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   <title>Form  4          PFIZER INC                For: Aug 31  Filed by: BOURLA ALBERT</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++4++++++++++PFIZER+INC++++++++++++++++For%3A+Aug+31++Filed+by%3A+BOURLA+ALBERT/27014049.html</link>
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   <title>Form  N-PX       PFIZER INC                For: Jun 30</title>
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   <title>Form  3          PFIZER INC                For: Aug 17  Filed by: Guegan Cecile</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++3++++++++++PFIZER+INC++++++++++++++++For%3A+Aug+17++Filed+by%3A+Guegan+Cecile/26996913.html</link>
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   <title>Form  3          PFIZER INC                For: Aug 17  Filed by: Guegan Cecile</title>
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   <title>FDA approves Pfizer-BioNTech XFG-targeted Covid-19 vaccine</title>
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&lt;p&gt;Pfizer Inc. (NYSE: PFE) and BioNTech SE (Nasdaq: BNTX) announced on August 27, 2026, that the U.S. Food and Drug Administration has approved a supplemental Biologics License Application for their 2026-2027 COVID-19 vaccine targeting the XFG variant, sold under the brand name Comirnaty.&lt;/p&gt;

&lt;p&gt;The approved vaccine is indicated for adults aged 65 and older, as well as individuals aged 5 through 64 who have at least one underlying condition placing them at high risk for severe COVID-19 outcomes.&lt;/p&gt;

&lt;p&gt;The FDA's decision is based on previously submitted clinical, non-clinical, and real-world data supporting the safety and effectiveness of Comirnaty, along with manufacturing and</description>
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   <title>FDA approves Pfizer-BioNTech XFG-targeted Covid-19 vaccine</title>
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&lt;p&gt;Pfizer Inc. (NYSE: PFE) and BioNTech SE (Nasdaq: BNTX) announced on August 27, 2026, that the U.S. Food and Drug Administration has approved a supplemental Biologics License Application for their 2026-2027 COVID-19 vaccine targeting the XFG variant, sold under the brand name Comirnaty.&lt;/p&gt;

&lt;p&gt;The approved vaccine is indicated for adults aged 65 and older, as well as individuals aged 5 through 64 who have at least one underlying condition placing them at high risk for severe COVID-19 outcomes.&lt;/p&gt;

&lt;p&gt;The FDA's decision is based on previously submitted clinical, non-clinical, and real-world data supporting the safety and effectiveness of Comirnaty, along with manufacturing and</description>
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   <title>FDA approves Pfizer-BioNTech XFG-targeted Covid-19 vaccine</title>
   <link>http://www.streetinsider.com/FDA/FDA+approves+Pfizer-BioNTech+XFG-targeted+Covid-19+vaccine/26990467.html</link>
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&lt;p&gt;Pfizer Inc. (NYSE: PFE) and BioNTech SE (Nasdaq: BNTX) announced on August 27, 2026, that the U.S. Food and Drug Administration has approved a supplemental Biologics License Application for their 2026-2027 COVID-19 vaccine targeting the XFG variant, sold under the brand name Comirnaty.&lt;/p&gt;

&lt;p&gt;The approved vaccine is indicated for adults aged 65 and older, as well as individuals aged 5 through 64 who have at least one underlying condition placing them at high risk for severe COVID-19 outcomes.&lt;/p&gt;

&lt;p&gt;The FDA's decision is based on previously submitted clinical, non-clinical, and real-world data supporting the safety and effectiveness of Comirnaty, along with manufacturing and</description>
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   <title>FDA approves Pfizer-BioNTech XFG-targeted Covid-19 vaccine</title>
   <link>http://www.streetinsider.com/FDA/FDA+approves+Pfizer-BioNTech+XFG-targeted+Covid-19+vaccine/26990467.html</link>
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&lt;p&gt;Pfizer Inc. (NYSE: PFE) and BioNTech SE (Nasdaq: BNTX) announced on August 27, 2026, that the U.S. Food and Drug Administration has approved a supplemental Biologics License Application for their 2026-2027 COVID-19 vaccine targeting the XFG variant, sold under the brand name Comirnaty.&lt;/p&gt;

&lt;p&gt;The approved vaccine is indicated for adults aged 65 and older, as well as individuals aged 5 through 64 who have at least one underlying condition placing them at high risk for severe COVID-19 outcomes.&lt;/p&gt;

&lt;p&gt;The FDA's decision is based on previously submitted clinical, non-clinical, and real-world data supporting the safety and effectiveness of Comirnaty, along with manufacturing and</description>
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   <title>FDA approves Pfizer-BioNTech XFG-targeted Covid-19 vaccine</title>
   <link>http://www.streetinsider.com/FDA/FDA+approves+Pfizer-BioNTech+XFG-targeted+Covid-19+vaccine/26990467.html</link>
   <description>

&lt;p&gt;Pfizer Inc. (NYSE: PFE) and BioNTech SE (Nasdaq: BNTX) announced on August 27, 2026, that the U.S. Food and Drug Administration has approved a supplemental Biologics License Application for their 2026-2027 COVID-19 vaccine targeting the XFG variant, sold under the brand name Comirnaty.&lt;/p&gt;

&lt;p&gt;The approved vaccine is indicated for adults aged 65 and older, as well as individuals aged 5 through 64 who have at least one underlying condition placing them at high risk for severe COVID-19 outcomes.&lt;/p&gt;

&lt;p&gt;The FDA's decision is based on previously submitted clinical, non-clinical, and real-world data supporting the safety and effectiveness of Comirnaty, along with manufacturing and</description>
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   <title>FDA approves Pfizer-BioNTech XFG-targeted Covid-19 vaccine</title>
   <link>http://www.streetinsider.com/FDA/FDA+approves+Pfizer-BioNTech+XFG-targeted+Covid-19+vaccine/26990467.html</link>
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&lt;p&gt;Pfizer Inc. (NYSE: PFE) and BioNTech SE (Nasdaq: BNTX) announced on August 27, 2026, that the U.S. Food and Drug Administration has approved a supplemental Biologics License Application for their 2026-2027 COVID-19 vaccine targeting the XFG variant, sold under the brand name Comirnaty.&lt;/p&gt;

&lt;p&gt;The approved vaccine is indicated for adults aged 65 and older, as well as individuals aged 5 through 64 who have at least one underlying condition placing them at high risk for severe COVID-19 outcomes.&lt;/p&gt;

&lt;p&gt;The FDA's decision is based on previously submitted clinical, non-clinical, and real-world data supporting the safety and effectiveness of Comirnaty, along with manufacturing and</description>
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   <title>FDA approves Pfizer-BioNTech XFG-targeted Covid-19 vaccine</title>
   <link>http://www.streetinsider.com/FDA/FDA+approves+Pfizer-BioNTech+XFG-targeted+Covid-19+vaccine/26990467.html</link>
   <description>

&lt;p&gt;Pfizer Inc. (NYSE: PFE) and BioNTech SE (Nasdaq: BNTX) announced on August 27, 2026, that the U.S. Food and Drug Administration has approved a supplemental Biologics License Application for their 2026-2027 COVID-19 vaccine targeting the XFG variant, sold under the brand name Comirnaty.&lt;/p&gt;

&lt;p&gt;The approved vaccine is indicated for adults aged 65 and older, as well as individuals aged 5 through 64 who have at least one underlying condition placing them at high risk for severe COVID-19 outcomes.&lt;/p&gt;

&lt;p&gt;The FDA's decision is based on previously submitted clinical, non-clinical, and real-world data supporting the safety and effectiveness of Comirnaty, along with manufacturing and</description>
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   <title>FDA approves Pfizer-BioNTech XFG-targeted Covid-19 vaccine</title>
   <link>http://www.streetinsider.com/FDA/FDA+approves+Pfizer-BioNTech+XFG-targeted+Covid-19+vaccine/26990467.html</link>
   <description>

&lt;p&gt;Pfizer Inc. (NYSE: PFE) and BioNTech SE (Nasdaq: BNTX) announced on August 27, 2026, that the U.S. Food and Drug Administration has approved a supplemental Biologics License Application for their 2026-2027 COVID-19 vaccine targeting the XFG variant, sold under the brand name Comirnaty.&lt;/p&gt;

&lt;p&gt;The approved vaccine is indicated for adults aged 65 and older, as well as individuals aged 5 through 64 who have at least one underlying condition placing them at high risk for severe COVID-19 outcomes.&lt;/p&gt;

&lt;p&gt;The FDA's decision is based on previously submitted clinical, non-clinical, and real-world data supporting the safety and effectiveness of Comirnaty, along with manufacturing and</description>
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   <title>FDA approves Pfizer-BioNTech XFG-targeted Covid-19 vaccine</title>
   <link>http://www.streetinsider.com/FDA/FDA+approves+Pfizer-BioNTech+XFG-targeted+Covid-19+vaccine/26990467.html</link>
   <description>

&lt;p&gt;Pfizer Inc. (NYSE: PFE) and BioNTech SE (Nasdaq: BNTX) announced on August 27, 2026, that the U.S. Food and Drug Administration has approved a supplemental Biologics License Application for their 2026-2027 COVID-19 vaccine targeting the XFG variant, sold under the brand name Comirnaty.&lt;/p&gt;

&lt;p&gt;The approved vaccine is indicated for adults aged 65 and older, as well as individuals aged 5 through 64 who have at least one underlying condition placing them at high risk for severe COVID-19 outcomes.&lt;/p&gt;

&lt;p&gt;The FDA's decision is based on previously submitted clinical, non-clinical, and real-world data supporting the safety and effectiveness of Comirnaty, along with manufacturing and</description>
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   <title>Form  4          PFIZER INC                For: Aug 14  Filed by: BOURLA ALBERT</title>
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   <pubDate>Mon, 17 Aug 2026 18:15:00 -0400</pubDate>
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   <title>Form  4          PFIZER INC                For: Aug 14  Filed by: BOURLA ALBERT</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++4++++++++++PFIZER+INC++++++++++++++++For%3A+Aug+14++Filed+by%3A+BOURLA+ALBERT/26939159.html</link>
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   <pubDate>Mon, 17 Aug 2026 18:15:00 -0400</pubDate>
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   <title>EMA validates Pfizer and Valneva's Lyme disease vaccine application</title>
   <link>http://www.streetinsider.com/FDA/EMA+validates+Pfizer+and+Valneva%27s+Lyme+disease+vaccine+application/26923320.html</link>
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&lt;p&gt;Pfizer Inc. (NYSE: PFE) and Valneva SE (Nasdaq: VALN; Euronext Paris: VLA) announced that the European Medicines Agency (EMA) has validated a Marketing Authorization Application (MAA) for their investigational Lyme disease vaccine candidate, PF-07307405, and will begin its formal assessment.&lt;/p&gt;

&lt;p&gt;The application is based on results from the Phase 3 VALOR trial, which reported efficacy of more than 70% in preventing Lyme disease in participants aged five years and older. The vaccine was reported to be well tolerated, with no safety concerns identified in the trial.&lt;/p&gt;

&lt;p&gt;The VALOR trial was a multicenter, placebo-controlled, randomized, observer-blinded study conducted across sites in the U.S.,</description>
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   <pubDate>Fri, 14 Aug 2026 01:00:15 -0400</pubDate>
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  <item>
   <title>Pfizer and Valneva’s Lyme Disease Vaccine Candidate Marketing Authorization Application Validated by European Medicines Agency</title>
   <link>http://www.streetinsider.com/Press+Releases/Pfizer+and+Valneva%E2%80%99s+Lyme+Disease+Vaccine+Candidate+Marketing+Authorization+Application+Validated+by+European+Medicines+Agency/26923316.html</link>
   <description>&lt;ul&gt;&lt;li style=&quot;margin-top:0cm; margin-bottom:0cm;&quot;&gt;&lt;i&gt;Submission based on favorable efficacy and safety results from Phase 3 VALOR trial&lt;/i&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p align=&quot;justify&quot;&gt;&lt;b&gt;NEW YORK &amp;amp; LYON, France, August, 14, 2026 &lt;/b&gt;Pfizer Inc. (NYSE: PFE) and Valneva SE (Nasdaq: VALN; Euronext Paris: VLA) today announced that the European Medicines Agency (EMA) has validated the Marketing Authorization Application (MAA) for PF-07307405, the companies’ 6-valent outer surface protein A (OspA)-based Lyme disease vaccine candidate and will begin its assessment of the application. &lt;/p&gt;  &lt;p&gt;The application is based on encouraging efficacy of more than 70% observed in the &lt;a href=&quot;https://www.globenewswire.com/Tracker?data=94NMu-Ed2WJO2C0bL8thnlJhIOVZiX3ychd_AnC4qadVvaZeE4bN0j641mIYwIvERswiJL0fFY-ENd2VeUZkKJFFBe2j7zYzCv3g7Pzq8JF-A5P1Adf-7e8sOfl6uKTsYzbUNGg_eC751rMS1KgF6WPppxx0BM1hqEn46Yqd2SQYnSg3SJ2_QAt6X36YVo_bvmsAY514PiIRX1mir2lEJrPZvZLLpVT47Gfj0JZ5hQg=&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;Phase 3 VALOR&lt;/a&gt; “Vaccine Against Lyme for Outdoor</description>
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   <pubDate>Fri, 14 Aug 2026 01:00:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">PFE</category>
   	  </item>
  <item>
   <title>Pfizer and Valneva’s Lyme Disease Vaccine Candidate Marketing Authorization Application Validated by European Medicines Agency</title>
   <link>http://www.streetinsider.com/Globe+Newswire/Pfizer+and+Valneva%E2%80%99s+Lyme+Disease+Vaccine+Candidate+Marketing+Authorization+Application+Validated+by+European+Medicines+Agency/26923316.html</link>
   <description>&lt;ul&gt;&lt;li style=&quot;margin-top:0cm; margin-bottom:0cm;&quot;&gt;&lt;i&gt;Submission based on favorable efficacy and safety results from Phase 3 VALOR trial&lt;/i&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p align=&quot;justify&quot;&gt;&lt;b&gt;NEW YORK &amp;amp; LYON, France, August, 14, 2026 &lt;/b&gt;Pfizer Inc. (NYSE: PFE) and Valneva SE (Nasdaq: VALN; Euronext Paris: VLA) today announced that the European Medicines Agency (EMA) has validated the Marketing Authorization Application (MAA) for PF-07307405, the companies’ 6-valent outer surface protein A (OspA)-based Lyme disease vaccine candidate and will begin its assessment of the application. &lt;/p&gt;  &lt;p&gt;The application is based on encouraging efficacy of more than 70% observed in the &lt;a href=&quot;https://www.globenewswire.com/Tracker?data=94NMu-Ed2WJO2C0bL8thnlJhIOVZiX3ychd_AnC4qadVvaZeE4bN0j641mIYwIvERswiJL0fFY-ENd2VeUZkKJFFBe2j7zYzCv3g7Pzq8JF-A5P1Adf-7e8sOfl6uKTsYzbUNGg_eC751rMS1KgF6WPppxx0BM1hqEn46Yqd2SQYnSg3SJ2_QAt6X36YVo_bvmsAY514PiIRX1mir2lEJrPZvZLLpVT47Gfj0JZ5hQg=&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;Phase 3 VALOR&lt;/a&gt; “Vaccine Against Lyme for Outdoor</description>
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   <pubDate>Fri, 14 Aug 2026 01:00:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">PFE</category>
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   <title>Form  13F-HR     PFIZER INC                For: Jun 30</title>
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   <pubDate>Thu, 13 Aug 2026 16:44:00 -0400</pubDate>
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   <title>Form  13F-HR     PFIZER INC                For: Jun 30</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++13F-HR+++++PFIZER+INC++++++++++++++++For%3A+Jun+30/26922279.html</link>
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   <pubDate>Thu, 13 Aug 2026 16:44:00 -0400</pubDate>
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   <title>Form  4          PFIZER INC                For: Aug 12  Filed by: BOURLA ALBERT</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++4++++++++++PFIZER+INC++++++++++++++++For%3A+Aug+12++Filed+by%3A+BOURLA+ALBERT/26912695.html</link>
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   <pubDate>Wed, 12 Aug 2026 16:04:00 -0400</pubDate>
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   <title>Form  4          PFIZER INC                For: Aug 12  Filed by: BOURLA ALBERT</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++4++++++++++PFIZER+INC++++++++++++++++For%3A+Aug+12++Filed+by%3A+BOURLA+ALBERT/26912695.html</link>
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   <pubDate>Wed, 12 Aug 2026 16:04:00 -0400</pubDate>
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   <title>PFE builds bull case at $26 after earnings beat and insider buys</title>
   <link>http://www.streetinsider.com/General+News/PFE+builds+bull+case+at+%2426+after+earnings+beat+and+insider+buys/26888642.html</link>
   <description>&lt;p&gt;Investing.com - Pfizer stock is trading at $26.20, up 1.51% on Friday, pressing the upper edge of a two-month base that bulls argue is coiling for a breakout.&lt;/p&gt;&lt;p&gt;The setup has quietly become one of the more debated large-cap pharmaceutical questions on Wall Street: after a roughly 45% decline over five years, is PFE finally cheap enough — and operationally sound enough — to own again? The evidence accumulated since Tuesday's Q2 report suggests the answer is tilting toward yes, though the path is not without landmines.&lt;/p&gt;&lt;p&gt;The Earnings Foundation&lt;/p&gt;&lt;p&gt;Pfizer's second-quarter results, reported on August 4, delivered the clearest proof yet that</description>
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   <pubDate>Fri, 07 Aug 2026 09:42:59 -0400</pubDate>
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   <title>Pfizer (PFE) PT Lowered to $29 at Bernstein SocGen Group</title>
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   <description>Bernstein SocGen Group analyst Courtney Breen lowered the price target on Pfizer (NYSE: PFE) to $29.00  (from $30.00) while maintaining a Market Perform rating.</description>
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   <pubDate>Fri, 07 Aug 2026 09:11:48 -0400</pubDate>
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   <title>Trump Administration Weighs Order On Autism And Vaccines - Bloomberg</title>
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   <description>&lt;p&gt;Trump Administration Weighs Order On Autism And Vaccines - Bloomberg&lt;/p&gt;</description>
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   <pubDate>Thu, 06 Aug 2026 16:36:01 -0400</pubDate>
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