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   <title>Form  4          PFIZER INC                For: Jun 09  Filed by: DAMICO JENNIFER B.</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++4++++++++++PFIZER+INC++++++++++++++++For%3A+Jun+09++Filed+by%3A+DAMICO+JENNIFER+B./26631245.html</link>
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   <pubDate>Wed, 10 Jun 2026 19:58:00 -0400</pubDate>
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   <title>Form  4          PFIZER INC                For: Jun 09  Filed by: DAMICO JENNIFER B.</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++4++++++++++PFIZER+INC++++++++++++++++For%3A+Jun+09++Filed+by%3A+DAMICO+JENNIFER+B./26631245.html</link>
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   <title>Pfizer upgraded by RBC as valuation resets ahead of key pipeline catalysts</title>
   <link>http://www.streetinsider.com/Investing/Pfizer+upgraded+by+RBC+as+valuation+resets+ahead+of+key+pipeline+catalysts/26629651.html</link>
   <description>&lt;p&gt;Investing.com -- Pfizer shares may have found a more balanced risk-reward profile after a sharp decline this year, prompting RBC Capital Markets to upgrade the drugmaker to Sector Perform from Underperform while maintaining its $25 price target. The brokerage said the stock&amp;amp;#39;s roughly 11% pullback from its 2026 highs has brought valuation in line with its expectations, reducing the downside risks it had previously highlighted.&lt;/p&gt;
&lt;p data-start=&quot;544&quot; data-end=&quot;874&quot;&gt;RBC said Pfizer&amp;amp;#39;s strong first-quarter results could support a higher 2026 outlook, while its dividend yield of nearly 7% should help underpin the shares. The firm believes concerns around revenue erosion and the company&amp;amp;#39;s lagging</description>
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   <pubDate>Wed, 10 Jun 2026 15:50:06 -0400</pubDate>
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   <title>Pfizer upgraded by RBC as valuation resets ahead of key pipeline catalysts</title>
   <link>http://www.streetinsider.com/General+News/Pfizer+upgraded+by+RBC+as+valuation+resets+ahead+of+key+pipeline+catalysts/26629651.html</link>
   <description>&lt;p&gt;Investing.com -- Pfizer shares may have found a more balanced risk-reward profile after a sharp decline this year, prompting RBC Capital Markets to upgrade the drugmaker to Sector Perform from Underperform while maintaining its $25 price target. The brokerage said the stock&amp;amp;#39;s roughly 11% pullback from its 2026 highs has brought valuation in line with its expectations, reducing the downside risks it had previously highlighted.&lt;/p&gt;
&lt;p data-start=&quot;544&quot; data-end=&quot;874&quot;&gt;RBC said Pfizer&amp;amp;#39;s strong first-quarter results could support a higher 2026 outlook, while its dividend yield of nearly 7% should help underpin the shares. The firm believes concerns around revenue erosion and the company&amp;amp;#39;s lagging</description>
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   <pubDate>Wed, 10 Jun 2026 15:50:06 -0400</pubDate>
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   <title>RBC Capital Upgrades Pfizer (PFE) to Sector Perform</title>
   <link>http://www.streetinsider.com/Upgrades/RBC+Capital+Upgrades+Pfizer+%28PFE%29+to+Sector+Perform/26625547.html</link>
   <description>&lt;p&gt;RBC Capital analyst Trung Huynh upgraded Pfizer (NYSE: PFE) from Underperform to Sector Perform with a price target of $25.00.&lt;/p&gt;&lt;p&gt;The analyst comments: “We upgrade PFE to Sector Perform from Underperform. Our overall thesis has not changed substantially, but the stock is down -11% from highs this year and is now trading in line with our 9x - 1Y fwd PE valuation. We think the risk reward is now more balanced going into two key catalysts: sigvotatug vedotin in 2L lung mid-26, and mevro 2H26. Additionally, strong 1Q26 fundamentals support a potential 2026 guidance upgrade, while the 7% dividend yield should</description>
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   <pubDate>Wed, 10 Jun 2026 02:29:54 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">PFE</category>
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   <title>RBC Capital Upgrades Pfizer (PFE) to Sector Perform</title>
   <link>http://www.streetinsider.com/Analyst+Comments/RBC+Capital+Upgrades+Pfizer+%28PFE%29+to+Sector+Perform/26625547.html</link>
   <description>&lt;p&gt;RBC Capital analyst Trung Huynh upgraded Pfizer (NYSE: PFE) from Underperform to Sector Perform with a price target of $25.00.&lt;/p&gt;&lt;p&gt;The analyst comments: “We upgrade PFE to Sector Perform from Underperform. Our overall thesis has not changed substantially, but the stock is down -11% from highs this year and is now trading in line with our 9x - 1Y fwd PE valuation. We think the risk reward is now more balanced going into two key catalysts: sigvotatug vedotin in 2L lung mid-26, and mevro 2H26. Additionally, strong 1Q26 fundamentals support a potential 2026 guidance upgrade, while the 7% dividend yield should</description>
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   <pubDate>Wed, 10 Jun 2026 02:29:54 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">PFE</category>
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   <title>Cancer's Toughest Targets Are Drawing Wall Street's Attention as Oncology Innovation Accelerates</title>
   <link>http://www.streetinsider.com/Press+Releases/Cancer%27s+Toughest+Targets+Are+Drawing+Wall+Street%27s+Attention+as+Oncology+Innovation+Accelerates/26621749.html</link>
   <description>&lt;p&gt;DENVER, June  09, 2026  (GLOBE NEWSWIRE) -- (&lt;a href=&quot;https://www.globenewswire.com/Tracker?data=XayG3E74G-kX2BQ0P2T-Sw1VCdiMiVcvUadWXSg2wi--MBPQY9M80Mp2Fpy_bCNadkdnxYOtvS_Aef_F0xa18IegbHaGsA9We_rndgb26sw=&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;&lt;u&gt;www.247marketnews.com&lt;/u&gt;&lt;/a&gt;) – Artificial intelligence continues to dominate healthcare headlines, but another transformative story is quietly unfolding across biotechnology: the race to develop more effective treatments for some of the deadliest forms of cancer. From precision oncology and targeted therapies to next-generation approaches designed to overcome treatment resistance, a new wave of innovation is emerging that could reshape cancer care over the next decade.&lt;/p&gt;  &lt;p&gt;One area drawing increasing attention is neuro-oncology, particularly therapies targeting glioblastoma multiforme (GBM) and other aggressive brain cancers. Despite decades of research and billions</description>
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   <pubDate>Tue, 09 Jun 2026 09:44:01 -0400</pubDate>
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   <title>Cancer's Toughest Targets Are Drawing Wall Street's Attention as Oncology Innovation Accelerates</title>
   <link>http://www.streetinsider.com/Press+Releases/Cancer%27s+Toughest+Targets+Are+Drawing+Wall+Street%27s+Attention+as+Oncology+Innovation+Accelerates/26621749.html</link>
   <description>&lt;p&gt;DENVER, June  09, 2026  (GLOBE NEWSWIRE) -- (&lt;a href=&quot;https://www.globenewswire.com/Tracker?data=XayG3E74G-kX2BQ0P2T-Sw1VCdiMiVcvUadWXSg2wi--MBPQY9M80Mp2Fpy_bCNadkdnxYOtvS_Aef_F0xa18IegbHaGsA9We_rndgb26sw=&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;&lt;u&gt;www.247marketnews.com&lt;/u&gt;&lt;/a&gt;) – Artificial intelligence continues to dominate healthcare headlines, but another transformative story is quietly unfolding across biotechnology: the race to develop more effective treatments for some of the deadliest forms of cancer. From precision oncology and targeted therapies to next-generation approaches designed to overcome treatment resistance, a new wave of innovation is emerging that could reshape cancer care over the next decade.&lt;/p&gt;  &lt;p&gt;One area drawing increasing attention is neuro-oncology, particularly therapies targeting glioblastoma multiforme (GBM) and other aggressive brain cancers. Despite decades of research and billions</description>
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   <pubDate>Tue, 09 Jun 2026 09:44:01 -0400</pubDate>
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   <title>Cancer's Toughest Targets Are Drawing Wall Street's Attention as Oncology Innovation Accelerates</title>
   <link>http://www.streetinsider.com/Press+Releases/Cancer%27s+Toughest+Targets+Are+Drawing+Wall+Street%27s+Attention+as+Oncology+Innovation+Accelerates/26621749.html</link>
   <description>&lt;p&gt;DENVER, June  09, 2026  (GLOBE NEWSWIRE) -- (&lt;a href=&quot;https://www.globenewswire.com/Tracker?data=XayG3E74G-kX2BQ0P2T-Sw1VCdiMiVcvUadWXSg2wi--MBPQY9M80Mp2Fpy_bCNadkdnxYOtvS_Aef_F0xa18IegbHaGsA9We_rndgb26sw=&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;&lt;u&gt;www.247marketnews.com&lt;/u&gt;&lt;/a&gt;) – Artificial intelligence continues to dominate healthcare headlines, but another transformative story is quietly unfolding across biotechnology: the race to develop more effective treatments for some of the deadliest forms of cancer. From precision oncology and targeted therapies to next-generation approaches designed to overcome treatment resistance, a new wave of innovation is emerging that could reshape cancer care over the next decade.&lt;/p&gt;  &lt;p&gt;One area drawing increasing attention is neuro-oncology, particularly therapies targeting glioblastoma multiforme (GBM) and other aggressive brain cancers. Despite decades of research and billions</description>
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   <pubDate>Tue, 09 Jun 2026 09:44:01 -0400</pubDate>
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   <title>Cancer's Toughest Targets Are Drawing Wall Street's Attention as Oncology Innovation Accelerates</title>
   <link>http://www.streetinsider.com/Globe+Newswire/Cancer%27s+Toughest+Targets+Are+Drawing+Wall+Street%27s+Attention+as+Oncology+Innovation+Accelerates/26621749.html</link>
   <description>&lt;p&gt;DENVER, June  09, 2026  (GLOBE NEWSWIRE) -- (&lt;a href=&quot;https://www.globenewswire.com/Tracker?data=XayG3E74G-kX2BQ0P2T-Sw1VCdiMiVcvUadWXSg2wi--MBPQY9M80Mp2Fpy_bCNadkdnxYOtvS_Aef_F0xa18IegbHaGsA9We_rndgb26sw=&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;&lt;u&gt;www.247marketnews.com&lt;/u&gt;&lt;/a&gt;) – Artificial intelligence continues to dominate healthcare headlines, but another transformative story is quietly unfolding across biotechnology: the race to develop more effective treatments for some of the deadliest forms of cancer. From precision oncology and targeted therapies to next-generation approaches designed to overcome treatment resistance, a new wave of innovation is emerging that could reshape cancer care over the next decade.&lt;/p&gt;  &lt;p&gt;One area drawing increasing attention is neuro-oncology, particularly therapies targeting glioblastoma multiforme (GBM) and other aggressive brain cancers. Despite decades of research and billions</description>
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   <pubDate>Tue, 09 Jun 2026 09:44:01 -0400</pubDate>
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   <title>Cancer's Toughest Targets Are Drawing Wall Street's Attention as Oncology Innovation Accelerates</title>
   <link>http://www.streetinsider.com/Globe+Newswire/Cancer%27s+Toughest+Targets+Are+Drawing+Wall+Street%27s+Attention+as+Oncology+Innovation+Accelerates/26621749.html</link>
   <description>&lt;p&gt;DENVER, June  09, 2026  (GLOBE NEWSWIRE) -- (&lt;a href=&quot;https://www.globenewswire.com/Tracker?data=XayG3E74G-kX2BQ0P2T-Sw1VCdiMiVcvUadWXSg2wi--MBPQY9M80Mp2Fpy_bCNadkdnxYOtvS_Aef_F0xa18IegbHaGsA9We_rndgb26sw=&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;&lt;u&gt;www.247marketnews.com&lt;/u&gt;&lt;/a&gt;) – Artificial intelligence continues to dominate healthcare headlines, but another transformative story is quietly unfolding across biotechnology: the race to develop more effective treatments for some of the deadliest forms of cancer. From precision oncology and targeted therapies to next-generation approaches designed to overcome treatment resistance, a new wave of innovation is emerging that could reshape cancer care over the next decade.&lt;/p&gt;  &lt;p&gt;One area drawing increasing attention is neuro-oncology, particularly therapies targeting glioblastoma multiforme (GBM) and other aggressive brain cancers. Despite decades of research and billions</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Globe+Newswire/Cancer%27s+Toughest+Targets+Are+Drawing+Wall+Street%27s+Attention+as+Oncology+Innovation+Accelerates/26621749.html</guid>
   <pubDate>Tue, 09 Jun 2026 09:44:01 -0400</pubDate>
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   <title>Cancer's Toughest Targets Are Drawing Wall Street's Attention as Oncology Innovation Accelerates</title>
   <link>http://www.streetinsider.com/Globe+Newswire/Cancer%27s+Toughest+Targets+Are+Drawing+Wall+Street%27s+Attention+as+Oncology+Innovation+Accelerates/26621749.html</link>
   <description>&lt;p&gt;DENVER, June  09, 2026  (GLOBE NEWSWIRE) -- (&lt;a href=&quot;https://www.globenewswire.com/Tracker?data=XayG3E74G-kX2BQ0P2T-Sw1VCdiMiVcvUadWXSg2wi--MBPQY9M80Mp2Fpy_bCNadkdnxYOtvS_Aef_F0xa18IegbHaGsA9We_rndgb26sw=&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;&lt;u&gt;www.247marketnews.com&lt;/u&gt;&lt;/a&gt;) – Artificial intelligence continues to dominate healthcare headlines, but another transformative story is quietly unfolding across biotechnology: the race to develop more effective treatments for some of the deadliest forms of cancer. From precision oncology and targeted therapies to next-generation approaches designed to overcome treatment resistance, a new wave of innovation is emerging that could reshape cancer care over the next decade.&lt;/p&gt;  &lt;p&gt;One area drawing increasing attention is neuro-oncology, particularly therapies targeting glioblastoma multiforme (GBM) and other aggressive brain cancers. Despite decades of research and billions</description>
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   <title>FDA approves expanded HYMPAVZI use for hemophilia patients with inhibitors</title>
   <link>http://www.streetinsider.com/FDA/FDA+approves+expanded+HYMPAVZI+use+for+hemophilia+patients+with+inhibitors/26613979.html</link>
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&lt;p&gt;Pfizer Inc. (NYSE: PFE) announced the U.S. Food and Drug Administration approved an expanded indication for HYMPAVZI to include patients with hemophilia A or B ages 12 years and older with inhibitors and pediatric patients ages 6 to 11 years with or without inhibitors.&lt;/p&gt;

&lt;p&gt;HYMPAVZI is now indicated for routine prophylaxis to prevent or reduce the frequency of bleeding episodes in adults and pediatric patients 6 years of age and older with hemophilia A or hemophilia B, with or without inhibitors. The treatment is administered subcutaneously once weekly.&lt;/p&gt;

&lt;p&gt;The approval was supported by results from the Phase 3 BASIS trial for adults</description>
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   <pubDate>Mon, 08 Jun 2026 06:45:20 -0400</pubDate>
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   <title>FDA approves expanded HYMPAVZI use for hemophilia patients with inhibitors</title>
   <link>http://www.streetinsider.com/FDA/FDA+approves+expanded+HYMPAVZI+use+for+hemophilia+patients+with+inhibitors/26613979.html</link>
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&lt;p&gt;Pfizer Inc. (NYSE: PFE) announced the U.S. Food and Drug Administration approved an expanded indication for HYMPAVZI to include patients with hemophilia A or B ages 12 years and older with inhibitors and pediatric patients ages 6 to 11 years with or without inhibitors.&lt;/p&gt;

&lt;p&gt;HYMPAVZI is now indicated for routine prophylaxis to prevent or reduce the frequency of bleeding episodes in adults and pediatric patients 6 years of age and older with hemophilia A or hemophilia B, with or without inhibitors. The treatment is administered subcutaneously once weekly.&lt;/p&gt;

&lt;p&gt;The approval was supported by results from the Phase 3 BASIS trial for adults</description>
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   <title>FDA approves expanded HYMPAVZI use for hemophilia patients with inhibitors</title>
   <link>http://www.streetinsider.com/FDA/FDA+approves+expanded+HYMPAVZI+use+for+hemophilia+patients+with+inhibitors/26613979.html</link>
   <description>

&lt;p&gt;Pfizer Inc. (NYSE: PFE) announced the U.S. Food and Drug Administration approved an expanded indication for HYMPAVZI to include patients with hemophilia A or B ages 12 years and older with inhibitors and pediatric patients ages 6 to 11 years with or without inhibitors.&lt;/p&gt;

&lt;p&gt;HYMPAVZI is now indicated for routine prophylaxis to prevent or reduce the frequency of bleeding episodes in adults and pediatric patients 6 years of age and older with hemophilia A or hemophilia B, with or without inhibitors. The treatment is administered subcutaneously once weekly.&lt;/p&gt;

&lt;p&gt;The approval was supported by results from the Phase 3 BASIS trial for adults</description>
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   <title>FDA approves expanded HYMPAVZI use for hemophilia patients with inhibitors</title>
   <link>http://www.streetinsider.com/FDA/FDA+approves+expanded+HYMPAVZI+use+for+hemophilia+patients+with+inhibitors/26613979.html</link>
   <description>

&lt;p&gt;Pfizer Inc. (NYSE: PFE) announced the U.S. Food and Drug Administration approved an expanded indication for HYMPAVZI to include patients with hemophilia A or B ages 12 years and older with inhibitors and pediatric patients ages 6 to 11 years with or without inhibitors.&lt;/p&gt;

&lt;p&gt;HYMPAVZI is now indicated for routine prophylaxis to prevent or reduce the frequency of bleeding episodes in adults and pediatric patients 6 years of age and older with hemophilia A or hemophilia B, with or without inhibitors. The treatment is administered subcutaneously once weekly.&lt;/p&gt;

&lt;p&gt;The approval was supported by results from the Phase 3 BASIS trial for adults</description>
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   <title>FDA approves expanded HYMPAVZI use for hemophilia patients with inhibitors</title>
   <link>http://www.streetinsider.com/FDA/FDA+approves+expanded+HYMPAVZI+use+for+hemophilia+patients+with+inhibitors/26613979.html</link>
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&lt;p&gt;Pfizer Inc. (NYSE: PFE) announced the U.S. Food and Drug Administration approved an expanded indication for HYMPAVZI to include patients with hemophilia A or B ages 12 years and older with inhibitors and pediatric patients ages 6 to 11 years with or without inhibitors.&lt;/p&gt;

&lt;p&gt;HYMPAVZI is now indicated for routine prophylaxis to prevent or reduce the frequency of bleeding episodes in adults and pediatric patients 6 years of age and older with hemophilia A or hemophilia B, with or without inhibitors. The treatment is administered subcutaneously once weekly.&lt;/p&gt;

&lt;p&gt;The approval was supported by results from the Phase 3 BASIS trial for adults</description>
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   <title>FDA approves expanded HYMPAVZI use for hemophilia patients with inhibitors</title>
   <link>http://www.streetinsider.com/FDA/FDA+approves+expanded+HYMPAVZI+use+for+hemophilia+patients+with+inhibitors/26613979.html</link>
   <description>

&lt;p&gt;Pfizer Inc. (NYSE: PFE) announced the U.S. Food and Drug Administration approved an expanded indication for HYMPAVZI to include patients with hemophilia A or B ages 12 years and older with inhibitors and pediatric patients ages 6 to 11 years with or without inhibitors.&lt;/p&gt;

&lt;p&gt;HYMPAVZI is now indicated for routine prophylaxis to prevent or reduce the frequency of bleeding episodes in adults and pediatric patients 6 years of age and older with hemophilia A or hemophilia B, with or without inhibitors. The treatment is administered subcutaneously once weekly.&lt;/p&gt;

&lt;p&gt;The approval was supported by results from the Phase 3 BASIS trial for adults</description>
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   <title>FDA approves expanded HYMPAVZI use for hemophilia patients with inhibitors</title>
   <link>http://www.streetinsider.com/FDA/FDA+approves+expanded+HYMPAVZI+use+for+hemophilia+patients+with+inhibitors/26613979.html</link>
   <description>

&lt;p&gt;Pfizer Inc. (NYSE: PFE) announced the U.S. Food and Drug Administration approved an expanded indication for HYMPAVZI to include patients with hemophilia A or B ages 12 years and older with inhibitors and pediatric patients ages 6 to 11 years with or without inhibitors.&lt;/p&gt;

&lt;p&gt;HYMPAVZI is now indicated for routine prophylaxis to prevent or reduce the frequency of bleeding episodes in adults and pediatric patients 6 years of age and older with hemophilia A or hemophilia B, with or without inhibitors. The treatment is administered subcutaneously once weekly.&lt;/p&gt;

&lt;p&gt;The approval was supported by results from the Phase 3 BASIS trial for adults</description>
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   <title>FDA approves expanded HYMPAVZI use for hemophilia patients with inhibitors</title>
   <link>http://www.streetinsider.com/FDA/FDA+approves+expanded+HYMPAVZI+use+for+hemophilia+patients+with+inhibitors/26613979.html</link>
   <description>

&lt;p&gt;Pfizer Inc. (NYSE: PFE) announced the U.S. Food and Drug Administration approved an expanded indication for HYMPAVZI to include patients with hemophilia A or B ages 12 years and older with inhibitors and pediatric patients ages 6 to 11 years with or without inhibitors.&lt;/p&gt;

&lt;p&gt;HYMPAVZI is now indicated for routine prophylaxis to prevent or reduce the frequency of bleeding episodes in adults and pediatric patients 6 years of age and older with hemophilia A or hemophilia B, with or without inhibitors. The treatment is administered subcutaneously once weekly.&lt;/p&gt;

&lt;p&gt;The approval was supported by results from the Phase 3 BASIS trial for adults</description>
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   <title>U.S. FDA Approves Pfizer’s HYMPAVZI for the Treatment of Two Additional Hemophilia A or B Patient Populations with Significant Medical Need</title>
   <link>http://www.streetinsider.com/Press+Releases/U.S.+FDA+Approves+Pfizer%E2%80%99s+HYMPAVZI+for+the+Treatment+of+Two+Additional+Hemophilia+A+or+B+Patient+Populations+with+Significant+Medical+Need/26613977.html</link>
   <description>
&lt;ul class=&quot;bwlistdisc&quot;&gt;
&lt;li&gt;
&lt;i&gt;Approval expands HYMPAVZI use to now include people with hemophilia A or B ages 12 years and older with inhibitors and pediatric patients (ages 6 to 11 years) with or without inhibitors&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;HYMPAVZI is the first subcutaneous non-factor therapy available for pediatric patients with hemophilia B ages 6 to 11 years old&lt;/i&gt;

&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;    NEW YORK--(BUSINESS WIRE)--
Pfizer Inc. (NYSE: PFE)&lt;b&gt; &lt;/b&gt;today announced that the U.S. Food and Drug Administration (FDA) has approved an expanded indication for HYMPAVZI® (marstacimab-hncq) to include the treatment of patients with hemophilia A or B 12 years and older with inhibitors and pediatric patients (ages</description>
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   <title>U.S. FDA Approves Pfizer’s HYMPAVZI for the Treatment of Two Additional Hemophilia A or B Patient Populations with Significant Medical Need</title>
   <link>http://www.streetinsider.com/Press+Releases/U.S.+FDA+Approves+Pfizer%E2%80%99s+HYMPAVZI+for+the+Treatment+of+Two+Additional+Hemophilia+A+or+B+Patient+Populations+with+Significant+Medical+Need/26613977.html</link>
   <description>
&lt;ul class=&quot;bwlistdisc&quot;&gt;
&lt;li&gt;
&lt;i&gt;Approval expands HYMPAVZI use to now include people with hemophilia A or B ages 12 years and older with inhibitors and pediatric patients (ages 6 to 11 years) with or without inhibitors&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;HYMPAVZI is the first subcutaneous non-factor therapy available for pediatric patients with hemophilia B ages 6 to 11 years old&lt;/i&gt;

&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;    NEW YORK--(BUSINESS WIRE)--
Pfizer Inc. (NYSE: PFE)&lt;b&gt; &lt;/b&gt;today announced that the U.S. Food and Drug Administration (FDA) has approved an expanded indication for HYMPAVZI® (marstacimab-hncq) to include the treatment of patients with hemophilia A or B 12 years and older with inhibitors and pediatric patients (ages</description>
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   <title>U.S. FDA Approves Pfizer’s HYMPAVZI for the Treatment of Two Additional Hemophilia A or B Patient Populations with Significant Medical Need</title>
   <link>http://www.streetinsider.com/Press+Releases/U.S.+FDA+Approves+Pfizer%E2%80%99s+HYMPAVZI+for+the+Treatment+of+Two+Additional+Hemophilia+A+or+B+Patient+Populations+with+Significant+Medical+Need/26613977.html</link>
   <description>
&lt;ul class=&quot;bwlistdisc&quot;&gt;
&lt;li&gt;
&lt;i&gt;Approval expands HYMPAVZI use to now include people with hemophilia A or B ages 12 years and older with inhibitors and pediatric patients (ages 6 to 11 years) with or without inhibitors&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;HYMPAVZI is the first subcutaneous non-factor therapy available for pediatric patients with hemophilia B ages 6 to 11 years old&lt;/i&gt;

&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;    NEW YORK--(BUSINESS WIRE)--
Pfizer Inc. (NYSE: PFE)&lt;b&gt; &lt;/b&gt;today announced that the U.S. Food and Drug Administration (FDA) has approved an expanded indication for HYMPAVZI® (marstacimab-hncq) to include the treatment of patients with hemophilia A or B 12 years and older with inhibitors and pediatric patients (ages</description>
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   <title>U.S. FDA Approves Pfizer’s HYMPAVZI for the Treatment of Two Additional Hemophilia A or B Patient Populations with Significant Medical Need</title>
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&lt;ul class=&quot;bwlistdisc&quot;&gt;
&lt;li&gt;
&lt;i&gt;Approval expands HYMPAVZI use to now include people with hemophilia A or B ages 12 years and older with inhibitors and pediatric patients (ages 6 to 11 years) with or without inhibitors&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;HYMPAVZI is the first subcutaneous non-factor therapy available for pediatric patients with hemophilia B ages 6 to 11 years old&lt;/i&gt;

&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;    NEW YORK--(BUSINESS WIRE)--
Pfizer Inc. (NYSE: PFE)&lt;b&gt; &lt;/b&gt;today announced that the U.S. Food and Drug Administration (FDA) has approved an expanded indication for HYMPAVZI® (marstacimab-hncq) to include the treatment of patients with hemophilia A or B 12 years and older with inhibitors and pediatric patients (ages</description>
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   <title>U.S. FDA Approves Pfizer’s HYMPAVZI for the Treatment of Two Additional Hemophilia A or B Patient Populations with Significant Medical Need</title>
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&lt;ul class=&quot;bwlistdisc&quot;&gt;
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&lt;i&gt;Approval expands HYMPAVZI use to now include people with hemophilia A or B ages 12 years and older with inhibitors and pediatric patients (ages 6 to 11 years) with or without inhibitors&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;HYMPAVZI is the first subcutaneous non-factor therapy available for pediatric patients with hemophilia B ages 6 to 11 years old&lt;/i&gt;

&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;    NEW YORK--(BUSINESS WIRE)--
Pfizer Inc. (NYSE: PFE)&lt;b&gt; &lt;/b&gt;today announced that the U.S. Food and Drug Administration (FDA) has approved an expanded indication for HYMPAVZI® (marstacimab-hncq) to include the treatment of patients with hemophilia A or B 12 years and older with inhibitors and pediatric patients (ages</description>
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