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    <title>AACR-NCI-EORTC Molecular Targets and Cancer Therapeutics</title>
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    <item>
      <title>ADCs’ breakout 2025 and their still-unfinished potential</title>
      <description>
        <![CDATA[Over the course of the year, and continuing into the latest scientific meetings, an extraordinary breadth of new antibody-drug conjugate (ADC) designs was reported, with innovations spanning targets, linkers, payloads, conjugation chemistries and overall architectures. Once defined by a simple “one target, one payload” model, the field is lately expanding into a more versatile and diverse therapeutic space.]]>
      </description>
      <guid>http://www.bioworld.com/articles/727720</guid>
      <pubDate>Fri, 02 Jan 2026 08:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/727720-adcs-breakout-2025-and-their-still-unfinished-potential</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/Antibody-drug-conjugate-cytotoxic-payload.webp?t=1690210650" type="image/jpeg" medium="image" fileSize="142424">
        <media:title type="plain">3D rendering of antibody drug conjugated with cytotoxic payload</media:title>
      </media:content>
    </item>
    <item>
      <title>ADCs’ breakout 2025 and their still-unfinished potential</title>
      <description>
        <![CDATA[Over the course of the year, and continuing into the latest scientific meetings, an extraordinary breadth of new antibody-drug conjugate (ADC) designs was reported, with innovations spanning targets, linkers, payloads, conjugation chemistries and overall architectures. Once defined by a simple “one target, one payload” model, the field is lately expanding into a more versatile and diverse therapeutic space.]]>
      </description>
      <guid>http://www.bioworld.com/articles/727478</guid>
      <pubDate>Tue, 30 Dec 2025 08:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/727478-adcs-breakout-2025-and-their-still-unfinished-potential</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/Antibody-drug-conjugate-cytotoxic-payload.webp?t=1690210650" type="image/jpeg" medium="image" fileSize="142424">
        <media:title type="plain">3D rendering of antibody drug conjugated with cytotoxic payload</media:title>
      </media:content>
    </item>
    <item>
      <title>New FGFR3 inhibitors offer best-in-class selectivity, potency</title>
      <description>
        <![CDATA[FGFR3 genomic alterations, including S249C as the most common, are recognized oncogenic drivers in 10%-60% of bladder cancers depending on the disease stage. Onco3r Therapeutics BV recently reported the identification of a novel series of highly potent, isoform-selective small-molecule FGFR3 inhibitors.]]>
      </description>
      <guid>http://www.bioworld.com/articles/726572</guid>
      <pubDate>Wed, 26 Nov 2025 08:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/726572-new-fgfr3-inhibitors-offer-best-in-class-selectivity-potency</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Urology/Bladder-illustration.webp?t=1615559821" type="image/png" medium="image" fileSize="432209">
        <media:title type="plain">Bladder </media:title>
      </media:content>
    </item>
    <item>
      <title>Selective CDK2 inhibitor is active in multiple solid tumor models</title>
      <description>
        <![CDATA[Researchers from Eilean Therapeutics LLC and collaborators presented the discovery and characterization of a new, selective CDK2 inhibitor showing potent in vitro and in vivo activity at the 2025 AACR-NCI-EORTC International Conference on Molecular Targets and Cancer Therapeutics.]]>
      </description>
      <guid>http://www.bioworld.com/articles/726528</guid>
      <pubDate>Mon, 24 Nov 2025 08:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/726528-selective-cdk2-inhibitor-is-active-in-multiple-solid-tumor-models</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Cancer/Targeted-cancer-cell.webp?t=1741213881" type="image/jpeg" medium="image" fileSize="269059">
        <media:title type="plain">Targeted cancer cell</media:title>
      </media:content>
    </item>
    <item>
      <title>Small-molecule SMARCA2 inhibitors to treat SMARCA4-mutant cancers</title>
      <description>
        <![CDATA[At the AACR-NCI-EORTC International Conference on Molecular Targets and Cancer Therapeutics, researchers from Onco3r Therapeutics BV presented a novel series of selective SMARCA2 small-molecule inhibitors with a best-in-class potency and selectivity profile.]]>
      </description>
      <guid>http://www.bioworld.com/articles/726526</guid>
      <pubDate>Mon, 24 Nov 2025 08:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/726526-small-molecule-smarca2-inhibitors-to-treat-smarca4-mutant-cancers</link>
    </item>
    <item>
      <title>Novel B7-H7-targeted ADC NPX-125 active in solid tumors</title>
      <description>
        <![CDATA[Nextpoint Therapeutics Inc. presented their novel B7-H7-directed antibody-drug conjugate (ADC).]]>
      </description>
      <guid>http://www.bioworld.com/articles/726413</guid>
      <pubDate>Fri, 21 Nov 2025 08:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/726413-novel-b7-h7-targeted-adc-npx-125-active-in-solid-tumors</link>
    </item>
    <item>
      <title>EP-102 METTL3 inhibitor shows efficacy in NSCLC models</title>
      <description>
        <![CDATA[METTL3, the enzyme that adds the m6A RNA modification, is a key regulator of RNA processing and protein synthesis. In cancer, METTL3 is often overexpressed, driving tumor growth, invasion and therapy resistance across multiple malignancies, including lung, pancreatic, ovarian, colorectal cancers and acute myeloid leukemia.]]>
      </description>
      <guid>http://www.bioworld.com/articles/726360</guid>
      <pubDate>Thu, 20 Nov 2025 08:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/726360-ep-102-mettl3-inhibitor-shows-efficacy-in-nsclc-models</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>Oral cyclin D1-selective inhibitors with antitumor activity, improved safety profile</title>
      <description>
        <![CDATA[At the AACR-NCI-EORTC International Conference on Molecular Targets and Cancer Therapeutics, researchers from Circle Pharma Inc. presented their recent work on developing novel compounds that specifically target cyclin D1 while avoiding the toxicity associated with targeting cyclin D3.]]>
      </description>
      <guid>http://www.bioworld.com/articles/726303</guid>
      <pubDate>Wed, 19 Nov 2025 08:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/726303-oral-cyclin-d1-selective-inhibitors-with-antitumor-activity-improved-safety-profile</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>
    </item>
    <item>
      <title>CEACAM5-targeting ADC with a highly potent pan-RAS(ON) inhibitor payload</title>
      <description>
        <![CDATA[Although tricomplex pan-RAS (ON) inhibitors, such as RMC-6236, constitute a promising class of therapeutics against RAS-driven cancers, their on-target, off-tumor toxicities challenge the dosing strategy and the safety of drug combinations.]]>
      </description>
      <guid>http://www.bioworld.com/articles/726287</guid>
      <pubDate>Tue, 18 Nov 2025 08:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/726287-ceacam5-targeting-adc-with-a-highly-potent-pan-rason-inhibitor-payload</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Research-and-science/Floating-antibody-drug-conjugates.webp?t=1737562655" type="image/jpeg" medium="image" fileSize="131818">
        <media:title type="plain">Floating antibody drug conjugates</media:title>
      </media:content>
    </item>
    <item>
      <title>Small-molecule p53 Y220C reactivators with enhanced potency presented</title>
      <description>
        <![CDATA[Inactivation of the tumor suppressor p53 occurs in approximately half of human cancer cases. In particular, the Y220C point mutation, which induces p53 misfolding and inactivation, is found in about 1% of solid tumors. Previous research identified a unique, druggable pocket on the p53 surface created by this mutation that constitutes a promising cancer therapeutic target.]]>
      </description>
      <guid>http://www.bioworld.com/articles/726285</guid>
      <pubDate>Tue, 18 Nov 2025 08:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/726285-small-molecule-p53-y220c-reactivators-with-enhanced-potency-presented</link>
    </item>
    <item>
      <title>RVU-305 shows potential against GBM in preclinical studies</title>
      <description>
        <![CDATA[In glioblastoma multiforme, MTAP loss leads to MTA accumulation, which partially inhibits PRMT5, making the cells reliant on residual PRMT5 activity for survival. Targeting this remaining PRMT5 with MTA-cooperative inhibitors induces synthetic lethality, representing a promising targeted approach for MTAP-deleted gliomas. Researchers from Ryvu Therapeutics SA reported the preclinical profile of RVU-305, a PRMT5 inhibitor, in MTAP-deleted cancer models.]]>
      </description>
      <guid>http://www.bioworld.com/articles/726283</guid>
      <pubDate>Tue, 18 Nov 2025 08:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/726283-rvu-305-shows-potential-against-gbm-in-preclinical-studies</link>
    </item>
    <item>
      <title>AB-801 enhances KRAS inhibitor antitumor activity</title>
      <description>
        <![CDATA[Researchers from Arcus Biosciences Inc. described the antitumor efficacy of AB-801, an AXL inhibitor in several cancer models.]]>
      </description>
      <guid>http://www.bioworld.com/articles/726085</guid>
      <pubDate>Mon, 17 Nov 2025 08:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/726085-ab-801-enhances-kras-inhibitor-antitumor-activity</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Cancer/Cancer-cell-tumor-target.webp?t=1692022386" type="image/jpeg" medium="image" fileSize="543788">
        <media:title type="plain">3D illustration of cancer in crosshairs</media:title>
      </media:content>
    </item>
    <item>
      <title>CDK2 degraders show activity in HR+/HER2- and CCNE1-amplified breast tumors</title>
      <description>
        <![CDATA[During the AACR-NCI-EORTC International Conference on Molecular Targets and Cancer Therapeutics, scientists from Plexium Inc. presented the identification of a new class of potent, selective, cereblon (CRBN)-based molecular glue degraders of CDK2 using its proprietary monovalent degrader platform.]]>
      </description>
      <guid>http://www.bioworld.com/articles/726066</guid>
      <pubDate>Fri, 14 Nov 2025 08:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/726066-cdk2-degraders-show-activity-in-hr-her2-and-ccne1-amplified-breast-tumors</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Cancer/Breast-cancer-illustration.webp?t=1755012743" type="image/jpeg" medium="image" fileSize="458149">
        <media:title type="plain">Breast cancer illustration</media:title>
      </media:content>
    </item>
    <item>
      <title>Macrocyclic KIF18A inhibitors show preclinical promise</title>
      <description>
        <![CDATA[At the recent AACR-NCI-EORTC International Conference on Molecular Targets and Cancer Therapeutics, researchers from Aurigene Oncology Ltd. presented the discovery and clinical characterization of novel macrocyclic KIF18A inhibitors.]]>
      </description>
      <guid>http://www.bioworld.com/articles/726003</guid>
      <pubDate>Fri, 14 Nov 2025 08:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/726003-macrocyclic-kif18a-inhibitors-show-preclinical-promise</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Cancer/Blue-cancer-cell.webp?t=1753195222" type="image/jpeg" medium="image" fileSize="246736">
        <media:title type="plain">Blue cancer cell</media:title>
      </media:content>
    </item>
    <item>
      <title>HMPL-A251 combines HER2 targeting with precision payload</title>
      <description>
        <![CDATA[Hutchmed (China) Ltd. has developed HMPL-A251, a novel HER2 antibody-drug conjugate (ADC) designed to deliver a potent PI3K/PIKK inhibitor directly to tumor cells.]]>
      </description>
      <guid>http://www.bioworld.com/articles/725997</guid>
      <pubDate>Fri, 14 Nov 2025 08:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/725997-hmpl-a251-combines-her2-targeting-with-precision-payload</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Drugs/ADC-antibody-drug-conjugate-cancer.webp?t=1750428816" type="image/jpeg" medium="image" fileSize="121146">
        <media:title type="plain">Concept art of an antibody-drug conjugate</media:title>
      </media:content>
    </item>
    <item>
      <title>CBO-001, a first-in-class L1CAM ADC with preclinical antitumor activity</title>
      <description>
        <![CDATA[CIS Biopharma AG recently presented an antibody-drug conjugate (ADC) targeting the L1 cell adhesion molecule (L1CAM/CD171) as a potential candidate for the treatment of advanced tumors.]]>
      </description>
      <guid>http://www.bioworld.com/articles/726039</guid>
      <pubDate>Thu, 13 Nov 2025 08:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/726039-cbo-001-a-first-in-class-l1cam-adc-with-preclinical-antitumor-activity</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Cancer/Antibodies-attacking-cancer-cell.webp?t=1621365766" type="image/png" medium="image" fileSize="566115">
        <media:title type="plain">Antibodies attacking cancer cell</media:title>
      </media:content>
    </item>
    <item>
      <title>ITGB6-targeted ADC shows antitumor activity in solid tumor models</title>
      <description>
        <![CDATA[Pinotbio Inc. recently reported a novel antibody-drug conjugate (ADC), named PBX-004, consisting of an ITGB6-targeting antibody conjugated to a potent topoisomerase I (TOP1) inhibitor payload.]]>
      </description>
      <guid>http://www.bioworld.com/articles/726037</guid>
      <pubDate>Thu, 13 Nov 2025 08:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/726037-itgb6-targeted-adc-shows-antitumor-activity-in-solid-tumor-models</link>
    </item>
    <item>
      <title>New oral KRAS G12C(ON) and G12V(ON) inhibitors presented</title>
      <description>
        <![CDATA[Researchers from Prospect Therapeutics Inc. have discovered PSTA-5204, a novel oral KRAS G12D(ON) inhibitor that exhibits potent in vitro activity, strong in vivo efficacy and high selectivity over wild-type KRAS.]]>
      </description>
      <guid>http://www.bioworld.com/articles/726019</guid>
      <pubDate>Wed, 12 Nov 2025 08:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/726019-new-oral-kras-g12con-and-g12von-inhibitors-presented</link>
    </item>
    <item>
      <title>Oral CBL-B inhibitor shows strong immune activation, favorable safety</title>
      <description>
        <![CDATA[Aurigene Oncology Ltd. recently provided details on the discovery and preclinical characterization of AUR-243, a novel CBL-B inhibitor with a distinct therapeutic profile and best-in-class potential compared to other inhibitors. AUR-243 was described as a structurally distinct, oral small molecule demonstrating excellent potency, functional activity and superior efficacy.]]>
      </description>
      <guid>http://www.bioworld.com/articles/726018</guid>
      <pubDate>Wed, 12 Nov 2025 08:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/726018-oral-cbl-b-inhibitor-shows-strong-immune-activation-favorable-safety</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Cancer/Cancer-immunotherapy-illustration.webp?t=1607379909" type="image/png" medium="image" fileSize="527250">
        <media:title type="plain">Cancer immunotherapy illustration</media:title>
      </media:content>
    </item>
    <item>
      <title>TRI-611 targets ALK fusion and TKI-resistant NSCLC </title>
      <description>
        <![CDATA[Researchers at Triana Biomedicines Inc. presented the preclinical characterization of TRI-611, a CNS-penetrant molecular glue degrader targeting ALK in models of ALK fusion-positive non-small-cell lung cancer.]]>
      </description>
      <guid>http://www.bioworld.com/articles/726061</guid>
      <pubDate>Tue, 11 Nov 2025 08:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/726061-tri-611-targets-alk-fusion-and-tki-resistant-nsclc</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Cancer/lung-cancer-tumor.webp?t=1756305616" type="image/jpeg" medium="image" fileSize="459046">
        <media:title type="plain">Illustration of lungs with cancer inset</media:title>
      </media:content>
    </item>
    <item>
      <title>MGC-026, a B7-H3-targeted ADC with potent activity in prostate cancer models</title>
      <description>
        <![CDATA[Researchers from Macrogenics Inc. presented preclinical efficacy data on MGC-026, an antibody-drug conjugate (ADC) consisting of a humanized monoclonal antibody (MGA017) targeting B7-H3, linked to a cytotoxic exatecan payload via a cleavable Val-Ala-PABC linker using Synaffix Glycoconnect technology.]]>
      </description>
      <guid>http://www.bioworld.com/articles/725932</guid>
      <pubDate>Mon, 10 Nov 2025 08:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/725932-mgc-026-a-b7-h3-targeted-adc-with-potent-activity-in-prostate-cancer-models</link>
    </item>
    <item>
      <title>ZE77-0273 shows broad activity against EGFR resistance mutations in NSCLC </title>
      <description>
        <![CDATA[Researchers from Chemdiv Inc. and Eilean Therapeutics LLC recently presented preclinical data on ZE77-0273, an AI-designed, reversible pan-EGFR inhibitor developed to address a key unmet need in the treatment of EGFR-mutant non-small-cell lung cancer.]]>
      </description>
      <guid>http://www.bioworld.com/articles/725930</guid>
      <pubDate>Mon, 10 Nov 2025 08:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/725930-ze77-0273-shows-broad-activity-against-egfr-resistance-mutations-in-nsclc</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/Lung-cancer-NSCLC-adenocarcinoma.webp?t=1673537444" type="image/png" medium="image" fileSize="1387734">
        <media:title type="plain">3D illustration and light micrograph of lung cancer.</media:title>
      </media:content>
    </item>
    <item>
      <title>Discovery of PSTA-2413, a potential best-in-class oral pan-RAS inhibitor</title>
      <description>
        <![CDATA[Prospect Therapeutics Inc.’s PSTA-2413 is a newly developed oral pan-RAS inhibitor that demonstrates selectivity over wild-type KRAS, along with strong in vitro potency and in vivo antitumor efficacy.]]>
      </description>
      <guid>http://www.bioworld.com/articles/725929</guid>
      <pubDate>Mon, 10 Nov 2025 08:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/725929-discovery-of-psta-2413-a-potential-best-in-class-oral-pan-ras-inhibitor</link>
    </item>
    <item>
      <title>Qurient presents data on QP-101, a dual-payload HER2-targeting ADC</title>
      <description>
        <![CDATA[Antibody-drug conjugates (ADCs) carrying topoisomerase I (TOP1) inhibitors, such as trastuzumab deruxtecan (T-DXd), have achieved notable clinical success in HER2-positive and HER2-low cancers, but their broader application is challenged by payload-related safety issues and emerging resistance.]]>
      </description>
      <guid>http://www.bioworld.com/articles/725912</guid>
      <pubDate>Fri, 07 Nov 2025 08:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/725912-qurient-presents-data-on-qp-101-a-dual-payload-her2-targeting-adc</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>MT-4561 exerts antitumor efficacy in NUT carcinoma</title>
      <description>
        <![CDATA[NUT carcinoma is a rare and aggressive cancer tied to the BRD4-NUT fusion protein, with poor prognosis and lack of effective therapy.]]>
      </description>
      <guid>http://www.bioworld.com/articles/725910</guid>
      <pubDate>Fri, 07 Nov 2025 08:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/725910-mt-4561-exerts-antitumor-efficacy-in-nut-carcinoma</link>
    </item>
    <item>
      <title>Acrivon Therapeutics reports preclinical data on ACR-2316</title>
      <description>
        <![CDATA[Acrivon Therapeutics Inc. has developed a new WEE1/PKMYT1 inhibitor, ACR-2316, to overcome the limitations observed with previous WEE1 and PKMYT1 inhibitors in the treatment of cancer.]]>
      </description>
      <guid>http://www.bioworld.com/articles/725856</guid>
      <pubDate>Thu, 06 Nov 2025 08:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/725856-acrivon-therapeutics-reports-preclinical-data-on-acr-2316</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>Accutar presents development of PI3Kα degrader-antibody conjugates</title>
      <description>
        <![CDATA[Accutar Biotechnology Inc. recently presented preclinical data on AC-4847, a first-in-class PI3Kα-targeting degrader-antibody conjugate (DAC) designed for selective treatment of PI3Kα-driven cancers.]]>
      </description>
      <guid>http://www.bioworld.com/articles/725855</guid>
      <pubDate>Thu, 06 Nov 2025 08:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/725855-accutar-presents-development-of-pi3k-degrader-antibody-conjugates</link>
    </item>
    <item>
      <title>CBB-120 shows potent TROP2 targeting with improved safety margin</title>
      <description>
        <![CDATA[Researchers at Crossbridge Bio Inc. have conducted preclinical evaluation of CBB-120, a novel TROP2-directed dual-payload ADC designed to combine TOP1i and ATR inhibitor (ATRi) mechanisms for enhanced therapeutic efficacy.]]>
      </description>
      <guid>http://www.bioworld.com/articles/725851</guid>
      <pubDate>Thu, 06 Nov 2025 08:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/725851-cbb-120-shows-potent-trop2-targeting-with-improved-safety-margin</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>Bispecific antibody-drug conjugate Gensci-143 shows promise in solid tumors</title>
      <description>
        <![CDATA[Changchung Genescience Pharmaceutical Co. Ltd., reported effects of the bispecific antibody-drug conjugate (ADC) of Gensci-143, is in metastatic castration-resistant prostate cancer (mCRPC) and other solid tumors.]]>
      </description>
      <guid>http://www.bioworld.com/articles/725837</guid>
      <pubDate>Wed, 05 Nov 2025 08:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/725837-bispecific-antibody-drug-conjugate-gensci-143-shows-promise-in-solid-tumors</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/Antibody-Drug-Conjugate-Molecules-ADC.webp?t=1671207526" type="image/png" medium="image" fileSize="887488">
        <media:title type="plain">3D illustration demonstrating antibody-drug conjugate.</media:title>
      </media:content>
    </item>
    <item>
      <title>Glycan-targeting ADC shows preclinical activity against HER2-low gastric cancer</title>
      <description>
        <![CDATA[Advanced gastric cancer continues to pose a significant medical challenge because of the scarcity of effective treatments and the frequent development of resistance to available drugs.]]>
      </description>
      <guid>http://www.bioworld.com/articles/725835</guid>
      <pubDate>Wed, 05 Nov 2025 08:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/725835-glycan-targeting-adc-shows-preclinical-activity-against-her2-low-gastric-cancer</link>
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