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   <title>Form  6-K        Pharming Group N.V.       For: Sep 11</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++6-K++++++++Pharming+Group+N.V.+++++++For%3A+Sep+11/27052571.html</link>
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   <pubDate>Fri, 11 Sep 2026 14:59:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">PHAR</category>
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   <title>FDA approves Pharming's Joenja for children ages 4 to 11 with APDS</title>
   <link>http://www.streetinsider.com/FDA/FDA+approves+Pharming%27s+Joenja+for+children+ages+4+to+11+with+APDS/27052335.html</link>
   <description>

&lt;p&gt;The U.S. Food and Drug Administration has approved a supplemental New Drug Application from Pharming Group N.V. (Euronext Amsterdam: PHARM, Nasdaq: PHAR) for 40 mg and 50 mg twice-daily doses of Joenja (leniolisib) to treat children aged 4 to 11 years weighing at least 27 kg with activated phosphoinositide 3-kinase delta syndrome, known as APDS, a rare primary immunodeficiency.&lt;/p&gt;

&lt;p&gt;The approval, announced September 11, 2026, expands the existing Joenja indication, which the FDA first granted in March 2023 for adults and pediatric patients 12 years and older. According to the company, the newly approved doses are expected to be available through</description>
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   <pubDate>Fri, 11 Sep 2026 14:00:16 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">PHAR</category>
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   <title>FDA approves Pharming’s Joenja® as first treatment for children with APDS in the U.S.</title>
   <link>http://www.streetinsider.com/Press+Releases/FDA+approves+Pharming%E2%80%99s+Joenja%C2%AE+as+first+treatment+for+children+with+APDS+in+the+U.S./27052331.html</link>
   <description>&lt;ul&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in; text-align:left;&quot;&gt;&lt;b&gt;FDA approval expands Joenja indication to include children with activated phosphoinositide 3-kinase delta (PI3Kδ) syndrome (APDS) ages 4 to 11 who weigh at least 27kg&lt;/b&gt;&lt;/li&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in; text-align:left;&quot;&gt;&lt;b&gt;Newly approved Joenja doses are expected to be available in October&lt;/b&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p align=&quot;justify&quot;&gt;&lt;b&gt;&lt;i&gt;Leiden, the Netherlands, September 11, 2026: &lt;/i&gt;&lt;/b&gt;Pharming (Euronext Amsterdam: PHARM/Nasdaq: PHAR), a global biotechnology company focused on rare immune and genetic diseases, today announced that the U.S. Food and Drug Administration (FDA) has approved its supplemental New Drug Application (sNDA) for 40 mg and 50 mg twice-daily dosing of Joenja® (leniolisib), an oral, selective phosphoinositide 3-kinase delta (PI3Kδ) inhibitor,</description>
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   <pubDate>Fri, 11 Sep 2026 14:00:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">PHAR</category>
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  <item>
   <title>FDA approves Pharming’s Joenja® as first treatment for children with APDS in the U.S.</title>
   <link>http://www.streetinsider.com/Globe+Newswire/FDA+approves+Pharming%E2%80%99s+Joenja%C2%AE+as+first+treatment+for+children+with+APDS+in+the+U.S./27052331.html</link>
   <description>&lt;ul&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in; text-align:left;&quot;&gt;&lt;b&gt;FDA approval expands Joenja indication to include children with activated phosphoinositide 3-kinase delta (PI3Kδ) syndrome (APDS) ages 4 to 11 who weigh at least 27kg&lt;/b&gt;&lt;/li&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in; text-align:left;&quot;&gt;&lt;b&gt;Newly approved Joenja doses are expected to be available in October&lt;/b&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p align=&quot;justify&quot;&gt;&lt;b&gt;&lt;i&gt;Leiden, the Netherlands, September 11, 2026: &lt;/i&gt;&lt;/b&gt;Pharming (Euronext Amsterdam: PHARM/Nasdaq: PHAR), a global biotechnology company focused on rare immune and genetic diseases, today announced that the U.S. Food and Drug Administration (FDA) has approved its supplemental New Drug Application (sNDA) for 40 mg and 50 mg twice-daily dosing of Joenja® (leniolisib), an oral, selective phosphoinositide 3-kinase delta (PI3Kδ) inhibitor,</description>
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   <pubDate>Fri, 11 Sep 2026 14:00:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">PHAR</category>
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   <title>Pharming Group to participate in September investor conferences</title>
   <link>http://www.streetinsider.com/Press+Releases/Pharming+Group+to+participate+in+September+investor+conferences/27038105.html</link>
   <description>&lt;p align=&quot;justify&quot;&gt;&lt;b&gt;Leiden, the &lt;/b&gt;&lt;b&gt;Netherlands, September 9, 2026: &lt;/b&gt;Pharming Group N.V. (“Pharming”) (Euronext Amsterdam: PHARM/Nasdaq: PHAR) today announced that its management will participate in the following investor conferences in the month of September:&lt;/p&gt;  &lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;margin-bottom:6pt; text-align:left;&quot;&gt;&lt;b&gt;H.C. Wainwright 28th Annual Global Investment Conference, New York, September 14, 2026&lt;/b&gt;&lt;br /&gt;Fabrice Chouraqui, Chief Executive Officer, will present on Monday, September 14 at 09:30 EDT/15:30 CEST. A live webcast and replay of the presentation will be made available in the “Events and presentations” and “Our news” sections of Pharming’s website. &lt;/li&gt;&lt;li style=&quot;margin-bottom:6pt; text-align:left;&quot;&gt;&lt;b&gt;Morgan Stanley&lt;/b&gt; &lt;b&gt;24th Annual Global Healthcare Conference, New York, September 15, 2026&lt;/b&gt;&lt;/li&gt;&lt;/ul&gt;</description>
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   <pubDate>Wed, 09 Sep 2026 02:00:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">PHAR</category>
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   <title>Pharming Group to participate in September investor conferences</title>
   <link>http://www.streetinsider.com/Globe+Newswire/Pharming+Group+to+participate+in+September+investor+conferences/27038105.html</link>
   <description>&lt;p align=&quot;justify&quot;&gt;&lt;b&gt;Leiden, the &lt;/b&gt;&lt;b&gt;Netherlands, September 9, 2026: &lt;/b&gt;Pharming Group N.V. (“Pharming”) (Euronext Amsterdam: PHARM/Nasdaq: PHAR) today announced that its management will participate in the following investor conferences in the month of September:&lt;/p&gt;  &lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;margin-bottom:6pt; text-align:left;&quot;&gt;&lt;b&gt;H.C. Wainwright 28th Annual Global Investment Conference, New York, September 14, 2026&lt;/b&gt;&lt;br /&gt;Fabrice Chouraqui, Chief Executive Officer, will present on Monday, September 14 at 09:30 EDT/15:30 CEST. A live webcast and replay of the presentation will be made available in the “Events and presentations” and “Our news” sections of Pharming’s website. &lt;/li&gt;&lt;li style=&quot;margin-bottom:6pt; text-align:left;&quot;&gt;&lt;b&gt;Morgan Stanley&lt;/b&gt; &lt;b&gt;24th Annual Global Healthcare Conference, New York, September 15, 2026&lt;/b&gt;&lt;/li&gt;&lt;/ul&gt;</description>
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   <pubDate>Wed, 09 Sep 2026 02:00:00 -0400</pubDate>
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   <title>Form  6-K        Pharming Group N.V.       For: Aug 13</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++6-K++++++++Pharming+Group+N.V.+++++++For%3A+Aug+13/26915804.html</link>
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   <pubDate>Thu, 13 Aug 2026 06:07:00 -0400</pubDate>
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   	   	<category domain="http://rss.financialcontent.com/stocksymbol">PHARM</category>
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   <title>Form  6-K        Pharming Group N.V.       For: Aug 13</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++6-K++++++++Pharming+Group+N.V.+++++++For%3A+Aug+13/26915804.html</link>
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   <pubDate>Thu, 13 Aug 2026 06:07:00 -0400</pubDate>
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   <title>Form  6-K        Pharming Group N.V.       For: Aug 13</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++6-K++++++++Pharming+Group+N.V.+++++++For%3A+Aug+13/26915804.html</link>
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   <pubDate>Thu, 13 Aug 2026 06:07:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">O.00551852</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">PHAR</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">PHARM</category>
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   <title>Pharming Group (PHAR) PT Raised to $38 at Canaccord</title>
   <link>http://www.streetinsider.com/Analyst+PT+Change/Pharming+Group+%28PHAR%29+PT+Raised+to+%2438+at+Canaccord/26853564.html</link>
   <description>Canaccord analyst Whitney Ijem raised the price target on Pharming Group (NASDAQ: PHAR) to $38.00  (from $37.00) while maintaining a Buy rating.</description>
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   <pubDate>Mon, 03 Aug 2026 06:42:05 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">PHAR</category>
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   <title>Pharming Group (PHAR) PT Lowered to $39 at Oppenheimer</title>
   <link>http://www.streetinsider.com/Analyst+PT+Change/Pharming+Group+%28PHAR%29+PT+Lowered+to+%2439+at+Oppenheimer/26842562.html</link>
   <description>(Updated - July 30, 2026 2:15 PM EDT)

&lt;p&gt;Oppenheimer analyst Jeff Jones lowered the price target on Pharming Group (NASDAQ: PHAR) to $39.00 (from $40.00) while maintaining a Outperform rating.&lt;/p&gt;&lt;p&gt;The analyst commented: &quot;On Thursday, PHAR reported (press release) 2Q26 revenue of $90.2M, in line with our estimates, but below consensus, $90.5/99.5M, respectively. Ruconest is seeing pressure from oral Ekterly, as expected, with $72.3M in revenue reported vs. OPCO/consensus of $72.5/82M. Management indicated an expectation for Ruconest to return to growth in 2H26, with ~93% of patients retained on the product during 2Q. Ruconest pressure was offset by strong Joenja performance of</description>
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   <pubDate>Thu, 30 Jul 2026 14:15:27 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">PHAR</category>
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   <title>Pharming Group (PHAR) PT Lowered to $39 at Oppenheimer</title>
   <link>http://www.streetinsider.com/Analyst+Comments/Pharming+Group+%28PHAR%29+PT+Lowered+to+%2439+at+Oppenheimer/26842562.html</link>
   <description>(Updated - July 30, 2026 2:15 PM EDT)

&lt;p&gt;Oppenheimer analyst Jeff Jones lowered the price target on Pharming Group (NASDAQ: PHAR) to $39.00 (from $40.00) while maintaining a Outperform rating.&lt;/p&gt;&lt;p&gt;The analyst commented: &quot;On Thursday, PHAR reported (press release) 2Q26 revenue of $90.2M, in line with our estimates, but below consensus, $90.5/99.5M, respectively. Ruconest is seeing pressure from oral Ekterly, as expected, with $72.3M in revenue reported vs. OPCO/consensus of $72.5/82M. Management indicated an expectation for Ruconest to return to growth in 2H26, with ~93% of patients retained on the product during 2Q. Ruconest pressure was offset by strong Joenja performance of</description>
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   <pubDate>Thu, 30 Jul 2026 14:15:27 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">PHAR</category>
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   <title>Pharming Group N.V. (PHAR) Misses Q2 EPS by 6c</title>
   <link>http://www.streetinsider.com/Earnings/Pharming+Group+N.V.+%28PHAR%29+Misses+Q2+EPS+by+6c/26838040.html</link>
   <description>&lt;p&gt;Pharming Group N.V. (NASDAQ: PHAR) reported Q2 EPS of $0.00, $0.06 worse than the analyst estimate of $0.06. Revenue for the quarter came in at $90.2 million versus the consensus estimate of $101.28 million.&lt;/p&gt;&lt;p&gt;For earnings history and earnings-related data on Pharming Group N.V. (PHAR) &lt;a href=&quot;http://www.streetinsider.com/ec_earnings.php?q=PHAR&quot;&gt;click here&lt;/a&gt;.&lt;/p&gt;</description>
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   <pubDate>Thu, 30 Jul 2026 06:23:14 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">PHAR</category>
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   <title>Form  6-K        Pharming Group N.V.       For: Jul 30</title>
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   <title>Form  6-K        Pharming Group N.V.       For: Jul 30</title>
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   <title>Form  6-K        Pharming Group N.V.       For: Jul 30</title>
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   <title>Form  6-K        Pharming Group N.V.       For: Jun 04</title>
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   <title>Form  6-K        Pharming Group N.V.       For: Jun 04</title>
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   <title>Form  6-K        Pharming Group N.V.       For: Jun 04</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++6-K++++++++Pharming+Group+N.V.+++++++For%3A+Jun+04/26601978.html</link>
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   <title>Pharming announces U.S. FDA acceptance of sNDA resubmission for Joenja® (leniolisib) to treat children aged 4 to 11 years with APDS</title>
   <link>http://www.streetinsider.com/Press+Releases/Pharming+announces+U.S.+FDA+acceptance+of+sNDA+resubmission+for+Joenja%C2%AE+%28leniolisib%29+to+treat+children+aged+4+to+11+years+with+APDS/26601280.html</link>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;margin-bottom:6pt; text-align:left;&quot;&gt;&lt;b&gt;If approved, Joenja will be the first approved treatment in the U.S. for children with activated phosphoinositide 3-kinase delta (PI3Kδ) syndrome (APDS), a rare primary immunodeficiency &lt;/b&gt;&lt;/li&gt;&lt;li style=&quot;margin-bottom:6pt; text-align:left;&quot;&gt;&lt;b&gt;Supplemental New Drug Application (sNDA) resubmission seeks approval for 40 mg and 50 mg twice-daily dosing&lt;/b&gt;&lt;/li&gt;&lt;li style=&quot;margin-bottom:6pt; text-align:left;&quot;&gt;&lt;b&gt;Separate sNDA for lower weight pediatric patients planned for second half 2026&lt;/b&gt;&lt;br/&gt;&lt;br/&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p align=&quot;justify&quot;&gt;&lt;b&gt;Leiden, the Netherlands, June 4, 2026: &lt;/b&gt;Pharming Group (Euronext: PHARM; Nasdaq: PHAR) today announced that the U.S. Food and Drug Administration (FDA) has accepted its resubmitted supplemental New Drug Application (sNDA) seeking approval for Joenja® (leniolisib), an oral, selective phosphoinositide 3-kinase delta (PI3Kδ) inhibitor, as a</description>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;margin-bottom:6pt; text-align:left;&quot;&gt;&lt;b&gt;If approved, Joenja will be the first approved treatment in the U.S. for children with activated phosphoinositide 3-kinase delta (PI3Kδ) syndrome (APDS), a rare primary immunodeficiency &lt;/b&gt;&lt;/li&gt;&lt;li style=&quot;margin-bottom:6pt; text-align:left;&quot;&gt;&lt;b&gt;Supplemental New Drug Application (sNDA) resubmission seeks approval for 40 mg and 50 mg twice-daily dosing&lt;/b&gt;&lt;/li&gt;&lt;li style=&quot;margin-bottom:6pt; text-align:left;&quot;&gt;&lt;b&gt;Separate sNDA for lower weight pediatric patients planned for second half 2026&lt;/b&gt;&lt;br/&gt;&lt;br/&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p align=&quot;justify&quot;&gt;&lt;b&gt;Leiden, the Netherlands, June 4, 2026: &lt;/b&gt;Pharming Group (Euronext: PHARM; Nasdaq: PHAR) today announced that the U.S. Food and Drug Administration (FDA) has accepted its resubmitted supplemental New Drug Application (sNDA) seeking approval for Joenja® (leniolisib), an oral, selective phosphoinositide 3-kinase delta (PI3Kδ) inhibitor, as a</description>
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   <title>Pharming announces U.S. FDA acceptance of sNDA resubmission for Joenja® (leniolisib) to treat children aged 4 to 11 years with APDS</title>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;margin-bottom:6pt; text-align:left;&quot;&gt;&lt;b&gt;If approved, Joenja will be the first approved treatment in the U.S. for children with activated phosphoinositide 3-kinase delta (PI3Kδ) syndrome (APDS), a rare primary immunodeficiency &lt;/b&gt;&lt;/li&gt;&lt;li style=&quot;margin-bottom:6pt; text-align:left;&quot;&gt;&lt;b&gt;Supplemental New Drug Application (sNDA) resubmission seeks approval for 40 mg and 50 mg twice-daily dosing&lt;/b&gt;&lt;/li&gt;&lt;li style=&quot;margin-bottom:6pt; text-align:left;&quot;&gt;&lt;b&gt;Separate sNDA for lower weight pediatric patients planned for second half 2026&lt;/b&gt;&lt;br/&gt;&lt;br/&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p align=&quot;justify&quot;&gt;&lt;b&gt;Leiden, the Netherlands, June 4, 2026: &lt;/b&gt;Pharming Group (Euronext: PHARM; Nasdaq: PHAR) today announced that the U.S. Food and Drug Administration (FDA) has accepted its resubmitted supplemental New Drug Application (sNDA) seeking approval for Joenja® (leniolisib), an oral, selective phosphoinositide 3-kinase delta (PI3Kδ) inhibitor, as a</description>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;margin-bottom:6pt; text-align:left;&quot;&gt;&lt;b&gt;If approved, Joenja will be the first approved treatment in the U.S. for children with activated phosphoinositide 3-kinase delta (PI3Kδ) syndrome (APDS), a rare primary immunodeficiency &lt;/b&gt;&lt;/li&gt;&lt;li style=&quot;margin-bottom:6pt; text-align:left;&quot;&gt;&lt;b&gt;Supplemental New Drug Application (sNDA) resubmission seeks approval for 40 mg and 50 mg twice-daily dosing&lt;/b&gt;&lt;/li&gt;&lt;li style=&quot;margin-bottom:6pt; text-align:left;&quot;&gt;&lt;b&gt;Separate sNDA for lower weight pediatric patients planned for second half 2026&lt;/b&gt;&lt;br/&gt;&lt;br/&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p align=&quot;justify&quot;&gt;&lt;b&gt;Leiden, the Netherlands, June 4, 2026: &lt;/b&gt;Pharming Group (Euronext: PHARM; Nasdaq: PHAR) today announced that the U.S. Food and Drug Administration (FDA) has accepted its resubmitted supplemental New Drug Application (sNDA) seeking approval for Joenja® (leniolisib), an oral, selective phosphoinositide 3-kinase delta (PI3Kδ) inhibitor, as a</description>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;margin-bottom:6pt; text-align:left;&quot;&gt;&lt;b&gt;If approved, Joenja will be the first approved treatment in the U.S. for children with activated phosphoinositide 3-kinase delta (PI3Kδ) syndrome (APDS), a rare primary immunodeficiency &lt;/b&gt;&lt;/li&gt;&lt;li style=&quot;margin-bottom:6pt; text-align:left;&quot;&gt;&lt;b&gt;Supplemental New Drug Application (sNDA) resubmission seeks approval for 40 mg and 50 mg twice-daily dosing&lt;/b&gt;&lt;/li&gt;&lt;li style=&quot;margin-bottom:6pt; text-align:left;&quot;&gt;&lt;b&gt;Separate sNDA for lower weight pediatric patients planned for second half 2026&lt;/b&gt;&lt;br/&gt;&lt;br/&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p align=&quot;justify&quot;&gt;&lt;b&gt;Leiden, the Netherlands, June 4, 2026: &lt;/b&gt;Pharming Group (Euronext: PHARM; Nasdaq: PHAR) today announced that the U.S. Food and Drug Administration (FDA) has accepted its resubmitted supplemental New Drug Application (sNDA) seeking approval for Joenja® (leniolisib), an oral, selective phosphoinositide 3-kinase delta (PI3Kδ) inhibitor, as a</description>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;margin-bottom:6pt; text-align:left;&quot;&gt;&lt;b&gt;If approved, Joenja will be the first approved treatment in the U.S. for children with activated phosphoinositide 3-kinase delta (PI3Kδ) syndrome (APDS), a rare primary immunodeficiency &lt;/b&gt;&lt;/li&gt;&lt;li style=&quot;margin-bottom:6pt; text-align:left;&quot;&gt;&lt;b&gt;Supplemental New Drug Application (sNDA) resubmission seeks approval for 40 mg and 50 mg twice-daily dosing&lt;/b&gt;&lt;/li&gt;&lt;li style=&quot;margin-bottom:6pt; text-align:left;&quot;&gt;&lt;b&gt;Separate sNDA for lower weight pediatric patients planned for second half 2026&lt;/b&gt;&lt;br/&gt;&lt;br/&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p align=&quot;justify&quot;&gt;&lt;b&gt;Leiden, the Netherlands, June 4, 2026: &lt;/b&gt;Pharming Group (Euronext: PHARM; Nasdaq: PHAR) today announced that the U.S. Food and Drug Administration (FDA) has accepted its resubmitted supplemental New Drug Application (sNDA) seeking approval for Joenja® (leniolisib), an oral, selective phosphoinositide 3-kinase delta (PI3Kδ) inhibitor, as a</description>
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