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   <title>CLINUVEL receives final EMA scientific advice for pivotal Phase III vitiligo study</title>
   <link>http://www.streetinsider.com/Press+Releases/CLINUVEL+receives+final+EMA+scientific+advice+for+pivotal+Phase+III+vitiligo+study/26361154.html</link>
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&lt;p align=&quot;left&quot;&gt;&lt;strong&gt;EXECUTIVE SUMMARY&lt;/strong&gt;&lt;/p&gt;  &lt;ul&gt;&lt;li style=&quot;margin-top:3pt; margin-bottom:0in;&quot;&gt;final European scientific advice received for pivotal Phase III vitiligo study&lt;/li&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in;&quot;&gt;EMA emphasised its “totality of evidence” approach&lt;/li&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in;&quot;&gt;central photographic review and validated disease assessment tools agreed&lt;/li&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in;&quot;&gt;CUV107 to compare SCENESSE® with adjunct NB-UVB vs NB-UVB monotherapy&lt;/li&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in;&quot;&gt;CUV107 study (n=300) to commence in 2H 2026&lt;/li&gt;&lt;/ul&gt;  &lt;p&gt;MELBOURNE, Australia, April  24, 2026  (GLOBE NEWSWIRE) -- CLINUVEL PHARMACEUTICALS LTD today announced that the European Medicines Agency (EMA) has provided final scientific advice on the design of the planned pivotal Phase III CUV107 study and anticipated evaluation of evidence of CLINUVEL’s</description>
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   <title>CLINUVEL receives final EMA scientific advice for pivotal Phase III vitiligo study</title>
   <link>http://www.streetinsider.com/Press+Releases/CLINUVEL+receives+final+EMA+scientific+advice+for+pivotal+Phase+III+vitiligo+study/26361154.html</link>
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&lt;p align=&quot;left&quot;&gt;&lt;strong&gt;EXECUTIVE SUMMARY&lt;/strong&gt;&lt;/p&gt;  &lt;ul&gt;&lt;li style=&quot;margin-top:3pt; margin-bottom:0in;&quot;&gt;final European scientific advice received for pivotal Phase III vitiligo study&lt;/li&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in;&quot;&gt;EMA emphasised its “totality of evidence” approach&lt;/li&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in;&quot;&gt;central photographic review and validated disease assessment tools agreed&lt;/li&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in;&quot;&gt;CUV107 to compare SCENESSE® with adjunct NB-UVB vs NB-UVB monotherapy&lt;/li&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in;&quot;&gt;CUV107 study (n=300) to commence in 2H 2026&lt;/li&gt;&lt;/ul&gt;  &lt;p&gt;MELBOURNE, Australia, April  24, 2026  (GLOBE NEWSWIRE) -- CLINUVEL PHARMACEUTICALS LTD today announced that the European Medicines Agency (EMA) has provided final scientific advice on the design of the planned pivotal Phase III CUV107 study and anticipated evaluation of evidence of CLINUVEL’s</description>
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   <title>CLINUVEL receives final EMA scientific advice for pivotal Phase III vitiligo study</title>
   <link>http://www.streetinsider.com/Press+Releases/CLINUVEL+receives+final+EMA+scientific+advice+for+pivotal+Phase+III+vitiligo+study/26361154.html</link>
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&lt;p align=&quot;left&quot;&gt;&lt;strong&gt;EXECUTIVE SUMMARY&lt;/strong&gt;&lt;/p&gt;  &lt;ul&gt;&lt;li style=&quot;margin-top:3pt; margin-bottom:0in;&quot;&gt;final European scientific advice received for pivotal Phase III vitiligo study&lt;/li&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in;&quot;&gt;EMA emphasised its “totality of evidence” approach&lt;/li&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in;&quot;&gt;central photographic review and validated disease assessment tools agreed&lt;/li&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in;&quot;&gt;CUV107 to compare SCENESSE® with adjunct NB-UVB vs NB-UVB monotherapy&lt;/li&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in;&quot;&gt;CUV107 study (n=300) to commence in 2H 2026&lt;/li&gt;&lt;/ul&gt;  &lt;p&gt;MELBOURNE, Australia, April  24, 2026  (GLOBE NEWSWIRE) -- CLINUVEL PHARMACEUTICALS LTD today announced that the European Medicines Agency (EMA) has provided final scientific advice on the design of the planned pivotal Phase III CUV107 study and anticipated evaluation of evidence of CLINUVEL’s</description>
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   <title>CLINUVEL receives final EMA scientific advice for pivotal Phase III vitiligo study</title>
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&lt;p align=&quot;left&quot;&gt;&lt;strong&gt;EXECUTIVE SUMMARY&lt;/strong&gt;&lt;/p&gt;  &lt;ul&gt;&lt;li style=&quot;margin-top:3pt; margin-bottom:0in;&quot;&gt;final European scientific advice received for pivotal Phase III vitiligo study&lt;/li&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in;&quot;&gt;EMA emphasised its “totality of evidence” approach&lt;/li&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in;&quot;&gt;central photographic review and validated disease assessment tools agreed&lt;/li&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in;&quot;&gt;CUV107 to compare SCENESSE® with adjunct NB-UVB vs NB-UVB monotherapy&lt;/li&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in;&quot;&gt;CUV107 study (n=300) to commence in 2H 2026&lt;/li&gt;&lt;/ul&gt;  &lt;p&gt;MELBOURNE, Australia, April  24, 2026  (GLOBE NEWSWIRE) -- CLINUVEL PHARMACEUTICALS LTD today announced that the European Medicines Agency (EMA) has provided final scientific advice on the design of the planned pivotal Phase III CUV107 study and anticipated evaluation of evidence of CLINUVEL’s</description>
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   <title>CLINUVEL receives final EMA scientific advice for pivotal Phase III vitiligo study</title>
   <link>http://www.streetinsider.com/Press+Releases/CLINUVEL+receives+final+EMA+scientific+advice+for+pivotal+Phase+III+vitiligo+study/26361154.html</link>
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&lt;p align=&quot;left&quot;&gt;&lt;strong&gt;EXECUTIVE SUMMARY&lt;/strong&gt;&lt;/p&gt;  &lt;ul&gt;&lt;li style=&quot;margin-top:3pt; margin-bottom:0in;&quot;&gt;final European scientific advice received for pivotal Phase III vitiligo study&lt;/li&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in;&quot;&gt;EMA emphasised its “totality of evidence” approach&lt;/li&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in;&quot;&gt;central photographic review and validated disease assessment tools agreed&lt;/li&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in;&quot;&gt;CUV107 to compare SCENESSE® with adjunct NB-UVB vs NB-UVB monotherapy&lt;/li&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in;&quot;&gt;CUV107 study (n=300) to commence in 2H 2026&lt;/li&gt;&lt;/ul&gt;  &lt;p&gt;MELBOURNE, Australia, April  24, 2026  (GLOBE NEWSWIRE) -- CLINUVEL PHARMACEUTICALS LTD today announced that the European Medicines Agency (EMA) has provided final scientific advice on the design of the planned pivotal Phase III CUV107 study and anticipated evaluation of evidence of CLINUVEL’s</description>
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   <title>CLINUVEL receives final EMA scientific advice for pivotal Phase III vitiligo study</title>
   <link>http://www.streetinsider.com/Press+Releases/CLINUVEL+receives+final+EMA+scientific+advice+for+pivotal+Phase+III+vitiligo+study/26361154.html</link>
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&lt;p align=&quot;left&quot;&gt;&lt;strong&gt;EXECUTIVE SUMMARY&lt;/strong&gt;&lt;/p&gt;  &lt;ul&gt;&lt;li style=&quot;margin-top:3pt; margin-bottom:0in;&quot;&gt;final European scientific advice received for pivotal Phase III vitiligo study&lt;/li&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in;&quot;&gt;EMA emphasised its “totality of evidence” approach&lt;/li&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in;&quot;&gt;central photographic review and validated disease assessment tools agreed&lt;/li&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in;&quot;&gt;CUV107 to compare SCENESSE® with adjunct NB-UVB vs NB-UVB monotherapy&lt;/li&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in;&quot;&gt;CUV107 study (n=300) to commence in 2H 2026&lt;/li&gt;&lt;/ul&gt;  &lt;p&gt;MELBOURNE, Australia, April  24, 2026  (GLOBE NEWSWIRE) -- CLINUVEL PHARMACEUTICALS LTD today announced that the European Medicines Agency (EMA) has provided final scientific advice on the design of the planned pivotal Phase III CUV107 study and anticipated evaluation of evidence of CLINUVEL’s</description>
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   <title>CLINUVEL receives final EMA scientific advice for pivotal Phase III vitiligo study</title>
   <link>http://www.streetinsider.com/Press+Releases/CLINUVEL+receives+final+EMA+scientific+advice+for+pivotal+Phase+III+vitiligo+study/26361154.html</link>
   <description>
&lt;p align=&quot;left&quot;&gt;&lt;strong&gt;EXECUTIVE SUMMARY&lt;/strong&gt;&lt;/p&gt;  &lt;ul&gt;&lt;li style=&quot;margin-top:3pt; margin-bottom:0in;&quot;&gt;final European scientific advice received for pivotal Phase III vitiligo study&lt;/li&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in;&quot;&gt;EMA emphasised its “totality of evidence” approach&lt;/li&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in;&quot;&gt;central photographic review and validated disease assessment tools agreed&lt;/li&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in;&quot;&gt;CUV107 to compare SCENESSE® with adjunct NB-UVB vs NB-UVB monotherapy&lt;/li&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in;&quot;&gt;CUV107 study (n=300) to commence in 2H 2026&lt;/li&gt;&lt;/ul&gt;  &lt;p&gt;MELBOURNE, Australia, April  24, 2026  (GLOBE NEWSWIRE) -- CLINUVEL PHARMACEUTICALS LTD today announced that the European Medicines Agency (EMA) has provided final scientific advice on the design of the planned pivotal Phase III CUV107 study and anticipated evaluation of evidence of CLINUVEL’s</description>
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   <title>CLINUVEL receives final EMA scientific advice for pivotal Phase III vitiligo study</title>
   <link>http://www.streetinsider.com/Globe+Newswire/CLINUVEL+receives+final+EMA+scientific+advice+for+pivotal+Phase+III+vitiligo+study/26361154.html</link>
   <description>
&lt;p align=&quot;left&quot;&gt;&lt;strong&gt;EXECUTIVE SUMMARY&lt;/strong&gt;&lt;/p&gt;  &lt;ul&gt;&lt;li style=&quot;margin-top:3pt; margin-bottom:0in;&quot;&gt;final European scientific advice received for pivotal Phase III vitiligo study&lt;/li&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in;&quot;&gt;EMA emphasised its “totality of evidence” approach&lt;/li&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in;&quot;&gt;central photographic review and validated disease assessment tools agreed&lt;/li&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in;&quot;&gt;CUV107 to compare SCENESSE® with adjunct NB-UVB vs NB-UVB monotherapy&lt;/li&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in;&quot;&gt;CUV107 study (n=300) to commence in 2H 2026&lt;/li&gt;&lt;/ul&gt;  &lt;p&gt;MELBOURNE, Australia, April  24, 2026  (GLOBE NEWSWIRE) -- CLINUVEL PHARMACEUTICALS LTD today announced that the European Medicines Agency (EMA) has provided final scientific advice on the design of the planned pivotal Phase III CUV107 study and anticipated evaluation of evidence of CLINUVEL’s</description>
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   <title>CLINUVEL receives final EMA scientific advice for pivotal Phase III vitiligo study</title>
   <link>http://www.streetinsider.com/Globe+Newswire/CLINUVEL+receives+final+EMA+scientific+advice+for+pivotal+Phase+III+vitiligo+study/26361154.html</link>
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&lt;p align=&quot;left&quot;&gt;&lt;strong&gt;EXECUTIVE SUMMARY&lt;/strong&gt;&lt;/p&gt;  &lt;ul&gt;&lt;li style=&quot;margin-top:3pt; margin-bottom:0in;&quot;&gt;final European scientific advice received for pivotal Phase III vitiligo study&lt;/li&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in;&quot;&gt;EMA emphasised its “totality of evidence” approach&lt;/li&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in;&quot;&gt;central photographic review and validated disease assessment tools agreed&lt;/li&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in;&quot;&gt;CUV107 to compare SCENESSE® with adjunct NB-UVB vs NB-UVB monotherapy&lt;/li&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in;&quot;&gt;CUV107 study (n=300) to commence in 2H 2026&lt;/li&gt;&lt;/ul&gt;  &lt;p&gt;MELBOURNE, Australia, April  24, 2026  (GLOBE NEWSWIRE) -- CLINUVEL PHARMACEUTICALS LTD today announced that the European Medicines Agency (EMA) has provided final scientific advice on the design of the planned pivotal Phase III CUV107 study and anticipated evaluation of evidence of CLINUVEL’s</description>
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   <title>CLINUVEL receives final EMA scientific advice for pivotal Phase III vitiligo study</title>
   <link>http://www.streetinsider.com/Globe+Newswire/CLINUVEL+receives+final+EMA+scientific+advice+for+pivotal+Phase+III+vitiligo+study/26361154.html</link>
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&lt;p align=&quot;left&quot;&gt;&lt;strong&gt;EXECUTIVE SUMMARY&lt;/strong&gt;&lt;/p&gt;  &lt;ul&gt;&lt;li style=&quot;margin-top:3pt; margin-bottom:0in;&quot;&gt;final European scientific advice received for pivotal Phase III vitiligo study&lt;/li&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in;&quot;&gt;EMA emphasised its “totality of evidence” approach&lt;/li&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in;&quot;&gt;central photographic review and validated disease assessment tools agreed&lt;/li&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in;&quot;&gt;CUV107 to compare SCENESSE® with adjunct NB-UVB vs NB-UVB monotherapy&lt;/li&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in;&quot;&gt;CUV107 study (n=300) to commence in 2H 2026&lt;/li&gt;&lt;/ul&gt;  &lt;p&gt;MELBOURNE, Australia, April  24, 2026  (GLOBE NEWSWIRE) -- CLINUVEL PHARMACEUTICALS LTD today announced that the European Medicines Agency (EMA) has provided final scientific advice on the design of the planned pivotal Phase III CUV107 study and anticipated evaluation of evidence of CLINUVEL’s</description>
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   <title>CLINUVEL receives final EMA scientific advice for pivotal Phase III vitiligo study</title>
   <link>http://www.streetinsider.com/Globe+Newswire/CLINUVEL+receives+final+EMA+scientific+advice+for+pivotal+Phase+III+vitiligo+study/26361154.html</link>
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&lt;p align=&quot;left&quot;&gt;&lt;strong&gt;EXECUTIVE SUMMARY&lt;/strong&gt;&lt;/p&gt;  &lt;ul&gt;&lt;li style=&quot;margin-top:3pt; margin-bottom:0in;&quot;&gt;final European scientific advice received for pivotal Phase III vitiligo study&lt;/li&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in;&quot;&gt;EMA emphasised its “totality of evidence” approach&lt;/li&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in;&quot;&gt;central photographic review and validated disease assessment tools agreed&lt;/li&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in;&quot;&gt;CUV107 to compare SCENESSE® with adjunct NB-UVB vs NB-UVB monotherapy&lt;/li&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in;&quot;&gt;CUV107 study (n=300) to commence in 2H 2026&lt;/li&gt;&lt;/ul&gt;  &lt;p&gt;MELBOURNE, Australia, April  24, 2026  (GLOBE NEWSWIRE) -- CLINUVEL PHARMACEUTICALS LTD today announced that the European Medicines Agency (EMA) has provided final scientific advice on the design of the planned pivotal Phase III CUV107 study and anticipated evaluation of evidence of CLINUVEL’s</description>
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   <pubDate>Fri, 24 Apr 2026 01:47:00 -0400</pubDate>
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   <title>CLINUVEL receives final EMA scientific advice for pivotal Phase III vitiligo study</title>
   <link>http://www.streetinsider.com/Globe+Newswire/CLINUVEL+receives+final+EMA+scientific+advice+for+pivotal+Phase+III+vitiligo+study/26361154.html</link>
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&lt;p align=&quot;left&quot;&gt;&lt;strong&gt;EXECUTIVE SUMMARY&lt;/strong&gt;&lt;/p&gt;  &lt;ul&gt;&lt;li style=&quot;margin-top:3pt; margin-bottom:0in;&quot;&gt;final European scientific advice received for pivotal Phase III vitiligo study&lt;/li&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in;&quot;&gt;EMA emphasised its “totality of evidence” approach&lt;/li&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in;&quot;&gt;central photographic review and validated disease assessment tools agreed&lt;/li&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in;&quot;&gt;CUV107 to compare SCENESSE® with adjunct NB-UVB vs NB-UVB monotherapy&lt;/li&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in;&quot;&gt;CUV107 study (n=300) to commence in 2H 2026&lt;/li&gt;&lt;/ul&gt;  &lt;p&gt;MELBOURNE, Australia, April  24, 2026  (GLOBE NEWSWIRE) -- CLINUVEL PHARMACEUTICALS LTD today announced that the European Medicines Agency (EMA) has provided final scientific advice on the design of the planned pivotal Phase III CUV107 study and anticipated evaluation of evidence of CLINUVEL’s</description>
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   <pubDate>Fri, 24 Apr 2026 01:47:00 -0400</pubDate>
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   <title>CLINUVEL receives final EMA scientific advice for pivotal Phase III vitiligo study</title>
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&lt;p align=&quot;left&quot;&gt;&lt;strong&gt;EXECUTIVE SUMMARY&lt;/strong&gt;&lt;/p&gt;  &lt;ul&gt;&lt;li style=&quot;margin-top:3pt; margin-bottom:0in;&quot;&gt;final European scientific advice received for pivotal Phase III vitiligo study&lt;/li&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in;&quot;&gt;EMA emphasised its “totality of evidence” approach&lt;/li&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in;&quot;&gt;central photographic review and validated disease assessment tools agreed&lt;/li&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in;&quot;&gt;CUV107 to compare SCENESSE® with adjunct NB-UVB vs NB-UVB monotherapy&lt;/li&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in;&quot;&gt;CUV107 study (n=300) to commence in 2H 2026&lt;/li&gt;&lt;/ul&gt;  &lt;p&gt;MELBOURNE, Australia, April  24, 2026  (GLOBE NEWSWIRE) -- CLINUVEL PHARMACEUTICALS LTD today announced that the European Medicines Agency (EMA) has provided final scientific advice on the design of the planned pivotal Phase III CUV107 study and anticipated evaluation of evidence of CLINUVEL’s</description>
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   <title>CLINUVEL receives final EMA scientific advice for pivotal Phase III vitiligo study</title>
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&lt;p align=&quot;left&quot;&gt;&lt;strong&gt;EXECUTIVE SUMMARY&lt;/strong&gt;&lt;/p&gt;  &lt;ul&gt;&lt;li style=&quot;margin-top:3pt; margin-bottom:0in;&quot;&gt;final European scientific advice received for pivotal Phase III vitiligo study&lt;/li&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in;&quot;&gt;EMA emphasised its “totality of evidence” approach&lt;/li&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in;&quot;&gt;central photographic review and validated disease assessment tools agreed&lt;/li&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in;&quot;&gt;CUV107 to compare SCENESSE® with adjunct NB-UVB vs NB-UVB monotherapy&lt;/li&gt;&lt;li style=&quot;margin-top:0in; margin-bottom:0in;&quot;&gt;CUV107 study (n=300) to commence in 2H 2026&lt;/li&gt;&lt;/ul&gt;  &lt;p&gt;MELBOURNE, Australia, April  24, 2026  (GLOBE NEWSWIRE) -- CLINUVEL PHARMACEUTICALS LTD today announced that the European Medicines Agency (EMA) has provided final scientific advice on the design of the planned pivotal Phase III CUV107 study and anticipated evaluation of evidence of CLINUVEL’s</description>
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   <title>CLINUVEL: advancing peptides for photomedicine and vitiligo care at AAD 2026</title>
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&lt;p&gt;MELBOURNE, Australia, April  15, 2026  (GLOBE NEWSWIRE) -- CLINUVEL’s innovative photomedicine and vitiligo programs featured extensively at the recent American Academy of Dermatology (AAD) Annual Meeting, the world’s largest gathering of dermatology professionals. Through the Company’s bespoke Pavilion of Photomedicine and conference sessions across five days, the development and commercialisation of CLINUVEL’s proprietary peptides in dermatology was presented to over 20,000 delegates.&lt;/p&gt;  &lt;p&gt;Building on momentum from the 2025 AAD meeting, AAD 2026 saw CLINUVEL’s ambition translate into deeper engagement with the medical community, with the Pavilion now an established hub for meaningful scientific exchange and candid dialogues.</description>
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   <title>CLINUVEL: advancing peptides for photomedicine and vitiligo care at AAD 2026</title>
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&lt;p&gt;MELBOURNE, Australia, April  15, 2026  (GLOBE NEWSWIRE) -- CLINUVEL’s innovative photomedicine and vitiligo programs featured extensively at the recent American Academy of Dermatology (AAD) Annual Meeting, the world’s largest gathering of dermatology professionals. Through the Company’s bespoke Pavilion of Photomedicine and conference sessions across five days, the development and commercialisation of CLINUVEL’s proprietary peptides in dermatology was presented to over 20,000 delegates.&lt;/p&gt;  &lt;p&gt;Building on momentum from the 2025 AAD meeting, AAD 2026 saw CLINUVEL’s ambition translate into deeper engagement with the medical community, with the Pavilion now an established hub for meaningful scientific exchange and candid dialogues.</description>
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&lt;p&gt;MELBOURNE, Australia, April  15, 2026  (GLOBE NEWSWIRE) -- CLINUVEL’s innovative photomedicine and vitiligo programs featured extensively at the recent American Academy of Dermatology (AAD) Annual Meeting, the world’s largest gathering of dermatology professionals. Through the Company’s bespoke Pavilion of Photomedicine and conference sessions across five days, the development and commercialisation of CLINUVEL’s proprietary peptides in dermatology was presented to over 20,000 delegates.&lt;/p&gt;  &lt;p&gt;Building on momentum from the 2025 AAD meeting, AAD 2026 saw CLINUVEL’s ambition translate into deeper engagement with the medical community, with the Pavilion now an established hub for meaningful scientific exchange and candid dialogues.</description>
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&lt;p&gt;MELBOURNE, Australia, April  15, 2026  (GLOBE NEWSWIRE) -- CLINUVEL’s innovative photomedicine and vitiligo programs featured extensively at the recent American Academy of Dermatology (AAD) Annual Meeting, the world’s largest gathering of dermatology professionals. Through the Company’s bespoke Pavilion of Photomedicine and conference sessions across five days, the development and commercialisation of CLINUVEL’s proprietary peptides in dermatology was presented to over 20,000 delegates.&lt;/p&gt;  &lt;p&gt;Building on momentum from the 2025 AAD meeting, AAD 2026 saw CLINUVEL’s ambition translate into deeper engagement with the medical community, with the Pavilion now an established hub for meaningful scientific exchange and candid dialogues.</description>
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&lt;p&gt;MELBOURNE, Australia, April  15, 2026  (GLOBE NEWSWIRE) -- CLINUVEL’s innovative photomedicine and vitiligo programs featured extensively at the recent American Academy of Dermatology (AAD) Annual Meeting, the world’s largest gathering of dermatology professionals. Through the Company’s bespoke Pavilion of Photomedicine and conference sessions across five days, the development and commercialisation of CLINUVEL’s proprietary peptides in dermatology was presented to over 20,000 delegates.&lt;/p&gt;  &lt;p&gt;Building on momentum from the 2025 AAD meeting, AAD 2026 saw CLINUVEL’s ambition translate into deeper engagement with the medical community, with the Pavilion now an established hub for meaningful scientific exchange and candid dialogues.</description>
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&lt;p&gt;MELBOURNE, Australia, April  15, 2026  (GLOBE NEWSWIRE) -- CLINUVEL’s innovative photomedicine and vitiligo programs featured extensively at the recent American Academy of Dermatology (AAD) Annual Meeting, the world’s largest gathering of dermatology professionals. Through the Company’s bespoke Pavilion of Photomedicine and conference sessions across five days, the development and commercialisation of CLINUVEL’s proprietary peptides in dermatology was presented to over 20,000 delegates.&lt;/p&gt;  &lt;p&gt;Building on momentum from the 2025 AAD meeting, AAD 2026 saw CLINUVEL’s ambition translate into deeper engagement with the medical community, with the Pavilion now an established hub for meaningful scientific exchange and candid dialogues.</description>
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