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   <title>Moderna shares continue to fall after early cancer vaccine data leak</title>
   <link>http://www.streetinsider.com/Investing/Moderna+shares+continue+to+fall+after+early+cancer+vaccine+data+leak/27225994.html</link>
   <description>&lt;p&gt;Moderna Inc. shares dropped 2.3% in morning trading on Friday, adding to sharp losses from the previous session after clinical trial results for its personalized melanoma vaccine were published early by a medical news website on Thursday.&lt;/p&gt;&lt;p&gt;The Phase 3 data for intismeran autogene, developed with Merck &amp; Co. (NYSE:MRK), was scheduled for presentation at the ESMO Congress in Madrid on Saturday. The information appeared on a medical news website Thursday afternoon before being removed, prompting Moderna and Merck to issue an official release of the results.&lt;/p&gt;&lt;p&gt;The INTerpath-001 trial showed the vaccine combined with Merck's Keytruda reduced the risk of melanoma</description>
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   <pubDate>Fri, 23 Oct 2026 09:50:17 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">MRK</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">MRNA</category>
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   <title>Moderna shares continue to fall after early cancer vaccine data leak</title>
   <link>http://www.streetinsider.com/Investing/Moderna+shares+continue+to+fall+after+early+cancer+vaccine+data+leak/27225994.html</link>
   <description>&lt;p&gt;Moderna Inc. shares dropped 2.3% in morning trading on Friday, adding to sharp losses from the previous session after clinical trial results for its personalized melanoma vaccine were published early by a medical news website on Thursday.&lt;/p&gt;&lt;p&gt;The Phase 3 data for intismeran autogene, developed with Merck &amp; Co. (NYSE:MRK), was scheduled for presentation at the ESMO Congress in Madrid on Saturday. The information appeared on a medical news website Thursday afternoon before being removed, prompting Moderna and Merck to issue an official release of the results.&lt;/p&gt;&lt;p&gt;The INTerpath-001 trial showed the vaccine combined with Merck's Keytruda reduced the risk of melanoma</description>
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   <pubDate>Fri, 23 Oct 2026 09:50:17 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">MRK</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">MRNA</category>
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   <title>Citi reiterates Sell rating on Moderna with $80 price target</title>
   <link>http://www.streetinsider.com/Hot+Comments/Citi+reiterates+Sell+rating+on+Moderna+with+%2480+price+target/27225988.html</link>
   <description>&lt;p&gt;Citi analyst Geoff Meacham reiterated a Sell rating and $80.00 price target on Moderna (NASDAQ: MRNA).&lt;/p&gt;&lt;p&gt;Meacham outlined ten reasons why positive melanoma trial data from the INTerpath-001 study do not address his concerns about the company's valuation. He noted that one successful study in melanoma does not validate individualized neoantigen therapy as a broadly applicable oncology platform, and that overall survival data remain immature.&lt;/p&gt;&lt;p&gt;The analyst said the therapy, intismeran, requires tumor sequencing, individualized manufacturing, and coordination across multiple medical disciplines, with pricing still unknown. He also pointed to neoadjuvant pembrolizumab as a simpler alternative, citing an event-free survival hazard ratio</description>
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   <pubDate>Fri, 23 Oct 2026 09:48:42 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">MRNA</category>
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   <title>Moderna Named a Top Employer by Science for Twelfth Consecutive Year</title>
   <link>http://www.streetinsider.com/Press+Releases/Moderna+Named+a+Top+Employer+by+Science+for+Twelfth+Consecutive+Year/27224857.html</link>
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      &lt;p&gt;&lt;strong id=&quot;dateline&quot;&gt;CAMBRIDGE, MA / &lt;a href='https://www.accessnewswire.com/'&gt;ACCESS Newswire&lt;/a&gt; / October 23, 2026 / &lt;/strong&gt;Moderna, Inc. (NASDAQ:MRNA) today announced it was ranked as a top employer in the global biopharmaceutical industry in Science and Science Careers' 2026 Top Employers Survey for the twelfth consecutive year. Moderna was recognized for its corporate image, leadership and direction, and work culture, reflecting its reputation for innovation and quality research, commitment to continuous improvement, and collaborative, data-driven environment.&lt;/p&gt;&lt;p&gt;&quot;At Moderna, we have always believed that the best science happens when talented people are given the opportunity to tackle important problems and</description>
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   <pubDate>Fri, 23 Oct 2026 07:00:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">MRNA</category>
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  <item>
   <title>Moderna Named a Top Employer by Science for Twelfth Consecutive Year</title>
   <link>http://www.streetinsider.com/ACCESS+Newswire/Moderna+Named+a+Top+Employer+by+Science+for+Twelfth+Consecutive+Year/27224857.html</link>
   <description>
      &lt;p&gt;&lt;strong id=&quot;dateline&quot;&gt;CAMBRIDGE, MA / &lt;a href='https://www.accessnewswire.com/'&gt;ACCESS Newswire&lt;/a&gt; / October 23, 2026 / &lt;/strong&gt;Moderna, Inc. (NASDAQ:MRNA) today announced it was ranked as a top employer in the global biopharmaceutical industry in Science and Science Careers' 2026 Top Employers Survey for the twelfth consecutive year. Moderna was recognized for its corporate image, leadership and direction, and work culture, reflecting its reputation for innovation and quality research, commitment to continuous improvement, and collaborative, data-driven environment.&lt;/p&gt;&lt;p&gt;&quot;At Moderna, we have always believed that the best science happens when talented people are given the opportunity to tackle important problems and</description>
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   <pubDate>Fri, 23 Oct 2026 07:00:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">MRNA</category>
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   <title>Moderna (MRNA) call put ratio 1 call to 1.4 puts amid wide share price movement</title>
   <link>http://www.streetinsider.com/Options/Moderna+%28MRNA%29+call+put+ratio+1+call+to+1.4+puts+amid+wide+share+price+movement/27224386.html</link>
   <description>&lt;p&gt;Moderna (NASDAQ: MRNA) 30-day option implied volatility is at 92; compared to its 52-week range of 57 to 138. Call put ratio 1 call to 1.4 puts amid wide share price movement.&lt;/p&gt;</description>
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   <pubDate>Fri, 23 Oct 2026 05:51:06 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">MRNA</category>
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   <title>RBC Capital Reiterates Sector Perform Rating on Merck (MRK)</title>
   <link>http://www.streetinsider.com/Analyst+Comments/RBC+Capital+Reiterates+Sector+Perform+Rating+on+Merck+%28MRK%29/27222559.html</link>
   <description>&lt;p&gt;RBC Capital analyst Trung Huynh reiterated a Sector Perform rating and $145.00 price target on Merck (NYSE: MRK).&lt;/p&gt;&lt;p&gt;The analyst comments &quot;Our View: The INTerpath-001 data is clinically meaningful and likely approvable, offering patients an important new treatment option in high-risk melanoma. An RFS hazard ratio of 0.58 with a well-tolerated safety profile should support regulatory filings in the US and Europe, and we expect FDA approval in 2027. Merck and Moderna are currently engaging with regulatory authorities. However, the data falls short of the high bar set by Phase 2 results and investor expectations. Going into the readout, investor expectations</description>
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   <pubDate>Thu, 22 Oct 2026 16:05:11 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">MRK</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">MRNA</category>
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   <title>RBC Capital Reiterates Sector Perform Rating on Merck (MRK)</title>
   <link>http://www.streetinsider.com/Analyst+Comments/RBC+Capital+Reiterates+Sector+Perform+Rating+on+Merck+%28MRK%29/27222559.html</link>
   <description>&lt;p&gt;RBC Capital analyst Trung Huynh reiterated a Sector Perform rating and $145.00 price target on Merck (NYSE: MRK).&lt;/p&gt;&lt;p&gt;The analyst comments &quot;Our View: The INTerpath-001 data is clinically meaningful and likely approvable, offering patients an important new treatment option in high-risk melanoma. An RFS hazard ratio of 0.58 with a well-tolerated safety profile should support regulatory filings in the US and Europe, and we expect FDA approval in 2027. Merck and Moderna are currently engaging with regulatory authorities. However, the data falls short of the high bar set by Phase 2 results and investor expectations. Going into the readout, investor expectations</description>
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   <pubDate>Thu, 22 Oct 2026 16:05:11 -0400</pubDate>
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   	   	<category domain="http://rss.financialcontent.com/stocksymbol">MRNA</category>
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   <title>Citi keeps Sell rating on Moderna after melanoma trial data, PT $80</title>
   <link>http://www.streetinsider.com/General+News/Citi+keeps+Sell+rating+on+Moderna+after+melanoma+trial+data%2C+PT+%2480/27222470.html</link>
   <description>&lt;p&gt;Citi analyst Geoff Meacham reiterated a Sell rating and $80.00 price target on Moderna (NASDAQ: MRNA) after phase 3 INTerpath-001 trial data showed the company's intismeran combined with pembrolizumab reduced the risk of recurrence or death by 42% compared to pembrolizumab alone in adjuvant melanoma, with a hazard ratio of 0.58.&lt;/p&gt;&lt;p&gt;Moderna shares fell 25% intraday following the data release, which was confirmed by the European Society for Medical Oncology. The broader XBI index and S&amp;P 500 each declined approximately 1% on the same day.&lt;/p&gt;&lt;p&gt;Meacham noted that while the trial results represent a clinically meaningful advance with consistent efficacy across lower-</description>
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   <pubDate>Thu, 22 Oct 2026 16:01:44 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">MRNA</category>
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   <title>Merck and Moderna report Phase 3 melanoma trial results</title>
   <link>http://www.streetinsider.com/Corporate+News/Merck+and+Moderna+report+Phase+3+melanoma+trial+results/27222416.html</link>
   <description>&lt;p&gt;Merck (NYSE: MRK) and Moderna (NASDAQ: MRNA) announced results from the Phase 3 INTerpath-001 trial evaluating intismeran autogene in combination with KEYTRUDA (pembrolizumab) as adjuvant treatment for patients with completely resected stage IIB-IV melanoma. The results were presented at the European Society for Medical Oncology (ESMO) Congress 2026 and accepted for publication in The New England Journal of Medicine.&lt;/p&gt;&lt;p&gt;The trial enrolled 1,137 patients randomized 2:1 to receive intismeran plus KEYTRUDA or placebo plus KEYTRUDA. At the primary pre-specified analysis, after a median follow-up of 24.6 months, intismeran combined with KEYTRUDA reduced the risk of recurrence or death by 42% (HR=0.58</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Corporate+News/Merck+and+Moderna+report+Phase+3+melanoma+trial+results/27222416.html</guid>
   <pubDate>Thu, 22 Oct 2026 15:59:27 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">MRK</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">MRNA</category>
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   <title>Merck and Moderna report Phase 3 melanoma trial results</title>
   <link>http://www.streetinsider.com/FDA/Merck+and+Moderna+report+Phase+3+melanoma+trial+results/27222416.html</link>
   <description>&lt;p&gt;Merck (NYSE: MRK) and Moderna (NASDAQ: MRNA) announced results from the Phase 3 INTerpath-001 trial evaluating intismeran autogene in combination with KEYTRUDA (pembrolizumab) as adjuvant treatment for patients with completely resected stage IIB-IV melanoma. The results were presented at the European Society for Medical Oncology (ESMO) Congress 2026 and accepted for publication in The New England Journal of Medicine.&lt;/p&gt;&lt;p&gt;The trial enrolled 1,137 patients randomized 2:1 to receive intismeran plus KEYTRUDA or placebo plus KEYTRUDA. At the primary pre-specified analysis, after a median follow-up of 24.6 months, intismeran combined with KEYTRUDA reduced the risk of recurrence or death by 42% (HR=0.58</description>
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   <pubDate>Thu, 22 Oct 2026 15:59:27 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">MRK</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">MRNA</category>
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  <item>
   <title>Merck and Moderna report Phase 3 melanoma trial results</title>
   <link>http://www.streetinsider.com/Hot+Corp.+News/Merck+and+Moderna+report+Phase+3+melanoma+trial+results/27222416.html</link>
   <description>&lt;p&gt;Merck (NYSE: MRK) and Moderna (NASDAQ: MRNA) announced results from the Phase 3 INTerpath-001 trial evaluating intismeran autogene in combination with KEYTRUDA (pembrolizumab) as adjuvant treatment for patients with completely resected stage IIB-IV melanoma. The results were presented at the European Society for Medical Oncology (ESMO) Congress 2026 and accepted for publication in The New England Journal of Medicine.&lt;/p&gt;&lt;p&gt;The trial enrolled 1,137 patients randomized 2:1 to receive intismeran plus KEYTRUDA or placebo plus KEYTRUDA. At the primary pre-specified analysis, after a median follow-up of 24.6 months, intismeran combined with KEYTRUDA reduced the risk of recurrence or death by 42% (HR=0.58</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Hot+Corp.+News/Merck+and+Moderna+report+Phase+3+melanoma+trial+results/27222416.html</guid>
   <pubDate>Thu, 22 Oct 2026 15:59:27 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">MRK</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">MRNA</category>
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   <title>Merck and Moderna report Phase 3 melanoma trial results</title>
   <link>http://www.streetinsider.com/Hot+FDA+News/Merck+and+Moderna+report+Phase+3+melanoma+trial+results/27222416.html</link>
   <description>&lt;p&gt;Merck (NYSE: MRK) and Moderna (NASDAQ: MRNA) announced results from the Phase 3 INTerpath-001 trial evaluating intismeran autogene in combination with KEYTRUDA (pembrolizumab) as adjuvant treatment for patients with completely resected stage IIB-IV melanoma. The results were presented at the European Society for Medical Oncology (ESMO) Congress 2026 and accepted for publication in The New England Journal of Medicine.&lt;/p&gt;&lt;p&gt;The trial enrolled 1,137 patients randomized 2:1 to receive intismeran plus KEYTRUDA or placebo plus KEYTRUDA. At the primary pre-specified analysis, after a median follow-up of 24.6 months, intismeran combined with KEYTRUDA reduced the risk of recurrence or death by 42% (HR=0.58</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Hot+FDA+News/Merck+and+Moderna+report+Phase+3+melanoma+trial+results/27222416.html</guid>
   <pubDate>Thu, 22 Oct 2026 15:59:27 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">MRK</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">MRNA</category>
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   <title>Merck and Moderna report Phase 3 melanoma trial results</title>
   <link>http://www.streetinsider.com/Corporate+News/Merck+and+Moderna+report+Phase+3+melanoma+trial+results/27222416.html</link>
   <description>&lt;p&gt;Merck (NYSE: MRK) and Moderna (NASDAQ: MRNA) announced results from the Phase 3 INTerpath-001 trial evaluating intismeran autogene in combination with KEYTRUDA (pembrolizumab) as adjuvant treatment for patients with completely resected stage IIB-IV melanoma. The results were presented at the European Society for Medical Oncology (ESMO) Congress 2026 and accepted for publication in The New England Journal of Medicine.&lt;/p&gt;&lt;p&gt;The trial enrolled 1,137 patients randomized 2:1 to receive intismeran plus KEYTRUDA or placebo plus KEYTRUDA. At the primary pre-specified analysis, after a median follow-up of 24.6 months, intismeran combined with KEYTRUDA reduced the risk of recurrence or death by 42% (HR=0.58</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Corporate+News/Merck+and+Moderna+report+Phase+3+melanoma+trial+results/27222416.html</guid>
   <pubDate>Thu, 22 Oct 2026 15:59:27 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">MRK</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">MRNA</category>
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   <title>Merck and Moderna report Phase 3 melanoma trial results</title>
   <link>http://www.streetinsider.com/FDA/Merck+and+Moderna+report+Phase+3+melanoma+trial+results/27222416.html</link>
   <description>&lt;p&gt;Merck (NYSE: MRK) and Moderna (NASDAQ: MRNA) announced results from the Phase 3 INTerpath-001 trial evaluating intismeran autogene in combination with KEYTRUDA (pembrolizumab) as adjuvant treatment for patients with completely resected stage IIB-IV melanoma. The results were presented at the European Society for Medical Oncology (ESMO) Congress 2026 and accepted for publication in The New England Journal of Medicine.&lt;/p&gt;&lt;p&gt;The trial enrolled 1,137 patients randomized 2:1 to receive intismeran plus KEYTRUDA or placebo plus KEYTRUDA. At the primary pre-specified analysis, after a median follow-up of 24.6 months, intismeran combined with KEYTRUDA reduced the risk of recurrence or death by 42% (HR=0.58</description>
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   <pubDate>Thu, 22 Oct 2026 15:59:27 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">MRK</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">MRNA</category>
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   <title>Merck and Moderna report Phase 3 melanoma trial results</title>
   <link>http://www.streetinsider.com/Hot+Corp.+News/Merck+and+Moderna+report+Phase+3+melanoma+trial+results/27222416.html</link>
   <description>&lt;p&gt;Merck (NYSE: MRK) and Moderna (NASDAQ: MRNA) announced results from the Phase 3 INTerpath-001 trial evaluating intismeran autogene in combination with KEYTRUDA (pembrolizumab) as adjuvant treatment for patients with completely resected stage IIB-IV melanoma. The results were presented at the European Society for Medical Oncology (ESMO) Congress 2026 and accepted for publication in The New England Journal of Medicine.&lt;/p&gt;&lt;p&gt;The trial enrolled 1,137 patients randomized 2:1 to receive intismeran plus KEYTRUDA or placebo plus KEYTRUDA. At the primary pre-specified analysis, after a median follow-up of 24.6 months, intismeran combined with KEYTRUDA reduced the risk of recurrence or death by 42% (HR=0.58</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Hot+Corp.+News/Merck+and+Moderna+report+Phase+3+melanoma+trial+results/27222416.html</guid>
   <pubDate>Thu, 22 Oct 2026 15:59:27 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">MRK</category>
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   <title>Merck and Moderna report Phase 3 melanoma trial results</title>
   <link>http://www.streetinsider.com/Hot+FDA+News/Merck+and+Moderna+report+Phase+3+melanoma+trial+results/27222416.html</link>
   <description>&lt;p&gt;Merck (NYSE: MRK) and Moderna (NASDAQ: MRNA) announced results from the Phase 3 INTerpath-001 trial evaluating intismeran autogene in combination with KEYTRUDA (pembrolizumab) as adjuvant treatment for patients with completely resected stage IIB-IV melanoma. The results were presented at the European Society for Medical Oncology (ESMO) Congress 2026 and accepted for publication in The New England Journal of Medicine.&lt;/p&gt;&lt;p&gt;The trial enrolled 1,137 patients randomized 2:1 to receive intismeran plus KEYTRUDA or placebo plus KEYTRUDA. At the primary pre-specified analysis, after a median follow-up of 24.6 months, intismeran combined with KEYTRUDA reduced the risk of recurrence or death by 42% (HR=0.58</description>
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   <pubDate>Thu, 22 Oct 2026 15:59:27 -0400</pubDate>
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   <title>Moderna (MRNA) call put ratio 1 call to 1.6 puts as share price down 22%</title>
   <link>http://www.streetinsider.com/Options/Moderna+%28MRNA%29+call+put+ratio+1+call+to+1.6+puts+as+share+price+down+22%25/27222270.html</link>
   <description>&lt;p&gt;Moderna (NASDAQ: MRNA) 30-day option implied volatility is at 95; compared to its 52-week range of 57 to 138. Call put ratio 1 call to 1.6 puts as share price down 22%.&lt;/p&gt;</description>
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   <pubDate>Thu, 22 Oct 2026 15:20:09 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">MRNA</category>
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   <title>Merck and Moderna melanoma drug combo cuts recurrence risk by 42%</title>
   <link>http://www.streetinsider.com/FDA/Merck+and+Moderna+melanoma+drug+combo+cuts+recurrence+risk+by+42%25/27222188.html</link>
   <description>

&lt;p&gt;Merck (NYSE: MRK) and Moderna (NASDAQ: MRNA) announced Phase 3 trial results showing that intismeran autogene combined with KEYTRUDA (pembrolizumab) reduced the risk of recurrence or death by 42% compared to KEYTRUDA alone in patients with completely resected stage IIB-IV melanoma.&lt;/p&gt;

&lt;p&gt;The INTerpath-001 trial enrolled 1,137 patients who were randomized 2:1 to receive intismeran plus KEYTRUDA or placebo plus KEYTRUDA for approximately one year. After a median follow-up of 24.6 months, the combination also reduced the risk of distant metastasis or death by 38% compared to KEYTRUDA alone. The two-year recurrence-free survival rate was 82.2% for the combination versus 70.0% for</description>
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   <pubDate>Thu, 22 Oct 2026 14:59:25 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">MRK</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">MRNA</category>
   	  </item>
  <item>
   <title>Merck and Moderna melanoma drug combo cuts recurrence risk by 42%</title>
   <link>http://www.streetinsider.com/FDA/Merck+and+Moderna+melanoma+drug+combo+cuts+recurrence+risk+by+42%25/27222188.html</link>
   <description>

&lt;p&gt;Merck (NYSE: MRK) and Moderna (NASDAQ: MRNA) announced Phase 3 trial results showing that intismeran autogene combined with KEYTRUDA (pembrolizumab) reduced the risk of recurrence or death by 42% compared to KEYTRUDA alone in patients with completely resected stage IIB-IV melanoma.&lt;/p&gt;

&lt;p&gt;The INTerpath-001 trial enrolled 1,137 patients who were randomized 2:1 to receive intismeran plus KEYTRUDA or placebo plus KEYTRUDA for approximately one year. After a median follow-up of 24.6 months, the combination also reduced the risk of distant metastasis or death by 38% compared to KEYTRUDA alone. The two-year recurrence-free survival rate was 82.2% for the combination versus 70.0% for</description>
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   <pubDate>Thu, 22 Oct 2026 14:59:25 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">MRK</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">MRNA</category>
   	  </item>
  <item>
   <title>Merck and Moderna Will Present Results From Landmark Phase 3 INTerpath-001 Trial for Intismeran Autogene Plus KEYTRUDA® (pembrolizumab) at ESMO 2026 Presidential Symposium</title>
   <link>http://www.streetinsider.com/Press+Releases/Merck+and+Moderna+Will+Present+Results+From+Landmark+Phase+3+INTerpath-001+Trial+for+Intismeran+Autogene+Plus+KEYTRUDA%C2%AE+%28pembrolizumab%29+at+ESMO+2026+Presidential+Symposium/27222185.html</link>
   <description>
&lt;p class=&quot;bwalignc&quot;&gt;
&lt;b&gt;Intismeran plus KEYTRUDA significantly reduced the risk of recurrence or death by 42% (HR=0.58 [95% CI, 0.45–0.75]; two-sided p&amp;lt;0.001) compared to KEYTRUDA alone for patients with completely resected stage IIB-IV melanoma&lt;/b&gt;

&lt;/p&gt;&lt;p class=&quot;bwalignc&quot;&gt;
&lt;b&gt;Benefit was greater after six months, following the intismeran immunization regimen, as intismeran plus KEYTRUDA reduced the risk of recurrence or death by 58% (piecewise HR=0.42 [95% CI, 0.30–0.58]) compared to KEYTRUDA alone in a pre-specified sensitivity analysis&lt;/b&gt;

&lt;/p&gt;
&lt;p&gt;    RAHWAY, N.J. &amp;amp; CAMBRIDGE, Mass.--(BUSINESS WIRE)--
Merck (NYSE: MRK), known as MSD outside of the United States and Canada, and Moderna, Inc. (NASDAQ: MRNA) today announced detailed positive</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Press+Releases/Merck+and+Moderna+Will+Present+Results+From+Landmark+Phase+3+INTerpath-001+Trial+for+Intismeran+Autogene+Plus+KEYTRUDA%C2%AE+%28pembrolizumab%29+at+ESMO+2026+Presidential+Symposium/27222185.html</guid>
   <pubDate>Thu, 22 Oct 2026 14:59:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">MRK</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">MRNA</category>
   	  </item>
  <item>
   <title>Merck and Moderna Will Present Results From Landmark Phase 3 INTerpath-001 Trial for Intismeran Autogene Plus KEYTRUDA® (pembrolizumab) at ESMO 2026 Presidential Symposium</title>
   <link>http://www.streetinsider.com/Business+Wire/Merck+and+Moderna+Will+Present+Results+From+Landmark+Phase+3+INTerpath-001+Trial+for+Intismeran+Autogene+Plus+KEYTRUDA%C2%AE+%28pembrolizumab%29+at+ESMO+2026+Presidential+Symposium/27222185.html</link>
   <description>
&lt;p class=&quot;bwalignc&quot;&gt;
&lt;b&gt;Intismeran plus KEYTRUDA significantly reduced the risk of recurrence or death by 42% (HR=0.58 [95% CI, 0.45–0.75]; two-sided p&amp;lt;0.001) compared to KEYTRUDA alone for patients with completely resected stage IIB-IV melanoma&lt;/b&gt;

&lt;/p&gt;&lt;p class=&quot;bwalignc&quot;&gt;
&lt;b&gt;Benefit was greater after six months, following the intismeran immunization regimen, as intismeran plus KEYTRUDA reduced the risk of recurrence or death by 58% (piecewise HR=0.42 [95% CI, 0.30–0.58]) compared to KEYTRUDA alone in a pre-specified sensitivity analysis&lt;/b&gt;

&lt;/p&gt;
&lt;p&gt;    RAHWAY, N.J. &amp;amp; CAMBRIDGE, Mass.--(BUSINESS WIRE)--
Merck (NYSE: MRK), known as MSD outside of the United States and Canada, and Moderna, Inc. (NASDAQ: MRNA) today announced detailed positive</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Business+Wire/Merck+and+Moderna+Will+Present+Results+From+Landmark+Phase+3+INTerpath-001+Trial+for+Intismeran+Autogene+Plus+KEYTRUDA%C2%AE+%28pembrolizumab%29+at+ESMO+2026+Presidential+Symposium/27222185.html</guid>
   <pubDate>Thu, 22 Oct 2026 14:59:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">MRK</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">MRNA</category>
   	  </item>
  <item>
   <title>Merck and Moderna Will Present Results From Landmark Phase 3 INTerpath-001 Trial for Intismeran Autogene Plus KEYTRUDA® (pembrolizumab) at ESMO 2026 Presidential Symposium</title>
   <link>http://www.streetinsider.com/Press+Releases/Merck+and+Moderna+Will+Present+Results+From+Landmark+Phase+3+INTerpath-001+Trial+for+Intismeran+Autogene+Plus+KEYTRUDA%C2%AE+%28pembrolizumab%29+at+ESMO+2026+Presidential+Symposium/27222185.html</link>
   <description>
&lt;p class=&quot;bwalignc&quot;&gt;
&lt;b&gt;Intismeran plus KEYTRUDA significantly reduced the risk of recurrence or death by 42% (HR=0.58 [95% CI, 0.45–0.75]; two-sided p&amp;lt;0.001) compared to KEYTRUDA alone for patients with completely resected stage IIB-IV melanoma&lt;/b&gt;

&lt;/p&gt;&lt;p class=&quot;bwalignc&quot;&gt;
&lt;b&gt;Benefit was greater after six months, following the intismeran immunization regimen, as intismeran plus KEYTRUDA reduced the risk of recurrence or death by 58% (piecewise HR=0.42 [95% CI, 0.30–0.58]) compared to KEYTRUDA alone in a pre-specified sensitivity analysis&lt;/b&gt;

&lt;/p&gt;
&lt;p&gt;    RAHWAY, N.J. &amp;amp; CAMBRIDGE, Mass.--(BUSINESS WIRE)--
Merck (NYSE: MRK), known as MSD outside of the United States and Canada, and Moderna, Inc. (NASDAQ: MRNA) today announced detailed positive</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Press+Releases/Merck+and+Moderna+Will+Present+Results+From+Landmark+Phase+3+INTerpath-001+Trial+for+Intismeran+Autogene+Plus+KEYTRUDA%C2%AE+%28pembrolizumab%29+at+ESMO+2026+Presidential+Symposium/27222185.html</guid>
   <pubDate>Thu, 22 Oct 2026 14:59:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">MRK</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">MRNA</category>
   	  </item>
  <item>
   <title>Merck and Moderna Will Present Results From Landmark Phase 3 INTerpath-001 Trial for Intismeran Autogene Plus KEYTRUDA® (pembrolizumab) at ESMO 2026 Presidential Symposium</title>
   <link>http://www.streetinsider.com/Business+Wire/Merck+and+Moderna+Will+Present+Results+From+Landmark+Phase+3+INTerpath-001+Trial+for+Intismeran+Autogene+Plus+KEYTRUDA%C2%AE+%28pembrolizumab%29+at+ESMO+2026+Presidential+Symposium/27222185.html</link>
   <description>
&lt;p class=&quot;bwalignc&quot;&gt;
&lt;b&gt;Intismeran plus KEYTRUDA significantly reduced the risk of recurrence or death by 42% (HR=0.58 [95% CI, 0.45–0.75]; two-sided p&amp;lt;0.001) compared to KEYTRUDA alone for patients with completely resected stage IIB-IV melanoma&lt;/b&gt;

&lt;/p&gt;&lt;p class=&quot;bwalignc&quot;&gt;
&lt;b&gt;Benefit was greater after six months, following the intismeran immunization regimen, as intismeran plus KEYTRUDA reduced the risk of recurrence or death by 58% (piecewise HR=0.42 [95% CI, 0.30–0.58]) compared to KEYTRUDA alone in a pre-specified sensitivity analysis&lt;/b&gt;

&lt;/p&gt;
&lt;p&gt;    RAHWAY, N.J. &amp;amp; CAMBRIDGE, Mass.--(BUSINESS WIRE)--
Merck (NYSE: MRK), known as MSD outside of the United States and Canada, and Moderna, Inc. (NASDAQ: MRNA) today announced detailed positive</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Business+Wire/Merck+and+Moderna+Will+Present+Results+From+Landmark+Phase+3+INTerpath-001+Trial+for+Intismeran+Autogene+Plus+KEYTRUDA%C2%AE+%28pembrolizumab%29+at+ESMO+2026+Presidential+Symposium/27222185.html</guid>
   <pubDate>Thu, 22 Oct 2026 14:59:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">MRK</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">MRNA</category>
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  <item>
   <title>Moderna shares plunge on cancer vaccine data leak</title>
   <link>http://www.streetinsider.com/Investing/Moderna+shares+plunge+on+cancer+vaccine+data+leak/27221804.html</link>
   <description>(Updated - October 22, 2026 2:34 PM EDT)

&lt;p data-pm-slice=&quot;1 1 []&quot;&gt;Investing.com -- Moderna shares plunged more than 25% on Thursday, while Merck fell over 3%, after what appeared to be an early release of closely watched clinical trial results for the companies' experimental cancer vaccine.&lt;/p&gt;&lt;p&gt;The results appeared on medical news website Oncology Central around 12:30 p.m. ET, but were taken down shortly afterward. The data had been scheduled for presentation at the ESMO Congress on Saturday.&lt;/p&gt;&lt;p&gt;According to the briefly published report, combining the companies' personalized mRNA cancer vaccine with Merck's blockbuster immunotherapy Keytruda reduced the risk of melanoma returning or</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Investing/Moderna+shares+plunge+on+cancer+vaccine+data+leak/27221804.html</guid>
   <pubDate>Thu, 22 Oct 2026 14:34:53 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">MRK</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">MRNA</category>
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