Galapagos N.V.

Galapagos N.V. (GLPG) Market Cap

Galapagos N.V. has a market capitalization of $1.94B, based on the latest available market data.

Financials updated on 2025-12-31

SectorHealthcare
IndustryBiotechnology
Employees704
ExchangeNASDAQ Global Select

Price: $29.42

▌ -0.34 (-1.14%)

Market Cap: 1.94B

NASDAQ · time unavailable

CEO: Henry Gosebruch

Sector: Healthcare

Industry: Biotechnology

IPO Date: 2012-02-27

Website: https://www.glpg.com

Galapagos N.V. (GLPG) - Company Information

Market Cap: 1.94B · Sector: Healthcare

Galapagos NV, an integrated biopharmaceutical company, engages in the discovery, development, and commercialization of various medicines for high unmet medical need. Its pipeline products include filgotinib, a JAK1 inhibitor that is in various phases of clinical trials for the treatment of rheumatoid arthritis, Crohn's disease, ulcerative colitis, small bowel CD, fistulizing CD, ankylosing spondylitis, psoriatic arthritis, and uveitis. The company's pipeline products also comprise GLPG1972 that has completed Phase 2b trial for treating osteoarthritis; Toledo molecules, including GLPG3970, GLPG4399, and GLPG4876 for inflammation; and GLPG4716 and Ziritaxestat to treat idiopathic pulmonary fibrosis. In addition, its other pipeline products include GLPG2737, a cystic fibrosis transmembrane conductance regulator that is in Phase 2 clinical trials to treat patients with autosomal dominant polycystic kidney disease; and GLPG0555, a JAK1 inhibitor, which is in Phase 1b for treatment of patients with osteoarthritis. The company has collaboration agreements with Gilead Sciences, Inc.; AbbVie S.Ă  r.l.; and Novartis Pharma AG. Galapagos NV was incorporated in 1999 and is headquartered in Mechelen, Belgium.

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AI-Generated Research: This report is for informational purposes only. Please validate all data using official SEC filings before making investment decisions.

📘 Galapagos N.V. (GLPG) — Investment Overview

đŸ§© Business Model Overview

Galapagos N.V. (GLPG) is a biopharmaceutical company focused on discovering, developing, and commercializing therapies with an emphasis on targeted, mechanism-driven medicines. The company’s model typically combines internal drug discovery and late-stage development with a partnership-led monetisation strategy. This structure allows Galapagos to share development risk, access capital efficiency through co-development or licensing arrangements, and potentially retain commercial upside in selected geographies or indications—depending on the agreement terms.

At a high level, Galapagos operates across the core stages of value creation: (1) discovery and translational science to identify tractable biological targets, (2) clinical development and evidence generation to validate efficacy and safety, and (3) commercialization planning and execution once assets reach approved indications. The pipeline is organized around the translation of scientific hypotheses into clinical candidates, followed by disciplined “go/no-go” decisions informed by clinical endpoints, biomarker signals (where relevant), and competitive context.

Importantly, Galapagos’ business model is not solely dependent on any single asset category. Instead, it is designed to balance near-term revenue contributions (from products and agreements) with longer-duration optionality stemming from ongoing development programs. This optionality is central to underwriting the company’s multi-year profile: successful clinical outcomes for successive candidates can expand the revenue base, extend platform credibility, and improve the bargaining position for future partnerships or commercial collaboration.

💰 Revenue Streams & Monetisation Model

Galapagos monetises value through a combination of product-related revenue and external deal structures. Revenue streams commonly include:

  • Commercial product revenue: Income generated from marketed therapies in relevant jurisdictions, where Galapagos holds commercial rights directly.
  • Licensing and collaboration revenue: Upfront payments, milestone-based payments, and ongoing research or development support under partnership agreements. These arrangements can reflect the transfer of rights, shared development responsibilities, or manufacturing and regulatory cost allocations.
  • Royalties and sales-sharing arrangements: Ongoing economics tied to partner sales where Galapagos retains certain rights to an asset or technology.
  • Reimbursement dynamics and commercial mix effects: Where applicable, net sales can be influenced by contracting structures, payer uptake, channel dynamics, and competitive reimbursement pressure.

A key feature of the Galapagos model is that it tends to employ partnerships strategically. This can create a “two-track” monetisation pathway: (1) nearer-term revenue from commercial activities or matured assets, and (2) longer-duration monetisation through milestones and royalties tied to assets that progress with partner support. This can reduce capital intensity compared with a purely independent commercialization strategy, while still enabling Galapagos to participate in value creation.

From an investor lens, the quality of monetisation is shaped by agreement terms—especially whether Galapagos bears significant costs for clinical and regulatory execution, and whether it retains pricing and commercialization control in high-value markets. Understanding the revenue contribution mix (products vs. deals) and the contractual basis for milestones or royalties is critical for assessing the durability of future cash generation.

🧠 Competitive Advantages & Market Positioning

Galapagos’ competitive posture is grounded in its biology-driven approach and an ability to advance candidates from target selection through clinical validation. In targeted therapeutics, competitive advantage typically comes from three interlocking factors: (1) scientific differentiation in mechanism or target engagement, (2) clinical evidence quality demonstrating meaningful outcomes for patients, and (3) operational execution that reduces time-to-decision and avoids late-stage surprises.

In market positioning, Galapagos generally targets therapeutic areas where precise mechanism alignment can translate into efficacy and tolerability. For such markets, differentiation can emerge through:

  • Clinical outcome evidence: Demonstration of robust endpoints, durable responses, and manageable safety profiles compared with standards of care.
  • Mechanistic clarity: A defensible rationale for patient selection, dosing strategy, and integration into treatment algorithms.
  • Development discipline: Efficient study design, biomarker-informed strategies (where relevant), and consistent translation from nonclinical signals to clinical performance.
  • Partnership and scaling capability: Commercial and development collaborations can enhance market reach and operational leverage.

Another important positioning element is pipeline continuity. Many biopharmaceutical companies exhibit “single-asset” risk where future outlook hinges on one late-stage program. Galapagos’ investment case is strengthened when the pipeline exhibits a credible sequence of catalysts—so that positive readouts in one program support confidence in subsequent programs, and negative outcomes do not fully impair the medium-term opportunity set.

Finally, competitive dynamics in pharma often hinge on payer and prescriber adoption. When therapies are differentiated by efficacy, safety, and convenience (e.g., dosing schedule, patient adherence implications), they can achieve earlier uptake and better pricing resilience. Galapagos’ ability to support access strategy—through evidence, health economic framing, and clinical education—becomes a competitive lever as products mature.

🚀 Multi-Year Growth Drivers

The multi-year growth narrative for Galapagos is best understood as a portfolio of drivers spanning commercialization, lifecycle management, and pipeline progression. The key growth channels generally include:

  • Commercial expansion and product lifecycle activities: Growth can come from increased penetration, expanded labeled indications, and/or improved patient segmentation. Lifecycle activities may include additional trial evidence, comparative data, and optimized positioning within treatment pathways.
  • Pipeline advancement into late-stage development: Each successful transition across clinical phases increases the probability-weighted value of future milestones and/or product revenue. Investors typically focus on whether programs demonstrate clear clinical differentiation and credible safety.
  • Partner-driven acceleration of asset value: Strategic collaborations can reduce capital burden while enabling faster execution. Well-structured partnerships can also increase the attractiveness of assets for broader commercial development.
  • Platform credibility and deal optionality: A consistent track record can improve future partnering terms and improve bargaining leverage—potentially increasing the proportion of economics retained by Galapagos and lowering development risk through better-resourced collaborations.
  • Geographic scaling and reimbursement execution: Broader access in key markets supports revenue durability. Strong payer outcomes and formulary coverage can reduce revenue volatility and extend product life cycles.

From a financial perspective, a crucial aspect of growth durability is managing the balance between spending (R&D, manufacturing scale-up, and commercialization support) and monetisation. In targeted biotech, growth can be self-reinforcing when clinical success improves funding flexibility, reduces perceived risk, and enables management to fund pipeline progression without sacrificing long-term economics.

In underwriting terms, the most constructive scenario is one where Galapagos maintains a steady pipeline of de-risked programs that can progressively contribute to revenue through both product expansion and partnership economics. The less constructive scenario would involve a pipeline with large “lumpy” value concentration, where a single event determines a significant portion of the long-term outlook.

⚠ Risk Factors to Monitor

Despite a structured approach to discovery and development, Galapagos faces the typical risk profile of biopharmaceutical companies—plus risks specific to portfolio composition, partnerships, and commercialization execution. Key risks to monitor include:

  • Clinical and regulatory risk: Efficacy and safety signals can change with broader patient populations or longer follow-up. Regulatory review outcomes can deviate from earlier clinical expectations.
  • Competitive and standard-of-care risk: New entrants, label expansions from competitors, or shifts in treatment paradigms can compress adoption or pricing power.
  • Commercial adoption risk: Even differentiated therapies require strong payer and prescriber engagement. Reimbursement hurdles, real-world persistence, and formulary dynamics can affect net sales durability.
  • Dependency on partnership economics: Milestones, royalties, and cost-sharing terms can materially influence cash flows. Contract structures may cap upside or shift future development costs.
  • Pipeline concentration and timing risk: The presence of one or two high-impact programs can dominate valuation. A setback in a major asset can reduce probability-weighted future value.
  • Manufacturing and supply chain execution: Scale-up, quality systems, and distribution logistics can affect product continuity and cost structure—particularly if demand exceeds initial assumptions.
  • Financing and capital allocation risk: Equity or debt financing can dilute shareholders if external funding becomes necessary. Capital allocation decisions among R&D, commercialization, and business development can influence long-term returns.
  • Intellectual property and legal risk: Patent life, exclusivity strategy, and freedom-to-operate analysis affect long-term economics and competitive landscape.

A disciplined investment process should treat these risks as dynamic variables. For example, the clinical risk of one program changes once it generates confirmatory evidence, while the commercialization risk can be monitored through adoption trends, payer behavior, and evidence in real-world settings. For partnership-driven economics, investors should track whether collaboration milestones remain achievable and whether rights and obligations remain favorable.

📊 Valuation & Market View

Valuing Galapagos requires an approach that reflects both operating revenues and the optionality embedded in its pipeline. A robust valuation framework typically combines:

  • Sum-of-the-parts (SOTP): Estimating value for marketed assets (based on sales assumptions, margins, and duration) plus separate valuation for late-stage pipeline programs (based on probability-weighted clinical success and expected peak sales or partnered economics).
  • Risk-adjusted discounting: Discounting future cash flows to reflect clinical/regulatory uncertainty. The discount rate can also incorporate financing risk and biotech-specific volatility.
  • Scenario analysis: Constructing bull/base/bear cases around (a) clinical progression, (b) commercialization trajectory, and (c) milestone/royalty realization under partnership agreements.
  • Assessment of deal economics: Incorporating the structure of collaborations (who pays for what, how royalties are shared, and what triggers milestones) to avoid overestimating revenue potential.

From a market view perspective, the investment debate often centers on how investors interpret the company’s probability-weighted pipeline progress relative to its cost base. When confidence increases around clinical differentiation and execution, the market tends to price the pipeline more aggressively. Conversely, when uncertainty rises—through safety signals, competitive read-throughs, or delays in development—valuation can become more sensitive to near-term cash burn and the probability distribution of pipeline outcomes.

Key underwriting questions include:

  • How much of the valuation is supported by current product revenue versus probability-weighted pipeline value?
  • Does the pipeline show credible evidence of differentiation that translates into durable adoption and pricing?
  • Are partnership terms likely to preserve upside for Galapagos as assets mature?
  • Is the cost trajectory aligned with expected catalyst timing and monetisation pathways?

In high-quality biotech underwriting, the most resilient valuation cases are those where cash-flow visibility is supported by a diversified set of revenue contributors and where pipeline catalysts reduce uncertainty incrementally.

🔍 Investment Takeaway

Galapagos N.V. represents a targeted biopharmaceutical investment profile combining (1) monetisation through commercialization and partnership economics and (2) multi-year value creation potential through ongoing pipeline development. The core investment thesis typically rests on the credibility of clinical differentiation, the durability of commercial adoption, and the favorable evolution of collaboration-based revenue mechanisms.

A favorable risk-reward setup generally emerges when the pipeline shows consistent evidence of tractable biology translating into meaningful clinical outcomes, when partnership economics remain attractive, and when commercialization execution supports durable payer adoption. Conversely, the most significant risks stem from clinical/regulatory uncertainty, competitive shifts in therapeutic standards, and the sensitivity of cash flows to deal terms and milestone realization.

For investors, the decision framework should emphasize portfolio diversification of catalysts, the probability-weighted valuation of pipeline assets, and rigorous monitoring of execution across clinical development, regulatory milestones, and commercialization access. With a disciplined underwriting process, Galapagos can be evaluated as an investable platform for targeted therapy development with optionality—while respecting the inherent volatility of biopharmaceutical timelines.


⚠ AI-generated — informational only. Validate using filings before investing.

Management’s tone is confident on transformation—highlighting ~EUR 3bn cash at year-end 2025 and a strong, constructive Gilead partnership that can fund both upfront and ongoing development costs beyond the stand-alone pool. However, the Q&A shows the real pressure points are execution and timing: cell therapy wind-down still requires meaningful cash outflows (up to EUR 50m in Q1 2026; EUR 125m–EUR 175m restructuring in 2026; plus EUR 35m–EUR 40m final restructuring costs), and management refused to promise the envelope will smooth out. On business development, there’s no specific deal deadline, but OLCA expiration (~3 years and change) is the de facto deadline, with an explicit consequence if they miss it. For GLPG3667, the internal “high bar” remains, but partner conversations are driven by a stated lack of full Phase III infrastructure—suggesting internal control is constrained and success depends on external deal-making and timing.

AI IconGrowth Catalysts

  • GLPG3667 (TYK2) Phase II topline results in dermatomyositis and SLE; pursuing potential partnerships to accelerate development toward Phase III
  • Transition from legacy cell therapy to a pipeline of derisked late-stage clinical assets (primarily i&i and oncology)

Business Development

  • Gilead collaboration remains a key strategic advantage; openness to contribute both upfront consideration and development/spend terms (explicitly stated as strong/constructive dialogue)
  • Exploring partnerships with other i&i players for GLPG3667 (management citing lack of full infrastructure internally to go through Phase III)

AI IconFinancial Highlights

  • 2025 operating profit from continuing operations: EUR 295.1m vs operating loss of EUR 188.3m in 2024
  • Revenue driver: release of remaining deferred income balance of EUR 1,069m tied to OLCA exclusive access rights granted to Gilead
  • OLCA accounting context: contract liability approx. EUR 2.3bn recognized to revenue straight-line over 10 years; 2025 amendments/wind-down assessment resulted in no remaining obligations justifying the liability in IFRS
  • No expected 2025 cash tax impact from the OLCA revenue recognition
  • Operating expense headwinds in 2025: EUR 399.8m negative impact, dominated by cell therapy wind-down EUR 275m (impairment EUR 228.1m; severance EUR 33.3m; early termination EUR 16.3m; deal cost EUR 10.1m; accelerated noncash cost EUR 1.5m; other EUR 7.5m) partly offset by contingent consideration fair value adjustment EUR 21.8m
  • Additional 2025 reorganization: small molecules strategic reorg for EUR 124.8m
  • Cash & cash equivalents + financial investments: EUR 2,998m at Dec 31 2025 vs EUR 3,317.8m at Dec 31 2024; USD cash increased vs prior year
  • 2026 cash-flow profile guidance: cash flow neutral to positive by end of 2026

AI IconCapital Funding

  • Year-end 2025 cash position: approx. EUR 3.0bn
  • 2026 cash runway guidance: approx. EUR 2.775bn to EUR 2.850bn in cash/cash equivalents/financial investments at Dec 31 2026 (excluding business development activities or currency fluctuations)
  • Currency allocation: as of Dec 31 2025, cash/financial investments included EUR 2,159m held in USD (vs EUR 726.9m at Dec 31 2024); management stated now holding ~72% USD / 28% EUR and expects to continue increasing USD portion

AI IconStrategy & Ops

  • Cell therapy wind-down execution: substantially completed by end of Q3 2026 (from works council processes completed last month)
  • Updated one-time restructuring cash range for cell therapy: reduced by EUR 25m to EUR 125m–EUR 175m in 2026 (down from prior EUR 150m–EUR 200m)
  • Near-term cash outflows: expect operating cash outflow up to EUR 50m in Q1 2026 related to wind-down
  • Final restructuring implementation costs: expected EUR 35m–EUR 40m
  • TYK2 (GLPG3667) cost guidance: up to EUR 40m in 2026 for completion of Phase II in DM/SLE and support toward Phase III

AI IconMarket Outlook

  • OLCA timing risk framing: OLCA expiration is ~3 years and change away; management emphasized no specific deal deadline but stated they need a transformative transaction ahead of OLCA expiration
  • Breakeven timing (cash flow): cash flow neutral to positive by end of 2026; no quarter-level operating income break-even provided

AI IconRisks & Headwinds

  • Deal-dependence / contract regime risk: OLCA expires in ~3 years and change; if a transformative transaction is not completed before OLCA expiration, management stated OLCA would expire and operations continue without it
  • Cost overhang / execution hurdle: cell therapy wind-down costs are 'chunky' throughout 2026 (despite reduced restructuring range); management did not provide further future guidance details beyond noting updates on future calls
  • GLPG3667 internal development hurdle: management cited lack of full infrastructure internally to take the program into Phase III, making partner talks a central decision driver
  • Currency/earnings rate sensitivity: management justified USD transition with higher interest earnings rates (management stated EUR ~2% vs USD ~4%), but noted EUR operating expenses still require retaining a portion in euros

Sentiment: MIXED

Note: This summary was synthesized by AI from the GLPG Q4 2025 earnings transcript. Financial data is complex; please verify all metrics against official SEC filings before making investment decisions.

đŸ§Ÿ Full Earnings Call Transcriptâ–Œ

Ticker: GLPG

Quarter: Q4 2025

Date: 2026-02-24 08:00:00

Operator: Good day, and thank you for standing by. Welcome to the Galapagos Year-End 2025 Financial Results Conference Call. [Operator Instructions] Please be advised that today's conference is being recorded. I would now like to hand the conference over to your speaker today, Glenn Schulman, Head of Investor Relations. Please go ahead.

Glenn Schulman: Good day, everyone. This is Glenn Schulman, Head of Investor Relations, and I'd like to thank you all for joining us today as we report Galapagos' full year 2025 financial results and fourth quarter business update. Last evening, we issued a press release outlining these results. This release, along with today's presentation, can be found on the Galapagos Investor website at www.glpg.com. Before we begin, I would like to remind everyone that we will be making forward-looking statements. These forward-looking statements include remarks concerning future developments of our company and our pipeline and possible changes in the industry and competitive environment. These forward-looking statements reflect our current views about our plans, intentions, expectations, strategies and prospects, which are based on the information currently available to us and on assumptions we have made. Actual results may differ materially from those indicated by these statements and are accurate only as of the date of this recording, February 24, 2026. Galapagos is not under any obligation to update statements regarding the future or to conform to these statements in relation to actual results unless required by law. You are cautioned not to place any undue reliance on these statements. Joining us on today's call from the executive team are Henry Gosebruch, Chief Executive Officer; Aaron Cox, Chief Financial Officer; Sooin Kwon, Chief Business Officer; and Dan Grossman, Chief Strategy Officer of the company, all of whom will be available during the Q&A session. With all that, let me now turn the call over to Henry Gosebruch, CEO of Galapagos. Henry?

Henry Gosebruch: Thank you, Glenn, and thank you all for joining us today. Galapagos had a transformative 2025, focused on turning the page from cell therapy, implementing a new strategic direction and laying a strong foundation for long-term value creation. We are entering this new chapter with approximately EUR 3 billion in cash at year-end 2025 in a strong position to pursue transformative business development opportunities with significant strategic flexibility. The new team is in place to execute on the strategic vision. We have been very deliberate in assembling the right leadership team to execute the strategy, and I could not be more pleased with the level of talent we've been able to attract to Galapagos. We've assembled a management team with world-class business development expertise and a shared mission of leveraging our unique position to create significant shareholder value. Collectively, our team has executed hundreds of transactions in the life sciences sector and is working well together with the goal of creating value for our shareholders. We have also evolved our Board composition, welcoming 5 new directors who bring the deep transaction, capital allocation and operating experiences needed for this next phase of growth. Our objective is not incremental rebuilding, but a fundamental reshaping of the company around programs we believe are capable of delivering meaningful patient impact and sustainable shareholder returns. We are aggressively evaluating opportunities across our focus areas and maintaining a broad dialogue with companies and innovators globally. We are encouraged by the level of potential transactions we have in our deal pipeline and our opportunity to become a unique player in the biotech deal ecosystem and carve out niches where we can be competitively differentiated. At the same time, we are disciplined and selective. We will allocate our capital carefully and thoughtfully with clear financial metrics in mind. Our focus remains on clinically derisked opportunities in areas where we are able to bring unique insights that represent competitive advantage. Lastly, our collaboration with Gilead remains a key strategic advantage and potential competitive differentiation. We are working very closely with Gilead and continue to have active and constructive dialogue as we evaluate opportunities. Their global development and commercialization expertise, combined with our capital base, agility and deal-making skills creates a powerful platform as we shape this next phase of growth for Galapagos. Let me briefly provide an update on our legacy R&D asset, TYK2 or GLPG3667. In December, we announced top line Phase II results for GLPG3667 in patients with dermatomyositis and systemic lupus erythematosus or SLE. GLPG3667 met the primary endpoint in the dermatomyositis study, demonstrating a statistically significant clinical benefit and meaningful improvement on secondary measures of disease activity compared to placebo. We are currently evaluating all strategic options for this program, including pursuing potential partnerships with other i&i players to accelerate the development of GLPG3667. In conclusion, Galapagos is well positioned for the future. Our year-end cash position of approximately EUR 3 billion, our strong business development and capital allocation experience provides the strategic flexibility to pursue business development opportunities while maintaining a disciplined focus on value creation. With that overview, I would like to now turn the call over to Aaron Cox, our CFO, to review our full year 2025 financial results and 2026 guidance. Aaron?

Aaron Cox: Thanks, Henry, and hello, everyone. In the press release issued last night, we detailed our full year 2025 results, provided an update on fourth quarter performance and shared our 2026 guidance. Total operating profit from continuing operations amounted to EUR 295.1 million in 2025 compared to an operating loss of EUR 188.3 million in 2024. This operating profit was primarily due to the release in revenue of the remaining deferred income balance of EUR 1,069 million associated with the exclusive access rights granted to Gilead under the OLCA. As a reminder, in conjunction with this transaction in 2019, Galapagos recognized a contract liability of approximately EUR 2.3 billion, which was to be recognized as revenue on a straight-line basis over the 10-year term of the agreement. Following the 2025 OLCA amendments, the intention to wind down and related events in 2025, as of December 31, it was assessed that there were no remaining obligations that would justify this specific contract liability to be maintained in our IFRS financial statements. We do not expect any cash tax impact in 2025 related to this recognition of revenue. Importantly, while the OLCA still remains in force, we expect that any future business development transaction will be completed under terms that would be different than the existing terms of the OLCA. Now turning to expenses. Operating expenses were negatively impacted for a total of EUR 399.8 million by the decision to wind down the cell therapy activities with an impact of EUR 275 million, consisting of an impairment of the cell therapy activities of EUR 228.1 million, severance costs of EUR 33.3 million, costs for early termination of collaborations of EUR 16.3 million, deal cost of EUR 10.1 million, EUR 1.5 million for additional accelerated noncash cost recognition for subscription right plans, and EUR 7.5 million of other costs, partly offset by a positive fair value adjustment of the contingent consideration payable of EUR 21.8 million. Additionally, the executed strategic reorganization related to the small molecules business announced in 2025 for EUR 124.8 million. Financial investments and cash and cash equivalents totaled EUR 2,998 million on December 31, 2025, as compared to EUR 3,317.8 million on December 31, 2024. Our cash and cash equivalents and current financial investments included EUR 2,159 million held in U.S. dollars versus EUR 726.9 million on December 31, 2024. These U.S. dollars were translated to euros at an exchange rate of 1.175. Since year-end, we have converted more euros to U.S. dollars and now hold approximately 72% of our cash in U.S. dollars and 28% in euros. We expect to continue increasing the portion of cash in U.S. dollars as the year progresses. Turning now to our guidance for 2026. As part of the transformation to the new Galapagos, we announced our intention to wind down our cell therapy activities last fall, and we are now executing on this process following the works council processes that were completed last month. Given the progress we've made on this execution, I can now share that we expect the cell therapy wind down to be substantially completed by the end of the third quarter of 2026. In connection with the wind down of the cell therapy activities, we expect an operating cash outflow of up to EUR 50 million in Q1 2026 as well as one-time restructuring cash impact of EUR 125 million to EUR 175 million in 2026. This reflects a EUR 25 million reduction compared to the prior guidance range of EUR 150 million to EUR 200 million. In addition, we anticipate cash costs of approximately EUR 35 million to EUR 40 million for the final implementation of the restructuring announced in January 2025. Costs related to the ongoing TYK2 program, including completion of the Phase II clinical trials in DM and SLE, as well as ongoing support to advance the program towards Phase III development are expected to be up to EUR 40 million in 2026. Away from the spend items, we continue to expect meaningful cash flow to come from interest income, royalties and tax credits. As a result, we expect to be cash flow neutral to positive by the end of 2026. We also anticipate we will have approximately EUR 2.775 billion to EUR [ 2.850 ] billion in cash, cash equivalents and financial investments at December 31, 2026, excluding any business development activities or currency fluctuations. Now let me turn it back to Henry to wrap up.

Henry Gosebruch: Thanks, Aaron. In closing, 2026 will be a pivotal year for Galapagos as we focus on building long-term value through transformative business development, leveraging our strong balance sheet, our deal-making expertise and our unique collaboration with Gilead. Our shares remain at a significant discount to the cash figures, Aaron just reviewed. We will be focused on closing the gap through execution on our business development plan, thoughtful capital allocation and engagement with shareholders to rebuild trust and confidence. We are encouraged by the momentum we've built so far as we reshape Galapagos with a clear strategy in place. With a disciplined approach to capital allocation, we remain focused on pursuing the right opportunities to build a pipeline of novel therapeutics designed to deliver meaningful benefits for patients and a sustainable value for shareholders. We are still early in this new chapter of our company, but we are off to a strong start, and we are excited about the future ahead. So with that, thank you all for your attention, and we will now open it up for your questions. Operator?

Operator: [Operator Instructions] And our first question comes from the line of Brian Abrahams from RBC Capital Markets.

Brian Abrahams: Just as you continue to progress on business development, just kind of curious if anything has evolved in terms of what you might be looking for? And then is there any deadline or any sort of change that we might expect based on the Gilead agreement if you're not able to identify assets to bring in by a certain time point?

Henry Gosebruch: Yes. Brian, it's Henry. I'll take those questions. So no, our strategy is really consistent with what we've been talking about since last fall in terms of focusing on derisked late-stage clinical assets, not exclusively, but primarily in the i&i and oncology space. And I'd say we continue to see a lot of good opportunity there. And as we said in the prepared remarks, we're focusing on opportunities where we think we can bring unique insight, unique competitive advantage. But I think there's, again, a lot of opportunity, and we're working through our deal funnel and remain confident that there's a lot of attractive opportunity for us. With respect to your second question, as we said previously, we're not going to set a deadline for a specific deal. Again, we'll remain patient, disciplined. Again, we do have some good activity going on, but it's more important to do the right deal than to do a deal by a certain period of time. The OLCA does expire. Now it doesn't expire for about 3 years and change. So ultimately, that is a deadline. But certainly, we're focused on getting an important transaction, transformative transaction done ahead of that ultimate expiration of OLCA.

Brian Abrahams: Got it. And if something does not happen before then?

Henry Gosebruch: Well, if something does not happen by then, despite working really hard on, trying to make it happen, then OLCA would expire, and we would go on without the OLCA in place.

Operator: Our next question comes from the line of Phil Nadeau from TD Cowen.

Philip Nadeau: Our question is on GLPG3667. In the past, you've suggested that the bar to moving that forward internally and investing in it further would be rather high. We're curious to get an update on your thoughts there. I know you said you're pursuing all possible avenues of moving that forward. But how does management weigh developing that internally and investing in it versus out-licensing?

Henry Gosebruch: Yes, Phil, I would say those comments also stands. We have a high bar. Frankly, we have a high bar, not just for 3667, but for any asset, be it internal or external, we really look at it with the same unbiased lens. Now with respect to where we are, again, it's still early. We, as you know, get the topline data just before the holiday. Data is still coming in. So we don't have the full package in place. We are in the process of talking to partners. Again, given that we don't have the full infrastructure required to really take this into Phase III, it makes sense to see where some of the players are that, that have that. And maybe in working with a partner, we can do more, do it faster, do it more capital efficient and ultimately create more value. So we're focused on looking at that. We're focused on getting our arms around the data that's still trickling in. But again, the bar is exactly the same bar that we've always set for ourselves.

Operator: [Operator Instructions] Our next question comes from the line of Sean McCutcheon from Raymond James.

Sean McCutcheon: Can you speak to your current view on capital allocation, specifically as it relates to the pool of capital you aim to put forth for acquisitions for BD? And how much you need to reserve for operating expenses going forward and how the Gilead partnership informs deal sizing and optionality on that front?

Henry Gosebruch: Yes, it's Henry. Thanks for the question. So look, at a high level, I mean, some of what I'm going to say is it's pretty obvious, but we have EUR 3 billion in capital. And as you point out, that capital needs to account both for any consideration to a partner or acquisition target and of course, our development expenses we would have in any transaction. Now when you say sort of how does the relationship with Gilead inform our capital allocation, as we said on calls previously, the dialogue with Gilead is quite strong. It's very, very constructive. They continue to indicate openness to contribute in both deal terms, meaning paying some of the upfront consideration as well as taking on some of the development spend operation. So ultimately, in working with Gilead, we can go beyond the EUR 3 billion we have. And I think that's one of the features we think is very attractive in working with Gilead. So as we think through it, we don't just think about our pool of capital. We also think about what in working with Gilead can we add to the pie and therefore, kind of go beyond what we could do on our own. I don't know if that's where you were going with your question or if you want to clarify maybe what I didn't answer.

Sean McCutcheon: No, I think that covers it.

Operator: There are no further questions at this time. So I'll hand the call back to Glenn for closing remarks.

Glenn Schulman: Thanks, [ Mel ]. I think in the Q&A queue, we do have one more or a couple more coming in, if possible, it would be great to take. I think there's a question from KBC.

Operator: Please go ahead Mathijs Geerts Danau from KBCS.

Mathijs Geerts Danau: Mathijs coming for Jacob. I had a question on the lower cell therapy wind-down costs. Do you maybe expect that to lower further in the future? Or do you see any possibility in that?

Henry Gosebruch: Yes, Mathijs, thanks. It's Henry. Thanks for getting the question, and I'll let Aaron answer that.

Aaron Cox: Yes, thanks. We're not providing future guidance here, but we'll obviously update folks on how that cost envelope is progressing on future calls. But yes, we did lower the range from a previous range of EUR 150 million to EUR 200 million in terms of one-time restructuring costs. We lowered that range by EUR 25 million with this release. And as we continue to progress through the wind down, we'll provide updated costs on future calls.

Operator: [Operator Instructions] Our next question comes from the line of Delphine Le Louet from Bernstein.

Delphine Le Louet: I was wondering and coming back to the capital allocation and the decision you've been taking especially regarding the cash and the cash allocation, the move from euro to dollar, considering the fact that you didn't gain as much as financial income as last year. And so I was questioning about what was the rationale on the back of that? What was the exact timing for us to be clear? And shall we consider the breakup of, let's say, 2/3 U.S., 1/3 euro as being a picture for your next investment portfolio or for the picture we should have from your investment income in the near future?

Aaron Cox: Yes. Thanks, Delphine. So mid last year, we started transitioning more euros to dollars, and that was primarily based on where we expected our BD activity to be driven and also where our cost base is starting to move towards, which is more U.S.-based. We provided a range on this call of EUR 2.775 billion to EUR [ 2.850 ] billion for the year. And as I mentioned before, we'll update that as we go through the year. In terms of continued transition to U.S. dollars, we did -- as you heard from my remarks, we do expect to transition more to U.S. dollars as the year progresses, but still keeping a portion in euros as we still have meaningful operating expenses in euro denomination over the year as we move through this wind down. We do see higher earnings rates in terms of what we're receiving on our U.S. dollars. As you look at rates across the environment, you could estimate euros earning around 2% and U.S. dollars earning around 4%. So while the exchange rate does move, we are seeing significant uptake in terms of the interest earned on the U.S. dollars versus euros.

Delphine Le Louet: Can I ask another one? Or do you have to go back in the queue?

Henry Gosebruch: Go ahead, Delphine. Go ahead.

Delphine Le Louet: I was wondering if you have or if you can communicate any expectation regarding your -- the breakeven in terms of operating income.

Henry Gosebruch: You cut out a little bit. You're asking about what regarding operating income?

Delphine Le Louet: Yes. When do you expect to breakeven for the operating income?

Aaron Cox: Yes. We've indicated we expect to be cash flow neutral to positive by year-end. Obviously, as we work through the wind down and associated costs, those costs are going to be chunky kind of throughout the year. So it's hard to predict exactly which quarter some of those costs are going to fall in, but we do expect to be cash flow neutral and positive by year-end.

Operator: [Operator Instructions] Our next question comes from the line of Nora Lazar from [indiscernible]. There are no further questions at this time. So please go ahead, Glenn, for closing remarks.

Glenn Schulman: Thanks, [ Mel ] and thanks, everyone, for taking the time to join us this morning on the call. Just a couple of upcoming activities on the Investor Relations front, the Galapagos team is going to be at the TD Cowen Conference next week up in Boston, attending the Jefferies by the Beach Conference in a couple of weeks, Kempen Conference coming up in April 15 and the Bank of America Conference in May. Those interested in meeting with the team, please feel free to reach out to your sales contact at those respective institutions to schedule a meeting. Lastly, I just want to mention that our annual report will be filed near the end of March, March 26. So there'll be additional information coming out then. And if you need anything in the meantime, don't hesitate to reach out to me. Thank you all for your attention today, and have a great week.

Operator: This concludes today's conference call. Thank you for participating. You may now disconnect.

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