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Alumis (NASDAQ: ALMS) details envudeucitinib psoriasis Phase 3 progress

Filing Impact
(Moderate)
Filing Sentiment
(Neutral)
Form Type
8-K

Rhea-AI Filing Summary

Alumis Inc. filed a report describing new communications about its oral psoriasis therapy envudeucitinib. The company issued a press release titled “Alumis’ Envudeucitinib Delivers Leading Skin Clearance Among Next-Generation Oral Plaque Psoriasis Therapies in Phase 3 Program” and furnished it as an exhibit. Alumis also posted an updated corporate presentation for investors and attached it as a separate exhibit.

The report notes that these materials contain forward-looking statements, including Alumis’s plans to submit a new drug application in the second half of 2026 and the potential for envudeucitinib to address IL-23/IL-17–driven diseases and those driven by Type I interferon. Alumis cautions that regulatory decisions, clinical trial outcomes, funding, and intellectual property protection could cause actual results to differ from these expectations.

Positive

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Insights

Alumis shares updated data narrative and timeline for its lead psoriasis drug.

Alumis highlights its oral plaque psoriasis candidate envudeucitinib, referencing a Phase 3 program described as delivering “leading skin clearance” versus other next-generation oral therapies. While detailed efficacy and safety numbers are not provided here, the company signals confidence by positioning the drug within IL-23/IL-17–driven diseases and conditions driven by Type I interferon.

The report reiterates a plan to submit a new drug application in the second half of 2026, which anchors management’s regulatory timeline for envudeucitinib. It also mentions timing for a topline readout in the LUMUS Phase 2b program and broader clinical pipeline plans, though specifics are contained in the attached materials.

Extensive risk language underscores that outcomes depend on regulatory acceptance of the planned NDA, determinations that envudeucitinib is sufficiently safe and efficacious in moderate-to-severe plaque psoriasis, successful clinical trial results, adequate funding, and effective intellectual property protection. Future SEC filings and presentations are likely to elaborate as trials progress and regulatory interactions advance.

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UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

Washington, D.C. 20549

 

FORM 8-K

 

CURRENT REPORT

Pursuant to Section 13 or 15(d)
of the Securities Exchange Act of 1934

 

Date of Report (Date of earliest event reported): January 6, 2026

 

Alumis Inc.

(Exact name of registrant as specified in its charter)

 

 

Delaware   001-42143   86-1771129
(State or other jurisdiction
of incorporation)
  (Commission
File Number)
  (IRS Employer
Identification No.)

 

280 East Grand Avenue

South San Francisco, California 94080

(Address of principal executive offices)

 

Registrant’s telephone number, including area code: (650) 231-6625

 

N/A

(Former name or former address, if changed since last report.)

 

Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions:

 

¨Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)

 

¨Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)

 

¨Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b))

 

¨Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c))

 

Securities registered pursuant to Section 12(b) of the Act:

 

Title of each class   Trading
Symbol(s)
  Name of each exchange
on which registered
Common Stock, $0.0001 par value per share   ALMS   The Nasdaq Global Select Market

 

Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§240.12b-2 of this chapter).

 

Emerging growth company x

 

If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. ¨

 

 

 

 

 

 

Item 8.01 Other Events.

 

On January 6, 2026, Alumis Inc. (the “Company” or “Alumis”) issued a press release titled “Alumis’ Envudeucitinib Delivers Leading Skin Clearance Among Next-Generation Oral Plaque Psoriasis Therapies in Phase 3 Program”. A copy of the press release is filed herewith as Exhibit 99.1 and is incorporated by reference.

 

Additionally, on January 6, 2026, the Company posted an updated corporate presentation to the investor section of its website. A copy of the corporate presentation is filed herewith as Exhibit 99.2 and is incorporated by reference.

 

The information contained in the slides is summary information that is intended to be considered in the context of the more complete information included in the Company’s filings with the Securities and Exchange Commission (“SEC”) and other public announcements that the Company has made and may make from time to time by press release or otherwise. The Company undertakes no duty or obligation to update or revise the information contained in the presentation in this Current Report on Form 8-K, although it may do so from time to time as its management believes is appropriate. Any such update may be made through the filing of other reports or documents with the SEC.

 

Forward-Looking Statements

 

This Current Report on Form 8-K contains forward-looking statements within the meaning of federal securities laws, including the “safe harbor” provisions of the Private Securities Litigation Reform Act of 1995. These statements may be identified by words such as “aims,” “anticipates,” “believes,” “could,” “estimates,” “expects,” “forecasts,” “goal,” “intends,” “may,” “plans,” “possible,” “potential,” “seeks,” “will” and variations of these words or similar expressions that are intended to identify forward-looking statements. All statements, other than statements of historical facts, including without limitation those regarding Alumis’s plans to submit an NDA in the second half of 2026, the potential for envudeucitinib to transform the treatment landscape for IL-23/IL-17–driven diseases as well as those driven by Type I interferon, the potential for envudeucitinib to meaningfully elevate care for and effectively reduce the full burden of disease for patients with moderate-to-severe plaque psoriasis, the timing of Alumis’ topline readout in its LUMUS Phase 2b program and statements regarding Alumis’ future plans and prospects, including development of its clinical pipeline; and any assumptions underlying any of the foregoing, are forward-looking statements. Any forward-looking statements in this press release are based on Alumis’ current expectations, estimates and projections only as of the date of this release and are subject to a number of risks and uncertainties that could cause actual results to differ materially and adversely from those set forth in or implied by such forward-looking statements. Readers are cautioned that actual results, levels of activity, safety, efficacy, performance or events and circumstances could differ materially from those expressed or implied in Alumis’ forward-looking statements due to a variety of risks and uncertainties, which include, without limitation, risks and uncertainties related to whether regulatory authorities determine that envudeucitinib in moderate-to-severe plaque psoriasis is sufficiently safe and efficacious and grant regulatory approval; whether regulatory authorities accept for filing Alumis’ planned NDA submission; Alumis’ ability to obtain regulatory approval of and ultimately commercialize Alumis’ clinical candidates, the timing and results of preclinical and clinical trials, Alumis’ ability to fund development activities and achieve development goals, and Alumis’ ability to protect its intellectual property. Additional information on the above risks and uncertainties and additional risks, uncertainties and factors that could cause actual results to differ materially from those in the forward-looking statements are contained in Alumis’ filings and reports with the SEC under the heading “Risk Factors” and elsewhere in such filings and reports, including any future reports Alumis may file with the SEC from time to time. Alumis explicitly disclaims any obligation to update any forward-looking statements except to the extent required by law. 

 

Item 9.01 Financial Statements and Exhibits.

 

(d)   Exhibits.

 

Exhibit No.   Description
     
99.1   Press Release, dated January 6, 2026, titled Alumis’ Envudeucitinib Delivers Leading Skin Clearance Among Next-Generation Oral Plaque Psoriasis Therapies in Phase 3 Program.
     
99.2   Corporate Presentation dated January 2026.
   
104   Cover Page Interactive Data File (embedded within the Inline XBRL Document).

 

 

 

 

SIGNATURES

 

Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.

 

  Alumis Inc.
     
  By: /s/ John Schroer
    John Schroer
    Chief Financial Officer

 

Dated: January 6, 2026

 

 

 

FAQ

What did Alumis Inc. (ALMS) report in this 8-K filing?

Alumis reported that it issued a press release on January 6, 2026 about its oral plaque psoriasis therapy envudeucitinib and posted an updated corporate investor presentation, both furnished as exhibits.

What is Alumis’ envudeucitinib and what stage is it in?

Envudeucitinib is Alumis’ oral therapy for moderate-to-severe plaque psoriasis. The company references a Phase 3 program and describes the press release as highlighting “leading skin clearance” among next-generation oral plaque psoriasis therapies.

What regulatory plans did Alumis (ALMS) outline for envudeucitinib?

Alumis stated plans to submit a new drug application (NDA) for envudeucitinib in the second half of 2026, subject to regulatory authorities accepting and ultimately approving the submission.

How does Alumis describe the potential of envudeucitinib beyond plaque psoriasis?

Alumis notes the potential for envudeucitinib to transform treatment for IL-23/IL-17–driven diseases and those driven by Type I interferon, and to reduce the overall burden of disease for patients with moderate-to-severe plaque psoriasis.

What risks and uncertainties does Alumis highlight around envudeucitinib?

The company cites risks that regulators may not find envudeucitinib sufficiently safe and efficacious, may not accept or approve the planned NDA, and emphasizes uncertainties around clinical trial timing and results, funding its development goals, and protecting intellectual property.

What exhibits are included with Alumis’ 8-K related to envudeucitinib?

The filing includes a press release dated January 6, 2026 as Exhibit 99.1, a corporate presentation dated January 2026 as Exhibit 99.2, and a cover page interactive data file as Exhibit 104.
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