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    <title>CAR T</title>
    <description></description>
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    <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>TI-0032 induces B-cell depletion in preclinical setting</title>
      <description>Therorna Shanghai Co. Ltd. has presented data on TI-0032, an anti-CD19 CAR circular RNA therapeutic delivered by lipid nanoparticles (LNPs) for the treatment of autoimmune and hematological disorders.</description>
      <content:encoded>
        <![CDATA[Therorna Shanghai Co. Ltd. has presented data on TI-0032, an anti-CD19 CAR circular RNA therapeutic delivered by lipid nanoparticles (LNPs) for the treatment of autoimmune and hematological disorders.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731781</guid>
      <pubDate>Wed, 10 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731781-ti-0032-induces-b-cell-depletion-in-preclinical-setting</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Research-and-science/RNA-strand.webp?t=1609964773" type="image/png" medium="image" fileSize="440899">
        <media:title type="plain">RNA strand</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>Series A financing at Waypoint Bio supports CAR T programs</title>
      <description>Waypoint Bio has closed a $20 million series A financing round to support its work developing next-generation in vivo CAR T therapeutics for solid tumors using a platform that integrates AI, computer vision and spatial pooled screening.</description>
      <content:encoded>
        <![CDATA[Waypoint Bio has closed a $20 million series A financing round to support its work developing next-generation in vivo CAR T therapeutics for solid tumors using a platform that integrates AI, computer vision and spatial pooled screening.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731579</guid>
      <pubDate>Tue, 02 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731579-series-a-financing-at-waypoint-bio-supports-car-t-programs</link>
    </item>
    <item>
      <title>Oricell’s OriC-902 shows robust results in HCC</title>
      <description>At the ongoing European Association for the Study of the Liver 2026 annual meeting in Barcelona, researchers from Oricell Therapeutics Co. Ltd. presented data on a CAR T-cell approach targeting glypican 3 (GPC3) – OriC-902 – for the treatment of GPC3+ hepatocellular carcinoma (HCC).</description>
      <content:encoded>
        <![CDATA[At the ongoing European Association for the Study of the Liver 2026 annual meeting in Barcelona, researchers from Oricell Therapeutics Co. Ltd. presented data on a CAR T-cell approach targeting glypican 3 (GPC3) – OriC-902 – for the treatment of GPC3+ hepatocellular carcinoma (HCC).]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731475</guid>
      <pubDate>Thu, 28 May 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731475-oricells-oric-902-shows-robust-results-in-hcc</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Research-and-science/Red-CAR-T-cell-on-blue-blackground.webp?t=1719844699" type="image/jpeg" medium="image" fileSize="121460">
        <media:title type="plain">Red CAR T cell on blue blackground</media:title>
      </media:content>
    </item>
    <item>
      <title>Dual-targeting, rapamycin-enhanced CAR T for multiple myeloma</title>
      <description>Umoja Biopharma Inc. performed preclinical studies to evaluate the antitumor activity of UB-VV500, an off-the-shell lentiviral vector CAR T-cell product. It is based on its Vivovec technology and designed to engineer fully human anti-B-cell maturation antigen (BCMA)/G protein-coupled receptor class C group 5 member D (GPRC5D) dual-targeting chimeric antigen receptor (CAR) T cells, for the potential treatment of multiple myeloma (MM).</description>
      <content:encoded>
        <![CDATA[Umoja Biopharma Inc. performed preclinical studies to evaluate the antitumor activity of UB-VV500, an off-the-shell lentiviral vector CAR T-cell product. It is based on its Vivovec technology and designed to engineer fully human anti-B-cell maturation antigen (BCMA)/G protein-coupled receptor class C group 5 member D (GPRC5D) dual-targeting chimeric antigen receptor (CAR) T cells, for the potential treatment of multiple myeloma (MM).]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731254</guid>
      <pubDate>Fri, 22 May 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731254-dual-targeting-rapamycin-enhanced-car-t-for-multiple-myeloma</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Cancer/Multiple-myeloma-illustration2.webp?t=1627495152" type="image/png" medium="image" fileSize="407028">
        <media:title type="plain">Multiple myeloma illustration</media:title>
      </media:content>
    </item>
    <item>
      <title>FDA clears Qihan Biotech’s CAR T therapy QT-019C for clinic</title>
      <description>Hangzhou Qihan Biotech Co. Ltd. has obtained IND clearance from the FDA for QT-019C, a universal allogeneic CAR T-cell therapy for autoimmune diseases. QT-019C cell injection is an off-the-shelf allogeneic CAR T-cell therapy engineered from healthy donor leukapheresis products to stably express two distinct CARs targeting CD19 and BCMA.</description>
      <content:encoded>
        <![CDATA[Hangzhou Qihan Biotech Co. Ltd. has obtained IND clearance from the FDA for QT-019C, a universal allogeneic CAR T-cell therapy for autoimmune diseases. QT-019C cell injection is an off-the-shelf allogeneic CAR T-cell therapy engineered from healthy donor leukapheresis products to stably express two distinct CARs targeting CD19 and BCMA.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731233</guid>
      <pubDate>Thu, 21 May 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731233-fda-clears-qihan-biotechs-car-t-therapy-qt-019c-for-clinic</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Immune/Autoimmune-CAR-T-cell-therapy-rheumatoid-arthritis.webp?t=1766588083" type="image/jpeg" medium="image" fileSize="1074495">
        <media:title type="plain">Illustration of CAR T cell therapy in rheumatoid arthritis</media:title>
      </media:content>
    </item>
    <item>
      <title>MD Anderson gains IND nod for CD94-targeted CAR T therapy </title>
      <description>The University of Texas MD Anderson Cancer Center has received IND clearance from the FDA to initiate a phase I trial of a novel CAR T-cell therapy, JV-394, for patients with relapsed or refractory CD94-positive T/natural killer (NK) cell lymphomas.</description>
      <content:encoded>
        <![CDATA[The University of Texas MD Anderson Cancer Center has received IND clearance from the FDA to initiate a phase I trial of a novel CAR T-cell therapy, JV-394, for patients with relapsed or refractory CD94-positive T/natural killer (NK) cell lymphomas.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731141</guid>
      <pubDate>Mon, 18 May 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731141-md-anderson-gains-ind-nod-for-cd94-targeted-car-t-therapy</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-source/CAR-T-cell-attacking-a-cancer-cell.webp?t=1759242499" type="image/jpeg" medium="image" fileSize="874683">
        <media:title type="plain">Computer visualization of a CAR T cell attacking a cancer cell.</media:title>
        <media:description type="plain">Computer visualization of a CAR T cell attacking a cancer cell. Credit: C. Bock, CeMM.</media:description>
      </media:content>
    </item>
    <item>
      <title>Financing at Create Medicines to advance in vivo CAR therapies</title>
      <description>Create Medicines Inc. has closed a $122 million series B funding round to support progression of its pipeline of in vivo CAR therapies across autoimmune disease and oncology. The company’s proprietary mRNA-LNP platform directly engineers T cells, NK cells and myeloid cells inside the body to enable scalable, repeat-dose, off-the-shelf immunotherapies.</description>
      <content:encoded>
        <![CDATA[Create Medicines Inc. has closed a $122 million series B funding round to support progression of its pipeline of in vivo CAR therapies across autoimmune disease and oncology. The company’s proprietary mRNA-LNP platform directly engineers T cells, NK cells and myeloid cells inside the body to enable scalable, repeat-dose, off-the-shelf immunotherapies.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731122</guid>
      <pubDate>Fri, 15 May 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731122-financing-at-create-medicines-to-advance-in-vivo-car-therapies</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Money/dollar-sign-dropper.webp?t=1593437965" type="image/png" medium="image" fileSize="1167950">
        <media:title type="plain">Dollar sign dropper and test tube</media:title>
      </media:content>
    </item>
    <item>
      <title>ASGCT 2026: Circular RNA, the new beast in gene and cell therapy</title>
      <description>Circular RNA (circRNA) is not a new concept, but it is a novel strategy in the field of gene and cell therapy. While mRNA vaccines have revolutionized medicine, this RNA fragment without free ends surpasses their performance in both efficacy and durability, bringing it to the attention of several pioneering companies. The latest advances in circRNA presented at the 29th Annual Meeting of the American Society of Gene and Cell Therapy (ASGCT) clearly surpass the performance achieved with linear mRNA.</description>
      <content:encoded>
        <![CDATA[Circular RNA (circRNA) is not a new concept, but it is a novel strategy in the field of gene and cell therapy. While mRNA vaccines have revolutionized medicine, this RNA fragment without free ends surpasses their performance in both efficacy and durability, bringing it to the attention of several pioneering companies. The latest advances in circRNA presented at the 29th Annual Meeting of the American Society of Gene and Cell Therapy (ASGCT) clearly surpass the performance achieved with linear mRNA.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731268</guid>
      <pubDate>Wed, 13 May 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731268-asgct-2026-circular-rna-the-new-beast-in-gene-and-cell-therapy</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/glowing-circle-illustration.webp?t=1778686093" type="image/png" medium="image" fileSize="673869">
        <media:title type="plain">Illustration of a glowing circle to represent circRNA</media:title>
      </media:content>
    </item>
    <item>
      <title>Seed financing at Parcelbio to advance mRNA medicines</title>
      <description>Parcelbio has raised $13 million in seed financing to continue its development of a new class of potent and durable mRNA medicines. The financing will support development of Parcelbio’s proprietary APEXm (Amplified and Prolonged EXpression mRNA) platform and advance its pipeline, including its lead in vivo CAR T program for autoimmune disease.</description>
      <content:encoded>
        <![CDATA[Parcelbio has raised $13 million in seed financing to continue its development of a new class of potent and durable mRNA medicines. The financing will support development of Parcelbio’s proprietary APEXm (Amplified and Prolonged EXpression mRNA) platform and advance its pipeline, including its lead in vivo CAR T program for autoimmune disease.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/730949</guid>
      <pubDate>Fri, 08 May 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/730949-seed-financing-at-parcelbio-to-advance-mrna-medicines</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>PD-L1 CAR T cells simultaneously target tumor cells and the immunosuppressive TME in CCA</title>
      <description>Although antibodies to PD-L1 are used in the clinic, their benefit is limited by immune exclusion within the local microenvironment. Objective response rates with anti-PD-L1 monotherapy are low due to the heterogeneity of PD-L1 expression, low tumor mutational burden and the highly immunosuppressive tumor microenvironment (TME) of cholangiocarcinoma (CCA).</description>
      <content:encoded>
        <![CDATA[<p>Although antibodies to PD-L1 are used in the clinic, their benefit is limited by immune exclusion within the local microenvironment. Objective response rates with anti-PD-L1 monotherapy are low due to the heterogeneity of PD-L1 expression, low tumor mutational burden and the highly immunosuppressive tumor microenvironment (TME) of cholangiocarcinoma (CCA).</p>]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/730516</guid>
      <pubDate>Mon, 20 Apr 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/730516-pd-l1-car-t-cells-simultaneously-target-tumor-cells-and-the-immunosuppressive-tme-in-cca</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/Chimeric-Antigen-Receptor-CAR-T-cell-therapy.webp?t=1776698265" type="image/jpeg" medium="image" fileSize="230403">
        <media:title type="plain">Illustration of CAR T cells</media:title>
      </media:content>
    </item>
    <item>
      <title>CGT-19 as an approach to expand CAR T-cell therapy accessibility</title>
      <description>The use of CAR T-cell therapy has transformed outcomes for relapsed or refractory B-cell malignancies, but access to it remains extremely limited in some countries. Cartogene Therapeutics Pvt Ltd. aimed to address this need by in-licensing CGT-19, a CD19 CAR T construct from Vector Biomed Inc.</description>
      <content:encoded>
        <![CDATA[The use of CAR T-cell therapy has transformed outcomes for relapsed or refractory B-cell malignancies, but access to it remains extremely limited in some countries. Cartogene Therapeutics Pvt Ltd. aimed to address this need by in-licensing CGT-19, a CD19 CAR T construct from Vector Biomed Inc.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/730015</guid>
      <pubDate>Mon, 30 Mar 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/730015-cgt-19-as-an-approach-to-expand-car-t-cell-therapy-accessibility</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/CAR-CD19-binding.webp?t=1665503757" type="image/png" medium="image" fileSize="2301092">
        <media:title type="plain">CD19 binding </media:title>
      </media:content>
    </item>
    <item>
      <title>CAR T targeting CD44E splicing variant shows potential for HCC treatment</title>
      <description>Previously, Chinese researchers used long-read RNA sequencing to identify a unique alternative splicing variant of CD44 transmembrane protein, named CD44E, which is highly expressed in hepatocellular carcinoma (HCC) tumors compared to adjacent nontumoral liver tissues. In a new study, the team analyzed the Genotype-Tissue Expression (GTEx) database and confirmed that CD44E expression is limited in essential normal organs, while CD44S standard isoform is broadly expressed on most cell types.</description>
      <content:encoded>
        <![CDATA[Previously, Chinese researchers used long-read RNA sequencing to identify a unique alternative splicing variant of CD44 transmembrane protein, named CD44E, which is highly expressed in hepatocellular carcinoma (HCC) tumors compared to adjacent nontumoral liver tissues. In a new study, the team analyzed the Genotype-Tissue Expression (GTEx) database and confirmed that CD44E expression is limited in essential normal organs, while CD44S standard isoform is broadly expressed on most cell types.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/730000</guid>
      <pubDate>Fri, 27 Mar 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/730000-car-t-targeting-cd44e-splicing-variant-shows-potential-for-hcc-treatment</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Cancer/HCC-hepatocellular-carcinoma-liver-cancer.webp?t=1722888982" type="image/jpeg" medium="image" fileSize="265067">
        <media:title type="plain">Illustration of tumor in the liver</media:title>
      </media:content>
    </item>
    <item>
      <title>Approach to enhance CAR T efficacy in infectious diseases and cancer</title>
      <description>CAR T-cell therapy can be applied to treat some chronic infectious diseases, particularly to provide a functional cure for HIV-1 in people living with HIV. However, the effectiveness of CAR T cells for persistent suppression of HIV still faces many constraints, including the high mutation rate of reverse transcriptase, which enables the emergence of immune escape viral variants.</description>
      <content:encoded>
        <![CDATA[CAR T-cell therapy can be applied to treat some chronic infectious diseases, particularly to provide a functional cure for HIV-1 in people living with HIV. However, the effectiveness of CAR T cells for persistent suppression of HIV still faces many constraints, including the high mutation rate of reverse transcriptase, which enables the emergence of immune escape viral variants.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/729932</guid>
      <pubDate>Thu, 26 Mar 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/729932-approach-to-enhance-car-t-efficacy-in-infectious-diseases-and-cancer</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/NIH-NIAID-HIV.webp?t=1724423365" type="image/jpeg" medium="image" fileSize="446919">
        <media:title type="plain">Transmission electron micrograph of HIV particles</media:title>
        <media:description type="plain">HIV-1 virus particles (colorized yellow) replicating from an HIV-infected H9 T cell (pink). Credit: NIAID, NIH</media:description>
      </media:content>
    </item>
    <item>
      <title>Overt Bio advances OVT-101 toward clinic</title>
      <description>Overt Bio Inc. is advancing lead asset OVT-101 toward the clinic. The allogeneic, potential first-in-class, off-the-shelf γδ CAR T therapy targets claudin-6, which is present in the majority of ovarian cancers and several other solid tumors.</description>
      <content:encoded>
        <![CDATA[Overt Bio Inc. is advancing lead asset OVT-101 toward the clinic. The allogeneic, potential first-in-class, off-the-shelf γδ CAR T therapy targets claudin-6, which is present in the majority of ovarian cancers and several other solid tumors.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/729861</guid>
      <pubDate>Tue, 24 Mar 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/729861-overt-bio-advances-ovt-101-toward-clinic</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Sexual-health/Ovarian-cancer.webp?t=1589293151" type="image/png" medium="image" fileSize="197603">
        <media:title type="plain">Ovarian cancer illustration</media:title>
      </media:content>
    </item>
    <item>
      <title>Nanobody CAR construct targeting CLL-1 shows preclinical activity against AML</title>
      <description>Researchers from the Sino-American Cancer Foundation and Taipei Medical University have developed a novel nanobody-based CAR T-cell platform directed against C-type lectin-like molecule-1 (CLL-1) for the possible treatment of acute myeloid leukemia (AML).</description>
      <content:encoded>
        <![CDATA[Researchers from the Sino-American Cancer Foundation and Taipei Medical University have developed a novel nanobody-based CAR T-cell platform directed against C-type lectin-like molecule-1 (CLL-1) for the possible treatment of acute myeloid leukemia (AML).]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/729694</guid>
      <pubDate>Wed, 18 Mar 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/729694-nanobody-car-construct-targeting-cll-1-shows-preclinical-activity-against-aml</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Research-and-science/Nanoparticle-illustration.webp?t=1735833924" type="image/jpeg" medium="image" fileSize="311893">
        <media:title type="plain">Nanoparticle illustration </media:title>
      </media:content>
    </item>
    <item>
      <title>DR5 as promising CAR T-cell target allowing inhibition of tumor cells and MDSCs</title>
      <description>University of Pennsylvania researchers investigated death receptor 5 (DR5 or CD262) as a chimeric antigen receptor (CAR) target for solid tumors.</description>
      <content:encoded>
        <![CDATA[University of Pennsylvania researchers investigated death receptor 5 (DR5 or CD262) as a chimeric antigen receptor (CAR) target for solid tumors.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/729594</guid>
      <pubDate>Wed, 11 Mar 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/729594-dr5-as-promising-car-t-cell-target-allowing-inhibition-of-tumor-cells-and-mdscs</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>HITting solid tumors with a closer look and a stronger CAR T cell</title>
      <description>CAR T cells have been groundbreaking for the treatment of B-cell cancers. But 8 years after Kymriah (tisagenlecleucel, Novartis AG) became the first CAR T-cell therapy to be approved, there are no CAR Ts approved for solid tumors.</description>
      <content:encoded>
        <![CDATA[CAR T cells have been groundbreaking for the treatment of B-cell cancers. But 8 years after Kymriah (tisagenlecleucel, Novartis AG) became the first CAR T-cell therapy to be approved, there are no CAR Ts approved for solid tumors.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/729130</guid>
      <pubDate>Mon, 02 Mar 2026 08:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/729130-hitting-solid-tumors-with-a-closer-look-and-a-stronger-car-t-cell</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Research-and-science/CAR-T-cell.webp?t=1671545711" type="image/png" medium="image" fileSize="497911">
        <media:title type="plain">CAR T cell attacking cancer cells</media:title>
        <media:description type="plain">Illustration of CAR T cell attacking cancer cells. 
Credit: La Jolla Institute
</media:description>
      </media:content>
    </item>
    <item>
      <title>Nanobody-based CLL-1-targeted CAR T cells enhance AML killing with reduced off-target effects</title>
      <description>To overcome the challenges of current CAR T-cell strategies and enhance their efficacy and specificity for acute myeloid leukemia, researchers at the Sino-American Cancer Foundation and collaborating institutions have developed a nanobody-based CAR T-cell platform directed against C-type lectin-like molecule-1 (CLL-1).</description>
      <content:encoded>
        <![CDATA[To overcome the challenges of current CAR T-cell strategies and enhance their efficacy and specificity for acute myeloid leukemia, researchers at the Sino-American Cancer Foundation and collaborating institutions have developed a nanobody-based CAR T-cell platform directed against C-type lectin-like molecule-1 (CLL-1).]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/729057</guid>
      <pubDate>Thu, 26 Feb 2026 08:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/729057-nanobody-based-cll-1-targeted-car-t-cells-enhance-aml-killing-with-reduced-off-target-effects</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Cancer/Acute-myeloid-leukemia-(AML).webp?t=1670008838" type="image/png" medium="image" fileSize="289455">
        <media:title type="plain">Acute myeloid leukemia</media:title>
      </media:content>
    </item>
    <item>
      <title>TRX-319 silences autoreactive B and T cells in multiple sclerosis</title>
      <description>Researchers from Tr1x Inc. presented the development of TRX-319, a novel allogeneic regulatory T-cell therapy designed for the treatment of autoimmune disorders.</description>
      <content:encoded>
        <![CDATA[Researchers from Tr1x Inc. presented the development of TRX-319, a novel allogeneic regulatory T-cell therapy designed for the treatment of autoimmune disorders.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/728788</guid>
      <pubDate>Wed, 11 Feb 2026 08:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/728788-trx-319-silences-autoreactive-b-and-t-cells-in-multiple-sclerosis</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/Lymphocyte-tcell-bcell.webp?t=1726498696" type="image/jpeg" medium="image" fileSize="222409">
        <media:title type="plain">Illustration of lymphocytes</media:title>
      </media:content>
    </item>
    <item>
      <title>Tempest Therapeutics outlines plans for acquired CAR T assets</title>
      <description>Tempest Therapeutics Inc. has outlined plans to advance its newly acquired CAR T assets. While prioritizing development of its clinical-stage dual-targeting CD19/BCMA CAR-T program, TPST-2003 (ERI-2003), the company will also expand its portfolio into next-generation modalities.</description>
      <content:encoded>
        <![CDATA[Tempest Therapeutics Inc. has outlined plans to advance its newly acquired CAR T assets. While prioritizing development of its clinical-stage dual-targeting CD19/BCMA CAR-T program, TPST-2003 (ERI-2003), the company will also expand its portfolio into next-generation modalities.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/728785</guid>
      <pubDate>Wed, 11 Feb 2026 08:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/728785-tempest-therapeutics-outlines-plans-for-acquired-car-t-assets</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/Cancer-Chimeric-Antigen-Receptor-CAR-T-Cell.webp?t=1691077403" type="image/jpeg" medium="image" fileSize="249886">
        <media:title type="plain">3D rendering of CAR T therapy in cell</media:title>
      </media:content>
    </item>
    <item>
      <title>In vivo CAR T cells reduce liver fibrosis</title>
      <description>Liver fibrosis in the course of metabolic dysfunction-associated steatohepatitis could be significantly reduced using CAR T-cells generated in vivo. Scientists at the Icahn School of Medicine at Mount Sinai have developed an experimental cell therapy that eliminates only one type of liver cell, the stellate cells that express fibroblast activation protein alpha. This strategy not only reduced fibrosis but also reversed liver damage.</description>
      <content:encoded>
        <![CDATA[Liver fibrosis in the course of metabolic dysfunction-associated steatohepatitis could be significantly reduced using CAR T-cells generated in vivo. Scientists at the Icahn School of Medicine at Mount Sinai have developed an experimental cell therapy that eliminates only one type of liver cell, the stellate cells that express fibroblast activation protein alpha. This strategy not only reduced fibrosis but also reversed liver damage.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/728597</guid>
      <pubDate>Mon, 02 Feb 2026 08:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/728597-in-vivo-car-t-cells-reduce-liver-fibrosis</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Gastrointestinal/Liver-damage-fibrosis-cirrhosis.webp?t=1769528466" type="image/jpeg" medium="image" fileSize="677639">
        <media:title type="plain">Art concept for liver damage, such as fatty liver, fibrosis or cirrhosis</media:title>
      </media:content>
    </item>
    <item>
      <title>Selective CAR T targeting mutant CALR shows preclinical activity against MPNs</title>
      <description>Despite the successful application of adoptive T-cell transfer with chimeric antigen receptor (CAR)-engineered T cells for the treatment of various hematologic malignancies, several other hematologic disorders, such as BCR::ABL1-negative myeloproliferative neoplasms (MPNs), still lack effective treatment options.</description>
      <content:encoded>
        <![CDATA[Despite the successful application of adoptive T-cell transfer with chimeric antigen receptor (CAR)-engineered T cells for the treatment of various hematologic malignancies, several other hematologic disorders, such as BCR::ABL1-negative myeloproliferative neoplasms (MPNs), still lack effective treatment options.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/728399</guid>
      <pubDate>Wed, 28 Jan 2026 08:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/728399-selective-car-t-targeting-mutant-calr-shows-preclinical-activity-against-mpns</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>In vivo CAR T cells reduce liver fibrosis</title>
      <description>Liver fibrosis in the course of metabolic dysfunction-associated steatohepatitis (MASH) could be significantly reduced using CAR T-cells generated in vivo. Scientists at the Icahn School of Medicine at Mount Sinai have developed an experimental cell therapy that eliminates only one type of liver cell, the stellate cells that express fibroblast activation protein alpha (FAP). This strategy not only reduced fibrosis but also reversed liver damage.</description>
      <content:encoded>
        <![CDATA[Liver fibrosis in the course of metabolic dysfunction-associated steatohepatitis (MASH) could be significantly reduced using CAR T-cells generated in vivo. Scientists at the Icahn School of Medicine at Mount Sinai have developed an experimental cell therapy that eliminates only one type of liver cell, the stellate cells that express fibroblast activation protein alpha (FAP). This strategy not only reduced fibrosis but also reversed liver damage.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/728373</guid>
      <pubDate>Tue, 27 Jan 2026 08:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/728373-in-vivo-car-t-cells-reduce-liver-fibrosis</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Gastrointestinal/Liver-damage-fibrosis-cirrhosis.webp?t=1769528466" type="image/jpeg" medium="image" fileSize="677639">
        <media:title type="plain">Art concept for liver damage, such as fatty liver, fibrosis or cirrhosis</media:title>
      </media:content>
    </item>
    <item>
      <title>Dispatch Bio’s DISP-10 gains IND clearance for solid tumors</title>
      <description>Dispatch Biotherapeutics Inc. has obtained IND clearance from the FDA for DISP-10, enabling the initiation of a phase I study in patients with solid tumors. Initial clinical evaluation will begin in gastrointestinal cancers, with plans to expand into multiple additional solid tumor indications following clinical proof of concept.</description>
      <content:encoded>
        <![CDATA[Dispatch Biotherapeutics Inc. has obtained IND clearance from the FDA for DISP-10, enabling the initiation of a phase I study in patients with solid tumors. Initial clinical evaluation will begin in gastrointestinal cancers, with plans to expand into multiple additional solid tumor indications following clinical proof of concept.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/727933</guid>
      <pubDate>Tue, 13 Jan 2026 08:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/727933-dispatch-bios-disp-10-gains-ind-clearance-for-solid-tumors</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/cancer-tumor-crosshairs-target.webp?t=1711120097" type="image/jpeg" medium="image" fileSize="283816">
        <media:title type="plain">Concept art for targeting cancer</media:title>
      </media:content>
    </item>
    <item>
      <title>Development and characterization of anti-CD19 in vivo CAR T therapy</title>
      <description>Shenzhen Grit Biotechnology Co. Ltd. and Shanghai Vitalgen Biopharma Co. Ltd. recently presented their work to develop and evaluate a novel anti-CD19 in vivo CAR T candidate, named GT-801.</description>
      <content:encoded>
        <![CDATA[Shenzhen Grit Biotechnology Co. Ltd. and Shanghai Vitalgen Biopharma Co. Ltd. recently presented their work to develop and evaluate a novel anti-CD19 in vivo CAR T candidate, named GT-801.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/727466</guid>
      <pubDate>Mon, 29 Dec 2025 08:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/727466-development-and-characterization-of-anti-cd19-in-vivo-car-t-therapy</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Research-and-science/CAR-T-cell.webp?t=1671545711" type="image/png" medium="image" fileSize="497911">
        <media:title type="plain">CAR T cell attacking cancer cells</media:title>
        <media:description type="plain">Illustration of CAR T cell attacking cancer cells. 
Credit: La Jolla Institute
</media:description>
      </media:content>
    </item>
    <item>
      <title>IMV-101 shows promise for B-cell malignancies</title>
      <description>IMV-101 is a new CAR T-cell therapy targeting CD19 developed by Suzhou Immunofoco Biotechnology Co. Ltd. for the potential treatment of B-cell malignancies and autoimmune diseases. The company has presented results of the evaluation of its in vitro and in vivo properties.</description>
      <content:encoded>
        <![CDATA[IMV-101 is a new CAR T-cell therapy targeting CD19 developed by Suzhou Immunofoco Biotechnology Co. Ltd. for the potential treatment of B-cell malignancies and autoimmune diseases. The company has presented results of the evaluation of its in vitro and in vivo properties.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/727445</guid>
      <pubDate>Wed, 24 Dec 2025 08:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/727445-imv-101-shows-promise-for-b-cell-malignancies</link>
    </item>
    <item>
      <title>Further financing at Vyriad to advance VV-169 into clinic</title>
      <description>Vyriad Inc. has announced the closing of a $25 million final tranche to its series B financing, bringing the total series B round to $85 million. This additional funding will support first-in-human testing of VV-169, Vyriad’s in vivo CAR T candidate, in patients with relapsed or treatment-refractory multiple myeloma.</description>
      <content:encoded>
        <![CDATA[Vyriad Inc. has announced the closing of a $25 million final tranche to its series B financing, bringing the total series B round to $85 million. This additional funding will support first-in-human testing of VV-169, Vyriad’s in vivo CAR T candidate, in patients with relapsed or treatment-refractory multiple myeloma.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/727442</guid>
      <pubDate>Wed, 24 Dec 2025 08:00:00 -0500</pubDate>
      <link>https://www.bioworld.com/articles/727442-further-financing-at-vyriad-to-advance-vv-169-into-clinic</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Research-and-science/RD-money.webp?t=1588877677" type="image/png" medium="image" fileSize="578436">
        <media:title type="plain">Dollar sign droplet above test tube</media:title>
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