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   <title>Guggenheim Downgrades Alumis Inc (ALMS) to Neutral</title>
   <link>http://www.streetinsider.com/Downgrades/Guggenheim+Downgrades+Alumis+Inc+%28ALMS%29+to+Neutral/27019680.html</link>
   <description>&lt;p&gt;Guggenheim analyst Yatin Suneja downgraded Alumis Inc (NASDAQ: ALMS) from Buy to Neutral.&lt;/p&gt;&lt;p&gt;The analyst comments &quot;ALMS's Phase IIb SLE study (n=408) evaluating Envudeucitinib (oral TYK2i) missed both primary and secondary endpoints in the overall population. Post-hoc subgroup analysis in IFNG-high patients showed encouraging clinical responses, which supports moving forward with Phase III development, per mgmt. While we think the most likely path forward is to conduct two Phase III studies (which would likely take ~2-3 years), we expect to hear future updates regarding Phase III design, sizing, dosing, and the enrollment criteria related to desired IFNGS status. Until then, we</description>
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   <pubDate>Wed, 02 Sep 2026 16:35:57 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">ALMS</category>
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   <title>Guggenheim Downgrades Alumis Inc (ALMS) to Neutral</title>
   <link>http://www.streetinsider.com/Analyst+Comments/Guggenheim+Downgrades+Alumis+Inc+%28ALMS%29+to+Neutral/27019680.html</link>
   <description>&lt;p&gt;Guggenheim analyst Yatin Suneja downgraded Alumis Inc (NASDAQ: ALMS) from Buy to Neutral.&lt;/p&gt;&lt;p&gt;The analyst comments &quot;ALMS's Phase IIb SLE study (n=408) evaluating Envudeucitinib (oral TYK2i) missed both primary and secondary endpoints in the overall population. Post-hoc subgroup analysis in IFNG-high patients showed encouraging clinical responses, which supports moving forward with Phase III development, per mgmt. While we think the most likely path forward is to conduct two Phase III studies (which would likely take ~2-3 years), we expect to hear future updates regarding Phase III design, sizing, dosing, and the enrollment criteria related to desired IFNGS status. Until then, we</description>
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   <pubDate>Wed, 02 Sep 2026 16:35:57 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">ALMS</category>
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   <title>Alumis Inc (ALMS) PT Lowered to $37 at Oppenheimer</title>
   <link>http://www.streetinsider.com/Analyst+PT+Change/Alumis+Inc+%28ALMS%29+PT+Lowered+to+%2437+at+Oppenheimer/27015755.html</link>
   <description>Oppenheimer analyst Jeff Jones lowered the price target on Alumis Inc (NASDAQ: ALMS) to $37.00  (from $55.00) while maintaining a Outperform rating.</description>
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   <pubDate>Wed, 02 Sep 2026 07:55:56 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">ALMS</category>
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   <title>Alumis Inc (ALMS) PT Lowered to $29 at Morgan Stanley</title>
   <link>http://www.streetinsider.com/Analyst+PT+Change/Alumis+Inc+%28ALMS%29+PT+Lowered+to+%2429+at+Morgan+Stanley/27015302.html</link>
   <description>&lt;p&gt;Morgan Stanley analyst Terence Flynn lowered the price target on Alumis Inc (NASDAQ: ALMS) to $29.00 (from $39.00) while maintaining a Overweight rating.&lt;/p&gt;&lt;p&gt;The analyst comments &quot;ALMS reported that a Ph2 SLE/lupus trial of key pipeline drug Envudeucitinib (Envu; oral TYK2i) failed to meet the primary and secondary endpoints and shares traded down -57% (vs. S&amp;P 500 -0.7%) - see our first take HERE. The company hosted a conference call and provided more details on the prespecified subgroup of patients with high interferon gene signature (IFNGS), placebo behavior, and imputation methodology and shared that they plan to discuss the Ph3 path</description>
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   <pubDate>Wed, 02 Sep 2026 06:26:14 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">ALMS</category>
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   <title>Alumis Inc (ALMS) PT Lowered to $29 at Morgan Stanley</title>
   <link>http://www.streetinsider.com/Analyst+Comments/Alumis+Inc+%28ALMS%29+PT+Lowered+to+%2429+at+Morgan+Stanley/27015302.html</link>
   <description>&lt;p&gt;Morgan Stanley analyst Terence Flynn lowered the price target on Alumis Inc (NASDAQ: ALMS) to $29.00 (from $39.00) while maintaining a Overweight rating.&lt;/p&gt;&lt;p&gt;The analyst comments &quot;ALMS reported that a Ph2 SLE/lupus trial of key pipeline drug Envudeucitinib (Envu; oral TYK2i) failed to meet the primary and secondary endpoints and shares traded down -57% (vs. S&amp;P 500 -0.7%) - see our first take HERE. The company hosted a conference call and provided more details on the prespecified subgroup of patients with high interferon gene signature (IFNGS), placebo behavior, and imputation methodology and shared that they plan to discuss the Ph3 path</description>
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   <pubDate>Wed, 02 Sep 2026 06:26:14 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">ALMS</category>
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   <title>Alumis Inc (ALMS) PT Lowered to $27 at Baird</title>
   <link>http://www.streetinsider.com/Analyst+PT+Change/Alumis+Inc+%28ALMS%29+PT+Lowered+to+%2427+at+Baird/27015256.html</link>
   <description>Baird analyst Brian Skorney lowered the price target on Alumis Inc (NASDAQ: ALMS) to $27.00  (from $35.00) while maintaining a Outperform rating.</description>
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   <pubDate>Wed, 02 Sep 2026 06:17:19 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">ALMS</category>
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   <title>Alumis Inc (ALMS) PT Lowered to $25 at Wells Fargo</title>
   <link>http://www.streetinsider.com/Analyst+PT+Change/Alumis+Inc+%28ALMS%29+PT+Lowered+to+%2425+at+Wells+Fargo/27014768.html</link>
   <description>&lt;p&gt;Wells Fargo analyst Derek Archila lowered the price target on Alumis Inc (NASDAQ: ALMS) to $25.00 (from $51.00) while maintaining a Overweight rating.&lt;/p&gt;&lt;p&gt;The analyst comments &quot;How we are thinking about valuation: This is the tricky part, envu's PsO oppty deserves value but how much? Assuming a co-co, we get to $13/shr as mgmt reiterated to us they do not plan to launch themselves. Mgmt had highlighted previously waiting for the SLE data prior to making strategic decisions, which is needed to add to their cash runway. We assign a 35% POS (from 75%) for SLE worth ~$6/sh based on today's</description>
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   <pubDate>Wed, 02 Sep 2026 05:13:49 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">ALMS</category>
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  <item>
   <title>Alumis Inc (ALMS) PT Lowered to $25 at Wells Fargo</title>
   <link>http://www.streetinsider.com/Analyst+Comments/Alumis+Inc+%28ALMS%29+PT+Lowered+to+%2425+at+Wells+Fargo/27014768.html</link>
   <description>&lt;p&gt;Wells Fargo analyst Derek Archila lowered the price target on Alumis Inc (NASDAQ: ALMS) to $25.00 (from $51.00) while maintaining a Overweight rating.&lt;/p&gt;&lt;p&gt;The analyst comments &quot;How we are thinking about valuation: This is the tricky part, envu's PsO oppty deserves value but how much? Assuming a co-co, we get to $13/shr as mgmt reiterated to us they do not plan to launch themselves. Mgmt had highlighted previously waiting for the SLE data prior to making strategic decisions, which is needed to add to their cash runway. We assign a 35% POS (from 75%) for SLE worth ~$6/sh based on today's</description>
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   <pubDate>Wed, 02 Sep 2026 05:13:49 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">ALMS</category>
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   <title>Alumis SLE trial fails primary endpoints; subgroup data guides Phase 3</title>
   <link>http://www.streetinsider.com/Trading+Halts/Alumis+SLE+trial+fails+primary+endpoints%3B+subgroup+data+guides+Phase+3/27008897.html</link>
   <description>&lt;p&gt;Alumis Inc. (Nasdaq: ALMS) announced that its Phase 2b LUMUS trial of envudeucitinib for moderate-to-severe systemic lupus erythematosus (SLE) did not meet its primary and secondary endpoints in the overall trial population, according to a company statement.&lt;/p&gt;&lt;p&gt;The trial enrolled 408 patients who received one of three envudeucitinib doses or placebo over 48 weeks. The primary endpoint measured overall disease activity using the British Isles Lupus Assessment Group-based Composite Lupus Assessment (BICLA) at Week 48.&lt;/p&gt;&lt;p&gt;A prespecified subgroup of patients with high interferon gene signature (IFNGS-high) showed responses on the primary endpoint and key secondary measures, including CLASI-50, SRI-4, and Lupus Low</description>
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   <pubDate>Tue, 01 Sep 2026 07:32:55 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">ALMS</category>
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   <title>Alumis SLE trial fails primary endpoints; subgroup data guides Phase 3</title>
   <link>http://www.streetinsider.com/Corporate+News/Alumis+SLE+trial+fails+primary+endpoints%3B+subgroup+data+guides+Phase+3/27008897.html</link>
   <description>&lt;p&gt;Alumis Inc. (Nasdaq: ALMS) announced that its Phase 2b LUMUS trial of envudeucitinib for moderate-to-severe systemic lupus erythematosus (SLE) did not meet its primary and secondary endpoints in the overall trial population, according to a company statement.&lt;/p&gt;&lt;p&gt;The trial enrolled 408 patients who received one of three envudeucitinib doses or placebo over 48 weeks. The primary endpoint measured overall disease activity using the British Isles Lupus Assessment Group-based Composite Lupus Assessment (BICLA) at Week 48.&lt;/p&gt;&lt;p&gt;A prespecified subgroup of patients with high interferon gene signature (IFNGS-high) showed responses on the primary endpoint and key secondary measures, including CLASI-50, SRI-4, and Lupus Low</description>
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   <pubDate>Tue, 01 Sep 2026 07:32:55 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">ALMS</category>
   	  </item>
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   <title>Alumis SLE trial fails primary endpoints; subgroup data guides Phase 3</title>
   <link>http://www.streetinsider.com/FDA/Alumis+SLE+trial+fails+primary+endpoints%3B+subgroup+data+guides+Phase+3/27008897.html</link>
   <description>&lt;p&gt;Alumis Inc. (Nasdaq: ALMS) announced that its Phase 2b LUMUS trial of envudeucitinib for moderate-to-severe systemic lupus erythematosus (SLE) did not meet its primary and secondary endpoints in the overall trial population, according to a company statement.&lt;/p&gt;&lt;p&gt;The trial enrolled 408 patients who received one of three envudeucitinib doses or placebo over 48 weeks. The primary endpoint measured overall disease activity using the British Isles Lupus Assessment Group-based Composite Lupus Assessment (BICLA) at Week 48.&lt;/p&gt;&lt;p&gt;A prespecified subgroup of patients with high interferon gene signature (IFNGS-high) showed responses on the primary endpoint and key secondary measures, including CLASI-50, SRI-4, and Lupus Low</description>
   <guid isPermaLink="true">http://www.streetinsider.com/FDA/Alumis+SLE+trial+fails+primary+endpoints%3B+subgroup+data+guides+Phase+3/27008897.html</guid>
   <pubDate>Tue, 01 Sep 2026 07:32:55 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">ALMS</category>
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   <title>Alumis SLE trial fails primary endpoints; subgroup data guides Phase 3</title>
   <link>http://www.streetinsider.com/Hot+Corp.+News/Alumis+SLE+trial+fails+primary+endpoints%3B+subgroup+data+guides+Phase+3/27008897.html</link>
   <description>&lt;p&gt;Alumis Inc. (Nasdaq: ALMS) announced that its Phase 2b LUMUS trial of envudeucitinib for moderate-to-severe systemic lupus erythematosus (SLE) did not meet its primary and secondary endpoints in the overall trial population, according to a company statement.&lt;/p&gt;&lt;p&gt;The trial enrolled 408 patients who received one of three envudeucitinib doses or placebo over 48 weeks. The primary endpoint measured overall disease activity using the British Isles Lupus Assessment Group-based Composite Lupus Assessment (BICLA) at Week 48.&lt;/p&gt;&lt;p&gt;A prespecified subgroup of patients with high interferon gene signature (IFNGS-high) showed responses on the primary endpoint and key secondary measures, including CLASI-50, SRI-4, and Lupus Low</description>
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   <pubDate>Tue, 01 Sep 2026 07:32:55 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">ALMS</category>
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  <item>
   <title>Alumis SLE trial fails primary endpoints; subgroup data guides Phase 3</title>
   <link>http://www.streetinsider.com/Hot+FDA+News/Alumis+SLE+trial+fails+primary+endpoints%3B+subgroup+data+guides+Phase+3/27008897.html</link>
   <description>&lt;p&gt;Alumis Inc. (Nasdaq: ALMS) announced that its Phase 2b LUMUS trial of envudeucitinib for moderate-to-severe systemic lupus erythematosus (SLE) did not meet its primary and secondary endpoints in the overall trial population, according to a company statement.&lt;/p&gt;&lt;p&gt;The trial enrolled 408 patients who received one of three envudeucitinib doses or placebo over 48 weeks. The primary endpoint measured overall disease activity using the British Isles Lupus Assessment Group-based Composite Lupus Assessment (BICLA) at Week 48.&lt;/p&gt;&lt;p&gt;A prespecified subgroup of patients with high interferon gene signature (IFNGS-high) showed responses on the primary endpoint and key secondary measures, including CLASI-50, SRI-4, and Lupus Low</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Hot+FDA+News/Alumis+SLE+trial+fails+primary+endpoints%3B+subgroup+data+guides+Phase+3/27008897.html</guid>
   <pubDate>Tue, 01 Sep 2026 07:32:55 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">ALMS</category>
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   <title>Alumis (ALMS) Halted, News Pending</title>
   <link>http://www.streetinsider.com/Trading+Halts/Alumis+%28ALMS%29+Halted%2C+News+Pending/27008839.html</link>
   <description>&lt;p&gt;Alumis (NASDAQ: ALMS) Halted, News Pending&lt;br /&gt; &lt;/p&gt;</description>
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   <pubDate>Tue, 01 Sep 2026 07:26:44 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">ALMS</category>
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   <title>H.C. Wainwright Reiterates Neutral Rating on Alumis Inc (ALMS)</title>
   <link>http://www.streetinsider.com/Analyst+Comments/H.C.+Wainwright+Reiterates+Neutral+Rating+on+Alumis+Inc+%28ALMS%29/26934543.html</link>
   <description>&lt;p&gt;H.C. Wainwright analyst Mitchell S. Kapoor reiterated a Neutral rating and $25.00 price target on Alumis Inc (NASDAQ: ALMS).&lt;/p&gt;&lt;p&gt;The analyst commented: &quot;Alumis is prioritizing Sjögren’s disease and systemic lupus erythematosus (SLE) as the next envu indications, contingent on 3Q26 LUMUS results and capital allocation. A convincing SLE result would provide clinical support for maximal TYK2 inhibition in Type I interferon-driven disease and justify follow-on development in related indications, giving Alumis a second path beyond psoriasis (PsO). A weak or mixed result would leave most near-term value tied to PsO, where the 4Q26 NDA and ONWARD3 durability support a strong approval</description>
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   <pubDate>Mon, 17 Aug 2026 06:43:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">ALMS</category>
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   <title>Form  SCHEDULE 13D  ALUMIS INC.                            Filed by: Foresite Capital Fund VI LP</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++SCHEDULE+13D++ALUMIS+INC.++++++++++++++++++++++++++++Filed+by%3A+Foresite+Capital+Fund+VI+LP/26934405.html</link>
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   <pubDate>Mon, 17 Aug 2026 06:10:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">ALMS</category>
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   <title>Form  SCHEDULE 13D  ALUMIS INC.                            Filed by: Foresite Capital Fund VI LP</title>
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   <pubDate>Mon, 17 Aug 2026 06:10:00 -0400</pubDate>
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   <title>Form  10-Q       ALUMIS INC.               For: Jun 30</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++10-Q+++++++ALUMIS+INC.+++++++++++++++For%3A+Jun+30/26921542.html</link>
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   <pubDate>Thu, 13 Aug 2026 16:20:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">ALMS</category>
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   <title>Form  10-Q       ALUMIS INC.               For: Jun 30</title>
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   <pubDate>Thu, 13 Aug 2026 16:20:00 -0400</pubDate>
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   <title>Form  8-K        ALUMIS INC.               For: Aug 13</title>
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   <pubDate>Thu, 13 Aug 2026 16:09:00 -0400</pubDate>
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   <title>Form  8-K        ALUMIS INC.               For: Aug 13</title>
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   <pubDate>Thu, 13 Aug 2026 16:09:00 -0400</pubDate>
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   <title>Alumis Reports Second Quarter 2026 Financial Results and  Highlights Recent Achievements</title>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;– ONWARD3: 54% of patients reached complete skin clearance (PASI 100) at 48 weeks, positioning envudeucitinib to set a new standard in PsO –&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;– Alumis remains on track to submit its New Drug Application to FDA for envudeucitinib in moderate-to-severe plaque psoriasis (PsO) in Q4 2026 –&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;&lt;em&gt;– Potentially pivotal Phase 2b LUMUS topline data for envudeucitinib in SLE anticipated in Q3 2026 –&lt;/em&gt;&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;&lt;br/&gt;SOUTH SAN FRANCISCO, Calif., Aug.  13, 2026  (GLOBE NEWSWIRE) --  Alumis Inc. (Nasdaq: ALMS), a late-stage biopharmaceutical company developing next-generation targeted therapies for patients with</description>
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   <title>Alumis Reports Second Quarter 2026 Financial Results and  Highlights Recent Achievements</title>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;– ONWARD3: 54% of patients reached complete skin clearance (PASI 100) at 48 weeks, positioning envudeucitinib to set a new standard in PsO –&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;– Alumis remains on track to submit its New Drug Application to FDA for envudeucitinib in moderate-to-severe plaque psoriasis (PsO) in Q4 2026 –&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;&lt;em&gt;– Potentially pivotal Phase 2b LUMUS topline data for envudeucitinib in SLE anticipated in Q3 2026 –&lt;/em&gt;&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;&lt;br/&gt;SOUTH SAN FRANCISCO, Calif., Aug.  13, 2026  (GLOBE NEWSWIRE) --  Alumis Inc. (Nasdaq: ALMS), a late-stage biopharmaceutical company developing next-generation targeted therapies for patients with</description>
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   <title>Alumis Reports Second Quarter 2026 Financial Results and  Highlights Recent Achievements</title>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;– ONWARD3: 54% of patients reached complete skin clearance (PASI 100) at 48 weeks, positioning envudeucitinib to set a new standard in PsO –&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;– Alumis remains on track to submit its New Drug Application to FDA for envudeucitinib in moderate-to-severe plaque psoriasis (PsO) in Q4 2026 –&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;&lt;em&gt;– Potentially pivotal Phase 2b LUMUS topline data for envudeucitinib in SLE anticipated in Q3 2026 –&lt;/em&gt;&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;&lt;br/&gt;SOUTH SAN FRANCISCO, Calif., Aug.  13, 2026  (GLOBE NEWSWIRE) --  Alumis Inc. (Nasdaq: ALMS), a late-stage biopharmaceutical company developing next-generation targeted therapies for patients with</description>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;– ONWARD3: 54% of patients reached complete skin clearance (PASI 100) at 48 weeks, positioning envudeucitinib to set a new standard in PsO –&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;– Alumis remains on track to submit its New Drug Application to FDA for envudeucitinib in moderate-to-severe plaque psoriasis (PsO) in Q4 2026 –&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;&lt;em&gt;– Potentially pivotal Phase 2b LUMUS topline data for envudeucitinib in SLE anticipated in Q3 2026 –&lt;/em&gt;&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;&lt;br/&gt;SOUTH SAN FRANCISCO, Calif., Aug.  13, 2026  (GLOBE NEWSWIRE) --  Alumis Inc. (Nasdaq: ALMS), a late-stage biopharmaceutical company developing next-generation targeted therapies for patients with</description>
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