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   <title>Grifols starts two Phase 3 trials to expand immunoglobulin labels</title>
   <link>http://www.streetinsider.com/FDA/Grifols+starts+two+Phase+3+trials+to+expand+immunoglobulin+labels/26776956.html</link>
   <description>

&lt;p&gt;Grifols (MCE: GRF, MCE: GRF.P, NASDAQ: GRFS) announced that the first patients have been dosed in two separate Phase 3 clinical trials aimed at expanding U.S. label indications for its immunoglobulin therapies, Gamunex-C and Xembify.&lt;/p&gt;

&lt;p&gt;The SIGMA trial will evaluate Gamunex-C, an intravenous immunoglobulin, in combination with standard-of-care treatment to prevent infections in patients with secondary immunodeficiency caused by blood cancers including Chronic Lymphocytic Leukemia, Multiple Myeloma, and Non-Hodgkin Lymphoma. The open-label, single-arm study will enroll 50 participants. The primary efficacy objective is to demonstrate that the rate of serious bacterial infections is less than one per participant per year. Expanding</description>
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   <pubDate>Thu, 16 Jul 2026 08:01:14 -0400</pubDate>
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   <title>Grifols starts two Phase 3 trials to expand immunoglobulin labels</title>
   <link>http://www.streetinsider.com/FDA/Grifols+starts+two+Phase+3+trials+to+expand+immunoglobulin+labels/26776956.html</link>
   <description>

&lt;p&gt;Grifols (MCE: GRF, MCE: GRF.P, NASDAQ: GRFS) announced that the first patients have been dosed in two separate Phase 3 clinical trials aimed at expanding U.S. label indications for its immunoglobulin therapies, Gamunex-C and Xembify.&lt;/p&gt;

&lt;p&gt;The SIGMA trial will evaluate Gamunex-C, an intravenous immunoglobulin, in combination with standard-of-care treatment to prevent infections in patients with secondary immunodeficiency caused by blood cancers including Chronic Lymphocytic Leukemia, Multiple Myeloma, and Non-Hodgkin Lymphoma. The open-label, single-arm study will enroll 50 participants. The primary efficacy objective is to demonstrate that the rate of serious bacterial infections is less than one per participant per year. Expanding</description>
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   <pubDate>Thu, 16 Jul 2026 08:01:14 -0400</pubDate>
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   <title>Grifols starts two Phase 3 trials to expand immunoglobulin labels</title>
   <link>http://www.streetinsider.com/FDA/Grifols+starts+two+Phase+3+trials+to+expand+immunoglobulin+labels/26776956.html</link>
   <description>

&lt;p&gt;Grifols (MCE: GRF, MCE: GRF.P, NASDAQ: GRFS) announced that the first patients have been dosed in two separate Phase 3 clinical trials aimed at expanding U.S. label indications for its immunoglobulin therapies, Gamunex-C and Xembify.&lt;/p&gt;

&lt;p&gt;The SIGMA trial will evaluate Gamunex-C, an intravenous immunoglobulin, in combination with standard-of-care treatment to prevent infections in patients with secondary immunodeficiency caused by blood cancers including Chronic Lymphocytic Leukemia, Multiple Myeloma, and Non-Hodgkin Lymphoma. The open-label, single-arm study will enroll 50 participants. The primary efficacy objective is to demonstrate that the rate of serious bacterial infections is less than one per participant per year. Expanding</description>
   <guid isPermaLink="true">http://www.streetinsider.com/FDA/Grifols+starts+two+Phase+3+trials+to+expand+immunoglobulin+labels/26776956.html</guid>
   <pubDate>Thu, 16 Jul 2026 08:01:14 -0400</pubDate>
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   <title>Grifols starts two Phase 3 trials to expand immunoglobulin labels</title>
   <link>http://www.streetinsider.com/FDA/Grifols+starts+two+Phase+3+trials+to+expand+immunoglobulin+labels/26776956.html</link>
   <description>

&lt;p&gt;Grifols (MCE: GRF, MCE: GRF.P, NASDAQ: GRFS) announced that the first patients have been dosed in two separate Phase 3 clinical trials aimed at expanding U.S. label indications for its immunoglobulin therapies, Gamunex-C and Xembify.&lt;/p&gt;

&lt;p&gt;The SIGMA trial will evaluate Gamunex-C, an intravenous immunoglobulin, in combination with standard-of-care treatment to prevent infections in patients with secondary immunodeficiency caused by blood cancers including Chronic Lymphocytic Leukemia, Multiple Myeloma, and Non-Hodgkin Lymphoma. The open-label, single-arm study will enroll 50 participants. The primary efficacy objective is to demonstrate that the rate of serious bacterial infections is less than one per participant per year. Expanding</description>
   <guid isPermaLink="true">http://www.streetinsider.com/FDA/Grifols+starts+two+Phase+3+trials+to+expand+immunoglobulin+labels/26776956.html</guid>
   <pubDate>Thu, 16 Jul 2026 08:01:14 -0400</pubDate>
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   <title>Grifols starts two Phase 3 trials to expand immunoglobulin labels</title>
   <link>http://www.streetinsider.com/FDA/Grifols+starts+two+Phase+3+trials+to+expand+immunoglobulin+labels/26776956.html</link>
   <description>

&lt;p&gt;Grifols (MCE: GRF, MCE: GRF.P, NASDAQ: GRFS) announced that the first patients have been dosed in two separate Phase 3 clinical trials aimed at expanding U.S. label indications for its immunoglobulin therapies, Gamunex-C and Xembify.&lt;/p&gt;

&lt;p&gt;The SIGMA trial will evaluate Gamunex-C, an intravenous immunoglobulin, in combination with standard-of-care treatment to prevent infections in patients with secondary immunodeficiency caused by blood cancers including Chronic Lymphocytic Leukemia, Multiple Myeloma, and Non-Hodgkin Lymphoma. The open-label, single-arm study will enroll 50 participants. The primary efficacy objective is to demonstrate that the rate of serious bacterial infections is less than one per participant per year. Expanding</description>
   <guid isPermaLink="true">http://www.streetinsider.com/FDA/Grifols+starts+two+Phase+3+trials+to+expand+immunoglobulin+labels/26776956.html</guid>
   <pubDate>Thu, 16 Jul 2026 08:01:14 -0400</pubDate>
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   <title>Grifols starts two Phase 3 trials to expand immunoglobulin labels</title>
   <link>http://www.streetinsider.com/FDA/Grifols+starts+two+Phase+3+trials+to+expand+immunoglobulin+labels/26776956.html</link>
   <description>

&lt;p&gt;Grifols (MCE: GRF, MCE: GRF.P, NASDAQ: GRFS) announced that the first patients have been dosed in two separate Phase 3 clinical trials aimed at expanding U.S. label indications for its immunoglobulin therapies, Gamunex-C and Xembify.&lt;/p&gt;

&lt;p&gt;The SIGMA trial will evaluate Gamunex-C, an intravenous immunoglobulin, in combination with standard-of-care treatment to prevent infections in patients with secondary immunodeficiency caused by blood cancers including Chronic Lymphocytic Leukemia, Multiple Myeloma, and Non-Hodgkin Lymphoma. The open-label, single-arm study will enroll 50 participants. The primary efficacy objective is to demonstrate that the rate of serious bacterial infections is less than one per participant per year. Expanding</description>
   <guid isPermaLink="true">http://www.streetinsider.com/FDA/Grifols+starts+two+Phase+3+trials+to+expand+immunoglobulin+labels/26776956.html</guid>
   <pubDate>Thu, 16 Jul 2026 08:01:14 -0400</pubDate>
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   <title>Grifols Doses First Patients in Two Phase 3 Trials to Expand Indications of its Flagship Immunoglobulins</title>
   <link>http://www.streetinsider.com/Press+Releases/Grifols+Doses+First+Patients+in+Two+Phase+3+Trials+to+Expand+Indications+of+its+Flagship+Immunoglobulins/26776938.html</link>
   <description>
&lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;&lt;strong&gt;&lt;em&gt;One trial, SIGMA, will evaluate Grifols’ intravenous immunoglobulin (Ig) GAMUNEX&lt;/em&gt;&lt;/strong&gt;&lt;strong&gt;&lt;em&gt;®&lt;/em&gt;&lt;/strong&gt;&lt;strong&gt;&lt;em&gt;-C (immune globulin injection [human], 10% caprylate chromatography purified) plus standard medical treatment in patients with secondary immunodeficiency&lt;/em&gt;&lt;/strong&gt;&lt;br/&gt;&lt;br/&gt;&lt;/li&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;&lt;strong&gt;&lt;em&gt;A second trial, XPERT, will determine whether Grifols’ subcutaneous Ig, XEMBIFY&lt;/em&gt;&lt;/strong&gt;&lt;strong&gt;&lt;em&gt;®&lt;/em&gt;&lt;/strong&gt;&lt;strong&gt;&lt;em&gt; (immune globulin subcutaneous human klhw) is non-inferior to GAMUNEX-C in patients with Chronic Inflammatory Demyelinating Polyradiculoneuropathy (CIDP)&lt;/em&gt;&lt;/strong&gt;&lt;br/&gt;&lt;br/&gt;&lt;/li&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;&lt;strong&gt;&lt;em&gt;Both studies are designed to support U.S. label expansion on these fast-growing Grifols Ig franchise therapies and offer patients more treatment options for their immune system disorders&lt;/em&gt;&lt;/strong&gt;&lt;br/&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p align=&quot;justify&quot;&gt;BARCELONA, Spain, July  16, 2026  (GLOBE NEWSWIRE) -- Grifols (MCE:GRF, MCE:GRF.P, NASDAQ:GRFS),</description>
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   <title>Grifols Doses First Patients in Two Phase 3 Trials to Expand Indications of its Flagship Immunoglobulins</title>
   <link>http://www.streetinsider.com/Press+Releases/Grifols+Doses+First+Patients+in+Two+Phase+3+Trials+to+Expand+Indications+of+its+Flagship+Immunoglobulins/26776938.html</link>
   <description>
&lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;&lt;strong&gt;&lt;em&gt;One trial, SIGMA, will evaluate Grifols’ intravenous immunoglobulin (Ig) GAMUNEX&lt;/em&gt;&lt;/strong&gt;&lt;strong&gt;&lt;em&gt;®&lt;/em&gt;&lt;/strong&gt;&lt;strong&gt;&lt;em&gt;-C (immune globulin injection [human], 10% caprylate chromatography purified) plus standard medical treatment in patients with secondary immunodeficiency&lt;/em&gt;&lt;/strong&gt;&lt;br/&gt;&lt;br/&gt;&lt;/li&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;&lt;strong&gt;&lt;em&gt;A second trial, XPERT, will determine whether Grifols’ subcutaneous Ig, XEMBIFY&lt;/em&gt;&lt;/strong&gt;&lt;strong&gt;&lt;em&gt;®&lt;/em&gt;&lt;/strong&gt;&lt;strong&gt;&lt;em&gt; (immune globulin subcutaneous human klhw) is non-inferior to GAMUNEX-C in patients with Chronic Inflammatory Demyelinating Polyradiculoneuropathy (CIDP)&lt;/em&gt;&lt;/strong&gt;&lt;br/&gt;&lt;br/&gt;&lt;/li&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;&lt;strong&gt;&lt;em&gt;Both studies are designed to support U.S. label expansion on these fast-growing Grifols Ig franchise therapies and offer patients more treatment options for their immune system disorders&lt;/em&gt;&lt;/strong&gt;&lt;br/&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p align=&quot;justify&quot;&gt;BARCELONA, Spain, July  16, 2026  (GLOBE NEWSWIRE) -- Grifols (MCE:GRF, MCE:GRF.P, NASDAQ:GRFS),</description>
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   <pubDate>Thu, 16 Jul 2026 08:00:00 -0400</pubDate>
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   <title>Grifols Doses First Patients in Two Phase 3 Trials to Expand Indications of its Flagship Immunoglobulins</title>
   <link>http://www.streetinsider.com/Press+Releases/Grifols+Doses+First+Patients+in+Two+Phase+3+Trials+to+Expand+Indications+of+its+Flagship+Immunoglobulins/26776938.html</link>
   <description>
&lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;&lt;strong&gt;&lt;em&gt;One trial, SIGMA, will evaluate Grifols’ intravenous immunoglobulin (Ig) GAMUNEX&lt;/em&gt;&lt;/strong&gt;&lt;strong&gt;&lt;em&gt;®&lt;/em&gt;&lt;/strong&gt;&lt;strong&gt;&lt;em&gt;-C (immune globulin injection [human], 10% caprylate chromatography purified) plus standard medical treatment in patients with secondary immunodeficiency&lt;/em&gt;&lt;/strong&gt;&lt;br/&gt;&lt;br/&gt;&lt;/li&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;&lt;strong&gt;&lt;em&gt;A second trial, XPERT, will determine whether Grifols’ subcutaneous Ig, XEMBIFY&lt;/em&gt;&lt;/strong&gt;&lt;strong&gt;&lt;em&gt;®&lt;/em&gt;&lt;/strong&gt;&lt;strong&gt;&lt;em&gt; (immune globulin subcutaneous human klhw) is non-inferior to GAMUNEX-C in patients with Chronic Inflammatory Demyelinating Polyradiculoneuropathy (CIDP)&lt;/em&gt;&lt;/strong&gt;&lt;br/&gt;&lt;br/&gt;&lt;/li&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;&lt;strong&gt;&lt;em&gt;Both studies are designed to support U.S. label expansion on these fast-growing Grifols Ig franchise therapies and offer patients more treatment options for their immune system disorders&lt;/em&gt;&lt;/strong&gt;&lt;br/&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p align=&quot;justify&quot;&gt;BARCELONA, Spain, July  16, 2026  (GLOBE NEWSWIRE) -- Grifols (MCE:GRF, MCE:GRF.P, NASDAQ:GRFS),</description>
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   <pubDate>Thu, 16 Jul 2026 08:00:00 -0400</pubDate>
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   <title>Grifols Doses First Patients in Two Phase 3 Trials to Expand Indications of its Flagship Immunoglobulins</title>
   <link>http://www.streetinsider.com/Press+Releases/Grifols+Doses+First+Patients+in+Two+Phase+3+Trials+to+Expand+Indications+of+its+Flagship+Immunoglobulins/26776938.html</link>
   <description>
&lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;&lt;strong&gt;&lt;em&gt;One trial, SIGMA, will evaluate Grifols’ intravenous immunoglobulin (Ig) GAMUNEX&lt;/em&gt;&lt;/strong&gt;&lt;strong&gt;&lt;em&gt;®&lt;/em&gt;&lt;/strong&gt;&lt;strong&gt;&lt;em&gt;-C (immune globulin injection [human], 10% caprylate chromatography purified) plus standard medical treatment in patients with secondary immunodeficiency&lt;/em&gt;&lt;/strong&gt;&lt;br/&gt;&lt;br/&gt;&lt;/li&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;&lt;strong&gt;&lt;em&gt;A second trial, XPERT, will determine whether Grifols’ subcutaneous Ig, XEMBIFY&lt;/em&gt;&lt;/strong&gt;&lt;strong&gt;&lt;em&gt;®&lt;/em&gt;&lt;/strong&gt;&lt;strong&gt;&lt;em&gt; (immune globulin subcutaneous human klhw) is non-inferior to GAMUNEX-C in patients with Chronic Inflammatory Demyelinating Polyradiculoneuropathy (CIDP)&lt;/em&gt;&lt;/strong&gt;&lt;br/&gt;&lt;br/&gt;&lt;/li&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;&lt;strong&gt;&lt;em&gt;Both studies are designed to support U.S. label expansion on these fast-growing Grifols Ig franchise therapies and offer patients more treatment options for their immune system disorders&lt;/em&gt;&lt;/strong&gt;&lt;br/&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p align=&quot;justify&quot;&gt;BARCELONA, Spain, July  16, 2026  (GLOBE NEWSWIRE) -- Grifols (MCE:GRF, MCE:GRF.P, NASDAQ:GRFS),</description>
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   <title>Grifols Doses First Patients in Two Phase 3 Trials to Expand Indications of its Flagship Immunoglobulins</title>
   <link>http://www.streetinsider.com/Press+Releases/Grifols+Doses+First+Patients+in+Two+Phase+3+Trials+to+Expand+Indications+of+its+Flagship+Immunoglobulins/26776938.html</link>
   <description>
&lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;&lt;strong&gt;&lt;em&gt;One trial, SIGMA, will evaluate Grifols’ intravenous immunoglobulin (Ig) GAMUNEX&lt;/em&gt;&lt;/strong&gt;&lt;strong&gt;&lt;em&gt;®&lt;/em&gt;&lt;/strong&gt;&lt;strong&gt;&lt;em&gt;-C (immune globulin injection [human], 10% caprylate chromatography purified) plus standard medical treatment in patients with secondary immunodeficiency&lt;/em&gt;&lt;/strong&gt;&lt;br/&gt;&lt;br/&gt;&lt;/li&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;&lt;strong&gt;&lt;em&gt;A second trial, XPERT, will determine whether Grifols’ subcutaneous Ig, XEMBIFY&lt;/em&gt;&lt;/strong&gt;&lt;strong&gt;&lt;em&gt;®&lt;/em&gt;&lt;/strong&gt;&lt;strong&gt;&lt;em&gt; (immune globulin subcutaneous human klhw) is non-inferior to GAMUNEX-C in patients with Chronic Inflammatory Demyelinating Polyradiculoneuropathy (CIDP)&lt;/em&gt;&lt;/strong&gt;&lt;br/&gt;&lt;br/&gt;&lt;/li&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;&lt;strong&gt;&lt;em&gt;Both studies are designed to support U.S. label expansion on these fast-growing Grifols Ig franchise therapies and offer patients more treatment options for their immune system disorders&lt;/em&gt;&lt;/strong&gt;&lt;br/&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p align=&quot;justify&quot;&gt;BARCELONA, Spain, July  16, 2026  (GLOBE NEWSWIRE) -- Grifols (MCE:GRF, MCE:GRF.P, NASDAQ:GRFS),</description>
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   <pubDate>Thu, 16 Jul 2026 08:00:00 -0400</pubDate>
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   <title>Grifols Doses First Patients in Two Phase 3 Trials to Expand Indications of its Flagship Immunoglobulins</title>
   <link>http://www.streetinsider.com/Press+Releases/Grifols+Doses+First+Patients+in+Two+Phase+3+Trials+to+Expand+Indications+of+its+Flagship+Immunoglobulins/26776938.html</link>
   <description>
&lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;&lt;strong&gt;&lt;em&gt;One trial, SIGMA, will evaluate Grifols’ intravenous immunoglobulin (Ig) GAMUNEX&lt;/em&gt;&lt;/strong&gt;&lt;strong&gt;&lt;em&gt;®&lt;/em&gt;&lt;/strong&gt;&lt;strong&gt;&lt;em&gt;-C (immune globulin injection [human], 10% caprylate chromatography purified) plus standard medical treatment in patients with secondary immunodeficiency&lt;/em&gt;&lt;/strong&gt;&lt;br/&gt;&lt;br/&gt;&lt;/li&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;&lt;strong&gt;&lt;em&gt;A second trial, XPERT, will determine whether Grifols’ subcutaneous Ig, XEMBIFY&lt;/em&gt;&lt;/strong&gt;&lt;strong&gt;&lt;em&gt;®&lt;/em&gt;&lt;/strong&gt;&lt;strong&gt;&lt;em&gt; (immune globulin subcutaneous human klhw) is non-inferior to GAMUNEX-C in patients with Chronic Inflammatory Demyelinating Polyradiculoneuropathy (CIDP)&lt;/em&gt;&lt;/strong&gt;&lt;br/&gt;&lt;br/&gt;&lt;/li&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;&lt;strong&gt;&lt;em&gt;Both studies are designed to support U.S. label expansion on these fast-growing Grifols Ig franchise therapies and offer patients more treatment options for their immune system disorders&lt;/em&gt;&lt;/strong&gt;&lt;br/&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p align=&quot;justify&quot;&gt;BARCELONA, Spain, July  16, 2026  (GLOBE NEWSWIRE) -- Grifols (MCE:GRF, MCE:GRF.P, NASDAQ:GRFS),</description>
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   <title>Grifols Doses First Patients in Two Phase 3 Trials to Expand Indications of its Flagship Immunoglobulins</title>
   <link>http://www.streetinsider.com/Globe+Newswire/Grifols+Doses+First+Patients+in+Two+Phase+3+Trials+to+Expand+Indications+of+its+Flagship+Immunoglobulins/26776938.html</link>
   <description>
&lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;&lt;strong&gt;&lt;em&gt;One trial, SIGMA, will evaluate Grifols’ intravenous immunoglobulin (Ig) GAMUNEX&lt;/em&gt;&lt;/strong&gt;&lt;strong&gt;&lt;em&gt;®&lt;/em&gt;&lt;/strong&gt;&lt;strong&gt;&lt;em&gt;-C (immune globulin injection [human], 10% caprylate chromatography purified) plus standard medical treatment in patients with secondary immunodeficiency&lt;/em&gt;&lt;/strong&gt;&lt;br/&gt;&lt;br/&gt;&lt;/li&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;&lt;strong&gt;&lt;em&gt;A second trial, XPERT, will determine whether Grifols’ subcutaneous Ig, XEMBIFY&lt;/em&gt;&lt;/strong&gt;&lt;strong&gt;&lt;em&gt;®&lt;/em&gt;&lt;/strong&gt;&lt;strong&gt;&lt;em&gt; (immune globulin subcutaneous human klhw) is non-inferior to GAMUNEX-C in patients with Chronic Inflammatory Demyelinating Polyradiculoneuropathy (CIDP)&lt;/em&gt;&lt;/strong&gt;&lt;br/&gt;&lt;br/&gt;&lt;/li&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;&lt;strong&gt;&lt;em&gt;Both studies are designed to support U.S. label expansion on these fast-growing Grifols Ig franchise therapies and offer patients more treatment options for their immune system disorders&lt;/em&gt;&lt;/strong&gt;&lt;br/&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p align=&quot;justify&quot;&gt;BARCELONA, Spain, July  16, 2026  (GLOBE NEWSWIRE) -- Grifols (MCE:GRF, MCE:GRF.P, NASDAQ:GRFS),</description>
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   <title>Grifols Doses First Patients in Two Phase 3 Trials to Expand Indications of its Flagship Immunoglobulins</title>
   <link>http://www.streetinsider.com/Globe+Newswire/Grifols+Doses+First+Patients+in+Two+Phase+3+Trials+to+Expand+Indications+of+its+Flagship+Immunoglobulins/26776938.html</link>
   <description>
&lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;&lt;strong&gt;&lt;em&gt;One trial, SIGMA, will evaluate Grifols’ intravenous immunoglobulin (Ig) GAMUNEX&lt;/em&gt;&lt;/strong&gt;&lt;strong&gt;&lt;em&gt;®&lt;/em&gt;&lt;/strong&gt;&lt;strong&gt;&lt;em&gt;-C (immune globulin injection [human], 10% caprylate chromatography purified) plus standard medical treatment in patients with secondary immunodeficiency&lt;/em&gt;&lt;/strong&gt;&lt;br/&gt;&lt;br/&gt;&lt;/li&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;&lt;strong&gt;&lt;em&gt;A second trial, XPERT, will determine whether Grifols’ subcutaneous Ig, XEMBIFY&lt;/em&gt;&lt;/strong&gt;&lt;strong&gt;&lt;em&gt;®&lt;/em&gt;&lt;/strong&gt;&lt;strong&gt;&lt;em&gt; (immune globulin subcutaneous human klhw) is non-inferior to GAMUNEX-C in patients with Chronic Inflammatory Demyelinating Polyradiculoneuropathy (CIDP)&lt;/em&gt;&lt;/strong&gt;&lt;br/&gt;&lt;br/&gt;&lt;/li&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;&lt;strong&gt;&lt;em&gt;Both studies are designed to support U.S. label expansion on these fast-growing Grifols Ig franchise therapies and offer patients more treatment options for their immune system disorders&lt;/em&gt;&lt;/strong&gt;&lt;br/&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p align=&quot;justify&quot;&gt;BARCELONA, Spain, July  16, 2026  (GLOBE NEWSWIRE) -- Grifols (MCE:GRF, MCE:GRF.P, NASDAQ:GRFS),</description>
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   <title>Grifols Doses First Patients in Two Phase 3 Trials to Expand Indications of its Flagship Immunoglobulins</title>
   <link>http://www.streetinsider.com/Globe+Newswire/Grifols+Doses+First+Patients+in+Two+Phase+3+Trials+to+Expand+Indications+of+its+Flagship+Immunoglobulins/26776938.html</link>
   <description>
&lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;&lt;strong&gt;&lt;em&gt;One trial, SIGMA, will evaluate Grifols’ intravenous immunoglobulin (Ig) GAMUNEX&lt;/em&gt;&lt;/strong&gt;&lt;strong&gt;&lt;em&gt;®&lt;/em&gt;&lt;/strong&gt;&lt;strong&gt;&lt;em&gt;-C (immune globulin injection [human], 10% caprylate chromatography purified) plus standard medical treatment in patients with secondary immunodeficiency&lt;/em&gt;&lt;/strong&gt;&lt;br/&gt;&lt;br/&gt;&lt;/li&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;&lt;strong&gt;&lt;em&gt;A second trial, XPERT, will determine whether Grifols’ subcutaneous Ig, XEMBIFY&lt;/em&gt;&lt;/strong&gt;&lt;strong&gt;&lt;em&gt;®&lt;/em&gt;&lt;/strong&gt;&lt;strong&gt;&lt;em&gt; (immune globulin subcutaneous human klhw) is non-inferior to GAMUNEX-C in patients with Chronic Inflammatory Demyelinating Polyradiculoneuropathy (CIDP)&lt;/em&gt;&lt;/strong&gt;&lt;br/&gt;&lt;br/&gt;&lt;/li&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;&lt;strong&gt;&lt;em&gt;Both studies are designed to support U.S. label expansion on these fast-growing Grifols Ig franchise therapies and offer patients more treatment options for their immune system disorders&lt;/em&gt;&lt;/strong&gt;&lt;br/&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p align=&quot;justify&quot;&gt;BARCELONA, Spain, July  16, 2026  (GLOBE NEWSWIRE) -- Grifols (MCE:GRF, MCE:GRF.P, NASDAQ:GRFS),</description>
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   <title>Grifols Doses First Patients in Two Phase 3 Trials to Expand Indications of its Flagship Immunoglobulins</title>
   <link>http://www.streetinsider.com/Globe+Newswire/Grifols+Doses+First+Patients+in+Two+Phase+3+Trials+to+Expand+Indications+of+its+Flagship+Immunoglobulins/26776938.html</link>
   <description>
&lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;&lt;strong&gt;&lt;em&gt;One trial, SIGMA, will evaluate Grifols’ intravenous immunoglobulin (Ig) GAMUNEX&lt;/em&gt;&lt;/strong&gt;&lt;strong&gt;&lt;em&gt;®&lt;/em&gt;&lt;/strong&gt;&lt;strong&gt;&lt;em&gt;-C (immune globulin injection [human], 10% caprylate chromatography purified) plus standard medical treatment in patients with secondary immunodeficiency&lt;/em&gt;&lt;/strong&gt;&lt;br/&gt;&lt;br/&gt;&lt;/li&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;&lt;strong&gt;&lt;em&gt;A second trial, XPERT, will determine whether Grifols’ subcutaneous Ig, XEMBIFY&lt;/em&gt;&lt;/strong&gt;&lt;strong&gt;&lt;em&gt;®&lt;/em&gt;&lt;/strong&gt;&lt;strong&gt;&lt;em&gt; (immune globulin subcutaneous human klhw) is non-inferior to GAMUNEX-C in patients with Chronic Inflammatory Demyelinating Polyradiculoneuropathy (CIDP)&lt;/em&gt;&lt;/strong&gt;&lt;br/&gt;&lt;br/&gt;&lt;/li&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;&lt;strong&gt;&lt;em&gt;Both studies are designed to support U.S. label expansion on these fast-growing Grifols Ig franchise therapies and offer patients more treatment options for their immune system disorders&lt;/em&gt;&lt;/strong&gt;&lt;br/&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p align=&quot;justify&quot;&gt;BARCELONA, Spain, July  16, 2026  (GLOBE NEWSWIRE) -- Grifols (MCE:GRF, MCE:GRF.P, NASDAQ:GRFS),</description>
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   <title>Grifols Doses First Patients in Two Phase 3 Trials to Expand Indications of its Flagship Immunoglobulins</title>
   <link>http://www.streetinsider.com/Globe+Newswire/Grifols+Doses+First+Patients+in+Two+Phase+3+Trials+to+Expand+Indications+of+its+Flagship+Immunoglobulins/26776938.html</link>
   <description>
&lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;&lt;strong&gt;&lt;em&gt;One trial, SIGMA, will evaluate Grifols’ intravenous immunoglobulin (Ig) GAMUNEX&lt;/em&gt;&lt;/strong&gt;&lt;strong&gt;&lt;em&gt;®&lt;/em&gt;&lt;/strong&gt;&lt;strong&gt;&lt;em&gt;-C (immune globulin injection [human], 10% caprylate chromatography purified) plus standard medical treatment in patients with secondary immunodeficiency&lt;/em&gt;&lt;/strong&gt;&lt;br/&gt;&lt;br/&gt;&lt;/li&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;&lt;strong&gt;&lt;em&gt;A second trial, XPERT, will determine whether Grifols’ subcutaneous Ig, XEMBIFY&lt;/em&gt;&lt;/strong&gt;&lt;strong&gt;&lt;em&gt;®&lt;/em&gt;&lt;/strong&gt;&lt;strong&gt;&lt;em&gt; (immune globulin subcutaneous human klhw) is non-inferior to GAMUNEX-C in patients with Chronic Inflammatory Demyelinating Polyradiculoneuropathy (CIDP)&lt;/em&gt;&lt;/strong&gt;&lt;br/&gt;&lt;br/&gt;&lt;/li&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;&lt;strong&gt;&lt;em&gt;Both studies are designed to support U.S. label expansion on these fast-growing Grifols Ig franchise therapies and offer patients more treatment options for their immune system disorders&lt;/em&gt;&lt;/strong&gt;&lt;br/&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p align=&quot;justify&quot;&gt;BARCELONA, Spain, July  16, 2026  (GLOBE NEWSWIRE) -- Grifols (MCE:GRF, MCE:GRF.P, NASDAQ:GRFS),</description>
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   <title>Grifols Doses First Patients in Two Phase 3 Trials to Expand Indications of its Flagship Immunoglobulins</title>
   <link>http://www.streetinsider.com/Globe+Newswire/Grifols+Doses+First+Patients+in+Two+Phase+3+Trials+to+Expand+Indications+of+its+Flagship+Immunoglobulins/26776938.html</link>
   <description>
&lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;&lt;strong&gt;&lt;em&gt;One trial, SIGMA, will evaluate Grifols’ intravenous immunoglobulin (Ig) GAMUNEX&lt;/em&gt;&lt;/strong&gt;&lt;strong&gt;&lt;em&gt;®&lt;/em&gt;&lt;/strong&gt;&lt;strong&gt;&lt;em&gt;-C (immune globulin injection [human], 10% caprylate chromatography purified) plus standard medical treatment in patients with secondary immunodeficiency&lt;/em&gt;&lt;/strong&gt;&lt;br/&gt;&lt;br/&gt;&lt;/li&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;&lt;strong&gt;&lt;em&gt;A second trial, XPERT, will determine whether Grifols’ subcutaneous Ig, XEMBIFY&lt;/em&gt;&lt;/strong&gt;&lt;strong&gt;&lt;em&gt;®&lt;/em&gt;&lt;/strong&gt;&lt;strong&gt;&lt;em&gt; (immune globulin subcutaneous human klhw) is non-inferior to GAMUNEX-C in patients with Chronic Inflammatory Demyelinating Polyradiculoneuropathy (CIDP)&lt;/em&gt;&lt;/strong&gt;&lt;br/&gt;&lt;br/&gt;&lt;/li&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;&lt;strong&gt;&lt;em&gt;Both studies are designed to support U.S. label expansion on these fast-growing Grifols Ig franchise therapies and offer patients more treatment options for their immune system disorders&lt;/em&gt;&lt;/strong&gt;&lt;br/&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p align=&quot;justify&quot;&gt;BARCELONA, Spain, July  16, 2026  (GLOBE NEWSWIRE) -- Grifols (MCE:GRF, MCE:GRF.P, NASDAQ:GRFS),</description>
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   <title>Form  6-K        Grifols SA                For: Jun 18</title>
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   <pubDate>Thu, 18 Jun 2026 16:00:00 -0400</pubDate>
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   <title>Form  6-K        Grifols SA                For: Jun 18</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++6-K++++++++Grifols+SA++++++++++++++++For%3A+Jun+18/26665768.html</link>
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   <pubDate>Thu, 18 Jun 2026 16:00:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">0RDU</category>
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   <title>Grifols launches FESILTY fibrinogen concentrate in the US</title>
   <link>http://www.streetinsider.com/Corporate+News/Grifols+launches+FESILTY+fibrinogen+concentrate+in+the+US/26644496.html</link>
   <description>&lt;p&gt;Grifols (MCE: GRF, NASDAQ: GRFS) announced the US launch of FESILTY, a fibrinogen concentrate approved by the Food and Drug Administration for treating acute bleeding episodes in pediatric and adult patients with congenital fibrinogen deficiency.&lt;/p&gt;&lt;p&gt;The FDA approved FESILTY in December for patients with congenital fibrinogen deficiency, including hypo- or afibrinogenemia, but not for dysfibrinogenemia. The treatment addresses a rare inherited condition caused by genetic mutations that impair fibrinogen production or function.&lt;/p&gt;&lt;p&gt;FESILTY provides a purified fibrinogen concentrate that enables rapid restoration of fibrinogen levels during bleeding events. The product can be stored at room temperature and reconstituted in approximately three minutes,</description>
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   <pubDate>Mon, 15 Jun 2026 08:02:13 -0400</pubDate>
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