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    <title>Immuno-oncology</title>
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    <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.]]>
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      <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>
    <item>
      <title>Shanghai Ruotuo Biotechnology discovers new anti-EGFR/HER3 ADCs</title>
      <description>Shanghai Ruotuo Biotechnology Co. Ltd. has patented antibody-drug conjugates (ADCs) comprising bispecific antibodies targeting epidermal growth factor receptors (EGFR; ERBB; HER) and receptor tyrosine-protein kinase erbb-3 (ERBB3; HER3) linked to a cytotoxic drug through a linker intended for use in the treatment of cancer.</description>
      <content:encoded>
        <![CDATA[Shanghai Ruotuo Biotechnology Co. Ltd. has patented antibody-drug conjugates (ADCs) comprising bispecific antibodies targeting epidermal growth factor receptors (EGFR; ERBB; HER) and receptor tyrosine-protein kinase erbb-3 (ERBB3; HER3) linked to a cytotoxic drug through a linker intended for use in the treatment of cancer.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731865</guid>
      <pubDate>Fri, 12 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731865-shanghai-ruotuo-biotechnology-discovers-new-anti-egfr-her3-adcs</link>
    </item>
    <item>
      <title>Tumor irradiation promotes CAR T-cell persistence and efficacy in lung metastases models</title>
      <description>A team of investigators at Icahn School of Medicine at Mount Sinai and collaborating institutions aimed to isolate the on-target activity of CAR T cells to target tumor cells.</description>
      <content:encoded>
        <![CDATA[A team of investigators at Icahn School of Medicine at Mount Sinai and collaborating institutions aimed to isolate the on-target activity of CAR T cells to target tumor cells.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731858</guid>
      <pubDate>Fri, 12 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731858-tumor-irradiation-promotes-car-t-cell-persistence-and-efficacy-in-lung-metastases-models</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Cancer/Cancer-cell-and-target.webp?t=1703001756" type="image/jpeg" medium="image" fileSize="313981">
        <media:title type="plain">Cancer cell targeted in crosshairs</media:title>
      </media:content>
    </item>
    <item>
      <title>T-Curx gains trial clearance for Siglec-6-targeted TCX-001</title>
      <description>T-Curx GmbH has obtained clinical trial approval from the Swiss agency Swissmedic for the company’s nonviral lead CAR T program, TCX-001. The first-in-human phase I study will open in Switzerland, and a submission to the EMA will seek to expand the trial to sites in Germany. The study will enroll adults with relapsed or refractory acute myeloid leukemia (AML) and chronic lymphocytic leukemia (CLL), including patients not eligible for stem cell transplantation.</description>
      <content:encoded>
        <![CDATA[T-Curx GmbH has obtained clinical trial approval from the Swiss agency Swissmedic for the company’s nonviral lead CAR T program, TCX-001. The first-in-human phase I study will open in Switzerland, and a submission to the EMA will seek to expand the trial to sites in Germany. The study will enroll adults with relapsed or refractory acute myeloid leukemia (AML) and chronic lymphocytic leukemia (CLL), including patients not eligible for stem cell transplantation.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731835</guid>
      <pubDate>Thu, 11 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731835-t-curx-gains-trial-clearance-for-siglec-6-targeted-tcx-001</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Cancer/CAR-T-cell-attacking-cancer-cell.webp?t=1691517857" type="image/jpeg" medium="image" fileSize="248197">
        <media:title type="plain">CAR T cells attacking cancer cell</media:title>
      </media:content>
    </item>
    <item>
      <title>Antengene’s ATG-201 gains IND clearance in China</title>
      <description>Antengene Corp. Ltd. has obtained IND approval from China’s National Medical Products Administration (NMPA) for ATG-201 for the treatment of B-cell related autoimmune diseases.</description>
      <content:encoded>
        <![CDATA[Antengene Corp. Ltd. has obtained IND approval from China’s National Medical Products Administration (NMPA) for ATG-201 for the treatment of B-cell related autoimmune diseases.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731780</guid>
      <pubDate>Wed, 10 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731780-antengenes-atg-201-gains-ind-clearance-in-china</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Drugs/3D-bispecific-antibodies.webp?t=1732120101" type="image/jpeg" medium="image" fileSize="146730">
        <media:title type="plain">3d rendering of bispecific antibodies</media:title>
      </media:content>
    </item>
    <item>
      <title>Pheon Therapeutics discovers new CDCP1-targeting ADCs</title>
      <description>Pheon Therapeutics Ltd. has patented antibody-drug conjugates, comprising an antibody targeting CDCP1 covalently linked to a cytotoxic drug through a linker, that are potentially useful for the treatment of cancer.</description>
      <content:encoded>
        <![CDATA[Pheon Therapeutics Ltd. has patented antibody-drug conjugates, comprising an antibody targeting CDCP1 covalently linked to a cytotoxic drug through a linker, that are potentially useful for the treatment of cancer.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731772</guid>
      <pubDate>Tue, 09 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731772-pheon-therapeutics-discovers-new-cdcp1-targeting-adcs</link>
    </item>
    <item>
      <title>Moderna’s mRNA-4194 cleared for clinic for Lynch syndrome</title>
      <description>The University of Oxford and Moderna Inc. have announced authorization by the U.K.’s Medicines and Healthcare products Regulatory Agency (MHRA) to initiate a phase I/II study of mRNA-4194, Moderna’s investigational mRNA-based cancer vaccine for Lynch syndrome.</description>
      <content:encoded>
        <![CDATA[The University of Oxford and Moderna Inc. have announced authorization by the U.K.’s Medicines and Healthcare products Regulatory Agency (MHRA) to initiate a phase I/II study of mRNA-4194, Moderna’s investigational mRNA-based cancer vaccine for Lynch syndrome. ]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731760</guid>
      <pubDate>Tue, 09 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731760-modernas-mrna-4194-cleared-for-clinic-for-lynch-syndrome</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/Mrna-therapeutic-illustration.webp?t=1778251655" type="image/png" medium="image" fileSize="958605">
        <media:title type="plain">Illustration of messenger RNA</media:title>
      </media:content>
    </item>
    <item>
      <title>AxS007 penetrates BBB for breast cancer brain metastases</title>
      <description>About 90% of brain metastases are often limited therapeutically speaking due to the impermeable blood-brain barrier (BBB). Nanocarry Therapeutics Ltd. has presented AxS007, a novel insulin-mediated nanocarrier that delivers multiple copies of trastuzumab and pertuzumab across the BBB, using native insulin as a brain transporter and increasing brain exposure.</description>
      <content:encoded>
        <![CDATA[About 90% of brain metastases are often limited therapeutically speaking due to the impermeable blood-brain barrier (BBB). Nanocarry Therapeutics Ltd. has presented AxS007, a novel insulin-mediated nanocarrier that delivers multiple copies of trastuzumab and pertuzumab across the BBB, using native insulin as a brain transporter and increasing brain exposure.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731675</guid>
      <pubDate>Fri, 05 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731675-axs007-penetrates-bbb-for-breast-cancer-brain-metastases</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/Blood-Brain-Barrier-Illustration.webp?t=1678203491" type="image/png" medium="image" fileSize="856287">
        <media:title type="plain">Illustration of brain in head highlighting the blood-brain barier.</media:title>
      </media:content>
    </item>
    <item>
      <title>Sotio Biotech’s SOT-106 designated orphan drug for osteosarcoma</title>
      <description>Sotio Biotech AS’s SOT-106 has been granted orphan drug designation by the FDA for the treatment of osteosarcoma. SOT-106 is a next-generation antibody-drug conjugate targeting leucine-rich repeat-containing 15 (LRRC15), a clinically validated target broadly expressed across sarcoma subtypes and in tumor-associated stroma.</description>
      <content:encoded>
        <![CDATA[Sotio Biotech AS’s SOT-106 has been granted orphan drug designation by the FDA for the treatment of osteosarcoma. SOT-106 is a next-generation antibody-drug conjugate targeting leucine-rich repeat-containing 15 (LRRC15), a clinically validated target broadly expressed across sarcoma subtypes and in tumor-associated stroma.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731653</guid>
      <pubDate>Thu, 04 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731653-sotio-biotechs-sot-106-designated-orphan-drug-for-osteosarcoma</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/osteosarcoma-bone-cancer-knee-illustration.webp?t=1780586547" type="image/jpeg" medium="image" fileSize="560760">
        <media:title type="plain">Illustration of bone cancer in the knee</media:title>
      </media:content>
    </item>
    <item>
      <title>IMU’s $53M series A to advance high-definition immune profiling tech</title>
      <description>IMU Biosciences Ltd. has closed its series A at £40 million (US$53.9 million), adding £28.5 million to the initial close in January 2024, and bringing the total raised since the company’s formation in 2021 to £45 million. Since that first close, IMU has built what is claimed as the world’s largest high-definition immune system dataset, with almost 25,000 profiles of healthy volunteers and disease-specific patient cohorts.</description>
      <content:encoded>
        <![CDATA[IMU Biosciences Ltd. has closed its series A at £40 million (US$53.9 million), adding £28.5 million to the initial close in January 2024, and bringing the total raised since the company’s formation in 2021 to £45 million. Since that first close, IMU has built what is claimed as the world’s largest high-definition immune system dataset, with almost 25,000 profiles of healthy volunteers and disease-specific patient cohorts.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731669</guid>
      <pubDate>Wed, 03 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731669-imus-53m-series-a-to-advance-high-definition-immune-profiling-tech</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Money/Pound-sign-on-tech-background.webp?t=1780434872" type="image/jpeg" medium="image" fileSize="224337">
        <media:title type="plain">Pound sign on tech background</media:title>
      </media:content>
    </item>
    <item>
      <title>CSPC’s SYS-6063 gains Chinese trial clearance for SLE</title>
      <description>CSPC Pharmaceutical Group Ltd. has obtained clinical trial clearance from China’s National Medical Products Administration (NMPA) for SYS-6063, an mRNA-LNP-based dual-target CAR T-cell injection for the treatment of relapsed or refractory systemic lupus erythematosus (SLE).</description>
      <content:encoded>
        <![CDATA[CSPC Pharmaceutical Group Ltd. has obtained clinical trial clearance from China’s National Medical Products Administration (NMPA) for SYS-6063, an mRNA-LNP-based dual-target CAR T-cell injection for the treatment of relapsed or refractory systemic lupus erythematosus (SLE).]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731596</guid>
      <pubDate>Wed, 03 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731596-cspcs-sys-6063-gains-chinese-trial-clearance-for-sle</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/Systemic-Lupus-Erythematosus.webp?t=1684937966" type="image/jpeg" medium="image" fileSize="100180">
        <media:title type="plain">Concept art for systemic lupus erythematosus R&amp;D</media:title>
      </media:content>
    </item>
    <item>
      <title>IMU’s $53M series A to advance high-definition immune profiling tech</title>
      <description>IMU Biosciences Ltd. has closed its series A at £40 million (US$53.9 million), adding £28.5 million to the initial close in January 2024, and bringing the total raised since the company’s formation in 2021 to £45 million. Since that first close, IMU has built what is claimed as the world’s largest high-definition immune system dataset, with almost 25,000 profiles of healthy volunteers and disease-specific patient cohorts.</description>
      <content:encoded>
        <![CDATA[IMU Biosciences Ltd. has closed its series A at £40 million (US$53.9 million), adding £28.5 million to the initial close in January 2024, and bringing the total raised since the company’s formation in 2021 to £45 million. Since that first close, IMU has built what is claimed as the world’s largest high-definition immune system dataset, with almost 25,000 profiles of healthy volunteers and disease-specific patient cohorts.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731528</guid>
      <pubDate>Tue, 02 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731528-imus-53m-series-a-to-advance-high-definition-immune-profiling-tech</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Money/Pound-sign-on-tech-background.webp?t=1780434872" type="image/jpeg" medium="image" fileSize="224337">
        <media:title type="plain">Pound sign on tech background</media:title>
      </media:content>
    </item>
    <item>
      <title>FDA approves IND for Iovance’s TIL therapy IOV-5001</title>
      <description>Iovance Biotherapeutics Inc. has received IND clearance from the FDA for IOV-5001, a next-generation interleukin-12 (IL-12)-tethered tumor-infiltrating lymphocyte (TIL) therapy.</description>
      <content:encoded>
        <![CDATA[Iovance Biotherapeutics Inc. has received IND clearance from the FDA for IOV-5001, a next-generation interleukin-12 (IL-12)-tethered tumor-infiltrating lymphocyte (TIL) therapy. ]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731580</guid>
      <pubDate>Tue, 02 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731580-fda-approves-ind-for-iovances-til-therapy-iov-5001</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/Cancer-research-microscope-pathology.webp?t=1669740694" type="image/png" medium="image" fileSize="1333240">
        <media:title type="plain">Microscope with laptop displaying histology image.</media:title>
      </media:content>
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