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   <title>Leerink Partners Reiterates Outperform Rating on BridgeBio Pharma (BBIO) after data presentation: &quot;risk/reward skewed to the upside&quot;</title>
   <link>http://www.streetinsider.com/Analyst+Comments/Leerink+Partners+Reiterates+Outperform+Rating+on+BridgeBio+Pharma+%28BBIO%29+after+data+presentation%3A+%22riskreward+skewed+to+the+upside%22/26150614.html</link>
   <description>&lt;p&gt;Leerink Partners analyst Mani Foroohar reiterated an Outperform rating and $98.00 price target on BridgeBio Pharma (NASDAQ: BBIO)&lt;/p&gt;&lt;p&gt;The analyst commented, &quot;The presentation is a net positive, albeit largely incremental – early 3-month 100MTT separation, granular CK normalization, and traditional approval path confirmation are the key additions. The LGMD2I/R9 opportunity remains a point of disconnect for the Street: we see a first-in-disease agent in a high unmet need indication, with a clean safety profile with a long lead-time to launch vs gene therapy alternatives still years away – a setup for a strong launch to establish a durable position as standard-of-care.</description>
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   <pubDate>Thu, 12 Mar 2026 09:24:45 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">BBIO</category>
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   <title>BridgeBio reports positive phase 3 results for LGMD2I/R9 drug BBP-418</title>
   <link>http://www.streetinsider.com/FDA/BridgeBio+reports+positive+phase+3+results+for+LGMD2IR9+drug+BBP-418/26145331.html</link>
   <description>

&lt;p&gt;BridgeBio Pharma Inc. (NASDAQ: BBIO) reported positive interim results from its phase 3 FORTIFY trial of BBP-418, an oral treatment for limb-girdle muscular dystrophy type 2I/R9 (LGMD2I/R9). The data were presented at the MDA Clinical and Scientific Conference.&lt;/p&gt;

&lt;p&gt;The study showed BBP-418 demonstrated early separation from placebo on the 100-meter timed test, with improvements in ambulation evident at three months. At 12 months, patients treated with BBP-418 completed the test approximately 31 seconds faster than those receiving placebo.&lt;/p&gt;

&lt;p&gt;Treatment resulted in sustained reduction in serum creatine kinase levels, with 59.6% of patients achieving levels within twice the upper limit of normal and</description>
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   <pubDate>Wed, 11 Mar 2026 14:00:16 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">BBIO</category>
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   <title>BBP-418 Demonstrates Consistent Efficacy and Favorable Safety Profile in Phase 3 FORTIFY Interim Analysis in LGMD2I/R9</title>
   <link>http://www.streetinsider.com/Press+Releases/BBP-418+Demonstrates+Consistent+Efficacy+and+Favorable+Safety+Profile+in+Phase+3+FORTIFY+Interim+Analysis+in+LGMD2IR9/26145323.html</link>
   <description>&lt;p&gt;&lt;em&gt;-&lt;/em&gt; &lt;em&gt;Phase 3 FORTIFY interim analysis results presented in a late-breaking oral presentation at MDA highlight the broad and consistent efficacy of BBP-418 across key clinical endpoints and prespecified subgroups&lt;/em&gt;&lt;/p&gt;  &lt;p&gt;&lt;em&gt;-&lt;/em&gt;&lt;em&gt; Early separation from placebo observed in 100MTT, with improvements in ambulation evident as early as three months following initiation of BBP-418 treatment&lt;/em&gt;&lt;/p&gt;  &lt;p&gt;&lt;em&gt;- Based on the positive interim analysis results, BridgeBio intends to submit an NDA to the FDA for traditional approval in the first half of 2026 with a U.S. launch anticipated in late 2026/early 2027&lt;/em&gt;&lt;/p&gt;  &lt;p&gt;&lt;em&gt;- If successful, BBP-418 could be the first approved therapy</description>
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   <pubDate>Wed, 11 Mar 2026 14:00:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">BBIO</category>
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   <title>BBP-418 Demonstrates Consistent Efficacy and Favorable Safety Profile in Phase 3 FORTIFY Interim Analysis in LGMD2I/R9</title>
   <link>http://www.streetinsider.com/Globe+Newswire/BBP-418+Demonstrates+Consistent+Efficacy+and+Favorable+Safety+Profile+in+Phase+3+FORTIFY+Interim+Analysis+in+LGMD2IR9/26145323.html</link>
   <description>&lt;p&gt;&lt;em&gt;-&lt;/em&gt; &lt;em&gt;Phase 3 FORTIFY interim analysis results presented in a late-breaking oral presentation at MDA highlight the broad and consistent efficacy of BBP-418 across key clinical endpoints and prespecified subgroups&lt;/em&gt;&lt;/p&gt;  &lt;p&gt;&lt;em&gt;-&lt;/em&gt;&lt;em&gt; Early separation from placebo observed in 100MTT, with improvements in ambulation evident as early as three months following initiation of BBP-418 treatment&lt;/em&gt;&lt;/p&gt;  &lt;p&gt;&lt;em&gt;- Based on the positive interim analysis results, BridgeBio intends to submit an NDA to the FDA for traditional approval in the first half of 2026 with a U.S. launch anticipated in late 2026/early 2027&lt;/em&gt;&lt;/p&gt;  &lt;p&gt;&lt;em&gt;- If successful, BBP-418 could be the first approved therapy</description>
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   <pubDate>Wed, 11 Mar 2026 14:00:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">BBIO</category>
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   <title>Form  144        BridgeBio Pharma, Inc.                 Filed by: Valantine Hannah</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++144++++++++BridgeBio+Pharma%2C+Inc.+++++++++++++++++Filed+by%3A+Valantine+Hannah/26139200.html</link>
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   <pubDate>Tue, 10 Mar 2026 16:02:00 -0400</pubDate>
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   <title>Form  144        BridgeBio Pharma, Inc.                 Filed by: Valantine Hannah</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++144++++++++BridgeBio+Pharma%2C+Inc.+++++++++++++++++Filed+by%3A+Valantine+Hannah/26139200.html</link>
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   <pubDate>Tue, 10 Mar 2026 16:02:00 -0400</pubDate>
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   <title>Barclays Reiterates Overweight Rating on BridgeBio Pharma (BBIO) amid tafamidis IP trial update</title>
   <link>http://www.streetinsider.com/Analyst+Comments/Barclays+Reiterates+Overweight+Rating+on+BridgeBio+Pharma+%28BBIO%29+amid+tafamidis+IP+trial+update/26138074.html</link>
   <description>&lt;p&gt;Barclays analyst Eliana Merle reiterated an Overweight rating and $157.00 price target on BridgeBio Pharma (NASDAQ: BBIO)&lt;/p&gt;&lt;p&gt;The analyst commented, &quot;On Tuesday 3/10, the judge in the PFE (covered by Emily Field) US tafamidis IP trial issued a memorandum opinion denying the ANDA filers' motion to exclude PFE expert testimony. We note from our prior work on taf IP, including a legal expert call (link) that the admissibility of PFE's expert testimony was flagged as a key swing factor in the case; the outcome now appears to be in PFE's favor in allowing the testimony (both Matzger's curve fitting &amp; Raman</description>
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   <pubDate>Tue, 10 Mar 2026 12:42:40 -0400</pubDate>
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   <title>BridgeBio Pharma (BBIO) PT Raised to $94 at JPMorgan</title>
   <link>http://www.streetinsider.com/Analyst+PT+Change/BridgeBio+Pharma+%28BBIO%29+PT+Raised+to+%2494+at+JPMorgan/26135478.html</link>
   <description>JPMorgan analyst Anupam Rama raised the price target on BridgeBio Pharma (NASDAQ: BBIO) to $94.00  (from $89.00) while maintaining a Overweight rating.</description>
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   <pubDate>Tue, 10 Mar 2026 07:58:15 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">BBIO</category>
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   <title>William Blair Starts BridgeBio Pharma (BBIO) at Outperform</title>
   <link>http://www.streetinsider.com/New+Coverage/William+Blair+Starts+BridgeBio+Pharma+%28BBIO%29+at+Outperform/26134955.html</link>
   <description>&lt;p&gt;William Blair analyst John Boyle initiates coverage on BridgeBio Pharma (NASDAQ: BBIO) with a Outperform rating.&lt;/p&gt;&lt;p&gt;The analyst comments &quot;We are initiating coverage of BridgeBio Therapeutics with an Outperform rating and fair value of $93.03 per share. BridgeBio is a commercial-stage biotech company in a unique position with an accelerating launch in Attruby, near-term NDA submissions for disease-modifying therapies (encaleret in ADH1 and BBP-418 in LGMD2I/R9) setting up late-2026/early-2027 launches, and regulatory submission for infigratinib in achondroplasia planned for second half 2026. Attruby is well positioned for growth in ATTR-CM. Attruby (a second-generation stabilizer) is launching alongside Alnylam’s Amvuttra (a silencer)</description>
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   <pubDate>Tue, 10 Mar 2026 06:34:51 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">BBIO</category>
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   <title>William Blair Starts BridgeBio Pharma (BBIO) at Outperform</title>
   <link>http://www.streetinsider.com/Analyst+Comments/William+Blair+Starts+BridgeBio+Pharma+%28BBIO%29+at+Outperform/26134955.html</link>
   <description>&lt;p&gt;William Blair analyst John Boyle initiates coverage on BridgeBio Pharma (NASDAQ: BBIO) with a Outperform rating.&lt;/p&gt;&lt;p&gt;The analyst comments &quot;We are initiating coverage of BridgeBio Therapeutics with an Outperform rating and fair value of $93.03 per share. BridgeBio is a commercial-stage biotech company in a unique position with an accelerating launch in Attruby, near-term NDA submissions for disease-modifying therapies (encaleret in ADH1 and BBP-418 in LGMD2I/R9) setting up late-2026/early-2027 launches, and regulatory submission for infigratinib in achondroplasia planned for second half 2026. Attruby is well positioned for growth in ATTR-CM. Attruby (a second-generation stabilizer) is launching alongside Alnylam’s Amvuttra (a silencer)</description>
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   <pubDate>Tue, 10 Mar 2026 06:34:51 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">BBIO</category>
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   <title>Form  4          BridgeBio Pharma, Inc.    For: Mar 04  Filed by: Ellis Andrea</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++4++++++++++BridgeBio+Pharma%2C+Inc.++++For%3A+Mar+04++Filed+by%3A+Ellis+Andrea/26126381.html</link>
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   <pubDate>Fri, 06 Mar 2026 16:58:00 -0400</pubDate>
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   <title>Form  4          BridgeBio Pharma, Inc.    For: Mar 04  Filed by: Ellis Andrea</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++4++++++++++BridgeBio+Pharma%2C+Inc.++++For%3A+Mar+04++Filed+by%3A+Ellis+Andrea/26126381.html</link>
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   <pubDate>Fri, 06 Mar 2026 16:58:00 -0400</pubDate>
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   <title>Form  144        BridgeBio Pharma, Inc.                 Filed by: Ellis Andrea</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++144++++++++BridgeBio+Pharma%2C+Inc.+++++++++++++++++Filed+by%3A+Ellis+Andrea/26111421.html</link>
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   <pubDate>Wed, 04 Mar 2026 16:18:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">BBIO</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">O.41347907</category>
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   <title>Form  144        BridgeBio Pharma, Inc.                 Filed by: Ellis Andrea</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++144++++++++BridgeBio+Pharma%2C+Inc.+++++++++++++++++Filed+by%3A+Ellis+Andrea/26111421.html</link>
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   <pubDate>Wed, 04 Mar 2026 16:18:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">BBIO</category>
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   <title>BridgeBio to present FORTIFY trial data at MDA conference</title>
   <link>http://www.streetinsider.com/FDA/BridgeBio+to+present+FORTIFY+trial+data+at+MDA+conference/26107173.html</link>
   <description>

&lt;p&gt;BridgeBio Pharma Inc. (NASDAQ: BBIO) will present additional data from its Phase 3 FORTIFY trial at the MDA Clinical &amp; Scientific Conference in Orlando, Florida from March 8-11, 2026, according to a company statement.&lt;/p&gt;

&lt;p&gt;The FORTIFY trial evaluates BBP-418 in patients with limb-girdle muscular dystrophy type 2I/R9 (LGMD2I/R9). Katherine Mathews, a professor at the University of Iowa's Roy J. and Lucille A. Carver College of Medicine, will deliver a late-breaking oral presentation titled &quot;Interim Analysis from Ongoing Phase 3 FORTIFY Study of BBP-418 for Patients with LGMD2I/R9 Meets Efficacy Endpoints&quot; on March 11 at 2:00 pm ET.&lt;/p&gt;

&lt;p&gt;Academic collaborators from Yale School</description>
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   <pubDate>Wed, 04 Mar 2026 07:30:44 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">BBIO</category>
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   <title>BridgeBio to present FORTIFY trial data at MDA conference</title>
   <link>http://www.streetinsider.com/FDA/BridgeBio+to+present+FORTIFY+trial+data+at+MDA+conference/26107173.html</link>
   <description>

&lt;p&gt;BridgeBio Pharma Inc. (NASDAQ: BBIO) will present additional data from its Phase 3 FORTIFY trial at the MDA Clinical &amp; Scientific Conference in Orlando, Florida from March 8-11, 2026, according to a company statement.&lt;/p&gt;

&lt;p&gt;The FORTIFY trial evaluates BBP-418 in patients with limb-girdle muscular dystrophy type 2I/R9 (LGMD2I/R9). Katherine Mathews, a professor at the University of Iowa's Roy J. and Lucille A. Carver College of Medicine, will deliver a late-breaking oral presentation titled &quot;Interim Analysis from Ongoing Phase 3 FORTIFY Study of BBP-418 for Patients with LGMD2I/R9 Meets Efficacy Endpoints&quot; on March 11 at 2:00 pm ET.&lt;/p&gt;

&lt;p&gt;Academic collaborators from Yale School</description>
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   <pubDate>Wed, 04 Mar 2026 07:30:44 -0400</pubDate>
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   <title>BridgeBio to present FORTIFY trial data at MDA conference</title>
   <link>http://www.streetinsider.com/FDA/BridgeBio+to+present+FORTIFY+trial+data+at+MDA+conference/26107162.html</link>
   <description>

&lt;p&gt;BridgeBio Pharma, Inc. (NASDAQ: BBIO) will present additional data from the interim analysis of its Phase 3 FORTIFY clinical trial at the MDA Clinical &amp; Scientific Conference in Orlando, Florida on March 8-11, 2026, according to a company statement.&lt;/p&gt;

&lt;p&gt;The FORTIFY trial evaluates BBP-418 in patients with limb-girdle muscular dystrophy type 2I/R9 (LGMD2I/R9). The data will be shared in a late-breaking oral presentation titled &quot;Interim Analysis from Ongoing Phase 3 FORTIFY Study of BBP-418 for Patients with LGMD2I/R9 Meets Efficacy Endpoints&quot; on March 11 at 2:00 pm ET.&lt;/p&gt;

&lt;p&gt;Katherine Mathews, M.D., Professor of Pediatrics and Neurology at the University of Iowa's Roy</description>
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   <pubDate>Wed, 04 Mar 2026 07:30:11 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">BBIO</category>
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   <title>BridgeBio to Present Additional Data from the Phase 3 FORTIFY Trial at the 2026 MDA Clinical &amp;amp; Scientific Conference</title>
   <link>http://www.streetinsider.com/Press+Releases/BridgeBio+to+Present+Additional+Data+from+the+Phase+3+FORTIFY+Trial+at+the+2026+MDA+Clinical+%26amp%3B+Scientific+Conference/26107170.html</link>
   <description>
&lt;p&gt;PALO ALTO, Calif., March  04, 2026  (GLOBE NEWSWIRE) -- BridgeBio Pharma, Inc. (Nasdaq: BBIO) (“BridgeBio” or the “Company”), a biopharmaceutical company focused on developing medicines for genetic conditions, announced today that additional data from the interim analysis of FORTIFY, the Phase 3 clinical trial of BBP-418 in patients with limb-girdle muscular dystrophy type 2I/R9 (LGMD2I/R9), will be shared in a late-breaking oral presentation at the MDA Clinical and Scientific Conference, taking place in Orlando, Florida on March 8-11, 2026. Additionally, an oral presentation from BridgeBio’s academic collaborators at Yale School of Medicine, along with four posters, will highlight</description>
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   <pubDate>Wed, 04 Mar 2026 07:30:00 -0400</pubDate>
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   <title>BridgeBio to Present Additional Data from the Phase 3 FORTIFY Trial at the 2026 MDA Clinical &amp;amp; Scientific Conference</title>
   <link>http://www.streetinsider.com/Press+Releases/BridgeBio+to+Present+Additional+Data+from+the+Phase+3+FORTIFY+Trial+at+the+2026+MDA+Clinical+%26amp%3B+Scientific+Conference/26107170.html</link>
   <description>
&lt;p&gt;PALO ALTO, Calif., March  04, 2026  (GLOBE NEWSWIRE) -- BridgeBio Pharma, Inc. (Nasdaq: BBIO) (“BridgeBio” or the “Company”), a biopharmaceutical company focused on developing medicines for genetic conditions, announced today that additional data from the interim analysis of FORTIFY, the Phase 3 clinical trial of BBP-418 in patients with limb-girdle muscular dystrophy type 2I/R9 (LGMD2I/R9), will be shared in a late-breaking oral presentation at the MDA Clinical and Scientific Conference, taking place in Orlando, Florida on March 8-11, 2026. Additionally, an oral presentation from BridgeBio’s academic collaborators at Yale School of Medicine, along with four posters, will highlight</description>
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   <pubDate>Wed, 04 Mar 2026 07:30:00 -0400</pubDate>
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   <title>BridgeBio to Present Additional Data from the Phase 3 FORTIFY Trial at the 2026 MDA Clinical &amp;amp; Scientific Conference</title>
   <link>http://www.streetinsider.com/Globe+Newswire/BridgeBio+to+Present+Additional+Data+from+the+Phase+3+FORTIFY+Trial+at+the+2026+MDA+Clinical+%26amp%3B+Scientific+Conference/26107170.html</link>
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&lt;p&gt;PALO ALTO, Calif., March  04, 2026  (GLOBE NEWSWIRE) -- BridgeBio Pharma, Inc. (Nasdaq: BBIO) (“BridgeBio” or the “Company”), a biopharmaceutical company focused on developing medicines for genetic conditions, announced today that additional data from the interim analysis of FORTIFY, the Phase 3 clinical trial of BBP-418 in patients with limb-girdle muscular dystrophy type 2I/R9 (LGMD2I/R9), will be shared in a late-breaking oral presentation at the MDA Clinical and Scientific Conference, taking place in Orlando, Florida on March 8-11, 2026. Additionally, an oral presentation from BridgeBio’s academic collaborators at Yale School of Medicine, along with four posters, will highlight</description>
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&lt;p&gt;PALO ALTO, Calif., March  04, 2026  (GLOBE NEWSWIRE) -- BridgeBio Pharma, Inc. (Nasdaq: BBIO) (“BridgeBio” or the “Company”), a biopharmaceutical company focused on developing medicines for genetic conditions, announced today that additional data from the interim analysis of FORTIFY, the Phase 3 clinical trial of BBP-418 in patients with limb-girdle muscular dystrophy type 2I/R9 (LGMD2I/R9), will be shared in a late-breaking oral presentation at the MDA Clinical and Scientific Conference, taking place in Orlando, Florida on March 8-11, 2026. Additionally, an oral presentation from BridgeBio’s academic collaborators at Yale School of Medicine, along with four posters, will highlight</description>
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   <description>&lt;p&gt;PALO ALTO, Calif., March  04, 2026  (GLOBE NEWSWIRE) -- BridgeBio Pharma, Inc. (Nasdaq: BBIO) (“BridgeBio” or the “Company”), a biopharmaceutical company focused on developing medicines for genetic conditions, announced today that additional data from the interim analysis of FORTIFY, the Phase 3 clinical trial of BBP-418 in patients with limb-girdle muscular dystrophy type 2I/R9 (LGMD2I/R9), will be shared in a late-breaking oral presentation at the MDA Clinical and Scientific Conference, taking place in Orlando, Florida on March 8-11, 2026. Additionally, an oral presentation from BridgeBio’s academic collaborators at Yale School of Medicine, along with four posters, will highlight</description>
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   <description>&lt;p&gt;PALO ALTO, Calif., March  04, 2026  (GLOBE NEWSWIRE) -- BridgeBio Pharma, Inc. (Nasdaq: BBIO) (“BridgeBio” or the “Company”), a biopharmaceutical company focused on developing medicines for genetic conditions, announced today that additional data from the interim analysis of FORTIFY, the Phase 3 clinical trial of BBP-418 in patients with limb-girdle muscular dystrophy type 2I/R9 (LGMD2I/R9), will be shared in a late-breaking oral presentation at the MDA Clinical and Scientific Conference, taking place in Orlando, Florida on March 8-11, 2026. Additionally, an oral presentation from BridgeBio’s academic collaborators at Yale School of Medicine, along with four posters, will highlight</description>
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