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   <title>Sernova Biotherapeutics Receives FDA Orphan Drug Designation for Autologous Islet Transplantation for Prevention of Diabetes Due to Total Pancreatectomy</title>
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&lt;p align=&quot;justify&quot;&gt;TORONTO and BOSTON, June  17, 2026  (GLOBE NEWSWIRE) -- Sernova Biotherapeutics Inc. (“Sernova” or the “Company”) (TSX: SVA) (OTC: SEOVF) (FSE/XETRA: PSHO), a leading regenerative medicine company focused on developing its Cell Pouch Bio-hybrid Organ as a functional cure for type 1 diabetes, today announced that the U.S. Food and Drug Administration (“FDA”) has granted orphan drug designation for autologous islet transplantation (“AIT”) for the prevention of diabetes due to total pancreatectomy.&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;Sernova’s proprietary Cell Pouch Bio-hybrid Organ is designed to support the engraftment and long-term function of transplanted therapeutic cells. Chronic Pancreatitis causes debilitating</description>
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&lt;p align=&quot;justify&quot;&gt;TORONTO and BOSTON, June  17, 2026  (GLOBE NEWSWIRE) -- Sernova Biotherapeutics Inc. (“Sernova” or the “Company”) (TSX: SVA) (OTC: SEOVF) (FSE/XETRA: PSHO), a leading regenerative medicine company focused on developing its Cell Pouch Bio-hybrid Organ as a functional cure for type 1 diabetes, today announced that the U.S. Food and Drug Administration (“FDA”) has granted orphan drug designation for autologous islet transplantation (“AIT”) for the prevention of diabetes due to total pancreatectomy.&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;Sernova’s proprietary Cell Pouch Bio-hybrid Organ is designed to support the engraftment and long-term function of transplanted therapeutic cells. Chronic Pancreatitis causes debilitating</description>
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   <title>Sernova Biotherapeutics Receives FDA Orphan Drug Designation for Autologous Islet Transplantation for Prevention of Diabetes Due to Total Pancreatectomy</title>
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&lt;p align=&quot;justify&quot;&gt;TORONTO and BOSTON, June  17, 2026  (GLOBE NEWSWIRE) -- Sernova Biotherapeutics Inc. (“Sernova” or the “Company”) (TSX: SVA) (OTC: SEOVF) (FSE/XETRA: PSHO), a leading regenerative medicine company focused on developing its Cell Pouch Bio-hybrid Organ as a functional cure for type 1 diabetes, today announced that the U.S. Food and Drug Administration (“FDA”) has granted orphan drug designation for autologous islet transplantation (“AIT”) for the prevention of diabetes due to total pancreatectomy.&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;Sernova’s proprietary Cell Pouch Bio-hybrid Organ is designed to support the engraftment and long-term function of transplanted therapeutic cells. Chronic Pancreatitis causes debilitating</description>
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&lt;p align=&quot;justify&quot;&gt;TORONTO and BOSTON, June  17, 2026  (GLOBE NEWSWIRE) -- Sernova Biotherapeutics Inc. (“Sernova” or the “Company”) (TSX: SVA) (OTC: SEOVF) (FSE/XETRA: PSHO), a leading regenerative medicine company focused on developing its Cell Pouch Bio-hybrid Organ as a functional cure for type 1 diabetes, today announced that the U.S. Food and Drug Administration (“FDA”) has granted orphan drug designation for autologous islet transplantation (“AIT”) for the prevention of diabetes due to total pancreatectomy.&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;Sernova’s proprietary Cell Pouch Bio-hybrid Organ is designed to support the engraftment and long-term function of transplanted therapeutic cells. Chronic Pancreatitis causes debilitating</description>
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&lt;p align=&quot;justify&quot;&gt;TORONTO and BOSTON, June  17, 2026  (GLOBE NEWSWIRE) -- Sernova Biotherapeutics Inc. (“Sernova” or the “Company”) (TSX: SVA) (OTC: SEOVF) (FSE/XETRA: PSHO), a leading regenerative medicine company focused on developing its Cell Pouch Bio-hybrid Organ as a functional cure for type 1 diabetes, today announced that the U.S. Food and Drug Administration (“FDA”) has granted orphan drug designation for autologous islet transplantation (“AIT”) for the prevention of diabetes due to total pancreatectomy.&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;Sernova’s proprietary Cell Pouch Bio-hybrid Organ is designed to support the engraftment and long-term function of transplanted therapeutic cells. Chronic Pancreatitis causes debilitating</description>
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&lt;p align=&quot;justify&quot;&gt;TORONTO and BOSTON, June  17, 2026  (GLOBE NEWSWIRE) -- Sernova Biotherapeutics Inc. (“Sernova” or the “Company”) (TSX: SVA) (OTC: SEOVF) (FSE/XETRA: PSHO), a leading regenerative medicine company focused on developing its Cell Pouch Bio-hybrid Organ as a functional cure for type 1 diabetes, today announced that the U.S. Food and Drug Administration (“FDA”) has granted orphan drug designation for autologous islet transplantation (“AIT”) for the prevention of diabetes due to total pancreatectomy.&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;Sernova’s proprietary Cell Pouch Bio-hybrid Organ is designed to support the engraftment and long-term function of transplanted therapeutic cells. Chronic Pancreatitis causes debilitating</description>
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&lt;p align=&quot;justify&quot;&gt;TORONTO and BOSTON, June  17, 2026  (GLOBE NEWSWIRE) -- Sernova Biotherapeutics Inc. (“Sernova” or the “Company”) (TSX: SVA) (OTC: SEOVF) (FSE/XETRA: PSHO), a leading regenerative medicine company focused on developing its Cell Pouch Bio-hybrid Organ as a functional cure for type 1 diabetes, today announced that the U.S. Food and Drug Administration (“FDA”) has granted orphan drug designation for autologous islet transplantation (“AIT”) for the prevention of diabetes due to total pancreatectomy.&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;Sernova’s proprietary Cell Pouch Bio-hybrid Organ is designed to support the engraftment and long-term function of transplanted therapeutic cells. Chronic Pancreatitis causes debilitating</description>
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&lt;p align=&quot;justify&quot;&gt;TORONTO and BOSTON, June  17, 2026  (GLOBE NEWSWIRE) -- Sernova Biotherapeutics Inc. (“Sernova” or the “Company”) (TSX: SVA) (OTC: SEOVF) (FSE/XETRA: PSHO), a leading regenerative medicine company focused on developing its Cell Pouch Bio-hybrid Organ as a functional cure for type 1 diabetes, today announced that the U.S. Food and Drug Administration (“FDA”) has granted orphan drug designation for autologous islet transplantation (“AIT”) for the prevention of diabetes due to total pancreatectomy.&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;Sernova’s proprietary Cell Pouch Bio-hybrid Organ is designed to support the engraftment and long-term function of transplanted therapeutic cells. Chronic Pancreatitis causes debilitating</description>
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&lt;p align=&quot;justify&quot;&gt;TORONTO and BOSTON, June  17, 2026  (GLOBE NEWSWIRE) -- Sernova Biotherapeutics Inc. (“Sernova” or the “Company”) (TSX: SVA) (OTC: SEOVF) (FSE/XETRA: PSHO), a leading regenerative medicine company focused on developing its Cell Pouch Bio-hybrid Organ as a functional cure for type 1 diabetes, today announced that the U.S. Food and Drug Administration (“FDA”) has granted orphan drug designation for autologous islet transplantation (“AIT”) for the prevention of diabetes due to total pancreatectomy.&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;Sernova’s proprietary Cell Pouch Bio-hybrid Organ is designed to support the engraftment and long-term function of transplanted therapeutic cells. Chronic Pancreatitis causes debilitating</description>
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   <title>Sernova Biotherapeutics Receives FDA Orphan Drug Designation for Autologous Islet Transplantation for Prevention of Diabetes Due to Total Pancreatectomy</title>
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&lt;p align=&quot;justify&quot;&gt;TORONTO and BOSTON, June  17, 2026  (GLOBE NEWSWIRE) -- Sernova Biotherapeutics Inc. (“Sernova” or the “Company”) (TSX: SVA) (OTC: SEOVF) (FSE/XETRA: PSHO), a leading regenerative medicine company focused on developing its Cell Pouch Bio-hybrid Organ as a functional cure for type 1 diabetes, today announced that the U.S. Food and Drug Administration (“FDA”) has granted orphan drug designation for autologous islet transplantation (“AIT”) for the prevention of diabetes due to total pancreatectomy.&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;Sernova’s proprietary Cell Pouch Bio-hybrid Organ is designed to support the engraftment and long-term function of transplanted therapeutic cells. Chronic Pancreatitis causes debilitating</description>
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   <title>Sernova Biotherapeutics Receives FDA Orphan Drug Designation for Autologous Islet Transplantation for Prevention of Diabetes Due to Total Pancreatectomy</title>
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&lt;p align=&quot;justify&quot;&gt;TORONTO and BOSTON, June  17, 2026  (GLOBE NEWSWIRE) -- Sernova Biotherapeutics Inc. (“Sernova” or the “Company”) (TSX: SVA) (OTC: SEOVF) (FSE/XETRA: PSHO), a leading regenerative medicine company focused on developing its Cell Pouch Bio-hybrid Organ as a functional cure for type 1 diabetes, today announced that the U.S. Food and Drug Administration (“FDA”) has granted orphan drug designation for autologous islet transplantation (“AIT”) for the prevention of diabetes due to total pancreatectomy.&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;Sernova’s proprietary Cell Pouch Bio-hybrid Organ is designed to support the engraftment and long-term function of transplanted therapeutic cells. Chronic Pancreatitis causes debilitating</description>
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   <title>Sernova Biotherapeutics Receives FDA Orphan Drug Designation for Autologous Islet Transplantation for Prevention of Diabetes Due to Total Pancreatectomy</title>
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&lt;p align=&quot;justify&quot;&gt;TORONTO and BOSTON, June  17, 2026  (GLOBE NEWSWIRE) -- Sernova Biotherapeutics Inc. (“Sernova” or the “Company”) (TSX: SVA) (OTC: SEOVF) (FSE/XETRA: PSHO), a leading regenerative medicine company focused on developing its Cell Pouch Bio-hybrid Organ as a functional cure for type 1 diabetes, today announced that the U.S. Food and Drug Administration (“FDA”) has granted orphan drug designation for autologous islet transplantation (“AIT”) for the prevention of diabetes due to total pancreatectomy.&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;Sernova’s proprietary Cell Pouch Bio-hybrid Organ is designed to support the engraftment and long-term function of transplanted therapeutic cells. Chronic Pancreatitis causes debilitating</description>
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   <title>Sernova Biotherapeutics Receives FDA Orphan Drug Designation for Autologous Islet Transplantation for Prevention of Diabetes Due to Total Pancreatectomy</title>
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&lt;p align=&quot;justify&quot;&gt;TORONTO and BOSTON, June  17, 2026  (GLOBE NEWSWIRE) -- Sernova Biotherapeutics Inc. (“Sernova” or the “Company”) (TSX: SVA) (OTC: SEOVF) (FSE/XETRA: PSHO), a leading regenerative medicine company focused on developing its Cell Pouch Bio-hybrid Organ as a functional cure for type 1 diabetes, today announced that the U.S. Food and Drug Administration (“FDA”) has granted orphan drug designation for autologous islet transplantation (“AIT”) for the prevention of diabetes due to total pancreatectomy.&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;Sernova’s proprietary Cell Pouch Bio-hybrid Organ is designed to support the engraftment and long-term function of transplanted therapeutic cells. Chronic Pancreatitis causes debilitating</description>
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   <title>Sernova Biotherapeutics Receives FDA Orphan Drug Designation for Autologous Islet Transplantation for Prevention of Diabetes Due to Total Pancreatectomy</title>
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&lt;p align=&quot;justify&quot;&gt;TORONTO and BOSTON, June  17, 2026  (GLOBE NEWSWIRE) -- Sernova Biotherapeutics Inc. (“Sernova” or the “Company”) (TSX: SVA) (OTC: SEOVF) (FSE/XETRA: PSHO), a leading regenerative medicine company focused on developing its Cell Pouch Bio-hybrid Organ as a functional cure for type 1 diabetes, today announced that the U.S. Food and Drug Administration (“FDA”) has granted orphan drug designation for autologous islet transplantation (“AIT”) for the prevention of diabetes due to total pancreatectomy.&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;Sernova’s proprietary Cell Pouch Bio-hybrid Organ is designed to support the engraftment and long-term function of transplanted therapeutic cells. Chronic Pancreatitis causes debilitating</description>
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   <title>SINOVAC regains Nasdaq compliance after filing annual report</title>
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   <description>&lt;p&gt;Sinovac Biotech Ltd. (NASDAQ: SVA) received notification that it has regained compliance with Nasdaq Global Market listing requirements, the Beijing-based biopharmaceutical company announced.&lt;/p&gt;&lt;p&gt;The company received a letter dated June 10, 2026, from a Nasdaq hearing advisor stating that Sinovac now complies with Listing Rule 5250(c)(1) and meets all listing requirements. The notification followed the company's filing of its annual report on Form 20-F for the year ended December 31, 2025, which was submitted on June 5, 2026.&lt;/p&gt;&lt;p&gt;A scheduled hearing before the Nasdaq Hearings Panel has been canceled as a result of the compliance restoration. However, Sinovac remains under a Mandatory</description>
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   <title>SINOVAC Regained Compliance With the Nasdaq Global Market’s Listing Requirements</title>
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&lt;p&gt;    BEIJING--(BUSINESS WIRE)--
Sinovac Biotech Ltd. (Nasdaq: SVA) (&quot;SINOVAC&quot; or the &quot;Company&quot;), a leading provider of biopharmaceutical products in China, today announced that it received a notification letter dated June 10, 2026 (the &quot;Notification Letter&quot;), from Hearing Advisor of The Nasdaq Stock Market LLC., indicating that the Company has regained compliance with Listing Rule 5250(c)(1) and that the Company is therefore in compliance with the Nasdaq Global Market's listing requirements. As noted in the Hearing Panel's May 20, 2026 compliance determination, the Company remains under a Mandatory Panel Monitor pursuant to Listing Rule 5815(d)(4)(B) until May 20, 2027.

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   <title>SINOVAC Regained Compliance With the Nasdaq Global Market’s Listing Requirements</title>
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&lt;p&gt;    BEIJING--(BUSINESS WIRE)--
Sinovac Biotech Ltd. (Nasdaq: SVA) (&quot;SINOVAC&quot; or the &quot;Company&quot;), a leading provider of biopharmaceutical products in China, today announced that it received a notification letter dated June 10, 2026 (the &quot;Notification Letter&quot;), from Hearing Advisor of The Nasdaq Stock Market LLC., indicating that the Company has regained compliance with Listing Rule 5250(c)(1) and that the Company is therefore in compliance with the Nasdaq Global Market's listing requirements. As noted in the Hearing Panel's May 20, 2026 compliance determination, the Company remains under a Mandatory Panel Monitor pursuant to Listing Rule 5815(d)(4)(B) until May 20, 2027.

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   <title>SINOVAC Regained Compliance With the Nasdaq Global Market’s Listing Requirements</title>
   <link>http://www.streetinsider.com/Press+Releases/SINOVAC+Regained+Compliance+With+the+Nasdaq+Global+Market%E2%80%99s+Listing+Requirements/26643464.html</link>
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&lt;p&gt;    BEIJING--(BUSINESS WIRE)--
Sinovac Biotech Ltd. (Nasdaq: SVA) (&quot;SINOVAC&quot; or the &quot;Company&quot;), a leading provider of biopharmaceutical products in China, today announced that it received a notification letter dated June 10, 2026 (the &quot;Notification Letter&quot;), from Hearing Advisor of The Nasdaq Stock Market LLC., indicating that the Company has regained compliance with Listing Rule 5250(c)(1) and that the Company is therefore in compliance with the Nasdaq Global Market's listing requirements. As noted in the Hearing Panel's May 20, 2026 compliance determination, the Company remains under a Mandatory Panel Monitor pursuant to Listing Rule 5815(d)(4)(B) until May 20, 2027.

&lt;/p&gt;&lt;p&gt;
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   <pubDate>Mon, 15 Jun 2026 06:00:00 -0400</pubDate>
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  <item>
   <title>SINOVAC Regained Compliance With the Nasdaq Global Market’s Listing Requirements</title>
   <link>http://www.streetinsider.com/Press+Releases/SINOVAC+Regained+Compliance+With+the+Nasdaq+Global+Market%E2%80%99s+Listing+Requirements/26643464.html</link>
   <description>
&lt;p&gt;    BEIJING--(BUSINESS WIRE)--
Sinovac Biotech Ltd. (Nasdaq: SVA) (&quot;SINOVAC&quot; or the &quot;Company&quot;), a leading provider of biopharmaceutical products in China, today announced that it received a notification letter dated June 10, 2026 (the &quot;Notification Letter&quot;), from Hearing Advisor of The Nasdaq Stock Market LLC., indicating that the Company has regained compliance with Listing Rule 5250(c)(1) and that the Company is therefore in compliance with the Nasdaq Global Market's listing requirements. As noted in the Hearing Panel's May 20, 2026 compliance determination, the Company remains under a Mandatory Panel Monitor pursuant to Listing Rule 5815(d)(4)(B) until May 20, 2027.

&lt;/p&gt;&lt;p&gt;
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   <pubDate>Mon, 15 Jun 2026 06:00:00 -0400</pubDate>
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