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   <title>Dizal to Present Emerging Data on ZEGFROVY® in Non-Small Cell Lung Cancer at WCLC 2026</title>
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   <title>Dizal to Present Emerging Data on ZEGFROVY® in Non-Small Cell Lung Cancer at WCLC 2026</title>
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   <title>Dizal to Present Emerging Data on ZEGFROVY® in Non-Small Cell Lung Cancer at WCLC 2026</title>
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   <title>Dizal to Present Emerging Data on ZEGFROVY® in Non-Small Cell Lung Cancer at WCLC 2026</title>
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   <title>Dizal to Present Emerging Data on ZEGFROVY® in Non-Small Cell Lung Cancer at WCLC 2026</title>
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   <title>Dizal to Present Emerging Data on ZEGFROVY® in Non-Small Cell Lung Cancer at WCLC 2026</title>
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   <title>Dizal to Present Emerging Data on ZEGFROVY® in Non-Small Cell Lung Cancer at WCLC 2026</title>
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   <title>Dizal to Present Emerging Data on ZEGFROVY® in Non-Small Cell Lung Cancer at WCLC 2026</title>
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   <title>Dizal to Present Emerging Data on ZEGFROVY® in Non-Small Cell Lung Cancer at WCLC 2026</title>
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   <title>Dizal to Present Emerging Data on ZEGFROVY® in Non-Small Cell Lung Cancer at WCLC 2026</title>
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   <title>Dizal Presents Positive NSCLC Data for Fourth-Generation EGFR TKI DZD6008 and Golidocitinib in Combination with Anti-PD-1 at ASCO 2026</title>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;i&gt;Oral presentation of &lt;money&gt;DZD6008&lt;/money&gt; demonstrated strong and durable anti-tumor activity, excellent BBB-penetrant properties, and a favorable safety profile in patients relapsed from third-generation EGFR TKI&lt;/i&gt;&lt;/li&gt;&lt;li&gt;&lt;i&gt;In treatment-naïve patients with advanced NSCLC without driver mutations, Golidocitinib, a JAK-only inhibitor, in combination with anti-PD-1 antibody enhanced anti-tumor response. &lt;/i&gt;&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/cn..shangh&quot; idsrc=&quot;xmltag.org&quot; &gt;SHANGHAI&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;May 30, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- Dizal (SSE:688192), a biopharmaceutical company committed to developing novel medicines for the treatment of oncology and hematological diseases, today announced the presentations of two studies in non-small cell lung cancer (NSCLC) at the 2026 &lt;span value=&quot;ACORN:5021672661&quot; idsrc=&quot;xmltag.org&quot; &gt;American Society of Clinical Oncology&lt;/span&gt; (ASCO)</description>
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   <pubDate>Sat, 30 May 2026 20:09:00 -0400</pubDate>
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   <title>Dizal Presents Positive NSCLC Data for Fourth-Generation EGFR TKI DZD6008 and Golidocitinib in Combination with Anti-PD-1 at ASCO 2026</title>
   <link>http://www.streetinsider.com/Press+Releases/Dizal+Presents+Positive+NSCLC+Data+for+Fourth-Generation+EGFR+TKI+DZD6008+and+Golidocitinib+in+Combination+with+Anti-PD-1+at+ASCO+2026/26577291.html</link>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;i&gt;Oral presentation of &lt;money&gt;DZD6008&lt;/money&gt; demonstrated strong and durable anti-tumor activity, excellent BBB-penetrant properties, and a favorable safety profile in patients relapsed from third-generation EGFR TKI&lt;/i&gt;&lt;/li&gt;&lt;li&gt;&lt;i&gt;In treatment-naïve patients with advanced NSCLC without driver mutations, Golidocitinib, a JAK-only inhibitor, in combination with anti-PD-1 antibody enhanced anti-tumor response. &lt;/i&gt;&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/cn..shangh&quot; idsrc=&quot;xmltag.org&quot; &gt;SHANGHAI&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;May 30, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- Dizal (SSE:688192), a biopharmaceutical company committed to developing novel medicines for the treatment of oncology and hematological diseases, today announced the presentations of two studies in non-small cell lung cancer (NSCLC) at the 2026 &lt;span value=&quot;ACORN:5021672661&quot; idsrc=&quot;xmltag.org&quot; &gt;American Society of Clinical Oncology&lt;/span&gt; (ASCO)</description>
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   <title>Dizal Presents Positive NSCLC Data for Fourth-Generation EGFR TKI DZD6008 and Golidocitinib in Combination with Anti-PD-1 at ASCO 2026</title>
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&lt;div class=&quot;xn-content&quot;&gt;
&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;i&gt;Oral presentation of &lt;money&gt;DZD6008&lt;/money&gt; demonstrated strong and durable anti-tumor activity, excellent BBB-penetrant properties, and a favorable safety profile in patients relapsed from third-generation EGFR TKI&lt;/i&gt;&lt;/li&gt;&lt;li&gt;&lt;i&gt;In treatment-naïve patients with advanced NSCLC without driver mutations, Golidocitinib, a JAK-only inhibitor, in combination with anti-PD-1 antibody enhanced anti-tumor response. &lt;/i&gt;&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/cn..shangh&quot; idsrc=&quot;xmltag.org&quot; &gt;SHANGHAI&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;May 30, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- Dizal (SSE:688192), a biopharmaceutical company committed to developing novel medicines for the treatment of oncology and hematological diseases, today announced the presentations of two studies in non-small cell lung cancer (NSCLC) at the 2026 &lt;span value=&quot;ACORN:5021672661&quot; idsrc=&quot;xmltag.org&quot; &gt;American Society of Clinical Oncology&lt;/span&gt; (ASCO)</description>
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   <title>Dizal Presents Positive NSCLC Data for Fourth-Generation EGFR TKI DZD6008 and Golidocitinib in Combination with Anti-PD-1 at ASCO 2026</title>
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&lt;div class=&quot;xn-content&quot;&gt;
&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;i&gt;Oral presentation of &lt;money&gt;DZD6008&lt;/money&gt; demonstrated strong and durable anti-tumor activity, excellent BBB-penetrant properties, and a favorable safety profile in patients relapsed from third-generation EGFR TKI&lt;/i&gt;&lt;/li&gt;&lt;li&gt;&lt;i&gt;In treatment-naïve patients with advanced NSCLC without driver mutations, Golidocitinib, a JAK-only inhibitor, in combination with anti-PD-1 antibody enhanced anti-tumor response. &lt;/i&gt;&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/cn..shangh&quot; idsrc=&quot;xmltag.org&quot; &gt;SHANGHAI&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;May 30, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- Dizal (SSE:688192), a biopharmaceutical company committed to developing novel medicines for the treatment of oncology and hematological diseases, today announced the presentations of two studies in non-small cell lung cancer (NSCLC) at the 2026 &lt;span value=&quot;ACORN:5021672661&quot; idsrc=&quot;xmltag.org&quot; &gt;American Society of Clinical Oncology&lt;/span&gt; (ASCO)</description>
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   <title>Dizal Presents Positive NSCLC Data for Fourth-Generation EGFR TKI DZD6008 and Golidocitinib in Combination with Anti-PD-1 at ASCO 2026</title>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;i&gt;Oral presentation of &lt;money&gt;DZD6008&lt;/money&gt; demonstrated strong and durable anti-tumor activity, excellent BBB-penetrant properties, and a favorable safety profile in patients relapsed from third-generation EGFR TKI&lt;/i&gt;&lt;/li&gt;&lt;li&gt;&lt;i&gt;In treatment-naïve patients with advanced NSCLC without driver mutations, Golidocitinib, a JAK-only inhibitor, in combination with anti-PD-1 antibody enhanced anti-tumor response. &lt;/i&gt;&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/cn..shangh&quot; idsrc=&quot;xmltag.org&quot; &gt;SHANGHAI&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;May 30, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- Dizal (SSE:688192), a biopharmaceutical company committed to developing novel medicines for the treatment of oncology and hematological diseases, today announced the presentations of two studies in non-small cell lung cancer (NSCLC) at the 2026 &lt;span value=&quot;ACORN:5021672661&quot; idsrc=&quot;xmltag.org&quot; &gt;American Society of Clinical Oncology&lt;/span&gt; (ASCO)</description>
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   <title>Dizal Presents Positive NSCLC Data for Fourth-Generation EGFR TKI DZD6008 and Golidocitinib in Combination with Anti-PD-1 at ASCO 2026</title>
   <link>http://www.streetinsider.com/PRNewswire/Dizal+Presents+Positive+NSCLC+Data+for+Fourth-Generation+EGFR+TKI+DZD6008+and+Golidocitinib+in+Combination+with+Anti-PD-1+at+ASCO+2026/26577291.html</link>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;i&gt;Oral presentation of &lt;money&gt;DZD6008&lt;/money&gt; demonstrated strong and durable anti-tumor activity, excellent BBB-penetrant properties, and a favorable safety profile in patients relapsed from third-generation EGFR TKI&lt;/i&gt;&lt;/li&gt;&lt;li&gt;&lt;i&gt;In treatment-naïve patients with advanced NSCLC without driver mutations, Golidocitinib, a JAK-only inhibitor, in combination with anti-PD-1 antibody enhanced anti-tumor response. &lt;/i&gt;&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/cn..shangh&quot; idsrc=&quot;xmltag.org&quot; &gt;SHANGHAI&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;May 30, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- Dizal (SSE:688192), a biopharmaceutical company committed to developing novel medicines for the treatment of oncology and hematological diseases, today announced the presentations of two studies in non-small cell lung cancer (NSCLC) at the 2026 &lt;span value=&quot;ACORN:5021672661&quot; idsrc=&quot;xmltag.org&quot; &gt;American Society of Clinical Oncology&lt;/span&gt; (ASCO)</description>
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   <title>Dizal's ZEGFROVY beats chemotherapy in lung cancer trial</title>
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&lt;p&gt;Dizal Pharmaceutical (SSE: 688192) announced that its drug ZEGFROVY demonstrated superior results compared to platinum-doublet chemotherapy in treating patients with a specific type of non-small cell lung cancer, according to results from a phase 3 clinical trial.&lt;/p&gt;

&lt;p&gt;The WU-KONG28 study evaluated ZEGFROVY as a first-line treatment for advanced non-small cell lung cancer patients with EGFR exon 20 insertion mutations. The trial included 324 patients randomized to receive either ZEGFROVY at 300 mg once daily or chemotherapy.&lt;/p&gt;

&lt;p&gt;Median progression-free survival was 10.3 months with ZEGFROVY versus 7.5 months with chemotherapy. The objective response rate was 68.1% with ZEGFROVY compared to 35.4% with chemotherapy.</description>
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&lt;p&gt;Dizal Pharmaceutical (SSE: 688192) announced that its drug ZEGFROVY demonstrated superior results compared to platinum-doublet chemotherapy in treating patients with a specific type of non-small cell lung cancer, according to results from a phase 3 clinical trial.&lt;/p&gt;

&lt;p&gt;The WU-KONG28 study evaluated ZEGFROVY as a first-line treatment for advanced non-small cell lung cancer patients with EGFR exon 20 insertion mutations. The trial included 324 patients randomized to receive either ZEGFROVY at 300 mg once daily or chemotherapy.&lt;/p&gt;

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&lt;p&gt;Dizal Pharmaceutical (SSE: 688192) announced that its drug ZEGFROVY demonstrated superior results compared to platinum-doublet chemotherapy in treating patients with a specific type of non-small cell lung cancer, according to results from a phase 3 clinical trial.&lt;/p&gt;

&lt;p&gt;The WU-KONG28 study evaluated ZEGFROVY as a first-line treatment for advanced non-small cell lung cancer patients with EGFR exon 20 insertion mutations. The trial included 324 patients randomized to receive either ZEGFROVY at 300 mg once daily or chemotherapy.&lt;/p&gt;

&lt;p&gt;Median progression-free survival was 10.3 months with ZEGFROVY versus 7.5 months with chemotherapy. The objective response rate was 68.1% with ZEGFROVY compared to 35.4% with chemotherapy.</description>
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&lt;p&gt;Dizal Pharmaceutical (SSE: 688192) announced that its drug ZEGFROVY demonstrated superior results compared to platinum-doublet chemotherapy in treating patients with a specific type of non-small cell lung cancer, according to results from a phase 3 clinical trial.&lt;/p&gt;

&lt;p&gt;The WU-KONG28 study evaluated ZEGFROVY as a first-line treatment for advanced non-small cell lung cancer patients with EGFR exon 20 insertion mutations. The trial included 324 patients randomized to receive either ZEGFROVY at 300 mg once daily or chemotherapy.&lt;/p&gt;

&lt;p&gt;Median progression-free survival was 10.3 months with ZEGFROVY versus 7.5 months with chemotherapy. The objective response rate was 68.1% with ZEGFROVY compared to 35.4% with chemotherapy.</description>
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   <title>Dizal's ZEGFROVY beats chemotherapy in lung cancer trial</title>
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&lt;p&gt;Dizal Pharmaceutical (SSE: 688192) announced that its drug ZEGFROVY demonstrated superior results compared to platinum-doublet chemotherapy in treating patients with a specific type of non-small cell lung cancer, according to results from a phase 3 clinical trial.&lt;/p&gt;

&lt;p&gt;The WU-KONG28 study evaluated ZEGFROVY as a first-line treatment for advanced non-small cell lung cancer patients with EGFR exon 20 insertion mutations. The trial included 324 patients randomized to receive either ZEGFROVY at 300 mg once daily or chemotherapy.&lt;/p&gt;

&lt;p&gt;Median progression-free survival was 10.3 months with ZEGFROVY versus 7.5 months with chemotherapy. The objective response rate was 68.1% with ZEGFROVY compared to 35.4% with chemotherapy.</description>
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&lt;p&gt;Dizal Pharmaceutical (SSE: 688192) announced that its drug ZEGFROVY demonstrated superior results compared to platinum-doublet chemotherapy in treating patients with a specific type of non-small cell lung cancer, according to results from a phase 3 clinical trial.&lt;/p&gt;

&lt;p&gt;The WU-KONG28 study evaluated ZEGFROVY as a first-line treatment for advanced non-small cell lung cancer patients with EGFR exon 20 insertion mutations. The trial included 324 patients randomized to receive either ZEGFROVY at 300 mg once daily or chemotherapy.&lt;/p&gt;

&lt;p&gt;Median progression-free survival was 10.3 months with ZEGFROVY versus 7.5 months with chemotherapy. The objective response rate was 68.1% with ZEGFROVY compared to 35.4% with chemotherapy.</description>
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&lt;p&gt;Dizal Pharmaceutical (SSE: 688192) announced that its drug ZEGFROVY demonstrated superior results compared to platinum-doublet chemotherapy in treating patients with a specific type of non-small cell lung cancer, according to results from a phase 3 clinical trial.&lt;/p&gt;

&lt;p&gt;The WU-KONG28 study evaluated ZEGFROVY as a first-line treatment for advanced non-small cell lung cancer patients with EGFR exon 20 insertion mutations. The trial included 324 patients randomized to receive either ZEGFROVY at 300 mg once daily or chemotherapy.&lt;/p&gt;

&lt;p&gt;Median progression-free survival was 10.3 months with ZEGFROVY versus 7.5 months with chemotherapy. The objective response rate was 68.1% with ZEGFROVY compared to 35.4% with chemotherapy.</description>
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   <title>Dizal's ZEGFROVY beats chemotherapy in lung cancer trial</title>
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&lt;p&gt;Dizal Pharmaceutical (SSE: 688192) announced that its drug ZEGFROVY demonstrated superior results compared to platinum-doublet chemotherapy in treating patients with a specific type of non-small cell lung cancer, according to results from a phase 3 clinical trial.&lt;/p&gt;

&lt;p&gt;The WU-KONG28 study evaluated ZEGFROVY as a first-line treatment for advanced non-small cell lung cancer patients with EGFR exon 20 insertion mutations. The trial included 324 patients randomized to receive either ZEGFROVY at 300 mg once daily or chemotherapy.&lt;/p&gt;

&lt;p&gt;Median progression-free survival was 10.3 months with ZEGFROVY versus 7.5 months with chemotherapy. The objective response rate was 68.1% with ZEGFROVY compared to 35.4% with chemotherapy.</description>
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   <title>Dizal's ZEGFROVY beats chemotherapy in lung cancer trial</title>
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   <description>

&lt;p&gt;Dizal Pharmaceutical (SSE: 688192) announced that its drug ZEGFROVY demonstrated superior results compared to platinum-doublet chemotherapy in treating patients with a specific type of non-small cell lung cancer, according to results from a phase 3 clinical trial.&lt;/p&gt;

&lt;p&gt;The WU-KONG28 study evaluated ZEGFROVY as a first-line treatment for advanced non-small cell lung cancer patients with EGFR exon 20 insertion mutations. The trial included 324 patients randomized to receive either ZEGFROVY at 300 mg once daily or chemotherapy.&lt;/p&gt;

&lt;p&gt;Median progression-free survival was 10.3 months with ZEGFROVY versus 7.5 months with chemotherapy. The objective response rate was 68.1% with ZEGFROVY compared to 35.4% with chemotherapy.</description>
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