pubDate>Fri, 19 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732039-chinese-scientists-identify-new-macrocyclic-compounds-as-kinase-inhibitors</link>
    </item>
    <item>
      <title>Hangzhou Innogate Pharma discovers new KAT inhibitors</title>
      <description>Hangzhou Innogate Pharma Co. Ltd. has patented inhibitors of histone acetyltransferase KAT5 (Tip60) and/or KAT6A (MOZ; MYST-3) and/or KAT6B (MOZ2; MYST-4) and/or KAT7 (HBO-1; MYST-2) and/or KAT8 (hMOF; MYST-1) reported to be useful for the treatment of cancer.</description>
      <content:encoded>
        <![CDATA[Hangzhou Innogate Pharma Co. Ltd. has patented inhibitors of histone acetyltransferase KAT5 (Tip60) and/or KAT6A (MOZ; MYST-3) and/or KAT6B (MOZ2; MYST-4) and/or KAT7 (HBO-1; MYST-2) and/or KAT8 (hMOF; MYST-1) reported to be useful for the treatment of cancer.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732037</guid>
      <pubDate>Fri, 19 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732037-hangzhou-innogate-pharma-discovers-new-kat-inhibitors</link>
    </item>
    <item>
      <title>Ellison Medical Institute signs license agreement for QED-203</title>
      <description>Uniquest Pty Ltd., the commercialization company of the University of Queensland, has entered into an exclusive license agreement with the Ellison Medical Institute (EMI) to develop and commercialize the University of Queensland’s QED-203 for metastatic castration-resistant prostate cancer.</description>
      <content:encoded>
        <![CDATA[Uniquest Pty Ltd., the commercialization company of the University of Queensland, has entered into an exclusive license agreement with the Ellison Medical Institute (EMI) to develop and commercialize the University of Queensland’s QED-203 for metastatic castration-resistant prostate cancer.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732032</guid>
      <pubDate>Fri, 19 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732032-ellison-medical-institute-signs-license-agreement-for-qed-203</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Cancer/Prostate-cancer-cells.webp?t=1765920543" type="image/png" medium="image" fileSize="389611">
        <media:title type="plain">Prostate cancer cells</media:title>
        <media:description type="plain">Prostate cancer cells</media:description>
      </media:content>
    </item>
    <item>
      <title>Evaxion shares data from characterization of EVX-04</title>
      <description>Evaxion A/S has developed EVX-04, an AI-designed DNA vaccine encoding 1β endogenous retroviruses (ERVs)-derived antigenic fragments to induce broad antigen-specific T-cell responses targeting acute myeloid leukemia blasts expressing ERV antigens.</description>
      <content:encoded>
        <![CDATA[Evaxion A/S has developed EVX-04, an AI-designed DNA vaccine encoding 1β endogenous retroviruses (ERVs)-derived antigenic fragments to induce broad antigen-specific T-cell responses targeting acute myeloid leukemia blasts expressing ERV antigens.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732031</guid>
      <pubDate>Fri, 19 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732031-evaxion-shares-data-from-characterization-of-evx-04</link>
    </item>
    <item>
      <title>J-Pharma drives first cancer LAT1 to phase III study with FDA nod </title>
      <description>J-Pharma Co. Ltd. is progressing the most clinically advanced L-type amino acid transport 1 (LAT1) inhibitor, nanvuranlat (JPH‑203), in a global phase III Beacon-BTC study of biliary tract cancer following U.S. FDA alignment.</description>
      <content:encoded>
        <![CDATA[J-Pharma Co. Ltd. is progressing the most clinically advanced L-type amino acid transport 1 (LAT1) inhibitor, nanvuranlat (JPH‑203), in a global phase III Beacon-BTC study of biliary tract cancer following U.S. FDA alignment.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731921</guid>
      <pubDate>Thu, 18 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731921-j-pharma-drives-first-cancer-lat1-to-phase-iii-study-with-fda-nod</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/Cholangiocarcinoma-Bile-Duct-Cancer.webp?t=1674573514" type="image/png" medium="image" fileSize="810777">
        <media:title type="plain">Illustration of cancer in the bile ducts</media:title>
      </media:content>
    </item>
    <item>
      <title>Sunshine Lake Pharma identifies new GTPase KRAS G12C inhibitors</title>
      <description>Sunshine Lake Pharma Co. Ltd. has patented GTPase KRAS (G12C mutant) inhibitors found to be potentially useful for the treatment of cancer.</description>
      <content:encoded>
        <![CDATA[Sunshine Lake Pharma Co. Ltd. has patented GTPase KRAS (G12C mutant) inhibitors found to be potentially useful for the treatment of cancer.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732023</guid>
      <pubDate>Thu, 18 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732023-sunshine-lake-pharma-identifies-new-gtpase-kras-g12c-inhibitors</link>
    </item>
    <item>
      <title>Convalife presents new dual CDK4/cyclin D1 and CDK9 inhibitors</title>
      <description>Researchers from Convalife Pharmaceuticals Co. Ltd. and Zhejiang Convalife Pharmaceutical Co. Ltd. have described dual CDK4/cyclin D1 and cyclin-dependent kinase 9 (CDK9) inhibitors reported to be useful for the treatment of cancer and inflammatory disorders.</description>
      <content:encoded>
        <![CDATA[Researchers from Convalife Pharmaceuticals Co. Ltd. and Zhejiang Convalife Pharmaceutical Co. Ltd. have described dual CDK4/cyclin D1 and cyclin-dependent kinase 9 (CDK9) inhibitors reported to be useful for the treatment of cancer and inflammatory disorders.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732021</guid>
      <pubDate>Thu, 18 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732021-convalife-presents-new-dual-cdk4-cyclin-d1-and-cdk9-inhibitors</link>
    </item>
    <item>
      <title>Sichuan Kelun-Biotech Biopharmaceutical patents new heterocyclic compounds</title>
      <description>Sichuan Kelun-Biotech Biopharmaceutical Co. Ltd. has disclosed heterocyclic compounds and their antibody-drug conjugates reported to be useful for the treatment of cancer.</description>
      <content:encoded>
        <![CDATA[Sichuan Kelun-Biotech Biopharmaceutical Co. Ltd. has disclosed heterocyclic compounds and their antibody-drug conjugates reported to be useful for the treatment of cancer.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732019</guid>
      <pubDate>Thu, 18 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732019-sichuan-kelun-biotech-biopharmaceutical-patents-new-heterocyclic-compounds</link>
    </item>
    <item>
      <title>KANSL2 is oncogene and actionable biomarker in multiple myeloma</title>
      <description>Due to the availability of drugs targeting histone acetylation and associated reader proteins, the equilibrium of histone acetylation and deacetylation has attracted attention in multiple myeloma as a potential therapeutic target. Therefore, the identification of novel predictive biomarkers for multiple myeloma patient selection for epigenetic therapies is urgently needed.</description>
      <content:encoded>
        <![CDATA[<p>Due to the availability of drugs targeting histone acetylation and associated reader proteins, the equilibrium of histone acetylation and deacetylation has attracted attention in multiple myeloma as a potential therapeutic target. Therefore, the identification of novel predictive biomarkers for multiple myeloma patient selection for epigenetic therapies is urgently needed.</p>]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732014</guid>
      <pubDate>Thu, 18 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732014-kansl2-is-oncogene-and-actionable-biomarker-in-multiple-myeloma</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Cancer/Multiple-myeloma-illustration.webp?t=1614631713" type="image/png" medium="image" fileSize="634062">
        <media:title type="plain">Multiple myeloma illustration</media:title>
      </media:content>
    </item>
    <item>
      <title>CC-3 antibody shows antitumoral activity in penile cancer</title>
      <description>Advanced penile cancer (PeCa) is a rare cancer affecting the genitourinary tract with a 5-year survival rate of about 10% when metastatic. First-line therapies achieve objective response rates of 40%-50%, while immunotherapy has not been established.</description>
      <content:encoded>
        <![CDATA[Advanced penile cancer (PeCa) is a rare cancer affecting the genitourinary tract with a 5-year survival rate of about 10% when metastatic. First-line therapies achieve objective response rates of 40%-50%, while immunotherapy has not been established. ]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732013</guid>
      <pubDate>Thu, 18 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732013-cc-3-antibody-shows-antitumoral-activity-in-penile-cancer</link>
    </item>
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