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   <title>Actinium reports ATNM-400 cancer therapy data at AACR meeting</title>
   <link>http://www.streetinsider.com/Corporate+News/Actinium+reports+ATNM-400+cancer+therapy+data+at+AACR+meeting/26347061.html</link>
   <description>&lt;p&gt;Actinium Pharmaceuticals Inc. (NYSE American: ATNM) presented preclinical data for its ATNM-400 targeted radiotherapy at the American Association for Cancer Research Annual Meeting in San Diego. The experimental treatment showed activity across prostate, lung, and breast cancer models in laboratory studies.&lt;/p&gt;&lt;p&gt;ATNM-400 uses the Actinium-225 radioisotope and targets a membrane antigen that the company states is overexpressed in treatment-resistant solid tumors. In prostate cancer models, the therapy demonstrated efficacy in both high and low PSMA-expressing cancers, as well as PSMA-negative models.&lt;/p&gt;&lt;p&gt;The treatment showed greater tumor growth inhibition than osimertinib plus chemotherapy in EGFR-mutant non-small cell lung cancer models. The company also</description>
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   <title>Actinium reports ATNM-400 cancer therapy data at AACR meeting</title>
   <link>http://www.streetinsider.com/Corporate+News/Actinium+reports+ATNM-400+cancer+therapy+data+at+AACR+meeting/26347061.html</link>
   <description>&lt;p&gt;Actinium Pharmaceuticals Inc. (NYSE American: ATNM) presented preclinical data for its ATNM-400 targeted radiotherapy at the American Association for Cancer Research Annual Meeting in San Diego. The experimental treatment showed activity across prostate, lung, and breast cancer models in laboratory studies.&lt;/p&gt;&lt;p&gt;ATNM-400 uses the Actinium-225 radioisotope and targets a membrane antigen that the company states is overexpressed in treatment-resistant solid tumors. In prostate cancer models, the therapy demonstrated efficacy in both high and low PSMA-expressing cancers, as well as PSMA-negative models.&lt;/p&gt;&lt;p&gt;The treatment showed greater tumor growth inhibition than osimertinib plus chemotherapy in EGFR-mutant non-small cell lung cancer models. The company also</description>
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   <pubDate>Wed, 22 Apr 2026 07:01:58 -0400</pubDate>
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   <title>Actinium reports ATNM-400 cancer therapy data at AACR meeting</title>
   <link>http://www.streetinsider.com/FDA/Actinium+reports+ATNM-400+cancer+therapy+data+at+AACR+meeting/26347061.html</link>
   <description>&lt;p&gt;Actinium Pharmaceuticals Inc. (NYSE American: ATNM) presented preclinical data for its ATNM-400 targeted radiotherapy at the American Association for Cancer Research Annual Meeting in San Diego. The experimental treatment showed activity across prostate, lung, and breast cancer models in laboratory studies.&lt;/p&gt;&lt;p&gt;ATNM-400 uses the Actinium-225 radioisotope and targets a membrane antigen that the company states is overexpressed in treatment-resistant solid tumors. In prostate cancer models, the therapy demonstrated efficacy in both high and low PSMA-expressing cancers, as well as PSMA-negative models.&lt;/p&gt;&lt;p&gt;The treatment showed greater tumor growth inhibition than osimertinib plus chemotherapy in EGFR-mutant non-small cell lung cancer models. The company also</description>
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   <title>Actinium reports ATNM-400 cancer therapy data at AACR meeting</title>
   <link>http://www.streetinsider.com/FDA/Actinium+reports+ATNM-400+cancer+therapy+data+at+AACR+meeting/26347061.html</link>
   <description>&lt;p&gt;Actinium Pharmaceuticals Inc. (NYSE American: ATNM) presented preclinical data for its ATNM-400 targeted radiotherapy at the American Association for Cancer Research Annual Meeting in San Diego. The experimental treatment showed activity across prostate, lung, and breast cancer models in laboratory studies.&lt;/p&gt;&lt;p&gt;ATNM-400 uses the Actinium-225 radioisotope and targets a membrane antigen that the company states is overexpressed in treatment-resistant solid tumors. In prostate cancer models, the therapy demonstrated efficacy in both high and low PSMA-expressing cancers, as well as PSMA-negative models.&lt;/p&gt;&lt;p&gt;The treatment showed greater tumor growth inhibition than osimertinib plus chemotherapy in EGFR-mutant non-small cell lung cancer models. The company also</description>
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   <title>Actinium Pharmaceuticals, Inc. Announces Compelling Pan-Tumor Data for ATNM-400 Demonstrating Broad Efficacy Across Prostate, Lung, and Breast Cancer Models at the 2026 American Association of Cancer </title>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;ATNM-400 demonstrates pan-tumor activity across prostate, lung, and breast cancer models, supporting multi-indication development potential&lt;/li&gt;&lt;li&gt;In prostate cancer, ATNM-400 demonstrates efficacy across both high PSMA-expressing and, importantly, low PSMA-expressing prostate cancer models, unlike many PSMA-targeted radioligand therapies that work only in PSMA-high settings&lt;/li&gt;&lt;li&gt;In EGFR-mutant non-small cell lung cancer, ATNM-400 demonstrates greater tumor growth inhibition than osimertinib (a tyrosine kinase inhibitor) plus chemotherapy and outperforms the approved Trop-2 ADC Dato-DXd (DATROWAY®), the EGFR-cMET bispecific antibody amivantamab (RYBREVANT®) and the experimental EGFR-HER3 ADC izalontamab brengitecan, supporting potential use across first-, second-, and third-line treatment settings&lt;/li&gt;&lt;li&gt;In breast cancer, new head-to-head data shows</description>
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   <title>Actinium Pharmaceuticals, Inc. Announces Compelling Pan-Tumor Data for ATNM-400 Demonstrating Broad Efficacy Across Prostate, Lung, and Breast Cancer Models at the 2026 American Association of Cancer </title>
   <link>http://www.streetinsider.com/Press+Releases/Actinium+Pharmaceuticals%2C+Inc.+Announces+Compelling+Pan-Tumor+Data+for+ATNM-400+Demonstrating+Broad+Efficacy+Across+Prostate%2C+Lung%2C+and+Breast+Cancer+Models+at+the+2026+American+Association+of+Cancer+/26347012.html</link>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;ATNM-400 demonstrates pan-tumor activity across prostate, lung, and breast cancer models, supporting multi-indication development potential&lt;/li&gt;&lt;li&gt;In prostate cancer, ATNM-400 demonstrates efficacy across both high PSMA-expressing and, importantly, low PSMA-expressing prostate cancer models, unlike many PSMA-targeted radioligand therapies that work only in PSMA-high settings&lt;/li&gt;&lt;li&gt;In EGFR-mutant non-small cell lung cancer, ATNM-400 demonstrates greater tumor growth inhibition than osimertinib (a tyrosine kinase inhibitor) plus chemotherapy and outperforms the approved Trop-2 ADC Dato-DXd (DATROWAY®), the EGFR-cMET bispecific antibody amivantamab (RYBREVANT®) and the experimental EGFR-HER3 ADC izalontamab brengitecan, supporting potential use across first-, second-, and third-line treatment settings&lt;/li&gt;&lt;li&gt;In breast cancer, new head-to-head data shows</description>
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   <title>Actinium Pharmaceuticals, Inc. Announces Compelling Pan-Tumor Data for ATNM-400 Demonstrating Broad Efficacy Across Prostate, Lung, and Breast Cancer Models at the 2026 American Association of Cancer </title>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;ATNM-400 demonstrates pan-tumor activity across prostate, lung, and breast cancer models, supporting multi-indication development potential&lt;/li&gt;&lt;li&gt;In prostate cancer, ATNM-400 demonstrates efficacy across both high PSMA-expressing and, importantly, low PSMA-expressing prostate cancer models, unlike many PSMA-targeted radioligand therapies that work only in PSMA-high settings&lt;/li&gt;&lt;li&gt;In EGFR-mutant non-small cell lung cancer, ATNM-400 demonstrates greater tumor growth inhibition than osimertinib (a tyrosine kinase inhibitor) plus chemotherapy and outperforms the approved Trop-2 ADC Dato-DXd (DATROWAY®), the EGFR-cMET bispecific antibody amivantamab (RYBREVANT®) and the experimental EGFR-HER3 ADC izalontamab brengitecan, supporting potential use across first-, second-, and third-line treatment settings&lt;/li&gt;&lt;li&gt;In breast cancer, new head-to-head data shows</description>
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   <title>Actinium Pharmaceuticals, Inc. Announces Compelling Pan-Tumor Data for ATNM-400 Demonstrating Broad Efficacy Across Prostate, Lung, and Breast Cancer Models at the 2026 American Association of Cancer </title>
   <link>http://www.streetinsider.com/Press+Releases/Actinium+Pharmaceuticals%2C+Inc.+Announces+Compelling+Pan-Tumor+Data+for+ATNM-400+Demonstrating+Broad+Efficacy+Across+Prostate%2C+Lung%2C+and+Breast+Cancer+Models+at+the+2026+American+Association+of+Cancer+/26347012.html</link>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;ATNM-400 demonstrates pan-tumor activity across prostate, lung, and breast cancer models, supporting multi-indication development potential&lt;/li&gt;&lt;li&gt;In prostate cancer, ATNM-400 demonstrates efficacy across both high PSMA-expressing and, importantly, low PSMA-expressing prostate cancer models, unlike many PSMA-targeted radioligand therapies that work only in PSMA-high settings&lt;/li&gt;&lt;li&gt;In EGFR-mutant non-small cell lung cancer, ATNM-400 demonstrates greater tumor growth inhibition than osimertinib (a tyrosine kinase inhibitor) plus chemotherapy and outperforms the approved Trop-2 ADC Dato-DXd (DATROWAY®), the EGFR-cMET bispecific antibody amivantamab (RYBREVANT®) and the experimental EGFR-HER3 ADC izalontamab brengitecan, supporting potential use across first-, second-, and third-line treatment settings&lt;/li&gt;&lt;li&gt;In breast cancer, new head-to-head data shows</description>
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   <title>Actinium Pharmaceuticals, Inc. Announces Compelling Pan-Tumor Data for ATNM-400 Demonstrating Broad Efficacy Across Prostate, Lung, and Breast Cancer Models at the 2026 American Association of Cancer </title>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;ATNM-400 demonstrates pan-tumor activity across prostate, lung, and breast cancer models, supporting multi-indication development potential&lt;/li&gt;&lt;li&gt;In prostate cancer, ATNM-400 demonstrates efficacy across both high PSMA-expressing and, importantly, low PSMA-expressing prostate cancer models, unlike many PSMA-targeted radioligand therapies that work only in PSMA-high settings&lt;/li&gt;&lt;li&gt;In EGFR-mutant non-small cell lung cancer, ATNM-400 demonstrates greater tumor growth inhibition than osimertinib (a tyrosine kinase inhibitor) plus chemotherapy and outperforms the approved Trop-2 ADC Dato-DXd (DATROWAY®), the EGFR-cMET bispecific antibody amivantamab (RYBREVANT®) and the experimental EGFR-HER3 ADC izalontamab brengitecan, supporting potential use across first-, second-, and third-line treatment settings&lt;/li&gt;&lt;li&gt;In breast cancer, new head-to-head data shows</description>
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   <title>Actinium Pharmaceuticals, Inc. Announces Compelling Pan-Tumor Data for ATNM-400 Demonstrating Broad Efficacy Across Prostate, Lung, and Breast Cancer Models at the 2026 American Association of Cancer </title>
   <link>http://www.streetinsider.com/Press+Releases/Actinium+Pharmaceuticals%2C+Inc.+Announces+Compelling+Pan-Tumor+Data+for+ATNM-400+Demonstrating+Broad+Efficacy+Across+Prostate%2C+Lung%2C+and+Breast+Cancer+Models+at+the+2026+American+Association+of+Cancer+/26347012.html</link>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;ATNM-400 demonstrates pan-tumor activity across prostate, lung, and breast cancer models, supporting multi-indication development potential&lt;/li&gt;&lt;li&gt;In prostate cancer, ATNM-400 demonstrates efficacy across both high PSMA-expressing and, importantly, low PSMA-expressing prostate cancer models, unlike many PSMA-targeted radioligand therapies that work only in PSMA-high settings&lt;/li&gt;&lt;li&gt;In EGFR-mutant non-small cell lung cancer, ATNM-400 demonstrates greater tumor growth inhibition than osimertinib (a tyrosine kinase inhibitor) plus chemotherapy and outperforms the approved Trop-2 ADC Dato-DXd (DATROWAY®), the EGFR-cMET bispecific antibody amivantamab (RYBREVANT®) and the experimental EGFR-HER3 ADC izalontamab brengitecan, supporting potential use across first-, second-, and third-line treatment settings&lt;/li&gt;&lt;li&gt;In breast cancer, new head-to-head data shows</description>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;ATNM-400 demonstrates pan-tumor activity across prostate, lung, and breast cancer models, supporting multi-indication development potential&lt;/li&gt;&lt;li&gt;In prostate cancer, ATNM-400 demonstrates efficacy across both high PSMA-expressing and, importantly, low PSMA-expressing prostate cancer models, unlike many PSMA-targeted radioligand therapies that work only in PSMA-high settings&lt;/li&gt;&lt;li&gt;In EGFR-mutant non-small cell lung cancer, ATNM-400 demonstrates greater tumor growth inhibition than osimertinib (a tyrosine kinase inhibitor) plus chemotherapy and outperforms the approved Trop-2 ADC Dato-DXd (DATROWAY®), the EGFR-cMET bispecific antibody amivantamab (RYBREVANT®) and the experimental EGFR-HER3 ADC izalontamab brengitecan, supporting potential use across first-, second-, and third-line treatment settings&lt;/li&gt;&lt;li&gt;In breast cancer, new head-to-head data shows</description>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;ATNM-400 demonstrates pan-tumor activity across prostate, lung, and breast cancer models, supporting multi-indication development potential&lt;/li&gt;&lt;li&gt;In prostate cancer, ATNM-400 demonstrates efficacy across both high PSMA-expressing and, importantly, low PSMA-expressing prostate cancer models, unlike many PSMA-targeted radioligand therapies that work only in PSMA-high settings&lt;/li&gt;&lt;li&gt;In EGFR-mutant non-small cell lung cancer, ATNM-400 demonstrates greater tumor growth inhibition than osimertinib (a tyrosine kinase inhibitor) plus chemotherapy and outperforms the approved Trop-2 ADC Dato-DXd (DATROWAY®), the EGFR-cMET bispecific antibody amivantamab (RYBREVANT®) and the experimental EGFR-HER3 ADC izalontamab brengitecan, supporting potential use across first-, second-, and third-line treatment settings&lt;/li&gt;&lt;li&gt;In breast cancer, new head-to-head data shows</description>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;ATNM-400 demonstrates pan-tumor activity across prostate, lung, and breast cancer models, supporting multi-indication development potential&lt;/li&gt;&lt;li&gt;In prostate cancer, ATNM-400 demonstrates efficacy across both high PSMA-expressing and, importantly, low PSMA-expressing prostate cancer models, unlike many PSMA-targeted radioligand therapies that work only in PSMA-high settings&lt;/li&gt;&lt;li&gt;In EGFR-mutant non-small cell lung cancer, ATNM-400 demonstrates greater tumor growth inhibition than osimertinib (a tyrosine kinase inhibitor) plus chemotherapy and outperforms the approved Trop-2 ADC Dato-DXd (DATROWAY®), the EGFR-cMET bispecific antibody amivantamab (RYBREVANT®) and the experimental EGFR-HER3 ADC izalontamab brengitecan, supporting potential use across first-, second-, and third-line treatment settings&lt;/li&gt;&lt;li&gt;In breast cancer, new head-to-head data shows</description>
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&lt;div class=&quot;xn-content&quot;&gt;
&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;ATNM-400 demonstrates pan-tumor activity across prostate, lung, and breast cancer models, supporting multi-indication development potential&lt;/li&gt;&lt;li&gt;In prostate cancer, ATNM-400 demonstrates efficacy across both high PSMA-expressing and, importantly, low PSMA-expressing prostate cancer models, unlike many PSMA-targeted radioligand therapies that work only in PSMA-high settings&lt;/li&gt;&lt;li&gt;In EGFR-mutant non-small cell lung cancer, ATNM-400 demonstrates greater tumor growth inhibition than osimertinib (a tyrosine kinase inhibitor) plus chemotherapy and outperforms the approved Trop-2 ADC Dato-DXd (DATROWAY®), the EGFR-cMET bispecific antibody amivantamab (RYBREVANT®) and the experimental EGFR-HER3 ADC izalontamab brengitecan, supporting potential use across first-, second-, and third-line treatment settings&lt;/li&gt;&lt;li&gt;In breast cancer, new head-to-head data shows</description>
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   <title>Actinium Pharmaceuticals, Inc. Announces Compelling Pan-Tumor Data for ATNM-400 Demonstrating Broad Efficacy Across Prostate, Lung, and Breast Cancer Models at the 2026 American Association of Cancer </title>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;ATNM-400 demonstrates pan-tumor activity across prostate, lung, and breast cancer models, supporting multi-indication development potential&lt;/li&gt;&lt;li&gt;In prostate cancer, ATNM-400 demonstrates efficacy across both high PSMA-expressing and, importantly, low PSMA-expressing prostate cancer models, unlike many PSMA-targeted radioligand therapies that work only in PSMA-high settings&lt;/li&gt;&lt;li&gt;In EGFR-mutant non-small cell lung cancer, ATNM-400 demonstrates greater tumor growth inhibition than osimertinib (a tyrosine kinase inhibitor) plus chemotherapy and outperforms the approved Trop-2 ADC Dato-DXd (DATROWAY®), the EGFR-cMET bispecific antibody amivantamab (RYBREVANT®) and the experimental EGFR-HER3 ADC izalontamab brengitecan, supporting potential use across first-, second-, and third-line treatment settings&lt;/li&gt;&lt;li&gt;In breast cancer, new head-to-head data shows</description>
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   <title>Actinium Pharmaceuticals, Inc. Announces Compelling Pan-Tumor Data for ATNM-400 Demonstrating Broad Efficacy Across Prostate, Lung, and Breast Cancer Models at the 2026 American Association of Cancer </title>
   <link>http://www.streetinsider.com/PRNewswire/Actinium+Pharmaceuticals%2C+Inc.+Announces+Compelling+Pan-Tumor+Data+for+ATNM-400+Demonstrating+Broad+Efficacy+Across+Prostate%2C+Lung%2C+and+Breast+Cancer+Models+at+the+2026+American+Association+of+Cancer+/26347012.html</link>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;ATNM-400 demonstrates pan-tumor activity across prostate, lung, and breast cancer models, supporting multi-indication development potential&lt;/li&gt;&lt;li&gt;In prostate cancer, ATNM-400 demonstrates efficacy across both high PSMA-expressing and, importantly, low PSMA-expressing prostate cancer models, unlike many PSMA-targeted radioligand therapies that work only in PSMA-high settings&lt;/li&gt;&lt;li&gt;In EGFR-mutant non-small cell lung cancer, ATNM-400 demonstrates greater tumor growth inhibition than osimertinib (a tyrosine kinase inhibitor) plus chemotherapy and outperforms the approved Trop-2 ADC Dato-DXd (DATROWAY®), the EGFR-cMET bispecific antibody amivantamab (RYBREVANT®) and the experimental EGFR-HER3 ADC izalontamab brengitecan, supporting potential use across first-, second-, and third-line treatment settings&lt;/li&gt;&lt;li&gt;In breast cancer, new head-to-head data shows</description>
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   <title>Actinium Pharmaceuticals, Inc. Announces Compelling Pan-Tumor Data for ATNM-400 Demonstrating Broad Efficacy Across Prostate, Lung, and Breast Cancer Models at the 2026 American Association of Cancer </title>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;ATNM-400 demonstrates pan-tumor activity across prostate, lung, and breast cancer models, supporting multi-indication development potential&lt;/li&gt;&lt;li&gt;In prostate cancer, ATNM-400 demonstrates efficacy across both high PSMA-expressing and, importantly, low PSMA-expressing prostate cancer models, unlike many PSMA-targeted radioligand therapies that work only in PSMA-high settings&lt;/li&gt;&lt;li&gt;In EGFR-mutant non-small cell lung cancer, ATNM-400 demonstrates greater tumor growth inhibition than osimertinib (a tyrosine kinase inhibitor) plus chemotherapy and outperforms the approved Trop-2 ADC Dato-DXd (DATROWAY®), the EGFR-cMET bispecific antibody amivantamab (RYBREVANT®) and the experimental EGFR-HER3 ADC izalontamab brengitecan, supporting potential use across first-, second-, and third-line treatment settings&lt;/li&gt;&lt;li&gt;In breast cancer, new head-to-head data shows</description>
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   <title>Actinium Pharmaceuticals, Inc. Announces Compelling Pan-Tumor Data for ATNM-400 Demonstrating Broad Efficacy Across Prostate, Lung, and Breast Cancer Models at the 2026 American Association of Cancer </title>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;ATNM-400 demonstrates pan-tumor activity across prostate, lung, and breast cancer models, supporting multi-indication development potential&lt;/li&gt;&lt;li&gt;In prostate cancer, ATNM-400 demonstrates efficacy across both high PSMA-expressing and, importantly, low PSMA-expressing prostate cancer models, unlike many PSMA-targeted radioligand therapies that work only in PSMA-high settings&lt;/li&gt;&lt;li&gt;In EGFR-mutant non-small cell lung cancer, ATNM-400 demonstrates greater tumor growth inhibition than osimertinib (a tyrosine kinase inhibitor) plus chemotherapy and outperforms the approved Trop-2 ADC Dato-DXd (DATROWAY®), the EGFR-cMET bispecific antibody amivantamab (RYBREVANT®) and the experimental EGFR-HER3 ADC izalontamab brengitecan, supporting potential use across first-, second-, and third-line treatment settings&lt;/li&gt;&lt;li&gt;In breast cancer, new head-to-head data shows</description>
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   <title>Actinium Pharmaceuticals, Inc. Announces Compelling Pan-Tumor Data for ATNM-400 Demonstrating Broad Efficacy Across Prostate, Lung, and Breast Cancer Models at the 2026 American Association of Cancer </title>
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&lt;div class=&quot;xn-content&quot;&gt;
&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;ATNM-400 demonstrates pan-tumor activity across prostate, lung, and breast cancer models, supporting multi-indication development potential&lt;/li&gt;&lt;li&gt;In prostate cancer, ATNM-400 demonstrates efficacy across both high PSMA-expressing and, importantly, low PSMA-expressing prostate cancer models, unlike many PSMA-targeted radioligand therapies that work only in PSMA-high settings&lt;/li&gt;&lt;li&gt;In EGFR-mutant non-small cell lung cancer, ATNM-400 demonstrates greater tumor growth inhibition than osimertinib (a tyrosine kinase inhibitor) plus chemotherapy and outperforms the approved Trop-2 ADC Dato-DXd (DATROWAY®), the EGFR-cMET bispecific antibody amivantamab (RYBREVANT®) and the experimental EGFR-HER3 ADC izalontamab brengitecan, supporting potential use across first-, second-, and third-line treatment settings&lt;/li&gt;&lt;li&gt;In breast cancer, new head-to-head data shows</description>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;Actimab-A combinations enhanced in vivo AML cell killing across multiple preclinical models, independent of mutation status, when combined with standard-of-care targeted and non-targeted therapies including revumenib (menin-KMT2A inhibitor), gilteritinib (FLT3 inhibitor), and azacitidine (hypomethylating agent) - three pillars of modern AML treatment - supporting its potential role as a universal combination backbone&lt;br /&gt;&lt;br /&gt;&lt;/li&gt;&lt;li&gt;Transcriptional reprogramming identified as a central mechanism showing that Actimab-A combinations don't just add cytotoxicity, they reprogram AML cells from proliferation toward differentiation and apoptosis, providing the mechanistic basis for deeper, more durable MRD-negative responses and reinforcing Actimab-A's role as a universal combination backbone across AML&lt;br</description>
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   <title>Actinium Highlights Transcriptional Reprogramming as a Key Mechanism Underpinning Mutation-Agnostic Activity of Actimab-A in AML at the 2026 American Association of Cancer Research Annual Meeting</title>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;Actimab-A combinations enhanced in vivo AML cell killing across multiple preclinical models, independent of mutation status, when combined with standard-of-care targeted and non-targeted therapies including revumenib (menin-KMT2A inhibitor), gilteritinib (FLT3 inhibitor), and azacitidine (hypomethylating agent) - three pillars of modern AML treatment - supporting its potential role as a universal combination backbone&lt;br /&gt;&lt;br /&gt;&lt;/li&gt;&lt;li&gt;Transcriptional reprogramming identified as a central mechanism showing that Actimab-A combinations don't just add cytotoxicity, they reprogram AML cells from proliferation toward differentiation and apoptosis, providing the mechanistic basis for deeper, more durable MRD-negative responses and reinforcing Actimab-A's role as a universal combination backbone across AML&lt;br</description>
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   <title>Actinium Highlights Transcriptional Reprogramming as a Key Mechanism Underpinning Mutation-Agnostic Activity of Actimab-A in AML at the 2026 American Association of Cancer Research Annual Meeting</title>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;Actimab-A combinations enhanced in vivo AML cell killing across multiple preclinical models, independent of mutation status, when combined with standard-of-care targeted and non-targeted therapies including revumenib (menin-KMT2A inhibitor), gilteritinib (FLT3 inhibitor), and azacitidine (hypomethylating agent) - three pillars of modern AML treatment - supporting its potential role as a universal combination backbone&lt;br /&gt;&lt;br /&gt;&lt;/li&gt;&lt;li&gt;Transcriptional reprogramming identified as a central mechanism showing that Actimab-A combinations don't just add cytotoxicity, they reprogram AML cells from proliferation toward differentiation and apoptosis, providing the mechanistic basis for deeper, more durable MRD-negative responses and reinforcing Actimab-A's role as a universal combination backbone across AML&lt;br</description>
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   <title>Actinium Highlights Transcriptional Reprogramming as a Key Mechanism Underpinning Mutation-Agnostic Activity of Actimab-A in AML at the 2026 American Association of Cancer Research Annual Meeting</title>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;Actimab-A combinations enhanced in vivo AML cell killing across multiple preclinical models, independent of mutation status, when combined with standard-of-care targeted and non-targeted therapies including revumenib (menin-KMT2A inhibitor), gilteritinib (FLT3 inhibitor), and azacitidine (hypomethylating agent) - three pillars of modern AML treatment - supporting its potential role as a universal combination backbone&lt;br /&gt;&lt;br /&gt;&lt;/li&gt;&lt;li&gt;Transcriptional reprogramming identified as a central mechanism showing that Actimab-A combinations don't just add cytotoxicity, they reprogram AML cells from proliferation toward differentiation and apoptosis, providing the mechanistic basis for deeper, more durable MRD-negative responses and reinforcing Actimab-A's role as a universal combination backbone across AML&lt;br</description>
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   <title>Actinium Highlights Transcriptional Reprogramming as a Key Mechanism Underpinning Mutation-Agnostic Activity of Actimab-A in AML at the 2026 American Association of Cancer Research Annual Meeting</title>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;Actimab-A combinations enhanced in vivo AML cell killing across multiple preclinical models, independent of mutation status, when combined with standard-of-care targeted and non-targeted therapies including revumenib (menin-KMT2A inhibitor), gilteritinib (FLT3 inhibitor), and azacitidine (hypomethylating agent) - three pillars of modern AML treatment - supporting its potential role as a universal combination backbone&lt;br /&gt;&lt;br /&gt;&lt;/li&gt;&lt;li&gt;Transcriptional reprogramming identified as a central mechanism showing that Actimab-A combinations don't just add cytotoxicity, they reprogram AML cells from proliferation toward differentiation and apoptosis, providing the mechanistic basis for deeper, more durable MRD-negative responses and reinforcing Actimab-A's role as a universal combination backbone across AML&lt;br</description>
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