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   <title>Raymond James: 'The topline numbers presented by Black Diamond today indicate that the company has a viable asset in our view'</title>
   <link>http://www.streetinsider.com/Analyst+Comments/Raymond+James%3A+%27The+topline+numbers+presented+by+Black+Diamond+today+indicate+that+the+company+has+a+viable+asset+in+our+view%27/26539334.html</link>
   <description>&lt;p&gt;Raymond James analyst Sean McCutcheon reiterated an Outperform rating and $11.00 price target on Black Diamond Therapeutics (NASDAQ: BDTX).&lt;/p&gt;&lt;p&gt;The analyst comments &quot;Thursday, after market close, ASCO 2026 regular abstracts were released, and in conjunction Black Diamond reported the topline result for the longer-term follow-up from their Phase 2 study testing silevertinib in 1L non-classical EGFR mutant (EGFR NCM) NSCLC. Management also hosted a call to discuss the disclosure. Recall we previously saw the initial response rate data during December 2025 (our commentary), which we think hit the mark in a highly heterogenous NCM population, though left some uncertainty on tolerability/ability</description>
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   <pubDate>Fri, 22 May 2026 09:38:44 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">BDTX</category>
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   <title>Raymond James: 'The topline numbers presented by Black Diamond today indicate that the company has a viable asset in our view'</title>
   <link>http://www.streetinsider.com/Hot+Comments/Raymond+James%3A+%27The+topline+numbers+presented+by+Black+Diamond+today+indicate+that+the+company+has+a+viable+asset+in+our+view%27/26539334.html</link>
   <description>&lt;p&gt;Raymond James analyst Sean McCutcheon reiterated an Outperform rating and $11.00 price target on Black Diamond Therapeutics (NASDAQ: BDTX).&lt;/p&gt;&lt;p&gt;The analyst comments &quot;Thursday, after market close, ASCO 2026 regular abstracts were released, and in conjunction Black Diamond reported the topline result for the longer-term follow-up from their Phase 2 study testing silevertinib in 1L non-classical EGFR mutant (EGFR NCM) NSCLC. Management also hosted a call to discuss the disclosure. Recall we previously saw the initial response rate data during December 2025 (our commentary), which we think hit the mark in a highly heterogenous NCM population, though left some uncertainty on tolerability/ability</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Hot+Comments/Raymond+James%3A+%27The+topline+numbers+presented+by+Black+Diamond+today+indicate+that+the+company+has+a+viable+asset+in+our+view%27/26539334.html</guid>
   <pubDate>Fri, 22 May 2026 09:38:44 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">BDTX</category>
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   <title>Stifel Defending Black Diamond Therapeutics (BDTX): 'we believe investors are underappreciating the breadth of mutation silevertinib is showing'</title>
   <link>http://www.streetinsider.com/Analyst+Comments/Stifel+Defending+Black+Diamond+Therapeutics+%28BDTX%29%3A+%27we+believe+investors+are+underappreciating+the+breadth+of+mutation+silevertinib+is+showing%27/26539329.html</link>
   <description>&lt;p&gt;Stifel analyst Laura Prendergast reiterated a Buy rating and $8.00 price target on Black Diamond Therapeutics (NASDAQ: BDTX).&lt;/p&gt;&lt;p&gt;The analyst comments &quot;We view the preliminary median PFS of 15.2 months as highly encouraging and perhaps practice changing - the DoR had not yet been reached. 44% of patients are progression free/still on drug with median follow up ~9.8 months, suggesting PFS could increase with longer follow up. What stands out to us the most is: • The breadth of mutations seen in patients who are progression free for ≥1 year (10 unique mutations across 8 patients). • The lack of any</description>
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   <pubDate>Fri, 22 May 2026 09:37:35 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">BDTX</category>
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   <title>Stifel Defending Black Diamond Therapeutics (BDTX): 'we believe investors are underappreciating the breadth of mutation silevertinib is showing'</title>
   <link>http://www.streetinsider.com/Hot+Comments/Stifel+Defending+Black+Diamond+Therapeutics+%28BDTX%29%3A+%27we+believe+investors+are+underappreciating+the+breadth+of+mutation+silevertinib+is+showing%27/26539329.html</link>
   <description>&lt;p&gt;Stifel analyst Laura Prendergast reiterated a Buy rating and $8.00 price target on Black Diamond Therapeutics (NASDAQ: BDTX).&lt;/p&gt;&lt;p&gt;The analyst comments &quot;We view the preliminary median PFS of 15.2 months as highly encouraging and perhaps practice changing - the DoR had not yet been reached. 44% of patients are progression free/still on drug with median follow up ~9.8 months, suggesting PFS could increase with longer follow up. What stands out to us the most is: • The breadth of mutations seen in patients who are progression free for ≥1 year (10 unique mutations across 8 patients). • The lack of any</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Hot+Comments/Stifel+Defending+Black+Diamond+Therapeutics+%28BDTX%29%3A+%27we+believe+investors+are+underappreciating+the+breadth+of+mutation+silevertinib+is+showing%27/26539329.html</guid>
   <pubDate>Fri, 22 May 2026 09:37:35 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">BDTX</category>
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   <title>TD Cowen on Black Diamond Therapeutics (BDTX) Amid 18% Drop: 'is unclear if the FDA will require Ph3 run-in or additional Ph2 dosing work extending competitor's lead'</title>
   <link>http://www.streetinsider.com/Analyst+Comments/TD+Cowen+on+Black+Diamond+Therapeutics+%28BDTX%29+Amid+18%25+Drop%3A+%27is+unclear+if+the+FDA+will+require+Ph3+run-in+or+additional+Ph2+dosing+work+extending+competitor%27s+lead%27/26539322.html</link>
   <description>&lt;p&gt;TD Cowen analyst Marc Frahm reiterated a Buy rating and {REMOVEPT} price target on Black Diamond Therapeutics (NASDAQ: BDTX).&lt;/p&gt;&lt;p&gt;The analyst comments &quot;BDTX shared updated 1L data for 200mg silevertinib, including a preliminary mPFS of 15.2m, 60% ORR (86% CNS), and slightly increased dose-reduction of 84%. Mgmt plans to discuss Ph3 pivotal plans including a proposed 150mg dose with the FDA in H2. While 150mg dose selection appears wise, it is unclear if the FDA will require Ph3 run-in or additional Ph2 dosing work extending competitor's lead.&quot;&lt;/p&gt;&lt;p&gt;For an analyst ratings summary and ratings history on Black Diamond Therapeutics &lt;a href=&quot;http://www.streetinsider.com/rating_history.php?q=BDTX&quot;&gt;click here&lt;/a&gt;.</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Analyst+Comments/TD+Cowen+on+Black+Diamond+Therapeutics+%28BDTX%29+Amid+18%25+Drop%3A+%27is+unclear+if+the+FDA+will+require+Ph3+run-in+or+additional+Ph2+dosing+work+extending+competitor%27s+lead%27/26539322.html</guid>
   <pubDate>Fri, 22 May 2026 09:36:24 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">BDTX</category>
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   <title>TD Cowen on Black Diamond Therapeutics (BDTX) Amid 18% Drop: 'is unclear if the FDA will require Ph3 run-in or additional Ph2 dosing work extending competitor's lead'</title>
   <link>http://www.streetinsider.com/Hot+Comments/TD+Cowen+on+Black+Diamond+Therapeutics+%28BDTX%29+Amid+18%25+Drop%3A+%27is+unclear+if+the+FDA+will+require+Ph3+run-in+or+additional+Ph2+dosing+work+extending+competitor%27s+lead%27/26539322.html</link>
   <description>&lt;p&gt;TD Cowen analyst Marc Frahm reiterated a Buy rating and {REMOVEPT} price target on Black Diamond Therapeutics (NASDAQ: BDTX).&lt;/p&gt;&lt;p&gt;The analyst comments &quot;BDTX shared updated 1L data for 200mg silevertinib, including a preliminary mPFS of 15.2m, 60% ORR (86% CNS), and slightly increased dose-reduction of 84%. Mgmt plans to discuss Ph3 pivotal plans including a proposed 150mg dose with the FDA in H2. While 150mg dose selection appears wise, it is unclear if the FDA will require Ph3 run-in or additional Ph2 dosing work extending competitor's lead.&quot;&lt;/p&gt;&lt;p&gt;For an analyst ratings summary and ratings history on Black Diamond Therapeutics &lt;a href=&quot;http://www.streetinsider.com/rating_history.php?q=BDTX&quot;&gt;click here&lt;/a&gt;.</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Hot+Comments/TD+Cowen+on+Black+Diamond+Therapeutics+%28BDTX%29+Amid+18%25+Drop%3A+%27is+unclear+if+the+FDA+will+require+Ph3+run-in+or+additional+Ph2+dosing+work+extending+competitor%27s+lead%27/26539322.html</guid>
   <pubDate>Fri, 22 May 2026 09:36:24 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">BDTX</category>
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   <title>Black Diamond Therapeutics to Participate in Jefferies Global Healthcare Conference</title>
   <link>http://www.streetinsider.com/Press+Releases/Black+Diamond+Therapeutics+to+Participate+in+Jefferies+Global+Healthcare+Conference/26538626.html</link>
   <description>&lt;p align=&quot;left&quot;&gt;CAMBRIDGE, Mass., May  22, 2026  (GLOBE NEWSWIRE) -- &lt;a href=&quot;https://www.globenewswire.com/Tracker?data=ZQbin8Z_Gn0aJZPccENEsfhOqYolFXddWs9pz9_gS8tMdMmqMAKzWgSn-dsVi52gfLI1LnqzR9BQCViCjPTUWsk_IoTxwsculL5U4mO-8tY=&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;&lt;u&gt;Black Diamond Therapeutics, Inc.&lt;/u&gt;&lt;/a&gt; (Nasdaq: BDTX), a clinical-stage oncology company developing MasterKey therapies that target families of oncogenic mutations in patients with cancer, today announced that its Chief Executive Officer, Mark Velleca, M.D., Ph.D., will participate in a fireside chat at the Jefferies Global Healthcare Conference on June 3, 2026, in New York, NY. In addition, the company will host one-on-one meetings with investors on the same day.&lt;/p&gt;  &lt;p&gt;Presentation details are as follows:&lt;/p&gt;  &lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;4:55-5:25pm ET on Wednesday, June 3&lt;br /&gt;&lt;br /&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p&gt;The</description>
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   <pubDate>Fri, 22 May 2026 08:00:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">BDTX</category>
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   <title>Black Diamond Therapeutics to Participate in Jefferies Global Healthcare Conference</title>
   <link>http://www.streetinsider.com/Globe+Newswire/Black+Diamond+Therapeutics+to+Participate+in+Jefferies+Global+Healthcare+Conference/26538626.html</link>
   <description>&lt;p align=&quot;left&quot;&gt;CAMBRIDGE, Mass., May  22, 2026  (GLOBE NEWSWIRE) -- &lt;a href=&quot;https://www.globenewswire.com/Tracker?data=ZQbin8Z_Gn0aJZPccENEsfhOqYolFXddWs9pz9_gS8tMdMmqMAKzWgSn-dsVi52gfLI1LnqzR9BQCViCjPTUWsk_IoTxwsculL5U4mO-8tY=&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;&lt;u&gt;Black Diamond Therapeutics, Inc.&lt;/u&gt;&lt;/a&gt; (Nasdaq: BDTX), a clinical-stage oncology company developing MasterKey therapies that target families of oncogenic mutations in patients with cancer, today announced that its Chief Executive Officer, Mark Velleca, M.D., Ph.D., will participate in a fireside chat at the Jefferies Global Healthcare Conference on June 3, 2026, in New York, NY. In addition, the company will host one-on-one meetings with investors on the same day.&lt;/p&gt;  &lt;p&gt;Presentation details are as follows:&lt;/p&gt;  &lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;4:55-5:25pm ET on Wednesday, June 3&lt;br /&gt;&lt;br /&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p&gt;The</description>
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   <pubDate>Fri, 22 May 2026 08:00:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">BDTX</category>
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   <title>H.C. Wainwright Reiterates Buy Rating on Black Diamond Therapeutics (BDTX)</title>
   <link>http://www.streetinsider.com/Analyst+Comments/H.C.+Wainwright+Reiterates+Buy+Rating+on+Black+Diamond+Therapeutics+%28BDTX%29/26538391.html</link>
   <description>&lt;p&gt;H.C. Wainwright analyst Raghuram Selvaraju reiterated a Buy rating and $11.00 price target on Black Diamond Therapeutics (NASDAQ: BDTX).&lt;/p&gt;&lt;p&gt;The analyst commented: &quot;Yesterday, Black Diamond presented updated Phase 2 results, including duration of response (DOR) and progression-free survival (PFS) results, for silevertinib (BDTX-1535) in 1L NSCLC patients harboring non-classical EGFR mutations. As seen in the company's presentation, silevertinib (n=43; 44% brain metastases; 74% Caucasian) achieved a 60% [26/43] confirmed objective response rate (cORR) and an 86% [6/7] intracranial cORR in NSCLC patients with non-classical EGFR mutations treated in the 1L setting (see Figure 1 overleaf). Responses were seen across 33 distinct</description>
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   <pubDate>Fri, 22 May 2026 06:57:27 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">BDTX</category>
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   <title>Form  8-K        Black Diamond Therapeuti  For: May 21</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++8-K++++++++Black+Diamond+Therapeuti++For%3A+May+21/26536895.html</link>
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   <pubDate>Thu, 21 May 2026 17:19:00 -0400</pubDate>
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   <title>Form  8-K        Black Diamond Therapeuti  For: May 21</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++8-K++++++++Black+Diamond+Therapeuti++For%3A+May+21/26536895.html</link>
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   <pubDate>Thu, 21 May 2026 17:19:00 -0400</pubDate>
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   <title>Black Diamond reports phase 2 lung cancer trial results for silevertinib</title>
   <link>http://www.streetinsider.com/FDA/Black+Diamond+reports+phase+2+lung+cancer+trial+results+for+silevertinib/26536825.html</link>
   <description>

&lt;p&gt;Black Diamond Therapeutics Inc. (NASDAQ: BDTX) announced results from a Phase 2 trial of silevertinib in treatment-naïve non-small cell lung cancer patients with epidermal growth factor receptor non-classical mutations.&lt;/p&gt;

&lt;p&gt;The trial enrolled 43 patients who received 200 mg once daily of silevertinib. Results showed a preliminary median progression-free survival of 15.2 months, with median duration of response not yet reached. The objective response rate was 60% and disease control rate was 91%.&lt;/p&gt;

&lt;p&gt;Among 19 patients with brain metastases, the central nervous system objective response rate was 86%. No patients developed new brain metastases during treatment.&lt;/p&gt;

&lt;p&gt;The safety profile showed treatment-related adverse events greater</description>
   <guid isPermaLink="true">http://www.streetinsider.com/FDA/Black+Diamond+reports+phase+2+lung+cancer+trial+results+for+silevertinib/26536825.html</guid>
   <pubDate>Thu, 21 May 2026 17:14:07 -0400</pubDate>
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   <title>Black Diamond reports phase 2 lung cancer trial results for silevertinib</title>
   <link>http://www.streetinsider.com/FDA/Black+Diamond+reports+phase+2+lung+cancer+trial+results+for+silevertinib/26536825.html</link>
   <description>

&lt;p&gt;Black Diamond Therapeutics Inc. (NASDAQ: BDTX) announced results from a Phase 2 trial of silevertinib in treatment-naïve non-small cell lung cancer patients with epidermal growth factor receptor non-classical mutations.&lt;/p&gt;

&lt;p&gt;The trial enrolled 43 patients who received 200 mg once daily of silevertinib. Results showed a preliminary median progression-free survival of 15.2 months, with median duration of response not yet reached. The objective response rate was 60% and disease control rate was 91%.&lt;/p&gt;

&lt;p&gt;Among 19 patients with brain metastases, the central nervous system objective response rate was 86%. No patients developed new brain metastases during treatment.&lt;/p&gt;

&lt;p&gt;The safety profile showed treatment-related adverse events greater</description>
   <guid isPermaLink="true">http://www.streetinsider.com/FDA/Black+Diamond+reports+phase+2+lung+cancer+trial+results+for+silevertinib/26536825.html</guid>
   <pubDate>Thu, 21 May 2026 17:14:07 -0400</pubDate>
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   <title>Black Diamond reports phase 2 lung cancer trial results for silevertinib</title>
   <link>http://www.streetinsider.com/FDA/Black+Diamond+reports+phase+2+lung+cancer+trial+results+for+silevertinib/26536825.html</link>
   <description>

&lt;p&gt;Black Diamond Therapeutics Inc. (NASDAQ: BDTX) announced results from a Phase 2 trial of silevertinib in treatment-naïve non-small cell lung cancer patients with epidermal growth factor receptor non-classical mutations.&lt;/p&gt;

&lt;p&gt;The trial enrolled 43 patients who received 200 mg once daily of silevertinib. Results showed a preliminary median progression-free survival of 15.2 months, with median duration of response not yet reached. The objective response rate was 60% and disease control rate was 91%.&lt;/p&gt;

&lt;p&gt;Among 19 patients with brain metastases, the central nervous system objective response rate was 86%. No patients developed new brain metastases during treatment.&lt;/p&gt;

&lt;p&gt;The safety profile showed treatment-related adverse events greater</description>
   <guid isPermaLink="true">http://www.streetinsider.com/FDA/Black+Diamond+reports+phase+2+lung+cancer+trial+results+for+silevertinib/26536825.html</guid>
   <pubDate>Thu, 21 May 2026 17:14:07 -0400</pubDate>
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   <title>Black Diamond reports phase 2 lung cancer trial results for silevertinib</title>
   <link>http://www.streetinsider.com/FDA/Black+Diamond+reports+phase+2+lung+cancer+trial+results+for+silevertinib/26536825.html</link>
   <description>

&lt;p&gt;Black Diamond Therapeutics Inc. (NASDAQ: BDTX) announced results from a Phase 2 trial of silevertinib in treatment-naïve non-small cell lung cancer patients with epidermal growth factor receptor non-classical mutations.&lt;/p&gt;

&lt;p&gt;The trial enrolled 43 patients who received 200 mg once daily of silevertinib. Results showed a preliminary median progression-free survival of 15.2 months, with median duration of response not yet reached. The objective response rate was 60% and disease control rate was 91%.&lt;/p&gt;

&lt;p&gt;Among 19 patients with brain metastases, the central nervous system objective response rate was 86%. No patients developed new brain metastases during treatment.&lt;/p&gt;

&lt;p&gt;The safety profile showed treatment-related adverse events greater</description>
   <guid isPermaLink="true">http://www.streetinsider.com/FDA/Black+Diamond+reports+phase+2+lung+cancer+trial+results+for+silevertinib/26536825.html</guid>
   <pubDate>Thu, 21 May 2026 17:14:07 -0400</pubDate>
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   <title>Black Diamond Therapeutics Announces Positive Phase 2 Results for Silevertinib in Frontline NSCLC Patients with EGFR Non-Classical Mutations</title>
   <link>http://www.streetinsider.com/Press+Releases/Black+Diamond+Therapeutics+Announces+Positive+Phase+2+Results+for+Silevertinib+in+Frontline+NSCLC+Patients+with+EGFR+Non-Classical+Mutations/26536822.html</link>
   <description>
&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;em&gt;Preliminary mPFS of 15.2 months; mDOR not reached&lt;/em&gt;&lt;/li&gt;&lt;li&gt;&lt;em&gt;Robust CNS activity, with 86% CNS ORR; no patients developed de novo brain metastases&lt;/em&gt;&lt;/li&gt;&lt;li&gt;&lt;em&gt;ORR 60% in patients with a broad spectrum of EGFR-NCMs, including PACC&lt;/em&gt;&lt;/li&gt;&lt;li&gt;&lt;em&gt;Dose dependent and manageable AE profile, no new safety signals observed&lt;/em&gt;&lt;/li&gt;&lt;li&gt;&lt;em&gt;Webcast on Thursday, May 21, 2026 at 5:30 pm EDT&lt;/em&gt;&lt;br/&gt;&lt;br/&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p&gt;CAMBRIDGE, Mass., May  21, 2026  (GLOBE NEWSWIRE) -- Black Diamond Therapeutics, Inc. (Nasdaq: BDTX), a clinical-stage oncology company developing MasterKey therapies that target families of oncogenic mutations in patients with cancer, today announced positive results from its Phase 2 trial of silevertinib in frontline (1L)</description>
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   <pubDate>Thu, 21 May 2026 17:13:00 -0400</pubDate>
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   <title>Black Diamond Therapeutics Announces Positive Phase 2 Results for Silevertinib in Frontline NSCLC Patients with EGFR Non-Classical Mutations</title>
   <link>http://www.streetinsider.com/Press+Releases/Black+Diamond+Therapeutics+Announces+Positive+Phase+2+Results+for+Silevertinib+in+Frontline+NSCLC+Patients+with+EGFR+Non-Classical+Mutations/26536822.html</link>
   <description>
&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;em&gt;Preliminary mPFS of 15.2 months; mDOR not reached&lt;/em&gt;&lt;/li&gt;&lt;li&gt;&lt;em&gt;Robust CNS activity, with 86% CNS ORR; no patients developed de novo brain metastases&lt;/em&gt;&lt;/li&gt;&lt;li&gt;&lt;em&gt;ORR 60% in patients with a broad spectrum of EGFR-NCMs, including PACC&lt;/em&gt;&lt;/li&gt;&lt;li&gt;&lt;em&gt;Dose dependent and manageable AE profile, no new safety signals observed&lt;/em&gt;&lt;/li&gt;&lt;li&gt;&lt;em&gt;Webcast on Thursday, May 21, 2026 at 5:30 pm EDT&lt;/em&gt;&lt;br/&gt;&lt;br/&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p&gt;CAMBRIDGE, Mass., May  21, 2026  (GLOBE NEWSWIRE) -- Black Diamond Therapeutics, Inc. (Nasdaq: BDTX), a clinical-stage oncology company developing MasterKey therapies that target families of oncogenic mutations in patients with cancer, today announced positive results from its Phase 2 trial of silevertinib in frontline (1L)</description>
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   <title>Black Diamond Therapeutics Announces Positive Phase 2 Results for Silevertinib in Frontline NSCLC Patients with EGFR Non-Classical Mutations</title>
   <link>http://www.streetinsider.com/Press+Releases/Black+Diamond+Therapeutics+Announces+Positive+Phase+2+Results+for+Silevertinib+in+Frontline+NSCLC+Patients+with+EGFR+Non-Classical+Mutations/26536822.html</link>
   <description>
&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;em&gt;Preliminary mPFS of 15.2 months; mDOR not reached&lt;/em&gt;&lt;/li&gt;&lt;li&gt;&lt;em&gt;Robust CNS activity, with 86% CNS ORR; no patients developed de novo brain metastases&lt;/em&gt;&lt;/li&gt;&lt;li&gt;&lt;em&gt;ORR 60% in patients with a broad spectrum of EGFR-NCMs, including PACC&lt;/em&gt;&lt;/li&gt;&lt;li&gt;&lt;em&gt;Dose dependent and manageable AE profile, no new safety signals observed&lt;/em&gt;&lt;/li&gt;&lt;li&gt;&lt;em&gt;Webcast on Thursday, May 21, 2026 at 5:30 pm EDT&lt;/em&gt;&lt;br/&gt;&lt;br/&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p&gt;CAMBRIDGE, Mass., May  21, 2026  (GLOBE NEWSWIRE) -- Black Diamond Therapeutics, Inc. (Nasdaq: BDTX), a clinical-stage oncology company developing MasterKey therapies that target families of oncogenic mutations in patients with cancer, today announced positive results from its Phase 2 trial of silevertinib in frontline (1L)</description>
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   <title>Black Diamond Therapeutics Announces Positive Phase 2 Results for Silevertinib in Frontline NSCLC Patients with EGFR Non-Classical Mutations</title>
   <link>http://www.streetinsider.com/Press+Releases/Black+Diamond+Therapeutics+Announces+Positive+Phase+2+Results+for+Silevertinib+in+Frontline+NSCLC+Patients+with+EGFR+Non-Classical+Mutations/26536822.html</link>
   <description>
&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;em&gt;Preliminary mPFS of 15.2 months; mDOR not reached&lt;/em&gt;&lt;/li&gt;&lt;li&gt;&lt;em&gt;Robust CNS activity, with 86% CNS ORR; no patients developed de novo brain metastases&lt;/em&gt;&lt;/li&gt;&lt;li&gt;&lt;em&gt;ORR 60% in patients with a broad spectrum of EGFR-NCMs, including PACC&lt;/em&gt;&lt;/li&gt;&lt;li&gt;&lt;em&gt;Dose dependent and manageable AE profile, no new safety signals observed&lt;/em&gt;&lt;/li&gt;&lt;li&gt;&lt;em&gt;Webcast on Thursday, May 21, 2026 at 5:30 pm EDT&lt;/em&gt;&lt;br/&gt;&lt;br/&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p&gt;CAMBRIDGE, Mass., May  21, 2026  (GLOBE NEWSWIRE) -- Black Diamond Therapeutics, Inc. (Nasdaq: BDTX), a clinical-stage oncology company developing MasterKey therapies that target families of oncogenic mutations in patients with cancer, today announced positive results from its Phase 2 trial of silevertinib in frontline (1L)</description>
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   <title>Black Diamond Therapeutics Announces Positive Phase 2 Results for Silevertinib in Frontline NSCLC Patients with EGFR Non-Classical Mutations</title>
   <link>http://www.streetinsider.com/Globe+Newswire/Black+Diamond+Therapeutics+Announces+Positive+Phase+2+Results+for+Silevertinib+in+Frontline+NSCLC+Patients+with+EGFR+Non-Classical+Mutations/26536822.html</link>
   <description>
&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;em&gt;Preliminary mPFS of 15.2 months; mDOR not reached&lt;/em&gt;&lt;/li&gt;&lt;li&gt;&lt;em&gt;Robust CNS activity, with 86% CNS ORR; no patients developed de novo brain metastases&lt;/em&gt;&lt;/li&gt;&lt;li&gt;&lt;em&gt;ORR 60% in patients with a broad spectrum of EGFR-NCMs, including PACC&lt;/em&gt;&lt;/li&gt;&lt;li&gt;&lt;em&gt;Dose dependent and manageable AE profile, no new safety signals observed&lt;/em&gt;&lt;/li&gt;&lt;li&gt;&lt;em&gt;Webcast on Thursday, May 21, 2026 at 5:30 pm EDT&lt;/em&gt;&lt;br/&gt;&lt;br/&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p&gt;CAMBRIDGE, Mass., May  21, 2026  (GLOBE NEWSWIRE) -- Black Diamond Therapeutics, Inc. (Nasdaq: BDTX), a clinical-stage oncology company developing MasterKey therapies that target families of oncogenic mutations in patients with cancer, today announced positive results from its Phase 2 trial of silevertinib in frontline (1L)</description>
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   <title>Black Diamond Therapeutics Announces Positive Phase 2 Results for Silevertinib in Frontline NSCLC Patients with EGFR Non-Classical Mutations</title>
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   <description>
&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;em&gt;Preliminary mPFS of 15.2 months; mDOR not reached&lt;/em&gt;&lt;/li&gt;&lt;li&gt;&lt;em&gt;Robust CNS activity, with 86% CNS ORR; no patients developed de novo brain metastases&lt;/em&gt;&lt;/li&gt;&lt;li&gt;&lt;em&gt;ORR 60% in patients with a broad spectrum of EGFR-NCMs, including PACC&lt;/em&gt;&lt;/li&gt;&lt;li&gt;&lt;em&gt;Dose dependent and manageable AE profile, no new safety signals observed&lt;/em&gt;&lt;/li&gt;&lt;li&gt;&lt;em&gt;Webcast on Thursday, May 21, 2026 at 5:30 pm EDT&lt;/em&gt;&lt;br/&gt;&lt;br/&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p&gt;CAMBRIDGE, Mass., May  21, 2026  (GLOBE NEWSWIRE) -- Black Diamond Therapeutics, Inc. (Nasdaq: BDTX), a clinical-stage oncology company developing MasterKey therapies that target families of oncogenic mutations in patients with cancer, today announced positive results from its Phase 2 trial of silevertinib in frontline (1L)</description>
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   <title>Black Diamond Therapeutics Announces Positive Phase 2 Results for Silevertinib in Frontline NSCLC Patients with EGFR Non-Classical Mutations</title>
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   <description>
&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;em&gt;Preliminary mPFS of 15.2 months; mDOR not reached&lt;/em&gt;&lt;/li&gt;&lt;li&gt;&lt;em&gt;Robust CNS activity, with 86% CNS ORR; no patients developed de novo brain metastases&lt;/em&gt;&lt;/li&gt;&lt;li&gt;&lt;em&gt;ORR 60% in patients with a broad spectrum of EGFR-NCMs, including PACC&lt;/em&gt;&lt;/li&gt;&lt;li&gt;&lt;em&gt;Dose dependent and manageable AE profile, no new safety signals observed&lt;/em&gt;&lt;/li&gt;&lt;li&gt;&lt;em&gt;Webcast on Thursday, May 21, 2026 at 5:30 pm EDT&lt;/em&gt;&lt;br/&gt;&lt;br/&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p&gt;CAMBRIDGE, Mass., May  21, 2026  (GLOBE NEWSWIRE) -- Black Diamond Therapeutics, Inc. (Nasdaq: BDTX), a clinical-stage oncology company developing MasterKey therapies that target families of oncogenic mutations in patients with cancer, today announced positive results from its Phase 2 trial of silevertinib in frontline (1L)</description>
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   <title>Black Diamond Therapeutics Announces Positive Phase 2 Results for Silevertinib in Frontline NSCLC Patients with EGFR Non-Classical Mutations</title>
   <link>http://www.streetinsider.com/Globe+Newswire/Black+Diamond+Therapeutics+Announces+Positive+Phase+2+Results+for+Silevertinib+in+Frontline+NSCLC+Patients+with+EGFR+Non-Classical+Mutations/26536822.html</link>
   <description>
&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;em&gt;Preliminary mPFS of 15.2 months; mDOR not reached&lt;/em&gt;&lt;/li&gt;&lt;li&gt;&lt;em&gt;Robust CNS activity, with 86% CNS ORR; no patients developed de novo brain metastases&lt;/em&gt;&lt;/li&gt;&lt;li&gt;&lt;em&gt;ORR 60% in patients with a broad spectrum of EGFR-NCMs, including PACC&lt;/em&gt;&lt;/li&gt;&lt;li&gt;&lt;em&gt;Dose dependent and manageable AE profile, no new safety signals observed&lt;/em&gt;&lt;/li&gt;&lt;li&gt;&lt;em&gt;Webcast on Thursday, May 21, 2026 at 5:30 pm EDT&lt;/em&gt;&lt;br/&gt;&lt;br/&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p&gt;CAMBRIDGE, Mass., May  21, 2026  (GLOBE NEWSWIRE) -- Black Diamond Therapeutics, Inc. (Nasdaq: BDTX), a clinical-stage oncology company developing MasterKey therapies that target families of oncogenic mutations in patients with cancer, today announced positive results from its Phase 2 trial of silevertinib in frontline (1L)</description>
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   <title>Black Diamond Therapeutics schedules investor webcast on silevertinib trial</title>
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&lt;p&gt;Black Diamond Therapeutics Inc. (NASDAQ: BDTX) will host an investor webcast on May 21, 2026, at 5:30 p.m. ET to present updated results from its Phase 2 trial of silevertinib in first-line patients with EGFR mutated non-small cell lung cancer.&lt;/p&gt;

&lt;p&gt;The Cambridge, Massachusetts-based clinical-stage oncology company announced the webcast will be accessible through the &quot;Events and Presentations&quot; section on its investor website. A replay will be available for a limited time following the event.&lt;/p&gt;

&lt;p&gt;Silevertinib is described by the company as a brain-penetrant fourth-generation EGFR inhibitor targeting EGFR-mutant NSCLC and glioblastoma multiforme. Black Diamond Therapeutics develops what it calls MasterKey therapies designed</description>
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   <pubDate>Tue, 19 May 2026 08:01:11 -0400</pubDate>
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   <title>Black Diamond Therapeutics schedules investor webcast on silevertinib trial</title>
   <link>http://www.streetinsider.com/FDA/Black+Diamond+Therapeutics+schedules+investor+webcast+on+silevertinib+trial/26517628.html</link>
   <description>

&lt;p&gt;Black Diamond Therapeutics Inc. (NASDAQ: BDTX) will host an investor webcast on May 21, 2026, at 5:30 p.m. ET to present updated results from its Phase 2 trial of silevertinib in first-line patients with EGFR mutated non-small cell lung cancer.&lt;/p&gt;

&lt;p&gt;The Cambridge, Massachusetts-based clinical-stage oncology company announced the webcast will be accessible through the &quot;Events and Presentations&quot; section on its investor website. A replay will be available for a limited time following the event.&lt;/p&gt;

&lt;p&gt;Silevertinib is described by the company as a brain-penetrant fourth-generation EGFR inhibitor targeting EGFR-mutant NSCLC and glioblastoma multiforme. Black Diamond Therapeutics develops what it calls MasterKey therapies designed</description>
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   <pubDate>Tue, 19 May 2026 08:01:11 -0400</pubDate>
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