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   <title>RBC Capital on Neurocrine Bio. (NBIX): 'We like the setup and remain buyers'</title>
   <link>http://www.streetinsider.com/Analyst+Comments/RBC+Capital+on+Neurocrine+Bio.+%28NBIX%29%3A+%27We+like+the+setup+and+remain+buyers%27/27034400.html</link>
   <description>&lt;p&gt;RBC Capital analyst Brian Abrahams reiterated an Outperform rating and $198.00 price target on Neurocrine Bio. (NASDAQ: NBIX).&lt;/p&gt;&lt;p&gt;The analyst commented: &quot;Getting Ahead of a Catalyst-Rich 2027 - Before a Potential Run-Up;  Following the recent pullback, NBIX now trades at a ~$16B cap, &lt;4x our durable annual Ingrezza+Crenessity sales est. - implying minimal embedded value for Vykat or the pipeline. We expect strong Ingrezza +Crenessity numbers to drive 2H26 appreciation, with any improved Vykat performance further catalyzing upside - but also see potential for shares to run up into the higher density of '27 pipeline catalysts. While data from the</description>
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   <pubDate>Tue, 08 Sep 2026 09:15:53 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">NBIX</category>
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   <title>Neurocrine Bio. (NBIX) PT Raised to $253 at Citi</title>
   <link>http://www.streetinsider.com/Analyst+PT+Change/Neurocrine+Bio.+%28NBIX%29+PT+Raised+to+%24253+at+Citi/27021188.html</link>
   <description>&lt;p&gt;Citi analyst Yigel Nochomovitz raised the price target on Neurocrine Bio. (NASDAQ: NBIX) to $253.00 (from $249.00) while maintaining a Buy rating.&lt;/p&gt;</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Analyst+PT+Change/Neurocrine+Bio.+%28NBIX%29+PT+Raised+to+%24253+at+Citi/27021188.html</guid>
   <pubDate>Thu, 03 Sep 2026 05:02:18 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">NBIX</category>
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   <title>Neurocrine Bio. (NBIX) PT Lowered to $182 at Morgan Stanley</title>
   <link>http://www.streetinsider.com/Analyst+PT+Change/Neurocrine+Bio.+%28NBIX%29+PT+Lowered+to+%24182+at+Morgan+Stanley/26916936.html</link>
   <description>Morgan Stanley analyst Jeffrey Hung lowered the price target on Neurocrine Bio. (NASDAQ: NBIX) to $182.00  (from $196.00) while maintaining a Equalweight rating.</description>
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   <pubDate>Thu, 13 Aug 2026 08:09:11 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">NBIX</category>
   	  </item>
  <item>
   <title>Neurocrine's Ingrezza study shows quality-of-life gains in TD patients</title>
   <link>http://www.streetinsider.com/Corporate+News/Neurocrine%27s+Ingrezza+study+shows+quality-of-life+gains+in+TD+patients/26909472.html</link>
   <description>&lt;p&gt;Neurocrine Biosciences (NASDAQ: NBIX) announced the publication of results from its KINECT-PRO Phase 4 open-label study, showing that once-daily Ingrezza (valbenazine) capsules produced improvements in patient-reported quality of life and daily functioning among people with tardive dyskinesia (TD). The findings were published in &lt;em&gt;CNS Spectrums&lt;/em&gt;.&lt;/p&gt;&lt;p&gt;The study enrolled 59 patients who received Ingrezza at doses of 40 mg, 60 mg, or 80 mg once daily for up to 24 weeks. Fifty-two patients completed the Week 24 visit, with 45 included in efficacy analyses. At baseline, approximately 41% of patients had mild TD movement severity, while 59% had moderate or severe TD.&lt;/p&gt;&lt;p&gt;Mean</description>
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   <pubDate>Wed, 12 Aug 2026 08:30:55 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">NBIX</category>
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   <title>Neurocrine's Ingrezza study shows quality-of-life gains in TD patients</title>
   <link>http://www.streetinsider.com/FDA/Neurocrine%27s+Ingrezza+study+shows+quality-of-life+gains+in+TD+patients/26909472.html</link>
   <description>&lt;p&gt;Neurocrine Biosciences (NASDAQ: NBIX) announced the publication of results from its KINECT-PRO Phase 4 open-label study, showing that once-daily Ingrezza (valbenazine) capsules produced improvements in patient-reported quality of life and daily functioning among people with tardive dyskinesia (TD). The findings were published in &lt;em&gt;CNS Spectrums&lt;/em&gt;.&lt;/p&gt;&lt;p&gt;The study enrolled 59 patients who received Ingrezza at doses of 40 mg, 60 mg, or 80 mg once daily for up to 24 weeks. Fifty-two patients completed the Week 24 visit, with 45 included in efficacy analyses. At baseline, approximately 41% of patients had mild TD movement severity, while 59% had moderate or severe TD.&lt;/p&gt;&lt;p&gt;Mean</description>
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   <pubDate>Wed, 12 Aug 2026 08:30:55 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">NBIX</category>
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   <title>Neurocrine Biosciences Announces Publication of KINECT-PRO™ Findings Demonstrating INGREZZA® (valbenazine) Capsules Improved Patient-Reported Quality of Life and Daily Functioning for People Living</title>
   <link>http://www.streetinsider.com/Press+Releases/Neurocrine+Biosciences+Announces+Publication+of+KINECT-PRO%E2%84%A2+Findings+Demonstrating+INGREZZA%C2%AE+%28valbenazine%29+Capsules+Improved+Patient-Reported+Quality+of+Life+and+Daily+Functioning+for+People+Living/26909422.html</link>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;INGREZZA is the only vesicular monoamine transporter 2 inhibitor with clinical trial data demonstrating improvements in quality of life and functionality in people living with tardive dyskinesia across multiple validated patient-reported outcomes&lt;/li&gt;&lt;li&gt;Mean improvements in the patient-reported impacts of tardive dyskinesia and clinician-rated movement severity exceeded established thresholds for clinically meaningful change at Week 24, with improvements observed regardless of underlying psychiatric diagnosis or baseline movement severity&lt;/li&gt;&lt;li&gt;Approximately 58% of patients met the threshold for tardive dyskinesia symptomatic remission at Week 24, based on clinician assessment of movement severity&lt;/li&gt;&lt;li&gt;Findings reinforce that even patients with mild tardive dyskinesia movements are impacted and</description>
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   <pubDate>Wed, 12 Aug 2026 08:30:00 -0400</pubDate>
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   <title>Neurocrine Biosciences Announces Publication of KINECT-PRO™ Findings Demonstrating INGREZZA® (valbenazine) Capsules Improved Patient-Reported Quality of Life and Daily Functioning for People Living</title>
   <link>http://www.streetinsider.com/PRNewswire/Neurocrine+Biosciences+Announces+Publication+of+KINECT-PRO%E2%84%A2+Findings+Demonstrating+INGREZZA%C2%AE+%28valbenazine%29+Capsules+Improved+Patient-Reported+Quality+of+Life+and+Daily+Functioning+for+People+Living/26909422.html</link>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;INGREZZA is the only vesicular monoamine transporter 2 inhibitor with clinical trial data demonstrating improvements in quality of life and functionality in people living with tardive dyskinesia across multiple validated patient-reported outcomes&lt;/li&gt;&lt;li&gt;Mean improvements in the patient-reported impacts of tardive dyskinesia and clinician-rated movement severity exceeded established thresholds for clinically meaningful change at Week 24, with improvements observed regardless of underlying psychiatric diagnosis or baseline movement severity&lt;/li&gt;&lt;li&gt;Approximately 58% of patients met the threshold for tardive dyskinesia symptomatic remission at Week 24, based on clinician assessment of movement severity&lt;/li&gt;&lt;li&gt;Findings reinforce that even patients with mild tardive dyskinesia movements are impacted and</description>
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   <pubDate>Wed, 12 Aug 2026 08:30:00 -0400</pubDate>
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   <title>Neurocrine Biosciences Announces Publication of KINECT-PRO™ Findings Demonstrating INGREZZA® (valbenazine) Capsules Improved Patient-Reported Quality of Life and Daily Functioning for People Living</title>
   <link>http://www.streetinsider.com/Press+Releases/Neurocrine+Biosciences+Announces+Publication+of+KINECT-PRO%E2%84%A2+Findings+Demonstrating+INGREZZA%C2%AE+%28valbenazine%29+Capsules+Improved+Patient-Reported+Quality+of+Life+and+Daily+Functioning+for+People+Living/26909422.html</link>
   <description>
&lt;div class=&quot;xn-content&quot;&gt;
&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;INGREZZA is the only vesicular monoamine transporter 2 inhibitor with clinical trial data demonstrating improvements in quality of life and functionality in people living with tardive dyskinesia across multiple validated patient-reported outcomes&lt;/li&gt;&lt;li&gt;Mean improvements in the patient-reported impacts of tardive dyskinesia and clinician-rated movement severity exceeded established thresholds for clinically meaningful change at Week 24, with improvements observed regardless of underlying psychiatric diagnosis or baseline movement severity&lt;/li&gt;&lt;li&gt;Approximately 58% of patients met the threshold for tardive dyskinesia symptomatic remission at Week 24, based on clinician assessment of movement severity&lt;/li&gt;&lt;li&gt;Findings reinforce that even patients with mild tardive dyskinesia movements are impacted and</description>
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   <pubDate>Wed, 12 Aug 2026 08:30:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">NBIX</category>
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   <title>Neurocrine Biosciences Announces Publication of KINECT-PRO™ Findings Demonstrating INGREZZA® (valbenazine) Capsules Improved Patient-Reported Quality of Life and Daily Functioning for People Living</title>
   <link>http://www.streetinsider.com/PRNewswire/Neurocrine+Biosciences+Announces+Publication+of+KINECT-PRO%E2%84%A2+Findings+Demonstrating+INGREZZA%C2%AE+%28valbenazine%29+Capsules+Improved+Patient-Reported+Quality+of+Life+and+Daily+Functioning+for+People+Living/26909422.html</link>
   <description>
&lt;div class=&quot;xn-content&quot;&gt;
&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;INGREZZA is the only vesicular monoamine transporter 2 inhibitor with clinical trial data demonstrating improvements in quality of life and functionality in people living with tardive dyskinesia across multiple validated patient-reported outcomes&lt;/li&gt;&lt;li&gt;Mean improvements in the patient-reported impacts of tardive dyskinesia and clinician-rated movement severity exceeded established thresholds for clinically meaningful change at Week 24, with improvements observed regardless of underlying psychiatric diagnosis or baseline movement severity&lt;/li&gt;&lt;li&gt;Approximately 58% of patients met the threshold for tardive dyskinesia symptomatic remission at Week 24, based on clinician assessment of movement severity&lt;/li&gt;&lt;li&gt;Findings reinforce that even patients with mild tardive dyskinesia movements are impacted and</description>
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   <pubDate>Wed, 12 Aug 2026 08:30:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">NBIX</category>
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   <title>Neurocrine starts Phase 1 trial of obesity drug NBIP-1968</title>
   <link>http://www.streetinsider.com/FDA/Neurocrine+starts+Phase+1+trial+of+obesity+drug+NBIP-1968/26888048.html</link>
   <description>

&lt;p&gt;Neurocrine Biosciences (NASDAQ: NBIX) has initiated a Phase 1 first-in-human clinical study evaluating the safety and tolerability of NBIP-1968, an investigational GLP-1/GIP/glucagon receptor triple agonist being developed as a treatment for obesity, according to a company statement.&lt;/p&gt;

&lt;p&gt;The study will initially assess single ascending doses of NBIP-1968 in adult participants across a range of body mass index categories, including overweight and obese individuals.&lt;/p&gt;

&lt;p&gt;NBIP-1968 is an internally discovered, investigational long-acting compound designed for once-weekly subcutaneous administration. It targets receptors for glucagon-like peptide-1 (GLP-1), glucose-dependent insulinotropic polypeptide (GIP), and glucagon, with the goal of influencing metabolic pathways involved in appetite regulation, energy balance,</description>
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   <pubDate>Fri, 07 Aug 2026 08:30:24 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">NBIX</category>
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   <title>Neurocrine starts Phase 1 trial of obesity drug NBIP-1968</title>
   <link>http://www.streetinsider.com/FDA/Neurocrine+starts+Phase+1+trial+of+obesity+drug+NBIP-1968/26888048.html</link>
   <description>

&lt;p&gt;Neurocrine Biosciences (NASDAQ: NBIX) has initiated a Phase 1 first-in-human clinical study evaluating the safety and tolerability of NBIP-1968, an investigational GLP-1/GIP/glucagon receptor triple agonist being developed as a treatment for obesity, according to a company statement.&lt;/p&gt;

&lt;p&gt;The study will initially assess single ascending doses of NBIP-1968 in adult participants across a range of body mass index categories, including overweight and obese individuals.&lt;/p&gt;

&lt;p&gt;NBIP-1968 is an internally discovered, investigational long-acting compound designed for once-weekly subcutaneous administration. It targets receptors for glucagon-like peptide-1 (GLP-1), glucose-dependent insulinotropic polypeptide (GIP), and glucagon, with the goal of influencing metabolic pathways involved in appetite regulation, energy balance,</description>
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   <pubDate>Fri, 07 Aug 2026 08:30:24 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">NBIX</category>
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   <title>Neurocrine Biosciences Announces Initiation of Phase 1 Clinical Study Evaluating NBIP-'1968, a GLP-1/GIP/Glucagon Receptor Triple Agonist</title>
   <link>http://www.streetinsider.com/Press+Releases/Neurocrine+Biosciences+Announces+Initiation+of+Phase+1+Clinical+Study+Evaluating+NBIP-%271968%2C+a+GLP-1GIPGlucagon+Receptor+Triple+Agonist/26888032.html</link>
   <description>
&lt;div class=&quot;xn-content&quot;&gt;
&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;Initiation of study marks an important milestone in advancing Neurocrine's obesity portfolio and investigational metabolic disease pipeline  &lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.ca.sandgo&quot; idsrc=&quot;xmltag.org&quot; &gt;SAN DIEGO&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Aug. 7, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;a target=&quot;_blank&quot; href=&quot;https://edge.prnewswire.com/c/link/?t=0&amp;amp;l=en&amp;amp;o=4747681-1&amp;amp;h=511099642&amp;amp;u=https%3A%2F%2Fwww.neurocrine.com%2F&amp;amp;a=Neurocrine+Biosciences%2C+Inc.&quot; target=&quot;_blank&quot; rel=&quot;nofollow&quot;&gt;&lt;span value=&quot;NASDAQ-NMS:NBIX&quot; idsrc=&quot;xmltag.org&quot; &gt;Neurocrine Biosciences, Inc.&lt;/span&gt;&lt;/a&gt; (Nasdaq: NBIX) today announced the initiation of a Phase 1 first-in-human clinical study evaluating the safety and tolerability of NBIP-'1968, an investigational &lt;span&gt;GLP-1&lt;/span&gt;/GIP/glucagon receptor triple agonist being developed as a therapy for obesity.&lt;/p&gt;
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   <pubDate>Fri, 07 Aug 2026 08:30:00 -0400</pubDate>
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   <title>Neurocrine Biosciences Announces Initiation of Phase 1 Clinical Study Evaluating NBIP-'1968, a GLP-1/GIP/Glucagon Receptor Triple Agonist</title>
   <link>http://www.streetinsider.com/PRNewswire/Neurocrine+Biosciences+Announces+Initiation+of+Phase+1+Clinical+Study+Evaluating+NBIP-%271968%2C+a+GLP-1GIPGlucagon+Receptor+Triple+Agonist/26888032.html</link>
   <description>
&lt;div class=&quot;xn-content&quot;&gt;
&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;Initiation of study marks an important milestone in advancing Neurocrine's obesity portfolio and investigational metabolic disease pipeline  &lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.ca.sandgo&quot; idsrc=&quot;xmltag.org&quot; &gt;SAN DIEGO&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Aug. 7, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;a target=&quot;_blank&quot; href=&quot;https://edge.prnewswire.com/c/link/?t=0&amp;amp;l=en&amp;amp;o=4747681-1&amp;amp;h=511099642&amp;amp;u=https%3A%2F%2Fwww.neurocrine.com%2F&amp;amp;a=Neurocrine+Biosciences%2C+Inc.&quot; target=&quot;_blank&quot; rel=&quot;nofollow&quot;&gt;&lt;span value=&quot;NASDAQ-NMS:NBIX&quot; idsrc=&quot;xmltag.org&quot; &gt;Neurocrine Biosciences, Inc.&lt;/span&gt;&lt;/a&gt; (Nasdaq: NBIX) today announced the initiation of a Phase 1 first-in-human clinical study evaluating the safety and tolerability of NBIP-'1968, an investigational &lt;span&gt;GLP-1&lt;/span&gt;/GIP/glucagon receptor triple agonist being developed as a therapy for obesity.&lt;/p&gt;
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   <title>Neurocrine Biosciences Announces Initiation of Phase 1 Clinical Study Evaluating NBIP-'1968, a GLP-1/GIP/Glucagon Receptor Triple Agonist</title>
   <link>http://www.streetinsider.com/Press+Releases/Neurocrine+Biosciences+Announces+Initiation+of+Phase+1+Clinical+Study+Evaluating+NBIP-%271968%2C+a+GLP-1GIPGlucagon+Receptor+Triple+Agonist/26888032.html</link>
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&lt;div class=&quot;xn-content&quot;&gt;
&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;Initiation of study marks an important milestone in advancing Neurocrine's obesity portfolio and investigational metabolic disease pipeline  &lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.ca.sandgo&quot; idsrc=&quot;xmltag.org&quot; &gt;SAN DIEGO&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Aug. 7, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;a target=&quot;_blank&quot; href=&quot;https://edge.prnewswire.com/c/link/?t=0&amp;amp;l=en&amp;amp;o=4747681-1&amp;amp;h=511099642&amp;amp;u=https%3A%2F%2Fwww.neurocrine.com%2F&amp;amp;a=Neurocrine+Biosciences%2C+Inc.&quot; target=&quot;_blank&quot; rel=&quot;nofollow&quot;&gt;&lt;span value=&quot;NASDAQ-NMS:NBIX&quot; idsrc=&quot;xmltag.org&quot; &gt;Neurocrine Biosciences, Inc.&lt;/span&gt;&lt;/a&gt; (Nasdaq: NBIX) today announced the initiation of a Phase 1 first-in-human clinical study evaluating the safety and tolerability of NBIP-'1968, an investigational &lt;span&gt;GLP-1&lt;/span&gt;/GIP/glucagon receptor triple agonist being developed as a therapy for obesity.&lt;/p&gt;
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   <pubDate>Fri, 07 Aug 2026 08:30:00 -0400</pubDate>
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   <title>Neurocrine Biosciences Announces Initiation of Phase 1 Clinical Study Evaluating NBIP-'1968, a GLP-1/GIP/Glucagon Receptor Triple Agonist</title>
   <link>http://www.streetinsider.com/PRNewswire/Neurocrine+Biosciences+Announces+Initiation+of+Phase+1+Clinical+Study+Evaluating+NBIP-%271968%2C+a+GLP-1GIPGlucagon+Receptor+Triple+Agonist/26888032.html</link>
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&lt;div class=&quot;xn-content&quot;&gt;
&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;Initiation of study marks an important milestone in advancing Neurocrine's obesity portfolio and investigational metabolic disease pipeline  &lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.ca.sandgo&quot; idsrc=&quot;xmltag.org&quot; &gt;SAN DIEGO&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Aug. 7, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;a target=&quot;_blank&quot; href=&quot;https://edge.prnewswire.com/c/link/?t=0&amp;amp;l=en&amp;amp;o=4747681-1&amp;amp;h=511099642&amp;amp;u=https%3A%2F%2Fwww.neurocrine.com%2F&amp;amp;a=Neurocrine+Biosciences%2C+Inc.&quot; target=&quot;_blank&quot; rel=&quot;nofollow&quot;&gt;&lt;span value=&quot;NASDAQ-NMS:NBIX&quot; idsrc=&quot;xmltag.org&quot; &gt;Neurocrine Biosciences, Inc.&lt;/span&gt;&lt;/a&gt; (Nasdaq: NBIX) today announced the initiation of a Phase 1 first-in-human clinical study evaluating the safety and tolerability of NBIP-'1968, an investigational &lt;span&gt;GLP-1&lt;/span&gt;/GIP/glucagon receptor triple agonist being developed as a therapy for obesity.&lt;/p&gt;
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   <title>Form  4          NEUROCRINE BIOSCIENCES    For: Aug 04  Filed by: Onyia Jude</title>
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   <pubDate>Wed, 05 Aug 2026 17:36:00 -0400</pubDate>
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   <pubDate>Wed, 05 Aug 2026 17:36:00 -0400</pubDate>
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   <title>Neurocrine Bio. (NBIX) PT Raised to $213 at Truist Securities</title>
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   <description>Truist Securities analyst Danielle Brill raised the price target on Neurocrine Bio. (NASDAQ: NBIX) to $213.00  (from $200.00) while maintaining a Buy rating.</description>
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   <pubDate>Mon, 03 Aug 2026 07:06:06 -0400</pubDate>
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   <title>H.C. Wainwright Reiterates Buy Rating on Neurocrine Bio. (NBIX)</title>
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   <description>&lt;p&gt;H.C. Wainwright analyst Andrew Fein reiterated a Buy rating and $215.00 price target on Neurocrine Bio. (NASDAQ: NBIX).&lt;/p&gt;&lt;p&gt;The analyst commented: &quot;Neurocrine reaffirmed 2H27 Phase 3 topline for both osavampator in major depressive disorder and the first direclidine study in schizophrenia, with a second schizophrenia Phase 3 in 2028, which we think are the two big binary catalysts that have the potential to change the course of the company. Note that direclidine (NBI-'568) is a selective M4 orthosteric agonist that in Phase 2 produced a 7.5-point placebo-adjusted PANSS improvement at 20 mg once daily, an effect size of 0.61, with GI</description>
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   <pubDate>Mon, 03 Aug 2026 06:54:57 -0400</pubDate>
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   <title>Neurocrine Bio. (NBIX) PT Raised to $210 at Canaccord</title>
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   <description>(Updated - August 3, 2026 6:44 AM EDT)

&lt;p&gt;Canaccord analyst Sumant Kulkarni raised the price target on Neurocrine Bio. (NASDAQ: NBIX) to $210.00 (from $200.00) while maintaining a Buy rating.&lt;/p&gt;&lt;p&gt;The analyst commented: &quot;NBIX reported its 2Q26 results after the close yesterday (7/30). Sales of Ingrezza (valbenazine for tardive dyskinesia/TD, Huntington's chorea)/Crenessity (crinecerfont for classic congenital adrenal) came in at $716mn/ $184mn, which blew past our $675mn/$146mn and consensus of $688mn/$169mn. This was the first quarter including the recent acquisition of Soleno, and Vykat XR (diazoxide choline extended release) for hyperphagia (excessive appetite) in Prader-Willi syndrome (PWS) had partial quarter sales of</description>
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   <pubDate>Mon, 03 Aug 2026 06:44:05 -0400</pubDate>
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   <title>Neurocrine Bio. (NBIX) PT Raised to $210 at Canaccord</title>
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   <description>(Updated - August 3, 2026 6:44 AM EDT)

&lt;p&gt;Canaccord analyst Sumant Kulkarni raised the price target on Neurocrine Bio. (NASDAQ: NBIX) to $210.00 (from $200.00) while maintaining a Buy rating.&lt;/p&gt;&lt;p&gt;The analyst commented: &quot;NBIX reported its 2Q26 results after the close yesterday (7/30). Sales of Ingrezza (valbenazine for tardive dyskinesia/TD, Huntington's chorea)/Crenessity (crinecerfont for classic congenital adrenal) came in at $716mn/ $184mn, which blew past our $675mn/$146mn and consensus of $688mn/$169mn. This was the first quarter including the recent acquisition of Soleno, and Vykat XR (diazoxide choline extended release) for hyperphagia (excessive appetite) in Prader-Willi syndrome (PWS) had partial quarter sales of</description>
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   <pubDate>Mon, 03 Aug 2026 06:44:05 -0400</pubDate>
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   <pubDate>Fri, 31 Jul 2026 16:11:00 -0400</pubDate>
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