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   <title>Form  6-K        Enlivex Ltd.              For: Jul 30</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++6-K++++++++Enlivex+Ltd.++++++++++++++For%3A+Jul+30/26839277.html</link>
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   <pubDate>Thu, 30 Jul 2026 08:02:00 -0400</pubDate>
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   <title>Form  6-K        Enlivex Ltd.              For: Jul 30</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++6-K++++++++Enlivex+Ltd.++++++++++++++For%3A+Jul+30/26839277.html</link>
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   <pubDate>Thu, 30 Jul 2026 08:02:00 -0400</pubDate>
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   <title>Form  6-K        Enlivex Ltd.              For: Jul 29</title>
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   <pubDate>Wed, 29 Jul 2026 08:02:00 -0400</pubDate>
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   <title>Form  6-K        Enlivex Ltd.              For: Jul 29</title>
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   <pubDate>Wed, 29 Jul 2026 08:02:00 -0400</pubDate>
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   <title>Form  6-K        Enlivex Ltd.              For: Jul 28</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++6-K++++++++Enlivex+Ltd.++++++++++++++For%3A+Jul+28/26827786.html</link>
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   <pubDate>Tue, 28 Jul 2026 16:40:00 -0400</pubDate>
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   <title>Form  6-K        Enlivex Ltd.              For: Jul 28</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++6-K++++++++Enlivex+Ltd.++++++++++++++For%3A+Jul+28/26827786.html</link>
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   <pubDate>Tue, 28 Jul 2026 16:40:00 -0400</pubDate>
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   <title>Enlivex plans $400M private placement tied to crypto tokens</title>
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   <description>&lt;p&gt;Enlivex Ltd. (NASDAQ: ENLV) has entered into a securities purchase agreement with a single institutional investor for a private placement of $400 million in ordinary shares, according to a company statement.&lt;/p&gt;&lt;p&gt;Shares are priced at $5.00 each for subscriptions funded in U.S. dollars, USDT, or USD Coin, and at $6.00 per share for subscriptions funded in RAIN tokens. The $5.00 price represents a 17.4% premium and the $6.00 price a 40.8% premium to the closing share price on July 27, 2026. The investor has elected to fund the purchase using RAIN tokens, though that election may be changed before closing.&lt;/p&gt;&lt;p&gt;The agreement</description>
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   <pubDate>Tue, 28 Jul 2026 08:02:48 -0400</pubDate>
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   <title>Enlivex plans $400M private placement tied to crypto tokens</title>
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   <description>&lt;p&gt;Enlivex Ltd. (NASDAQ: ENLV) has entered into a securities purchase agreement with a single institutional investor for a private placement of $400 million in ordinary shares, according to a company statement.&lt;/p&gt;&lt;p&gt;Shares are priced at $5.00 each for subscriptions funded in U.S. dollars, USDT, or USD Coin, and at $6.00 per share for subscriptions funded in RAIN tokens. The $5.00 price represents a 17.4% premium and the $6.00 price a 40.8% premium to the closing share price on July 27, 2026. The investor has elected to fund the purchase using RAIN tokens, though that election may be changed before closing.&lt;/p&gt;&lt;p&gt;The agreement</description>
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   <pubDate>Tue, 28 Jul 2026 08:02:48 -0400</pubDate>
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   <title>Form  6-K        Enlivex Ltd.              For: Jul 28</title>
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   <pubDate>Tue, 28 Jul 2026 08:02:00 -0400</pubDate>
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   <title>Form  6-K        Enlivex Ltd.              For: Jul 28</title>
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   <pubDate>Tue, 28 Jul 2026 08:02:00 -0400</pubDate>
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   <title>Form  6-K        Enlivex Ltd.              For: Jul 20</title>
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   <pubDate>Mon, 20 Jul 2026 08:02:00 -0400</pubDate>
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   <title>Form  6-K        Enlivex Ltd.              For: Jul 20</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++6-K++++++++Enlivex+Ltd.++++++++++++++For%3A+Jul+20/26787346.html</link>
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   <pubDate>Mon, 20 Jul 2026 08:02:00 -0400</pubDate>
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   <title>FDA grants RMAT designation to Enlivex's Allocetra for knee OA</title>
   <link>http://www.streetinsider.com/Corporate+News/FDA+grants+RMAT+designation+to+Enlivex%27s+Allocetra+for+knee+OA/26760107.html</link>
   <description>&lt;p&gt;Enlivex Ltd. (NASDAQ: ENLV) announced that the U.S. Food and Drug Administration has granted Regenerative Medicine Advanced Therapy (RMAT) designation to its clinical-stage immunotherapy Allocetra™ for the treatment of age-related symptomatic knee osteoarthritis in patients aged 64 and older.&lt;/p&gt;&lt;p&gt;The FDA based the designation on clinical evidence from a completed Phase I/IIa trial, in which patients with primary age-related knee osteoarthritis treated with Allocetra™ showed statistically significant and clinically meaningful improvements in knee pain and physical function compared with placebo, with efficacy that was durable through at least six months.&lt;/p&gt;&lt;p&gt;RMAT designation makes a therapy potentially eligible for accelerated approval, priority review,</description>
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   <pubDate>Mon, 13 Jul 2026 08:01:06 -0400</pubDate>
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   <title>FDA grants RMAT designation to Enlivex's Allocetra for knee OA</title>
   <link>http://www.streetinsider.com/FDA/FDA+grants+RMAT+designation+to+Enlivex%27s+Allocetra+for+knee+OA/26760107.html</link>
   <description>&lt;p&gt;Enlivex Ltd. (NASDAQ: ENLV) announced that the U.S. Food and Drug Administration has granted Regenerative Medicine Advanced Therapy (RMAT) designation to its clinical-stage immunotherapy Allocetra™ for the treatment of age-related symptomatic knee osteoarthritis in patients aged 64 and older.&lt;/p&gt;&lt;p&gt;The FDA based the designation on clinical evidence from a completed Phase I/IIa trial, in which patients with primary age-related knee osteoarthritis treated with Allocetra™ showed statistically significant and clinically meaningful improvements in knee pain and physical function compared with placebo, with efficacy that was durable through at least six months.&lt;/p&gt;&lt;p&gt;RMAT designation makes a therapy potentially eligible for accelerated approval, priority review,</description>
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   <pubDate>Mon, 13 Jul 2026 08:01:06 -0400</pubDate>
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   <title>Enlivex Receives FDA Regenerative Medicine Advanced Therapy (RMAT) Designation for Allocetra™ in Age-Related Knee Osteoarthritis</title>
   <link>http://www.streetinsider.com/Press+Releases/Enlivex+Receives+FDA+Regenerative+Medicine+Advanced+Therapy+%28RMAT%29+Designation+for+Allocetra%E2%84%A2+in+Age-Related+Knee+Osteoarthritis/26760078.html</link>
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&lt;ul&gt;&lt;li&gt;FDA grant of RMAT designation to Allocetra™ reinforces the potential of this program to deliver a meaningful, disease-modifying impact in age-related primary knee osteoarthritis, where patients face declined quality-of-life and limited treatment options.&lt;/li&gt;&lt;li&gt;RMAT designation provides the benefit of intensive, early FDA engagement and guidance for efficient drug development including potential eligibility for accelerated approval, priority review and other opportunities to expedite review and approval.&lt;/li&gt;&lt;/ul&gt;  &lt;p&gt;Nes-Ziona, Israel, July  13, 2026  (GLOBE NEWSWIRE) -- Enlivex Ltd. (Nasdaq: ENLV) (&amp;quot;Enlivex&amp;quot; or the &amp;quot;Company&amp;quot;), a quality longevity company, today announced that the U.S. Food and Drug Administration (FDA) has granted Regenerative</description>
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   <title>Enlivex Receives FDA Regenerative Medicine Advanced Therapy (RMAT) Designation for Allocetra™ in Age-Related Knee Osteoarthritis</title>
   <link>http://www.streetinsider.com/Press+Releases/Enlivex+Receives+FDA+Regenerative+Medicine+Advanced+Therapy+%28RMAT%29+Designation+for+Allocetra%E2%84%A2+in+Age-Related+Knee+Osteoarthritis/26760078.html</link>
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&lt;ul&gt;&lt;li&gt;FDA grant of RMAT designation to Allocetra™ reinforces the potential of this program to deliver a meaningful, disease-modifying impact in age-related primary knee osteoarthritis, where patients face declined quality-of-life and limited treatment options.&lt;/li&gt;&lt;li&gt;RMAT designation provides the benefit of intensive, early FDA engagement and guidance for efficient drug development including potential eligibility for accelerated approval, priority review and other opportunities to expedite review and approval.&lt;/li&gt;&lt;/ul&gt;  &lt;p&gt;Nes-Ziona, Israel, July  13, 2026  (GLOBE NEWSWIRE) -- Enlivex Ltd. (Nasdaq: ENLV) (&amp;quot;Enlivex&amp;quot; or the &amp;quot;Company&amp;quot;), a quality longevity company, today announced that the U.S. Food and Drug Administration (FDA) has granted Regenerative</description>
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   <title>Enlivex Receives FDA Regenerative Medicine Advanced Therapy (RMAT) Designation for Allocetra™ in Age-Related Knee Osteoarthritis</title>
   <link>http://www.streetinsider.com/Press+Releases/Enlivex+Receives+FDA+Regenerative+Medicine+Advanced+Therapy+%28RMAT%29+Designation+for+Allocetra%E2%84%A2+in+Age-Related+Knee+Osteoarthritis/26760078.html</link>
   <description>
&lt;ul&gt;&lt;li&gt;FDA grant of RMAT designation to Allocetra™ reinforces the potential of this program to deliver a meaningful, disease-modifying impact in age-related primary knee osteoarthritis, where patients face declined quality-of-life and limited treatment options.&lt;/li&gt;&lt;li&gt;RMAT designation provides the benefit of intensive, early FDA engagement and guidance for efficient drug development including potential eligibility for accelerated approval, priority review and other opportunities to expedite review and approval.&lt;/li&gt;&lt;/ul&gt;  &lt;p&gt;Nes-Ziona, Israel, July  13, 2026  (GLOBE NEWSWIRE) -- Enlivex Ltd. (Nasdaq: ENLV) (&amp;quot;Enlivex&amp;quot; or the &amp;quot;Company&amp;quot;), a quality longevity company, today announced that the U.S. Food and Drug Administration (FDA) has granted Regenerative</description>
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   <title>Enlivex Receives FDA Regenerative Medicine Advanced Therapy (RMAT) Designation for Allocetra™ in Age-Related Knee Osteoarthritis</title>
   <link>http://www.streetinsider.com/Press+Releases/Enlivex+Receives+FDA+Regenerative+Medicine+Advanced+Therapy+%28RMAT%29+Designation+for+Allocetra%E2%84%A2+in+Age-Related+Knee+Osteoarthritis/26760078.html</link>
   <description>
&lt;ul&gt;&lt;li&gt;FDA grant of RMAT designation to Allocetra™ reinforces the potential of this program to deliver a meaningful, disease-modifying impact in age-related primary knee osteoarthritis, where patients face declined quality-of-life and limited treatment options.&lt;/li&gt;&lt;li&gt;RMAT designation provides the benefit of intensive, early FDA engagement and guidance for efficient drug development including potential eligibility for accelerated approval, priority review and other opportunities to expedite review and approval.&lt;/li&gt;&lt;/ul&gt;  &lt;p&gt;Nes-Ziona, Israel, July  13, 2026  (GLOBE NEWSWIRE) -- Enlivex Ltd. (Nasdaq: ENLV) (&amp;quot;Enlivex&amp;quot; or the &amp;quot;Company&amp;quot;), a quality longevity company, today announced that the U.S. Food and Drug Administration (FDA) has granted Regenerative</description>
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   <title>Enlivex Receives FDA Regenerative Medicine Advanced Therapy (RMAT) Designation for Allocetra™ in Age-Related Knee Osteoarthritis</title>
   <link>http://www.streetinsider.com/Globe+Newswire/Enlivex+Receives+FDA+Regenerative+Medicine+Advanced+Therapy+%28RMAT%29+Designation+for+Allocetra%E2%84%A2+in+Age-Related+Knee+Osteoarthritis/26760078.html</link>
   <description>
&lt;ul&gt;&lt;li&gt;FDA grant of RMAT designation to Allocetra™ reinforces the potential of this program to deliver a meaningful, disease-modifying impact in age-related primary knee osteoarthritis, where patients face declined quality-of-life and limited treatment options.&lt;/li&gt;&lt;li&gt;RMAT designation provides the benefit of intensive, early FDA engagement and guidance for efficient drug development including potential eligibility for accelerated approval, priority review and other opportunities to expedite review and approval.&lt;/li&gt;&lt;/ul&gt;  &lt;p&gt;Nes-Ziona, Israel, July  13, 2026  (GLOBE NEWSWIRE) -- Enlivex Ltd. (Nasdaq: ENLV) (&amp;quot;Enlivex&amp;quot; or the &amp;quot;Company&amp;quot;), a quality longevity company, today announced that the U.S. Food and Drug Administration (FDA) has granted Regenerative</description>
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   <title>Enlivex Receives FDA Regenerative Medicine Advanced Therapy (RMAT) Designation for Allocetra™ in Age-Related Knee Osteoarthritis</title>
   <link>http://www.streetinsider.com/Globe+Newswire/Enlivex+Receives+FDA+Regenerative+Medicine+Advanced+Therapy+%28RMAT%29+Designation+for+Allocetra%E2%84%A2+in+Age-Related+Knee+Osteoarthritis/26760078.html</link>
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&lt;ul&gt;&lt;li&gt;FDA grant of RMAT designation to Allocetra™ reinforces the potential of this program to deliver a meaningful, disease-modifying impact in age-related primary knee osteoarthritis, where patients face declined quality-of-life and limited treatment options.&lt;/li&gt;&lt;li&gt;RMAT designation provides the benefit of intensive, early FDA engagement and guidance for efficient drug development including potential eligibility for accelerated approval, priority review and other opportunities to expedite review and approval.&lt;/li&gt;&lt;/ul&gt;  &lt;p&gt;Nes-Ziona, Israel, July  13, 2026  (GLOBE NEWSWIRE) -- Enlivex Ltd. (Nasdaq: ENLV) (&amp;quot;Enlivex&amp;quot; or the &amp;quot;Company&amp;quot;), a quality longevity company, today announced that the U.S. Food and Drug Administration (FDA) has granted Regenerative</description>
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   <title>Enlivex Receives FDA Regenerative Medicine Advanced Therapy (RMAT) Designation for Allocetra™ in Age-Related Knee Osteoarthritis</title>
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&lt;ul&gt;&lt;li&gt;FDA grant of RMAT designation to Allocetra™ reinforces the potential of this program to deliver a meaningful, disease-modifying impact in age-related primary knee osteoarthritis, where patients face declined quality-of-life and limited treatment options.&lt;/li&gt;&lt;li&gt;RMAT designation provides the benefit of intensive, early FDA engagement and guidance for efficient drug development including potential eligibility for accelerated approval, priority review and other opportunities to expedite review and approval.&lt;/li&gt;&lt;/ul&gt;  &lt;p&gt;Nes-Ziona, Israel, July  13, 2026  (GLOBE NEWSWIRE) -- Enlivex Ltd. (Nasdaq: ENLV) (&amp;quot;Enlivex&amp;quot; or the &amp;quot;Company&amp;quot;), a quality longevity company, today announced that the U.S. Food and Drug Administration (FDA) has granted Regenerative</description>
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   <title>Enlivex Receives FDA Regenerative Medicine Advanced Therapy (RMAT) Designation for Allocetra™ in Age-Related Knee Osteoarthritis</title>
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&lt;ul&gt;&lt;li&gt;FDA grant of RMAT designation to Allocetra™ reinforces the potential of this program to deliver a meaningful, disease-modifying impact in age-related primary knee osteoarthritis, where patients face declined quality-of-life and limited treatment options.&lt;/li&gt;&lt;li&gt;RMAT designation provides the benefit of intensive, early FDA engagement and guidance for efficient drug development including potential eligibility for accelerated approval, priority review and other opportunities to expedite review and approval.&lt;/li&gt;&lt;/ul&gt;  &lt;p&gt;Nes-Ziona, Israel, July  13, 2026  (GLOBE NEWSWIRE) -- Enlivex Ltd. (Nasdaq: ENLV) (&amp;quot;Enlivex&amp;quot; or the &amp;quot;Company&amp;quot;), a quality longevity company, today announced that the U.S. Food and Drug Administration (FDA) has granted Regenerative</description>
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   <title>Form  6-K        Enlivex Ltd.              For: Jul 13</title>
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   <title> Enlivex Receives FDA Regenerative Medicine Advanced Therapy (RMAT) Designation for Allocetra™ in Age-Related Knee Osteoarthritis</title>
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   <description>&lt;ul&gt;&lt;li&gt;FDA grant of RMAT designation to Allocetra™ reinforces the potential of this program to deliver a meaningful, disease-modifying impact in age-related primary knee osteoarthritis, where patients face declined quality-of-life and limited treatment options.&lt;/li&gt;&lt;li&gt;RMAT designation provides the benefit of intensive, early FDA engagement and guidance for efficient drug development including potential eligibility for accelerated approval, priority review and other opportunities to expedite review and approval.&lt;/li&gt;&lt;/ul&gt;  &lt;p&gt;Nes-Ziona, Israel, July  13, 2026  (GLOBE NEWSWIRE) -- Enlivex Ltd. (Nasdaq: ENLV) (&quot;Enlivex&quot; or the &quot;Company&quot;), a quality longevity company, today announced that the U.S. Food and Drug Administration (FDA) has granted Regenerative</description>
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