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   <title>Form  4          Spero Therapeutics, Inc.  For: Feb 06  Filed by: Rajavelu Esther</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++4++++++++++Spero+Therapeutics%2C+Inc.++For%3A+Feb+06++Filed+by%3A+Rajavelu+Esther/25969788.html</link>
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   <title>Form  4          Spero Therapeutics, Inc.  For: Feb 06  Filed by: Rajavelu Esther</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++4++++++++++Spero+Therapeutics%2C+Inc.++For%3A+Feb+06++Filed+by%3A+Rajavelu+Esther/25969788.html</link>
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   <title>Form  4          Spero Therapeutics, Inc.  For: Feb 06  Filed by: Keutzer Timothy</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++4++++++++++Spero+Therapeutics%2C+Inc.++For%3A+Feb+06++Filed+by%3A+Keutzer+Timothy/25969765.html</link>
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   <title>Form  4          Spero Therapeutics, Inc.  For: Feb 06  Filed by: Keutzer Timothy</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++4++++++++++Spero+Therapeutics%2C+Inc.++For%3A+Feb+06++Filed+by%3A+Keutzer+Timothy/25969765.html</link>
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   <title>Form  4          Spero Therapeutics, Inc.  For: Feb 02  Filed by: Keutzer Timothy</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++4++++++++++Spero+Therapeutics%2C+Inc.++For%3A+Feb+02++Filed+by%3A+Keutzer+Timothy/25950032.html</link>
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   <title>Form  4          Spero Therapeutics, Inc.  For: Feb 02  Filed by: Keutzer Timothy</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++4++++++++++Spero+Therapeutics%2C+Inc.++For%3A+Feb+02++Filed+by%3A+Keutzer+Timothy/25950032.html</link>
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   <pubDate>Thu, 05 Feb 2026 06:30:00 -0500</pubDate>
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   <title>Form  4          Spero Therapeutics, Inc.  For: Feb 02  Filed by: Rajavelu Esther</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++4++++++++++Spero+Therapeutics%2C+Inc.++For%3A+Feb+02++Filed+by%3A+Rajavelu+Esther/25948906.html</link>
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   <pubDate>Wed, 04 Feb 2026 21:44:00 -0500</pubDate>
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   <title>Form  4          Spero Therapeutics, Inc.  For: Feb 02  Filed by: Rajavelu Esther</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++4++++++++++Spero+Therapeutics%2C+Inc.++For%3A+Feb+02++Filed+by%3A+Rajavelu+Esther/25948906.html</link>
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   <pubDate>Wed, 04 Feb 2026 21:44:00 -0500</pubDate>
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   <title>Form  8-K        Spero Therapeutics, Inc.  For: Jan 30</title>
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   <pubDate>Fri, 30 Jan 2026 17:01:00 -0500</pubDate>
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   <title>Form  8-K        Spero Therapeutics, Inc.  For: Jan 30</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++8-K++++++++Spero+Therapeutics%2C+Inc.++For%3A+Jan+30/25924369.html</link>
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   <title>Form  8-K        Spero Therapeutics, Inc.  For: Dec 19</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++8-K++++++++Spero+Therapeutics%2C+Inc.++For%3A+Dec+19/25762373.html</link>
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   <pubDate>Fri, 19 Dec 2025 08:26:00 -0500</pubDate>
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   <title>Form  8-K        Spero Therapeutics, Inc.  For: Dec 19</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++8-K++++++++Spero+Therapeutics%2C+Inc.++For%3A+Dec+19/25762373.html</link>
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   <pubDate>Fri, 19 Dec 2025 08:26:00 -0500</pubDate>
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   <title>GSK resubmits drug application for Spero's antibiotic treatment</title>
   <link>http://www.streetinsider.com/Corporate+News/GSK+resubmits+drug+application+for+Spero%27s+antibiotic+treatment/25762287.html</link>
   <description>&lt;p&gt;Spero Therapeutics Inc. (NASDAQ: SPRO) announced that development partner GSK filed a New Drug Application resubmission to the FDA for tebipenem HBr, an oral carbapenem antibiotic for treating complicated urinary tract infections, including pyelonephritis.&lt;/p&gt;&lt;p&gt;The resubmission triggers a $25 million milestone payment to Spero, expected in the first quarter of 2026, according to the company's statement.&lt;/p&gt;&lt;p&gt;The application is supported by results from the Phase 3 PIVOT-PO trial, which was stopped early for efficacy in May 2025 following a planned interim analysis. Trial results were presented at the IDWeek conference in October 2025.&lt;/p&gt;&lt;p&gt;Spero has granted GSK exclusive licensing rights to commercialize tebipenem</description>
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   <pubDate>Fri, 19 Dec 2025 08:01:39 -0500</pubDate>
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   <title>GSK resubmits drug application for Spero's antibiotic treatment</title>
   <link>http://www.streetinsider.com/FDA/GSK+resubmits+drug+application+for+Spero%27s+antibiotic+treatment/25762287.html</link>
   <description>&lt;p&gt;Spero Therapeutics Inc. (NASDAQ: SPRO) announced that development partner GSK filed a New Drug Application resubmission to the FDA for tebipenem HBr, an oral carbapenem antibiotic for treating complicated urinary tract infections, including pyelonephritis.&lt;/p&gt;&lt;p&gt;The resubmission triggers a $25 million milestone payment to Spero, expected in the first quarter of 2026, according to the company's statement.&lt;/p&gt;&lt;p&gt;The application is supported by results from the Phase 3 PIVOT-PO trial, which was stopped early for efficacy in May 2025 following a planned interim analysis. Trial results were presented at the IDWeek conference in October 2025.&lt;/p&gt;&lt;p&gt;Spero has granted GSK exclusive licensing rights to commercialize tebipenem</description>
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   <pubDate>Fri, 19 Dec 2025 08:01:39 -0500</pubDate>
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   <title>Spero Announces NDA Resubmission of Tebipenem HBr by GSK to the FDA for the Treatment of Complicated Urinary Tract Infections, Including Pyelonephritis</title>
   <link>http://www.streetinsider.com/Press+Releases/Spero+Announces+NDA+Resubmission+of+Tebipenem+HBr+by+GSK+to+the+FDA+for+the+Treatment+of+Complicated+Urinary+Tract+Infections%2C+Including+Pyelonephritis/25762252.html</link>
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&lt;p&gt;CAMBRIDGE, Mass., Dec.  19, 2025  (GLOBE NEWSWIRE) -- &lt;a target=&quot;_blank&quot; href=&quot;https://www.globenewswire.com/Tracker?data=FfytJI_Ad87-lr8QvTd773C2kdbCLXqABVVzCviWa05XdXi0KRmk9Px16EmxhKFI0MUh_jImLW4X3RInUj94kCBC1F5XcXnLk7-WuwnhkHs=&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;Spero Therapeutics&lt;/a&gt;, Inc. (Nasdaq: SPRO), a clinical-stage biopharmaceutical company focused on identifying and developing novel treatments for rare diseases and multi-drug resistant (MDR) bacterial infections, today announced that its development partner, GSK, filed a New Drug Application (NDA) resubmission to the U.S. Food and Drug Administration (FDA) for tebipenem HBr, an investigational oral carbapenem antibiotic being developed for the treatment of complicated urinary tract infections (cUTI), including pyelonephritis. The NDA submission triggers a $25 million milestone payment to Spero, expected to be received in Q1 2026.&lt;/p&gt; </description>
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   <title>Spero Announces NDA Resubmission of Tebipenem HBr by GSK to the FDA for the Treatment of Complicated Urinary Tract Infections, Including Pyelonephritis</title>
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&lt;p&gt;CAMBRIDGE, Mass., Dec.  19, 2025  (GLOBE NEWSWIRE) -- &lt;a target=&quot;_blank&quot; href=&quot;https://www.globenewswire.com/Tracker?data=FfytJI_Ad87-lr8QvTd773C2kdbCLXqABVVzCviWa05XdXi0KRmk9Px16EmxhKFI0MUh_jImLW4X3RInUj94kCBC1F5XcXnLk7-WuwnhkHs=&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;Spero Therapeutics&lt;/a&gt;, Inc. (Nasdaq: SPRO), a clinical-stage biopharmaceutical company focused on identifying and developing novel treatments for rare diseases and multi-drug resistant (MDR) bacterial infections, today announced that its development partner, GSK, filed a New Drug Application (NDA) resubmission to the U.S. Food and Drug Administration (FDA) for tebipenem HBr, an investigational oral carbapenem antibiotic being developed for the treatment of complicated urinary tract infections (cUTI), including pyelonephritis. The NDA submission triggers a $25 million milestone payment to Spero, expected to be received in Q1 2026.&lt;/p&gt; </description>
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   <title>Spero Announces NDA Resubmission of Tebipenem HBr by GSK to the FDA for the Treatment of Complicated Urinary Tract Infections, Including Pyelonephritis</title>
   <link>http://www.streetinsider.com/Press+Releases/Spero+Announces+NDA+Resubmission+of+Tebipenem+HBr+by+GSK+to+the+FDA+for+the+Treatment+of+Complicated+Urinary+Tract+Infections%2C+Including+Pyelonephritis/25762252.html</link>
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&lt;p&gt;CAMBRIDGE, Mass., Dec.  19, 2025  (GLOBE NEWSWIRE) -- &lt;a target=&quot;_blank&quot; href=&quot;https://www.globenewswire.com/Tracker?data=FfytJI_Ad87-lr8QvTd773C2kdbCLXqABVVzCviWa05XdXi0KRmk9Px16EmxhKFI0MUh_jImLW4X3RInUj94kCBC1F5XcXnLk7-WuwnhkHs=&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;Spero Therapeutics&lt;/a&gt;, Inc. (Nasdaq: SPRO), a clinical-stage biopharmaceutical company focused on identifying and developing novel treatments for rare diseases and multi-drug resistant (MDR) bacterial infections, today announced that its development partner, GSK, filed a New Drug Application (NDA) resubmission to the U.S. Food and Drug Administration (FDA) for tebipenem HBr, an investigational oral carbapenem antibiotic being developed for the treatment of complicated urinary tract infections (cUTI), including pyelonephritis. The NDA submission triggers a $25 million milestone payment to Spero, expected to be received in Q1 2026.&lt;/p&gt; </description>
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   <title>Spero Announces NDA Resubmission of Tebipenem HBr by GSK to the FDA for the Treatment of Complicated Urinary Tract Infections, Including Pyelonephritis</title>
   <link>http://www.streetinsider.com/Press+Releases/Spero+Announces+NDA+Resubmission+of+Tebipenem+HBr+by+GSK+to+the+FDA+for+the+Treatment+of+Complicated+Urinary+Tract+Infections%2C+Including+Pyelonephritis/25762252.html</link>
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&lt;p&gt;CAMBRIDGE, Mass., Dec.  19, 2025  (GLOBE NEWSWIRE) -- &lt;a target=&quot;_blank&quot; href=&quot;https://www.globenewswire.com/Tracker?data=FfytJI_Ad87-lr8QvTd773C2kdbCLXqABVVzCviWa05XdXi0KRmk9Px16EmxhKFI0MUh_jImLW4X3RInUj94kCBC1F5XcXnLk7-WuwnhkHs=&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;Spero Therapeutics&lt;/a&gt;, Inc. (Nasdaq: SPRO), a clinical-stage biopharmaceutical company focused on identifying and developing novel treatments for rare diseases and multi-drug resistant (MDR) bacterial infections, today announced that its development partner, GSK, filed a New Drug Application (NDA) resubmission to the U.S. Food and Drug Administration (FDA) for tebipenem HBr, an investigational oral carbapenem antibiotic being developed for the treatment of complicated urinary tract infections (cUTI), including pyelonephritis. The NDA submission triggers a $25 million milestone payment to Spero, expected to be received in Q1 2026.&lt;/p&gt; </description>
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   <title>Spero Announces NDA Resubmission of Tebipenem HBr by GSK to the FDA for the Treatment of Complicated Urinary Tract Infections, Including Pyelonephritis</title>
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&lt;p&gt;CAMBRIDGE, Mass., Dec.  19, 2025  (GLOBE NEWSWIRE) -- &lt;a target=&quot;_blank&quot; href=&quot;https://www.globenewswire.com/Tracker?data=FfytJI_Ad87-lr8QvTd773C2kdbCLXqABVVzCviWa05XdXi0KRmk9Px16EmxhKFI0MUh_jImLW4X3RInUj94kCBC1F5XcXnLk7-WuwnhkHs=&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;Spero Therapeutics&lt;/a&gt;, Inc. (Nasdaq: SPRO), a clinical-stage biopharmaceutical company focused on identifying and developing novel treatments for rare diseases and multi-drug resistant (MDR) bacterial infections, today announced that its development partner, GSK, filed a New Drug Application (NDA) resubmission to the U.S. Food and Drug Administration (FDA) for tebipenem HBr, an investigational oral carbapenem antibiotic being developed for the treatment of complicated urinary tract infections (cUTI), including pyelonephritis. The NDA submission triggers a $25 million milestone payment to Spero, expected to be received in Q1 2026.&lt;/p&gt; </description>
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   <title>Spero Announces NDA Resubmission of Tebipenem HBr by GSK to the FDA for the Treatment of Complicated Urinary Tract Infections, Including Pyelonephritis</title>
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&lt;p&gt;CAMBRIDGE, Mass., Dec.  19, 2025  (GLOBE NEWSWIRE) -- &lt;a target=&quot;_blank&quot; href=&quot;https://www.globenewswire.com/Tracker?data=FfytJI_Ad87-lr8QvTd773C2kdbCLXqABVVzCviWa05XdXi0KRmk9Px16EmxhKFI0MUh_jImLW4X3RInUj94kCBC1F5XcXnLk7-WuwnhkHs=&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;Spero Therapeutics&lt;/a&gt;, Inc. (Nasdaq: SPRO), a clinical-stage biopharmaceutical company focused on identifying and developing novel treatments for rare diseases and multi-drug resistant (MDR) bacterial infections, today announced that its development partner, GSK, filed a New Drug Application (NDA) resubmission to the U.S. Food and Drug Administration (FDA) for tebipenem HBr, an investigational oral carbapenem antibiotic being developed for the treatment of complicated urinary tract infections (cUTI), including pyelonephritis. The NDA submission triggers a $25 million milestone payment to Spero, expected to be received in Q1 2026.&lt;/p&gt; </description>
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   <title>Spero Announces NDA Resubmission of Tebipenem HBr by GSK to the FDA for the Treatment of Complicated Urinary Tract Infections, Including Pyelonephritis</title>
   <link>http://www.streetinsider.com/Globe+Newswire/Spero+Announces+NDA+Resubmission+of+Tebipenem+HBr+by+GSK+to+the+FDA+for+the+Treatment+of+Complicated+Urinary+Tract+Infections%2C+Including+Pyelonephritis/25762252.html</link>
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&lt;p&gt;CAMBRIDGE, Mass., Dec.  19, 2025  (GLOBE NEWSWIRE) -- &lt;a target=&quot;_blank&quot; href=&quot;https://www.globenewswire.com/Tracker?data=FfytJI_Ad87-lr8QvTd773C2kdbCLXqABVVzCviWa05XdXi0KRmk9Px16EmxhKFI0MUh_jImLW4X3RInUj94kCBC1F5XcXnLk7-WuwnhkHs=&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;Spero Therapeutics&lt;/a&gt;, Inc. (Nasdaq: SPRO), a clinical-stage biopharmaceutical company focused on identifying and developing novel treatments for rare diseases and multi-drug resistant (MDR) bacterial infections, today announced that its development partner, GSK, filed a New Drug Application (NDA) resubmission to the U.S. Food and Drug Administration (FDA) for tebipenem HBr, an investigational oral carbapenem antibiotic being developed for the treatment of complicated urinary tract infections (cUTI), including pyelonephritis. The NDA submission triggers a $25 million milestone payment to Spero, expected to be received in Q1 2026.&lt;/p&gt; </description>
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   <title>Spero Announces NDA Resubmission of Tebipenem HBr by GSK to the FDA for the Treatment of Complicated Urinary Tract Infections, Including Pyelonephritis</title>
   <link>http://www.streetinsider.com/Globe+Newswire/Spero+Announces+NDA+Resubmission+of+Tebipenem+HBr+by+GSK+to+the+FDA+for+the+Treatment+of+Complicated+Urinary+Tract+Infections%2C+Including+Pyelonephritis/25762252.html</link>
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&lt;p&gt;CAMBRIDGE, Mass., Dec.  19, 2025  (GLOBE NEWSWIRE) -- &lt;a target=&quot;_blank&quot; href=&quot;https://www.globenewswire.com/Tracker?data=FfytJI_Ad87-lr8QvTd773C2kdbCLXqABVVzCviWa05XdXi0KRmk9Px16EmxhKFI0MUh_jImLW4X3RInUj94kCBC1F5XcXnLk7-WuwnhkHs=&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;Spero Therapeutics&lt;/a&gt;, Inc. (Nasdaq: SPRO), a clinical-stage biopharmaceutical company focused on identifying and developing novel treatments for rare diseases and multi-drug resistant (MDR) bacterial infections, today announced that its development partner, GSK, filed a New Drug Application (NDA) resubmission to the U.S. Food and Drug Administration (FDA) for tebipenem HBr, an investigational oral carbapenem antibiotic being developed for the treatment of complicated urinary tract infections (cUTI), including pyelonephritis. The NDA submission triggers a $25 million milestone payment to Spero, expected to be received in Q1 2026.&lt;/p&gt; </description>
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   <title>Spero Announces NDA Resubmission of Tebipenem HBr by GSK to the FDA for the Treatment of Complicated Urinary Tract Infections, Including Pyelonephritis</title>
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&lt;p&gt;CAMBRIDGE, Mass., Dec.  19, 2025  (GLOBE NEWSWIRE) -- &lt;a target=&quot;_blank&quot; href=&quot;https://www.globenewswire.com/Tracker?data=FfytJI_Ad87-lr8QvTd773C2kdbCLXqABVVzCviWa05XdXi0KRmk9Px16EmxhKFI0MUh_jImLW4X3RInUj94kCBC1F5XcXnLk7-WuwnhkHs=&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;Spero Therapeutics&lt;/a&gt;, Inc. (Nasdaq: SPRO), a clinical-stage biopharmaceutical company focused on identifying and developing novel treatments for rare diseases and multi-drug resistant (MDR) bacterial infections, today announced that its development partner, GSK, filed a New Drug Application (NDA) resubmission to the U.S. Food and Drug Administration (FDA) for tebipenem HBr, an investigational oral carbapenem antibiotic being developed for the treatment of complicated urinary tract infections (cUTI), including pyelonephritis. The NDA submission triggers a $25 million milestone payment to Spero, expected to be received in Q1 2026.&lt;/p&gt; </description>
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   <title>Spero Announces NDA Resubmission of Tebipenem HBr by GSK to the FDA for the Treatment of Complicated Urinary Tract Infections, Including Pyelonephritis</title>
   <link>http://www.streetinsider.com/Globe+Newswire/Spero+Announces+NDA+Resubmission+of+Tebipenem+HBr+by+GSK+to+the+FDA+for+the+Treatment+of+Complicated+Urinary+Tract+Infections%2C+Including+Pyelonephritis/25762252.html</link>
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&lt;p&gt;CAMBRIDGE, Mass., Dec.  19, 2025  (GLOBE NEWSWIRE) -- &lt;a target=&quot;_blank&quot; href=&quot;https://www.globenewswire.com/Tracker?data=FfytJI_Ad87-lr8QvTd773C2kdbCLXqABVVzCviWa05XdXi0KRmk9Px16EmxhKFI0MUh_jImLW4X3RInUj94kCBC1F5XcXnLk7-WuwnhkHs=&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;Spero Therapeutics&lt;/a&gt;, Inc. (Nasdaq: SPRO), a clinical-stage biopharmaceutical company focused on identifying and developing novel treatments for rare diseases and multi-drug resistant (MDR) bacterial infections, today announced that its development partner, GSK, filed a New Drug Application (NDA) resubmission to the U.S. Food and Drug Administration (FDA) for tebipenem HBr, an investigational oral carbapenem antibiotic being developed for the treatment of complicated urinary tract infections (cUTI), including pyelonephritis. The NDA submission triggers a $25 million milestone payment to Spero, expected to be received in Q1 2026.&lt;/p&gt; </description>
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   <title>Spero Announces NDA Resubmission of Tebipenem HBr by GSK to the FDA for the Treatment of Complicated Urinary Tract Infections, Including Pyelonephritis</title>
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&lt;p&gt;CAMBRIDGE, Mass., Dec.  19, 2025  (GLOBE NEWSWIRE) -- &lt;a target=&quot;_blank&quot; href=&quot;https://www.globenewswire.com/Tracker?data=FfytJI_Ad87-lr8QvTd773C2kdbCLXqABVVzCviWa05XdXi0KRmk9Px16EmxhKFI0MUh_jImLW4X3RInUj94kCBC1F5XcXnLk7-WuwnhkHs=&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;Spero Therapeutics&lt;/a&gt;, Inc. (Nasdaq: SPRO), a clinical-stage biopharmaceutical company focused on identifying and developing novel treatments for rare diseases and multi-drug resistant (MDR) bacterial infections, today announced that its development partner, GSK, filed a New Drug Application (NDA) resubmission to the U.S. Food and Drug Administration (FDA) for tebipenem HBr, an investigational oral carbapenem antibiotic being developed for the treatment of complicated urinary tract infections (cUTI), including pyelonephritis. The NDA submission triggers a $25 million milestone payment to Spero, expected to be received in Q1 2026.&lt;/p&gt; </description>
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