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   <title>Tivic Health Systems (TIVC) enters GMP manufacturing agreement with Scorpius Bio</title>
   <link>http://www.streetinsider.com/Corporate+News/Tivic+Health+Systems+%28TIVC%29+enters+GMP+manufacturing+agreement+with+Scorpius+Bio/24793343.html</link>
   <description>&lt;p&gt;&lt;span data-silink=&quot;1&quot; target=&quot;_blank&quot; rel=&quot;nofollow&quot; href=&quot;https://cts.businesswire.com/ct/CT?id=smartlink&amp;amp;url=https%3A%2F%2Fwww.tivichealth.com%2F&amp;amp;esheet=54254631&amp;amp;newsitemid=20250514637661&amp;amp;lan=en-US&amp;amp;anchor=Tivic+Health%26%23174%3B+Systems%2C+Inc.&amp;amp;index=1&amp;amp;md5=d4aba0585fc1d150035e1c00a7f0e1c0&quot; shape=&quot;rect&quot;&gt;Tivic Health® Systems, Inc.&lt;/span&gt; (Nasdaq: TIVC), a diversified therapeutics company, announced today it has entered a definitive agreement with Scorpius BioManufacturing to complete the GMP manufacturing validation of the lead candidate from its TLR5 program, Entolimod™, for treatment of Acute Radiation Syndrome, or ARS, in preparation for filing a Biological Licensing application, or BLA, with the U.S. Food &amp; Drug Administration.&lt;/p&gt;&lt;p&gt;Scorpius BioManufacturing, Inc. is an integrated contract development and manufacturing organization (CDMO) and subsidiary of Scorpius Holdings Inc. (OTC:SCPX), which will be the primary U.S. manufacturer for Entolimod™. Scorpius plans to utilize its scientific and</description>
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   <pubDate>Wed, 14 May 2025 08:31:36 -0400</pubDate>
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   <title>Tivic Health Systems (TIVC) enters GMP manufacturing agreement with Scorpius Bio</title>
   <link>http://www.streetinsider.com/Corporate+News/Tivic+Health+Systems+%28TIVC%29+enters+GMP+manufacturing+agreement+with+Scorpius+Bio/24793343.html</link>
   <description>&lt;p&gt;&lt;span data-silink=&quot;1&quot; target=&quot;_blank&quot; rel=&quot;nofollow&quot; href=&quot;https://cts.businesswire.com/ct/CT?id=smartlink&amp;amp;url=https%3A%2F%2Fwww.tivichealth.com%2F&amp;amp;esheet=54254631&amp;amp;newsitemid=20250514637661&amp;amp;lan=en-US&amp;amp;anchor=Tivic+Health%26%23174%3B+Systems%2C+Inc.&amp;amp;index=1&amp;amp;md5=d4aba0585fc1d150035e1c00a7f0e1c0&quot; shape=&quot;rect&quot;&gt;Tivic Health® Systems, Inc.&lt;/span&gt; (Nasdaq: TIVC), a diversified therapeutics company, announced today it has entered a definitive agreement with Scorpius BioManufacturing to complete the GMP manufacturing validation of the lead candidate from its TLR5 program, Entolimod™, for treatment of Acute Radiation Syndrome, or ARS, in preparation for filing a Biological Licensing application, or BLA, with the U.S. Food &amp; Drug Administration.&lt;/p&gt;&lt;p&gt;Scorpius BioManufacturing, Inc. is an integrated contract development and manufacturing organization (CDMO) and subsidiary of Scorpius Holdings Inc. (OTC:SCPX), which will be the primary U.S. manufacturer for Entolimod™. Scorpius plans to utilize its scientific and</description>
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   <pubDate>Wed, 14 May 2025 08:31:36 -0400</pubDate>
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   <title>Tivic Health Enters GMP Manufacturing Validation Agreement with Scorpius BioManufacturing in Preparation for FDA Submission</title>
   <link>http://www.streetinsider.com/Press+Releases/Tivic+Health+Enters+GMP+Manufacturing+Validation+Agreement+with+Scorpius+BioManufacturing+in+Preparation+for+FDA+Submission/24793293.html</link>
   <description>
&lt;p&gt;    FREMONT, Calif.--(BUSINESS WIRE)--
&lt;a target=&quot;_blank&quot; rel=&quot;nofollow&quot; href=&quot;https://cts.businesswire.com/ct/CT?id=smartlink&amp;amp;url=https%3A%2F%2Fwww.tivichealth.com%2F&amp;amp;esheet=54254631&amp;amp;newsitemid=20250514637661&amp;amp;lan=en-US&amp;amp;anchor=Tivic+Health%26%23174%3B+Systems%2C+Inc.&amp;amp;index=1&amp;amp;md5=d4aba0585fc1d150035e1c00a7f0e1c0&quot; shape=&quot;rect&quot;&gt;Tivic Health® Systems, Inc.&lt;/a&gt; (Nasdaq: TIVC), a diversified therapeutics company, announced today it has entered a definitive agreement with Scorpius BioManufacturing to complete the GMP manufacturing validation of the lead candidate from its TLR5 program, Entolimod™, for treatment of Acute Radiation Syndrome, or ARS, in preparation for filing a Biological Licensing application, or BLA, with the U.S. Food &amp;amp; Drug Administration.
&lt;/p&gt;&lt;p&gt;
Scorpius BioManufacturing, Inc. is an integrated contract development and manufacturing organization (CDMO) and subsidiary of Scorpius Holdings Inc. (OTC:SCPX), which will be the primary U.S. manufacturer for Entolimod™. Scorpius plans</description>
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   <title>Tivic Health Enters GMP Manufacturing Validation Agreement with Scorpius BioManufacturing in Preparation for FDA Submission</title>
   <link>http://www.streetinsider.com/Press+Releases/Tivic+Health+Enters+GMP+Manufacturing+Validation+Agreement+with+Scorpius+BioManufacturing+in+Preparation+for+FDA+Submission/24793293.html</link>
   <description>
&lt;p&gt;    FREMONT, Calif.--(BUSINESS WIRE)--
&lt;a target=&quot;_blank&quot; rel=&quot;nofollow&quot; href=&quot;https://cts.businesswire.com/ct/CT?id=smartlink&amp;amp;url=https%3A%2F%2Fwww.tivichealth.com%2F&amp;amp;esheet=54254631&amp;amp;newsitemid=20250514637661&amp;amp;lan=en-US&amp;amp;anchor=Tivic+Health%26%23174%3B+Systems%2C+Inc.&amp;amp;index=1&amp;amp;md5=d4aba0585fc1d150035e1c00a7f0e1c0&quot; shape=&quot;rect&quot;&gt;Tivic Health® Systems, Inc.&lt;/a&gt; (Nasdaq: TIVC), a diversified therapeutics company, announced today it has entered a definitive agreement with Scorpius BioManufacturing to complete the GMP manufacturing validation of the lead candidate from its TLR5 program, Entolimod™, for treatment of Acute Radiation Syndrome, or ARS, in preparation for filing a Biological Licensing application, or BLA, with the U.S. Food &amp;amp; Drug Administration.
&lt;/p&gt;&lt;p&gt;
Scorpius BioManufacturing, Inc. is an integrated contract development and manufacturing organization (CDMO) and subsidiary of Scorpius Holdings Inc. (OTC:SCPX), which will be the primary U.S. manufacturer for Entolimod™. Scorpius plans</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Press+Releases/Tivic+Health+Enters+GMP+Manufacturing+Validation+Agreement+with+Scorpius+BioManufacturing+in+Preparation+for+FDA+Submission/24793293.html</guid>
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   <title>Tivic Health Enters GMP Manufacturing Validation Agreement with Scorpius BioManufacturing in Preparation for FDA Submission</title>
   <link>http://www.streetinsider.com/Press+Releases/Tivic+Health+Enters+GMP+Manufacturing+Validation+Agreement+with+Scorpius+BioManufacturing+in+Preparation+for+FDA+Submission/24793293.html</link>
   <description>
&lt;p&gt;    FREMONT, Calif.--(BUSINESS WIRE)--
&lt;a target=&quot;_blank&quot; rel=&quot;nofollow&quot; href=&quot;https://cts.businesswire.com/ct/CT?id=smartlink&amp;amp;url=https%3A%2F%2Fwww.tivichealth.com%2F&amp;amp;esheet=54254631&amp;amp;newsitemid=20250514637661&amp;amp;lan=en-US&amp;amp;anchor=Tivic+Health%26%23174%3B+Systems%2C+Inc.&amp;amp;index=1&amp;amp;md5=d4aba0585fc1d150035e1c00a7f0e1c0&quot; shape=&quot;rect&quot;&gt;Tivic Health® Systems, Inc.&lt;/a&gt; (Nasdaq: TIVC), a diversified therapeutics company, announced today it has entered a definitive agreement with Scorpius BioManufacturing to complete the GMP manufacturing validation of the lead candidate from its TLR5 program, Entolimod™, for treatment of Acute Radiation Syndrome, or ARS, in preparation for filing a Biological Licensing application, or BLA, with the U.S. Food &amp;amp; Drug Administration.
&lt;/p&gt;&lt;p&gt;
Scorpius BioManufacturing, Inc. is an integrated contract development and manufacturing organization (CDMO) and subsidiary of Scorpius Holdings Inc. (OTC:SCPX), which will be the primary U.S. manufacturer for Entolimod™. Scorpius plans</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Press+Releases/Tivic+Health+Enters+GMP+Manufacturing+Validation+Agreement+with+Scorpius+BioManufacturing+in+Preparation+for+FDA+Submission/24793293.html</guid>
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   <title>Tivic Health Enters GMP Manufacturing Validation Agreement with Scorpius BioManufacturing in Preparation for FDA Submission</title>
   <link>http://www.streetinsider.com/Press+Releases/Tivic+Health+Enters+GMP+Manufacturing+Validation+Agreement+with+Scorpius+BioManufacturing+in+Preparation+for+FDA+Submission/24793293.html</link>
   <description>
&lt;p&gt;    FREMONT, Calif.--(BUSINESS WIRE)--
&lt;a target=&quot;_blank&quot; rel=&quot;nofollow&quot; href=&quot;https://cts.businesswire.com/ct/CT?id=smartlink&amp;amp;url=https%3A%2F%2Fwww.tivichealth.com%2F&amp;amp;esheet=54254631&amp;amp;newsitemid=20250514637661&amp;amp;lan=en-US&amp;amp;anchor=Tivic+Health%26%23174%3B+Systems%2C+Inc.&amp;amp;index=1&amp;amp;md5=d4aba0585fc1d150035e1c00a7f0e1c0&quot; shape=&quot;rect&quot;&gt;Tivic Health® Systems, Inc.&lt;/a&gt; (Nasdaq: TIVC), a diversified therapeutics company, announced today it has entered a definitive agreement with Scorpius BioManufacturing to complete the GMP manufacturing validation of the lead candidate from its TLR5 program, Entolimod™, for treatment of Acute Radiation Syndrome, or ARS, in preparation for filing a Biological Licensing application, or BLA, with the U.S. Food &amp;amp; Drug Administration.
&lt;/p&gt;&lt;p&gt;
Scorpius BioManufacturing, Inc. is an integrated contract development and manufacturing organization (CDMO) and subsidiary of Scorpius Holdings Inc. (OTC:SCPX), which will be the primary U.S. manufacturer for Entolimod™. Scorpius plans</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Press+Releases/Tivic+Health+Enters+GMP+Manufacturing+Validation+Agreement+with+Scorpius+BioManufacturing+in+Preparation+for+FDA+Submission/24793293.html</guid>
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   <title>Tivic Health Enters GMP Manufacturing Validation Agreement with Scorpius BioManufacturing in Preparation for FDA Submission</title>
   <link>http://www.streetinsider.com/Press+Releases/Tivic+Health+Enters+GMP+Manufacturing+Validation+Agreement+with+Scorpius+BioManufacturing+in+Preparation+for+FDA+Submission/24793293.html</link>
   <description>
&lt;p&gt;    FREMONT, Calif.--(BUSINESS WIRE)--
&lt;a target=&quot;_blank&quot; rel=&quot;nofollow&quot; href=&quot;https://cts.businesswire.com/ct/CT?id=smartlink&amp;amp;url=https%3A%2F%2Fwww.tivichealth.com%2F&amp;amp;esheet=54254631&amp;amp;newsitemid=20250514637661&amp;amp;lan=en-US&amp;amp;anchor=Tivic+Health%26%23174%3B+Systems%2C+Inc.&amp;amp;index=1&amp;amp;md5=d4aba0585fc1d150035e1c00a7f0e1c0&quot; shape=&quot;rect&quot;&gt;Tivic Health® Systems, Inc.&lt;/a&gt; (Nasdaq: TIVC), a diversified therapeutics company, announced today it has entered a definitive agreement with Scorpius BioManufacturing to complete the GMP manufacturing validation of the lead candidate from its TLR5 program, Entolimod™, for treatment of Acute Radiation Syndrome, or ARS, in preparation for filing a Biological Licensing application, or BLA, with the U.S. Food &amp;amp; Drug Administration.
&lt;/p&gt;&lt;p&gt;
Scorpius BioManufacturing, Inc. is an integrated contract development and manufacturing organization (CDMO) and subsidiary of Scorpius Holdings Inc. (OTC:SCPX), which will be the primary U.S. manufacturer for Entolimod™. Scorpius plans</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Press+Releases/Tivic+Health+Enters+GMP+Manufacturing+Validation+Agreement+with+Scorpius+BioManufacturing+in+Preparation+for+FDA+Submission/24793293.html</guid>
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   <title>Tivic Health Enters GMP Manufacturing Validation Agreement with Scorpius BioManufacturing in Preparation for FDA Submission</title>
   <link>http://www.streetinsider.com/Press+Releases/Tivic+Health+Enters+GMP+Manufacturing+Validation+Agreement+with+Scorpius+BioManufacturing+in+Preparation+for+FDA+Submission/24793293.html</link>
   <description>
&lt;p&gt;    FREMONT, Calif.--(BUSINESS WIRE)--
&lt;a target=&quot;_blank&quot; rel=&quot;nofollow&quot; href=&quot;https://cts.businesswire.com/ct/CT?id=smartlink&amp;amp;url=https%3A%2F%2Fwww.tivichealth.com%2F&amp;amp;esheet=54254631&amp;amp;newsitemid=20250514637661&amp;amp;lan=en-US&amp;amp;anchor=Tivic+Health%26%23174%3B+Systems%2C+Inc.&amp;amp;index=1&amp;amp;md5=d4aba0585fc1d150035e1c00a7f0e1c0&quot; shape=&quot;rect&quot;&gt;Tivic Health® Systems, Inc.&lt;/a&gt; (Nasdaq: TIVC), a diversified therapeutics company, announced today it has entered a definitive agreement with Scorpius BioManufacturing to complete the GMP manufacturing validation of the lead candidate from its TLR5 program, Entolimod™, for treatment of Acute Radiation Syndrome, or ARS, in preparation for filing a Biological Licensing application, or BLA, with the U.S. Food &amp;amp; Drug Administration.
&lt;/p&gt;&lt;p&gt;
Scorpius BioManufacturing, Inc. is an integrated contract development and manufacturing organization (CDMO) and subsidiary of Scorpius Holdings Inc. (OTC:SCPX), which will be the primary U.S. manufacturer for Entolimod™. Scorpius plans</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Press+Releases/Tivic+Health+Enters+GMP+Manufacturing+Validation+Agreement+with+Scorpius+BioManufacturing+in+Preparation+for+FDA+Submission/24793293.html</guid>
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   <title>Tivic Health Enters GMP Manufacturing Validation Agreement with Scorpius BioManufacturing in Preparation for FDA Submission</title>
   <link>http://www.streetinsider.com/Press+Releases/Tivic+Health+Enters+GMP+Manufacturing+Validation+Agreement+with+Scorpius+BioManufacturing+in+Preparation+for+FDA+Submission/24793293.html</link>
   <description>
&lt;p&gt;    FREMONT, Calif.--(BUSINESS WIRE)--
&lt;a target=&quot;_blank&quot; rel=&quot;nofollow&quot; href=&quot;https://cts.businesswire.com/ct/CT?id=smartlink&amp;amp;url=https%3A%2F%2Fwww.tivichealth.com%2F&amp;amp;esheet=54254631&amp;amp;newsitemid=20250514637661&amp;amp;lan=en-US&amp;amp;anchor=Tivic+Health%26%23174%3B+Systems%2C+Inc.&amp;amp;index=1&amp;amp;md5=d4aba0585fc1d150035e1c00a7f0e1c0&quot; shape=&quot;rect&quot;&gt;Tivic Health® Systems, Inc.&lt;/a&gt; (Nasdaq: TIVC), a diversified therapeutics company, announced today it has entered a definitive agreement with Scorpius BioManufacturing to complete the GMP manufacturing validation of the lead candidate from its TLR5 program, Entolimod™, for treatment of Acute Radiation Syndrome, or ARS, in preparation for filing a Biological Licensing application, or BLA, with the U.S. Food &amp;amp; Drug Administration.
&lt;/p&gt;&lt;p&gt;
Scorpius BioManufacturing, Inc. is an integrated contract development and manufacturing organization (CDMO) and subsidiary of Scorpius Holdings Inc. (OTC:SCPX), which will be the primary U.S. manufacturer for Entolimod™. Scorpius plans</description>
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   <title>Tivic Health Enters GMP Manufacturing Validation Agreement with Scorpius BioManufacturing in Preparation for FDA Submission</title>
   <link>http://www.streetinsider.com/Business+Wire/Tivic+Health+Enters+GMP+Manufacturing+Validation+Agreement+with+Scorpius+BioManufacturing+in+Preparation+for+FDA+Submission/24793293.html</link>
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&lt;p&gt;    FREMONT, Calif.--(BUSINESS WIRE)--
&lt;a target=&quot;_blank&quot; rel=&quot;nofollow&quot; href=&quot;https://cts.businesswire.com/ct/CT?id=smartlink&amp;amp;url=https%3A%2F%2Fwww.tivichealth.com%2F&amp;amp;esheet=54254631&amp;amp;newsitemid=20250514637661&amp;amp;lan=en-US&amp;amp;anchor=Tivic+Health%26%23174%3B+Systems%2C+Inc.&amp;amp;index=1&amp;amp;md5=d4aba0585fc1d150035e1c00a7f0e1c0&quot; shape=&quot;rect&quot;&gt;Tivic Health® Systems, Inc.&lt;/a&gt; (Nasdaq: TIVC), a diversified therapeutics company, announced today it has entered a definitive agreement with Scorpius BioManufacturing to complete the GMP manufacturing validation of the lead candidate from its TLR5 program, Entolimod™, for treatment of Acute Radiation Syndrome, or ARS, in preparation for filing a Biological Licensing application, or BLA, with the U.S. Food &amp;amp; Drug Administration.
&lt;/p&gt;&lt;p&gt;
Scorpius BioManufacturing, Inc. is an integrated contract development and manufacturing organization (CDMO) and subsidiary of Scorpius Holdings Inc. (OTC:SCPX), which will be the primary U.S. manufacturer for Entolimod™. Scorpius plans</description>
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   <title>Tivic Health Enters GMP Manufacturing Validation Agreement with Scorpius BioManufacturing in Preparation for FDA Submission</title>
   <link>http://www.streetinsider.com/Business+Wire/Tivic+Health+Enters+GMP+Manufacturing+Validation+Agreement+with+Scorpius+BioManufacturing+in+Preparation+for+FDA+Submission/24793293.html</link>
   <description>
&lt;p&gt;    FREMONT, Calif.--(BUSINESS WIRE)--
&lt;a target=&quot;_blank&quot; rel=&quot;nofollow&quot; href=&quot;https://cts.businesswire.com/ct/CT?id=smartlink&amp;amp;url=https%3A%2F%2Fwww.tivichealth.com%2F&amp;amp;esheet=54254631&amp;amp;newsitemid=20250514637661&amp;amp;lan=en-US&amp;amp;anchor=Tivic+Health%26%23174%3B+Systems%2C+Inc.&amp;amp;index=1&amp;amp;md5=d4aba0585fc1d150035e1c00a7f0e1c0&quot; shape=&quot;rect&quot;&gt;Tivic Health® Systems, Inc.&lt;/a&gt; (Nasdaq: TIVC), a diversified therapeutics company, announced today it has entered a definitive agreement with Scorpius BioManufacturing to complete the GMP manufacturing validation of the lead candidate from its TLR5 program, Entolimod™, for treatment of Acute Radiation Syndrome, or ARS, in preparation for filing a Biological Licensing application, or BLA, with the U.S. Food &amp;amp; Drug Administration.
&lt;/p&gt;&lt;p&gt;
Scorpius BioManufacturing, Inc. is an integrated contract development and manufacturing organization (CDMO) and subsidiary of Scorpius Holdings Inc. (OTC:SCPX), which will be the primary U.S. manufacturer for Entolimod™. Scorpius plans</description>
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   <title>Tivic Health Enters GMP Manufacturing Validation Agreement with Scorpius BioManufacturing in Preparation for FDA Submission</title>
   <link>http://www.streetinsider.com/Business+Wire/Tivic+Health+Enters+GMP+Manufacturing+Validation+Agreement+with+Scorpius+BioManufacturing+in+Preparation+for+FDA+Submission/24793293.html</link>
   <description>
&lt;p&gt;    FREMONT, Calif.--(BUSINESS WIRE)--
&lt;a target=&quot;_blank&quot; rel=&quot;nofollow&quot; href=&quot;https://cts.businesswire.com/ct/CT?id=smartlink&amp;amp;url=https%3A%2F%2Fwww.tivichealth.com%2F&amp;amp;esheet=54254631&amp;amp;newsitemid=20250514637661&amp;amp;lan=en-US&amp;amp;anchor=Tivic+Health%26%23174%3B+Systems%2C+Inc.&amp;amp;index=1&amp;amp;md5=d4aba0585fc1d150035e1c00a7f0e1c0&quot; shape=&quot;rect&quot;&gt;Tivic Health® Systems, Inc.&lt;/a&gt; (Nasdaq: TIVC), a diversified therapeutics company, announced today it has entered a definitive agreement with Scorpius BioManufacturing to complete the GMP manufacturing validation of the lead candidate from its TLR5 program, Entolimod™, for treatment of Acute Radiation Syndrome, or ARS, in preparation for filing a Biological Licensing application, or BLA, with the U.S. Food &amp;amp; Drug Administration.
&lt;/p&gt;&lt;p&gt;
Scorpius BioManufacturing, Inc. is an integrated contract development and manufacturing organization (CDMO) and subsidiary of Scorpius Holdings Inc. (OTC:SCPX), which will be the primary U.S. manufacturer for Entolimod™. Scorpius plans</description>
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   <title>Tivic Health Enters GMP Manufacturing Validation Agreement with Scorpius BioManufacturing in Preparation for FDA Submission</title>
   <link>http://www.streetinsider.com/Business+Wire/Tivic+Health+Enters+GMP+Manufacturing+Validation+Agreement+with+Scorpius+BioManufacturing+in+Preparation+for+FDA+Submission/24793293.html</link>
   <description>
&lt;p&gt;    FREMONT, Calif.--(BUSINESS WIRE)--
&lt;a target=&quot;_blank&quot; rel=&quot;nofollow&quot; href=&quot;https://cts.businesswire.com/ct/CT?id=smartlink&amp;amp;url=https%3A%2F%2Fwww.tivichealth.com%2F&amp;amp;esheet=54254631&amp;amp;newsitemid=20250514637661&amp;amp;lan=en-US&amp;amp;anchor=Tivic+Health%26%23174%3B+Systems%2C+Inc.&amp;amp;index=1&amp;amp;md5=d4aba0585fc1d150035e1c00a7f0e1c0&quot; shape=&quot;rect&quot;&gt;Tivic Health® Systems, Inc.&lt;/a&gt; (Nasdaq: TIVC), a diversified therapeutics company, announced today it has entered a definitive agreement with Scorpius BioManufacturing to complete the GMP manufacturing validation of the lead candidate from its TLR5 program, Entolimod™, for treatment of Acute Radiation Syndrome, or ARS, in preparation for filing a Biological Licensing application, or BLA, with the U.S. Food &amp;amp; Drug Administration.
&lt;/p&gt;&lt;p&gt;
Scorpius BioManufacturing, Inc. is an integrated contract development and manufacturing organization (CDMO) and subsidiary of Scorpius Holdings Inc. (OTC:SCPX), which will be the primary U.S. manufacturer for Entolimod™. Scorpius plans</description>
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   <title>Tivic Health Enters GMP Manufacturing Validation Agreement with Scorpius BioManufacturing in Preparation for FDA Submission</title>
   <link>http://www.streetinsider.com/Business+Wire/Tivic+Health+Enters+GMP+Manufacturing+Validation+Agreement+with+Scorpius+BioManufacturing+in+Preparation+for+FDA+Submission/24793293.html</link>
   <description>
&lt;p&gt;    FREMONT, Calif.--(BUSINESS WIRE)--
&lt;a target=&quot;_blank&quot; rel=&quot;nofollow&quot; href=&quot;https://cts.businesswire.com/ct/CT?id=smartlink&amp;amp;url=https%3A%2F%2Fwww.tivichealth.com%2F&amp;amp;esheet=54254631&amp;amp;newsitemid=20250514637661&amp;amp;lan=en-US&amp;amp;anchor=Tivic+Health%26%23174%3B+Systems%2C+Inc.&amp;amp;index=1&amp;amp;md5=d4aba0585fc1d150035e1c00a7f0e1c0&quot; shape=&quot;rect&quot;&gt;Tivic Health® Systems, Inc.&lt;/a&gt; (Nasdaq: TIVC), a diversified therapeutics company, announced today it has entered a definitive agreement with Scorpius BioManufacturing to complete the GMP manufacturing validation of the lead candidate from its TLR5 program, Entolimod™, for treatment of Acute Radiation Syndrome, or ARS, in preparation for filing a Biological Licensing application, or BLA, with the U.S. Food &amp;amp; Drug Administration.
&lt;/p&gt;&lt;p&gt;
Scorpius BioManufacturing, Inc. is an integrated contract development and manufacturing organization (CDMO) and subsidiary of Scorpius Holdings Inc. (OTC:SCPX), which will be the primary U.S. manufacturer for Entolimod™. Scorpius plans</description>
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   <title>Tivic Health Enters GMP Manufacturing Validation Agreement with Scorpius BioManufacturing in Preparation for FDA Submission</title>
   <link>http://www.streetinsider.com/Business+Wire/Tivic+Health+Enters+GMP+Manufacturing+Validation+Agreement+with+Scorpius+BioManufacturing+in+Preparation+for+FDA+Submission/24793293.html</link>
   <description>
&lt;p&gt;    FREMONT, Calif.--(BUSINESS WIRE)--
&lt;a target=&quot;_blank&quot; rel=&quot;nofollow&quot; href=&quot;https://cts.businesswire.com/ct/CT?id=smartlink&amp;amp;url=https%3A%2F%2Fwww.tivichealth.com%2F&amp;amp;esheet=54254631&amp;amp;newsitemid=20250514637661&amp;amp;lan=en-US&amp;amp;anchor=Tivic+Health%26%23174%3B+Systems%2C+Inc.&amp;amp;index=1&amp;amp;md5=d4aba0585fc1d150035e1c00a7f0e1c0&quot; shape=&quot;rect&quot;&gt;Tivic Health® Systems, Inc.&lt;/a&gt; (Nasdaq: TIVC), a diversified therapeutics company, announced today it has entered a definitive agreement with Scorpius BioManufacturing to complete the GMP manufacturing validation of the lead candidate from its TLR5 program, Entolimod™, for treatment of Acute Radiation Syndrome, or ARS, in preparation for filing a Biological Licensing application, or BLA, with the U.S. Food &amp;amp; Drug Administration.
&lt;/p&gt;&lt;p&gt;
Scorpius BioManufacturing, Inc. is an integrated contract development and manufacturing organization (CDMO) and subsidiary of Scorpius Holdings Inc. (OTC:SCPX), which will be the primary U.S. manufacturer for Entolimod™. Scorpius plans</description>
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   <title>Tivic Health Enters GMP Manufacturing Validation Agreement with Scorpius BioManufacturing in Preparation for FDA Submission</title>
   <link>http://www.streetinsider.com/Business+Wire/Tivic+Health+Enters+GMP+Manufacturing+Validation+Agreement+with+Scorpius+BioManufacturing+in+Preparation+for+FDA+Submission/24793293.html</link>
   <description>
&lt;p&gt;    FREMONT, Calif.--(BUSINESS WIRE)--
&lt;a target=&quot;_blank&quot; rel=&quot;nofollow&quot; href=&quot;https://cts.businesswire.com/ct/CT?id=smartlink&amp;amp;url=https%3A%2F%2Fwww.tivichealth.com%2F&amp;amp;esheet=54254631&amp;amp;newsitemid=20250514637661&amp;amp;lan=en-US&amp;amp;anchor=Tivic+Health%26%23174%3B+Systems%2C+Inc.&amp;amp;index=1&amp;amp;md5=d4aba0585fc1d150035e1c00a7f0e1c0&quot; shape=&quot;rect&quot;&gt;Tivic Health® Systems, Inc.&lt;/a&gt; (Nasdaq: TIVC), a diversified therapeutics company, announced today it has entered a definitive agreement with Scorpius BioManufacturing to complete the GMP manufacturing validation of the lead candidate from its TLR5 program, Entolimod™, for treatment of Acute Radiation Syndrome, or ARS, in preparation for filing a Biological Licensing application, or BLA, with the U.S. Food &amp;amp; Drug Administration.
&lt;/p&gt;&lt;p&gt;
Scorpius BioManufacturing, Inc. is an integrated contract development and manufacturing organization (CDMO) and subsidiary of Scorpius Holdings Inc. (OTC:SCPX), which will be the primary U.S. manufacturer for Entolimod™. Scorpius plans</description>
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   <title>Scorpius Holdings Provides 2024 Year-End Business Update; Implements Strategic Cost Reductions and Operational Streamlining</title>
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&lt;p align=&quot;left&quot;&gt;SAN ANTONIO, April  30, 2025  (GLOBE NEWSWIRE) -- &lt;a target=&quot;_blank&quot; href=&quot;https://www.globenewswire.com/Tracker?data=NLKPQj5YXIvdjAC7cVSc81A8FtfqwP9Y3nEMpEftVwLVCReAwTeG_TgDyuU46otIrHWHf2kFqBp5g7N7h7MKQ5H3FlTSCSZ-iMHZvaEi2cWu58zl69ww3fZmnlEbi4SF&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;&lt;strong&gt;Scorpius Holdings, Inc&lt;/strong&gt;&lt;/a&gt;&lt;strong&gt; (OTC:&lt;/strong&gt; &lt;strong&gt;SCPX) &lt;/strong&gt;(“Scorpius” or “the Company”), an integrated contract development and manufacturing organization (&amp;quot;CDMO”), today provided strategic, financial, and operational updates for the year ended December 31, 2024.&lt;/p&gt;  &lt;p&gt;Jeff Wolf, CEO of Scorpius Holdings, Inc., stated, &amp;quot;The current biotech funding environment has created real headwinds for many of our clients, particularly when it comes to advancing drug development and clinical trials. In response, we took decisive steps to streamline our operations, reduce our cost structure, and refocus on our core CDMO</description>
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   <title>Scorpius Holdings Provides 2024 Year-End Business Update; Implements Strategic Cost Reductions and Operational Streamlining</title>
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&lt;p align=&quot;left&quot;&gt;SAN ANTONIO, April  30, 2025  (GLOBE NEWSWIRE) -- &lt;a target=&quot;_blank&quot; href=&quot;https://www.globenewswire.com/Tracker?data=NLKPQj5YXIvdjAC7cVSc81A8FtfqwP9Y3nEMpEftVwLVCReAwTeG_TgDyuU46otIrHWHf2kFqBp5g7N7h7MKQ5H3FlTSCSZ-iMHZvaEi2cWu58zl69ww3fZmnlEbi4SF&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;&lt;strong&gt;Scorpius Holdings, Inc&lt;/strong&gt;&lt;/a&gt;&lt;strong&gt; (OTC:&lt;/strong&gt; &lt;strong&gt;SCPX) &lt;/strong&gt;(“Scorpius” or “the Company”), an integrated contract development and manufacturing organization (&amp;quot;CDMO”), today provided strategic, financial, and operational updates for the year ended December 31, 2024.&lt;/p&gt;  &lt;p&gt;Jeff Wolf, CEO of Scorpius Holdings, Inc., stated, &amp;quot;The current biotech funding environment has created real headwinds for many of our clients, particularly when it comes to advancing drug development and clinical trials. In response, we took decisive steps to streamline our operations, reduce our cost structure, and refocus on our core CDMO</description>
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   <title>Scorpius Holdings Provides 2024 Year-End Business Update; Implements Strategic Cost Reductions and Operational Streamlining</title>
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&lt;p align=&quot;left&quot;&gt;SAN ANTONIO, April  30, 2025  (GLOBE NEWSWIRE) -- &lt;a target=&quot;_blank&quot; href=&quot;https://www.globenewswire.com/Tracker?data=NLKPQj5YXIvdjAC7cVSc81A8FtfqwP9Y3nEMpEftVwLVCReAwTeG_TgDyuU46otIrHWHf2kFqBp5g7N7h7MKQ5H3FlTSCSZ-iMHZvaEi2cWu58zl69ww3fZmnlEbi4SF&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;&lt;strong&gt;Scorpius Holdings, Inc&lt;/strong&gt;&lt;/a&gt;&lt;strong&gt; (OTC:&lt;/strong&gt; &lt;strong&gt;SCPX) &lt;/strong&gt;(“Scorpius” or “the Company”), an integrated contract development and manufacturing organization (&amp;quot;CDMO”), today provided strategic, financial, and operational updates for the year ended December 31, 2024.&lt;/p&gt;  &lt;p&gt;Jeff Wolf, CEO of Scorpius Holdings, Inc., stated, &amp;quot;The current biotech funding environment has created real headwinds for many of our clients, particularly when it comes to advancing drug development and clinical trials. In response, we took decisive steps to streamline our operations, reduce our cost structure, and refocus on our core CDMO</description>
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   <title>Scorpius Holdings Provides 2024 Year-End Business Update; Implements Strategic Cost Reductions and Operational Streamlining</title>
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&lt;p align=&quot;left&quot;&gt;SAN ANTONIO, April  30, 2025  (GLOBE NEWSWIRE) -- &lt;a target=&quot;_blank&quot; href=&quot;https://www.globenewswire.com/Tracker?data=NLKPQj5YXIvdjAC7cVSc81A8FtfqwP9Y3nEMpEftVwLVCReAwTeG_TgDyuU46otIrHWHf2kFqBp5g7N7h7MKQ5H3FlTSCSZ-iMHZvaEi2cWu58zl69ww3fZmnlEbi4SF&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;&lt;strong&gt;Scorpius Holdings, Inc&lt;/strong&gt;&lt;/a&gt;&lt;strong&gt; (OTC:&lt;/strong&gt; &lt;strong&gt;SCPX) &lt;/strong&gt;(“Scorpius” or “the Company”), an integrated contract development and manufacturing organization (&amp;quot;CDMO”), today provided strategic, financial, and operational updates for the year ended December 31, 2024.&lt;/p&gt;  &lt;p&gt;Jeff Wolf, CEO of Scorpius Holdings, Inc., stated, &amp;quot;The current biotech funding environment has created real headwinds for many of our clients, particularly when it comes to advancing drug development and clinical trials. In response, we took decisive steps to streamline our operations, reduce our cost structure, and refocus on our core CDMO</description>
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&lt;p align=&quot;left&quot;&gt;SAN ANTONIO, April  30, 2025  (GLOBE NEWSWIRE) -- &lt;a target=&quot;_blank&quot; href=&quot;https://www.globenewswire.com/Tracker?data=NLKPQj5YXIvdjAC7cVSc81A8FtfqwP9Y3nEMpEftVwLVCReAwTeG_TgDyuU46otIrHWHf2kFqBp5g7N7h7MKQ5H3FlTSCSZ-iMHZvaEi2cWu58zl69ww3fZmnlEbi4SF&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;&lt;strong&gt;Scorpius Holdings, Inc&lt;/strong&gt;&lt;/a&gt;&lt;strong&gt; (OTC:&lt;/strong&gt; &lt;strong&gt;SCPX) &lt;/strong&gt;(“Scorpius” or “the Company”), an integrated contract development and manufacturing organization (&amp;quot;CDMO”), today provided strategic, financial, and operational updates for the year ended December 31, 2024.&lt;/p&gt;  &lt;p&gt;Jeff Wolf, CEO of Scorpius Holdings, Inc., stated, &amp;quot;The current biotech funding environment has created real headwinds for many of our clients, particularly when it comes to advancing drug development and clinical trials. In response, we took decisive steps to streamline our operations, reduce our cost structure, and refocus on our core CDMO</description>
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   <title>Scorpius Holdings Provides 2024 Year-End Business Update; Implements Strategic Cost Reductions and Operational Streamlining</title>
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   <title>Scorpius Holdings Provides 2024 Year-End Business Update; Implements Strategic Cost Reductions and Operational Streamlining</title>
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   <title>Scorpius Holdings Provides 2024 Year-End Business Update; Implements Strategic Cost Reductions and Operational Streamlining</title>
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   <title>Scorpius Holdings Provides 2024 Year-End Business Update; Implements Strategic Cost Reductions and Operational Streamlining</title>
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