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   <title>Form  8-K        Kyverna Therapeutics,     For: Jul 08</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++8-K++++++++Kyverna+Therapeutics%2C+++++For%3A+Jul+08/26749553.html</link>
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   <pubDate>Thu, 09 Jul 2026 06:03:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">KYTX</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">O.46871589</category>
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   <title>Form  8-K        Kyverna Therapeutics,     For: Jul 08</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++8-K++++++++Kyverna+Therapeutics%2C+++++For%3A+Jul+08/26749553.html</link>
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   <pubDate>Thu, 09 Jul 2026 06:03:00 -0400</pubDate>
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   <title>Kyverna Therapeutics names Ritesh Srivastava as chief legal officer</title>
   <link>http://www.streetinsider.com/Management+Changes/Kyverna+Therapeutics+names+Ritesh+Srivastava+as+chief+legal+officer/26670211.html</link>
   <description>&lt;p&gt;Kyverna Therapeutics (Nasdaq: KYTX) appointed Ritesh Srivastava as Chief Legal and Compliance Officer, effective June 22, 2026, according to a company statement.&lt;/p&gt;&lt;p&gt;Srivastava joins from BPGbio, where he served as General Counsel. Before that, he was Global Compliance Officer at Spectrum Pharmaceuticals, advising the board on corporate governance, risk management, and public company disclosure matters. He also previously served as Director of Compliance and Investigations at Avanir Pharmaceuticals.&lt;/p&gt;&lt;p&gt;Earlier in his career, Srivastava was a federal prosecutor with the U.S. Department of Justice, where he led investigations into healthcare fraud and anti-kickback cases. He also practiced as a litigator at Cooley LLP</description>
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   <pubDate>Mon, 22 Jun 2026 08:02:08 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">KYTX</category>
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   <title>Kyverna Therapeutics Appoints Ritesh Srivastava as Chief Legal and Compliance Officer, Adding Leadership Strength to Support Commercial-Stage Transition</title>
   <link>http://www.streetinsider.com/Press+Releases/Kyverna+Therapeutics+Appoints+Ritesh+Srivastava+as+Chief+Legal+and+Compliance+Officer%2C+Adding+Leadership+Strength+to+Support+Commercial-Stage+Transition/26670022.html</link>
   <description>&lt;p align=&quot;left&quot;&gt;EMERYVILLE, Calif., June  22, 2026  (GLOBE NEWSWIRE) -- Kyverna Therapeutics, Inc. (Nasdaq: KYTX), a late-stage clinical biopharmaceutical company developing cell therapies for patients with autoimmune diseases, today announced the appointment of Ritesh Srivastava as Chief Legal and Compliance Officer, effective June 22, 2026. Mr. Srivastava brings extensive experience spanning legal, corporate strategy, compliance, and risk management, which will further support Kyverna as it advances miv-cel (mivocabtagene autoleucel, KYV-101) towards a potential first approval in stiff person syndrome and transitions to a commercial-stage organization.&lt;/p&gt;  &lt;p&gt;“Ritesh is a key addition to Kyverna as we prepare for commercialization and</description>
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   <pubDate>Mon, 22 Jun 2026 08:00:00 -0400</pubDate>
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   <title>Kyverna Therapeutics Appoints Ritesh Srivastava as Chief Legal and Compliance Officer, Adding Leadership Strength to Support Commercial-Stage Transition</title>
   <link>http://www.streetinsider.com/Press+Releases/Kyverna+Therapeutics+Appoints+Ritesh+Srivastava+as+Chief+Legal+and+Compliance+Officer%2C+Adding+Leadership+Strength+to+Support+Commercial-Stage+Transition/26670022.html</link>
   <description>&lt;p align=&quot;left&quot;&gt;EMERYVILLE, Calif., June  22, 2026  (GLOBE NEWSWIRE) -- Kyverna Therapeutics, Inc. (Nasdaq: KYTX), a late-stage clinical biopharmaceutical company developing cell therapies for patients with autoimmune diseases, today announced the appointment of Ritesh Srivastava as Chief Legal and Compliance Officer, effective June 22, 2026. Mr. Srivastava brings extensive experience spanning legal, corporate strategy, compliance, and risk management, which will further support Kyverna as it advances miv-cel (mivocabtagene autoleucel, KYV-101) towards a potential first approval in stiff person syndrome and transitions to a commercial-stage organization.&lt;/p&gt;  &lt;p&gt;“Ritesh is a key addition to Kyverna as we prepare for commercialization and</description>
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   <pubDate>Mon, 22 Jun 2026 08:00:00 -0400</pubDate>
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   <title>Kyverna Therapeutics Appoints Ritesh Srivastava as Chief Legal and Compliance Officer, Adding Leadership Strength to Support Commercial-Stage Transition</title>
   <link>http://www.streetinsider.com/Globe+Newswire/Kyverna+Therapeutics+Appoints+Ritesh+Srivastava+as+Chief+Legal+and+Compliance+Officer%2C+Adding+Leadership+Strength+to+Support+Commercial-Stage+Transition/26670022.html</link>
   <description>&lt;p align=&quot;left&quot;&gt;EMERYVILLE, Calif., June  22, 2026  (GLOBE NEWSWIRE) -- Kyverna Therapeutics, Inc. (Nasdaq: KYTX), a late-stage clinical biopharmaceutical company developing cell therapies for patients with autoimmune diseases, today announced the appointment of Ritesh Srivastava as Chief Legal and Compliance Officer, effective June 22, 2026. Mr. Srivastava brings extensive experience spanning legal, corporate strategy, compliance, and risk management, which will further support Kyverna as it advances miv-cel (mivocabtagene autoleucel, KYV-101) towards a potential first approval in stiff person syndrome and transitions to a commercial-stage organization.&lt;/p&gt;  &lt;p&gt;“Ritesh is a key addition to Kyverna as we prepare for commercialization and</description>
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   <pubDate>Mon, 22 Jun 2026 08:00:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">KYTX</category>
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   <title>Kyverna Therapeutics Appoints Ritesh Srivastava as Chief Legal and Compliance Officer, Adding Leadership Strength to Support Commercial-Stage Transition</title>
   <link>http://www.streetinsider.com/Globe+Newswire/Kyverna+Therapeutics+Appoints+Ritesh+Srivastava+as+Chief+Legal+and+Compliance+Officer%2C+Adding+Leadership+Strength+to+Support+Commercial-Stage+Transition/26670022.html</link>
   <description>&lt;p align=&quot;left&quot;&gt;EMERYVILLE, Calif., June  22, 2026  (GLOBE NEWSWIRE) -- Kyverna Therapeutics, Inc. (Nasdaq: KYTX), a late-stage clinical biopharmaceutical company developing cell therapies for patients with autoimmune diseases, today announced the appointment of Ritesh Srivastava as Chief Legal and Compliance Officer, effective June 22, 2026. Mr. Srivastava brings extensive experience spanning legal, corporate strategy, compliance, and risk management, which will further support Kyverna as it advances miv-cel (mivocabtagene autoleucel, KYV-101) towards a potential first approval in stiff person syndrome and transitions to a commercial-stage organization.&lt;/p&gt;  &lt;p&gt;“Ritesh is a key addition to Kyverna as we prepare for commercialization and</description>
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   <pubDate>Mon, 22 Jun 2026 08:00:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">KYTX</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">KYTX</category>
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   <title>H.C. Wainwright Reiterates Buy Rating on Kyverna Therapeutics Inc (KYTX)</title>
   <link>http://www.streetinsider.com/Analyst+Comments/H.C.+Wainwright+Reiterates+Buy+Rating+on+Kyverna+Therapeutics+Inc+%28KYTX%29/26602144.html</link>
   <description>&lt;p&gt;H.C. Wainwright analyst Mitchell S. Kapoor reiterated a Buy rating and $25.00 price target on Kyverna Therapeutics Inc (NASDAQ: KYTX).&lt;/p&gt;&lt;p&gt;The analyst commented: &quot;Kyverna’s updated Phase 1 COMPARE data at EULAR look meaningfully positive for miv-cel’s broader autoimmune activity: all six ACPA-positive, treatment-refractory RA patients had reduced disease activity after one infusion, 66.6% achieved ACR70 by Week 36, disease-associated autoantibodies declined for up to 52 weeks, B cells repopulated with a naïve/transitional phenotype, and there were no high-grade CRS or ICANS events. It is important to consider that these were difficult-to-treat patients who had failed a median of 6.5 prior biologic</description>
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   <pubDate>Thu, 04 Jun 2026 06:41:37 -0400</pubDate>
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   <title>Kyverna presents updated data on miv-cel for rheumatoid arthritis</title>
   <link>http://www.streetinsider.com/Corporate+News/Kyverna+presents+updated+data+on+miv-cel+for+rheumatoid+arthritis/26595749.html</link>
   <description>&lt;p&gt;Kyverna Therapeutics Inc. (NASDAQ: KYTX) presented updated data from its Phase 1 trial of miv-cel in patients with treatment-refractory rheumatoid arthritis at the European Alliance of Associations for Rheumatology Congress in London.&lt;/p&gt;&lt;p&gt;The COMPARE trial enrolled six patients with anti-citrullinated protein antibody-positive rheumatoid arthritis who had failed a median of 6.5 prior biologic treatments. Patients received a single infusion of miv-cel CAR T cells following lymphodepletion, with follow-up ranging up to 52 weeks.&lt;/p&gt;&lt;p&gt;According to the company, 66.6% of patients met the American College of Rheumatology improvement criteria response by Week 36. The treatment resulted in depletion of CD19+ B cells and</description>
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   <pubDate>Wed, 03 Jun 2026 08:03:57 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">KYTX</category>
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   <title>Kyverna presents updated data on miv-cel for rheumatoid arthritis</title>
   <link>http://www.streetinsider.com/FDA/Kyverna+presents+updated+data+on+miv-cel+for+rheumatoid+arthritis/26595749.html</link>
   <description>&lt;p&gt;Kyverna Therapeutics Inc. (NASDAQ: KYTX) presented updated data from its Phase 1 trial of miv-cel in patients with treatment-refractory rheumatoid arthritis at the European Alliance of Associations for Rheumatology Congress in London.&lt;/p&gt;&lt;p&gt;The COMPARE trial enrolled six patients with anti-citrullinated protein antibody-positive rheumatoid arthritis who had failed a median of 6.5 prior biologic treatments. Patients received a single infusion of miv-cel CAR T cells following lymphodepletion, with follow-up ranging up to 52 weeks.&lt;/p&gt;&lt;p&gt;According to the company, 66.6% of patients met the American College of Rheumatology improvement criteria response by Week 36. The treatment resulted in depletion of CD19+ B cells and</description>
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   <pubDate>Wed, 03 Jun 2026 08:03:57 -0400</pubDate>
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   <title>Kyverna Therapeutics Highlights Updated Miv-cel Data at EULAR Demonstrating Substantial Reduction in Disease Activity in ACPA-Positive, Treatment Refractory Rheumatoid Arthritis</title>
   <link>http://www.streetinsider.com/Press+Releases/Kyverna+Therapeutics+Highlights+Updated+Miv-cel+Data+at+EULAR+Demonstrating+Substantial+Reduction+in+Disease+Activity+in+ACPA-Positive%2C+Treatment+Refractory+Rheumatoid+Arthritis/26595540.html</link>
   <description>&lt;p align=&quot;center&quot;&gt;&lt;em&gt;Majority of patients met the American College of Rheumatology improvement criteria (ACR70) response by Week 36&lt;/em&gt;&lt;/p&gt;    &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Single-dose of miv-cel delivered deep B-cell depletion with evidence of immune reset&lt;/em&gt;&lt;/p&gt;    &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Miv-cel continues to demonstrate a well-tolerated safety profile, consistent with observations from over 100 patients treated to date&lt;/em&gt;&lt;sup&gt;&lt;em&gt;1&lt;/em&gt;&lt;/sup&gt;&lt;/p&gt;    &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Data reinforce miv-cel’s differentiated clinical profile and opportunity to change the treatment paradigm across a variety of autoimmune diseases&lt;/em&gt;&lt;/p&gt;    &lt;p&gt;EMERYVILLE, Calif., June  03, 2026  (GLOBE NEWSWIRE) -- Kyverna Therapeutics, Inc. (Nasdaq: KYTX), a late-stage clinical biopharmaceutical</description>
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   <pubDate>Wed, 03 Jun 2026 08:00:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">KYTX</category>
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   <title>Kyverna Therapeutics Highlights Updated Miv-cel Data at EULAR Demonstrating Substantial Reduction in Disease Activity in ACPA-Positive, Treatment Refractory Rheumatoid Arthritis</title>
   <link>http://www.streetinsider.com/Press+Releases/Kyverna+Therapeutics+Highlights+Updated+Miv-cel+Data+at+EULAR+Demonstrating+Substantial+Reduction+in+Disease+Activity+in+ACPA-Positive%2C+Treatment+Refractory+Rheumatoid+Arthritis/26595540.html</link>
   <description>&lt;p align=&quot;center&quot;&gt;&lt;em&gt;Majority of patients met the American College of Rheumatology improvement criteria (ACR70) response by Week 36&lt;/em&gt;&lt;/p&gt;    &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Single-dose of miv-cel delivered deep B-cell depletion with evidence of immune reset&lt;/em&gt;&lt;/p&gt;    &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Miv-cel continues to demonstrate a well-tolerated safety profile, consistent with observations from over 100 patients treated to date&lt;/em&gt;&lt;sup&gt;&lt;em&gt;1&lt;/em&gt;&lt;/sup&gt;&lt;/p&gt;    &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Data reinforce miv-cel’s differentiated clinical profile and opportunity to change the treatment paradigm across a variety of autoimmune diseases&lt;/em&gt;&lt;/p&gt;    &lt;p&gt;EMERYVILLE, Calif., June  03, 2026  (GLOBE NEWSWIRE) -- Kyverna Therapeutics, Inc. (Nasdaq: KYTX), a late-stage clinical biopharmaceutical</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Press+Releases/Kyverna+Therapeutics+Highlights+Updated+Miv-cel+Data+at+EULAR+Demonstrating+Substantial+Reduction+in+Disease+Activity+in+ACPA-Positive%2C+Treatment+Refractory+Rheumatoid+Arthritis/26595540.html</guid>
   <pubDate>Wed, 03 Jun 2026 08:00:00 -0400</pubDate>
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   <title>Kyverna Therapeutics Highlights Updated Miv-cel Data at EULAR Demonstrating Substantial Reduction in Disease Activity in ACPA-Positive, Treatment Refractory Rheumatoid Arthritis</title>
   <link>http://www.streetinsider.com/Globe+Newswire/Kyverna+Therapeutics+Highlights+Updated+Miv-cel+Data+at+EULAR+Demonstrating+Substantial+Reduction+in+Disease+Activity+in+ACPA-Positive%2C+Treatment+Refractory+Rheumatoid+Arthritis/26595540.html</link>
   <description>&lt;p align=&quot;center&quot;&gt;&lt;em&gt;Majority of patients met the American College of Rheumatology improvement criteria (ACR70) response by Week 36&lt;/em&gt;&lt;/p&gt;    &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Single-dose of miv-cel delivered deep B-cell depletion with evidence of immune reset&lt;/em&gt;&lt;/p&gt;    &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Miv-cel continues to demonstrate a well-tolerated safety profile, consistent with observations from over 100 patients treated to date&lt;/em&gt;&lt;sup&gt;&lt;em&gt;1&lt;/em&gt;&lt;/sup&gt;&lt;/p&gt;    &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Data reinforce miv-cel’s differentiated clinical profile and opportunity to change the treatment paradigm across a variety of autoimmune diseases&lt;/em&gt;&lt;/p&gt;    &lt;p&gt;EMERYVILLE, Calif., June  03, 2026  (GLOBE NEWSWIRE) -- Kyverna Therapeutics, Inc. (Nasdaq: KYTX), a late-stage clinical biopharmaceutical</description>
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   <pubDate>Wed, 03 Jun 2026 08:00:00 -0400</pubDate>
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   <title>Kyverna Therapeutics Highlights Updated Miv-cel Data at EULAR Demonstrating Substantial Reduction in Disease Activity in ACPA-Positive, Treatment Refractory Rheumatoid Arthritis</title>
   <link>http://www.streetinsider.com/Globe+Newswire/Kyverna+Therapeutics+Highlights+Updated+Miv-cel+Data+at+EULAR+Demonstrating+Substantial+Reduction+in+Disease+Activity+in+ACPA-Positive%2C+Treatment+Refractory+Rheumatoid+Arthritis/26595540.html</link>
   <description>&lt;p align=&quot;center&quot;&gt;&lt;em&gt;Majority of patients met the American College of Rheumatology improvement criteria (ACR70) response by Week 36&lt;/em&gt;&lt;/p&gt;    &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Single-dose of miv-cel delivered deep B-cell depletion with evidence of immune reset&lt;/em&gt;&lt;/p&gt;    &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Miv-cel continues to demonstrate a well-tolerated safety profile, consistent with observations from over 100 patients treated to date&lt;/em&gt;&lt;sup&gt;&lt;em&gt;1&lt;/em&gt;&lt;/sup&gt;&lt;/p&gt;    &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Data reinforce miv-cel’s differentiated clinical profile and opportunity to change the treatment paradigm across a variety of autoimmune diseases&lt;/em&gt;&lt;/p&gt;    &lt;p&gt;EMERYVILLE, Calif., June  03, 2026  (GLOBE NEWSWIRE) -- Kyverna Therapeutics, Inc. (Nasdaq: KYTX), a late-stage clinical biopharmaceutical</description>
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   <title>Form  8-K        Kyverna Therapeutics,     For: May 27</title>
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   <pubDate>Tue, 02 Jun 2026 16:30:00 -0400</pubDate>
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   <title>Form  8-K        Kyverna Therapeutics,     For: May 27</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++8-K++++++++Kyverna+Therapeutics%2C+++++For%3A+May+27/26592222.html</link>
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   <pubDate>Tue, 02 Jun 2026 16:30:00 -0400</pubDate>
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   <title>Form  4          Kyverna Therapeutics,     For: May 27  Filed by: SEIDENBERG BETH C</title>
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