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   <title>Form  SCHEDULE 13G/A  Abivax S.A.                            Filed by: TCG Crossover GP I, LLC</title>
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   <title>Form  SCHEDULE 13G/A  Abivax S.A.                            Filed by: TCG Crossover GP I, LLC</title>
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   <title>Form  SCHEDULE 13G/A  Abivax S.A.                            Filed by: TCG Crossover GP I, LLC</title>
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   <title>Form  SCHEDULE 13G/A  Abivax S.A.                            Filed by: Invus Global Management, LLC</title>
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   <pubDate>Thu, 13 Aug 2026 10:55:00 -0400</pubDate>
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   <title>Form  SCHEDULE 13G/A  Abivax S.A.                            Filed by: Invus Global Management, LLC</title>
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   <title>Form  SCHEDULE 13G/A  Abivax S.A.                            Filed by: Invus Global Management, LLC</title>
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   <pubDate>Thu, 13 Aug 2026 10:55:00 -0400</pubDate>
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   <title>Abivax completes pre-NDA meeting with FDA for ulcerative colitis drug</title>
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   <description>&lt;p&gt;Abivax SA (Nasdaq: ABVX) announced it has completed a pre-New Drug Application (NDA) meeting with the U.S. Food and Drug Administration (FDA) for obefazimod, its drug candidate for the treatment of adults with moderately to severely active ulcerative colitis.&lt;/p&gt;&lt;p&gt;According to a statement from the company, the FDA provided feedback that resulted in alignment on the planned NDA submission strategy, including the content and format of the submission. Abivax said it remains on track to file its first NDA for obefazimod by the end of 2026.&lt;/p&gt;&lt;p&gt;Marc de Garidel, Chief Executive Officer of Abivax, said: &quot;Achieving alignment with the FDA on our</description>
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   <pubDate>Thu, 30 Jul 2026 16:07:24 -0400</pubDate>
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   <title>Abivax completes pre-NDA meeting with FDA for ulcerative colitis drug</title>
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   <description>&lt;p&gt;Abivax SA (Nasdaq: ABVX) announced it has completed a pre-New Drug Application (NDA) meeting with the U.S. Food and Drug Administration (FDA) for obefazimod, its drug candidate for the treatment of adults with moderately to severely active ulcerative colitis.&lt;/p&gt;&lt;p&gt;According to a statement from the company, the FDA provided feedback that resulted in alignment on the planned NDA submission strategy, including the content and format of the submission. Abivax said it remains on track to file its first NDA for obefazimod by the end of 2026.&lt;/p&gt;&lt;p&gt;Marc de Garidel, Chief Executive Officer of Abivax, said: &quot;Achieving alignment with the FDA on our</description>
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   <pubDate>Thu, 30 Jul 2026 16:07:24 -0400</pubDate>
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   <title>Abivax Announces Positive Pre-NDA Interaction with the FDA for Obefazimod</title>
   <link>http://www.streetinsider.com/Press+Releases/Abivax+Announces+Positive+Pre-NDA+Interaction+with+the+FDA+for+Obefazimod/26843503.html</link>
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&lt;p align=&quot;center&quot;&gt;&lt;b&gt;Abivax Announces Positive Pre-NDA &lt;/b&gt;&lt;b&gt;Interaction with the FDA for Obefazimod&lt;/b&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;i&gt;Company remains on track to submit its first New Drug Application for obefazimod for the treatment of moderately to severely active ulcerative colitis by the end of 2026&lt;/i&gt;&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;&lt;b&gt;PARIS, France – July 30, 2026 – 10:05 p.m. CEST&lt;/b&gt; – &lt;a target=&quot;_blank&quot; href=&quot;https://www.globenewswire.com/Tracker?data=KmygmJaiY5aeeB8E5kVOeVsUE7wqTY4WDszWoHGU74MDaN7qQuNfThU18KXh4BFHhdiK7ri-Xr96VmULH1Xx8A==&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;Abivax SA&lt;/a&gt; (Euronext Paris: FR0012333284 – ABVX / Nasdaq: ABVX) (“Abivax” or the “Company”), a clinical-stage biotechnology company focused on developing therapeutics that harness the body’s natural regulatory mechanisms to stabilize the immune response in patients with chronic inflammatory diseases, today announced</description>
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   <title>Abivax Announces Positive Pre-NDA Interaction with the FDA for Obefazimod</title>
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&lt;p align=&quot;center&quot;&gt;&lt;b&gt;Abivax Announces Positive Pre-NDA &lt;/b&gt;&lt;b&gt;Interaction with the FDA for Obefazimod&lt;/b&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;i&gt;Company remains on track to submit its first New Drug Application for obefazimod for the treatment of moderately to severely active ulcerative colitis by the end of 2026&lt;/i&gt;&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;&lt;b&gt;PARIS, France – July 30, 2026 – 10:05 p.m. CEST&lt;/b&gt; – &lt;a target=&quot;_blank&quot; href=&quot;https://www.globenewswire.com/Tracker?data=KmygmJaiY5aeeB8E5kVOeVsUE7wqTY4WDszWoHGU74MDaN7qQuNfThU18KXh4BFHhdiK7ri-Xr96VmULH1Xx8A==&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;Abivax SA&lt;/a&gt; (Euronext Paris: FR0012333284 – ABVX / Nasdaq: ABVX) (“Abivax” or the “Company”), a clinical-stage biotechnology company focused on developing therapeutics that harness the body’s natural regulatory mechanisms to stabilize the immune response in patients with chronic inflammatory diseases, today announced</description>
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   <title>Abivax Announces Positive Pre-NDA Interaction with the FDA for Obefazimod</title>
   <link>http://www.streetinsider.com/Press+Releases/Abivax+Announces+Positive+Pre-NDA+Interaction+with+the+FDA+for+Obefazimod/26843503.html</link>
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&lt;p align=&quot;center&quot;&gt;&lt;b&gt;Abivax Announces Positive Pre-NDA &lt;/b&gt;&lt;b&gt;Interaction with the FDA for Obefazimod&lt;/b&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;i&gt;Company remains on track to submit its first New Drug Application for obefazimod for the treatment of moderately to severely active ulcerative colitis by the end of 2026&lt;/i&gt;&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;&lt;b&gt;PARIS, France – July 30, 2026 – 10:05 p.m. CEST&lt;/b&gt; – &lt;a target=&quot;_blank&quot; href=&quot;https://www.globenewswire.com/Tracker?data=KmygmJaiY5aeeB8E5kVOeVsUE7wqTY4WDszWoHGU74MDaN7qQuNfThU18KXh4BFHhdiK7ri-Xr96VmULH1Xx8A==&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;Abivax SA&lt;/a&gt; (Euronext Paris: FR0012333284 – ABVX / Nasdaq: ABVX) (“Abivax” or the “Company”), a clinical-stage biotechnology company focused on developing therapeutics that harness the body’s natural regulatory mechanisms to stabilize the immune response in patients with chronic inflammatory diseases, today announced</description>
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   <title>Abivax Announces Positive Pre-NDA Interaction with the FDA for Obefazimod</title>
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&lt;p align=&quot;center&quot;&gt;&lt;b&gt;Abivax Announces Positive Pre-NDA &lt;/b&gt;&lt;b&gt;Interaction with the FDA for Obefazimod&lt;/b&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;i&gt;Company remains on track to submit its first New Drug Application for obefazimod for the treatment of moderately to severely active ulcerative colitis by the end of 2026&lt;/i&gt;&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;&lt;b&gt;PARIS, France – July 30, 2026 – 10:05 p.m. CEST&lt;/b&gt; – &lt;a target=&quot;_blank&quot; href=&quot;https://www.globenewswire.com/Tracker?data=KmygmJaiY5aeeB8E5kVOeVsUE7wqTY4WDszWoHGU74MDaN7qQuNfThU18KXh4BFHhdiK7ri-Xr96VmULH1Xx8A==&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;Abivax SA&lt;/a&gt; (Euronext Paris: FR0012333284 – ABVX / Nasdaq: ABVX) (“Abivax” or the “Company”), a clinical-stage biotechnology company focused on developing therapeutics that harness the body’s natural regulatory mechanisms to stabilize the immune response in patients with chronic inflammatory diseases, today announced</description>
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   <title>Abivax Announces Positive Pre-NDA Interaction with the FDA for Obefazimod</title>
   <link>http://www.streetinsider.com/Press+Releases/Abivax+Announces+Positive+Pre-NDA+Interaction+with+the+FDA+for+Obefazimod/26843503.html</link>
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&lt;p align=&quot;center&quot;&gt;&lt;b&gt;Abivax Announces Positive Pre-NDA &lt;/b&gt;&lt;b&gt;Interaction with the FDA for Obefazimod&lt;/b&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;i&gt;Company remains on track to submit its first New Drug Application for obefazimod for the treatment of moderately to severely active ulcerative colitis by the end of 2026&lt;/i&gt;&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;&lt;b&gt;PARIS, France – July 30, 2026 – 10:05 p.m. CEST&lt;/b&gt; – &lt;a target=&quot;_blank&quot; href=&quot;https://www.globenewswire.com/Tracker?data=KmygmJaiY5aeeB8E5kVOeVsUE7wqTY4WDszWoHGU74MDaN7qQuNfThU18KXh4BFHhdiK7ri-Xr96VmULH1Xx8A==&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;Abivax SA&lt;/a&gt; (Euronext Paris: FR0012333284 – ABVX / Nasdaq: ABVX) (“Abivax” or the “Company”), a clinical-stage biotechnology company focused on developing therapeutics that harness the body’s natural regulatory mechanisms to stabilize the immune response in patients with chronic inflammatory diseases, today announced</description>
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   <title>Abivax Announces Positive Pre-NDA Interaction with the FDA for Obefazimod</title>
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&lt;p align=&quot;center&quot;&gt;&lt;b&gt;Abivax Announces Positive Pre-NDA &lt;/b&gt;&lt;b&gt;Interaction with the FDA for Obefazimod&lt;/b&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;i&gt;Company remains on track to submit its first New Drug Application for obefazimod for the treatment of moderately to severely active ulcerative colitis by the end of 2026&lt;/i&gt;&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;&lt;b&gt;PARIS, France – July 30, 2026 – 10:05 p.m. CEST&lt;/b&gt; – &lt;a target=&quot;_blank&quot; href=&quot;https://www.globenewswire.com/Tracker?data=KmygmJaiY5aeeB8E5kVOeVsUE7wqTY4WDszWoHGU74MDaN7qQuNfThU18KXh4BFHhdiK7ri-Xr96VmULH1Xx8A==&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;Abivax SA&lt;/a&gt; (Euronext Paris: FR0012333284 – ABVX / Nasdaq: ABVX) (“Abivax” or the “Company”), a clinical-stage biotechnology company focused on developing therapeutics that harness the body’s natural regulatory mechanisms to stabilize the immune response in patients with chronic inflammatory diseases, today announced</description>
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   <title>Abivax Announces Positive Pre-NDA Interaction with the FDA for Obefazimod</title>
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&lt;p align=&quot;center&quot;&gt;&lt;b&gt;Abivax Announces Positive Pre-NDA &lt;/b&gt;&lt;b&gt;Interaction with the FDA for Obefazimod&lt;/b&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;i&gt;Company remains on track to submit its first New Drug Application for obefazimod for the treatment of moderately to severely active ulcerative colitis by the end of 2026&lt;/i&gt;&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;&lt;b&gt;PARIS, France – July 30, 2026 – 10:05 p.m. CEST&lt;/b&gt; – &lt;a target=&quot;_blank&quot; href=&quot;https://www.globenewswire.com/Tracker?data=KmygmJaiY5aeeB8E5kVOeVsUE7wqTY4WDszWoHGU74MDaN7qQuNfThU18KXh4BFHhdiK7ri-Xr96VmULH1Xx8A==&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;Abivax SA&lt;/a&gt; (Euronext Paris: FR0012333284 – ABVX / Nasdaq: ABVX) (“Abivax” or the “Company”), a clinical-stage biotechnology company focused on developing therapeutics that harness the body’s natural regulatory mechanisms to stabilize the immune response in patients with chronic inflammatory diseases, today announced</description>
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   <title>Abivax Announces Positive Pre-NDA Interaction with the FDA for Obefazimod</title>
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&lt;p align=&quot;center&quot;&gt;&lt;b&gt;Abivax Announces Positive Pre-NDA &lt;/b&gt;&lt;b&gt;Interaction with the FDA for Obefazimod&lt;/b&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;i&gt;Company remains on track to submit its first New Drug Application for obefazimod for the treatment of moderately to severely active ulcerative colitis by the end of 2026&lt;/i&gt;&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;&lt;b&gt;PARIS, France – July 30, 2026 – 10:05 p.m. CEST&lt;/b&gt; – &lt;a target=&quot;_blank&quot; href=&quot;https://www.globenewswire.com/Tracker?data=KmygmJaiY5aeeB8E5kVOeVsUE7wqTY4WDszWoHGU74MDaN7qQuNfThU18KXh4BFHhdiK7ri-Xr96VmULH1Xx8A==&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;Abivax SA&lt;/a&gt; (Euronext Paris: FR0012333284 – ABVX / Nasdaq: ABVX) (“Abivax” or the “Company”), a clinical-stage biotechnology company focused on developing therapeutics that harness the body’s natural regulatory mechanisms to stabilize the immune response in patients with chronic inflammatory diseases, today announced</description>
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   <title>Abivax Announces Positive Pre-NDA Interaction with the FDA for Obefazimod</title>
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&lt;p align=&quot;center&quot;&gt;&lt;b&gt;Abivax Announces Positive Pre-NDA &lt;/b&gt;&lt;b&gt;Interaction with the FDA for Obefazimod&lt;/b&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;i&gt;Company remains on track to submit its first New Drug Application for obefazimod for the treatment of moderately to severely active ulcerative colitis by the end of 2026&lt;/i&gt;&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;&lt;b&gt;PARIS, France – July 30, 2026 – 10:05 p.m. CEST&lt;/b&gt; – &lt;a target=&quot;_blank&quot; href=&quot;https://www.globenewswire.com/Tracker?data=KmygmJaiY5aeeB8E5kVOeVsUE7wqTY4WDszWoHGU74MDaN7qQuNfThU18KXh4BFHhdiK7ri-Xr96VmULH1Xx8A==&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;Abivax SA&lt;/a&gt; (Euronext Paris: FR0012333284 – ABVX / Nasdaq: ABVX) (“Abivax” or the “Company”), a clinical-stage biotechnology company focused on developing therapeutics that harness the body’s natural regulatory mechanisms to stabilize the immune response in patients with chronic inflammatory diseases, today announced</description>
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   <title>Abivax Announces Positive Pre-NDA Interaction with the FDA for Obefazimod</title>
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&lt;p align=&quot;center&quot;&gt;&lt;b&gt;Abivax Announces Positive Pre-NDA &lt;/b&gt;&lt;b&gt;Interaction with the FDA for Obefazimod&lt;/b&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;i&gt;Company remains on track to submit its first New Drug Application for obefazimod for the treatment of moderately to severely active ulcerative colitis by the end of 2026&lt;/i&gt;&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;&lt;b&gt;PARIS, France – July 30, 2026 – 10:05 p.m. CEST&lt;/b&gt; – &lt;a target=&quot;_blank&quot; href=&quot;https://www.globenewswire.com/Tracker?data=KmygmJaiY5aeeB8E5kVOeVsUE7wqTY4WDszWoHGU74MDaN7qQuNfThU18KXh4BFHhdiK7ri-Xr96VmULH1Xx8A==&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;Abivax SA&lt;/a&gt; (Euronext Paris: FR0012333284 – ABVX / Nasdaq: ABVX) (“Abivax” or the “Company”), a clinical-stage biotechnology company focused on developing therapeutics that harness the body’s natural regulatory mechanisms to stabilize the immune response in patients with chronic inflammatory diseases, today announced</description>
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   <title>Abivax Announces Positive Pre-NDA Interaction with the FDA for Obefazimod</title>
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&lt;p align=&quot;center&quot;&gt;&lt;b&gt;Abivax Announces Positive Pre-NDA &lt;/b&gt;&lt;b&gt;Interaction with the FDA for Obefazimod&lt;/b&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;i&gt;Company remains on track to submit its first New Drug Application for obefazimod for the treatment of moderately to severely active ulcerative colitis by the end of 2026&lt;/i&gt;&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;&lt;b&gt;PARIS, France – July 30, 2026 – 10:05 p.m. CEST&lt;/b&gt; – &lt;a target=&quot;_blank&quot; href=&quot;https://www.globenewswire.com/Tracker?data=KmygmJaiY5aeeB8E5kVOeVsUE7wqTY4WDszWoHGU74MDaN7qQuNfThU18KXh4BFHhdiK7ri-Xr96VmULH1Xx8A==&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;Abivax SA&lt;/a&gt; (Euronext Paris: FR0012333284 – ABVX / Nasdaq: ABVX) (“Abivax” or the “Company”), a clinical-stage biotechnology company focused on developing therapeutics that harness the body’s natural regulatory mechanisms to stabilize the immune response in patients with chronic inflammatory diseases, today announced</description>
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   <title>Abivax Announces Positive Pre-NDA Interaction with the FDA for Obefazimod</title>
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&lt;p align=&quot;center&quot;&gt;&lt;b&gt;Abivax Announces Positive Pre-NDA &lt;/b&gt;&lt;b&gt;Interaction with the FDA for Obefazimod&lt;/b&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;i&gt;Company remains on track to submit its first New Drug Application for obefazimod for the treatment of moderately to severely active ulcerative colitis by the end of 2026&lt;/i&gt;&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;&lt;b&gt;PARIS, France – July 30, 2026 – 10:05 p.m. CEST&lt;/b&gt; – &lt;a target=&quot;_blank&quot; href=&quot;https://www.globenewswire.com/Tracker?data=KmygmJaiY5aeeB8E5kVOeVsUE7wqTY4WDszWoHGU74MDaN7qQuNfThU18KXh4BFHhdiK7ri-Xr96VmULH1Xx8A==&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;Abivax SA&lt;/a&gt; (Euronext Paris: FR0012333284 – ABVX / Nasdaq: ABVX) (“Abivax” or the “Company”), a clinical-stage biotechnology company focused on developing therapeutics that harness the body’s natural regulatory mechanisms to stabilize the immune response in patients with chronic inflammatory diseases, today announced</description>
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   <title>Abivax Announces Positive Pre-NDA Interaction with the FDA for Obefazimod</title>
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&lt;p align=&quot;center&quot;&gt;&lt;b&gt;Abivax Announces Positive Pre-NDA &lt;/b&gt;&lt;b&gt;Interaction with the FDA for Obefazimod&lt;/b&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;i&gt;Company remains on track to submit its first New Drug Application for obefazimod for the treatment of moderately to severely active ulcerative colitis by the end of 2026&lt;/i&gt;&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;&lt;b&gt;PARIS, France – July 30, 2026 – 10:05 p.m. CEST&lt;/b&gt; – &lt;a target=&quot;_blank&quot; href=&quot;https://www.globenewswire.com/Tracker?data=KmygmJaiY5aeeB8E5kVOeVsUE7wqTY4WDszWoHGU74MDaN7qQuNfThU18KXh4BFHhdiK7ri-Xr96VmULH1Xx8A==&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;Abivax SA&lt;/a&gt; (Euronext Paris: FR0012333284 – ABVX / Nasdaq: ABVX) (“Abivax” or the “Company”), a clinical-stage biotechnology company focused on developing therapeutics that harness the body’s natural regulatory mechanisms to stabilize the immune response in patients with chronic inflammatory diseases, today announced</description>
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   <title>Abivax Announces Positive Pre-NDA Interaction with the FDA for Obefazimod</title>
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&lt;p align=&quot;center&quot;&gt;&lt;b&gt;Abivax Announces Positive Pre-NDA &lt;/b&gt;&lt;b&gt;Interaction with the FDA for Obefazimod&lt;/b&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;i&gt;Company remains on track to submit its first New Drug Application for obefazimod for the treatment of moderately to severely active ulcerative colitis by the end of 2026&lt;/i&gt;&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;&lt;b&gt;PARIS, France – July 30, 2026 – 10:05 p.m. CEST&lt;/b&gt; – &lt;a target=&quot;_blank&quot; href=&quot;https://www.globenewswire.com/Tracker?data=KmygmJaiY5aeeB8E5kVOeVsUE7wqTY4WDszWoHGU74MDaN7qQuNfThU18KXh4BFHhdiK7ri-Xr96VmULH1Xx8A==&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;Abivax SA&lt;/a&gt; (Euronext Paris: FR0012333284 – ABVX / Nasdaq: ABVX) (“Abivax” or the “Company”), a clinical-stage biotechnology company focused on developing therapeutics that harness the body’s natural regulatory mechanisms to stabilize the immune response in patients with chronic inflammatory diseases, today announced</description>
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   <description>Morgan Stanley analyst Judah Frommer raised the price target on Abivax (NASDAQ: ABVX) to $180.00  (from $132.00) while maintaining a Overweight rating.</description>
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   <description>&lt;p&gt;Abivax SA (Nasdaq: ABVX) has appointed four executives to its commercial leadership team as the company prepares for a potential U.S. commercialization of its drug candidate obefazimod, with a New Drug Application submission to the FDA planned for the fourth quarter of 2026.&lt;/p&gt;&lt;p&gt;According to a company statement, the four appointments are:&lt;/p&gt;&lt;p&gt;&lt;strong&gt;James Berger&lt;/strong&gt; as Global Head of Marketing. Berger previously served as Global Franchise Head for TEZSPIRE at Amgen and spent more than a decade at Takeda working on ENTYVIO. He also held roles at Merck and Bristol Myers Squibb.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Ivan Nuñez-Pacheco&lt;/strong&gt; as Global Head of Patient Services. Nuñez-Pacheco previously served as</description>
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   <description>&lt;p&gt;Abivax SA (Nasdaq: ABVX) has appointed four executives to its commercial leadership team as the company prepares for a potential U.S. commercialization of its drug candidate obefazimod, with a New Drug Application submission to the FDA planned for the fourth quarter of 2026.&lt;/p&gt;&lt;p&gt;According to a company statement, the four appointments are:&lt;/p&gt;&lt;p&gt;&lt;strong&gt;James Berger&lt;/strong&gt; as Global Head of Marketing. Berger previously served as Global Franchise Head for TEZSPIRE at Amgen and spent more than a decade at Takeda working on ENTYVIO. He also held roles at Merck and Bristol Myers Squibb.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Ivan Nuñez-Pacheco&lt;/strong&gt; as Global Head of Patient Services. Nuñez-Pacheco previously served as</description>
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