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   <title>Capricor Therapeutics (CAPR) Reiterated at Overweight by Cantor Fitzgerald </title>
   <link>http://www.streetinsider.com/Analyst+Comments/Capricor+Therapeutics+%28CAPR%29+Reiterated+at+Overweight+by+Cantor+Fitzgerald+/26770977.html</link>
   <description>&lt;p&gt;Cantor Fitzgerald analyst Kristen Kluska reiterated an Overweight rating and $62.00 price target on Capricor Therapeutics (NASDAQ: CAPR).&lt;/p&gt;&lt;p&gt;The analyst commented, &quot;Why meet? This could serve as one of the first Fireside Chats and chances to meet with management after the PDUFA for deramiocel (cardiosphere-derived cell therapy) for DMD (severe muscle weakness and wasting condition) on August 22nd. Investors can digest the FDA decision at length with the company, as well as hear what the latest is related to the litigation with NS Pharma (NC). Where we'll differentiate: Our expectation at this time is an approval, and we will be able</description>
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   <pubDate>Wed, 15 Jul 2026 07:48:02 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">CAPR</category>
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   <title>Form  8-K        CAPRICOR THERAPEUTICS,    For: Jul 09</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++8-K++++++++CAPRICOR+THERAPEUTICS%2C++++For%3A+Jul+09/26768985.html</link>
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   <pubDate>Tue, 14 Jul 2026 17:06:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">CAPR</category>
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   <title>Form  8-K        CAPRICOR THERAPEUTICS,    For: Jul 09</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++8-K++++++++CAPRICOR+THERAPEUTICS%2C++++For%3A+Jul+09/26768985.html</link>
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   <pubDate>Tue, 14 Jul 2026 17:06:00 -0400</pubDate>
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   <title>Capricor Therapeutics (CAPR) Reiterates Overweight Rating Ahead of Upcoming PDUFA </title>
   <link>http://www.streetinsider.com/Analyst+Comments/Capricor+Therapeutics+%28CAPR%29+Reiterates+Overweight+Rating+Ahead+of+Upcoming+PDUFA+/26738299.html</link>
   <description>&lt;p&gt;Cantor Fitzgerald analyst Kristen Kluska reiterated an Overweight rating and $62.00 price target on Capricor Therapeutics (NASDAQ: CAPR).&lt;/p&gt;&lt;p&gt;The analyst commented, &quot;CAPR has an upcoming regulatory catalyst: PDUFA for deramiocel (CAP-1002; cardiosphere-derived cell therapy) in DMD on 8/22/26. The upcoming PDUFA has become an even greater focus for investors following the recent scheduling of an AdCom on 7/29/26 and the ongoing litigation with NS Pharma (NC). Against this backdrop, we are publishing our latest thoughts on the stock and why we believe deramiocel's data package is compelling and well positioned to support approval. We'd be buyers of the stock right now,</description>
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   <pubDate>Tue, 07 Jul 2026 07:18:44 -0400</pubDate>
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   <title>Form  4          CAPRICOR THERAPEUTICS,    For: Jun 25  Filed by: Bergmann Anthony</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++4++++++++++CAPRICOR+THERAPEUTICS%2C++++For%3A+Jun+25++Filed+by%3A+Bergmann+Anthony/26708137.html</link>
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   <pubDate>Mon, 29 Jun 2026 21:30:00 -0400</pubDate>
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   <pubDate>Mon, 29 Jun 2026 21:30:00 -0400</pubDate>
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   <title>Form  4          CAPRICOR THERAPEUTICS,    For: Jun 25  Filed by: Krasney Karen</title>
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   <title>Form  4          CAPRICOR THERAPEUTICS,    For: Jun 25  Filed by: Krasney Karen</title>
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   <pubDate>Mon, 29 Jun 2026 21:30:00 -0400</pubDate>
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   <title>Capricor Therapeutics (CAPR) 4500 contracts of August 30 calls and 2900 contracts of August 20 puts trade</title>
   <link>http://www.streetinsider.com/Options/Capricor+Therapeutics+%28CAPR%29+4500+contracts+of+August+30+calls+and+2900+contracts+of+August+20+puts+trade/26701188.html</link>
   <description>&lt;p&gt;Capricor Therapeutics (NASDAQ: CAPR) 30-day option implied volatility is at 131; compared to its 52-week range of 66 to 422. Call put ratio 1 1call to 1 put with a focus on 4500 contracts of August 30 calls and 2900 contracts of August 20 puts.&lt;/p&gt;</description>
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   <pubDate>Mon, 29 Jun 2026 05:58:53 -0400</pubDate>
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   <title>Form  8-K        CAPRICOR THERAPEUTICS,    For: Jun 26</title>
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   <pubDate>Fri, 26 Jun 2026 17:15:00 -0400</pubDate>
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   <title>Form  8-K        CAPRICOR THERAPEUTICS,    For: Jun 26</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++8-K++++++++CAPRICOR+THERAPEUTICS%2C++++For%3A+Jun+26/26699912.html</link>
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   <pubDate>Fri, 26 Jun 2026 17:15:00 -0400</pubDate>
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   <title>FDA to review Capricor's DMD therapy at July advisory meeting</title>
   <link>http://www.streetinsider.com/FDA/FDA+to+review+Capricor%27s+DMD+therapy+at+July+advisory+meeting/26695914.html</link>
   <description>

&lt;p&gt;Capricor Therapeutics (NASDAQ: CAPR) announced that the FDA's Cellular, Tissue, and Gene Therapies Advisory Committee (CTGTAC) is scheduled to meet July 29, 2026, to discuss the company's Biologics License Application (BLA) for deramiocel, an investigational cell therapy for Duchenne muscular dystrophy (DMD).&lt;/p&gt;

&lt;p&gt;The BLA carries a Prescription Drug User Fee Act (PDUFA) target action date of August 22, 2026. The advisory committee meeting will be available for live streaming.&lt;/p&gt;

&lt;p&gt;The BLA is supported by data from the Phase 2 HOPE-2 trial, long-term outcomes from the HOPE-2-OLE trial, and results from the Phase 3 HOPE-3 trial. According to the company, HOPE-3 achieved statistical</description>
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   <title>FDA to review Capricor's DMD therapy at July advisory meeting</title>
   <link>http://www.streetinsider.com/FDA/FDA+to+review+Capricor%27s+DMD+therapy+at+July+advisory+meeting/26695914.html</link>
   <description>

&lt;p&gt;Capricor Therapeutics (NASDAQ: CAPR) announced that the FDA's Cellular, Tissue, and Gene Therapies Advisory Committee (CTGTAC) is scheduled to meet July 29, 2026, to discuss the company's Biologics License Application (BLA) for deramiocel, an investigational cell therapy for Duchenne muscular dystrophy (DMD).&lt;/p&gt;

&lt;p&gt;The BLA carries a Prescription Drug User Fee Act (PDUFA) target action date of August 22, 2026. The advisory committee meeting will be available for live streaming.&lt;/p&gt;

&lt;p&gt;The BLA is supported by data from the Phase 2 HOPE-2 trial, long-term outcomes from the HOPE-2-OLE trial, and results from the Phase 3 HOPE-3 trial. According to the company, HOPE-3 achieved statistical</description>
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   <title>FDA to review Capricor's DMD therapy at July advisory meeting</title>
   <link>http://www.streetinsider.com/FDA/FDA+to+review+Capricor%27s+DMD+therapy+at+July+advisory+meeting/26695914.html</link>
   <description>

&lt;p&gt;Capricor Therapeutics (NASDAQ: CAPR) announced that the FDA's Cellular, Tissue, and Gene Therapies Advisory Committee (CTGTAC) is scheduled to meet July 29, 2026, to discuss the company's Biologics License Application (BLA) for deramiocel, an investigational cell therapy for Duchenne muscular dystrophy (DMD).&lt;/p&gt;

&lt;p&gt;The BLA carries a Prescription Drug User Fee Act (PDUFA) target action date of August 22, 2026. The advisory committee meeting will be available for live streaming.&lt;/p&gt;

&lt;p&gt;The BLA is supported by data from the Phase 2 HOPE-2 trial, long-term outcomes from the HOPE-2-OLE trial, and results from the Phase 3 HOPE-3 trial. According to the company, HOPE-3 achieved statistical</description>
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   <title>FDA to review Capricor's DMD therapy at July advisory meeting</title>
   <link>http://www.streetinsider.com/FDA/FDA+to+review+Capricor%27s+DMD+therapy+at+July+advisory+meeting/26695914.html</link>
   <description>

&lt;p&gt;Capricor Therapeutics (NASDAQ: CAPR) announced that the FDA's Cellular, Tissue, and Gene Therapies Advisory Committee (CTGTAC) is scheduled to meet July 29, 2026, to discuss the company's Biologics License Application (BLA) for deramiocel, an investigational cell therapy for Duchenne muscular dystrophy (DMD).&lt;/p&gt;

&lt;p&gt;The BLA carries a Prescription Drug User Fee Act (PDUFA) target action date of August 22, 2026. The advisory committee meeting will be available for live streaming.&lt;/p&gt;

&lt;p&gt;The BLA is supported by data from the Phase 2 HOPE-2 trial, long-term outcomes from the HOPE-2-OLE trial, and results from the Phase 3 HOPE-3 trial. According to the company, HOPE-3 achieved statistical</description>
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   <title>FDA to review Capricor's DMD therapy at July advisory meeting</title>
   <link>http://www.streetinsider.com/FDA/FDA+to+review+Capricor%27s+DMD+therapy+at+July+advisory+meeting/26695914.html</link>
   <description>

&lt;p&gt;Capricor Therapeutics (NASDAQ: CAPR) announced that the FDA's Cellular, Tissue, and Gene Therapies Advisory Committee (CTGTAC) is scheduled to meet July 29, 2026, to discuss the company's Biologics License Application (BLA) for deramiocel, an investigational cell therapy for Duchenne muscular dystrophy (DMD).&lt;/p&gt;

&lt;p&gt;The BLA carries a Prescription Drug User Fee Act (PDUFA) target action date of August 22, 2026. The advisory committee meeting will be available for live streaming.&lt;/p&gt;

&lt;p&gt;The BLA is supported by data from the Phase 2 HOPE-2 trial, long-term outcomes from the HOPE-2-OLE trial, and results from the Phase 3 HOPE-3 trial. According to the company, HOPE-3 achieved statistical</description>
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   <title>FDA to review Capricor's DMD therapy at July advisory meeting</title>
   <link>http://www.streetinsider.com/FDA/FDA+to+review+Capricor%27s+DMD+therapy+at+July+advisory+meeting/26695914.html</link>
   <description>

&lt;p&gt;Capricor Therapeutics (NASDAQ: CAPR) announced that the FDA's Cellular, Tissue, and Gene Therapies Advisory Committee (CTGTAC) is scheduled to meet July 29, 2026, to discuss the company's Biologics License Application (BLA) for deramiocel, an investigational cell therapy for Duchenne muscular dystrophy (DMD).&lt;/p&gt;

&lt;p&gt;The BLA carries a Prescription Drug User Fee Act (PDUFA) target action date of August 22, 2026. The advisory committee meeting will be available for live streaming.&lt;/p&gt;

&lt;p&gt;The BLA is supported by data from the Phase 2 HOPE-2 trial, long-term outcomes from the HOPE-2-OLE trial, and results from the Phase 3 HOPE-3 trial. According to the company, HOPE-3 achieved statistical</description>
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   <title>FDA to review Capricor's DMD therapy at July advisory meeting</title>
   <link>http://www.streetinsider.com/FDA/FDA+to+review+Capricor%27s+DMD+therapy+at+July+advisory+meeting/26695914.html</link>
   <description>

&lt;p&gt;Capricor Therapeutics (NASDAQ: CAPR) announced that the FDA's Cellular, Tissue, and Gene Therapies Advisory Committee (CTGTAC) is scheduled to meet July 29, 2026, to discuss the company's Biologics License Application (BLA) for deramiocel, an investigational cell therapy for Duchenne muscular dystrophy (DMD).&lt;/p&gt;

&lt;p&gt;The BLA carries a Prescription Drug User Fee Act (PDUFA) target action date of August 22, 2026. The advisory committee meeting will be available for live streaming.&lt;/p&gt;

&lt;p&gt;The BLA is supported by data from the Phase 2 HOPE-2 trial, long-term outcomes from the HOPE-2-OLE trial, and results from the Phase 3 HOPE-3 trial. According to the company, HOPE-3 achieved statistical</description>
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   <title>FDA to review Capricor's DMD therapy at July advisory meeting</title>
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&lt;p&gt;Capricor Therapeutics (NASDAQ: CAPR) announced that the FDA's Cellular, Tissue, and Gene Therapies Advisory Committee (CTGTAC) is scheduled to meet July 29, 2026, to discuss the company's Biologics License Application (BLA) for deramiocel, an investigational cell therapy for Duchenne muscular dystrophy (DMD).&lt;/p&gt;

&lt;p&gt;The BLA carries a Prescription Drug User Fee Act (PDUFA) target action date of August 22, 2026. The advisory committee meeting will be available for live streaming.&lt;/p&gt;

&lt;p&gt;The BLA is supported by data from the Phase 2 HOPE-2 trial, long-term outcomes from the HOPE-2-OLE trial, and results from the Phase 3 HOPE-3 trial. According to the company, HOPE-3 achieved statistical</description>
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   <title>Capricor Therapeutics Announces FDA Advisory Committee Meeting to Review BLA for Deramiocel for the Treatment of Duchenne Muscular Dystrophy</title>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;–Advisory Committee meeting scheduled for July 29, 2026–&lt;/em&gt;&lt;br/&gt;&lt;em&gt;–Company&amp;apos;s Biologics License Application on track with PDUFA target action date of August 22, 2026–&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;SAN DIEGO, June  26, 2026  (GLOBE NEWSWIRE) -- &lt;a target=&quot;_blank&quot; href=&quot;https://www.globenewswire.com/Tracker?data=AZcayUcDGZHovCSDoZdE7qPvZOqELzOSExPNopIqX1qKQQKSEWJRQ4LLvXP6FsP1omF3c_iOv4TkY_Iif9If9xqEfRhfp7sL19uZ2dNdLmdJAow914iFJTObmSM2ROKqXwgSbkmsZptlnShlYy8KWryZWI7hUzHPR4g5hj_x1vTdQLCyyczizUgf09B5kLmANdi8dutE9USComoAVelaQlLdJ304Gznwpab0wDkuj27J1BPmTshgs5AojjZEnOzoyDZbT8JzY_YiQgTlBqYO5oDfUoQzChMFa5M20N-AzGfZxXo2Uq28iMS8cw0lat82RZ0qjD72Px58vdVEm_qAmrB9XbiaK4V6miEUQZ78QvhiVQP4zW-CZxm4n8MsX7KGYV5LWOaQWan0BP1RmhAl_9XTBY94HN34cpcV2YVrIiVG3KnVsHPifyjBrwCLjUKE&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;Capricor Therapeutics&lt;/a&gt; (NASDAQ: CAPR), a biotechnology company developing transformative cell and exosome-based therapeutics for rare diseases, today announced that the Cellular, Tissue, and Gene Therapies Advisory Committee (CTGTAC) of the U.S. Food and Drug Administration (FDA) is planning to convene an advisory committee meeting to discuss the Company&amp;apos;s Biologics License Application (BLA) seeking approval of Deramiocel, an investigational cell therapy for</description>
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   <title>Capricor Therapeutics Announces FDA Advisory Committee Meeting to Review BLA for Deramiocel for the Treatment of Duchenne Muscular Dystrophy</title>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;–Advisory Committee meeting scheduled for July 29, 2026–&lt;/em&gt;&lt;br/&gt;&lt;em&gt;–Company&amp;apos;s Biologics License Application on track with PDUFA target action date of August 22, 2026–&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;SAN DIEGO, June  26, 2026  (GLOBE NEWSWIRE) -- &lt;a target=&quot;_blank&quot; href=&quot;https://www.globenewswire.com/Tracker?data=AZcayUcDGZHovCSDoZdE7qPvZOqELzOSExPNopIqX1qKQQKSEWJRQ4LLvXP6FsP1omF3c_iOv4TkY_Iif9If9xqEfRhfp7sL19uZ2dNdLmdJAow914iFJTObmSM2ROKqXwgSbkmsZptlnShlYy8KWryZWI7hUzHPR4g5hj_x1vTdQLCyyczizUgf09B5kLmANdi8dutE9USComoAVelaQlLdJ304Gznwpab0wDkuj27J1BPmTshgs5AojjZEnOzoyDZbT8JzY_YiQgTlBqYO5oDfUoQzChMFa5M20N-AzGfZxXo2Uq28iMS8cw0lat82RZ0qjD72Px58vdVEm_qAmrB9XbiaK4V6miEUQZ78QvhiVQP4zW-CZxm4n8MsX7KGYV5LWOaQWan0BP1RmhAl_9XTBY94HN34cpcV2YVrIiVG3KnVsHPifyjBrwCLjUKE&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;Capricor Therapeutics&lt;/a&gt; (NASDAQ: CAPR), a biotechnology company developing transformative cell and exosome-based therapeutics for rare diseases, today announced that the Cellular, Tissue, and Gene Therapies Advisory Committee (CTGTAC) of the U.S. Food and Drug Administration (FDA) is planning to convene an advisory committee meeting to discuss the Company&amp;apos;s Biologics License Application (BLA) seeking approval of Deramiocel, an investigational cell therapy for</description>
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   <title>Capricor Therapeutics Announces FDA Advisory Committee Meeting to Review BLA for Deramiocel for the Treatment of Duchenne Muscular Dystrophy</title>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;–Advisory Committee meeting scheduled for July 29, 2026–&lt;/em&gt;&lt;br/&gt;&lt;em&gt;–Company&amp;apos;s Biologics License Application on track with PDUFA target action date of August 22, 2026–&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;SAN DIEGO, June  26, 2026  (GLOBE NEWSWIRE) -- &lt;a target=&quot;_blank&quot; href=&quot;https://www.globenewswire.com/Tracker?data=AZcayUcDGZHovCSDoZdE7qPvZOqELzOSExPNopIqX1qKQQKSEWJRQ4LLvXP6FsP1omF3c_iOv4TkY_Iif9If9xqEfRhfp7sL19uZ2dNdLmdJAow914iFJTObmSM2ROKqXwgSbkmsZptlnShlYy8KWryZWI7hUzHPR4g5hj_x1vTdQLCyyczizUgf09B5kLmANdi8dutE9USComoAVelaQlLdJ304Gznwpab0wDkuj27J1BPmTshgs5AojjZEnOzoyDZbT8JzY_YiQgTlBqYO5oDfUoQzChMFa5M20N-AzGfZxXo2Uq28iMS8cw0lat82RZ0qjD72Px58vdVEm_qAmrB9XbiaK4V6miEUQZ78QvhiVQP4zW-CZxm4n8MsX7KGYV5LWOaQWan0BP1RmhAl_9XTBY94HN34cpcV2YVrIiVG3KnVsHPifyjBrwCLjUKE&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;Capricor Therapeutics&lt;/a&gt; (NASDAQ: CAPR), a biotechnology company developing transformative cell and exosome-based therapeutics for rare diseases, today announced that the Cellular, Tissue, and Gene Therapies Advisory Committee (CTGTAC) of the U.S. Food and Drug Administration (FDA) is planning to convene an advisory committee meeting to discuss the Company&amp;apos;s Biologics License Application (BLA) seeking approval of Deramiocel, an investigational cell therapy for</description>
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   <title>Capricor Therapeutics Announces FDA Advisory Committee Meeting to Review BLA for Deramiocel for the Treatment of Duchenne Muscular Dystrophy</title>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;–Advisory Committee meeting scheduled for July 29, 2026–&lt;/em&gt;&lt;br/&gt;&lt;em&gt;–Company&amp;apos;s Biologics License Application on track with PDUFA target action date of August 22, 2026–&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;SAN DIEGO, June  26, 2026  (GLOBE NEWSWIRE) -- &lt;a target=&quot;_blank&quot; href=&quot;https://www.globenewswire.com/Tracker?data=AZcayUcDGZHovCSDoZdE7qPvZOqELzOSExPNopIqX1qKQQKSEWJRQ4LLvXP6FsP1omF3c_iOv4TkY_Iif9If9xqEfRhfp7sL19uZ2dNdLmdJAow914iFJTObmSM2ROKqXwgSbkmsZptlnShlYy8KWryZWI7hUzHPR4g5hj_x1vTdQLCyyczizUgf09B5kLmANdi8dutE9USComoAVelaQlLdJ304Gznwpab0wDkuj27J1BPmTshgs5AojjZEnOzoyDZbT8JzY_YiQgTlBqYO5oDfUoQzChMFa5M20N-AzGfZxXo2Uq28iMS8cw0lat82RZ0qjD72Px58vdVEm_qAmrB9XbiaK4V6miEUQZ78QvhiVQP4zW-CZxm4n8MsX7KGYV5LWOaQWan0BP1RmhAl_9XTBY94HN34cpcV2YVrIiVG3KnVsHPifyjBrwCLjUKE&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;Capricor Therapeutics&lt;/a&gt; (NASDAQ: CAPR), a biotechnology company developing transformative cell and exosome-based therapeutics for rare diseases, today announced that the Cellular, Tissue, and Gene Therapies Advisory Committee (CTGTAC) of the U.S. Food and Drug Administration (FDA) is planning to convene an advisory committee meeting to discuss the Company&amp;apos;s Biologics License Application (BLA) seeking approval of Deramiocel, an investigational cell therapy for</description>
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   <title>Capricor Therapeutics Announces FDA Advisory Committee Meeting to Review BLA for Deramiocel for the Treatment of Duchenne Muscular Dystrophy</title>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;–Advisory Committee meeting scheduled for July 29, 2026–&lt;/em&gt;&lt;br/&gt;&lt;em&gt;–Company&amp;apos;s Biologics License Application on track with PDUFA target action date of August 22, 2026–&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;SAN DIEGO, June  26, 2026  (GLOBE NEWSWIRE) -- &lt;a target=&quot;_blank&quot; href=&quot;https://www.globenewswire.com/Tracker?data=AZcayUcDGZHovCSDoZdE7qPvZOqELzOSExPNopIqX1qKQQKSEWJRQ4LLvXP6FsP1omF3c_iOv4TkY_Iif9If9xqEfRhfp7sL19uZ2dNdLmdJAow914iFJTObmSM2ROKqXwgSbkmsZptlnShlYy8KWryZWI7hUzHPR4g5hj_x1vTdQLCyyczizUgf09B5kLmANdi8dutE9USComoAVelaQlLdJ304Gznwpab0wDkuj27J1BPmTshgs5AojjZEnOzoyDZbT8JzY_YiQgTlBqYO5oDfUoQzChMFa5M20N-AzGfZxXo2Uq28iMS8cw0lat82RZ0qjD72Px58vdVEm_qAmrB9XbiaK4V6miEUQZ78QvhiVQP4zW-CZxm4n8MsX7KGYV5LWOaQWan0BP1RmhAl_9XTBY94HN34cpcV2YVrIiVG3KnVsHPifyjBrwCLjUKE&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;Capricor Therapeutics&lt;/a&gt; (NASDAQ: CAPR), a biotechnology company developing transformative cell and exosome-based therapeutics for rare diseases, today announced that the Cellular, Tissue, and Gene Therapies Advisory Committee (CTGTAC) of the U.S. Food and Drug Administration (FDA) is planning to convene an advisory committee meeting to discuss the Company&amp;apos;s Biologics License Application (BLA) seeking approval of Deramiocel, an investigational cell therapy for</description>
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   <title>Capricor Therapeutics Announces FDA Advisory Committee Meeting to Review BLA for Deramiocel for the Treatment of Duchenne Muscular Dystrophy</title>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;–Advisory Committee meeting scheduled for July 29, 2026–&lt;/em&gt;&lt;br/&gt;&lt;em&gt;–Company&amp;apos;s Biologics License Application on track with PDUFA target action date of August 22, 2026–&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;SAN DIEGO, June  26, 2026  (GLOBE NEWSWIRE) -- &lt;a target=&quot;_blank&quot; href=&quot;https://www.globenewswire.com/Tracker?data=AZcayUcDGZHovCSDoZdE7qPvZOqELzOSExPNopIqX1qKQQKSEWJRQ4LLvXP6FsP1omF3c_iOv4TkY_Iif9If9xqEfRhfp7sL19uZ2dNdLmdJAow914iFJTObmSM2ROKqXwgSbkmsZptlnShlYy8KWryZWI7hUzHPR4g5hj_x1vTdQLCyyczizUgf09B5kLmANdi8dutE9USComoAVelaQlLdJ304Gznwpab0wDkuj27J1BPmTshgs5AojjZEnOzoyDZbT8JzY_YiQgTlBqYO5oDfUoQzChMFa5M20N-AzGfZxXo2Uq28iMS8cw0lat82RZ0qjD72Px58vdVEm_qAmrB9XbiaK4V6miEUQZ78QvhiVQP4zW-CZxm4n8MsX7KGYV5LWOaQWan0BP1RmhAl_9XTBY94HN34cpcV2YVrIiVG3KnVsHPifyjBrwCLjUKE&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;Capricor Therapeutics&lt;/a&gt; (NASDAQ: CAPR), a biotechnology company developing transformative cell and exosome-based therapeutics for rare diseases, today announced that the Cellular, Tissue, and Gene Therapies Advisory Committee (CTGTAC) of the U.S. Food and Drug Administration (FDA) is planning to convene an advisory committee meeting to discuss the Company&amp;apos;s Biologics License Application (BLA) seeking approval of Deramiocel, an investigational cell therapy for</description>
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