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   <title>Cogent (COGT) Reiterated at Buy by Stifel After ASCO Presentation on Bezuclastinib </title>
   <link>http://www.streetinsider.com/Analyst+Comments/Cogent+%28COGT%29+Reiterated+at+Buy+by+Stifel+After+ASCO+Presentation+on+Bezuclastinib+/26579256.html</link>
   <description>&lt;p&gt;Stifel analyst Laura Prendergast reiterated a Buy rating and $45.00 price target on Cogent (NASDAQ: COGT).&lt;/p&gt;&lt;p&gt;The analyst commented, &quot; At ASCO, COGT presented promising primary results from the Ph3 PEAK study of bezuclastinib + sunitinib vs sunitinib in 2L GIST (slides here &amp; PR here). Last week, COGT announced the FDA accepted their NDA in imatinib pretreated GIST under priority review (here); PDUFA date set for November 30, 2026.We model peak sales of ~$2.4B by 2035, inclusive of ~$1.5B of 2L GIST revenue, and make no change to our Buy rating and $45 TP. While we expect the initial launch</description>
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   <pubDate>Mon, 01 Jun 2026 07:31:40 -0400</pubDate>
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   <title>H.C. Wainwright Reiterates Buy Rating on Cogent (COGT)</title>
   <link>http://www.streetinsider.com/Analyst+Comments/H.C.+Wainwright+Reiterates+Buy+Rating+on+Cogent+%28COGT%29/26578820.html</link>
   <description>&lt;p&gt;H.C. Wainwright analyst Robert Burns reiterated a Buy rating and $55.00 price target on Cogent (NASDAQ: COGT).&lt;/p&gt;&lt;p&gt;The analyst commented: &quot;At ASCO, Cogent presented the primary results from the Phase 3 PEAK trial, which evaluated bezuclastinib + Sutent (sunitinib) vs. Sutent in 2L, imatinib-resistant gastrointestinal stromal tumors (GIST). Treatment with bezuclastinib + Sutent (n=204) generated a statistically significant improvement compared to Sutent monotherapy in both ORR (45.6% vs 25.8%; p&lt;0.0001) and PFS (16.5 months vs. 9.2 months [HR=0.50; 95% CI: 0.39-0.65; p&lt;0.0001]), with a relatively consistent efficacy profile across genotype subgroups (see Figure 1 overleaf). The combination also reduced the risk</description>
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   <pubDate>Mon, 01 Jun 2026 06:57:55 -0400</pubDate>
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   <title>Cogent Biosciences reports positive Phase 3 trial data for GIST treatment</title>
   <link>http://www.streetinsider.com/FDA/Cogent+Biosciences+reports+positive+Phase+3+trial+data+for+GIST+treatment/26577190.html</link>
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&lt;p&gt;Cogent Biosciences Inc. (NASDAQ: COGT) announced results from its PEAK Phase 3 trial showing bezuclastinib combined with sunitinib demonstrated superior progression-free survival compared to sunitinib alone in patients with gastrointestinal stromal tumors who previously received imatinib treatment.&lt;/p&gt;

&lt;p&gt;The trial met its primary endpoint with median progression-free survival of 16.5 months for the combination therapy versus 9.2 months for sunitinib monotherapy, representing a 50% reduction in risk of disease progression or death with a hazard ratio of 0.50. The objective response rate reached 46% for patients receiving the combination compared to 26% for those on sunitinib alone.&lt;/p&gt;

&lt;p&gt;The bezuclastinib combination showed efficacy across</description>
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   <title>Cogent Biosciences reports positive Phase 3 trial data for GIST treatment</title>
   <link>http://www.streetinsider.com/FDA/Cogent+Biosciences+reports+positive+Phase+3+trial+data+for+GIST+treatment/26577190.html</link>
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&lt;p&gt;Cogent Biosciences Inc. (NASDAQ: COGT) announced results from its PEAK Phase 3 trial showing bezuclastinib combined with sunitinib demonstrated superior progression-free survival compared to sunitinib alone in patients with gastrointestinal stromal tumors who previously received imatinib treatment.&lt;/p&gt;

&lt;p&gt;The trial met its primary endpoint with median progression-free survival of 16.5 months for the combination therapy versus 9.2 months for sunitinib monotherapy, representing a 50% reduction in risk of disease progression or death with a hazard ratio of 0.50. The objective response rate reached 46% for patients receiving the combination compared to 26% for those on sunitinib alone.&lt;/p&gt;

&lt;p&gt;The bezuclastinib combination showed efficacy across</description>
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   <title>Cogent Biosciences reports positive Phase 3 trial data for GIST treatment</title>
   <link>http://www.streetinsider.com/FDA/Cogent+Biosciences+reports+positive+Phase+3+trial+data+for+GIST+treatment/26577190.html</link>
   <description>

&lt;p&gt;Cogent Biosciences Inc. (NASDAQ: COGT) announced results from its PEAK Phase 3 trial showing bezuclastinib combined with sunitinib demonstrated superior progression-free survival compared to sunitinib alone in patients with gastrointestinal stromal tumors who previously received imatinib treatment.&lt;/p&gt;

&lt;p&gt;The trial met its primary endpoint with median progression-free survival of 16.5 months for the combination therapy versus 9.2 months for sunitinib monotherapy, representing a 50% reduction in risk of disease progression or death with a hazard ratio of 0.50. The objective response rate reached 46% for patients receiving the combination compared to 26% for those on sunitinib alone.&lt;/p&gt;

&lt;p&gt;The bezuclastinib combination showed efficacy across</description>
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   <title>Cogent Biosciences reports positive Phase 3 trial data for GIST treatment</title>
   <link>http://www.streetinsider.com/FDA/Cogent+Biosciences+reports+positive+Phase+3+trial+data+for+GIST+treatment/26577190.html</link>
   <description>

&lt;p&gt;Cogent Biosciences Inc. (NASDAQ: COGT) announced results from its PEAK Phase 3 trial showing bezuclastinib combined with sunitinib demonstrated superior progression-free survival compared to sunitinib alone in patients with gastrointestinal stromal tumors who previously received imatinib treatment.&lt;/p&gt;

&lt;p&gt;The trial met its primary endpoint with median progression-free survival of 16.5 months for the combination therapy versus 9.2 months for sunitinib monotherapy, representing a 50% reduction in risk of disease progression or death with a hazard ratio of 0.50. The objective response rate reached 46% for patients receiving the combination compared to 26% for those on sunitinib alone.&lt;/p&gt;

&lt;p&gt;The bezuclastinib combination showed efficacy across</description>
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   <title>Cogent Biosciences reports positive Phase 3 trial data for GIST treatment</title>
   <link>http://www.streetinsider.com/FDA/Cogent+Biosciences+reports+positive+Phase+3+trial+data+for+GIST+treatment/26577190.html</link>
   <description>

&lt;p&gt;Cogent Biosciences Inc. (NASDAQ: COGT) announced results from its PEAK Phase 3 trial showing bezuclastinib combined with sunitinib demonstrated superior progression-free survival compared to sunitinib alone in patients with gastrointestinal stromal tumors who previously received imatinib treatment.&lt;/p&gt;

&lt;p&gt;The trial met its primary endpoint with median progression-free survival of 16.5 months for the combination therapy versus 9.2 months for sunitinib monotherapy, representing a 50% reduction in risk of disease progression or death with a hazard ratio of 0.50. The objective response rate reached 46% for patients receiving the combination compared to 26% for those on sunitinib alone.&lt;/p&gt;

&lt;p&gt;The bezuclastinib combination showed efficacy across</description>
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   <title>Cogent Biosciences reports positive Phase 3 trial data for GIST treatment</title>
   <link>http://www.streetinsider.com/FDA/Cogent+Biosciences+reports+positive+Phase+3+trial+data+for+GIST+treatment/26577190.html</link>
   <description>

&lt;p&gt;Cogent Biosciences Inc. (NASDAQ: COGT) announced results from its PEAK Phase 3 trial showing bezuclastinib combined with sunitinib demonstrated superior progression-free survival compared to sunitinib alone in patients with gastrointestinal stromal tumors who previously received imatinib treatment.&lt;/p&gt;

&lt;p&gt;The trial met its primary endpoint with median progression-free survival of 16.5 months for the combination therapy versus 9.2 months for sunitinib monotherapy, representing a 50% reduction in risk of disease progression or death with a hazard ratio of 0.50. The objective response rate reached 46% for patients receiving the combination compared to 26% for those on sunitinib alone.&lt;/p&gt;

&lt;p&gt;The bezuclastinib combination showed efficacy across</description>
   <guid isPermaLink="true">http://www.streetinsider.com/FDA/Cogent+Biosciences+reports+positive+Phase+3+trial+data+for+GIST+treatment/26577190.html</guid>
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   <title>Cogent Biosciences reports positive Phase 3 trial data for GIST treatment</title>
   <link>http://www.streetinsider.com/FDA/Cogent+Biosciences+reports+positive+Phase+3+trial+data+for+GIST+treatment/26577190.html</link>
   <description>

&lt;p&gt;Cogent Biosciences Inc. (NASDAQ: COGT) announced results from its PEAK Phase 3 trial showing bezuclastinib combined with sunitinib demonstrated superior progression-free survival compared to sunitinib alone in patients with gastrointestinal stromal tumors who previously received imatinib treatment.&lt;/p&gt;

&lt;p&gt;The trial met its primary endpoint with median progression-free survival of 16.5 months for the combination therapy versus 9.2 months for sunitinib monotherapy, representing a 50% reduction in risk of disease progression or death with a hazard ratio of 0.50. The objective response rate reached 46% for patients receiving the combination compared to 26% for those on sunitinib alone.&lt;/p&gt;

&lt;p&gt;The bezuclastinib combination showed efficacy across</description>
   <guid isPermaLink="true">http://www.streetinsider.com/FDA/Cogent+Biosciences+reports+positive+Phase+3+trial+data+for+GIST+treatment/26577190.html</guid>
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   <title>Cogent Biosciences reports positive Phase 3 trial data for GIST treatment</title>
   <link>http://www.streetinsider.com/FDA/Cogent+Biosciences+reports+positive+Phase+3+trial+data+for+GIST+treatment/26577190.html</link>
   <description>

&lt;p&gt;Cogent Biosciences Inc. (NASDAQ: COGT) announced results from its PEAK Phase 3 trial showing bezuclastinib combined with sunitinib demonstrated superior progression-free survival compared to sunitinib alone in patients with gastrointestinal stromal tumors who previously received imatinib treatment.&lt;/p&gt;

&lt;p&gt;The trial met its primary endpoint with median progression-free survival of 16.5 months for the combination therapy versus 9.2 months for sunitinib monotherapy, representing a 50% reduction in risk of disease progression or death with a hazard ratio of 0.50. The objective response rate reached 46% for patients receiving the combination compared to 26% for those on sunitinib alone.&lt;/p&gt;

&lt;p&gt;The bezuclastinib combination showed efficacy across</description>
   <guid isPermaLink="true">http://www.streetinsider.com/FDA/Cogent+Biosciences+reports+positive+Phase+3+trial+data+for+GIST+treatment/26577190.html</guid>
   <pubDate>Sat, 30 May 2026 08:00:17 -0400</pubDate>
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   <title>Cogent Biosciences Announces Detailed Clinical Data from PEAK Phase 3 Trial with Bezuclastinib in Combination with Sunitinib in Gastrointestinal Stromal Tumors (GIST) at 2026 American Society of Clini</title>
   <link>http://www.streetinsider.com/Press+Releases/Cogent+Biosciences+Announces+Detailed+Clinical+Data+from+PEAK+Phase+3+Trial+with+Bezuclastinib+in+Combination+with+Sunitinib+in+Gastrointestinal+Stromal+Tumors+%28GIST%29+at+2026+American+Society+of+Clini/26577178.html</link>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;Bezuclastinib combination is first treatment ever to demonstrate statistically significant advantage against active comparator in GIST patients; median PFS of 16.5 months versus 9.2 months (HR=0.50, CI: 0.39-0.65, p&amp;lt;0.0001) for bezuclastinib combination compared to sunitinib alone&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Bezuclastinib combination provides clear PFS benefit regardless of primary or secondary KIT mutations &lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Mean duration of treatment estimated at 21.4 months for patients receiving bezuclastinib combination&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Bezuclastinib combination well tolerated with no unique risks observed with the combination when compared to the known safety profile of sunitinib&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Priority Review granted following FDA acceptance of</description>
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   <title>Cogent Biosciences Announces Detailed Clinical Data from PEAK Phase 3 Trial with Bezuclastinib in Combination with Sunitinib in Gastrointestinal Stromal Tumors (GIST) at 2026 American Society of Clini</title>
   <link>http://www.streetinsider.com/Press+Releases/Cogent+Biosciences+Announces+Detailed+Clinical+Data+from+PEAK+Phase+3+Trial+with+Bezuclastinib+in+Combination+with+Sunitinib+in+Gastrointestinal+Stromal+Tumors+%28GIST%29+at+2026+American+Society+of+Clini/26577178.html</link>
   <description>
&lt;p align=&quot;center&quot;&gt;&lt;em&gt;Bezuclastinib combination is first treatment ever to demonstrate statistically significant advantage against active comparator in GIST patients; median PFS of 16.5 months versus 9.2 months (HR=0.50, CI: 0.39-0.65, p&amp;lt;0.0001) for bezuclastinib combination compared to sunitinib alone&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Bezuclastinib combination provides clear PFS benefit regardless of primary or secondary KIT mutations &lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Mean duration of treatment estimated at 21.4 months for patients receiving bezuclastinib combination&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Bezuclastinib combination well tolerated with no unique risks observed with the combination when compared to the known safety profile of sunitinib&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Priority Review granted following FDA acceptance of</description>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;Bezuclastinib combination is first treatment ever to demonstrate statistically significant advantage against active comparator in GIST patients; median PFS of 16.5 months versus 9.2 months (HR=0.50, CI: 0.39-0.65, p&amp;lt;0.0001) for bezuclastinib combination compared to sunitinib alone&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Bezuclastinib combination provides clear PFS benefit regardless of primary or secondary KIT mutations &lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Mean duration of treatment estimated at 21.4 months for patients receiving bezuclastinib combination&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Bezuclastinib combination well tolerated with no unique risks observed with the combination when compared to the known safety profile of sunitinib&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Priority Review granted following FDA acceptance of</description>
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   <title>Cogent Biosciences Announces Detailed Clinical Data from PEAK Phase 3 Trial with Bezuclastinib in Combination with Sunitinib in Gastrointestinal Stromal Tumors (GIST) at 2026 American Society of Clini</title>
   <link>http://www.streetinsider.com/Globe+Newswire/Cogent+Biosciences+Announces+Detailed+Clinical+Data+from+PEAK+Phase+3+Trial+with+Bezuclastinib+in+Combination+with+Sunitinib+in+Gastrointestinal+Stromal+Tumors+%28GIST%29+at+2026+American+Society+of+Clini/26577178.html</link>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;Bezuclastinib combination is first treatment ever to demonstrate statistically significant advantage against active comparator in GIST patients; median PFS of 16.5 months versus 9.2 months (HR=0.50, CI: 0.39-0.65, p&amp;lt;0.0001) for bezuclastinib combination compared to sunitinib alone&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Bezuclastinib combination provides clear PFS benefit regardless of primary or secondary KIT mutations &lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Mean duration of treatment estimated at 21.4 months for patients receiving bezuclastinib combination&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Bezuclastinib combination well tolerated with no unique risks observed with the combination when compared to the known safety profile of sunitinib&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Priority Review granted following FDA acceptance of</description>
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   <title>Cogent Biosciences Announces Detailed Clinical Data from PEAK Phase 3 Trial with Bezuclastinib in Combination with Sunitinib in Gastrointestinal Stromal Tumors (GIST) at 2026 American Society of Clini</title>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;Bezuclastinib combination is first treatment ever to demonstrate statistically significant advantage against active comparator in GIST patients; median PFS of 16.5 months versus 9.2 months (HR=0.50, CI: 0.39-0.65, p&amp;lt;0.0001) for bezuclastinib combination compared to sunitinib alone&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Bezuclastinib combination provides clear PFS benefit regardless of primary or secondary KIT mutations &lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Mean duration of treatment estimated at 21.4 months for patients receiving bezuclastinib combination&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Bezuclastinib combination well tolerated with no unique risks observed with the combination when compared to the known safety profile of sunitinib&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Priority Review granted following FDA acceptance of</description>
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   <title>Cogent Biosciences Announces Detailed Clinical Data from PEAK Phase 3 Trial with Bezuclastinib in Combination with Sunitinib in Gastrointestinal Stromal Tumors (GIST) at 2026 American Society of Clini</title>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;Bezuclastinib combination is first treatment ever to demonstrate statistically significant advantage against active comparator in GIST patients; median PFS of 16.5 months versus 9.2 months (HR=0.50, CI: 0.39-0.65, p&amp;lt;0.0001) for bezuclastinib combination compared to sunitinib alone&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Bezuclastinib combination provides clear PFS benefit regardless of primary or secondary KIT mutations &lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Mean duration of treatment estimated at 21.4 months for patients receiving bezuclastinib combination&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Bezuclastinib combination well tolerated with no unique risks observed with the combination when compared to the known safety profile of sunitinib&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Priority Review granted following FDA acceptance of</description>
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