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   <title>Lexeo phase I/II data for Friedreich ataxia gene therapy published</title>
   <link>http://www.streetinsider.com/Corporate+News/Lexeo+phase+III+data+for+Friedreich+ataxia+gene+therapy+published/26659716.html</link>
   <description>&lt;p&gt;Lexeo Therapeutics (Nasdaq: LXEO) announced that Phase I/II study results for its LX2006 gene therapy in Friedreich ataxia (FA) have been published in JAMA Cardiology.&lt;/p&gt;&lt;p&gt;The publication combines data from 17 participants across two independent studies: nine from a Weill Cornell Medicine study funded by the National Heart, Lung, and Blood Institute, and eight from Lexeo's own SUNRISE-FA study. Patients received a one-hour intravenous infusion of LX2006 and were evaluated over periods ranging from 6 to 36 months across three dose cohorts.&lt;/p&gt;&lt;p&gt;Among participants with abnormal baseline left ventricular mass index (LVMI) in mid- and high-dose cohorts, the data showed a 28%</description>
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   <pubDate>Wed, 17 Jun 2026 16:01:46 -0400</pubDate>
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   <title>Lexeo phase I/II data for Friedreich ataxia gene therapy published</title>
   <link>http://www.streetinsider.com/FDA/Lexeo+phase+III+data+for+Friedreich+ataxia+gene+therapy+published/26659716.html</link>
   <description>&lt;p&gt;Lexeo Therapeutics (Nasdaq: LXEO) announced that Phase I/II study results for its LX2006 gene therapy in Friedreich ataxia (FA) have been published in JAMA Cardiology.&lt;/p&gt;&lt;p&gt;The publication combines data from 17 participants across two independent studies: nine from a Weill Cornell Medicine study funded by the National Heart, Lung, and Blood Institute, and eight from Lexeo's own SUNRISE-FA study. Patients received a one-hour intravenous infusion of LX2006 and were evaluated over periods ranging from 6 to 36 months across three dose cohorts.&lt;/p&gt;&lt;p&gt;Among participants with abnormal baseline left ventricular mass index (LVMI) in mid- and high-dose cohorts, the data showed a 28%</description>
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   <pubDate>Wed, 17 Jun 2026 16:01:46 -0400</pubDate>
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   <title>Lexeo Therapeutics Announces Publication in JAMA Cardiology of Phase I/II Data for LX2006 in Friedreich Ataxia</title>
   <link>http://www.streetinsider.com/Press+Releases/Lexeo+Therapeutics+Announces+Publication+in+JAMA+Cardiology+of+Phase+III+Data+for+LX2006+in+Friedreich+Ataxia/26659704.html</link>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;Published findings in JAMA Cardiology demonstrate LX2006 generally well tolerated, with early signs of efficacy in Phase I/II studies&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;SUNRISE-FA 2 pivotal study for LX2006 on track to initiate in Q2 2026 with topline data expected in 2H 2027 &lt;/em&gt;&lt;/p&gt;  &lt;p&gt;NEW YORK, June  17, 2026  (GLOBE NEWSWIRE) -- &lt;a target=&quot;_blank&quot; href=&quot;https://www.globenewswire.com/Tracker?data=grCcmqeAqMqmhQ9hP5ERbrG6eN4eevOTwZ08umR-lYhfwmsM-5qD4qNetasAzfbKp2_mpdpSM7KUQosz7jgzmv01aRYpMfjCfySvZjQTfnI=&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;Lexeo Therapeutics, Inc.&lt;/a&gt; (Nasdaq: LXEO), a clinical stage genetic medicine company dedicated to pioneering novel treatments for cardiovascular diseases, today announced that key results from Phase I/II studies of LX2006 gene therapy in Friedreich ataxia (FA) have been published in the Journal</description>
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   <title>Lexeo Therapeutics Announces Publication in JAMA Cardiology of Phase I/II Data for LX2006 in Friedreich Ataxia</title>
   <link>http://www.streetinsider.com/Press+Releases/Lexeo+Therapeutics+Announces+Publication+in+JAMA+Cardiology+of+Phase+III+Data+for+LX2006+in+Friedreich+Ataxia/26659704.html</link>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;Published findings in JAMA Cardiology demonstrate LX2006 generally well tolerated, with early signs of efficacy in Phase I/II studies&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;SUNRISE-FA 2 pivotal study for LX2006 on track to initiate in Q2 2026 with topline data expected in 2H 2027 &lt;/em&gt;&lt;/p&gt;  &lt;p&gt;NEW YORK, June  17, 2026  (GLOBE NEWSWIRE) -- &lt;a target=&quot;_blank&quot; href=&quot;https://www.globenewswire.com/Tracker?data=grCcmqeAqMqmhQ9hP5ERbrG6eN4eevOTwZ08umR-lYhfwmsM-5qD4qNetasAzfbKp2_mpdpSM7KUQosz7jgzmv01aRYpMfjCfySvZjQTfnI=&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;Lexeo Therapeutics, Inc.&lt;/a&gt; (Nasdaq: LXEO), a clinical stage genetic medicine company dedicated to pioneering novel treatments for cardiovascular diseases, today announced that key results from Phase I/II studies of LX2006 gene therapy in Friedreich ataxia (FA) have been published in the Journal</description>
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   <title>Lexeo Therapeutics Announces Publication in JAMA Cardiology of Phase I/II Data for LX2006 in Friedreich Ataxia</title>
   <link>http://www.streetinsider.com/Press+Releases/Lexeo+Therapeutics+Announces+Publication+in+JAMA+Cardiology+of+Phase+III+Data+for+LX2006+in+Friedreich+Ataxia/26659704.html</link>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;Published findings in JAMA Cardiology demonstrate LX2006 generally well tolerated, with early signs of efficacy in Phase I/II studies&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;SUNRISE-FA 2 pivotal study for LX2006 on track to initiate in Q2 2026 with topline data expected in 2H 2027 &lt;/em&gt;&lt;/p&gt;  &lt;p&gt;NEW YORK, June  17, 2026  (GLOBE NEWSWIRE) -- &lt;a target=&quot;_blank&quot; href=&quot;https://www.globenewswire.com/Tracker?data=grCcmqeAqMqmhQ9hP5ERbrG6eN4eevOTwZ08umR-lYhfwmsM-5qD4qNetasAzfbKp2_mpdpSM7KUQosz7jgzmv01aRYpMfjCfySvZjQTfnI=&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;Lexeo Therapeutics, Inc.&lt;/a&gt; (Nasdaq: LXEO), a clinical stage genetic medicine company dedicated to pioneering novel treatments for cardiovascular diseases, today announced that key results from Phase I/II studies of LX2006 gene therapy in Friedreich ataxia (FA) have been published in the Journal</description>
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   <title>Lexeo Therapeutics Announces Publication in JAMA Cardiology of Phase I/II Data for LX2006 in Friedreich Ataxia</title>
   <link>http://www.streetinsider.com/Press+Releases/Lexeo+Therapeutics+Announces+Publication+in+JAMA+Cardiology+of+Phase+III+Data+for+LX2006+in+Friedreich+Ataxia/26659704.html</link>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;Published findings in JAMA Cardiology demonstrate LX2006 generally well tolerated, with early signs of efficacy in Phase I/II studies&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;SUNRISE-FA 2 pivotal study for LX2006 on track to initiate in Q2 2026 with topline data expected in 2H 2027 &lt;/em&gt;&lt;/p&gt;  &lt;p&gt;NEW YORK, June  17, 2026  (GLOBE NEWSWIRE) -- &lt;a target=&quot;_blank&quot; href=&quot;https://www.globenewswire.com/Tracker?data=grCcmqeAqMqmhQ9hP5ERbrG6eN4eevOTwZ08umR-lYhfwmsM-5qD4qNetasAzfbKp2_mpdpSM7KUQosz7jgzmv01aRYpMfjCfySvZjQTfnI=&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;Lexeo Therapeutics, Inc.&lt;/a&gt; (Nasdaq: LXEO), a clinical stage genetic medicine company dedicated to pioneering novel treatments for cardiovascular diseases, today announced that key results from Phase I/II studies of LX2006 gene therapy in Friedreich ataxia (FA) have been published in the Journal</description>
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   <title>Lexeo Therapeutics Announces Publication in JAMA Cardiology of Phase I/II Data for LX2006 in Friedreich Ataxia</title>
   <link>http://www.streetinsider.com/Globe+Newswire/Lexeo+Therapeutics+Announces+Publication+in+JAMA+Cardiology+of+Phase+III+Data+for+LX2006+in+Friedreich+Ataxia/26659704.html</link>
   <description>
&lt;p align=&quot;center&quot;&gt;&lt;em&gt;Published findings in JAMA Cardiology demonstrate LX2006 generally well tolerated, with early signs of efficacy in Phase I/II studies&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;SUNRISE-FA 2 pivotal study for LX2006 on track to initiate in Q2 2026 with topline data expected in 2H 2027 &lt;/em&gt;&lt;/p&gt;  &lt;p&gt;NEW YORK, June  17, 2026  (GLOBE NEWSWIRE) -- &lt;a target=&quot;_blank&quot; href=&quot;https://www.globenewswire.com/Tracker?data=grCcmqeAqMqmhQ9hP5ERbrG6eN4eevOTwZ08umR-lYhfwmsM-5qD4qNetasAzfbKp2_mpdpSM7KUQosz7jgzmv01aRYpMfjCfySvZjQTfnI=&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;Lexeo Therapeutics, Inc.&lt;/a&gt; (Nasdaq: LXEO), a clinical stage genetic medicine company dedicated to pioneering novel treatments for cardiovascular diseases, today announced that key results from Phase I/II studies of LX2006 gene therapy in Friedreich ataxia (FA) have been published in the Journal</description>
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   <title>Lexeo Therapeutics Announces Publication in JAMA Cardiology of Phase I/II Data for LX2006 in Friedreich Ataxia</title>
   <link>http://www.streetinsider.com/Globe+Newswire/Lexeo+Therapeutics+Announces+Publication+in+JAMA+Cardiology+of+Phase+III+Data+for+LX2006+in+Friedreich+Ataxia/26659704.html</link>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;Published findings in JAMA Cardiology demonstrate LX2006 generally well tolerated, with early signs of efficacy in Phase I/II studies&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;SUNRISE-FA 2 pivotal study for LX2006 on track to initiate in Q2 2026 with topline data expected in 2H 2027 &lt;/em&gt;&lt;/p&gt;  &lt;p&gt;NEW YORK, June  17, 2026  (GLOBE NEWSWIRE) -- &lt;a target=&quot;_blank&quot; href=&quot;https://www.globenewswire.com/Tracker?data=grCcmqeAqMqmhQ9hP5ERbrG6eN4eevOTwZ08umR-lYhfwmsM-5qD4qNetasAzfbKp2_mpdpSM7KUQosz7jgzmv01aRYpMfjCfySvZjQTfnI=&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;Lexeo Therapeutics, Inc.&lt;/a&gt; (Nasdaq: LXEO), a clinical stage genetic medicine company dedicated to pioneering novel treatments for cardiovascular diseases, today announced that key results from Phase I/II studies of LX2006 gene therapy in Friedreich ataxia (FA) have been published in the Journal</description>
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   <title>Lexeo Therapeutics Announces Publication in JAMA Cardiology of Phase I/II Data for LX2006 in Friedreich Ataxia</title>
   <link>http://www.streetinsider.com/Globe+Newswire/Lexeo+Therapeutics+Announces+Publication+in+JAMA+Cardiology+of+Phase+III+Data+for+LX2006+in+Friedreich+Ataxia/26659704.html</link>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;Published findings in JAMA Cardiology demonstrate LX2006 generally well tolerated, with early signs of efficacy in Phase I/II studies&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;SUNRISE-FA 2 pivotal study for LX2006 on track to initiate in Q2 2026 with topline data expected in 2H 2027 &lt;/em&gt;&lt;/p&gt;  &lt;p&gt;NEW YORK, June  17, 2026  (GLOBE NEWSWIRE) -- &lt;a target=&quot;_blank&quot; href=&quot;https://www.globenewswire.com/Tracker?data=grCcmqeAqMqmhQ9hP5ERbrG6eN4eevOTwZ08umR-lYhfwmsM-5qD4qNetasAzfbKp2_mpdpSM7KUQosz7jgzmv01aRYpMfjCfySvZjQTfnI=&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;Lexeo Therapeutics, Inc.&lt;/a&gt; (Nasdaq: LXEO), a clinical stage genetic medicine company dedicated to pioneering novel treatments for cardiovascular diseases, today announced that key results from Phase I/II studies of LX2006 gene therapy in Friedreich ataxia (FA) have been published in the Journal</description>
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   <title>Lexeo Therapeutics Announces Publication in JAMA Cardiology of Phase I/II Data for LX2006 in Friedreich Ataxia</title>
   <link>http://www.streetinsider.com/Globe+Newswire/Lexeo+Therapeutics+Announces+Publication+in+JAMA+Cardiology+of+Phase+III+Data+for+LX2006+in+Friedreich+Ataxia/26659704.html</link>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;Published findings in JAMA Cardiology demonstrate LX2006 generally well tolerated, with early signs of efficacy in Phase I/II studies&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;SUNRISE-FA 2 pivotal study for LX2006 on track to initiate in Q2 2026 with topline data expected in 2H 2027 &lt;/em&gt;&lt;/p&gt;  &lt;p&gt;NEW YORK, June  17, 2026  (GLOBE NEWSWIRE) -- &lt;a target=&quot;_blank&quot; href=&quot;https://www.globenewswire.com/Tracker?data=grCcmqeAqMqmhQ9hP5ERbrG6eN4eevOTwZ08umR-lYhfwmsM-5qD4qNetasAzfbKp2_mpdpSM7KUQosz7jgzmv01aRYpMfjCfySvZjQTfnI=&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;Lexeo Therapeutics, Inc.&lt;/a&gt; (Nasdaq: LXEO), a clinical stage genetic medicine company dedicated to pioneering novel treatments for cardiovascular diseases, today announced that key results from Phase I/II studies of LX2006 gene therapy in Friedreich ataxia (FA) have been published in the Journal</description>
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   <title>Form  8-K        Lexeo Therapeutics, Inc.  For: Jun 15</title>
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   <title>Form  8-K        Lexeo Therapeutics, Inc.  For: Jun 15</title>
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   <title>Lexeo finalizes pivotal trial design for gene therapy in heart condition</title>
   <link>http://www.streetinsider.com/Corporate+News/Lexeo+finalizes+pivotal+trial+design+for+gene+therapy+in+heart+condition/26644083.html</link>
   <description>&lt;p&gt;Lexeo Therapeutics Inc. (NASDAQ: LXEO) announced it has completed the protocol and statistical analysis plan for its SUNRISE-FA 2 pivotal trial of gene therapy candidate LX2006 for Friedreich ataxia cardiomyopathy, according to a company statement.&lt;/p&gt;&lt;p&gt;The open-label study will enroll 13 participants aged 16 years and older to receive a single intravenous dose of LX2006, compared with 13 untreated control participants. The primary endpoint measures left ventricular mass index through cardiac magnetic resonance imaging, with efficacy results expected at six months post-treatment.&lt;/p&gt;&lt;p&gt;Participants will have abnormal baseline left ventricular mass index, defined as at least two standard deviations above normal. The study</description>
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   <pubDate>Mon, 15 Jun 2026 07:01:08 -0400</pubDate>
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   <title>Lexeo finalizes pivotal trial design for gene therapy in heart condition</title>
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   <description>&lt;p&gt;Lexeo Therapeutics Inc. (NASDAQ: LXEO) announced it has completed the protocol and statistical analysis plan for its SUNRISE-FA 2 pivotal trial of gene therapy candidate LX2006 for Friedreich ataxia cardiomyopathy, according to a company statement.&lt;/p&gt;&lt;p&gt;The open-label study will enroll 13 participants aged 16 years and older to receive a single intravenous dose of LX2006, compared with 13 untreated control participants. The primary endpoint measures left ventricular mass index through cardiac magnetic resonance imaging, with efficacy results expected at six months post-treatment.&lt;/p&gt;&lt;p&gt;Participants will have abnormal baseline left ventricular mass index, defined as at least two standard deviations above normal. The study</description>
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   <pubDate>Mon, 15 Jun 2026 07:01:08 -0400</pubDate>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;SUNRISE-FA 2 study parameters include LVMI primary endpoint, 6-month topline efficacy analysis, inclusion criteria focused on abnormal baseline LVMI and open-label trial design &lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;BLA supportive manufacturing strategy includes flexible process validation, including reduced PPQ manufacturing batches&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;SUNRISE-FA 2 initiation on track for Q2 2026, with first patient expected to be enrolled by end of June&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Company to host webcast today at 8:00 AM ET&lt;/em&gt;&lt;/p&gt;  &lt;p&gt;NEW YORK, June  15, 2026  (GLOBE NEWSWIRE) -- &lt;a target=&quot;_blank&quot; href=&quot;https://www.globenewswire.com/Tracker?data=yCPeaIqvIQE16A5goRU48E30GNmuTS7GfVEZFB9gXaQ_PwpAhj14vHEIKg1y7a0p0MHXpBx-Jj_95AVdjAaXSOC6MDAtYJmLahXQwifEovk=&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;Lexeo Therapeutics, Inc.&lt;/a&gt; (Nasdaq: LXEO), a clinical stage genetic medicine company dedicated to pioneering</description>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;SUNRISE-FA 2 study parameters include LVMI primary endpoint, 6-month topline efficacy analysis, inclusion criteria focused on abnormal baseline LVMI and open-label trial design &lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;BLA supportive manufacturing strategy includes flexible process validation, including reduced PPQ manufacturing batches&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;SUNRISE-FA 2 initiation on track for Q2 2026, with first patient expected to be enrolled by end of June&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Company to host webcast today at 8:00 AM ET&lt;/em&gt;&lt;/p&gt;  &lt;p&gt;NEW YORK, June  15, 2026  (GLOBE NEWSWIRE) -- &lt;a target=&quot;_blank&quot; href=&quot;https://www.globenewswire.com/Tracker?data=yCPeaIqvIQE16A5goRU48E30GNmuTS7GfVEZFB9gXaQ_PwpAhj14vHEIKg1y7a0p0MHXpBx-Jj_95AVdjAaXSOC6MDAtYJmLahXQwifEovk=&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;Lexeo Therapeutics, Inc.&lt;/a&gt; (Nasdaq: LXEO), a clinical stage genetic medicine company dedicated to pioneering</description>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;SUNRISE-FA 2 study parameters include LVMI primary endpoint, 6-month topline efficacy analysis, inclusion criteria focused on abnormal baseline LVMI and open-label trial design &lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;BLA supportive manufacturing strategy includes flexible process validation, including reduced PPQ manufacturing batches&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;SUNRISE-FA 2 initiation on track for Q2 2026, with first patient expected to be enrolled by end of June&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Company to host webcast today at 8:00 AM ET&lt;/em&gt;&lt;/p&gt;  &lt;p&gt;NEW YORK, June  15, 2026  (GLOBE NEWSWIRE) -- &lt;a target=&quot;_blank&quot; href=&quot;https://www.globenewswire.com/Tracker?data=yCPeaIqvIQE16A5goRU48E30GNmuTS7GfVEZFB9gXaQ_PwpAhj14vHEIKg1y7a0p0MHXpBx-Jj_95AVdjAaXSOC6MDAtYJmLahXQwifEovk=&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;Lexeo Therapeutics, Inc.&lt;/a&gt; (Nasdaq: LXEO), a clinical stage genetic medicine company dedicated to pioneering</description>
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   <title>Lexeo Therapeutics Announces Regulatory Update and Registrational Trial Design for LX2006 Gene Therapy in Friedreich Ataxia</title>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;SUNRISE-FA 2 study parameters include LVMI primary endpoint, 6-month topline efficacy analysis, inclusion criteria focused on abnormal baseline LVMI and open-label trial design &lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;BLA supportive manufacturing strategy includes flexible process validation, including reduced PPQ manufacturing batches&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;SUNRISE-FA 2 initiation on track for Q2 2026, with first patient expected to be enrolled by end of June&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Company to host webcast today at 8:00 AM ET&lt;/em&gt;&lt;/p&gt;  &lt;p&gt;NEW YORK, June  15, 2026  (GLOBE NEWSWIRE) -- &lt;a target=&quot;_blank&quot; href=&quot;https://www.globenewswire.com/Tracker?data=yCPeaIqvIQE16A5goRU48E30GNmuTS7GfVEZFB9gXaQ_PwpAhj14vHEIKg1y7a0p0MHXpBx-Jj_95AVdjAaXSOC6MDAtYJmLahXQwifEovk=&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;Lexeo Therapeutics, Inc.&lt;/a&gt; (Nasdaq: LXEO), a clinical stage genetic medicine company dedicated to pioneering</description>
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   <title>Lexeo Therapeutics Announces Regulatory Update and Registrational Trial Design for LX2006 Gene Therapy in Friedreich Ataxia</title>
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   <title>Lexeo Therapeutics Announces Regulatory Update and Registrational Trial Design for LX2006 Gene Therapy in Friedreich Ataxia</title>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;SUNRISE-FA 2 study parameters include LVMI primary endpoint, 6-month topline efficacy analysis, inclusion criteria focused on abnormal baseline LVMI and open-label trial design &lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;BLA supportive manufacturing strategy includes flexible process validation, including reduced PPQ manufacturing batches&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;SUNRISE-FA 2 initiation on track for Q2 2026, with first patient expected to be enrolled by end of June&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Company to host webcast today at 8:00 AM ET&lt;/em&gt;&lt;/p&gt;  &lt;p&gt;NEW YORK, June  15, 2026  (GLOBE NEWSWIRE) -- &lt;a target=&quot;_blank&quot; href=&quot;https://www.globenewswire.com/Tracker?data=yCPeaIqvIQE16A5goRU48E30GNmuTS7GfVEZFB9gXaQ_PwpAhj14vHEIKg1y7a0p0MHXpBx-Jj_95AVdjAaXSOC6MDAtYJmLahXQwifEovk=&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;Lexeo Therapeutics, Inc.&lt;/a&gt; (Nasdaq: LXEO), a clinical stage genetic medicine company dedicated to pioneering</description>
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   <title>Lexeo Therapeutics Announces Regulatory Update and Registrational Trial Design for LX2006 Gene Therapy in Friedreich Ataxia</title>
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   <title>Lexeo Therapeutics Announces Regulatory Update and Registrational Trial Design for LX2006 Gene Therapy in Friedreich Ataxia</title>
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