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   <title>Three-Year Real-World Study Compares Burosumab Treatment with Oral Phosphate and Active Vitamin D in Adults with XLH</title>
   <link>http://www.streetinsider.com/Press+Releases/Three-Year+Real-World+Study+Compares+Burosumab+Treatment+with+Oral+Phosphate+and+Active+Vitamin+D+in+Adults+with+XLH/27184920.html</link>
   <description>
&lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;margin-bottom:8pt;&quot;&gt;&lt;em&gt;Publication in the Journal of Bone and Mineral Research offers new insight into the long-term XLH treatment experience&lt;/em&gt;&lt;br&gt;&lt;/br&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p&gt;PRINCETON, N.J., Oct.  14, 2026  (GLOBE NEWSWIRE) -- Kyowa Kirin, Inc., a wholly owned subsidiary of Kyowa Kirin Co., Ltd. (TSE:4151, Kyowa Kirin), today announced the publication of three-year real-world findings from an interim analysis of the XLH Disease Monitoring Program (DMP) in the &lt;em&gt;Journal of Bone and Mineral Research&lt;/em&gt;. The analysis assessed serum phosphate levels and patient-reported pain, stiffness, and physical function at years 1 and 3 among adults with X-linked hypophosphatemia (XLH) treated with burosumab or</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Press+Releases/Three-Year+Real-World+Study+Compares+Burosumab+Treatment+with+Oral+Phosphate+and+Active+Vitamin+D+in+Adults+with+XLH/27184920.html</guid>
   <pubDate>Wed, 14 Oct 2026 09:05:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">KNBWY</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">KYKOY</category>
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   <title>Three-Year Real-World Study Compares Burosumab Treatment with Oral Phosphate and Active Vitamin D in Adults with XLH</title>
   <link>http://www.streetinsider.com/Globe+Newswire/Three-Year+Real-World+Study+Compares+Burosumab+Treatment+with+Oral+Phosphate+and+Active+Vitamin+D+in+Adults+with+XLH/27184920.html</link>
   <description>
&lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;margin-bottom:8pt;&quot;&gt;&lt;em&gt;Publication in the Journal of Bone and Mineral Research offers new insight into the long-term XLH treatment experience&lt;/em&gt;&lt;br&gt;&lt;/br&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p&gt;PRINCETON, N.J., Oct.  14, 2026  (GLOBE NEWSWIRE) -- Kyowa Kirin, Inc., a wholly owned subsidiary of Kyowa Kirin Co., Ltd. (TSE:4151, Kyowa Kirin), today announced the publication of three-year real-world findings from an interim analysis of the XLH Disease Monitoring Program (DMP) in the &lt;em&gt;Journal of Bone and Mineral Research&lt;/em&gt;. The analysis assessed serum phosphate levels and patient-reported pain, stiffness, and physical function at years 1 and 3 among adults with X-linked hypophosphatemia (XLH) treated with burosumab or</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Globe+Newswire/Three-Year+Real-World+Study+Compares+Burosumab+Treatment+with+Oral+Phosphate+and+Active+Vitamin+D+in+Adults+with+XLH/27184920.html</guid>
   <pubDate>Wed, 14 Oct 2026 09:05:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">KNBWY</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">KYKOY</category>
   	  </item>
  <item>
   <title>Three-Year Real-World Study Compares Burosumab Treatment with Oral Phosphate and Active Vitamin D in Adults with XLH</title>
   <link>http://www.streetinsider.com/Press+Releases/Three-Year+Real-World+Study+Compares+Burosumab+Treatment+with+Oral+Phosphate+and+Active+Vitamin+D+in+Adults+with+XLH/27184920.html</link>
   <description>
&lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;margin-bottom:8pt;&quot;&gt;&lt;em&gt;Publication in the Journal of Bone and Mineral Research offers new insight into the long-term XLH treatment experience&lt;/em&gt;&lt;br&gt;&lt;/br&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p&gt;PRINCETON, N.J., Oct.  14, 2026  (GLOBE NEWSWIRE) -- Kyowa Kirin, Inc., a wholly owned subsidiary of Kyowa Kirin Co., Ltd. (TSE:4151, Kyowa Kirin), today announced the publication of three-year real-world findings from an interim analysis of the XLH Disease Monitoring Program (DMP) in the &lt;em&gt;Journal of Bone and Mineral Research&lt;/em&gt;. The analysis assessed serum phosphate levels and patient-reported pain, stiffness, and physical function at years 1 and 3 among adults with X-linked hypophosphatemia (XLH) treated with burosumab or</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Press+Releases/Three-Year+Real-World+Study+Compares+Burosumab+Treatment+with+Oral+Phosphate+and+Active+Vitamin+D+in+Adults+with+XLH/27184920.html</guid>
   <pubDate>Wed, 14 Oct 2026 09:05:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">KNBWY</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">KYKOY</category>
   	  </item>
  <item>
   <title>Three-Year Real-World Study Compares Burosumab Treatment with Oral Phosphate and Active Vitamin D in Adults with XLH</title>
   <link>http://www.streetinsider.com/Globe+Newswire/Three-Year+Real-World+Study+Compares+Burosumab+Treatment+with+Oral+Phosphate+and+Active+Vitamin+D+in+Adults+with+XLH/27184920.html</link>
   <description>
&lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;margin-bottom:8pt;&quot;&gt;&lt;em&gt;Publication in the Journal of Bone and Mineral Research offers new insight into the long-term XLH treatment experience&lt;/em&gt;&lt;br&gt;&lt;/br&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p&gt;PRINCETON, N.J., Oct.  14, 2026  (GLOBE NEWSWIRE) -- Kyowa Kirin, Inc., a wholly owned subsidiary of Kyowa Kirin Co., Ltd. (TSE:4151, Kyowa Kirin), today announced the publication of three-year real-world findings from an interim analysis of the XLH Disease Monitoring Program (DMP) in the &lt;em&gt;Journal of Bone and Mineral Research&lt;/em&gt;. The analysis assessed serum phosphate levels and patient-reported pain, stiffness, and physical function at years 1 and 3 among adults with X-linked hypophosphatemia (XLH) treated with burosumab or</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Globe+Newswire/Three-Year+Real-World+Study+Compares+Burosumab+Treatment+with+Oral+Phosphate+and+Active+Vitamin+D+in+Adults+with+XLH/27184920.html</guid>
   <pubDate>Wed, 14 Oct 2026 09:05:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">KNBWY</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">KYKOY</category>
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   <title>Final MINT Study Results Strengthen Real-World Evidence for Mogamulizumab (Poteligeo®) in Patients With Mycosis Fungoides and Sézary Syndrome</title>
   <link>http://www.streetinsider.com/Press+Releases/Final+MINT+Study+Results+Strengthen+Real-World+Evidence+for+Mogamulizumab+%28Poteligeo%C2%AE%29+in+Patients+With+Mycosis+Fungoides+and+S%C3%A9zary+Syndrome/27173082.html</link>
   <description>
&lt;ul class=&quot;bwlistdisc&quot;&gt;
&lt;li&gt;
&lt;i&gt;Final analysis of 109 patients from 18 German centres demonstrates durable treatment outcomes in routine clinical practice1&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;Median time-to-next-treatment&lt;/i&gt; &lt;i&gt;(TTNT), the study's primary endpoint, was 14.9 months, alongside a 62.4% best overall response rate, 20.2-month overall median progression-free survival and improved quality of life from baseline reported in routine care1&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;Exploratory analyses show meaningful responses in clinically relevant subgroups, including large cell transformation, folliculotropic mycosis fungoides and mogamulizumab-associated rash status, supporting individualised treatment for patients with mycosis fungoides and Sézary syndrome1&lt;/i&gt;

&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;    GALASHIELS, Scotland &amp;amp; MARLOW, England--(BUSINESS WIRE)--
Kyowa Kirin International plc, a wholly owned subsidiary of Kyowa Kirin Co.,</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Press+Releases/Final+MINT+Study+Results+Strengthen+Real-World+Evidence+for+Mogamulizumab+%28Poteligeo%C2%AE%29+in+Patients+With+Mycosis+Fungoides+and+S%C3%A9zary+Syndrome/27173082.html</guid>
   <pubDate>Mon, 12 Oct 2026 02:00:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">KNBWY</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">KYKOY</category>
   	  </item>
  <item>
   <title>Final MINT Study Results Strengthen Real-World Evidence for Mogamulizumab (Poteligeo®) in Patients With Mycosis Fungoides and Sézary Syndrome</title>
   <link>http://www.streetinsider.com/Business+Wire/Final+MINT+Study+Results+Strengthen+Real-World+Evidence+for+Mogamulizumab+%28Poteligeo%C2%AE%29+in+Patients+With+Mycosis+Fungoides+and+S%C3%A9zary+Syndrome/27173082.html</link>
   <description>
&lt;ul class=&quot;bwlistdisc&quot;&gt;
&lt;li&gt;
&lt;i&gt;Final analysis of 109 patients from 18 German centres demonstrates durable treatment outcomes in routine clinical practice1&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;Median time-to-next-treatment&lt;/i&gt; &lt;i&gt;(TTNT), the study's primary endpoint, was 14.9 months, alongside a 62.4% best overall response rate, 20.2-month overall median progression-free survival and improved quality of life from baseline reported in routine care1&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;Exploratory analyses show meaningful responses in clinically relevant subgroups, including large cell transformation, folliculotropic mycosis fungoides and mogamulizumab-associated rash status, supporting individualised treatment for patients with mycosis fungoides and Sézary syndrome1&lt;/i&gt;

&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;    GALASHIELS, Scotland &amp;amp; MARLOW, England--(BUSINESS WIRE)--
Kyowa Kirin International plc, a wholly owned subsidiary of Kyowa Kirin Co.,</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Business+Wire/Final+MINT+Study+Results+Strengthen+Real-World+Evidence+for+Mogamulizumab+%28Poteligeo%C2%AE%29+in+Patients+With+Mycosis+Fungoides+and+S%C3%A9zary+Syndrome/27173082.html</guid>
   <pubDate>Mon, 12 Oct 2026 02:00:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">KNBWY</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">KYKOY</category>
   	  </item>
  <item>
   <title>Final MINT Study Results Strengthen Real-World Evidence for Mogamulizumab (Poteligeo®) in Patients With Mycosis Fungoides and Sézary Syndrome</title>
   <link>http://www.streetinsider.com/Press+Releases/Final+MINT+Study+Results+Strengthen+Real-World+Evidence+for+Mogamulizumab+%28Poteligeo%C2%AE%29+in+Patients+With+Mycosis+Fungoides+and+S%C3%A9zary+Syndrome/27173082.html</link>
   <description>
&lt;ul class=&quot;bwlistdisc&quot;&gt;
&lt;li&gt;
&lt;i&gt;Final analysis of 109 patients from 18 German centres demonstrates durable treatment outcomes in routine clinical practice1&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;Median time-to-next-treatment&lt;/i&gt; &lt;i&gt;(TTNT), the study's primary endpoint, was 14.9 months, alongside a 62.4% best overall response rate, 20.2-month overall median progression-free survival and improved quality of life from baseline reported in routine care1&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;Exploratory analyses show meaningful responses in clinically relevant subgroups, including large cell transformation, folliculotropic mycosis fungoides and mogamulizumab-associated rash status, supporting individualised treatment for patients with mycosis fungoides and Sézary syndrome1&lt;/i&gt;

&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;    GALASHIELS, Scotland &amp;amp; MARLOW, England--(BUSINESS WIRE)--
Kyowa Kirin International plc, a wholly owned subsidiary of Kyowa Kirin Co.,</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Press+Releases/Final+MINT+Study+Results+Strengthen+Real-World+Evidence+for+Mogamulizumab+%28Poteligeo%C2%AE%29+in+Patients+With+Mycosis+Fungoides+and+S%C3%A9zary+Syndrome/27173082.html</guid>
   <pubDate>Mon, 12 Oct 2026 02:00:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">KNBWY</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">KYKOY</category>
   	  </item>
  <item>
   <title>Final MINT Study Results Strengthen Real-World Evidence for Mogamulizumab (Poteligeo®) in Patients With Mycosis Fungoides and Sézary Syndrome</title>
   <link>http://www.streetinsider.com/Business+Wire/Final+MINT+Study+Results+Strengthen+Real-World+Evidence+for+Mogamulizumab+%28Poteligeo%C2%AE%29+in+Patients+With+Mycosis+Fungoides+and+S%C3%A9zary+Syndrome/27173082.html</link>
   <description>
&lt;ul class=&quot;bwlistdisc&quot;&gt;
&lt;li&gt;
&lt;i&gt;Final analysis of 109 patients from 18 German centres demonstrates durable treatment outcomes in routine clinical practice1&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;Median time-to-next-treatment&lt;/i&gt; &lt;i&gt;(TTNT), the study's primary endpoint, was 14.9 months, alongside a 62.4% best overall response rate, 20.2-month overall median progression-free survival and improved quality of life from baseline reported in routine care1&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;Exploratory analyses show meaningful responses in clinically relevant subgroups, including large cell transformation, folliculotropic mycosis fungoides and mogamulizumab-associated rash status, supporting individualised treatment for patients with mycosis fungoides and Sézary syndrome1&lt;/i&gt;

&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;    GALASHIELS, Scotland &amp;amp; MARLOW, England--(BUSINESS WIRE)--
Kyowa Kirin International plc, a wholly owned subsidiary of Kyowa Kirin Co.,</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Business+Wire/Final+MINT+Study+Results+Strengthen+Real-World+Evidence+for+Mogamulizumab+%28Poteligeo%C2%AE%29+in+Patients+With+Mycosis+Fungoides+and+S%C3%A9zary+Syndrome/27173082.html</guid>
   <pubDate>Mon, 12 Oct 2026 02:00:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">KNBWY</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">KYKOY</category>
   	  </item>
  <item>
   <title>Kyowa Kirin and Knight Therapeutics Enter Into Exclusive Distribution Agreement for POTELIGEO® (mogamulizumab) for Cutaneous T-Cell Lymphoma (CTCL) Patients Across Latin America</title>
   <link>http://www.streetinsider.com/Press+Releases/Kyowa+Kirin+and+Knight+Therapeutics+Enter+Into+Exclusive+Distribution+Agreement+for+POTELIGEO%C2%AE+%28mogamulizumab%29+for+Cutaneous+T-Cell+Lymphoma+%28CTCL%29+Patients+Across+Latin+America/27117587.html</link>
   <description>
&lt;ul class=&quot;bwlistdisc&quot;&gt;
&lt;li&gt;
&lt;i&gt;This agreement marks the first introduction of Kyowa Kirin's POTELIGEO® in Latin America and expands access for patients.&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;Knight Therapeutics to exclusively distribute POTELIGEO® across Argentina, Brazil, Colombia and Mexico.&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;The agreement supports Kyowa Kirin’s mission to address barriers to diagnosis, treatment access and disease awareness for CTCL patients across the region.&lt;/i&gt;

&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;    GALASHIELS &amp;amp; MARLOW, U.K.--(BUSINESS WIRE)--
Kyowa Kirin International, a wholly owned subsidiary of Kyowa Kirin Co., Ltd. (TSE:4151, Kyowa Kirin), today announced the signing of an exclusive distribution agreement with Knight Therapeutics (“Knight”) (TSX: GUD) for the distribution of mogamulizumab in select countries in Latin America.

&lt;/p&gt;&lt;p&gt;
Under the</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Press+Releases/Kyowa+Kirin+and+Knight+Therapeutics+Enter+Into+Exclusive+Distribution+Agreement+for+POTELIGEO%C2%AE+%28mogamulizumab%29+for+Cutaneous+T-Cell+Lymphoma+%28CTCL%29+Patients+Across+Latin+America/27117587.html</guid>
   <pubDate>Tue, 29 Sep 2026 08:00:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">GUD</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">KNBWY</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">KYKOY</category>
   	  </item>
  <item>
   <title>Kyowa Kirin and Knight Therapeutics Enter Into Exclusive Distribution Agreement for POTELIGEO® (mogamulizumab) for Cutaneous T-Cell Lymphoma (CTCL) Patients Across Latin America</title>
   <link>http://www.streetinsider.com/Business+Wire/Kyowa+Kirin+and+Knight+Therapeutics+Enter+Into+Exclusive+Distribution+Agreement+for+POTELIGEO%C2%AE+%28mogamulizumab%29+for+Cutaneous+T-Cell+Lymphoma+%28CTCL%29+Patients+Across+Latin+America/27117587.html</link>
   <description>
&lt;ul class=&quot;bwlistdisc&quot;&gt;
&lt;li&gt;
&lt;i&gt;This agreement marks the first introduction of Kyowa Kirin's POTELIGEO® in Latin America and expands access for patients.&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;Knight Therapeutics to exclusively distribute POTELIGEO® across Argentina, Brazil, Colombia and Mexico.&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;The agreement supports Kyowa Kirin’s mission to address barriers to diagnosis, treatment access and disease awareness for CTCL patients across the region.&lt;/i&gt;

&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;    GALASHIELS &amp;amp; MARLOW, U.K.--(BUSINESS WIRE)--
Kyowa Kirin International, a wholly owned subsidiary of Kyowa Kirin Co., Ltd. (TSE:4151, Kyowa Kirin), today announced the signing of an exclusive distribution agreement with Knight Therapeutics (“Knight”) (TSX: GUD) for the distribution of mogamulizumab in select countries in Latin America.

&lt;/p&gt;&lt;p&gt;
Under the</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Business+Wire/Kyowa+Kirin+and+Knight+Therapeutics+Enter+Into+Exclusive+Distribution+Agreement+for+POTELIGEO%C2%AE+%28mogamulizumab%29+for+Cutaneous+T-Cell+Lymphoma+%28CTCL%29+Patients+Across+Latin+America/27117587.html</guid>
   <pubDate>Tue, 29 Sep 2026 08:00:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">GUD</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">KNBWY</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">KYKOY</category>
   	  </item>
  <item>
   <title>Kyowa Kirin and Knight Therapeutics Enter Into Exclusive Distribution Agreement for POTELIGEO® (mogamulizumab) for Cutaneous T-Cell Lymphoma (CTCL) Patients Across Latin America</title>
   <link>http://www.streetinsider.com/Press+Releases/Kyowa+Kirin+and+Knight+Therapeutics+Enter+Into+Exclusive+Distribution+Agreement+for+POTELIGEO%C2%AE+%28mogamulizumab%29+for+Cutaneous+T-Cell+Lymphoma+%28CTCL%29+Patients+Across+Latin+America/27117587.html</link>
   <description>
&lt;ul class=&quot;bwlistdisc&quot;&gt;
&lt;li&gt;
&lt;i&gt;This agreement marks the first introduction of Kyowa Kirin's POTELIGEO® in Latin America and expands access for patients.&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;Knight Therapeutics to exclusively distribute POTELIGEO® across Argentina, Brazil, Colombia and Mexico.&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;The agreement supports Kyowa Kirin’s mission to address barriers to diagnosis, treatment access and disease awareness for CTCL patients across the region.&lt;/i&gt;

&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;    GALASHIELS &amp;amp; MARLOW, U.K.--(BUSINESS WIRE)--
Kyowa Kirin International, a wholly owned subsidiary of Kyowa Kirin Co., Ltd. (TSE:4151, Kyowa Kirin), today announced the signing of an exclusive distribution agreement with Knight Therapeutics (“Knight”) (TSX: GUD) for the distribution of mogamulizumab in select countries in Latin America.

&lt;/p&gt;&lt;p&gt;
Under the</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Press+Releases/Kyowa+Kirin+and+Knight+Therapeutics+Enter+Into+Exclusive+Distribution+Agreement+for+POTELIGEO%C2%AE+%28mogamulizumab%29+for+Cutaneous+T-Cell+Lymphoma+%28CTCL%29+Patients+Across+Latin+America/27117587.html</guid>
   <pubDate>Tue, 29 Sep 2026 08:00:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">GUD</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">KNBWY</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">KYKOY</category>
   	  </item>
  <item>
   <title>Kyowa Kirin and Knight Therapeutics Enter Into Exclusive Distribution Agreement for POTELIGEO® (mogamulizumab) for Cutaneous T-Cell Lymphoma (CTCL) Patients Across Latin America</title>
   <link>http://www.streetinsider.com/Business+Wire/Kyowa+Kirin+and+Knight+Therapeutics+Enter+Into+Exclusive+Distribution+Agreement+for+POTELIGEO%C2%AE+%28mogamulizumab%29+for+Cutaneous+T-Cell+Lymphoma+%28CTCL%29+Patients+Across+Latin+America/27117587.html</link>
   <description>
&lt;ul class=&quot;bwlistdisc&quot;&gt;
&lt;li&gt;
&lt;i&gt;This agreement marks the first introduction of Kyowa Kirin's POTELIGEO® in Latin America and expands access for patients.&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;Knight Therapeutics to exclusively distribute POTELIGEO® across Argentina, Brazil, Colombia and Mexico.&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;The agreement supports Kyowa Kirin’s mission to address barriers to diagnosis, treatment access and disease awareness for CTCL patients across the region.&lt;/i&gt;

&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;    GALASHIELS &amp;amp; MARLOW, U.K.--(BUSINESS WIRE)--
Kyowa Kirin International, a wholly owned subsidiary of Kyowa Kirin Co., Ltd. (TSE:4151, Kyowa Kirin), today announced the signing of an exclusive distribution agreement with Knight Therapeutics (“Knight”) (TSX: GUD) for the distribution of mogamulizumab in select countries in Latin America.

&lt;/p&gt;&lt;p&gt;
Under the</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Business+Wire/Kyowa+Kirin+and+Knight+Therapeutics+Enter+Into+Exclusive+Distribution+Agreement+for+POTELIGEO%C2%AE+%28mogamulizumab%29+for+Cutaneous+T-Cell+Lymphoma+%28CTCL%29+Patients+Across+Latin+America/27117587.html</guid>
   <pubDate>Tue, 29 Sep 2026 08:00:00 -0400</pubDate>
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  <item>
   <title>Kyowa Kirin and Knight Therapeutics Enter Into Exclusive Distribution Agreement for POTELIGEO® (mogamulizumab) for Cutaneous T-Cell Lymphoma (CTCL) Patients Across Latin America</title>
   <link>http://www.streetinsider.com/Press+Releases/Kyowa+Kirin+and+Knight+Therapeutics+Enter+Into+Exclusive+Distribution+Agreement+for+POTELIGEO%C2%AE+%28mogamulizumab%29+for+Cutaneous+T-Cell+Lymphoma+%28CTCL%29+Patients+Across+Latin+America/27117587.html</link>
   <description>
&lt;ul class=&quot;bwlistdisc&quot;&gt;
&lt;li&gt;
&lt;i&gt;This agreement marks the first introduction of Kyowa Kirin's POTELIGEO® in Latin America and expands access for patients.&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;Knight Therapeutics to exclusively distribute POTELIGEO® across Argentina, Brazil, Colombia and Mexico.&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;The agreement supports Kyowa Kirin’s mission to address barriers to diagnosis, treatment access and disease awareness for CTCL patients across the region.&lt;/i&gt;

&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;    GALASHIELS &amp;amp; MARLOW, U.K.--(BUSINESS WIRE)--
Kyowa Kirin International, a wholly owned subsidiary of Kyowa Kirin Co., Ltd. (TSE:4151, Kyowa Kirin), today announced the signing of an exclusive distribution agreement with Knight Therapeutics (“Knight”) (TSX: GUD) for the distribution of mogamulizumab in select countries in Latin America.

&lt;/p&gt;&lt;p&gt;
Under the</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Press+Releases/Kyowa+Kirin+and+Knight+Therapeutics+Enter+Into+Exclusive+Distribution+Agreement+for+POTELIGEO%C2%AE+%28mogamulizumab%29+for+Cutaneous+T-Cell+Lymphoma+%28CTCL%29+Patients+Across+Latin+America/27117587.html</guid>
   <pubDate>Tue, 29 Sep 2026 08:00:00 -0400</pubDate>
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  <item>
   <title>Kyowa Kirin and Knight Therapeutics Enter Into Exclusive Distribution Agreement for POTELIGEO® (mogamulizumab) for Cutaneous T-Cell Lymphoma (CTCL) Patients Across Latin America</title>
   <link>http://www.streetinsider.com/Business+Wire/Kyowa+Kirin+and+Knight+Therapeutics+Enter+Into+Exclusive+Distribution+Agreement+for+POTELIGEO%C2%AE+%28mogamulizumab%29+for+Cutaneous+T-Cell+Lymphoma+%28CTCL%29+Patients+Across+Latin+America/27117587.html</link>
   <description>
&lt;ul class=&quot;bwlistdisc&quot;&gt;
&lt;li&gt;
&lt;i&gt;This agreement marks the first introduction of Kyowa Kirin's POTELIGEO® in Latin America and expands access for patients.&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;Knight Therapeutics to exclusively distribute POTELIGEO® across Argentina, Brazil, Colombia and Mexico.&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;The agreement supports Kyowa Kirin’s mission to address barriers to diagnosis, treatment access and disease awareness for CTCL patients across the region.&lt;/i&gt;

&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;    GALASHIELS &amp;amp; MARLOW, U.K.--(BUSINESS WIRE)--
Kyowa Kirin International, a wholly owned subsidiary of Kyowa Kirin Co., Ltd. (TSE:4151, Kyowa Kirin), today announced the signing of an exclusive distribution agreement with Knight Therapeutics (“Knight”) (TSX: GUD) for the distribution of mogamulizumab in select countries in Latin America.

&lt;/p&gt;&lt;p&gt;
Under the</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Business+Wire/Kyowa+Kirin+and+Knight+Therapeutics+Enter+Into+Exclusive+Distribution+Agreement+for+POTELIGEO%C2%AE+%28mogamulizumab%29+for+Cutaneous+T-Cell+Lymphoma+%28CTCL%29+Patients+Across+Latin+America/27117587.html</guid>
   <pubDate>Tue, 29 Sep 2026 08:00:00 -0400</pubDate>
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   <title>European Commission Approves Crysvita® (burosumab) for Infants with X-linked Hypophosphataemia in the European Union</title>
   <link>http://www.streetinsider.com/Press+Releases/European+Commission+Approves+Crysvita%C2%AE+%28burosumab%29+for+Infants+with+X-linked+Hypophosphataemia+in+the+European+Union/26791018.html</link>
   <description>
&lt;ul class=&quot;bwlistdisc&quot;&gt;
&lt;li&gt;
&lt;i&gt;Approval expands the approved indication for Crysvita to include infants from 1 month to 1 year of age, enabling earlier intervention in a rare, progressive disease that can impact skeletal development from infancy.&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;Approval applies across the European Union and European Economic Area, expanding access to treatment for the youngest patients living with XLH.&lt;/i&gt;

&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;    GALASHIELS, Scotland &amp;amp; MARLOW, England--(BUSINESS WIRE)--
Kyowa Kirin EMEA, a wholly owned subsidiary of Kyowa Kirin Co., Ltd. (TSE:4151), today announced that the European Commission (EC) has approved an expansion of the indication for Crysvita® (burosumab) for the treatment of X-linked hypophosphataemia (XLH), to</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Press+Releases/European+Commission+Approves+Crysvita%C2%AE+%28burosumab%29+for+Infants+with+X-linked+Hypophosphataemia+in+the+European+Union/26791018.html</guid>
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   <title>European Commission Approves Crysvita® (burosumab) for Infants with X-linked Hypophosphataemia in the European Union</title>
   <link>http://www.streetinsider.com/Business+Wire/European+Commission+Approves+Crysvita%C2%AE+%28burosumab%29+for+Infants+with+X-linked+Hypophosphataemia+in+the+European+Union/26791018.html</link>
   <description>
&lt;ul class=&quot;bwlistdisc&quot;&gt;
&lt;li&gt;
&lt;i&gt;Approval expands the approved indication for Crysvita to include infants from 1 month to 1 year of age, enabling earlier intervention in a rare, progressive disease that can impact skeletal development from infancy.&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;Approval applies across the European Union and European Economic Area, expanding access to treatment for the youngest patients living with XLH.&lt;/i&gt;

&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;    GALASHIELS, Scotland &amp;amp; MARLOW, England--(BUSINESS WIRE)--
Kyowa Kirin EMEA, a wholly owned subsidiary of Kyowa Kirin Co., Ltd. (TSE:4151), today announced that the European Commission (EC) has approved an expansion of the indication for Crysvita® (burosumab) for the treatment of X-linked hypophosphataemia (XLH), to</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Business+Wire/European+Commission+Approves+Crysvita%C2%AE+%28burosumab%29+for+Infants+with+X-linked+Hypophosphataemia+in+the+European+Union/26791018.html</guid>
   <pubDate>Tue, 21 Jul 2026 03:00:00 -0400</pubDate>
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   <title>European Commission Approves Crysvita® (burosumab) for Infants with X-linked Hypophosphataemia in the European Union</title>
   <link>http://www.streetinsider.com/Press+Releases/European+Commission+Approves+Crysvita%C2%AE+%28burosumab%29+for+Infants+with+X-linked+Hypophosphataemia+in+the+European+Union/26791018.html</link>
   <description>
&lt;ul class=&quot;bwlistdisc&quot;&gt;
&lt;li&gt;
&lt;i&gt;Approval expands the approved indication for Crysvita to include infants from 1 month to 1 year of age, enabling earlier intervention in a rare, progressive disease that can impact skeletal development from infancy.&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;Approval applies across the European Union and European Economic Area, expanding access to treatment for the youngest patients living with XLH.&lt;/i&gt;

&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;    GALASHIELS, Scotland &amp;amp; MARLOW, England--(BUSINESS WIRE)--
Kyowa Kirin EMEA, a wholly owned subsidiary of Kyowa Kirin Co., Ltd. (TSE:4151), today announced that the European Commission (EC) has approved an expansion of the indication for Crysvita® (burosumab) for the treatment of X-linked hypophosphataemia (XLH), to</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Press+Releases/European+Commission+Approves+Crysvita%C2%AE+%28burosumab%29+for+Infants+with+X-linked+Hypophosphataemia+in+the+European+Union/26791018.html</guid>
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   <title>European Commission Approves Crysvita® (burosumab) for Infants with X-linked Hypophosphataemia in the European Union</title>
   <link>http://www.streetinsider.com/Business+Wire/European+Commission+Approves+Crysvita%C2%AE+%28burosumab%29+for+Infants+with+X-linked+Hypophosphataemia+in+the+European+Union/26791018.html</link>
   <description>
&lt;ul class=&quot;bwlistdisc&quot;&gt;
&lt;li&gt;
&lt;i&gt;Approval expands the approved indication for Crysvita to include infants from 1 month to 1 year of age, enabling earlier intervention in a rare, progressive disease that can impact skeletal development from infancy.&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;Approval applies across the European Union and European Economic Area, expanding access to treatment for the youngest patients living with XLH.&lt;/i&gt;

&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;    GALASHIELS, Scotland &amp;amp; MARLOW, England--(BUSINESS WIRE)--
Kyowa Kirin EMEA, a wholly owned subsidiary of Kyowa Kirin Co., Ltd. (TSE:4151), today announced that the European Commission (EC) has approved an expansion of the indication for Crysvita® (burosumab) for the treatment of X-linked hypophosphataemia (XLH), to</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Business+Wire/European+Commission+Approves+Crysvita%C2%AE+%28burosumab%29+for+Infants+with+X-linked+Hypophosphataemia+in+the+European+Union/26791018.html</guid>
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   <title>European Commission Approves Crysvita® (burosumab) for Infants with X-linked Hypophosphataemia in the European Union</title>
   <link>http://www.streetinsider.com/Press+Releases/European+Commission+Approves+Crysvita%C2%AE+%28burosumab%29+for+Infants+with+X-linked+Hypophosphataemia+in+the+European+Union/26791018.html</link>
   <description>
&lt;ul class=&quot;bwlistdisc&quot;&gt;
&lt;li&gt;
&lt;i&gt;Approval expands the approved indication for Crysvita to include infants from 1 month to 1 year of age, enabling earlier intervention in a rare, progressive disease that can impact skeletal development from infancy.&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;Approval applies across the European Union and European Economic Area, expanding access to treatment for the youngest patients living with XLH.&lt;/i&gt;

&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;    GALASHIELS, Scotland &amp;amp; MARLOW, England--(BUSINESS WIRE)--
Kyowa Kirin EMEA, a wholly owned subsidiary of Kyowa Kirin Co., Ltd. (TSE:4151), today announced that the European Commission (EC) has approved an expansion of the indication for Crysvita® (burosumab) for the treatment of X-linked hypophosphataemia (XLH), to</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Press+Releases/European+Commission+Approves+Crysvita%C2%AE+%28burosumab%29+for+Infants+with+X-linked+Hypophosphataemia+in+the+European+Union/26791018.html</guid>
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  <item>
   <title>European Commission Approves Crysvita® (burosumab) for Infants with X-linked Hypophosphataemia in the European Union</title>
   <link>http://www.streetinsider.com/Business+Wire/European+Commission+Approves+Crysvita%C2%AE+%28burosumab%29+for+Infants+with+X-linked+Hypophosphataemia+in+the+European+Union/26791018.html</link>
   <description>
&lt;ul class=&quot;bwlistdisc&quot;&gt;
&lt;li&gt;
&lt;i&gt;Approval expands the approved indication for Crysvita to include infants from 1 month to 1 year of age, enabling earlier intervention in a rare, progressive disease that can impact skeletal development from infancy.&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;Approval applies across the European Union and European Economic Area, expanding access to treatment for the youngest patients living with XLH.&lt;/i&gt;

&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;    GALASHIELS, Scotland &amp;amp; MARLOW, England--(BUSINESS WIRE)--
Kyowa Kirin EMEA, a wholly owned subsidiary of Kyowa Kirin Co., Ltd. (TSE:4151), today announced that the European Commission (EC) has approved an expansion of the indication for Crysvita® (burosumab) for the treatment of X-linked hypophosphataemia (XLH), to</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Business+Wire/European+Commission+Approves+Crysvita%C2%AE+%28burosumab%29+for+Infants+with+X-linked+Hypophosphataemia+in+the+European+Union/26791018.html</guid>
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  <item>
   <title>European Commission Approves Crysvita® (burosumab) for Infants with X-linked Hypophosphataemia in the European Union</title>
   <link>http://www.streetinsider.com/Press+Releases/European+Commission+Approves+Crysvita%C2%AE+%28burosumab%29+for+Infants+with+X-linked+Hypophosphataemia+in+the+European+Union/26791018.html</link>
   <description>
&lt;ul class=&quot;bwlistdisc&quot;&gt;
&lt;li&gt;
&lt;i&gt;Approval expands the approved indication for Crysvita to include infants from 1 month to 1 year of age, enabling earlier intervention in a rare, progressive disease that can impact skeletal development from infancy.&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;Approval applies across the European Union and European Economic Area, expanding access to treatment for the youngest patients living with XLH.&lt;/i&gt;

&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;    GALASHIELS, Scotland &amp;amp; MARLOW, England--(BUSINESS WIRE)--
Kyowa Kirin EMEA, a wholly owned subsidiary of Kyowa Kirin Co., Ltd. (TSE:4151), today announced that the European Commission (EC) has approved an expansion of the indication for Crysvita® (burosumab) for the treatment of X-linked hypophosphataemia (XLH), to</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Press+Releases/European+Commission+Approves+Crysvita%C2%AE+%28burosumab%29+for+Infants+with+X-linked+Hypophosphataemia+in+the+European+Union/26791018.html</guid>
   <pubDate>Tue, 21 Jul 2026 03:00:00 -0400</pubDate>
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   <title>European Commission Approves Crysvita® (burosumab) for Infants with X-linked Hypophosphataemia in the European Union</title>
   <link>http://www.streetinsider.com/Business+Wire/European+Commission+Approves+Crysvita%C2%AE+%28burosumab%29+for+Infants+with+X-linked+Hypophosphataemia+in+the+European+Union/26791018.html</link>
   <description>
&lt;ul class=&quot;bwlistdisc&quot;&gt;
&lt;li&gt;
&lt;i&gt;Approval expands the approved indication for Crysvita to include infants from 1 month to 1 year of age, enabling earlier intervention in a rare, progressive disease that can impact skeletal development from infancy.&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;Approval applies across the European Union and European Economic Area, expanding access to treatment for the youngest patients living with XLH.&lt;/i&gt;

&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;    GALASHIELS, Scotland &amp;amp; MARLOW, England--(BUSINESS WIRE)--
Kyowa Kirin EMEA, a wholly owned subsidiary of Kyowa Kirin Co., Ltd. (TSE:4151), today announced that the European Commission (EC) has approved an expansion of the indication for Crysvita® (burosumab) for the treatment of X-linked hypophosphataemia (XLH), to</description>
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   <pubDate>Tue, 21 Jul 2026 03:00:00 -0400</pubDate>
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   <title>European Commission Approves Crysvita® (burosumab) for Infants with X-linked Hypophosphataemia in the European Union</title>
   <link>http://www.streetinsider.com/Press+Releases/European+Commission+Approves+Crysvita%C2%AE+%28burosumab%29+for+Infants+with+X-linked+Hypophosphataemia+in+the+European+Union/26791018.html</link>
   <description>
&lt;ul class=&quot;bwlistdisc&quot;&gt;
&lt;li&gt;
&lt;i&gt;Approval expands the approved indication for Crysvita to include infants from 1 month to 1 year of age, enabling earlier intervention in a rare, progressive disease that can impact skeletal development from infancy.&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;Approval applies across the European Union and European Economic Area, expanding access to treatment for the youngest patients living with XLH.&lt;/i&gt;

&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;    GALASHIELS, Scotland &amp;amp; MARLOW, England--(BUSINESS WIRE)--
Kyowa Kirin EMEA, a wholly owned subsidiary of Kyowa Kirin Co., Ltd. (TSE:4151), today announced that the European Commission (EC) has approved an expansion of the indication for Crysvita® (burosumab) for the treatment of X-linked hypophosphataemia (XLH), to</description>
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   <pubDate>Tue, 21 Jul 2026 03:00:00 -0400</pubDate>
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   <title>European Commission Approves Crysvita® (burosumab) for Infants with X-linked Hypophosphataemia in the European Union</title>
   <link>http://www.streetinsider.com/Business+Wire/European+Commission+Approves+Crysvita%C2%AE+%28burosumab%29+for+Infants+with+X-linked+Hypophosphataemia+in+the+European+Union/26791018.html</link>
   <description>
&lt;ul class=&quot;bwlistdisc&quot;&gt;
&lt;li&gt;
&lt;i&gt;Approval expands the approved indication for Crysvita to include infants from 1 month to 1 year of age, enabling earlier intervention in a rare, progressive disease that can impact skeletal development from infancy.&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;Approval applies across the European Union and European Economic Area, expanding access to treatment for the youngest patients living with XLH.&lt;/i&gt;

&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;    GALASHIELS, Scotland &amp;amp; MARLOW, England--(BUSINESS WIRE)--
Kyowa Kirin EMEA, a wholly owned subsidiary of Kyowa Kirin Co., Ltd. (TSE:4151), today announced that the European Commission (EC) has approved an expansion of the indication for Crysvita® (burosumab) for the treatment of X-linked hypophosphataemia (XLH), to</description>
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   <title>European Commission Approves Crysvita® (burosumab) for Infants with X-linked Hypophosphataemia in the European Union</title>
   <link>http://www.streetinsider.com/Press+Releases/European+Commission+Approves+Crysvita%C2%AE+%28burosumab%29+for+Infants+with+X-linked+Hypophosphataemia+in+the+European+Union/26791018.html</link>
   <description>
&lt;ul class=&quot;bwlistdisc&quot;&gt;
&lt;li&gt;
&lt;i&gt;Approval expands the approved indication for Crysvita to include infants from 1 month to 1 year of age, enabling earlier intervention in a rare, progressive disease that can impact skeletal development from infancy.&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;Approval applies across the European Union and European Economic Area, expanding access to treatment for the youngest patients living with XLH.&lt;/i&gt;

&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;    GALASHIELS, Scotland &amp;amp; MARLOW, England--(BUSINESS WIRE)--
Kyowa Kirin EMEA, a wholly owned subsidiary of Kyowa Kirin Co., Ltd. (TSE:4151), today announced that the European Commission (EC) has approved an expansion of the indication for Crysvita® (burosumab) for the treatment of X-linked hypophosphataemia (XLH), to</description>
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