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   <title>Form  4          JOHNSON &amp;amp; JOHNSON     For: Sep 02  Filed by: Schmid Timothy</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++4++++++++++JOHNSON+%26amp%3B+JOHNSON+++++For%3A+Sep+02++Filed+by%3A+Schmid+Timothy/27028024.html</link>
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   <pubDate>Fri, 04 Sep 2026 09:08:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">JNJ</category>
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   <title>Johnson &amp;amp; Johnson to Participate in the Deutsche Bank 2026 Healthcare Summit</title>
   <link>http://www.streetinsider.com/Press+Releases/Johnson+%26amp%3B+Johnson+to+Participate+in+the+Deutsche+Bank+2026+Healthcare+Summit/27019335.html</link>
   <description>
&lt;p&gt;    NEW BRUNSWICK, N.J.--(BUSINESS WIRE)--
Johnson &amp;amp; Johnson (NYSE: JNJ) will present at the Deutsche Bank 2026 Healthcare Summit on Thursday, September 17th, 2026. Management will participate in a Fireside Chat at 12:00 p.m. Eastern Time.

&lt;/p&gt;&lt;p&gt;
A live audio webcast of the presentation will be accessible through Johnson &amp;amp; Johnson’s Investor Relations website at &lt;a target=&quot;_blank&quot; rel=&quot;nofollow&quot; href=&quot;https://cts.businesswire.com/ct/CT?id=smartlink&amp;amp;url=http%3A%2F%2Fwww.investor.jnj.com&amp;amp;esheet=54598276&amp;amp;newsitemid=20260902938660&amp;amp;lan=en-US&amp;amp;anchor=www.investor.jnj.com&amp;amp;index=1&amp;amp;md5=5132a302092e1ec05641409bf1cb9c2a&quot; shape=&quot;rect&quot;&gt;www.investor.jnj.com&lt;/a&gt;. An archived edition of the session will be available later that day.

&lt;/p&gt;&lt;p&gt;
The audio webcast replay will be available approximately 48 hours after the webcast.

&lt;/p&gt;&lt;p&gt;&lt;img alt=&quot;&quot; src=&quot;https://cts.businesswire.com/ct/CT?id=bwnews&amp;amp;sty=20260902938660r1&amp;amp;sid=acqr8&amp;amp;distro=nx&amp;amp;lang=en&quot; style=&quot;width:0;height:0&quot; /&gt;&lt;span class=&quot;bwct31415&quot; /&gt;&lt;/p&gt;&lt;p id=&quot;mmgallerylink&quot;&gt;&lt;span id=&quot;mmgallerylink-phrase&quot;&gt;View source version on &lt;a target=&quot;_blank&quot; href=&quot;http://businesswire.com&quot;&gt;businesswire.com&lt;/a&gt;: &lt;/span&gt;&lt;span id=&quot;mmgallerylink-link&quot;&gt;&lt;a</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Press+Releases/Johnson+%26amp%3B+Johnson+to+Participate+in+the+Deutsche+Bank+2026+Healthcare+Summit/27019335.html</guid>
   <pubDate>Wed, 02 Sep 2026 16:21:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">JNJ</category>
   	  </item>
  <item>
   <title>Johnson &amp;amp; Johnson to Participate in the Deutsche Bank 2026 Healthcare Summit</title>
   <link>http://www.streetinsider.com/Business+Wire/Johnson+%26amp%3B+Johnson+to+Participate+in+the+Deutsche+Bank+2026+Healthcare+Summit/27019335.html</link>
   <description>
&lt;p&gt;    NEW BRUNSWICK, N.J.--(BUSINESS WIRE)--
Johnson &amp;amp; Johnson (NYSE: JNJ) will present at the Deutsche Bank 2026 Healthcare Summit on Thursday, September 17th, 2026. Management will participate in a Fireside Chat at 12:00 p.m. Eastern Time.

&lt;/p&gt;&lt;p&gt;
A live audio webcast of the presentation will be accessible through Johnson &amp;amp; Johnson’s Investor Relations website at &lt;a target=&quot;_blank&quot; rel=&quot;nofollow&quot; href=&quot;https://cts.businesswire.com/ct/CT?id=smartlink&amp;amp;url=http%3A%2F%2Fwww.investor.jnj.com&amp;amp;esheet=54598276&amp;amp;newsitemid=20260902938660&amp;amp;lan=en-US&amp;amp;anchor=www.investor.jnj.com&amp;amp;index=1&amp;amp;md5=5132a302092e1ec05641409bf1cb9c2a&quot; shape=&quot;rect&quot;&gt;www.investor.jnj.com&lt;/a&gt;. An archived edition of the session will be available later that day.

&lt;/p&gt;&lt;p&gt;
The audio webcast replay will be available approximately 48 hours after the webcast.

&lt;/p&gt;&lt;p&gt;&lt;img alt=&quot;&quot; src=&quot;https://cts.businesswire.com/ct/CT?id=bwnews&amp;amp;sty=20260902938660r1&amp;amp;sid=acqr8&amp;amp;distro=nx&amp;amp;lang=en&quot; style=&quot;width:0;height:0&quot; /&gt;&lt;span class=&quot;bwct31415&quot; /&gt;&lt;/p&gt;&lt;p id=&quot;mmgallerylink&quot;&gt;&lt;span id=&quot;mmgallerylink-phrase&quot;&gt;View source version on &lt;a target=&quot;_blank&quot; href=&quot;http://businesswire.com&quot;&gt;businesswire.com&lt;/a&gt;: &lt;/span&gt;&lt;span id=&quot;mmgallerylink-link&quot;&gt;&lt;a</description>
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   <pubDate>Wed, 02 Sep 2026 16:21:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">JNJ</category>
   	  </item>
  <item>
   <title>Form  144        JOHNSON &amp;amp; JOHNSON                  Filed by: Schmid Timothy</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++144++++++++JOHNSON+%26amp%3B+JOHNSON++++++++++++++++++Filed+by%3A+Schmid+Timothy/27017381.html</link>
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   <pubDate>Wed, 02 Sep 2026 11:27:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">JNJ</category>
   	  </item>
  <item>
   <title>Form  3          JOHNSON &amp;amp; JOHNSON     For: Sep 01  Filed by: Cavanaugh Thomas</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++3++++++++++JOHNSON+%26amp%3B+JOHNSON+++++For%3A+Sep+01++Filed+by%3A+Cavanaugh+Thomas/27013591.html</link>
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   <pubDate>Tue, 01 Sep 2026 16:52:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">JNJ</category>
   	  </item>
  <item>
   <title>Johnson &amp;amp; Johnson to Host Investor Conference Call on Third-Quarter Results</title>
   <link>http://www.streetinsider.com/Press+Releases/Johnson+%26amp%3B+Johnson+to+Host+Investor+Conference+Call+on+Third-Quarter+Results/27006721.html</link>
   <description>
&lt;p&gt;    NEW BRUNSWICK, N.J.--(BUSINESS WIRE)--
Johnson &amp;amp; Johnson (NYSE: JNJ) will host a conference call for investors at &lt;b&gt;8:30 a.m. (Eastern Time) on Tuesday, October 13th &lt;/b&gt;to review third-quarter results. Joaquin Duato, Chairman and Chief Executive Officer, Joseph J. Wolk, Executive Vice President and Chief Financial Officer and Ryan Koors, Vice President, Investor Relations will host the call. The question and answer portion of the call will also include additional members of Johnson &amp;amp; Johnson’s executive team.

&lt;/p&gt;&lt;p&gt;
Investors and other interested parties can access the webcast/conference call in the following ways:

&lt;/p&gt;&lt;ul class=&quot;bwlistdisc&quot;&gt;
&lt;li&gt;
The webcast and presentation material are accessible at</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Press+Releases/Johnson+%26amp%3B+Johnson+to+Host+Investor+Conference+Call+on+Third-Quarter+Results/27006721.html</guid>
   <pubDate>Mon, 31 Aug 2026 17:08:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">JNJ</category>
   	  </item>
  <item>
   <title>Johnson &amp;amp; Johnson to Host Investor Conference Call on Third-Quarter Results</title>
   <link>http://www.streetinsider.com/Business+Wire/Johnson+%26amp%3B+Johnson+to+Host+Investor+Conference+Call+on+Third-Quarter+Results/27006721.html</link>
   <description>
&lt;p&gt;    NEW BRUNSWICK, N.J.--(BUSINESS WIRE)--
Johnson &amp;amp; Johnson (NYSE: JNJ) will host a conference call for investors at &lt;b&gt;8:30 a.m. (Eastern Time) on Tuesday, October 13th &lt;/b&gt;to review third-quarter results. Joaquin Duato, Chairman and Chief Executive Officer, Joseph J. Wolk, Executive Vice President and Chief Financial Officer and Ryan Koors, Vice President, Investor Relations will host the call. The question and answer portion of the call will also include additional members of Johnson &amp;amp; Johnson’s executive team.

&lt;/p&gt;&lt;p&gt;
Investors and other interested parties can access the webcast/conference call in the following ways:

&lt;/p&gt;&lt;ul class=&quot;bwlistdisc&quot;&gt;
&lt;li&gt;
The webcast and presentation material are accessible at</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Business+Wire/Johnson+%26amp%3B+Johnson+to+Host+Investor+Conference+Call+on+Third-Quarter+Results/27006721.html</guid>
   <pubDate>Mon, 31 Aug 2026 17:08:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">JNJ</category>
   	  </item>
  <item>
   <title>FDA: issues early alert on Abiomed heart pump controller purge cassette issue</title>
   <link>http://www.streetinsider.com/FDA/FDA%3A+issues+early+alert+on+Abiomed+heart+pump+controller+purge+cassette+issue/26980479.html</link>
   <description>(Updated - August 26, 2026 2:00 PM EDT)

&lt;p&gt;FDA: issues early alert on Abiomed heart pump controller purge cassette issue&lt;/p&gt;&lt;ul&gt;&lt;li&gt;FDA: as of August 17, Abiomed has reported 37 serious injuries &amp; 3 deaths associated with heart pump controller purge cassette issue.&lt;br /&gt;&lt;/li&gt;&lt;/ul&gt;&lt;p&gt; &lt;/p&gt;</description>
   <guid isPermaLink="true">http://www.streetinsider.com/FDA/FDA%3A+issues+early+alert+on+Abiomed+heart+pump+controller+purge+cassette+issue/26980479.html</guid>
   <pubDate>Wed, 26 Aug 2026 14:00:37 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">JNJ</category>
   	  </item>
  <item>
   <title>FDA: issues early alert on Abiomed heart pump controller purge cassette issue</title>
   <link>http://www.streetinsider.com/Trader+Talk/FDA%3A+issues+early+alert+on+Abiomed+heart+pump+controller+purge+cassette+issue/26980479.html</link>
   <description>(Updated - August 26, 2026 2:00 PM EDT)

&lt;p&gt;FDA: issues early alert on Abiomed heart pump controller purge cassette issue&lt;/p&gt;&lt;ul&gt;&lt;li&gt;FDA: as of August 17, Abiomed has reported 37 serious injuries &amp; 3 deaths associated with heart pump controller purge cassette issue.&lt;br /&gt;&lt;/li&gt;&lt;/ul&gt;&lt;p&gt; &lt;/p&gt;</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Trader+Talk/FDA%3A+issues+early+alert+on+Abiomed+heart+pump+controller+purge+cassette+issue/26980479.html</guid>
   <pubDate>Wed, 26 Aug 2026 14:00:37 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">JNJ</category>
   	  </item>
  <item>
   <title>FDA approves Johnson &amp; Johnson drug for rare blood disorder</title>
   <link>http://www.streetinsider.com/FDA/FDA+approves+Johnson+%26+Johnson+drug+for+rare+blood+disorder/26969487.html</link>
   <description>

&lt;p&gt;The U.S. Food and Drug Administration has approved Johnson &amp; Johnson's (NYSE: JNJ) IMAAVY (nipocalimab-aahu) for the treatment of warm autoimmune hemolytic anemia (wAIHA), a rare condition in which autoantibodies destroy red blood cells, causing severe anemia. The approval marks the first time a therapy has been cleared specifically for wAIHA.&lt;/p&gt;

&lt;p&gt;The drug is approved for adults and pediatric patients aged 12 and older who are currently or previously treated with corticosteroids. The FDA granted Priority Review for the application.&lt;/p&gt;

&lt;p&gt;The approval is based on results from the Phase 2/3 ENERGY study, a randomized, double-blind, placebo-controlled trial involving 115 adults. The primary</description>
   <guid isPermaLink="true">http://www.streetinsider.com/FDA/FDA+approves+Johnson+%26+Johnson+drug+for+rare+blood+disorder/26969487.html</guid>
   <pubDate>Mon, 24 Aug 2026 19:13:04 -0400</pubDate>
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   <title>FDA approves Johnson &amp; Johnson drug for rare blood disorder</title>
   <link>http://www.streetinsider.com/FDA/FDA+approves+Johnson+%26+Johnson+drug+for+rare+blood+disorder/26969487.html</link>
   <description>

&lt;p&gt;The U.S. Food and Drug Administration has approved Johnson &amp; Johnson's (NYSE: JNJ) IMAAVY (nipocalimab-aahu) for the treatment of warm autoimmune hemolytic anemia (wAIHA), a rare condition in which autoantibodies destroy red blood cells, causing severe anemia. The approval marks the first time a therapy has been cleared specifically for wAIHA.&lt;/p&gt;

&lt;p&gt;The drug is approved for adults and pediatric patients aged 12 and older who are currently or previously treated with corticosteroids. The FDA granted Priority Review for the application.&lt;/p&gt;

&lt;p&gt;The approval is based on results from the Phase 2/3 ENERGY study, a randomized, double-blind, placebo-controlled trial involving 115 adults. The primary</description>
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   <title>FDA approves Johnson &amp; Johnson drug for rare blood disorder</title>
   <link>http://www.streetinsider.com/FDA/FDA+approves+Johnson+%26+Johnson+drug+for+rare+blood+disorder/26969487.html</link>
   <description>

&lt;p&gt;The U.S. Food and Drug Administration has approved Johnson &amp; Johnson's (NYSE: JNJ) IMAAVY (nipocalimab-aahu) for the treatment of warm autoimmune hemolytic anemia (wAIHA), a rare condition in which autoantibodies destroy red blood cells, causing severe anemia. The approval marks the first time a therapy has been cleared specifically for wAIHA.&lt;/p&gt;

&lt;p&gt;The drug is approved for adults and pediatric patients aged 12 and older who are currently or previously treated with corticosteroids. The FDA granted Priority Review for the application.&lt;/p&gt;

&lt;p&gt;The approval is based on results from the Phase 2/3 ENERGY study, a randomized, double-blind, placebo-controlled trial involving 115 adults. The primary</description>
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   <title>FDA approves Johnson &amp; Johnson drug for rare blood disorder</title>
   <link>http://www.streetinsider.com/FDA/FDA+approves+Johnson+%26+Johnson+drug+for+rare+blood+disorder/26969487.html</link>
   <description>

&lt;p&gt;The U.S. Food and Drug Administration has approved Johnson &amp; Johnson's (NYSE: JNJ) IMAAVY (nipocalimab-aahu) for the treatment of warm autoimmune hemolytic anemia (wAIHA), a rare condition in which autoantibodies destroy red blood cells, causing severe anemia. The approval marks the first time a therapy has been cleared specifically for wAIHA.&lt;/p&gt;

&lt;p&gt;The drug is approved for adults and pediatric patients aged 12 and older who are currently or previously treated with corticosteroids. The FDA granted Priority Review for the application.&lt;/p&gt;

&lt;p&gt;The approval is based on results from the Phase 2/3 ENERGY study, a randomized, double-blind, placebo-controlled trial involving 115 adults. The primary</description>
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   <title>FDA approves Johnson &amp; Johnson drug for rare blood disorder</title>
   <link>http://www.streetinsider.com/FDA/FDA+approves+Johnson+%26+Johnson+drug+for+rare+blood+disorder/26969487.html</link>
   <description>

&lt;p&gt;The U.S. Food and Drug Administration has approved Johnson &amp; Johnson's (NYSE: JNJ) IMAAVY (nipocalimab-aahu) for the treatment of warm autoimmune hemolytic anemia (wAIHA), a rare condition in which autoantibodies destroy red blood cells, causing severe anemia. The approval marks the first time a therapy has been cleared specifically for wAIHA.&lt;/p&gt;

&lt;p&gt;The drug is approved for adults and pediatric patients aged 12 and older who are currently or previously treated with corticosteroids. The FDA granted Priority Review for the application.&lt;/p&gt;

&lt;p&gt;The approval is based on results from the Phase 2/3 ENERGY study, a randomized, double-blind, placebo-controlled trial involving 115 adults. The primary</description>
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   <title>FDA approves Johnson &amp; Johnson drug for rare blood disorder</title>
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&lt;p&gt;The U.S. Food and Drug Administration has approved Johnson &amp; Johnson's (NYSE: JNJ) IMAAVY (nipocalimab-aahu) for the treatment of warm autoimmune hemolytic anemia (wAIHA), a rare condition in which autoantibodies destroy red blood cells, causing severe anemia. The approval marks the first time a therapy has been cleared specifically for wAIHA.&lt;/p&gt;

&lt;p&gt;The drug is approved for adults and pediatric patients aged 12 and older who are currently or previously treated with corticosteroids. The FDA granted Priority Review for the application.&lt;/p&gt;

&lt;p&gt;The approval is based on results from the Phase 2/3 ENERGY study, a randomized, double-blind, placebo-controlled trial involving 115 adults. The primary</description>
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   <title>FDA approves Johnson &amp; Johnson drug for rare blood disorder</title>
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&lt;p&gt;The U.S. Food and Drug Administration has approved Johnson &amp; Johnson's (NYSE: JNJ) IMAAVY (nipocalimab-aahu) for the treatment of warm autoimmune hemolytic anemia (wAIHA), a rare condition in which autoantibodies destroy red blood cells, causing severe anemia. The approval marks the first time a therapy has been cleared specifically for wAIHA.&lt;/p&gt;

&lt;p&gt;The drug is approved for adults and pediatric patients aged 12 and older who are currently or previously treated with corticosteroids. The FDA granted Priority Review for the application.&lt;/p&gt;

&lt;p&gt;The approval is based on results from the Phase 2/3 ENERGY study, a randomized, double-blind, placebo-controlled trial involving 115 adults. The primary</description>
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   <title>FDA approves Johnson &amp; Johnson drug for rare blood disorder</title>
   <link>http://www.streetinsider.com/FDA/FDA+approves+Johnson+%26+Johnson+drug+for+rare+blood+disorder/26969487.html</link>
   <description>

&lt;p&gt;The U.S. Food and Drug Administration has approved Johnson &amp; Johnson's (NYSE: JNJ) IMAAVY (nipocalimab-aahu) for the treatment of warm autoimmune hemolytic anemia (wAIHA), a rare condition in which autoantibodies destroy red blood cells, causing severe anemia. The approval marks the first time a therapy has been cleared specifically for wAIHA.&lt;/p&gt;

&lt;p&gt;The drug is approved for adults and pediatric patients aged 12 and older who are currently or previously treated with corticosteroids. The FDA granted Priority Review for the application.&lt;/p&gt;

&lt;p&gt;The approval is based on results from the Phase 2/3 ENERGY study, a randomized, double-blind, placebo-controlled trial involving 115 adults. The primary</description>
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   <title>FDA approves Johnson &amp; Johnson drug for rare blood disorder</title>
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   <description>

&lt;p&gt;The U.S. Food and Drug Administration has approved Johnson &amp; Johnson's (NYSE: JNJ) IMAAVY (nipocalimab-aahu) for the treatment of warm autoimmune hemolytic anemia (wAIHA), a rare condition in which autoantibodies destroy red blood cells, causing severe anemia. The approval marks the first time a therapy has been cleared specifically for wAIHA.&lt;/p&gt;

&lt;p&gt;The drug is approved for adults and pediatric patients aged 12 and older who are currently or previously treated with corticosteroids. The FDA granted Priority Review for the application.&lt;/p&gt;

&lt;p&gt;The approval is based on results from the Phase 2/3 ENERGY study, a randomized, double-blind, placebo-controlled trial involving 115 adults. The primary</description>
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   <title>FDA approves Johnson &amp; Johnson drug for rare blood disorder</title>
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   <description>

&lt;p&gt;The U.S. Food and Drug Administration has approved Johnson &amp; Johnson's (NYSE: JNJ) IMAAVY (nipocalimab-aahu) for the treatment of warm autoimmune hemolytic anemia (wAIHA), a rare condition in which autoantibodies destroy red blood cells, causing severe anemia. The approval marks the first time a therapy has been cleared specifically for wAIHA.&lt;/p&gt;

&lt;p&gt;The drug is approved for adults and pediatric patients aged 12 and older who are currently or previously treated with corticosteroids. The FDA granted Priority Review for the application.&lt;/p&gt;

&lt;p&gt;The approval is based on results from the Phase 2/3 ENERGY study, a randomized, double-blind, placebo-controlled trial involving 115 adults. The primary</description>
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   <title>FDA approves Johnson &amp; Johnson drug for rare blood disorder</title>
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   <description>

&lt;p&gt;The U.S. Food and Drug Administration has approved Johnson &amp; Johnson's (NYSE: JNJ) IMAAVY (nipocalimab-aahu) for the treatment of warm autoimmune hemolytic anemia (wAIHA), a rare condition in which autoantibodies destroy red blood cells, causing severe anemia. The approval marks the first time a therapy has been cleared specifically for wAIHA.&lt;/p&gt;

&lt;p&gt;The drug is approved for adults and pediatric patients aged 12 and older who are currently or previously treated with corticosteroids. The FDA granted Priority Review for the application.&lt;/p&gt;

&lt;p&gt;The approval is based on results from the Phase 2/3 ENERGY study, a randomized, double-blind, placebo-controlled trial involving 115 adults. The primary</description>
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   <title>FDA approves Johnson &amp; Johnson drug for rare blood disorder</title>
   <link>http://www.streetinsider.com/FDA/FDA+approves+Johnson+%26+Johnson+drug+for+rare+blood+disorder/26969487.html</link>
   <description>

&lt;p&gt;The U.S. Food and Drug Administration has approved Johnson &amp; Johnson's (NYSE: JNJ) IMAAVY (nipocalimab-aahu) for the treatment of warm autoimmune hemolytic anemia (wAIHA), a rare condition in which autoantibodies destroy red blood cells, causing severe anemia. The approval marks the first time a therapy has been cleared specifically for wAIHA.&lt;/p&gt;

&lt;p&gt;The drug is approved for adults and pediatric patients aged 12 and older who are currently or previously treated with corticosteroids. The FDA granted Priority Review for the application.&lt;/p&gt;

&lt;p&gt;The approval is based on results from the Phase 2/3 ENERGY study, a randomized, double-blind, placebo-controlled trial involving 115 adults. The primary</description>
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   <title>FDA approves IMAAVY® (nipocalimab-aahu) as first-ever treatment for warm autoimmune hemolytic anemia (wAIHA), representing a landmark advancement for patients</title>
   <link>http://www.streetinsider.com/Press+Releases/FDA+approves+IMAAVY%C2%AE+%28nipocalimab-aahu%29+as+first-ever+treatment+for+warm+autoimmune+hemolytic+anemia+%28wAIHA%29%2C+representing+a+landmark+advancement+for+patients/26969485.html</link>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;i&gt;IMAAVY is an immunoselective FcRn blocker designed to target and reduce pathogenic immunoglobulin G (IgG) autoantibodies while also preserving B-cell function&lt;/i&gt;&lt;/li&gt;&lt;li&gt;&lt;i&gt;Warm autoimmune hemolytic anemia is a rare, life-threatening disease in which autoantibodies cause the destruction of red blood cells, leading to severe anemia and debilitating fatigue&lt;/i&gt;&lt;/li&gt;&lt;li&gt;&lt;i&gt;The approval is based on the pivotal Phase 2/3 study which demonstrated durable hemoglobin response&lt;/i&gt;&lt;i&gt;&lt;sup&gt;a&lt;/sup&gt;&lt;/i&gt;&lt;/li&gt;&lt;li&gt;&lt;i&gt;A mean increase in hemoglobin of 1 g/dL at Week 1&lt;/i&gt;&lt;i&gt;&lt;sup&gt;b&lt;/sup&gt;&lt;/i&gt; &lt;i&gt;and improvement in FACIT-Fatigue&lt;/i&gt;&lt;i&gt;&lt;sup&gt;c&lt;/sup&gt;&lt;/i&gt; &lt;i&gt;score at Week 24 were observed in IMAAVY-treated patients&lt;/i&gt;&lt;i&gt;&lt;sup&gt;d&lt;/sup&gt;&lt;/i&gt;&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.pa.spruse&quot; idsrc=&quot;xmltag.org&quot; &gt;SPRING HOUSE, Pa.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Aug. 24, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;NYSE:JNJ&quot; idsrc=&quot;xmltag.org&quot;</description>
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   <title>FDA approves IMAAVY® (nipocalimab-aahu) as first-ever treatment for warm autoimmune hemolytic anemia (wAIHA), representing a landmark advancement for patients</title>
   <link>http://www.streetinsider.com/Press+Releases/FDA+approves+IMAAVY%C2%AE+%28nipocalimab-aahu%29+as+first-ever+treatment+for+warm+autoimmune+hemolytic+anemia+%28wAIHA%29%2C+representing+a+landmark+advancement+for+patients/26969485.html</link>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;i&gt;IMAAVY is an immunoselective FcRn blocker designed to target and reduce pathogenic immunoglobulin G (IgG) autoantibodies while also preserving B-cell function&lt;/i&gt;&lt;/li&gt;&lt;li&gt;&lt;i&gt;Warm autoimmune hemolytic anemia is a rare, life-threatening disease in which autoantibodies cause the destruction of red blood cells, leading to severe anemia and debilitating fatigue&lt;/i&gt;&lt;/li&gt;&lt;li&gt;&lt;i&gt;The approval is based on the pivotal Phase 2/3 study which demonstrated durable hemoglobin response&lt;/i&gt;&lt;i&gt;&lt;sup&gt;a&lt;/sup&gt;&lt;/i&gt;&lt;/li&gt;&lt;li&gt;&lt;i&gt;A mean increase in hemoglobin of 1 g/dL at Week 1&lt;/i&gt;&lt;i&gt;&lt;sup&gt;b&lt;/sup&gt;&lt;/i&gt; &lt;i&gt;and improvement in FACIT-Fatigue&lt;/i&gt;&lt;i&gt;&lt;sup&gt;c&lt;/sup&gt;&lt;/i&gt; &lt;i&gt;score at Week 24 were observed in IMAAVY-treated patients&lt;/i&gt;&lt;i&gt;&lt;sup&gt;d&lt;/sup&gt;&lt;/i&gt;&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.pa.spruse&quot; idsrc=&quot;xmltag.org&quot; &gt;SPRING HOUSE, Pa.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Aug. 24, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;NYSE:JNJ&quot; idsrc=&quot;xmltag.org&quot;</description>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;i&gt;IMAAVY is an immunoselective FcRn blocker designed to target and reduce pathogenic immunoglobulin G (IgG) autoantibodies while also preserving B-cell function&lt;/i&gt;&lt;/li&gt;&lt;li&gt;&lt;i&gt;Warm autoimmune hemolytic anemia is a rare, life-threatening disease in which autoantibodies cause the destruction of red blood cells, leading to severe anemia and debilitating fatigue&lt;/i&gt;&lt;/li&gt;&lt;li&gt;&lt;i&gt;The approval is based on the pivotal Phase 2/3 study which demonstrated durable hemoglobin response&lt;/i&gt;&lt;i&gt;&lt;sup&gt;a&lt;/sup&gt;&lt;/i&gt;&lt;/li&gt;&lt;li&gt;&lt;i&gt;A mean increase in hemoglobin of 1 g/dL at Week 1&lt;/i&gt;&lt;i&gt;&lt;sup&gt;b&lt;/sup&gt;&lt;/i&gt; &lt;i&gt;and improvement in FACIT-Fatigue&lt;/i&gt;&lt;i&gt;&lt;sup&gt;c&lt;/sup&gt;&lt;/i&gt; &lt;i&gt;score at Week 24 were observed in IMAAVY-treated patients&lt;/i&gt;&lt;i&gt;&lt;sup&gt;d&lt;/sup&gt;&lt;/i&gt;&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.pa.spruse&quot; idsrc=&quot;xmltag.org&quot; &gt;SPRING HOUSE, Pa.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Aug. 24, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;NYSE:JNJ&quot; idsrc=&quot;xmltag.org&quot;</description>
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   <pubDate>Mon, 24 Aug 2026 19:12:00 -0400</pubDate>
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   <title>FDA approves IMAAVY® (nipocalimab-aahu) as first-ever treatment for warm autoimmune hemolytic anemia (wAIHA), representing a landmark advancement for patients</title>
   <link>http://www.streetinsider.com/Press+Releases/FDA+approves+IMAAVY%C2%AE+%28nipocalimab-aahu%29+as+first-ever+treatment+for+warm+autoimmune+hemolytic+anemia+%28wAIHA%29%2C+representing+a+landmark+advancement+for+patients/26969485.html</link>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;i&gt;IMAAVY is an immunoselective FcRn blocker designed to target and reduce pathogenic immunoglobulin G (IgG) autoantibodies while also preserving B-cell function&lt;/i&gt;&lt;/li&gt;&lt;li&gt;&lt;i&gt;Warm autoimmune hemolytic anemia is a rare, life-threatening disease in which autoantibodies cause the destruction of red blood cells, leading to severe anemia and debilitating fatigue&lt;/i&gt;&lt;/li&gt;&lt;li&gt;&lt;i&gt;The approval is based on the pivotal Phase 2/3 study which demonstrated durable hemoglobin response&lt;/i&gt;&lt;i&gt;&lt;sup&gt;a&lt;/sup&gt;&lt;/i&gt;&lt;/li&gt;&lt;li&gt;&lt;i&gt;A mean increase in hemoglobin of 1 g/dL at Week 1&lt;/i&gt;&lt;i&gt;&lt;sup&gt;b&lt;/sup&gt;&lt;/i&gt; &lt;i&gt;and improvement in FACIT-Fatigue&lt;/i&gt;&lt;i&gt;&lt;sup&gt;c&lt;/sup&gt;&lt;/i&gt; &lt;i&gt;score at Week 24 were observed in IMAAVY-treated patients&lt;/i&gt;&lt;i&gt;&lt;sup&gt;d&lt;/sup&gt;&lt;/i&gt;&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.pa.spruse&quot; idsrc=&quot;xmltag.org&quot; &gt;SPRING HOUSE, Pa.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Aug. 24, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;NYSE:JNJ&quot; idsrc=&quot;xmltag.org&quot;</description>
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   <pubDate>Mon, 24 Aug 2026 19:12:00 -0400</pubDate>
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