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    <title>Immuno-oncology</title>
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    <item>
      <title>TICTACs remodel TAMs, reduce tumor burden and metastasis</title>
      <description>In a recent study, scientists from Stanford University and collaborators aimed to develop a platform for specific tumor-immune cell targeting, focusing on tumor-associated macrophages (TAMs), with the eventual goal of interfacing with existing immune checkpoint inhibitor technologies.</description>
      <content:encoded>
        <![CDATA[In a recent study, scientists from Stanford University and collaborators aimed to develop a platform for specific tumor-immune cell targeting, focusing on tumor-associated macrophages (TAMs), with the eventual goal of interfacing with existing immune checkpoint inhibitor technologies.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732625</guid>
      <pubDate>Tue, 14 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732625-tictacs-remodel-tams-reduce-tumor-burden-and-metastasis</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Cancer/Cancer-tumor-blood-vessels.webp?t=1691420296" type="image/jpeg" medium="image" fileSize="242637">
        <media:title type="plain">3D illustration of tumor</media:title>
      </media:content>
    </item>
    <item>
      <title>SL Science seeks US orphan drug designation for γδ T-cell therapy</title>
      <description>SL Science Holding Ltd. has submitted an orphan drug designation request to the FDA for its γδ T-cell therapy product, Vδ2+ γδ T cells, for the treatment of glioblastoma multiforme.</description>
      <content:encoded>
        <![CDATA[SL Science Holding Ltd. has submitted an orphan drug designation request to the FDA for its γδ T-cell therapy product, Vδ2+ γδ T cells, for the treatment of glioblastoma multiforme.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732565</guid>
      <pubDate>Mon, 13 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732565-sl-science-seeks-us-orphan-drug-designation-for-t-cell-therapy</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Cancer/tcells-attacking-tumor.webp?t=1734452639" type="image/jpeg" medium="image" fileSize="727452">
        <media:title type="plain">Illustration of T cells attacking tumor</media:title>
      </media:content>
    </item>
    <item>
      <title>Microbial ecology reshapes cancer care, diagnostics and therapies</title>
      <description>Cancer researchers are increasingly turning to the microbiome to understand why some patients respond well to treatment while others face severe complications. Gut microbial communities shift during intensive therapies such as bone marrow transplantation, and those changes influence infection risk, immune recovery and long‑term survival. New advances in microbial sequencing and engineering redefine this community as a measurable clinical parameter that can be monitored, modeled, and even therapeutically reshaped to improve outcomes in oncology and other conditions.</description>
      <content:encoded>
        <![CDATA[Cancer researchers are increasingly turning to the microbiome to understand why some patients respond well to treatment while others face severe complications. Gut microbial communities shift during intensive therapies such as bone marrow transplantation, and those changes influence infection risk, immune recovery and long‑term survival. New advances in microbial sequencing and engineering redefine this community as a measurable clinical parameter that can be monitored, modeled, and even therapeutically reshaped to improve outcomes in oncology and other conditions.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732621</guid>
      <pubDate>Fri, 10 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732621-microbial-ecology-reshapes-cancer-care-diagnostics-and-therapies</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/Gut-Microbiome-Dysbiosis.webp?t=1783522730" type="image/jpeg" medium="image" fileSize="516866">
        <media:title type="plain">Illustration of bacteria, microorganisms in the gastrointestinal system</media:title>
      </media:content>
    </item>
    <item>
      <title>Grant supports Rybodyn’s antibody therapies for lung cancer</title>
      <description>Rybodyn Inc. has been awarded $1.3 million from the U.S. Department of War to advance preclinical development of two novel antibody-based therapies for lung cancer.</description>
      <content:encoded>
        <![CDATA[Rybodyn Inc. has been awarded $1.3 million from the U.S. Department of War to advance preclinical development of two novel antibody-based therapies for lung cancer.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732500</guid>
      <pubDate>Thu, 09 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732500-grant-supports-rybodyns-antibody-therapies-for-lung-cancer</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Cancer/lung-cancer.webp?t=1588881354" type="image/png" medium="image" fileSize="422296">
        <media:title type="plain">Lung cancer illustration</media:title>
      </media:content>
    </item>
    <item>
      <title>Urogen’s UGN-501 gains IND clearance for bladder cancer</title>
      <description>Urogen Pharma Ltd. has obtained IND approval from the FDA for UGN-501, a next-generation investigational oncolytic virus. A phase I study evaluating intravesical administration of UGN-501 in patients with non-muscle invasive bladder cancer (NMIBC) is expected to begin in the fourth quarter.</description>
      <content:encoded>
        <![CDATA[Urogen Pharma Ltd. has obtained IND approval from the FDA for UGN-501, a next-generation investigational oncolytic virus. A phase I study evaluating intravesical administration of UGN-501 in patients with non-muscle invasive bladder cancer (NMIBC) is expected to begin in the fourth quarter.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732499</guid>
      <pubDate>Thu, 09 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732499-urogens-ugn-501-gains-ind-clearance-for-bladder-cancer</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Urology/Art-concept-for-bladder.webp?t=1733435225" type="image/jpeg" medium="image" fileSize="250443">
        <media:title type="plain">Art concept for bladder</media:title>
      </media:content>
    </item>
    <item>
      <title>Beijing Mabworks Biotech discloses new DLL3-targeting ADCs</title>
      <description>A Beijing Mabworks Biotech Co. Ltd. patent describes new antibody-drug conjugates (ADCs) comprising antigen-binding fragments or antibodies targeting delta-like protein 3 (DLL3) linked to a cytotoxic drug potentially useful for the treatment of small-cell lung cancer (SCLC).</description>
      <content:encoded>
        <![CDATA[A Beijing Mabworks Biotech Co. Ltd. patent describes new antibody-drug conjugates (ADCs) comprising antigen-binding fragments or antibodies targeting delta-like protein 3 (DLL3) linked to a cytotoxic drug potentially useful for the treatment of small-cell lung cancer (SCLC).]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732495</guid>
      <pubDate>Wed, 08 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732495-beijing-mabworks-biotech-discloses-new-dll3-targeting-adcs</link>
    </item>
    <item>
      <title>Targeting VSIG4-high TAMs in colorectal cancer immunotherapy</title>
      <description>Researchers from Hainan Medical University and collaborators have demonstrated that PGE2-EP2/EP4-G α s-PKA signaling drove the expansion of immunosuppressive VSIG4-high macrophages and promoted immunotherapy resistance in colorectal cancer (CRC).</description>
      <content:encoded>
        <![CDATA[Researchers from Hainan Medical University and collaborators have demonstrated that PGE2-EP2/EP4-G α s-PKA signaling drove the expansion of immunosuppressive VSIG4-high macrophages and promoted immunotherapy resistance in colorectal cancer (CRC).]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732486</guid>
      <pubDate>Wed, 08 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732486-targeting-vsig4-high-tams-in-colorectal-cancer-immunotherapy</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Cancer/Colorectal-cancer-tumor-ilustration.webp?t=1769011739" type="image/jpeg" medium="image" fileSize="677067">
        <media:title type="plain">Illustration of cancer inside colon</media:title>
      </media:content>
    </item>
    <item>
      <title>Coregen’s CRG-150 gains IND clearance for solid tumors</title>
      <description>Coregen Inc. has obtained IND clearance from the FDA for CRG-150, a novel adoptive cell therapy targeting SRC-3 (steroid receptor coactivator 3).</description>
      <content:encoded>
        <![CDATA[Coregen Inc. has obtained IND clearance from the FDA for CRG-150, a novel adoptive cell therapy targeting SRC-3 (steroid receptor coactivator 3).]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732484</guid>
      <pubDate>Wed, 08 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732484-coregens-crg-150-gains-ind-clearance-for-solid-tumors</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/Immunotherapy-cancer-targeted-by-immune-cells.webp?t=1783522893" type="image/jpeg" medium="image" fileSize="1094429">
        <media:title type="plain">Illustration of lymphocytes attacking cancer cell</media:title>
      </media:content>
    </item>
    <item>
      <title>FDA clears IND for LTZ Therapeutics’ LTZ-232</title>
      <description>LTZ Therapeutics Inc.’s LTZ-232 has gained IND clearance from the FDA, enabling initiation of a phase I study in patients with advanced metastatic colorectal cancer and other solid tumors.</description>
      <content:encoded>
        <![CDATA[LTZ Therapeutics Inc.’s LTZ-232 has gained IND clearance from the FDA, enabling initiation of a phase I study in patients with advanced metastatic colorectal cancer and other solid tumors.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732481</guid>
      <pubDate>Wed, 08 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732481-fda-clears-ind-for-ltz-therapeutics-ltz-232</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Cancer/Macrophage-and-cancer-cell.webp?t=1628531599" type="image/png" medium="image" fileSize="457280">
        <media:title type="plain">Macrophage and cancer cell </media:title>
      </media:content>
    </item>
    <item>
      <title>Microbial ecology reshapes cancer care, diagnostics and therapies</title>
      <description>Cancer researchers are increasingly turning to the microbiome to understand why some patients respond well to treatment while others face severe complications. Gut microbial communities shift during intensive therapies such as bone marrow transplantation, and those changes influence infection risk, immune recovery and long‑term survival. New advances in microbial sequencing and engineering redefine this community as a measurable clinical parameter that can be monitored, modeled, and even therapeutically reshaped to improve outcomes in oncology and other conditions.</description>
      <content:encoded>
        <![CDATA[Cancer researchers are increasingly turning to the microbiome to understand why some patients respond well to treatment while others face severe complications. Gut microbial communities shift during intensive therapies such as bone marrow transplantation, and those changes influence infection risk, immune recovery and long‑term survival. New advances in microbial sequencing and engineering redefine this community as a measurable clinical parameter that can be monitored, modeled, and even therapeutically reshaped to improve outcomes in oncology and other conditions.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732480</guid>
      <pubDate>Wed, 08 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732480-microbial-ecology-reshapes-cancer-care-diagnostics-and-therapies</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/Gut-Microbiome-Dysbiosis.webp?t=1783522730" type="image/jpeg" medium="image" fileSize="516866">
        <media:title type="plain">Illustration of bacteria, microorganisms in the gastrointestinal system</media:title>
      </media:content>
    </item>
    <item>
      <title>‘Target-high but uptake-defective’ state identified in ADC resistance</title>
      <description>Separate research teams have reported new insights into resistance mechanisms to the antibody-drug conjugate (ADC) Padcev (enfortumab vedotin, Astellas Pharma Inc./Pfizer Inc.), and possibly to ADCs more broadly. Urothelial cancer drug Padcev, which targets the cell adhesion molecule Nectin-4, was approved in 2019 and is currently one of Pfizer’s top 10 medicines and vaccines, generating $1.94 billion in 2025.</description>
      <content:encoded>
        <![CDATA[Separate research teams have reported new insights into resistance mechanisms to the antibody-drug conjugate (ADC) Padcev (enfortumab vedotin, Astellas Pharma Inc./Pfizer Inc.), and possibly to ADCs more broadly. Urothelial cancer drug Padcev, which targets the cell adhesion molecule Nectin-4, was approved in 2019 and is currently one of Pfizer’s top 10 medicines and vaccines, generating $1.94 billion in 2025.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732450</guid>
      <pubDate>Tue, 07 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732450-target-high-but-uptake-defective-state-identified-in-adc-resistance</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Drugs/Antibody-drug-conjugates-ADCs-3D.webp?t=1751620465" type="image/jpeg" medium="image" fileSize="160333">
        <media:title type="plain">3D rendering of an antibody-drug conjugate</media:title>
      </media:content>
    </item>
    <item>
      <title>Chinese, Australian researchers disclose GD2 ganglioside-targeting ADCs</title>
      <description>Children’s Hospital of Fudan University, Sydney Children’s Hospital and the University of Sydney have jointly patented new antibody-drug conjugates comprising an antibody targeting GD2 ganglioside covalently linked to cytotoxic drugs potentially useful for the treatment of osteosarcoma.</description>
      <content:encoded>
        <![CDATA[Children’s Hospital of Fudan University, Sydney Children’s Hospital and the University of Sydney have jointly patented new antibody-drug conjugates comprising an antibody targeting GD2 ganglioside covalently linked to cytotoxic drugs potentially useful for the treatment of osteosarcoma.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732411</guid>
      <pubDate>Mon, 06 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732411-chinese-australian-researchers-disclose-gd2-ganglioside-targeting-adcs</link>
    </item>
    <item>
      <title>Brightpath files IND application for BP-2202 for multiple myeloma</title>
      <description>Brightpath Biotherapeutics Co. Ltd. has submitted an IND application to the FDA to initiate a phase I trial of BP-2202 in the U.S. (NCT07667868).</description>
      <content:encoded>
        <![CDATA[Brightpath Biotherapeutics Co. Ltd. has submitted an IND application to the FDA to initiate a phase I trial of BP-2202 in the U.S. (NCT07667868).]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732376</guid>
      <pubDate>Fri, 03 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732376-brightpath-files-ind-application-for-bp-2202-for-multiple-myeloma</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/3D-CAR-T-cells-floating.webp?t=1783089402" type="image/jpeg" medium="image" fileSize="329594">
        <media:title type="plain">Illustration of CAR T</media:title>
      </media:content>
    </item>
    <item>
      <title>With GPNMB, CAR T makes further inroads in solid tumors</title>
      <description>Two papers published in the July 1, 2026, issues of Nature and Nature Cancer have reported on preclinical and early clinical data with glycoprotein nonmetastatic melanoma protein B (GPNMB)-targeting CAR T cells in two separate solid tumor types.</description>
      <content:encoded>
        <![CDATA[Two papers published in the July 1, 2026, issues of <em>Nature</em> and <em>Nature Cancer</em> have reported on preclinical and early clinical data with glycoprotein nonmetastatic melanoma protein B (GPNMB)-targeting CAR T cells in two separate solid tumor types.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732356</guid>
      <pubDate>Thu, 02 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732356-with-gpnmb-car-t-makes-further-inroads-in-solid-tumors</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/CAR-T-cell-Y-shaped-chimeric-antigen-receptors.webp?t=1783004848" type="image/jpeg" medium="image" fileSize="323438">
        <media:title type="plain">Illustration of CAR T</media:title>
      </media:content>
    </item>
    <item>
      <title>SUCNR1 antagonist reverses tumor immune suppression</title>
      <description>Researchers at East China Normal University and collaborators reported the discovery and optimization of a series of SUCNR1 antagonists for cancer immunotherapy.</description>
      <content:encoded>
        <![CDATA[Researchers at East China Normal University and collaborators reported the discovery and optimization of a series of SUCNR1 antagonists for cancer immunotherapy.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732335</guid>
      <pubDate>Wed, 01 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732335-sucnr1-antagonist-reverses-tumor-immune-suppression</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Cancer/TME-tumor-microenvironment-3D.webp?t=1699370810" type="image/jpeg" medium="image" fileSize="457538">
        <media:title type="plain">3D Rendering of tumor microenvironment</media:title>
      </media:content>
    </item>
    <item>
      <title>Grant supports Aptevo’s immunotherapy APVO-451 for solid tumors</title>
      <description>Aptevo Therapeutics Inc. has been awarded a $1.5 million research grant from the Andy Hill Cancer Research Endowment (CARE) Fund to support IND-enabling work for APVO-451, Aptevo’s trispecific antibody-like immunotherapy candidate for solid tumors.</description>
      <content:encoded>
        <![CDATA[Aptevo Therapeutics Inc. has been awarded a $1.5 million research grant from the Andy Hill Cancer Research Endowment (CARE) Fund to support IND-enabling work for APVO-451, Aptevo’s trispecific antibody-like immunotherapy candidate for solid tumors.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732334</guid>
      <pubDate>Wed, 01 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732334-grant-supports-aptevos-immunotherapy-apvo-451-for-solid-tumors</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Cancer/Cancer-cell-target-destroy.webp?t=1731081970" type="image/jpeg" medium="image" fileSize="520172">
        <media:title type="plain">Illustration of cancer cell in crosshairs being destroyed</media:title>
      </media:content>
    </item>
    <item>
      <title>GPC3-targeting ADC for HCC shows superior efficacy in preclinical models</title>
      <description>Salubris Biotechnology Co. have reported the development of novel antibody-drug conjugates (ADCs) against glypican-3 (GPC3), an oncofetal glycoprotein overexpressed in approximately 70%-85% of hepatocellular carcinoma (HCC) cases but absent in normal adult tissues.</description>
      <content:encoded>
        <![CDATA[Salubris Biotechnology Co. have reported the development of novel antibody-drug conjugates (ADCs) against glypican-3 (GPC3), an oncofetal glycoprotein overexpressed in approximately 70%-85% of hepatocellular carcinoma (HCC) cases but absent in normal adult tissues.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732189</guid>
      <pubDate>Fri, 26 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732189-gpc3-targeting-adc-for-hcc-shows-superior-efficacy-in-preclinical-models</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>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>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>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>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>Calidi receives pre-IND feedback from FDA on CLD-401</title>
      <description>Calidi Biotherapeutics Inc. has received pre-IND regulatory feedback from the FDA on Calidi’s IND-enabling preclinical plans and clinical strategy for CLD-401. The parties agreed on key aspects of the CMC and nonclinical programs, as well as the overall design for the proposed first-in-human study.</description>
      <content:encoded>
        <![CDATA[Calidi Biotherapeutics Inc. has received pre-IND regulatory feedback from the FDA on Calidi’s IND-enabling preclinical plans and clinical strategy for CLD-401. The parties agreed on key aspects of the CMC and nonclinical programs, as well as the overall design for the proposed first-in-human study.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731994</guid>
      <pubDate>Wed, 17 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731994-calidi-receives-pre-ind-feedback-from-fda-on-cld-401</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/Oncolytic-virus.webp?t=1729781802" type="image/jpeg" medium="image" fileSize="349995">
        <media:title type="plain">Oncolytic virus concept illustration</media:title>
      </media:content>
    </item>
    <item>
      <title>Hengrui Pharmaceuticals prepares new ADCs for cancer</title>
      <description>A patent from Jiangsu Hengrui Pharmaceuticals Co. Ltd. and Shanghai Hengrui Pharmaceutical Co. Ltd. has divulged new antibody-drug conjugates comprising antibodies covalently linked to N-myristoyltransferase 1 (NMT1) inhibitors for potential use in the treatment of cancer.</description>
      <content:encoded>
        <![CDATA[A patent from Jiangsu Hengrui Pharmaceuticals Co. Ltd. and Shanghai Hengrui Pharmaceutical Co. Ltd. has divulged new antibody-drug conjugates comprising antibodies covalently linked to <em>N</em>-myristoyltransferase 1 (NMT1) inhibitors for potential use in the treatment of cancer.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731971</guid>
      <pubDate>Tue, 16 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731971-hengrui-pharmaceuticals-prepares-new-adcs-for-cancer</link>
    </item>
    <item>
      <title>Bendao Biotechnology reports data on BTL-101 in multiple myeloma models</title>
      <description>Clinical responses to BCMA- or GPRC5D-directed T-cell engagers in relapsed/refractory multiple myeloma (MM) are often limited by disease relapse and antigen escape, underscoring the need for dual-targeting strategies that enhance durability while mitigating cytokine-driven toxicity.</description>
      <content:encoded>
        <![CDATA[Clinical responses to BCMA- or GPRC5D-directed T-cell engagers in relapsed/refractory multiple myeloma (MM) are often limited by disease relapse and antigen escape, underscoring the need for dual-targeting strategies that enhance durability while mitigating cytokine-driven toxicity.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731964</guid>
      <pubDate>Tue, 16 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731964-bendao-biotechnology-reports-data-on-btl-101-in-multiple-myeloma-models</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Cancer/multiple-myeloma-bone.webp?t=1725463101" type="image/jpeg" medium="image" fileSize="516109">
        <media:title type="plain">Multiple myeloma art concept</media:title>
      </media:content>
    </item>
    <item>
      <title>Signal rewiring turns ovarian cancer against itself</title>
      <description>Harnessing an oncolytic signal and redirecting it against the tumor itself could be developed as a selective strategy for certain cancer types, as occurs with ErbB hyperactivity, a form of signaling that drives many carcinomas. Inspired by this idea, scientists at Stanford University have engineered a virus that replicates only in ErbB-hyperactive ovarian cancer cells. This allowed them to precisely kill this specific tumor population, achieving greater efficacy and safety than previous oncolytic viruses.</description>
      <content:encoded>
        <![CDATA[Harnessing an oncolytic signal and redirecting it against the tumor itself could be developed as a selective strategy for certain cancer types, as occurs with ErbB hyperactivity, a form of signaling that drives many carcinomas. Inspired by this idea, scientists at Stanford University have engineered a virus that replicates only in ErbB-hyperactive ovarian cancer cells. This allowed them to precisely kill this specific tumor population, achieving greater efficacy and safety than previous oncolytic viruses.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731852</guid>
      <pubDate>Tue, 16 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731852-signal-rewiring-turns-ovarian-cancer-against-itself</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Cancer/Ovarian-cancer-ovary-tumor.webp?t=1781621742" type="image/jpeg" medium="image" fileSize="217654">
        <media:title type="plain">Illustration of cancer on ovary</media:title>
      </media:content>
    </item>
    <item>
      <title>Dual-epitope anti-LILRB4 STAR-T-cell therapy for R/R AML</title>
      <description>Researchers from Peking University and Bristar Immunotech Ltd. recently presented the development of a synthetic T-cell receptor and antigen receptor-T (STAR-T) cell therapy targeting leukocyte immunoglobulin-like receptor B4 (LILRB4) for acute myeloid leukemia (AML).</description>
      <content:encoded>
        <![CDATA[Researchers from Peking University and Bristar Immunotech Ltd. recently presented the development of a synthetic T-cell receptor and antigen receptor-T (STAR-T) cell therapy targeting leukocyte immunoglobulin-like receptor B4 (LILRB4) for acute myeloid leukemia (AML).]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731934</guid>
      <pubDate>Mon, 15 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731934-dual-epitope-anti-lilrb4-star-t-cell-therapy-for-r-r-aml</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Cancer/Cancer-acute-myeloid-leukemia-cell-field.webp?t=1777996415" type="image/jpeg" medium="image" fileSize="1044829">
        <media:title type="plain">Illustration of acute myeloid leukemia (AML) cells in the blood stream</media:title>
      </media:content>
    </item>
    <item>
      <title>Fortvita and Innovent patent new anti-TROP2/B7-H4 ADCs</title>
      <description>Fortvita Biologics Inc. and Innovent Biologics (Suzhou) Co. Ltd. have jointly reported new antibody-drug conjugates (ADCs) comprising a bispecific antibody or antigen-binding fragments targeting V-set domain-containing T-cell activation inhibitor 1 (VTCN1, B7-H4) and tumor-associated calcium signal transducer 2 (TACSTD2; TROP2) linked to cytotoxic drug. They are described as potentially useful for the treatment of cancer.</description>
      <content:encoded>
        <![CDATA[Fortvita Biologics Inc. and Innovent Biologics (Suzhou) Co. Ltd. have jointly reported new antibody-drug conjugates (ADCs) comprising a bispecific antibody or antigen-binding fragments targeting V-set domain-containing T-cell activation inhibitor 1 (VTCN1, B7-H4) and tumor-associated calcium signal transducer 2 (TACSTD2; TROP2) linked to cytotoxic drug. They are described as potentially useful for the treatment of cancer.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731868</guid>
      <pubDate>Fri, 12 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731868-fortvita-and-innovent-patent-new-anti-trop2-b7-h4-adcs</link>
    </item>
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