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   <title>H.C. Wainwright Reiterates Buy Rating on Opus Genetics (IRD)</title>
   <link>http://www.streetinsider.com/Analyst+Comments/H.C.+Wainwright+Reiterates+Buy+Rating+on+Opus+Genetics+%28IRD%29/26142221.html</link>
   <description>&lt;p&gt;H.C. Wainwright analyst Matthew Caufield reiterated a Buy rating and $8.00 price target on Opus Genetics (NASDAQ: IRD).&lt;/p&gt;&lt;p&gt;The analyst commented: &quot;The company continues advancement across its inherited retinal disease (IRD) platform demonstrating positive initial datasets: (i) OPGx-LCA5 for treating LCA5-related mutations; and (ii) OPGx-BEST1 for treating BEST1-related retinal degeneration. Moreover, the company maintains development for preclinical IRD gene therapies targeting RHO, CNGB1, RDH12-LCA, and NMNAT1, which we presently view as upside. We highlight the preclinical pipeline builds on additional clinical development plans for OPGx-MERTK for MERTK-related retinitis pigmentosa (RP), a disease which otherwise leads to progressive vision loss and subsequent</description>
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   <title>Form  8-K        Opus Genetics, Inc.       For: Mar 10</title>
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   <pubDate>Tue, 10 Mar 2026 07:17:00 -0400</pubDate>
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   <title>Form  8-K        Opus Genetics, Inc.       For: Mar 10</title>
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   <title>Opus Genetics Announces Financial Results for Full Year 2025 and Provides Corporate Update</title>
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&lt;p align=&quot;center&quot;&gt;- Favorable early safety and initial efficacy data from BEST1 program highlighted at premier gathering of global retinal experts with additional data expected mid-year 2026 -&lt;/p&gt;    &lt;p align=&quot;center&quot;&gt;- Reauthorization of FDA’s Rare Pediatric Disease Priority Review Voucher (PRV) program provides opportunity for Opus’ deep pipeline in rare inherited retinal diseases -&lt;br/&gt;&lt;br/&gt;- FDA Prescription Drug User Fee Act (PDUFA) date in October 2026 for Phentolamine Ophthalmic Solution 0.75% for the treatment of presbyopia -&lt;br/&gt;&lt;br/&gt;- Funding from prominent healthcare investors expected to extend cash runway into 2028 -&lt;/p&gt;    &lt;p&gt;RESEARCH TRIANGLE PARK, N.C., March  10,</description>
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   <title>Opus Genetics Announces Financial Results for Full Year 2025 and Provides Corporate Update</title>
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&lt;p align=&quot;center&quot;&gt;- Favorable early safety and initial efficacy data from BEST1 program highlighted at premier gathering of global retinal experts with additional data expected mid-year 2026 -&lt;/p&gt;    &lt;p align=&quot;center&quot;&gt;- Reauthorization of FDA’s Rare Pediatric Disease Priority Review Voucher (PRV) program provides opportunity for Opus’ deep pipeline in rare inherited retinal diseases -&lt;br/&gt;&lt;br/&gt;- FDA Prescription Drug User Fee Act (PDUFA) date in October 2026 for Phentolamine Ophthalmic Solution 0.75% for the treatment of presbyopia -&lt;br/&gt;&lt;br/&gt;- Funding from prominent healthcare investors expected to extend cash runway into 2028 -&lt;/p&gt;    &lt;p&gt;RESEARCH TRIANGLE PARK, N.C., March  10,</description>
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   <title>Opus Genetics Announces Financial Results for Full Year 2025 and Provides Corporate Update</title>
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&lt;p align=&quot;center&quot;&gt;- Favorable early safety and initial efficacy data from BEST1 program highlighted at premier gathering of global retinal experts with additional data expected mid-year 2026 -&lt;/p&gt;    &lt;p align=&quot;center&quot;&gt;- Reauthorization of FDA’s Rare Pediatric Disease Priority Review Voucher (PRV) program provides opportunity for Opus’ deep pipeline in rare inherited retinal diseases -&lt;br/&gt;&lt;br/&gt;- FDA Prescription Drug User Fee Act (PDUFA) date in October 2026 for Phentolamine Ophthalmic Solution 0.75% for the treatment of presbyopia -&lt;br/&gt;&lt;br/&gt;- Funding from prominent healthcare investors expected to extend cash runway into 2028 -&lt;/p&gt;    &lt;p&gt;RESEARCH TRIANGLE PARK, N.C., March  10,</description>
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   <title>Opus Genetics Announces Financial Results for Full Year 2025 and Provides Corporate Update</title>
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   <title>Opus Genetics Announces Financial Results for Full Year 2025 and Provides Corporate Update</title>
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&lt;p align=&quot;center&quot;&gt;- Favorable early safety and initial efficacy data from BEST1 program highlighted at premier gathering of global retinal experts with additional data expected mid-year 2026 -&lt;/p&gt;    &lt;p align=&quot;center&quot;&gt;- Reauthorization of FDA’s Rare Pediatric Disease Priority Review Voucher (PRV) program provides opportunity for Opus’ deep pipeline in rare inherited retinal diseases -&lt;br/&gt;&lt;br/&gt;- FDA Prescription Drug User Fee Act (PDUFA) date in October 2026 for Phentolamine Ophthalmic Solution 0.75% for the treatment of presbyopia -&lt;br/&gt;&lt;br/&gt;- Funding from prominent healthcare investors expected to extend cash runway into 2028 -&lt;/p&gt;    &lt;p&gt;RESEARCH TRIANGLE PARK, N.C., March  10,</description>
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&lt;p align=&quot;center&quot;&gt;- Favorable early safety and initial efficacy data from BEST1 program highlighted at premier gathering of global retinal experts with additional data expected mid-year 2026 -&lt;/p&gt;    &lt;p align=&quot;center&quot;&gt;- Reauthorization of FDA’s Rare Pediatric Disease Priority Review Voucher (PRV) program provides opportunity for Opus’ deep pipeline in rare inherited retinal diseases -&lt;br/&gt;&lt;br/&gt;- FDA Prescription Drug User Fee Act (PDUFA) date in October 2026 for Phentolamine Ophthalmic Solution 0.75% for the treatment of presbyopia -&lt;br/&gt;&lt;br/&gt;- Funding from prominent healthcare investors expected to extend cash runway into 2028 -&lt;/p&gt;    &lt;p&gt;RESEARCH TRIANGLE PARK, N.C., March  10,</description>
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   <title>Opus Genetics Announces Financial Results for Full Year 2025 and Provides Corporate Update</title>
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