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   <title>SCYNEXIS Announces Inducement Award Under Nasdaq Listing Rule 5635(c)(4)</title>
   <link>http://www.streetinsider.com/Press+Releases/SCYNEXIS+Announces+Inducement+Award+Under+Nasdaq+Listing+Rule+5635%28c%29%284%29/26976014.html</link>
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&lt;p align=&quot;left&quot;&gt;JERSEY CITY, N.J., Aug.  25, 2026  (GLOBE NEWSWIRE) -- SCYNEXIS, Inc. (Nasdaq: SCYX), a clinical-stage biotechnology company focused on developing innovative therapies for severe and difficult-to-treat diseases with significant unmet medical need, today announced the grant of an inducement equity award to a new Senior Director, with a grant date of August 24, 2026. The award was granted in connection with the commencement of the Senior Director’s employment with the Company, as a material inducement to the employee’s acceptance of employment, and was approved in accordance with Nasdaq Listing Rule 5635(c)(4).&lt;/p&gt;  &lt;p align=&quot;left&quot;&gt;The award was granted</description>
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   <pubDate>Tue, 25 Aug 2026 19:06:00 -0400</pubDate>
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   <title>SCYNEXIS Announces Inducement Award Under Nasdaq Listing Rule 5635(c)(4)</title>
   <link>http://www.streetinsider.com/Press+Releases/SCYNEXIS+Announces+Inducement+Award+Under+Nasdaq+Listing+Rule+5635%28c%29%284%29/26976014.html</link>
   <description>
&lt;p align=&quot;left&quot;&gt;JERSEY CITY, N.J., Aug.  25, 2026  (GLOBE NEWSWIRE) -- SCYNEXIS, Inc. (Nasdaq: SCYX), a clinical-stage biotechnology company focused on developing innovative therapies for severe and difficult-to-treat diseases with significant unmet medical need, today announced the grant of an inducement equity award to a new Senior Director, with a grant date of August 24, 2026. The award was granted in connection with the commencement of the Senior Director’s employment with the Company, as a material inducement to the employee’s acceptance of employment, and was approved in accordance with Nasdaq Listing Rule 5635(c)(4).&lt;/p&gt;  &lt;p align=&quot;left&quot;&gt;The award was granted</description>
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   <pubDate>Tue, 25 Aug 2026 19:06:00 -0400</pubDate>
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   <title>SCYNEXIS Announces Inducement Award Under Nasdaq Listing Rule 5635(c)(4)</title>
   <link>http://www.streetinsider.com/Globe+Newswire/SCYNEXIS+Announces+Inducement+Award+Under+Nasdaq+Listing+Rule+5635%28c%29%284%29/26976014.html</link>
   <description>
&lt;p align=&quot;left&quot;&gt;JERSEY CITY, N.J., Aug.  25, 2026  (GLOBE NEWSWIRE) -- SCYNEXIS, Inc. (Nasdaq: SCYX), a clinical-stage biotechnology company focused on developing innovative therapies for severe and difficult-to-treat diseases with significant unmet medical need, today announced the grant of an inducement equity award to a new Senior Director, with a grant date of August 24, 2026. The award was granted in connection with the commencement of the Senior Director’s employment with the Company, as a material inducement to the employee’s acceptance of employment, and was approved in accordance with Nasdaq Listing Rule 5635(c)(4).&lt;/p&gt;  &lt;p align=&quot;left&quot;&gt;The award was granted</description>
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   <pubDate>Tue, 25 Aug 2026 19:06:00 -0400</pubDate>
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   <title>SCYNEXIS Announces Inducement Award Under Nasdaq Listing Rule 5635(c)(4)</title>
   <link>http://www.streetinsider.com/Globe+Newswire/SCYNEXIS+Announces+Inducement+Award+Under+Nasdaq+Listing+Rule+5635%28c%29%284%29/26976014.html</link>
   <description>
&lt;p align=&quot;left&quot;&gt;JERSEY CITY, N.J., Aug.  25, 2026  (GLOBE NEWSWIRE) -- SCYNEXIS, Inc. (Nasdaq: SCYX), a clinical-stage biotechnology company focused on developing innovative therapies for severe and difficult-to-treat diseases with significant unmet medical need, today announced the grant of an inducement equity award to a new Senior Director, with a grant date of August 24, 2026. The award was granted in connection with the commencement of the Senior Director’s employment with the Company, as a material inducement to the employee’s acceptance of employment, and was approved in accordance with Nasdaq Listing Rule 5635(c)(4).&lt;/p&gt;  &lt;p align=&quot;left&quot;&gt;The award was granted</description>
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   <pubDate>Tue, 25 Aug 2026 19:06:00 -0400</pubDate>
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   <title>Form  SCHEDULE 13G/A  SCYNEXIS INC                           Filed by: CVI Investments, Inc.</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++SCHEDULE+13GA++SCYNEXIS+INC+++++++++++++++++++++++++++Filed+by%3A+CVI+Investments%2C+Inc./26929154.html</link>
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   <pubDate>Fri, 14 Aug 2026 14:45:00 -0400</pubDate>
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   <title>Form  SCHEDULE 13G/A  SCYNEXIS INC                           Filed by: CVI Investments, Inc.</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++SCHEDULE+13GA++SCYNEXIS+INC+++++++++++++++++++++++++++Filed+by%3A+CVI+Investments%2C+Inc./26929154.html</link>
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   <pubDate>Fri, 14 Aug 2026 14:45:00 -0400</pubDate>
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   <title>Form  SCHEDULE 13G/A  SCYNEXIS INC                           Filed by: GREAT POINT PARTNERS LLC</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++SCHEDULE+13GA++SCYNEXIS+INC+++++++++++++++++++++++++++Filed+by%3A+GREAT+POINT+PARTNERS+LLC/26925867.html</link>
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   <pubDate>Fri, 14 Aug 2026 09:33:00 -0400</pubDate>
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   <title>Form  SCHEDULE 13G/A  SCYNEXIS INC                           Filed by: GREAT POINT PARTNERS LLC</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++SCHEDULE+13GA++SCYNEXIS+INC+++++++++++++++++++++++++++Filed+by%3A+GREAT+POINT+PARTNERS+LLC/26925867.html</link>
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   <pubDate>Fri, 14 Aug 2026 09:33:00 -0400</pubDate>
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   <title>SCYNEXIS (SCYX) PT Raised to $33 at Guggenheim</title>
   <link>http://www.streetinsider.com/Analyst+PT+Change/SCYNEXIS+%28SCYX%29+PT+Raised+to+%2433+at+Guggenheim/26916024.html</link>
   <description>(Updated - August 13, 2026 6:47 AM EDT)

&lt;p&gt;Guggenheim analyst Vamil Divan raised the price target on SCYNEXIS (NASDAQ: SCYX) to $33.00 (from $24.00) while maintaining a Buy rating.&lt;/p&gt;&lt;p&gt;The analyst commented: &quot;We are increasing our price target on SCYX shares to $33 (from $24) and reiterating our Buy rating following multiple conversations with nephrologists that leave us more optimistic on both the mechanistic rationale and commercial opportunity for SCY-770 (formerly PXL-770) in autosomal dominant polycystic kidney disease (ADPKD). The transaction for SCY-770 with Poxel fundamentally reoriented SCYX from an antifungal-focused company to a rare renal disease company, with ADPKD the lead</description>
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   <pubDate>Thu, 13 Aug 2026 06:47:48 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">SCYX</category>
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   <title>SCYNEXIS (SCYX) PT Raised to $33 at Guggenheim</title>
   <link>http://www.streetinsider.com/Analyst+Comments/SCYNEXIS+%28SCYX%29+PT+Raised+to+%2433+at+Guggenheim/26916024.html</link>
   <description>(Updated - August 13, 2026 6:47 AM EDT)

&lt;p&gt;Guggenheim analyst Vamil Divan raised the price target on SCYNEXIS (NASDAQ: SCYX) to $33.00 (from $24.00) while maintaining a Buy rating.&lt;/p&gt;&lt;p&gt;The analyst commented: &quot;We are increasing our price target on SCYX shares to $33 (from $24) and reiterating our Buy rating following multiple conversations with nephrologists that leave us more optimistic on both the mechanistic rationale and commercial opportunity for SCY-770 (formerly PXL-770) in autosomal dominant polycystic kidney disease (ADPKD). The transaction for SCY-770 with Poxel fundamentally reoriented SCYX from an antifungal-focused company to a rare renal disease company, with ADPKD the lead</description>
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   <pubDate>Thu, 13 Aug 2026 06:47:48 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">SCYX</category>
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   <title>Form  SCHEDULE 13G  SCYNEXIS INC                           Filed by: Adage Capital Management, L.P.</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++SCHEDULE+13G++SCYNEXIS+INC+++++++++++++++++++++++++++Filed+by%3A+Adage+Capital+Management%2C+L.P./26911271.html</link>
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   <pubDate>Wed, 12 Aug 2026 12:09:00 -0400</pubDate>
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   <title>Form  SCHEDULE 13G  SCYNEXIS INC                           Filed by: Adage Capital Management, L.P.</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++SCHEDULE+13G++SCYNEXIS+INC+++++++++++++++++++++++++++Filed+by%3A+Adage+Capital+Management%2C+L.P./26911271.html</link>
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   <pubDate>Wed, 12 Aug 2026 12:09:00 -0400</pubDate>
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   <title>Scynexis (SCYX) Tops Q2 EPS by 114c</title>
   <link>http://www.streetinsider.com/Earnings/Scynexis+%28SCYX%29+Tops+Q2+EPS+by+114c/26899211.html</link>
   <description>&lt;p&gt;Scynexis (NASDAQ: SCYX) reported Q2 EPS of $0.63, $1.14 better than the analyst estimate of ($0.51). Revenue for the quarter came in at $240 thousand versus the consensus estimate of $80.33 thousand.&lt;/p&gt;&lt;p&gt;For earnings history and earnings-related data on Scynexis (SCYX) &lt;a href=&quot;http://www.streetinsider.com/ec_earnings.php?q=SCYX&quot;&gt;click here&lt;/a&gt;.&lt;/p&gt;</description>
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   <pubDate>Mon, 10 Aug 2026 17:21:17 -0400</pubDate>
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   <title>SCYNEXIS Reports Second Quarter 2026 Financial Results and Provides Corporate Update</title>
   <link>http://www.streetinsider.com/Press+Releases/SCYNEXIS+Reports+Second+Quarter+2026+Financial+Results+and+Provides+Corporate+Update/26898442.html</link>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;margin-top:6pt; margin-bottom:6pt; text-align:justify;&quot;&gt;Initiated a Phase 1 study of SCY-770, a first-in-class, potent and direct AMPK activator for treatment of ADPKD; topline data are expected in Q3 2026 and are anticipated to inform dose selection for the planned Phase 2 study &lt;br/&gt;&lt;br/&gt;&lt;/li&gt;&lt;li style=&quot;margin-top:6pt; margin-bottom:6pt; text-align:justify;&quot;&gt;The Phase 2 proof-of-concept study of SCY-770 in patients with ADPKD remains on track for initiation in Q4 2026, with an early efficacy read-out expected in the second half of 2027&lt;br/&gt;&lt;br/&gt;&lt;/li&gt;&lt;li style=&quot;margin-top:6pt; margin-bottom:6pt; text-align:justify;&quot;&gt;Completed dosing in the Phase 1 study of the IV formulation of second-generation antifungal SCY-247, with topline data on track for Q3</description>
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   <title>SCYNEXIS Reports Second Quarter 2026 Financial Results and Provides Corporate Update</title>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;margin-top:6pt; margin-bottom:6pt; text-align:justify;&quot;&gt;Initiated a Phase 1 study of SCY-770, a first-in-class, potent and direct AMPK activator for treatment of ADPKD; topline data are expected in Q3 2026 and are anticipated to inform dose selection for the planned Phase 2 study &lt;br/&gt;&lt;br/&gt;&lt;/li&gt;&lt;li style=&quot;margin-top:6pt; margin-bottom:6pt; text-align:justify;&quot;&gt;The Phase 2 proof-of-concept study of SCY-770 in patients with ADPKD remains on track for initiation in Q4 2026, with an early efficacy read-out expected in the second half of 2027&lt;br/&gt;&lt;br/&gt;&lt;/li&gt;&lt;li style=&quot;margin-top:6pt; margin-bottom:6pt; text-align:justify;&quot;&gt;Completed dosing in the Phase 1 study of the IV formulation of second-generation antifungal SCY-247, with topline data on track for Q3</description>
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   <title>SCYNEXIS Reports Second Quarter 2026 Financial Results and Provides Corporate Update</title>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;margin-top:6pt; margin-bottom:6pt; text-align:justify;&quot;&gt;Initiated a Phase 1 study of SCY-770, a first-in-class, potent and direct AMPK activator for treatment of ADPKD; topline data are expected in Q3 2026 and are anticipated to inform dose selection for the planned Phase 2 study &lt;br/&gt;&lt;br/&gt;&lt;/li&gt;&lt;li style=&quot;margin-top:6pt; margin-bottom:6pt; text-align:justify;&quot;&gt;The Phase 2 proof-of-concept study of SCY-770 in patients with ADPKD remains on track for initiation in Q4 2026, with an early efficacy read-out expected in the second half of 2027&lt;br/&gt;&lt;br/&gt;&lt;/li&gt;&lt;li style=&quot;margin-top:6pt; margin-bottom:6pt; text-align:justify;&quot;&gt;Completed dosing in the Phase 1 study of the IV formulation of second-generation antifungal SCY-247, with topline data on track for Q3</description>
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   <title>SCYNEXIS Reports Second Quarter 2026 Financial Results and Provides Corporate Update</title>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;margin-top:6pt; margin-bottom:6pt; text-align:justify;&quot;&gt;Initiated a Phase 1 study of SCY-770, a first-in-class, potent and direct AMPK activator for treatment of ADPKD; topline data are expected in Q3 2026 and are anticipated to inform dose selection for the planned Phase 2 study &lt;br/&gt;&lt;br/&gt;&lt;/li&gt;&lt;li style=&quot;margin-top:6pt; margin-bottom:6pt; text-align:justify;&quot;&gt;The Phase 2 proof-of-concept study of SCY-770 in patients with ADPKD remains on track for initiation in Q4 2026, with an early efficacy read-out expected in the second half of 2027&lt;br/&gt;&lt;br/&gt;&lt;/li&gt;&lt;li style=&quot;margin-top:6pt; margin-bottom:6pt; text-align:justify;&quot;&gt;Completed dosing in the Phase 1 study of the IV formulation of second-generation antifungal SCY-247, with topline data on track for Q3</description>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;margin-top:6pt; margin-bottom:6pt; text-align:justify;&quot;&gt;Initiated a Phase 1 study of SCY-770, a first-in-class, potent and direct AMPK activator for treatment of ADPKD; topline data are expected in Q3 2026 and are anticipated to inform dose selection for the planned Phase 2 study &lt;br/&gt;&lt;br/&gt;&lt;/li&gt;&lt;li style=&quot;margin-top:6pt; margin-bottom:6pt; text-align:justify;&quot;&gt;The Phase 2 proof-of-concept study of SCY-770 in patients with ADPKD remains on track for initiation in Q4 2026, with an early efficacy read-out expected in the second half of 2027&lt;br/&gt;&lt;br/&gt;&lt;/li&gt;&lt;li style=&quot;margin-top:6pt; margin-bottom:6pt; text-align:justify;&quot;&gt;Completed dosing in the Phase 1 study of the IV formulation of second-generation antifungal SCY-247, with topline data on track for Q3</description>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;margin-top:6pt; margin-bottom:6pt; text-align:justify;&quot;&gt;Initiated a Phase 1 study of SCY-770, a first-in-class, potent and direct AMPK activator for treatment of ADPKD; topline data are expected in Q3 2026 and are anticipated to inform dose selection for the planned Phase 2 study &lt;br/&gt;&lt;br/&gt;&lt;/li&gt;&lt;li style=&quot;margin-top:6pt; margin-bottom:6pt; text-align:justify;&quot;&gt;The Phase 2 proof-of-concept study of SCY-770 in patients with ADPKD remains on track for initiation in Q4 2026, with an early efficacy read-out expected in the second half of 2027&lt;br/&gt;&lt;br/&gt;&lt;/li&gt;&lt;li style=&quot;margin-top:6pt; margin-bottom:6pt; text-align:justify;&quot;&gt;Completed dosing in the Phase 1 study of the IV formulation of second-generation antifungal SCY-247, with topline data on track for Q3</description>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;margin-top:6pt; margin-bottom:6pt; text-align:justify;&quot;&gt;Initiated a Phase 1 study of SCY-770, a first-in-class, potent and direct AMPK activator for treatment of ADPKD; topline data are expected in Q3 2026 and are anticipated to inform dose selection for the planned Phase 2 study &lt;br/&gt;&lt;br/&gt;&lt;/li&gt;&lt;li style=&quot;margin-top:6pt; margin-bottom:6pt; text-align:justify;&quot;&gt;The Phase 2 proof-of-concept study of SCY-770 in patients with ADPKD remains on track for initiation in Q4 2026, with an early efficacy read-out expected in the second half of 2027&lt;br/&gt;&lt;br/&gt;&lt;/li&gt;&lt;li style=&quot;margin-top:6pt; margin-bottom:6pt; text-align:justify;&quot;&gt;Completed dosing in the Phase 1 study of the IV formulation of second-generation antifungal SCY-247, with topline data on track for Q3</description>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;margin-top:6pt; margin-bottom:6pt; text-align:justify;&quot;&gt;Initiated a Phase 1 study of SCY-770, a first-in-class, potent and direct AMPK activator for treatment of ADPKD; topline data are expected in Q3 2026 and are anticipated to inform dose selection for the planned Phase 2 study &lt;br/&gt;&lt;br/&gt;&lt;/li&gt;&lt;li style=&quot;margin-top:6pt; margin-bottom:6pt; text-align:justify;&quot;&gt;The Phase 2 proof-of-concept study of SCY-770 in patients with ADPKD remains on track for initiation in Q4 2026, with an early efficacy read-out expected in the second half of 2027&lt;br/&gt;&lt;br/&gt;&lt;/li&gt;&lt;li style=&quot;margin-top:6pt; margin-bottom:6pt; text-align:justify;&quot;&gt;Completed dosing in the Phase 1 study of the IV formulation of second-generation antifungal SCY-247, with topline data on track for Q3</description>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;margin-top:6pt; margin-bottom:6pt; text-align:justify;&quot;&gt;Initiated a Phase 1 study of SCY-770, a first-in-class, potent and direct AMPK activator for treatment of ADPKD; topline data are expected in Q3 2026 and are anticipated to inform dose selection for the planned Phase 2 study &lt;br/&gt;&lt;br/&gt;&lt;/li&gt;&lt;li style=&quot;margin-top:6pt; margin-bottom:6pt; text-align:justify;&quot;&gt;The Phase 2 proof-of-concept study of SCY-770 in patients with ADPKD remains on track for initiation in Q4 2026, with an early efficacy read-out expected in the second half of 2027&lt;br/&gt;&lt;br/&gt;&lt;/li&gt;&lt;li style=&quot;margin-top:6pt; margin-bottom:6pt; text-align:justify;&quot;&gt;Completed dosing in the Phase 1 study of the IV formulation of second-generation antifungal SCY-247, with topline data on track for Q3</description>
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