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argenx (NASDAQ: ARGX) seals Forte deal for first-in-class autoimmune antibody

(Neutral)
(Neutral)
Form Type
6-K

Rhea-AI Filing Summary

ARGENX SE (ARGX) completed the acquisition of Forte Biosciences, Inc. through a cash tender offer followed by a merger, making Forte a wholly owned subsidiary and removing its common stock from trading on the Nasdaq Capital Market. The deal brings FB102, a first-in-class anti-CD122 monoclonal antibody with clinical proof-of-concept in vitiligo and celiac disease, into the argenx immunology pipeline.

Through a subsidiary, argenx purchased all validly tendered Forte shares at $77.00 per share in cash. As of the tender expiration, 19,894,879 Forte shares had been validly tendered and not withdrawn, representing 87.13% of Forte’s issued and outstanding common stock together with shares already owned by argenx and its affiliates. All remaining Forte shares were converted into the right to receive the same cash amount per share in the subsequent merger. FB102 is being evaluated in Phase 2 celiac disease and Phase 1b alopecia areata studies, with data expected in the second half of 2026.

Positive

  • Strategic pipeline expansion: Completion of the Forte acquisition adds FB102, a first-in-class anti-CD122 antibody with clinical proof-of-concept in vitiligo and celiac disease, broadening ARGX’s immunology portfolio and targeting additional autoimmune indications.

Negative

  • None.
Tender offer price per share $77.00 per share Cash purchase price for each share of Forte common stock in tender offer and merger
Shares tendered 19,894,879 shares Forte common shares validly tendered and not withdrawn as of offer expiration
Ownership percentage acquired via tender and existing holdings 87.13% Portion of Forte’s issued and outstanding common stock represented by tendered shares plus shares already owned by argenx and affiliates
Tender offer expiration time One minute after 11:59 p.m. Eastern Time on August 26, 2026 Expiration of the cash tender offer for Forte shares
FB102 Phase 2 celiac disease data timing Second half of 2026 Expected timing for data readout from FB102 Phase 2 celiac disease study
FB102 Phase 1b alopecia areata data timing Second half of 2026 Expected timing for data readout from FB102 Phase 1b alopecia areata trial
cash tender offer financial
"argenx completed the cash tender offer, through a subsidiary, for all the outstanding shares"
A cash tender offer is a public proposal in which an individual or group offers to buy a set number of a company's shares directly from shareholders for a specified cash price during a limited time. It matters to investors because it gives a clear, immediate chance to sell shares at a known price — like a store offering to buy back items at a posted rate — and can affect the stock’s market price, ownership control and liquidity.
clinical proof-of-concept medical
"FB102, a first-in-class anti-CD122 antibody with clinical proof-of-concept in vitiligo"
An early clinical proof-of-concept is initial human trial evidence showing a drug or medical treatment produces the intended biological effect or meaningful patient benefit. Think of it as the first successful test drive that proves the idea works in real-world conditions rather than just in the lab. For investors, it meaningfully lowers scientific risk and can boost a program’s valuation, partner interest, and likelihood of further funding or approval.
anti-CD122 antibody medical
"FB102, a first-in-class anti-CD122 antibody with clinical proof-of-concept"
A laboratory-made antibody that binds to CD122, the protein also known as the beta chain of certain immune-cell receptors, to change how immune cells respond. Think of it like a key designed to fit a specific lock on immune cells to dial immune activity up or down. Investors encounter this term because such antibodies are drug candidates whose clinical progress, safety results, and regulatory decisions can affect a biotech company’s value and future revenue prospects.
Phase 2 celiac disease study medical
"A Phase 2 celiac disease study has been initiated with data expected"
Phase 1b alopecia areata trial medical
"A Phase 1b alopecia areata trial is ongoing with data expected"
neonatal Fc receptor (FcRn) blocker medical
"argenx developed and is commercializing the first approved neonatal Fc receptor (FcRn) blocker"

FAQ

What transaction did ARGENX (ARGX) announce in this Form 6-K?

ARGENX announced the completion of its acquisition of Forte Biosciences, Inc. It first conducted a cash tender offer and then merged a wholly owned subsidiary into Forte, making Forte a wholly owned subsidiary and delisting its common stock from the Nasdaq Capital Market.

What price did ARGENX (ARGX) pay per share for Forte Biosciences?

ARGENX, through a subsidiary, paid $77.00 per share in cash for each share of Forte Biosciences common stock, in both the tender offer and the follow-on merger, without interest and subject to any applicable tax withholding.

How many Forte Biosciences shares were tendered to ARGENX (ARGX)?

At expiration of the tender offer, 19,894,879 shares of Forte Biosciences common stock were validly tendered and not validly withdrawn. Together with shares already owned by ARGENX and its affiliates, this represented about 87.13% of Forte’s issued and outstanding common stock.

What happens to Forte Biosciences’ stock after the ARGENX (ARGX) acquisition?

Following the merger, Forte Biosciences became a wholly owned subsidiary of ARGENX, and Forte’s common stock will no longer be listed or traded on the Nasdaq Capital Market. Remaining Forte shares were converted into the right to receive $77.00 per share in cash.

What is FB102 and why is it important to ARGENX (ARGX)?

FB102 is a proprietary, first-in-class anti-CD122 monoclonal antibody with clinical proof-of-concept in vitiligo and celiac disease. It has potentially broad autoimmune applications and complements ARGENX’s existing antibody-based programs by targeting pathogenic T-cell and NK-cell activity.

What are the key clinical timelines for FB102 after the ARGENX (ARGX) acquisition?

FB102 is in a Phase 2 celiac disease study with data expected in the second half of 2026. A Phase 1b alopecia areata trial is also ongoing, with data expected in the second half of 2026, and vitiligo data were reported in July 2026.

AI-generated analysis. How Rhea-AI works. Not financial advice.

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UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
WASHINGTON, D.C. 20549



FORM 6-K



REPORT OF FOREIGN PRIVATE ISSUER
PURSUANT TO RULE 13a-16 OR 15d-16
UNDER THE SECURITIES EXCHANGE ACT OF 1934

For the Month of August 2026

Commission File Number: 001-38097



ARGENX SE
(Translation of registrant’s name into English)



Laarderhoogtweg 25
1101 EB Amsterdam, the Netherlands
(Address of principal executive offices)



Indicate by check mark whether the registrant files or will file annual reports under cover of Form 20-F or Form 40-F.

Form 20-F ☒ Form 40-F ☐

Indicate by check mark if the registrant is submitting the Form 6-K in paper as permitted by Regulation S-T Rule 101(b)(1): ☐

Indicate by check mark if the registrant is submitting the Form 6-K in paper as permitted by Regulation S-T Rule 101(b)(7): ☐



EXPLANATORY NOTE

On August 27, 2026, argenx SE (the “Company”) issued a press release, a copy of which is attached hereto as Exhibit 99.1 and is incorporated by reference herein.

The information contained in this Current Report on Form 6-K, including Exhibit 99.1, shall be deemed to be incorporated by reference into the Company’s Registration Statements on Forms S-8 (File Nos. 333-225375, 333-258253, 333-274721, and 333-292200), and to be part thereof from the date on which this Current Report on Form 6-K is filed, to the extent not superseded by documents or reports subsequently filed or furnished.

Exhibit
 
Description
     
99.1
 
Press Release August 27, 2026


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, thereunto duly authorized.

 
ARGENX SE
     
Date: August 27, 2026
By:
/s/ Hemamalini (Malini) Moorthy
   
Name: Hemamalini (Malini) Moorthy
Title: General Counsel




Exhibit 99.1

argenx Completes Acquisition of Forte Biosciences, Inc.

Acquisition adds first-in-class anti-CD122 Antibody, FB102, to argenx’s immunology pipeline

August 27, 2026 – 8:50 AM ET

Amsterdam, the Netherlands – argenx (Euronext & Nasdaq: ARGX), a global immunology innovation company today announced the successful completion of the acquisition of Forte Biosciences, Inc. (“Forte”) (Nasdaq: FBRX).

The acquisition expands argenx’s portfolio of differentiated immunology medicines, adding FB102, a first-in-class anti-CD122 antibody with clinical proof-of-concept in vitiligo and celiac disease and potential to address multiple autoimmune diseases. The acquisition reflects argenx’s disciplined approach to identifying and advancing breakthrough science for patients with the potential to redefine standards of care in diseases that have lacked meaningful innovation for decades.

“At argenx, we measure our progress through patient impact, and the Forte acquisition deepens that impact,” said Karen Massey, Chief Executive Officer of argenx. “As we advance toward Vision 2030, our ambition is to build a pipeline that extends our reach for patients across immunology. FB102 does exactly that with a potential first-in-class molecule targeting diseases with few treatment options today. This acquisition marks an important step in our long-term strategy to be the leading immunology innovation company.”

FB102 complements argenx’s existing portfolio of antibody-based programs, including efgartigimod, empasiprubart, adimanebart, and ARGX-121, as well as several additional early-stage molecules, by adding a mechanism focused on pathogenic T-cell and NK-cell activity, broadening the company’s ability to pursue diseases driven by different dimensions of the immune system.

Transaction details

argenx completed the cash tender offer, through a subsidiary, for all the outstanding shares of common stock of Forte at a purchase price of $77.00 per share, without interest and subject to any applicable tax withholding. As of the tender offer expiration at one minute after 11:59 p.m., Eastern Time, on August 26, 2026, 19,894,879 shares of Forte common stock were validly tendered and not validly withdrawn, representing, together with the shares owned by argenx and its affiliates, approximately 87.13% of the total number of Forte’s issued and outstanding shares of common stock as of such date and time. All such shares have been accepted for payment in accordance with the terms of the tender offer, and argenx, on behalf of its subsidiary, will promptly pay for such shares.


Following the completion of the tender offer, argenx completed the acquisition of Forte through a merger of argenx’s wholly owned subsidiary with and into Forte, with Forte being the surviving corporation, in which all shares of Forte common stock issued and outstanding at the effective time of the merger were converted into the right to receive cash equal to the $77.00 offer price per share, without interest and subject to any applicable tax withholding. At the completion of the merger, Forte became a wholly owned subsidiary of argenx and Forte’s common stock will no longer be listed or traded on the Nasdaq Capital Market.

About FB102

FB102 is a proprietary molecule with potentially broad autoimmune and autoimmune-related applications. In June 2025, Forte announced positive data from the FB102 celiac disease study. A Phase 2 celiac disease study has been initiated with data expected in the second half of 2026. Data from a vitiligo trial were reported in July 2026. A Phase 1b alopecia areata trial is ongoing with data expected in the second half of 2026.

About argenx

argenx is a global immunology innovation company committed to improving the lives of people suffering from severe autoimmune diseases. Partnering with leading academic researchers through its Immunology Innovation Program (IIP), argenx aims to translate immunology breakthroughs into a world-class portfolio of novel antibody-based medicines. argenx developed and is commercializing the first approved neonatal Fc receptor (FcRn) blocker and is evaluating its broad potential in multiple serious autoimmune diseases while advancing several earlier stage experimental medicines within its therapeutic franchises. For more information, visit  www.argenx.com  and follow us on LinkedIn, Instagram, Facebook, and YouTube.

About Forte

Forte Biosciences, Inc. is a clinical-stage biopharmaceutical company that is advancing FB102, which is a proprietary anti-CD122 monoclonal antibody therapeutic candidate with potentially broad autoimmune and autoimmune-related indications.

Contacts

Media:
Ben Petok
bpetok@argenx.com

Investors:
Alexandra Roy
aroy@argenx.com


Forward Looking Statements

The contents of this press release include statements that are, or may be deemed to be, “forward-looking statements.” These forward-looking statements generally can be identified by the use of forward-looking words, such as “aim”, “anticipate”, “aspire”, “believe”, “can”, “continue”, “could”, “estimate”, “expect”, “entail”, “forecast”, “future”, “goals”, “hope”, “intend”, “is designed to”, “likely”, “may”, “might”, “objective”, “plan”, “possible”, “potential”, “pursue”, “project”, “predict”, “seek”, “should”, “strategy”, “target”, “will” and other words and terms of similar meaning and expression, including in connection with any discussion of future operating or financial performance. By their nature, forward-looking statements involve risks and uncertainties and readers are cautioned that any such forward-looking statements are not guarantees of future performance. Forward-looking statements include, without limitation, statements regarding the tender offer, the merger and other related matters; prospective performance and opportunities; post-closing operations and the outlook for the businesses of Forte and argenx, including, without limitation, results from clinical trials, regulatory applications and related timelines, the ability of argenx to advance Forte’s product pipeline; and any assumptions underlying any of the foregoing. argenx’s actual results may differ materially from those predicted by the forward-looking statements as a result of various important factors, including but not limited to,  the effect of the announcement on argenx’s business; the effect of the announcement on Forte’s business, its ability to retain and hire key personnel, its ability to maintain relationships with its suppliers and others with whom it does business, or its operating results and business generally; risks related to diverting management’s attention from argenx’s ongoing business operations; expectations regarding the inherent uncertainties associated with the development of novel drug therapies; preclinical and clinical trial and product development activities and regulatory approval requirements; the acceptance of its products and product candidates by its patients as safe, effective and cost-effective; the impact of governmental laws and regulations, including tariffs, export controls, sanctions and other regulations on its business; its reliance on third-party suppliers, service providers and manufacturers; inflation and deflation and the corresponding fluctuations in interest rates; and regional instability and conflicts.

A further list and description of these and other risks, uncertainties, and factors that could cause actual results to differ materially from those referred to in the forward-looking statements can be found in argenx’s SEC filings and reports, including in argenx’s most recent annual report on Form 20-F filed with the SEC as well as subsequent filings and reports filed by argenx with the SEC. Given these risks and uncertainties, the reader is advised not to place undue reliance on such forward-looking statements. These forward-looking statements speak only as of the date of publication of this press release. argenx undertakes no obligation to publicly update or revise the information in this press release, including any forward-looking statements, except as may be required by law.



Filing Exhibits & Attachments

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