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 October 2023
Commission File Number: 001-37384
GALAPAGOS NV
(Translation of registrant's name
into English)
Generaal De Wittelaan L11 A3 2800 Mechelen, Belgium
(Address of principal executive
office)
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
[ X ] Form 40-F [ ]
The information contained in this Report on Form 6-K, including Exhibit 99.1, except for the quotes of Dr. Paul Stoffels, Thad Huston and Francesco Balestrieri, included in Exhibit 99.1, is hereby incorporated by reference into the Company's
Registration Statements on Form S-8 (File Nos. 333-204567, 333-208697, 333-211834, 333-215783, 333-218160, 333-225263, 333-231765, 333-249416,
333-260500, and 333-268756).
On October 30, 2023, the Registrant issued a press release, a copy of which is attached hereto as Exhibit 99.1 and is incorporated
herein by reference.
(c) Exhibit 99.1. Press release dated October 30, 2023
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.
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GALAPAGOS NV |
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(Registrant) |
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Date: November 2, 2023 |
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/s/ Annelies Denecker |
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Annelies Denecker |
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Company Secretary |
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EXHIBIT 99.1
Galapagos concludes strategic evaluation and signs letter of intent to transfer Jyseleca®
business to Alfasigma
- Transaction would enable Galapagos to realize considerable annualized savings and accelerate its
pipeline focused on developing transformational medicines
- Aims to preserve the Jyseleca® (filgotinib) business and a significant number of positions
- Galapagos plans to streamline its remaining operations and further build efficiencies
Mechelen, Belgium; 30 October 2023, 21:01 CET; regulated information – inside information
– Galapagos NV (Euronext & NASDAQ: GLPG) and Alfasigma S.p.A. today announced that they have signed a letter of intent
contemplating a transfer of the Jyseleca® business to Alfasigma, including the European and UK Marketing Authorizations, the commercial,
medical and development activities for Jyseleca® and approximately 400 positions in 14 European countries.
In the contemplated transaction, Galapagos will receive a €50 million upfront, potential milestone payments totaling
€120 million and mid-single to mid-double-digit royalties on European sales. Galapagos will pay up to €40 million by June
2025 to Alfasigma for Jyseleca® related development activities. In addition, Galapagos plans to streamline its remaining operations
and further build efficiencies, with an envisaged reduction of approximately 100 positions across the organization. Galapagos estimates
annualized savings ranging between €150 million and €200 million.
This repositioning of the company marks yet another significant milestone in Galapagos’ ongoing transformation
into an innovative biotechnology company with a patient-centric research and development pipeline focused on immunology and oncology.
While Galapagos’ commitment to transforming patient outcomes with life changing science and innovation remains unchanged, its ability
to work efficiently across streamlined operations and portfolio are expected to accelerate these efforts.
“Today’s news is the result of a thoughtful, in-depth analysis, and represents the successful conclusion
of the strategic evaluation process for Jyseleca®. We are confident this is the best possible outcome for our employees, patients
and their prescribers, our other stakeholders and Jyseleca®. I want to recognize the tremendous efforts and valuable contributions
of our talented workforce, and in particular the Jyseleca® team, who we believe can thrive within Alfasigma,” said Dr. Paul
Stoffels1, CEO and Chairman of Galapagos. “Looking ahead, the planned transaction is expected to free-up significant
resources across the organization, enabling us to invest more in our R&D growth areas, business development and M&A. This will
support and accelerate our transformation into a global innovative biotech company with a pipeline of best-in-class medicines to address
high unmet needs.”
Mr. Francesco Balestrieri, Chief Executive Officer of Alfasigma, added, “We are very pleased to have signed
a letter of intent with Galapagos and we are excited to acquire Galapagos’ Jyseleca® business. The acquisition of Galapagos'
Jyseleca® business represents another important milestone in Alfasigma's international transformation and growth path and fits perfectly
with our Company's core business areas.
We believe this will benefit both companies and ensure that Jyseleca® will continue
to be available to patients who can benefit from it. Galapagos has a skilled workforce dedicated to improving the lives of many patients,
and we look forward to welcoming them following completion of the process.”
Thad Huston, CFO and COO of Galapagos, said, “While decisions that affect our colleagues are never easy, these
changes are necessary to build a stronger future for our company. It is essential that we drive operational efficiencies in our remaining
operations and intend to implement a focused, rightsized organization that is approximately half the size of our current organization.
We will focus our efforts on internal research and development and disciplined business development as we work to expand our innovative
pipeline and generate value for our shareholders.”
Process and timing
The completion of the intended transaction is subject to the execution of
a definitive agreement and customary conditions, including regulatory approvals and consultations with works councils. There can be no
assurance regarding the completion of the transaction. The letter of intent includes a customary break-up fee in the event either party
does not proceed to a definitive agreement on terms consistent with the letter of intent. Galapagos will organize its Q3 2023 earnings
call on Friday, 3 November 2023 at 08:00 ET/ 13:00 CET.
Information on Related Party Transaction: amendment of Galapagos-Gilead filgotinib agreement
The following information is provided by Galapagos pursuant to article 7:97, paragraphs 3 and 4 of the Belgian Companies
and Association Code in connection with the amending of the Second Amended and Restated License and Collaboration Agreement between Gilead
and Galapagos for the development and commercialization of filgotinib (the “Filgotinib Agreement”). Galapagos
and Gilead have agreed to amend the Filgotinib Agreement to terminate the existing 50/50 global development cost sharing arrangement with
Galapagos bearing the costs going forward, and to terminate Galapagos’ obligation to pay tiered royalties to Gilead on net sales
of Jyseleca® in Europe, in addition to other amendments. It is the intention in the contemplated transaction between Galapagos and
Alfasigma that the amended Filgotinib Agreement will be assigned by Galapagos to Alfasigma.
Gilead has two representatives on the Board of Directors of Galapagos (Daniel O'Day and Linda Higgins). In addition,
Gilead holds (indirectly, through one of its subsidiaries) more than 25% of the shares in Galapagos. Hence, Gilead is considered a “related
party” of Galapagos in accordance with the International Financial Reporting Standards as adopted by the European Union. In view
hereof, the Board of Directors of Galapagos applied the procedure of article 7:97 of the Belgian Companies and Association Code and the
two representatives of Gilead on the Board of Directors of Galapagos did not participate in the deliberation and voting by the Board of
Directors in relation to the amendment of the Filgotinib Agreement.
Within the context of the aforementioned procedure, a committee of three independent members of the Board of Directors
of Galapagos (the “Committee”) issued an advice to the Board of Directors in which the Committee assessed the amended terms
of the Filgotinib Agreement. In its advice to the Board of Directors, the Committee concluded the following: “The Committee
believes that, under the circumstances, the proposed amendments to the filgotinib collaboration between Gilead and Galapagos are reasonable
and fair from the point of view of Galapagos and its shareholders, and in line with the strategy of the Company. The proposed amendments
offer an important opportunity to have autonomy on development and commercial activities in Europe in its ongoing collaboration with Gilead.
The proposed amendments also come with a number of challenges and risks, but these are not unreasonable and can be managed going forward.
The Committee therefore believes that the proposed amendments to the collaboration with Gilead in relation to filgotinib are in the interest
of Galapagos, and in any event not manifestly abusive. In view hereof, the Committee issues a favourable and unqualified opinion to the
Board of Directors of Galapagos.” The Board of Directors did not deviate from the Committee’s advice.
The assessment by the Statutory Auditor of Galapagos of the advice of the Committee and the minutes of the Board of
Directors is as follows: “Based on our assessment, nothing has come to our attention that causes us to believe that the financial
and accounting data reported in the advice of the Ad hoc committee of the independent members of the Board of Directors dated 30 October
2023 and in the minutes of the Board of Directors dated 30 October 2023, which justify the proposed transaction, are not consistent, in
all material respects, compared to the information we possess in the context of our assignment.”
About filgotinib
Filgotinib is marketed as Jyseleca® in Europe and Japan for the treatment of adults with moderate
to severe active RA who have responded inadequately or are intolerant to one or more disease modifying anti-rheumatic drugs. Filgotinib
is also marketed as Jyseleca® in Europe and Japan for the treatment of adult patients with moderate to severe active ulcerative
colitis (UC) who have had an inadequate response with, lost response to, or were intolerant to either conventional therapy or a biologic
agent. Jyseleca® 100mg and 200mg are registered in the above-mentioned territories. The European Summary of Product
Characteristics for filgotinib, which includes contraindications and special warnings and precautions, is available at www.ema.europa.eu.
The Great Britain Summary of Product Characteristics for filgotinib can be found at www.medicines.org.uk/emc and the Northern Ireland
Summary of Product Characteristics for filgotinib can be found at www.emcmedicines.com/en-GB/northernireland, respectively. The interview
form from the Japanese Ministry of Health, Labour and Welfare is available at www.info.pmda.go.jp.
Jyseleca® is a trademark of Galapagos NV and Gilead Sciences, Inc. or its related companies. Except for filgotinib’s
approval as Jyseleca® for the treatment of moderate to severe active RA and UC by the relevant regulatory authorities in the European
Union, Great Britain, and Japan, our drug candidates are investigational; their efficacy and safety have not been fully evaluated by any
regulatory authority.
About Galapagos
We are a global biotechnology company with operations in Europe and the US dedicated
to developing transformational medicines for more years of life and quality of life. Focusing on high unmet medical needs, we synergize
the most compelling science, technology, and collaborative approaches to create a deep pipeline of best-in-class small molecules, CAR-T
therapies, and biologics in oncology and immunology. With capabilities from lab to patient, including a decentralized, point-of-care CAR-T
manufacturing network, we are committed to challenging the status quo and delivering results for our patients, employees and shareholders.
For additional information, please visit www.glpg.com or follow us on LinkedIn or X (formerly
Twitter).
About Alfasigma
Alfasigma is one of Italy's leading pharmaceutical companies with a strong international
positioning. The Group has a worldwide presence in over 100 countries where about 3000 people work in research, development, production
and distribution. In Italy, Alfasigma is a leader in the prescription products market where, in addition to its strong focus on gastro-intestinal
products, it is present in several primary care therapeutic areas. It is popular with the consumer public for a number of nutraceuticals
& food supplements that respond to different needs, and that are well known and deeply rooted in the Italian families’ experience.
Its historical headquarters is in Bologna, to which is added Milan, while the production sites are: in Italy, in Pomezia (RM), Alanno
(PE), Sermoneta (LT) and Trezzano Rosa (MI) and abroad in Tortosa in Spain and in Shreveport (Louisiana) in the United States. The R&D
laboratories are in Pomezia and in the Parco Scientifico Tecnologico Kilometro Rosso in Bergamo. Alfasigma's mission is to improve people's
health and quality of life by offering caregivers and healthcare personnel therapeutic solutions according to the highest standards of
quality and safety.
This press release contains inside information within the meaning of Regulation (EU) No 596/2014 of the European
Parliament and of the Council of 16 April 2014 on market abuse (market abuse regulation).
Contact
Media inquiries: Marieke Vermeersch +32 479
490 603 media@glpg.com |
Investor inquiries: Sofie Van Gijsel +1 781
296 1143
ir@glpg.com
Sandra Cauwenberghs ir@glpg.com
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Forward-looking statements
This press release includes forward-looking statements within the meaning of the Private Securities Litigation
Reform Act of 1995, as amended, including statements related to the contemplated transaction between Galapagos and Alfasigma and the planned
reduction in force, statements related to the expected cost savings and efficiencies resulting from the foregoing, and statements related
to anticipated future research and development and business development activities. Forward-looking statements are subject to risks, uncertainties
and other factors that could cause actual results to differ materially from those referred to in the forward-looking statements
and, therefore, the reader should not place undue reliance on them. These risks, uncertainties and other factors include, without limitation,
the risk that the contemplated transaction between Galapagos and Alfasigma may be delayed or never consummated, the risk that the planned
reduction in force may be delayed or never consummated, the risk that the expected cost savings and efficiencies described in this press
release will not be realized and the risk that Galapagos will not successfully achieve its anticipated future research and development
and business development activities, as well as those risks and uncertainties identified in our Annual Report on Form 20-F for the year
ended 31 December 2022 and our subsequent filings with the SEC. All statements other than statements of historical fact are statements
that could be deemed forward-looking statements. The forward-looking statements contained herein are based on management’s current
expectations and beliefs and speak only as of the date hereof, and Galapagos makes no commitment to update or publicly release any revisions
to forward-looking statements in order to reflect new information or subsequent events, circumstances or changes in expectations.
1 Throughout this press release, ‘Dr. Paul Stoffels’ should be read as ‘Dr. Paul Stoffels, acting via
Stoffels IMC BV’
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