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    <title>European Hematology Association</title>
    <description></description>
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    <item>
      <title>Viva in vivo! At EHA, in vivo CAR T data continues to impress</title>
      <description>Treatment with first-generation CAR T cells regularly sent patients to the intensive care unit. Now, investigators are envisioning a future where CAR T treatment could occur on an outpatient basis.</description>
      <content:encoded>
        <![CDATA[Treatment with first-generation CAR T cells regularly sent patients to the intensive care unit. Now, investigators are envisioning a future where CAR T treatment could occur on an outpatient basis. ]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731988</guid>
      <pubDate>Tue, 16 Jun 2026 11:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731988-viva-in-vivo-at-eha-in-vivo-car-t-data-continues-to-impress</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Hematologic/CAR-T-and-red-blood-cells.webp?t=1781543267" type="image/jpeg" medium="image" fileSize="110320">
        <media:title type="plain">CAR T and red blood cells</media:title>
      </media:content>
    </item>
    <item>
      <title>For clonal hematopoiesis, epigenetics can be in driver’s seat </title>
      <description>Clonal hematopoiesis (CH), where few blood stem cells produce a significant fraction of mature blood cells that are genetically identical, is partly an inevitable feature of aging. Certainly, it is near universal in those older than 60. CH is not itself a disease, but 1%-2% of CH cases progress to acute myeloid leukemia, and it raises the risk of some other types of cancer as well. A total of eight genes are responsible for 95% of CH cases, George Vassiliou told the audience in Saturday’s plenary session at the 2026 Annual Congress of the European Hematology Association (EHA 2026).</description>
      <content:encoded>
        <![CDATA[Clonal hematopoiesis (CH), where few blood stem cells produce a significant fraction of mature blood cells that are genetically identical, is partly an inevitable feature of aging. Certainly, it is near universal in those older than 60. CH is not itself a disease, but 1%-2% of CH cases progress to acute myeloid leukemia, and it raises the risk of some other types of cancer as well. A total of eight genes are responsible for 95% of CH cases, George Vassiliou told the audience in Saturday’s plenary session at the 2026 Annual Congress of the European Hematology Association (EHA 2026).]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731978</guid>
      <pubDate>Tue, 16 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731978-for-clonal-hematopoiesis-epigenetics-can-be-in-drivers-seat</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Hematologic/Red-blood-cell-DNA.webp?t=1623189044" type="image/png" medium="image" fileSize="588772">
        <media:title type="plain">Red blood cells, DNA</media:title>
      </media:content>
    </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>CGT-1145 shows disease-modifying potential in JAK2 V617F models</title>
      <description>At the recently concluded congress of the European Hematology Association, researchers at Cogent Biosciences Inc. presented preclinical data on CGT-1145, a JAK2 V617F-mutant-selective inhibitor designed to preferentially target the mutant kinase while sparing wild-type JAK2.</description>
      <content:encoded>
        <![CDATA[At the recently concluded congress of the European Hematology Association, researchers at Cogent Biosciences Inc. presented preclinical data on CGT-1145, a JAK2 V617F-mutant-selective inhibitor designed to preferentially target the mutant kinase while sparing wild-type JAK2.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731959</guid>
      <pubDate>Tue, 16 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731959-cgt-1145-shows-disease-modifying-potential-in-jak2-v617f-models</link>
    </item>
    <item>
      <title>For clonal hematopoiesis, epigenetics can be in driver’s seat </title>
      <description>Clonal hematopoiesis (CH), where few blood stem cells produce a significant fraction of mature blood cells that are genetically identical, is partly an inevitable feature of aging. Certainly, it is near universal in those older than 60. CH is not itself a disease, but 1%-2% of CH cases progress to acute myeloid leukemia, and it raises the risk of some other types of cancer as well. A total of eight genes are responsible for 95% of CH cases, George Vassiliou told the audience in Saturday’s plenary session at the 2026 Annual Congress of the European Hematology Association (EHA 2026).</description>
      <content:encoded>
        <![CDATA[Clonal hematopoiesis (CH), where few blood stem cells produce a significant fraction of mature blood cells that are genetically identical, is partly an inevitable feature of aging. Certainly, it is near universal in those older than 60. CH is not itself a disease, but 1%-2% of CH cases progress to acute myeloid leukemia, and it raises the risk of some other types of cancer as well. A total of eight genes are responsible for 95% of CH cases, George Vassiliou told the audience in Saturday’s plenary session at the 2026 Annual Congress of the European Hematology Association (EHA 2026).]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731932</guid>
      <pubDate>Mon, 15 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731932-for-clonal-hematopoiesis-epigenetics-can-be-in-drivers-seat</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Hematologic/Red-blood-cell-DNA.webp?t=1623189044" type="image/png" medium="image" fileSize="588772">
        <media:title type="plain">Red blood cells, DNA</media:title>
      </media:content>
    </item>
    <item>
      <title>Viva in vivo! At EHA, in vivo CAR T data continues to impress</title>
      <description>Treatment with first-generation CAR T cells regularly sent patients to the intensive care unit. Now, investigators are envisioning a future where CAR T treatment could occur on an outpatient basis. At Sunday’s late-breaking oral session of the 2026 Annual Congress of the European Hematology Association (EHA2026), Lei Fan told his audience that the first-in-human data “support further development of LB-2501 as a potential first-in-class, off-the-shelf, single infusion, no lymphodepletion, outpatient use CAR T therapy.” Fan is a professor of hematology at the First Affiliated Hospital of Nanjing Medical University.</description>
      <content:encoded>
        <![CDATA[Treatment with first-generation CAR T cells regularly sent patients to the intensive care unit. Now, investigators are envisioning a future where CAR T treatment could occur on an outpatient basis. At Sunday’s late-breaking oral session of the 2026 Annual Congress of the European Hematology Association (EHA2026), Lei Fan told his audience that the first-in-human data “support further development of LB-2501 as a potential first-in-class, off-the-shelf, single infusion, no lymphodepletion, outpatient use CAR T therapy.” Fan is a professor of hematology at the First Affiliated Hospital of Nanjing Medical University.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731976</guid>
      <pubDate>Sun, 14 Jun 2026 11:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731976-viva-in-vivo-at-eha-in-vivo-car-t-data-continues-to-impress</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Hematologic/CAR-T-and-red-blood-cells.webp?t=1781543267" type="image/jpeg" medium="image" fileSize="110320">
        <media:title type="plain">CAR T and red blood cells</media:title>
      </media:content>
    </item>
    <item>
      <title>EHA 2026: With new lenses, a changing view on pediatric cancers</title>
      <description>In the most simplistic view, adult cancers occur because “immature cells are exposed to mutagens, accumulate mutations, and across life ultimately transform into cancer cells,” Franck Bourdeaut told his audience at the 2026 Annual Congress of the European Hematology Association (EHA 2026). “On the contrary, in pediatric cancers, it is assumed that very few mutations are responsible for a maturation block, make these cells derail from their normal differentiation trajectory and ultimately result in an early onset typical pediatric cancer.”</description>
      <content:encoded>
        <![CDATA[In the most simplistic view, adult cancers occur because “immature cells are exposed to mutagens, accumulate mutations, and across life ultimately transform into cancer cells,” Franck Bourdeaut told his audience at the 2026 Annual Congress of the European Hematology Association (EHA 2026). “On the contrary, in pediatric cancers, it is assumed that very few mutations are responsible for a maturation block, make these cells derail from their normal differentiation trajectory and ultimately result in an early onset typical pediatric cancer.”]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731957</guid>
      <pubDate>Fri, 12 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731957-eha-2026-with-new-lenses-a-changing-view-on-pediatric-cancers</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Research-and-science/Genome-sequence-map.webp?t=1754944094" type="image/jpeg" medium="image" fileSize="562692">
        <media:title type="plain">Genome sequence map</media:title>
      </media:content>
    </item>
    <item>
      <title>Enliven’s phase I CML data Enable phase III with BCR/ABL1 bid</title>
      <description>Tolerability is a key factor in the appeal of Enliven Therapeutics Inc.’s ELVN-001 for previously treated chronic myeloid leukemia (CML), which yielded positive updated phase I data from the Enable trial. Dennis Kim, hematologist from Princess Margaret Cancer Center in Toronto, said he would use the drug for a patient “who doesn’t have any other options.”</description>
      <content:encoded>
        <![CDATA[Tolerability is a key factor in the appeal of Enliven Therapeutics Inc.’s ELVN-001 for previously treated chronic myeloid leukemia (CML), which yielded positive updated phase I data from the Enable trial. Dennis Kim, hematologist from Princess Margaret Cancer Center in Toronto, said he would use the drug for a patient “who doesn’t have any other options.”]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/731799</guid>
      <pubDate>Thu, 11 Jun 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/731799-enlivens-phase-i-cml-data-enable-phase-iii-with-bcr-abl1-bid</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Cancer/Chronic-myeloid-leukemia-.webp?t=1781213329" type="image/jpeg" medium="image" fileSize="170113">
        <media:title type="plain">Microscopic image of chronic myeloid leukemia </media:title>
      </media:content>
    </item>
    <item>
      <title>Rgenta’s RGT-61159 shows promise for MYB-expressing cancers</title>
      <description>MYB is an oncogenic transcription factor that is often aberrantly expressed in hematologic malignancies, mostly in acute myeloid leukemia (AML). Rgenta Therapeutics Inc. recently presented data for RGT-61159, a potent and selective MYB inhibitor compound that demonstrated cell killing across a panel of MYB-overexpressing leukemic cell lines.</description>
      <content:encoded>
        <![CDATA[MYB is an oncogenic transcription factor that is often aberrantly expressed in hematologic malignancies, mostly in acute myeloid leukemia (AML). Rgenta Therapeutics Inc. recently presented data for RGT-61159, a potent and selective MYB inhibitor compound that demonstrated cell killing across a panel of MYB-overexpressing leukemic cell lines.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/721418</guid>
      <pubDate>Wed, 25 Jun 2025 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/721418-rgentas-rgt-61159-shows-promise-for-myb-expressing-cancers</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Cancer/Leukemia.webp?t=1588713330" type="image/png" medium="image" fileSize="421137">
        <media:title type="plain">Leukemia illustration</media:title>
      </media:content>
    </item>
    <item>
      <title>APG-5918 shows potent activity against T-cell lymphoma</title>
      <description>Therapies against aggressive T-cell lymphomas (TCLs) are limited and treatment resistance to histone deacetylase (HDAC) inhibitors often occurs. Polycomb protein EED is a key member of the polycomb repressive complex 2 (PRC2) complex and is an attractive therapeutic target for TCLs. APG-5918 is an EED inhibitor from Ascentage Pharma Group International Co. Ltd. that has been proven to disrupt the PRC2 functioning and has been tested in preclinical TCL models as a promising approach.</description>
      <content:encoded>
        <![CDATA[Therapies against aggressive T-cell lymphomas (TCLs) are limited and treatment resistance to histone deacetylase (HDAC) inhibitors often occurs. Polycomb protein EED is a key member of the polycomb repressive complex 2 (PRC2) complex and is an attractive therapeutic target for TCLs. APG-5918 is an EED inhibitor from Ascentage Pharma Group International Co. Ltd. that has been proven to disrupt the PRC2 functioning and has been tested in preclinical TCL models as a promising approach.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/721395</guid>
      <pubDate>Mon, 23 Jun 2025 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/721395-apg-5918-shows-potent-activity-against-t-cell-lymphoma</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Cancer/leukemia-lymphoma-blood-cancer.webp?t=1724424490" type="image/jpeg" medium="image" fileSize="506006">
        <media:title type="plain">Art concept for hematologic cancer</media:title>
      </media:content>
    </item>
    <item>
      <title>COG5 unveiled as a therapeutic target in multiple myeloma</title>
      <description>Multiple myeloma bone disease (MBD) lacks effective biomarkers; recent evidence involves exosomal circRNAs in the progression of cancer, but their roles in the field have not been deeply explored. The aim of this study was to explore the role of component of oligomeric golgi complex 5 (COG5) and shed light on its osteolytic mechanism.</description>
      <content:encoded>
        <![CDATA[Multiple myeloma bone disease (MBD) lacks effective biomarkers; recent evidence involves exosomal circRNAs in the progression of cancer, but their roles in the field have not been deeply explored. The aim of this study was to explore the role of component of oligomeric golgi complex 5 (COG5) and shed light on its osteolytic mechanism.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/721372</guid>
      <pubDate>Fri, 20 Jun 2025 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/721372-cog5-unveiled-as-a-therapeutic-target-in-multiple-myeloma</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>BAL-0891 induces potent antileukemic effect in preclinical AML</title>
      <description>Sillajen Inc. has recently presented data regarding their threonine tyrosine kinase (TTK) and Polo-like kinase 1 (PLK1) dual inhibitor BAL-0891 as a therapeutic approach for acute myeloid leukemia (AML) treatment. The compound was tested both in vitro and in vivo in the preclinical setting.</description>
      <content:encoded>
        <![CDATA[<p>Sillajen Inc. has recently presented data regarding their threonine tyrosine kinase (TTK) and Polo-like kinase 1 (PLK1) dual inhibitor BAL-0891 as a therapeutic approach for acute myeloid leukemia (AML) treatment. The compound was tested both in vitro and in vivo in the preclinical setting.</p>]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/721355</guid>
      <pubDate>Thu, 19 Jun 2025 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/721355-bal-0891-induces-potent-antileukemic-effect-in-preclinical-aml</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Cancer/Acute-myeloid-leukemia.webp?t=1588879994" type="image/png" medium="image" fileSize="485631">
        <media:title type="plain">Acute myeloid leukemia illustration</media:title>
      </media:content>
    </item>
    <item>
      <title>HPK1 inhibitor BGB-15025 exerts antileukemic activity in mice</title>
      <description>Despite an initial complete remission of 60%-80% in patients receiving anthracycline/cytarabine induction, acute myeloid leukemia (AML) shows a suboptimal long-term outcome rate. Serine/threonine kinase HPK1 has emerged as a promising therapeutic target, demonstrating pan-cancer prognostic significance.</description>
      <content:encoded>
        <![CDATA[Despite an initial complete remission of 60%-80% in patients receiving anthracycline/cytarabine induction, acute myeloid leukemia (AML) shows a suboptimal long-term outcome rate. Serine/threonine kinase HPK1 has emerged as a promising therapeutic target, demonstrating pan-cancer prognostic significance.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/721297</guid>
      <pubDate>Wed, 18 Jun 2025 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/721297-hpk1-inhibitor-bgb-15025-exerts-antileukemic-activity-in-mice</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/AML-cells-acute-myeloid-leukemia.webp?t=1663340307" type="image/png" medium="image" fileSize="1258935">
        <media:title type="plain">Microscopic image of acute myeloid leukemia (AML) cells.</media:title>
        <media:description type="plain">Acute myeloid leukemia cells. Credit: Cincinnati Children's
</media:description>
      </media:content>
    </item>
    <item>
      <title>At EHA 2025, ways to bring immune therapy to AML</title>
      <description>“The lack of therapeutic precision in treatment of myeloid malignancies is in sharp contrast with the fact that myeloid cancers represent the perhaps best characterized cancers of all at the cellular, molecular, and genetic levels,” Johanna Olweus told her audience at the Friday plenary session of the European Hematology Association 2025 Annual Congress.</description>
      <content:encoded>
        <![CDATA[“The lack of therapeutic precision in treatment of myeloid malignancies is in sharp contrast with the fact that myeloid cancers represent the perhaps best characterized cancers of all at the cellular, molecular, and genetic levels,” Johanna Olweus told her audience at the Friday plenary session of the European Hematology Association 2025 Annual Congress.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/721407</guid>
      <pubDate>Mon, 16 Jun 2025 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/721407-at-eha-2025-ways-to-bring-immune-therapy-to-aml</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Cancer/Cancer-AML-acute-myeloid-leukemia-myeloblasts.webp?t=1760622065" type="image/jpeg" medium="image" fileSize="197137">
        <media:title type="plain">Photomicrograph of bone marrow aspirate showing myeloblasts of acute myeloid leukemia</media:title>
        <media:description type="plain">Acute myeloid leukemia.</media:description>
      </media:content>
    </item>
    <item>
      <title>At EHA 2025, ways to bring immune therapy to AML</title>
      <description>“The lack of therapeutic precision in treatment of myeloid malignancies is in sharp contrast with the fact that myeloid cancers represent the perhaps best characterized cancers of all at the cellular, molecular, and genetic levels,” Johanna Olweus told her audience at the Friday plenary session of the European Hematology Association 2025 Annual Congress.</description>
      <content:encoded>
        <![CDATA[“The lack of therapeutic precision in treatment of myeloid malignancies is in sharp contrast with the fact that myeloid cancers represent the perhaps best characterized cancers of all at the cellular, molecular, and genetic levels,” Johanna Olweus told her audience at the Friday plenary session of the European Hematology Association 2025 Annual Congress.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/721093</guid>
      <pubDate>Fri, 13 Jun 2025 11:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/721093-at-eha-2025-ways-to-bring-immune-therapy-to-aml</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Cancer/Cancer-AML-acute-myeloid-leukemia-myeloblasts.webp?t=1760622065" type="image/jpeg" medium="image" fileSize="197137">
        <media:title type="plain">Photomicrograph of bone marrow aspirate showing myeloblasts of acute myeloid leukemia</media:title>
        <media:description type="plain">Acute myeloid leukemia.</media:description>
      </media:content>
    </item>
    <item>
      <title>PA2G4-MYC signaling axis involved in pathogenesis of 3q26 AML, study shows</title>
      <description>The treatment of subtypes of acute myeloid leukemia (AML) characterized by aberrantly activated transcription factors is still challenging.</description>
      <content:encoded>
        <![CDATA[The treatment of subtypes of acute myeloid leukemia (AML) characterized by aberrantly activated transcription factors is still challenging.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/709868</guid>
      <pubDate>Wed, 26 Jun 2024 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/709868-pa2g4-myc-signaling-axis-involved-in-pathogenesis-of-3q26-aml-study-shows</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Research-and-science/Drug-research-illustration.webp?t=1711382891" type="image/jpeg" medium="image" fileSize="249152">
        <media:title type="plain">Drug discovery illustration</media:title>
      </media:content>
    </item>
    <item>
      <title>Blimp-1 ablation enhances antitumoral efficacy of ARI-0002-h CAR T cells</title>
      <description>CAR T-cell therapy that targets BCMA is an effective option for treating relapsed/refractory multiple myeloma, but there is a lack of persistence due to the inability to develop a memory phenotype.</description>
      <content:encoded>
        <![CDATA[CAR T-cell therapy that targets BCMA is an effective option for treating relapsed/refractory multiple myeloma, but there is a lack of persistence due to the inability to develop a memory phenotype.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/709866</guid>
      <pubDate>Wed, 26 Jun 2024 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/709866-blimp-1-ablation-enhances-antitumoral-efficacy-of-ari-0002-h-car-t-cells</link>
    </item>
    <item>
      <title>REGN-7999 reverses liver iron overload, improves bone health in mouse model of beta-thalassemia</title>
      <description>Transmembrane serine protease 6 (TMPRSS6) is a negative regulator of hepcidin, which is the main iron homeostasis-regulating hormone. Regeneron Pharmaceuticals Inc. has recently presented preclinical data for the monoclonal antibody targeting TMPRSS6, REGN-7999, which is being developed for the treatment of iron overload.</description>
      <content:encoded>
        <![CDATA[Transmembrane serine protease 6 (TMPRSS6) is a negative regulator of hepcidin, which is the main iron homeostasis-regulating hormone. Regeneron Pharmaceuticals Inc. has recently presented preclinical data for the monoclonal antibody targeting TMPRSS6, REGN-7999, which is being developed for the treatment of iron overload.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/709860</guid>
      <pubDate>Wed, 26 Jun 2024 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/709860-regn-7999-reverses-liver-iron-overload-improves-bone-health-in-mouse-model-of-beta-thalassemia</link>
    </item>
    <item>
      <title>Six months out, new EU rules still raising feasibility concerns</title>
      <description>The industry is again raising concerns that new EU health technology assessment rules coming into force on Jan. 12, 2025, will have the opposite of the desired effect and slow down access to innovative therapies.</description>
      <content:encoded>
        <![CDATA[The industry is again raising concerns that new EU health technology assessment rules coming into force on Jan. 12, 2025, will have the opposite of the desired effect and slow down access to innovative therapies.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/709931</guid>
      <pubDate>Tue, 25 Jun 2024 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/709931-six-months-out-new-eu-rules-still-raising-feasibility-concerns</link>
    </item>
    <item>
      <title>Kinase inhibitor AD-80 shows antileukemic effects in FLT3-ITD AML</title>
      <description>Acute myeloid leukemia (AML) is characterized by the accumulation of immature blasts in the bone marrow or in the peripheral blood.</description>
      <content:encoded>
        <![CDATA[Acute myeloid leukemia (AML) is characterized by the accumulation of immature blasts in the bone marrow or in the peripheral blood.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/709813</guid>
      <pubDate>Tue, 25 Jun 2024 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/709813-kinase-inhibitor-ad-80-shows-antileukemic-effects-in-flt3-itd-aml</link>
    </item>
    <item>
      <title>Potential first-in-class agent for JAK2 V617F mutant myeloproliferative neoplasms</title>
      <description>Researchers from Incyte Corp. and collaborators presented the preclinical profile of INCB-160058, an ATP-competitive small-molecule inhibitor of the JAK2 V617F mutant sparing its wild-type (WT) form, designed for the treatment of JAC2 V617F mutation-positive myeloproliferative neoplasms with potential as a first-in-class JAK2 V617-inhibiting drug.</description>
      <content:encoded>
        <![CDATA[Researchers from Incyte Corp. and collaborators presented the preclinical profile of INCB-160058, an ATP-competitive small-molecule inhibitor of the JAK2 V617F mutant sparing its wild-type (WT) form, designed for the treatment of JAC2 V617F mutation-positive myeloproliferative neoplasms with potential as a first-in-class JAK2 V617-inhibiting drug.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/709751</guid>
      <pubDate>Fri, 21 Jun 2024 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/709751-potential-first-in-class-agent-for-jak2-v617f-mutant-myeloproliferative-neoplasms</link>
    </item>
    <item>
      <title>Astrazeneca’s first-in-class T-cell engager circumvents associated toxicities</title>
      <description>Bispecific CD20×CD3 T-cell engagers have shown efficacy in hematological malignancies; however, associated toxicities such as cytokine release syndrome and immune effector-associated neurotoxicity syndrome limit their use.</description>
      <content:encoded>
        <![CDATA[Bispecific CD20×CD3 T-cell engagers have shown efficacy in hematological malignancies; however, associated toxicities such as cytokine release syndrome and immune effector-associated neurotoxicity syndrome limit their use.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/709747</guid>
      <pubDate>Fri, 21 Jun 2024 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/709747-astrazenecas-first-in-class-t-cell-engager-circumvents-associated-toxicities</link>
    </item>
    <item>
      <title>New anti-TIM-3 antibody-drug conjugate displays efficacy in AML models </title>
      <description>Residual leukemic stem cells (LSCs) are leukemia relapse-initiating cells that mediate treatment resistance in response to therapy stress. Different from normal hematopoietic stem cells (HSCs), both blasts and LSCs express T-cell immunoglobulin mucin-3 (TIM-3) on the surface.</description>
      <content:encoded>
        <![CDATA[Residual leukemic stem cells (LSCs) are leukemia relapse-initiating cells that mediate treatment resistance in response to therapy stress. Different from normal hematopoietic stem cells (HSCs), both blasts and LSCs express T-cell immunoglobulin mucin-3 (TIM-3) on the surface.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/709713</guid>
      <pubDate>Thu, 20 Jun 2024 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/709713-new-anti-tim-3-antibody-drug-conjugate-displays-efficacy-in-aml-models</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Drugs/Antibody-drug-conjugate-illustration.webp?t=1643920520" type="image/png" medium="image" fileSize="124892">
        <media:title type="plain">Antibody-drug conjugate illustration</media:title>
      </media:content>
    </item>
    <item>
      <title>Anticancer quinolone yields antileukemia effects and overcomes venetoclax resistance</title>
      <description>Targeting topoisomerase 2 (TOP2) is crucial in AML, and researchers from Wakunaga Pharmaceutical Co. Ltd. have developed and tested racemic WAC-224, a quinolone TOP2 inhibitor, and (R)-WAC-224 as a potential approach for AML treatment.</description>
      <content:encoded>
        <![CDATA[Targeting topoisomerase 2 (TOP2) is crucial in AML, and researchers from Wakunaga Pharmaceutical Co. Ltd. have developed and tested racemic WAC-224, a quinolone TOP2 inhibitor, and (<em>R</em>)-WAC-224 as a potential approach for AML treatment.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/709712</guid>
      <pubDate>Thu, 20 Jun 2024 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/709712-anticancer-quinolone-yields-antileukemia-effects-and-overcomes-venetoclax-resistance</link>
    </item>
    <item>
      <title>Incyte’s anti-CALR displays robust antimyeloproliferative effect</title>
      <description>Among the acquired mutations in the calreticulin (CALR) gene, both 52 bp deletion (del52) and 5 bp insertion (ins5) are among the most frequent and are linked to two different types of myeloproliferative neoplasms (MPNs).</description>
      <content:encoded>
        <![CDATA[Among the acquired mutations in the calreticulin (CALR) gene, both 52 bp deletion (del52) and 5 bp insertion (ins5) are among the most frequent and are linked to two different types of myeloproliferative neoplasms (MPNs).]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/709704</guid>
      <pubDate>Thu, 20 Jun 2024 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/709704-incytes-anti-calr-displays-robust-antimyeloproliferative-effect</link>
    </item>
    <item>
      <title>EHA 2024: Movers and shakers in the AML landscape </title>
      <description>During the basic science morning track on the last day of this year’s Annual Congress of the European Hematology Association (EHA), the attention was focused on oncogenic transcription factors and complexes considered turning points within the acute myeloid leukemia (AML) arena.</description>
      <content:encoded>
        <![CDATA[During the basic science morning track on the last day of this year’s Annual Congress of the European Hematology Association (EHA), the attention was focused on oncogenic transcription factors and complexes considered turning points within the acute myeloid leukemia (AML) arena.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/709691</guid>
      <pubDate>Wed, 19 Jun 2024 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/709691-eha-2024-movers-and-shakers-in-the-aml-landscape</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Cancer/AML-Acute-Myekoid-Leukemia-Cells.webp?t=1718809128" type="image/jpeg" medium="image" fileSize="305580">
        <media:title type="plain">3D illustration of acute myeloid leukemia cells</media:title>
      </media:content>
    </item>
    <item>
      <title>lncMALAT1 behind multiple myeloma and its prognosis</title>
      <description>Angiogenesis plays a crucial role in multiple myeloma and its prognosis, with the success of antiangiogenic therapies being limited. Exosomes mediate cell-to-cell cross talk during the progression of cancer by transporting their molecular cargo, which include long non-coding RNAs (lncRNAs); their role in multiple myeloma was investigated.</description>
      <content:encoded>
        <![CDATA[Angiogenesis plays a crucial role in multiple myeloma and its prognosis, with the success of antiangiogenic therapies being limited. Exosomes mediate cell-to-cell cross talk during the progression of cancer by transporting their molecular cargo, which include long non-coding RNAs (lncRNAs); their role in multiple myeloma was investigated.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/709662</guid>
      <pubDate>Tue, 18 Jun 2024 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/709662-lncmalat1-behind-multiple-myeloma-and-its-prognosis</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>KF-1601 outperforms ponatinib in chronic myeloid leukemia models </title>
      <description>The development of resistance and relapse during the blast phase of chronic myeloid leukemia poses a challenge in the management of this pathology, with half of the cases accounting for FLT3 pathway activation that, in turn, contributes to tyrosine kinase inhibitor resistance.</description>
      <content:encoded>
        <![CDATA[The development of resistance and relapse during the blast phase of chronic myeloid leukemia poses a challenge in the management of this pathology, with half of the cases accounting for FLT3 pathway activation that, in turn, contributes to tyrosine kinase inhibitor resistance.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/709659</guid>
      <pubDate>Tue, 18 Jun 2024 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/709659-kf-1601-outperforms-ponatinib-in-chronic-myeloid-leukemia-models</link>
    </item>
    <item>
      <title>Arvina’s BCL6 protein degrader shows high antiproliferative activity</title>
      <description>B-cell lymphoma 6 (BCL6) is up-regulated in several B-cell malignancies where it acts as a transcription factor activity mediator to induce and maintain lymphomagenesis.</description>
      <content:encoded>
        <![CDATA[B-cell lymphoma 6 (BCL6) is up-regulated in several B-cell malignancies where it acts as a transcription factor activity mediator to induce and maintain lymphomagenesis.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/709658</guid>
      <pubDate>Tue, 18 Jun 2024 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/709658-arvinas-bcl6-protein-degrader-shows-high-antiproliferative-activity</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Cancer/cancer-diffuse-large-B-cell-lymphoma-DLBCL.webp?t=1682690773" type="image/jpeg" medium="image" fileSize="436230">
        <media:title type="plain">Photomicrograph of diffuse large B-cell lymphoma</media:title>
      </media:content>
    </item>
    <item>
      <title>SLAMF6-targeting immunotherapy as therapeutic strategy against AML</title>
      <description>Researchers from Lund University presented data from a study that aimed to identify novel targets for immunotherapy in acute myeloid leukemia (AML). To identify differentially expressed cell surface proteins in the primitive CD34+CD38- cell populations, an arrayed antibody screen was performed on primary bone marrow samples from patients with AML as well as healthy donors.</description>
      <content:encoded>
        <![CDATA[Researchers from Lund University presented data from a study that aimed to identify novel targets for immunotherapy in acute myeloid leukemia (AML). To identify differentially expressed cell surface proteins in the primitive CD34+CD38- cell populations, an arrayed antibody screen was performed on primary bone marrow samples from patients with AML as well as healthy donors.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/709585</guid>
      <pubDate>Mon, 17 Jun 2024 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/709585-slamf6-targeting-immunotherapy-as-therapeutic-strategy-against-aml</link>
    </item>
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