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   <title>Travere presents long-term FILSPARI data at European kidney conference</title>
   <link>http://www.streetinsider.com/FDA/Travere+presents+long-term+FILSPARI+data+at+European+kidney+conference/26603817.html</link>
   <description>

&lt;p&gt;Travere Therapeutics (NASDAQ: TVTX) presented extended results from its Phase 3 DUPLEX study of FILSPARI at the European Renal Association Congress. The data showed patients with focal segmental glomerulosclerosis who remained on the drug maintained proteinuria reductions over approximately five years of treatment.&lt;/p&gt;

&lt;p&gt;In the open-label extension study, 37.5% of patients who continued FILSPARI from the initial trial achieved complete remission at some point during treatment, while 87.5% achieved partial remission. Patients who switched from the control drug irbesartan to FILSPARI showed similar improvements, with 28.9% achieving complete remission and 74.6% achieving partial remission.&lt;/p&gt;

&lt;p&gt;The DUPLEX study enrolled 371 patients ages 8</description>
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   <pubDate>Thu, 04 Jun 2026 10:09:15 -0400</pubDate>
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   <title>Travere presents long-term FILSPARI data at European kidney conference</title>
   <link>http://www.streetinsider.com/FDA/Travere+presents+long-term+FILSPARI+data+at+European+kidney+conference/26603817.html</link>
   <description>

&lt;p&gt;Travere Therapeutics (NASDAQ: TVTX) presented extended results from its Phase 3 DUPLEX study of FILSPARI at the European Renal Association Congress. The data showed patients with focal segmental glomerulosclerosis who remained on the drug maintained proteinuria reductions over approximately five years of treatment.&lt;/p&gt;

&lt;p&gt;In the open-label extension study, 37.5% of patients who continued FILSPARI from the initial trial achieved complete remission at some point during treatment, while 87.5% achieved partial remission. Patients who switched from the control drug irbesartan to FILSPARI showed similar improvements, with 28.9% achieving complete remission and 74.6% achieving partial remission.&lt;/p&gt;

&lt;p&gt;The DUPLEX study enrolled 371 patients ages 8</description>
   <guid isPermaLink="true">http://www.streetinsider.com/FDA/Travere+presents+long-term+FILSPARI+data+at+European+kidney+conference/26603817.html</guid>
   <pubDate>Thu, 04 Jun 2026 10:09:15 -0400</pubDate>
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   <title>Travere presents long-term FILSPARI data at European kidney conference</title>
   <link>http://www.streetinsider.com/FDA/Travere+presents+long-term+FILSPARI+data+at+European+kidney+conference/26603817.html</link>
   <description>

&lt;p&gt;Travere Therapeutics (NASDAQ: TVTX) presented extended results from its Phase 3 DUPLEX study of FILSPARI at the European Renal Association Congress. The data showed patients with focal segmental glomerulosclerosis who remained on the drug maintained proteinuria reductions over approximately five years of treatment.&lt;/p&gt;

&lt;p&gt;In the open-label extension study, 37.5% of patients who continued FILSPARI from the initial trial achieved complete remission at some point during treatment, while 87.5% achieved partial remission. Patients who switched from the control drug irbesartan to FILSPARI showed similar improvements, with 28.9% achieving complete remission and 74.6% achieving partial remission.&lt;/p&gt;

&lt;p&gt;The DUPLEX study enrolled 371 patients ages 8</description>
   <guid isPermaLink="true">http://www.streetinsider.com/FDA/Travere+presents+long-term+FILSPARI+data+at+European+kidney+conference/26603817.html</guid>
   <pubDate>Thu, 04 Jun 2026 10:09:15 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">A.50215103</category>
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  <item>
   <title>Travere presents long-term FILSPARI data at European kidney conference</title>
   <link>http://www.streetinsider.com/FDA/Travere+presents+long-term+FILSPARI+data+at+European+kidney+conference/26603817.html</link>
   <description>

&lt;p&gt;Travere Therapeutics (NASDAQ: TVTX) presented extended results from its Phase 3 DUPLEX study of FILSPARI at the European Renal Association Congress. The data showed patients with focal segmental glomerulosclerosis who remained on the drug maintained proteinuria reductions over approximately five years of treatment.&lt;/p&gt;

&lt;p&gt;In the open-label extension study, 37.5% of patients who continued FILSPARI from the initial trial achieved complete remission at some point during treatment, while 87.5% achieved partial remission. Patients who switched from the control drug irbesartan to FILSPARI showed similar improvements, with 28.9% achieving complete remission and 74.6% achieving partial remission.&lt;/p&gt;

&lt;p&gt;The DUPLEX study enrolled 371 patients ages 8</description>
   <guid isPermaLink="true">http://www.streetinsider.com/FDA/Travere+presents+long-term+FILSPARI+data+at+European+kidney+conference/26603817.html</guid>
   <pubDate>Thu, 04 Jun 2026 10:09:15 -0400</pubDate>
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   <title>Travere Therapeutics Presents Long-Term Open-Label Extension Data from the Phase 3 DUPLEX Study at the 63rd European Renal Association (ERA) 2026 Congress</title>
   <link>http://www.streetinsider.com/Press+Releases/Travere+Therapeutics+Presents+Long-Term+Open-Label+Extension+Data+from+the+Phase+3+DUPLEX+Study+at+the+63rd+European+Renal+Association+%28ERA%29+2026+Congress/26603813.html</link>
   <description>
&lt;p class=&quot;bwalignc&quot;&gt;
&lt;i&gt;Patients in the study who initiated and remained on FILSPARI maintained durable and deepened proteinuria reductions, resulting in further achievement of clinically meaningful low proteinuria thresholds over time&lt;/i&gt;

&lt;/p&gt;&lt;p class=&quot;bwalignc&quot;&gt;
&lt;i&gt;Patients who transitioned from active control maximum labeled dose irbesartan to FILSPARI after the double-blind study period demonstrated rapid and sustained reductions in proteinuria&lt;/i&gt;

&lt;/p&gt;&lt;p class=&quot;bwalignc&quot;&gt;
&lt;i&gt;FILSPARI was generally well tolerated for up to five years of follow-up in the study&lt;/i&gt;

&lt;/p&gt;
&lt;p&gt;    SAN DIEGO--(BUSINESS WIRE)--
Travere Therapeutics, Inc., (Nasdaq: TVTX) today announced long-term results from the ongoing Phase 3 DUPLEX Study open-label extension (OLE) of FILSPARI® (sparsentan) in the treatment of focal</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Press+Releases/Travere+Therapeutics+Presents+Long-Term+Open-Label+Extension+Data+from+the+Phase+3+DUPLEX+Study+at+the+63rd+European+Renal+Association+%28ERA%29+2026+Congress/26603813.html</guid>
   <pubDate>Thu, 04 Jun 2026 10:09:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">A.50215103</category>
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   	   	<category domain="http://rss.financialcontent.com/stocksymbol">TVTX</category>
   	  </item>
  <item>
   <title>Travere Therapeutics Presents Long-Term Open-Label Extension Data from the Phase 3 DUPLEX Study at the 63rd European Renal Association (ERA) 2026 Congress</title>
   <link>http://www.streetinsider.com/Press+Releases/Travere+Therapeutics+Presents+Long-Term+Open-Label+Extension+Data+from+the+Phase+3+DUPLEX+Study+at+the+63rd+European+Renal+Association+%28ERA%29+2026+Congress/26603813.html</link>
   <description>
&lt;p class=&quot;bwalignc&quot;&gt;
&lt;i&gt;Patients in the study who initiated and remained on FILSPARI maintained durable and deepened proteinuria reductions, resulting in further achievement of clinically meaningful low proteinuria thresholds over time&lt;/i&gt;

&lt;/p&gt;&lt;p class=&quot;bwalignc&quot;&gt;
&lt;i&gt;Patients who transitioned from active control maximum labeled dose irbesartan to FILSPARI after the double-blind study period demonstrated rapid and sustained reductions in proteinuria&lt;/i&gt;

&lt;/p&gt;&lt;p class=&quot;bwalignc&quot;&gt;
&lt;i&gt;FILSPARI was generally well tolerated for up to five years of follow-up in the study&lt;/i&gt;

&lt;/p&gt;
&lt;p&gt;    SAN DIEGO--(BUSINESS WIRE)--
Travere Therapeutics, Inc., (Nasdaq: TVTX) today announced long-term results from the ongoing Phase 3 DUPLEX Study open-label extension (OLE) of FILSPARI® (sparsentan) in the treatment of focal</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Press+Releases/Travere+Therapeutics+Presents+Long-Term+Open-Label+Extension+Data+from+the+Phase+3+DUPLEX+Study+at+the+63rd+European+Renal+Association+%28ERA%29+2026+Congress/26603813.html</guid>
   <pubDate>Thu, 04 Jun 2026 10:09:00 -0400</pubDate>
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   	   	<category domain="http://rss.financialcontent.com/stocksymbol">TVTX</category>
   	  </item>
  <item>
   <title>Travere Therapeutics Presents Long-Term Open-Label Extension Data from the Phase 3 DUPLEX Study at the 63rd European Renal Association (ERA) 2026 Congress</title>
   <link>http://www.streetinsider.com/Press+Releases/Travere+Therapeutics+Presents+Long-Term+Open-Label+Extension+Data+from+the+Phase+3+DUPLEX+Study+at+the+63rd+European+Renal+Association+%28ERA%29+2026+Congress/26603813.html</link>
   <description>
&lt;p class=&quot;bwalignc&quot;&gt;
&lt;i&gt;Patients in the study who initiated and remained on FILSPARI maintained durable and deepened proteinuria reductions, resulting in further achievement of clinically meaningful low proteinuria thresholds over time&lt;/i&gt;

&lt;/p&gt;&lt;p class=&quot;bwalignc&quot;&gt;
&lt;i&gt;Patients who transitioned from active control maximum labeled dose irbesartan to FILSPARI after the double-blind study period demonstrated rapid and sustained reductions in proteinuria&lt;/i&gt;

&lt;/p&gt;&lt;p class=&quot;bwalignc&quot;&gt;
&lt;i&gt;FILSPARI was generally well tolerated for up to five years of follow-up in the study&lt;/i&gt;

&lt;/p&gt;
&lt;p&gt;    SAN DIEGO--(BUSINESS WIRE)--
Travere Therapeutics, Inc., (Nasdaq: TVTX) today announced long-term results from the ongoing Phase 3 DUPLEX Study open-label extension (OLE) of FILSPARI® (sparsentan) in the treatment of focal</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Press+Releases/Travere+Therapeutics+Presents+Long-Term+Open-Label+Extension+Data+from+the+Phase+3+DUPLEX+Study+at+the+63rd+European+Renal+Association+%28ERA%29+2026+Congress/26603813.html</guid>
   <pubDate>Thu, 04 Jun 2026 10:09:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">A.50215103</category>
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   	   	<category domain="http://rss.financialcontent.com/stocksymbol">O.28798549</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">TVTX</category>
   	  </item>
  <item>
   <title>Travere Therapeutics Presents Long-Term Open-Label Extension Data from the Phase 3 DUPLEX Study at the 63rd European Renal Association (ERA) 2026 Congress</title>
   <link>http://www.streetinsider.com/Press+Releases/Travere+Therapeutics+Presents+Long-Term+Open-Label+Extension+Data+from+the+Phase+3+DUPLEX+Study+at+the+63rd+European+Renal+Association+%28ERA%29+2026+Congress/26603813.html</link>
   <description>
&lt;p class=&quot;bwalignc&quot;&gt;
&lt;i&gt;Patients in the study who initiated and remained on FILSPARI maintained durable and deepened proteinuria reductions, resulting in further achievement of clinically meaningful low proteinuria thresholds over time&lt;/i&gt;

&lt;/p&gt;&lt;p class=&quot;bwalignc&quot;&gt;
&lt;i&gt;Patients who transitioned from active control maximum labeled dose irbesartan to FILSPARI after the double-blind study period demonstrated rapid and sustained reductions in proteinuria&lt;/i&gt;

&lt;/p&gt;&lt;p class=&quot;bwalignc&quot;&gt;
&lt;i&gt;FILSPARI was generally well tolerated for up to five years of follow-up in the study&lt;/i&gt;

&lt;/p&gt;
&lt;p&gt;    SAN DIEGO--(BUSINESS WIRE)--
Travere Therapeutics, Inc., (Nasdaq: TVTX) today announced long-term results from the ongoing Phase 3 DUPLEX Study open-label extension (OLE) of FILSPARI® (sparsentan) in the treatment of focal</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Press+Releases/Travere+Therapeutics+Presents+Long-Term+Open-Label+Extension+Data+from+the+Phase+3+DUPLEX+Study+at+the+63rd+European+Renal+Association+%28ERA%29+2026+Congress/26603813.html</guid>
   <pubDate>Thu, 04 Jun 2026 10:09:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">A.50215103</category>
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   	   	<category domain="http://rss.financialcontent.com/stocksymbol">O.28798549</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">TVTX</category>
   	  </item>
  <item>
   <title>Travere Therapeutics Presents Long-Term Open-Label Extension Data from the Phase 3 DUPLEX Study at the 63rd European Renal Association (ERA) 2026 Congress</title>
   <link>http://www.streetinsider.com/Business+Wire/Travere+Therapeutics+Presents+Long-Term+Open-Label+Extension+Data+from+the+Phase+3+DUPLEX+Study+at+the+63rd+European+Renal+Association+%28ERA%29+2026+Congress/26603813.html</link>
   <description>
&lt;p class=&quot;bwalignc&quot;&gt;
&lt;i&gt;Patients in the study who initiated and remained on FILSPARI maintained durable and deepened proteinuria reductions, resulting in further achievement of clinically meaningful low proteinuria thresholds over time&lt;/i&gt;

&lt;/p&gt;&lt;p class=&quot;bwalignc&quot;&gt;
&lt;i&gt;Patients who transitioned from active control maximum labeled dose irbesartan to FILSPARI after the double-blind study period demonstrated rapid and sustained reductions in proteinuria&lt;/i&gt;

&lt;/p&gt;&lt;p class=&quot;bwalignc&quot;&gt;
&lt;i&gt;FILSPARI was generally well tolerated for up to five years of follow-up in the study&lt;/i&gt;

&lt;/p&gt;
&lt;p&gt;    SAN DIEGO--(BUSINESS WIRE)--
Travere Therapeutics, Inc., (Nasdaq: TVTX) today announced long-term results from the ongoing Phase 3 DUPLEX Study open-label extension (OLE) of FILSPARI® (sparsentan) in the treatment of focal</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Business+Wire/Travere+Therapeutics+Presents+Long-Term+Open-Label+Extension+Data+from+the+Phase+3+DUPLEX+Study+at+the+63rd+European+Renal+Association+%28ERA%29+2026+Congress/26603813.html</guid>
   <pubDate>Thu, 04 Jun 2026 10:09:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">A.50215103</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">O.09235062</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">O.28798549</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">TVTX</category>
   	  </item>
  <item>
   <title>Travere Therapeutics Presents Long-Term Open-Label Extension Data from the Phase 3 DUPLEX Study at the 63rd European Renal Association (ERA) 2026 Congress</title>
   <link>http://www.streetinsider.com/Business+Wire/Travere+Therapeutics+Presents+Long-Term+Open-Label+Extension+Data+from+the+Phase+3+DUPLEX+Study+at+the+63rd+European+Renal+Association+%28ERA%29+2026+Congress/26603813.html</link>
   <description>
&lt;p class=&quot;bwalignc&quot;&gt;
&lt;i&gt;Patients in the study who initiated and remained on FILSPARI maintained durable and deepened proteinuria reductions, resulting in further achievement of clinically meaningful low proteinuria thresholds over time&lt;/i&gt;

&lt;/p&gt;&lt;p class=&quot;bwalignc&quot;&gt;
&lt;i&gt;Patients who transitioned from active control maximum labeled dose irbesartan to FILSPARI after the double-blind study period demonstrated rapid and sustained reductions in proteinuria&lt;/i&gt;

&lt;/p&gt;&lt;p class=&quot;bwalignc&quot;&gt;
&lt;i&gt;FILSPARI was generally well tolerated for up to five years of follow-up in the study&lt;/i&gt;

&lt;/p&gt;
&lt;p&gt;    SAN DIEGO--(BUSINESS WIRE)--
Travere Therapeutics, Inc., (Nasdaq: TVTX) today announced long-term results from the ongoing Phase 3 DUPLEX Study open-label extension (OLE) of FILSPARI® (sparsentan) in the treatment of focal</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Business+Wire/Travere+Therapeutics+Presents+Long-Term+Open-Label+Extension+Data+from+the+Phase+3+DUPLEX+Study+at+the+63rd+European+Renal+Association+%28ERA%29+2026+Congress/26603813.html</guid>
   <pubDate>Thu, 04 Jun 2026 10:09:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">A.50215103</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">O.09235062</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">O.28798549</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">TVTX</category>
   	  </item>
  <item>
   <title>Travere Therapeutics Presents Long-Term Open-Label Extension Data from the Phase 3 DUPLEX Study at the 63rd European Renal Association (ERA) 2026 Congress</title>
   <link>http://www.streetinsider.com/Business+Wire/Travere+Therapeutics+Presents+Long-Term+Open-Label+Extension+Data+from+the+Phase+3+DUPLEX+Study+at+the+63rd+European+Renal+Association+%28ERA%29+2026+Congress/26603813.html</link>
   <description>
&lt;p class=&quot;bwalignc&quot;&gt;
&lt;i&gt;Patients in the study who initiated and remained on FILSPARI maintained durable and deepened proteinuria reductions, resulting in further achievement of clinically meaningful low proteinuria thresholds over time&lt;/i&gt;

&lt;/p&gt;&lt;p class=&quot;bwalignc&quot;&gt;
&lt;i&gt;Patients who transitioned from active control maximum labeled dose irbesartan to FILSPARI after the double-blind study period demonstrated rapid and sustained reductions in proteinuria&lt;/i&gt;

&lt;/p&gt;&lt;p class=&quot;bwalignc&quot;&gt;
&lt;i&gt;FILSPARI was generally well tolerated for up to five years of follow-up in the study&lt;/i&gt;

&lt;/p&gt;
&lt;p&gt;    SAN DIEGO--(BUSINESS WIRE)--
Travere Therapeutics, Inc., (Nasdaq: TVTX) today announced long-term results from the ongoing Phase 3 DUPLEX Study open-label extension (OLE) of FILSPARI® (sparsentan) in the treatment of focal</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Business+Wire/Travere+Therapeutics+Presents+Long-Term+Open-Label+Extension+Data+from+the+Phase+3+DUPLEX+Study+at+the+63rd+European+Renal+Association+%28ERA%29+2026+Congress/26603813.html</guid>
   <pubDate>Thu, 04 Jun 2026 10:09:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">A.50215103</category>
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   	   	<category domain="http://rss.financialcontent.com/stocksymbol">O.28798549</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">TVTX</category>
   	  </item>
  <item>
   <title>Travere Therapeutics Presents Long-Term Open-Label Extension Data from the Phase 3 DUPLEX Study at the 63rd European Renal Association (ERA) 2026 Congress</title>
   <link>http://www.streetinsider.com/Business+Wire/Travere+Therapeutics+Presents+Long-Term+Open-Label+Extension+Data+from+the+Phase+3+DUPLEX+Study+at+the+63rd+European+Renal+Association+%28ERA%29+2026+Congress/26603813.html</link>
   <description>
&lt;p class=&quot;bwalignc&quot;&gt;
&lt;i&gt;Patients in the study who initiated and remained on FILSPARI maintained durable and deepened proteinuria reductions, resulting in further achievement of clinically meaningful low proteinuria thresholds over time&lt;/i&gt;

&lt;/p&gt;&lt;p class=&quot;bwalignc&quot;&gt;
&lt;i&gt;Patients who transitioned from active control maximum labeled dose irbesartan to FILSPARI after the double-blind study period demonstrated rapid and sustained reductions in proteinuria&lt;/i&gt;

&lt;/p&gt;&lt;p class=&quot;bwalignc&quot;&gt;
&lt;i&gt;FILSPARI was generally well tolerated for up to five years of follow-up in the study&lt;/i&gt;

&lt;/p&gt;
&lt;p&gt;    SAN DIEGO--(BUSINESS WIRE)--
Travere Therapeutics, Inc., (Nasdaq: TVTX) today announced long-term results from the ongoing Phase 3 DUPLEX Study open-label extension (OLE) of FILSPARI® (sparsentan) in the treatment of focal</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Business+Wire/Travere+Therapeutics+Presents+Long-Term+Open-Label+Extension+Data+from+the+Phase+3+DUPLEX+Study+at+the+63rd+European+Renal+Association+%28ERA%29+2026+Congress/26603813.html</guid>
   <pubDate>Thu, 04 Jun 2026 10:09:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">A.50215103</category>
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   	   	<category domain="http://rss.financialcontent.com/stocksymbol">O.28798549</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">TVTX</category>
   	  </item>
  <item>
   <title>Travere Therapeutics (TVTX) PT Raised to $62 at Citi</title>
   <link>http://www.streetinsider.com/Analyst+PT+Change/Travere+Therapeutics+%28TVTX%29+PT+Raised+to+%2462+at+Citi/26597788.html</link>
   <description>&lt;p&gt;Citi analyst Yigal Nochomovitz raised the price target on Travere Therapeutics (NASDAQ: TVTX) to $62.00 (from $59.00) while maintaining a Buy rating.&lt;/p&gt;</description>
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   <pubDate>Wed, 03 Jun 2026 12:53:31 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">TVTX</category>
   	  </item>
  <item>
   <title>Travere Therapeutics (TVTX) PT Raised to $67 at H.C. Wainwright</title>
   <link>http://www.streetinsider.com/Analyst+PT+Change/Travere+Therapeutics+%28TVTX%29+PT+Raised+to+%2467+at+H.C.+Wainwright/26589837.html</link>
   <description>&lt;p&gt;H.C. Wainwright analyst Joseph Pantginis raised the price target on Travere Therapeutics (NASDAQ: TVTX) to $67.00 (from $57.00) while maintaining a Buy rating.&lt;/p&gt;&lt;p&gt;The analyst comments &quot;We reiterate our Buy rating and are increasing our price target to $67 from $57 based on the addition of civerobrutinib to our overall valuation, but just for the PMN indication. We see potential upside from the inclusion of additional indications. Our valuation of Travere is now split into two components. First regarding current sales of FILSPARI, our valuation is based on a risk-adjusted net present value (rNPV) analysis of projected future revenues; we assume</description>
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   <pubDate>Tue, 02 Jun 2026 11:38:13 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">TVTX</category>
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   <title>Travere Therapeutics (TVTX) PT Raised to $67 at H.C. Wainwright</title>
   <link>http://www.streetinsider.com/Analyst+Comments/Travere+Therapeutics+%28TVTX%29+PT+Raised+to+%2467+at+H.C.+Wainwright/26589837.html</link>
   <description>&lt;p&gt;H.C. Wainwright analyst Joseph Pantginis raised the price target on Travere Therapeutics (NASDAQ: TVTX) to $67.00 (from $57.00) while maintaining a Buy rating.&lt;/p&gt;&lt;p&gt;The analyst comments &quot;We reiterate our Buy rating and are increasing our price target to $67 from $57 based on the addition of civerobrutinib to our overall valuation, but just for the PMN indication. We see potential upside from the inclusion of additional indications. Our valuation of Travere is now split into two components. First regarding current sales of FILSPARI, our valuation is based on a risk-adjusted net present value (rNPV) analysis of projected future revenues; we assume</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Analyst+Comments/Travere+Therapeutics+%28TVTX%29+PT+Raised+to+%2467+at+H.C.+Wainwright/26589837.html</guid>
   <pubDate>Tue, 02 Jun 2026 11:38:13 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">TVTX</category>
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   <title>Form  8-K        Travere Therapeutics,     For: Jun 01</title>
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   <pubDate>Tue, 02 Jun 2026 07:05:00 -0400</pubDate>
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   	   	<category domain="http://rss.financialcontent.com/stocksymbol">TVTX</category>
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   <title>Form  8-K        Travere Therapeutics,     For: Jun 01</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++8-K++++++++Travere+Therapeutics%2C+++++For%3A+Jun+01/26587298.html</link>
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   <pubDate>Tue, 02 Jun 2026 07:05:00 -0400</pubDate>
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   <title>Travere licenses BTK inhibitor from Everest for rare kidney diseases</title>
   <link>http://www.streetinsider.com/Corporate+News/Travere+licenses+BTK+inhibitor+from+Everest+for+rare+kidney+diseases/26587241.html</link>
   <description>&lt;p&gt;Travere Therapeutics Inc. (NASDAQ: TVTX) entered into an exclusive licensing agreement with Everest Medicines for civorebrutinib, an investigational oral BTK inhibitor for rare kidney diseases in markets outside China and certain East and Southeast Asian countries.&lt;/p&gt;&lt;p&gt;Under the agreement, Everest will receive an upfront payment of $112.5 million and is eligible for up to approximately $1.03 billion in additional milestone payments across up to five indications. Travere will pay tiered royalties on future sales ranging from high single-digit to double-digit percentages based on annual net sales thresholds.&lt;/p&gt;&lt;p&gt;Civorebrutinib is a covalent reversible Bruton's tyrosine kinase inhibitor designed for immune-mediated kidney diseases. The</description>
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   <pubDate>Tue, 02 Jun 2026 07:01:35 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">TVTX</category>
   	  </item>
  <item>
   <title>Travere licenses BTK inhibitor from Everest for rare kidney diseases</title>
   <link>http://www.streetinsider.com/FDA/Travere+licenses+BTK+inhibitor+from+Everest+for+rare+kidney+diseases/26587241.html</link>
   <description>&lt;p&gt;Travere Therapeutics Inc. (NASDAQ: TVTX) entered into an exclusive licensing agreement with Everest Medicines for civorebrutinib, an investigational oral BTK inhibitor for rare kidney diseases in markets outside China and certain East and Southeast Asian countries.&lt;/p&gt;&lt;p&gt;Under the agreement, Everest will receive an upfront payment of $112.5 million and is eligible for up to approximately $1.03 billion in additional milestone payments across up to five indications. Travere will pay tiered royalties on future sales ranging from high single-digit to double-digit percentages based on annual net sales thresholds.&lt;/p&gt;&lt;p&gt;Civorebrutinib is a covalent reversible Bruton's tyrosine kinase inhibitor designed for immune-mediated kidney diseases. The</description>
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   <pubDate>Tue, 02 Jun 2026 07:01:35 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">TVTX</category>
   	  </item>
  <item>
   <title>Travere Therapeutics Enters Into Exclusive Licensing Agreement with Everest Medicines for Civorebrutinib a Potential Best-in-Class BTK Inhibitor for Rare Kidney Diseases</title>
   <link>http://www.streetinsider.com/Press+Releases/Travere+Therapeutics+Enters+Into+Exclusive+Licensing+Agreement+with+Everest+Medicines+for+Civorebrutinib+a+Potential+Best-in-Class+BTK+Inhibitor+for+Rare+Kidney+Diseases/26587232.html</link>
   <description>
&lt;p class=&quot;bwalignc&quot;&gt;
&lt;i&gt;Civorebrutinib is an investigational oral, covalent reversible BTK inhibitor designed to provide differentiated efficacy, safety and convenience in immune-mediated kidney diseases&lt;/i&gt;

&lt;/p&gt;&lt;p class=&quot;bwalignc&quot;&gt;
&lt;i&gt;Civorebrutinib adds pipeline-in-a-product potential across multiple rare kidney diseases, expanding and diversifying Travere’s pipeline&lt;/i&gt;

&lt;/p&gt;&lt;p class=&quot;bwalignc&quot;&gt;
&lt;i&gt;Company to host conference call June 2, 2026 at 8:30 a.m. ET&lt;/i&gt;

&lt;/p&gt;
&lt;p&gt;    SAN DIEGO--(BUSINESS WIRE)--
Travere Therapeutics, Inc., (Nasdaq: TVTX) today announced that it has entered into an exclusive licensing and collaboration agreement with Everest Medicines for the development and commercialization of civorebrutinib (also known as EVER001), a potential best-in-class oral, covalent reversible Bruton’s tyrosine kinase (BTK) inhibitor in all markets outside</description>
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   <pubDate>Tue, 02 Jun 2026 07:01:00 -0400</pubDate>
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   	   	<category domain="http://rss.financialcontent.com/stocksymbol">TVTX</category>
   	  </item>
  <item>
   <title>Travere Therapeutics Enters Into Exclusive Licensing Agreement with Everest Medicines for Civorebrutinib a Potential Best-in-Class BTK Inhibitor for Rare Kidney Diseases</title>
   <link>http://www.streetinsider.com/Press+Releases/Travere+Therapeutics+Enters+Into+Exclusive+Licensing+Agreement+with+Everest+Medicines+for+Civorebrutinib+a+Potential+Best-in-Class+BTK+Inhibitor+for+Rare+Kidney+Diseases/26587232.html</link>
   <description>
&lt;p class=&quot;bwalignc&quot;&gt;
&lt;i&gt;Civorebrutinib is an investigational oral, covalent reversible BTK inhibitor designed to provide differentiated efficacy, safety and convenience in immune-mediated kidney diseases&lt;/i&gt;

&lt;/p&gt;&lt;p class=&quot;bwalignc&quot;&gt;
&lt;i&gt;Civorebrutinib adds pipeline-in-a-product potential across multiple rare kidney diseases, expanding and diversifying Travere’s pipeline&lt;/i&gt;

&lt;/p&gt;&lt;p class=&quot;bwalignc&quot;&gt;
&lt;i&gt;Company to host conference call June 2, 2026 at 8:30 a.m. ET&lt;/i&gt;

&lt;/p&gt;
&lt;p&gt;    SAN DIEGO--(BUSINESS WIRE)--
Travere Therapeutics, Inc., (Nasdaq: TVTX) today announced that it has entered into an exclusive licensing and collaboration agreement with Everest Medicines for the development and commercialization of civorebrutinib (also known as EVER001), a potential best-in-class oral, covalent reversible Bruton’s tyrosine kinase (BTK) inhibitor in all markets outside</description>
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   <pubDate>Tue, 02 Jun 2026 07:01:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">O.09235062</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">TVTX</category>
   	  </item>
  <item>
   <title>Travere Therapeutics Enters Into Exclusive Licensing Agreement with Everest Medicines for Civorebrutinib a Potential Best-in-Class BTK Inhibitor for Rare Kidney Diseases</title>
   <link>http://www.streetinsider.com/Business+Wire/Travere+Therapeutics+Enters+Into+Exclusive+Licensing+Agreement+with+Everest+Medicines+for+Civorebrutinib+a+Potential+Best-in-Class+BTK+Inhibitor+for+Rare+Kidney+Diseases/26587232.html</link>
   <description>
&lt;p class=&quot;bwalignc&quot;&gt;
&lt;i&gt;Civorebrutinib is an investigational oral, covalent reversible BTK inhibitor designed to provide differentiated efficacy, safety and convenience in immune-mediated kidney diseases&lt;/i&gt;

&lt;/p&gt;&lt;p class=&quot;bwalignc&quot;&gt;
&lt;i&gt;Civorebrutinib adds pipeline-in-a-product potential across multiple rare kidney diseases, expanding and diversifying Travere’s pipeline&lt;/i&gt;

&lt;/p&gt;&lt;p class=&quot;bwalignc&quot;&gt;
&lt;i&gt;Company to host conference call June 2, 2026 at 8:30 a.m. ET&lt;/i&gt;

&lt;/p&gt;
&lt;p&gt;    SAN DIEGO--(BUSINESS WIRE)--
Travere Therapeutics, Inc., (Nasdaq: TVTX) today announced that it has entered into an exclusive licensing and collaboration agreement with Everest Medicines for the development and commercialization of civorebrutinib (also known as EVER001), a potential best-in-class oral, covalent reversible Bruton’s tyrosine kinase (BTK) inhibitor in all markets outside</description>
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   <pubDate>Tue, 02 Jun 2026 07:01:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">O.09235062</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">TVTX</category>
   	  </item>
  <item>
   <title>Travere Therapeutics Enters Into Exclusive Licensing Agreement with Everest Medicines for Civorebrutinib a Potential Best-in-Class BTK Inhibitor for Rare Kidney Diseases</title>
   <link>http://www.streetinsider.com/Business+Wire/Travere+Therapeutics+Enters+Into+Exclusive+Licensing+Agreement+with+Everest+Medicines+for+Civorebrutinib+a+Potential+Best-in-Class+BTK+Inhibitor+for+Rare+Kidney+Diseases/26587232.html</link>
   <description>
&lt;p class=&quot;bwalignc&quot;&gt;
&lt;i&gt;Civorebrutinib is an investigational oral, covalent reversible BTK inhibitor designed to provide differentiated efficacy, safety and convenience in immune-mediated kidney diseases&lt;/i&gt;

&lt;/p&gt;&lt;p class=&quot;bwalignc&quot;&gt;
&lt;i&gt;Civorebrutinib adds pipeline-in-a-product potential across multiple rare kidney diseases, expanding and diversifying Travere’s pipeline&lt;/i&gt;

&lt;/p&gt;&lt;p class=&quot;bwalignc&quot;&gt;
&lt;i&gt;Company to host conference call June 2, 2026 at 8:30 a.m. ET&lt;/i&gt;

&lt;/p&gt;
&lt;p&gt;    SAN DIEGO--(BUSINESS WIRE)--
Travere Therapeutics, Inc., (Nasdaq: TVTX) today announced that it has entered into an exclusive licensing and collaboration agreement with Everest Medicines for the development and commercialization of civorebrutinib (also known as EVER001), a potential best-in-class oral, covalent reversible Bruton’s tyrosine kinase (BTK) inhibitor in all markets outside</description>
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   <pubDate>Tue, 02 Jun 2026 07:01:00 -0400</pubDate>
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   	   	<category domain="http://rss.financialcontent.com/stocksymbol">TVTX</category>
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   <title>Travere receives patent allowance for FILSPARI use in kidney disease</title>
   <link>http://www.streetinsider.com/Corporate+News/Travere+receives+patent+allowance+for+FILSPARI+use+in+kidney+disease/26557744.html</link>
   <description>

&lt;p&gt;Travere Therapeutics Inc. (NASDAQ: TVTX) received a Notice of Allowance from the U.S. Patent and Trademark Office for U.S. Patent Application No. 19/253,088, which covers certain methods of using FILSPARI (sparsentan) in IgA nephropathy treatment.&lt;/p&gt;

&lt;p&gt;The patent application, titled &quot;Biphenyl Sulfonamide Compounds for the Treatment of Kidney Diseases or Disorders,&quot; is expected to provide U.S. patent coverage for specific methods of using sparsentan in IgA nephropathy until October 2037, according to the company's statement.&lt;/p&gt;

&lt;p&gt;The application will become a U.S. patent following payment of the issue fee and standard USPTO post-allowance processing. Travere plans to submit the issued patent for listing in</description>
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   <pubDate>Wed, 27 May 2026 16:05:15 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">O.09235062</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">TVTX</category>
   	  </item>
  <item>
   <title>Travere receives patent allowance for FILSPARI use in kidney disease</title>
   <link>http://www.streetinsider.com/Corporate+News/Travere+receives+patent+allowance+for+FILSPARI+use+in+kidney+disease/26557744.html</link>
   <description>

&lt;p&gt;Travere Therapeutics Inc. (NASDAQ: TVTX) received a Notice of Allowance from the U.S. Patent and Trademark Office for U.S. Patent Application No. 19/253,088, which covers certain methods of using FILSPARI (sparsentan) in IgA nephropathy treatment.&lt;/p&gt;

&lt;p&gt;The patent application, titled &quot;Biphenyl Sulfonamide Compounds for the Treatment of Kidney Diseases or Disorders,&quot; is expected to provide U.S. patent coverage for specific methods of using sparsentan in IgA nephropathy until October 2037, according to the company's statement.&lt;/p&gt;

&lt;p&gt;The application will become a U.S. patent following payment of the issue fee and standard USPTO post-allowance processing. Travere plans to submit the issued patent for listing in</description>
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   <pubDate>Wed, 27 May 2026 16:05:15 -0400</pubDate>
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