Interim / Quarterly Report • Aug 21, 2025
Interim / Quarterly Report
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Q2 results exceeded expectations, driven by an improved momentum for tablets and adrenaline autoinjectors. Sales in Europe were ahead of plan, supporting 12% overall revenue growth, despite phasing of product shipments to International markets. The operating profit (EBIT) increased by 41%, and the full-year revenue outlook has been upgraded.
Comparative figures for Q2 2024 are shown in brackets. Growth rates are stated in local currencies (l.c.), unless otherwise indicated.
| Growth | Growth | ||||||
|---|---|---|---|---|---|---|---|
| In DKKm | Q2 2025 | l.c. | r.c. | H1 2025 | l.c. | r.c. | |
| Revenue | 1,527 | 12% | 11% | 3,049 | 12% | 12% | |
| EBIT | 375 | 41% | 42% | 844 | 46% | 46% | |
| EBIT margin – % | 25% | 28% |
l.c.: local currency; r.c.: reported currency
On 12 August 2025, ALK upgraded the full-year outlook based on the better-than-expected performance in Q2 and an improved outlook for the remainder of the year:
Commenting on the Q2 results, CEO Peter Halling said: "Q2 marked a step change in the execution of key strategic growth initiatives, notably the rollout of our respiratory tablets for young children, the launch of the neffy® adrenaline spray, and the deployment of a dedicated paediatric sales force in the US. While these efforts are still at an early stage, they have started contributing to growth, and we expect their impact to increase from the second half-year onwards. This reinforces our confidence in our ability to deliver sustained, profitable growth by reaching more patients with evidence-based allergy and anaphylaxis solutions."

Investor Relations: Per Plotnikof, tel. +45 4574 7527, mobile +45 2261 2525 Media: Maiken Riise Andersen, tel. +45 5054 1434
ALK is hosting a conference call for analysts and investors at 1.30 p.m. (CEST) on 21 August 2025 at which Management will review the financial results and the outlook. The conference call will be audio cast on https://ir.alk.net where the relevant presentation will be available shortly before the call begins.
To register for the conference call, please use this link and follow the registration instructions. You will receive an email from [email protected] with dial-in details, including a passcode and a pin code. Please make sure to whitelist [email protected] and/or check your spam filter. We advise you to register well in advance and to call in before 1.25 p.m. (CEST).

| Q2 | Q2 | H1 | H1 | Full year | |
|---|---|---|---|---|---|
| Amounts in DKKm | 2025 | 2024 | 2025 | 2024 | 2024 |
| Income statement Revenue |
1,527 | 1,374 | 3,049 | 2,725 | 5,537 |
| Revenue growth (local currencies) | 12% | 21% | 12% | 15% | 15% |
| Revenue growth (reported) | 11% | 21% | 12% | 15% | 15% |
| Operating profit (EBIT) | 375 | 264 | 844 | 580 | 1,091 |
| EBIT growth (local currencies) | 41% | 189% | 46% | 84% | 65% |
| EBIT growth (reported) | 42% | 172% | 46% | 78% | 64% |
| Operating profit before depreciation and amortisation (EBITDA) | 450 | 331 | 990 | 713 | 1,363 |
| Net financial items | (25) | 5 | (21) | (2) | (34) |
| Profit before tax (EBT) | 350 | 269 | 823 | 578 | 1,057 |
| Net profit | 263 | 201 | 617 | 433 | 815 |
| Average number of employees (FTE) | 2,782 | 2,811 | 2,782 | 2,806 | 2,789 |
| Balance sheet | |||||
| Total assets | 8,272 | 7,045 | 8,272 | 7,045 | 8,246 |
| Invested capital | 5,023 | 4,025 | 5,023 | 4,025 | 5,003 |
| Net interest bearing debt (NIBD) | 83 | 87 | 83 | 87 | 598 |
| Equity | 5,847 | 4,919 | 5,847 | 4,919 | 5,373 |
| Cash flow and investments | |||||
| Cash flow from operating activities |
320 | 259 | 709 | 542 | 1,213 |
| Cash flow from investing activities |
(104) | (98) | (163) | (270) | (1,417) |
| - of w hich investment in intangible assets |
(48) | (13) | (57) | (23) | (1,043) |
| - of w hich investment in tangible assets |
(58) | (84) | (106) | (133) | (260) |
| - of w hich acquisitions of companies and operations |
- | - | - | (115) | (115) |
| Free cash flow | 216 | 161 | 546 | 272 | (204) |
| Information on shares | |||||
| Share capital | 111 | 111 | 111 | 111 | 111 |
| Shares in thousands of DKK 0.5 each | 222,824 | 222,824 | 222,824 | 222,824 | 222,824 |
| Share price, end of period | 187 | 153 | 187 | 153 | 159 |
| Net asset value per share | 26 | 22 | 26 | 22 | 24 |
| Key figures | 65 | 66 | |||
| Gross margin – % | 25 | 63 | 28 | 64 | 64 |
| EBIT margin – % | 71 | 19 | 71 | 21 | 20 |
| Equity ratio – % | 30 | 70 | 30 | 70 | 65 |
| Return on invested capital (ROIC) % - rolling four quarters | 1.2 | 24 | 2.8 | 24 | 25 |
| Earnings per share (EPS) | 1.2 | 0.9 | 2.8 | 2.0 | 3.7 |
| Earnings per share (DEPS), diluted | 0.1 | 0.9 | 0.1 | 2.0 | 3.7 |
| NIBD/EBITDA - rolling four quarters | 7.1 | 0.1 | 7.1 | 0.1 | 0.4 |
| Share price/Net asset value | 6.9 | 6.9 | 6.6 |

| Q2 | % of | Q2 | % of | H1 | % of | H1 | % of | |
|---|---|---|---|---|---|---|---|---|
| 2025 | revenue | 2024 | revenue | Amounts in DKKm | 2025 | revenue | 2024 | revenue |
| 1,527 | 100 | 1,374 | 100 | Revenue | 3,049 | 100 | 2,725 | 100 |
| 532 | 35 | 507 | 37 | Cost of sales | 1,038 | 34 | 969 | 36 |
| 995 | 65 | 867 | 63 | Gross profit | 2,011 | 66 | 1,756 | 64 |
| 146 | 9 | 125 | 9 | Research and development expenses | 275 | 9 | 255 | 9 |
| 474 | 31 | 480 | 35 | Sales, marketing and administrative expenses | 892 | 29 | 924 | 34 |
| - | - | 2 | - | Other operating items, net | - | - | 3 | - |
| 375 | 25 | 264 | 19 | Operating profit (EBIT) | 844 | 28 | 580 | 21 |
| (25) | (2) | 5 | 1 | Net financial items | (21) | (1) | (2) | - |
| 350 | 23 | 269 | 20 | Profit before tax (EBT) | 823 | 27 | 578 | 21 |
| 87 | 6 | 68 | 5 | Tax on profit | 206 | 7 | 145 | 5 |
| 263 | 17 | 201 | 15 | Net profit | 617 | 20 | 433 | 16 |
| Operating profit before depreciation | ||||||||
| 450 | 29 | 331 | 24 | and amortisation (EBITDA) | 990 | 32 | 713 | 26 |
ALK continued to execute its Allergy+ strategy in Q2, supported by last year's recalibration of the business platform to focus on high-potential growth levers. Q2 efforts were particularly centred around paediatric tablet launches and the commercialisation of neffy® . Progress was seen across all disease areas.
The rollout of the house dust mite (HDM) allergy tablet for children continued the positive progress in Q2, based on the regulatory approvals and subsequent market access processes in the EU, Switzerland, the USA, Canada, and other markets. At the end of Q2, the tablet had been launched in 10 European and two North American markets served directly by ALK as well as three Southeast Asian partner markets.
Additional market launches are planned for the second half-year. Pricing and reimbursement processes are well underway in countries covered by the EU approval, and ALK has also filed for approvals in European countries outside the EU and other markets.
The rollout of the tree pollen allergy tablet ITULAZAX® for children also started in Q2. The tablet has been approved in 17 EU countries, Switzerland, Canada and the UK for young children and adolescents aged five to 17 and is launched in nine of these markets. This builds a solid base for the main initiation season for pollen tablets which typically starts in the third quarter.
So far, all key indicators – endorsements from key opinion leaders, number of patients initiated on treatment, interactions with caregivers, number of prescribers, etc. – continue to exceed expectations. End-June, more than 2,000 prescribers in markets served directly by ALK were estimated to have prescribed the HDM and/or tree pollen tablets for children.
While the ongoing launch activities for the HDM and tree pollen allergy tablets focus on existing prescribers, ALK is also working on expansion into new prescribers. Additionally, ALK will increasingly focus on the halo effects of having a complete tablet portfolio covering five of the most common respiratory allergies and being indicated for all age groups in relevant markets.
Further to the rollouts of tablets for children, ALK continued to expand in selected geographies.
In the USA, ALK has built a new dedicated sales force to target paediatricians (refer to the section 'Anaphylaxis'). The extended sales reach is expected to provide attractive synergies for the respiratory tablets indicated for use in children and adolescents.
In China, the country with the highest prevalence of HDM allergy world-wide, ALK still expects to initiate a bridging trial in Q3 to facilitate the approval of the HDM tablet. The trial is planned to enrol 300 subjects.
In Japan, ALK's partner Torii expects to start operations at a new API manufacturing facility in Q3 with a view to roughly double capacity and enable Torii to incrementally increase market supply of CEDARCURE™. Torii is about to become a whollyowned subsidiary of Shionogi & Co. Ltd., and the new owner is in the process of dissolving its partnership with a competitor and will focus on ALK's tablets going forward. The phase 3 registration study with ALK's GRAZAX® tablet is moving forward according to plan.
In the UK, the National Institute for Health and Care Excellence (NICE) endorsed ITULAZAX® in July for treatment of uncontrolled tree pollen allergy in adults. The tablet will now become accessible through the National Health Service systems in England, Wales and Northern Ireland with general reimbursement. In Q1, ACARIZAX® became the first Allergy

Immunotherapy (AIT) product to be recommended by NICE, and the two tablets' admission to the public healthcare systems represents a paradigm shift in a market, where AIT is significantly underutilised compared to other European countries. ALK plans to make submissions to extend the approvals of the two tablets to include children, while also taking steps to make GRAZAX® widely available in the UK.
ALK launched the neffy® adrenaline nasal spray in the first EU market end-June. German physicians were the first to prescribe the 2 mg EURneffy® (the EU trade name) spray to adults and children (≥ 30 kg) facing potentially life-threatening type 1 allergic reactions, including anaphylaxis.
Additional launches are planned for the second halfyear in other EU countries. Market access negotiations are progressing as planned, and a price premium for EURneffy® relative to adrenaline autoinjectors has been secured in Germany and Slovenia, which were the first markets to settle pricing and reimbursement. The initial market response to ALK's pre-launch and launch activities is encouraging and the interest among allergy specialists is generally high.
Furthermore, an application has been submitted to expand the EU approval of EURneffy® to include a 1 mg version for children aged four or older and weighing 15-30 kg.
Outside the EU, the 2 mg version was approved in July in the UK, where a launch is expected in the second half-year. The UK is Europe's – and ALK's – largest anaphylaxis market. A filing has also been made for approval in Canada, and ALK further intends to make neffy® available in other territories covered by the license agreement with ARS Pharma.
On 2 May, ALK entered into a four-year agreement with ARS Pharma to co-promote neffy® to US paediatricians. The agreement allows ALK to accelerate the build-up of a dedicated US paediatric sales force in a balanced way, based on performancebased cost and revenue sharing with ARS Pharma. The new paediatric sales force, comprising around 60 people, has been onboarded, trained, and deployed in the field. Customer engagement progresses as planned, and initial market feedback is positive.
Patient recruitment for the phase 2 trial of the peanut allergy tablet has been completed ahead of target with 150 subjects. The trial is expected to report topline data in H1 2026, after which ALK plans to proceed the programme into phase 3.
Work continues to develop treatments for adjacent diseases through in-house innovation, licensing, and partnerships. Patient recruitment has been initiated for ARS Pharma's phase 2b trial to investigate neffy®'s efficacy in acute flares in patients with chronic spontaneous urticaria. The agreement with ARS Pharma grants ALK exclusive rights to this and other new indications.
(Comparative figures for Q2 2024 are shown in brackets. Growth rates are stated in local currencies, unless otherwise indicated)
| DKKm | Q2 | Share of | Q2 | |
|---|---|---|---|---|
| 2025 | Growth* | revenue | 2024 | |
| Europe | 1,024 | 13% | 67% | 900 |
| North America | 269 | 17% | 18% | 241 |
| Int'l markets | 234 | 1% | 15% | 233 |
| Revenue | 1,527 | 12% | 100% | 1,374 |
* In local currencies
Revenue in Europe grew by 13% in local currencies to DKK 1,024 million (900). The region's largest markets, Germany and France, reported double-digit growth, while single- or double-digit growth was observed in most other markets. Tablets and anaphylaxis products were the main sources of growth and sales of both product groups exceeded expectations.
Tablet sales increased by 17% on broad-based growth across markets. Progress was mainly driven by higher volumes following the 2024/25 initiation season for tablets where the intake of new patients exceeded the previous season by more than 10%. Volume growth was reinforced by an inflow of particularly new ACARIZAX® patients in Q2, as ALK continued to mobilise patients and prescribers, and strengthen advocacy for evidence-based, registered AIT products. The new paediatric indications for ACARIZAX® and ITULAZAX® contributed positively to this development, although the input was modest, reflecting the early stage of the ongoing launches.
Conversely, there was a reduced impact from price and rebate adjustments compared to last year, when these factors accounted for approximately half of tablet sales growth in Europe.
Tablet sales growth was identical to Q1 although the impact from inventory build-ups at wholesalers is estimated to have declined in Q2 compared to Q1.
Combined sales of SCIT/SLIT drops increased by 1%. Sales of SLIT-drops, which are mainly marketed in France, increased, whereas SCIT sales fell short of expectations with a modest decrease. In line with Q1, this decrease was linked to fewer patients having started treatment, combined with reduced effects from price and rebate adjustments.
Sales of Other products and services (anaphylaxis, diagnostics, etc.) increased by 51%, driven by the anaphylaxis portfolio, which reported 62% growth.

Sales of Jext® autoinjectors benefited from favourable market dynamics, including a competitor's supply issues, while sales of EURneffy® reflected inventory build-up at wholesalers ahead of the launch in Germany.
Revenue in North America increased by 17% in local currencies to DKK 269 million (241). Sales in the USA continued to recover from last year's stagnancy and reported solid double-digit growth, based on progress in all product lines. In Canada, where tablets constitute the predominant product line, growth was higher.
Tablet sales in the region grew by 32%. US tablet sales benefited from the new paediatric indication for ODACTRA® which led to a higher uptake among both existing allergist prescribers and – to a minor extent – new paediatric prescribers. Canadian tablet sales growth mirrored sustained underlying demand, combined with some stockpiling at wholesalers ahead of price increases.
Sales of SCIT bulk allergen extracts to primarily US allergists grew by 2% witnessing an improved momentum with a continued focus on pricing optimisations.
Sales of Other products increased by 23%. Sales of PRE-PEN® for diagnosis of penicillin allergy continued the positive trend, and sales of life science products also regained momentum following last year's phaseout of a major low-margin account. Revenue from Other products also included a minor, estimated cost compensation from ARS Pharma for sales force activities under the co-promotion agreement for neffy® .
Revenue in International markets grew modestly, by 1%, to DKK 234 million (233), mainly reflecting the phasing of product shipments to China.
Tablet revenue increased by 9%. The primary market, Japan, delivered low double-digit growth in revenue from product shipment and sales royalties, partly impacted by the phasing of product shipments. Inmarket sales in Japan grew by double digits, still reflecting CEDARCURE™ capacity limitations at ALK's partner.
SCIT revenue decreased by 20%. In Q2, ALK resumed shipments to China, the region's largest SCIT market, after the recent renewal of ALK's import license, but shipments – as expected – were at a lower level than last year. Chinese in-market sales of SCIT continued to grow by double digits based on existing wholesaler inventories.
| DKKm | Q2 | Share of | Q2 | |
|---|---|---|---|---|
| 2025 | Growth* | revenue | 2024 | |
| SLIT tablets | 831 | 16% | 54% | 716 |
| SCIT/ | ||||
| SLIT-drops | 481 | -1% | 32% | 490 |
| Others incl. | ||||
| anaphylaxis | 215 | 30% | 14% | 168 |
| Revenue | 1,527 | 12% | 100% | 1,374 |
* In local currencies
(Comparative figures for H1 2024 are shown in brackets. Growth rates are stated in local currencies, unless otherwise indicated)
Revenue increased by 12% in local currencies to DKK 3,049 million (2,725), driven by double-digit growth in tablet and anaphylaxis revenue. Exchange rates impacted reported revenue growth negatively by less than 1 percentage point.
Cost of sales increased by 7% in local currencies to DKK 1,038 million (969). The gross profit of DKK 2,011 million (1,756) yielded a gross margin of 66% (64%), mirroring higher sales volumes, changes to the sales mix, and production efficiencies. These factors were to some extent offset by higher input costs.
Capacity costs to R&D, Sales & Marketing and Administration decreased by 1% in local currencies to DKK 1,167 million (1,179). The decrease was enabled by last year's optimisation and prioritisation initiatives, where ALK downsized operations in certain markets with limited immediate growth prospects for AIT, and further adapted the Chinese organisation to the new timeline for the ACARIZAX® launch.
R&D expenses increased by 8% to DKK 275 million (255) and mainly reflected funding of the peanut tablet programme, pre-clinical development projects, and preparations for the clinical trial with ACARIZAX® in China. Sales and marketing expenses decreased by 2% in local currencies to DKK 724 million (741), as savings offset growth investments in e.g. the paediatric tablet launches and the neffy® rollout. Administrative costs of DKK 168 million (183) decreased by 8% compared to H1 2024 where costs included activities to the Allergy+ strategy process.
EBIT (operating profit) improved by 46% in local currencies to DKK 844 million (580), raising the EBIT margin from 21% to 28%. Progress was driven by higher sales, improved gross margin, and a lower capacity cost-to-revenue ratio of 38% (43%). The first half-year 2024 EBIT included DKK 38 million in oneoffs to optimisation efforts, while no such costs were recognised this year. Exchange rates impacted growth in reported EBIT negatively by approximately 0.5 percentage point.

Net financials showed a loss of DKK 21 million (a loss of 2) related to interest expenses and currency losses.
Tax on the profit totalled DKK 206 million (145), and net profit increased to DKK 617 million (433).
Cash flow from operating activities was DKK 709 million (542) as higher earnings offset changes in working capital, mainly related to planned inventory build-up in support of future revenue growth. Cash flow from investing activities was DKK minus 163 million (minus 270 which included the DKK 115 million PRE-PEN® acquisition) reflecting the continued buildup of capacity for tablet production, upgrades to legacy production, as well as a milestone payment to ARS Pharma of DKK 35 million (USD 5 million) related to first commercial sale of EURneffy® in the licensed territory and investments in the next generation adrenaline auto-injector. Free cash flow was positive at DKK 546 million (positive at 272).
Cash flow from financing activities amounted to DKK minus 608 million (minus 329), mainly related to repayment of loans.
At the end of June, ALK held 1,261,283 of its own shares or 0.6% of the share capital, which is 0.1 percentage point down compared to year-end and June 2024.
Equity totalled DKK 5,847 million (4,919) at the end of June, and the equity ratio was 71% (70%).
On 12 August 2025, ALK upgraded the full-year outlook based on the better-than-expected performance in Q2 and an improved outlook for the remainder of the year:
The upgraded outlook mainly reflects higher sales of adrenaline autoinjectors and the momentum for tablets in Europe. Moreover, the upgrade reflects reduced risks associated with market conditions in Europe. On the basis of the improved revenue outlook, ALK has decided to allocate additional funds to strategic growth initiatives in the second half-year.
The outlook is based on the following assumptions:
Tablet sales are expected to grow by double digits. Growth will be fuelled by a growing number of patients in treatment, including children and adolescents, while the impact from price and rebate adjustments compared to 2024 is expected to be less.
Combined SCIT/SLIT drops sales are still projected to grow by single digits with growth in all three sales regions, although timing of SCIT shipments to China may influence growth in International markets.
Sales of Other Products (anaphylaxis, diagnostics, and life science products) are projected to grow by double digits, primarily driven by the anaphylaxis portfolio (Jext® and EURneffy® ). EURneffy® is expected to increasingly contribute to revenue growth in the second half-year, while investments in market building activities will adversely impact the EBIT margin.
The timing of product shipments as well as inventory variations at wholesalers may lead to quarterly fluctuations in revenue.
The gross margin is projected to further improve, driven by higher revenue, sales mix changes, and production efficiencies. These factors will be somewhat offset by inflationary cost pressure and the in-licensing of EURneffy® , which holds a lower gross margin.
R&D expenses are expected to increase by double digits in support of the peanut tablet programme, the clinical trial with ACARIZAX® in China, and pre-clinical development projects, however, R&D expenses are expected to remain at around 10% of the projected revenue. Sales and marketing as well as administrative expenses are expected to increase by single digits. No one-off costs for optimisation and prioritisation initiatives are planned. In 2024, such costs totalled DKK 75 million.

The outlook is based on current exchange rates, which are expected to negatively impact reported revenue growth by approximately 1 percentage point and to have only a minor effect on the EBIT result.
This interim report contains forward-looking statements, including forecasts of future revenue, operating profit, and cash flows as well as expected business-related events. Such statements are subject to risks and uncertainties, as various factors, some of which are outside ALK's control, may cause actual
results and performance to differ materially from the forecasts made. Such factors include, but are not limited to, consequences of pandemics, general economic and business-related conditions including: legal issues, uncertainty relating to demand, pricing, reimbursement rules, partners' plans and forecasts, fluctuations in exchange rates, competitive factors, reliance on suppliers and tariffs. Additional factors include the risks associated with the sourcing and manufacturing of ALK's products, as well as the potential for side effects from the use of ALK's products, as allergy immunotherapy may be associated with allergic reactions of differing extent, duration, and severity.
ALK maintains focus on broadening its core business within respiratory allergies and gradually expanding into the wider allergy field, including anaphylaxis, food allergy, and new adjacent disease areas.
| Therapeutic area and project name |
Target indication | Phase |
|---|---|---|
| Respiratory allergy | ||
| HDM SLIT-tablet | House dust mite allergic rhinitis – paediatric label extension | (p)(1)(2)(3)(R) |
| Tree SLIT-tablet | Tree pollen allergic rhinitis - paediatric label extension | (1)(2)(3)(R |
| Grass SLIT-tablet | Grass pollen allergic rhinitis in Japan | (1)(2)(3)(R)(R)(2)(2)(3)(R)(2)(2)(2)(2)(2)(2)(2)(2)(2)(2)(2)(2)(2)(2)(2)(2)(2)(2)(2)(2)(2)(2)(2)(2)(2)(2)(2)(2)(2)(2)(2)(2)(2)(2)(2)(2)(2)(2)(2)(2)(2)(2)(2)(2)(2)(2)(2)(2)(2) |
| HDM SLIT-tablet | House dust mite allergic rhinitis in China | (P)(1)(2)(3)(R) |
| Food allergy | ||
| Peanut SLIT-tablet | Peanut allergy | (P)(1)(2 (3)(R) |
| Tree nut SLIT-tablet | Tree nut allergy | P (1)(2)(3)(R) |
| ALK 014 (biologic) | Food allergy | P (1)(2)(3)(R)(R) |
| Anaphylaxis | ||
| Adrenaline autoinjector | Emergency treatment of anaphylaxis | (p)(1)(2)(3)(B) |
| Adrenaline nasal spray1) | Emergency treatment of anaphylaxis in Canada and other markets | (p)(1)(2)(3)(R |
| New therapeutic areas | ||
| Adrenaline nasal spray1) | Acute flares in chronic spontaneous urticaria (CSU) | (P)(1)(2 (3)(R) |
| ALK 014 (biologic) | Not disclosed | (1)(2)(3) |
| Silent period | 16 October 2025 |
|---|---|
| Nine-month interim report (Q3) | 13 November 2025 |

The Board of Directors and Board of Management today considered and approved the interim report of ALK-Abelló A/S for the period 1 January to 30 June 2025. The interim report has not been audited or reviewed by the company's independent auditor.
The consolidated interim report has been prepared in accordance with IAS 34 'Interim financial reporting' and additional Danish disclosure requirements for the presentation of quarterly interim reports by listed companies.
In our opinion, the interim report gives a true and fair view of the ALK Group's assets, equity and liabilities, financial position, results of operations and cash flow for the period 1 January to 30 June 2025. We further consider that the Management review in the preceding pages gives a true and fair statement of the development in the ALK Group's activities and business, the profit for the period and the ALK Group's financial position as a whole, and a description of the most significant risks and uncertainties to which the ALK Group is subject. Besides what has been disclosed in the interim report, no changes in the ALK Group's most significant risks and uncertainties have occurred relative to what was disclosed in the consolidated annual report 2024.
Hørsholm, 21 August 2025
| Peter Halling | |||
|---|---|---|---|
| President & CEO |
Henriette Mersebach Executive Vice President Research & Development Søren Daniel Niegel Executive Vice President Commercial Operations
Claus Steensen Sølje CFO & Executive Vice President
Board of Directors
Anders Hedegaard Chair
Lene Skole Vice Chair
Gitte Aabo
Katja Barnkob Nanna Rassov Carlson Lars Holmqvist
Jesper Høiland Bertil Lindmark Alan Main
Lise Lund Mærkedahl Johan Smedsrud

| Q2 | Q2 | H1 | H1 | |
|---|---|---|---|---|
| 2025 | 2024 | Amounts in DKKm | 2025 | 2024 |
| 1,527 | 1,374 | Revenue | 3,049 | 2,725 |
| 532 | 507 | Cost of sales | 1,038 | 969 |
| 995 | 867 | Gross profit | 2,011 | 1,756 |
| 146 | 125 | Research and development expenses | 275 | 255 |
| 385 | 387 | Sales and marketing expenses | 724 | 741 |
| 89 | 93 | Administrative expenses | 168 | 183 |
| - | 2 | Other operating items, net | - | 3 |
| 375 | 264 | Operating profit (EBIT) | 844 | 580 |
| (25) | 5 | Net financial items | (21) | (2) |
| 350 | 269 | Profit before tax (EBT) | 823 | 578 |
| 87 | 68 | Tax on profit | 206 | 145 |
| 263 | 201 | Net profit | 617 | 433 |
| Earnings per share (EPS) | ||||
| 1.2 | 0.9 | Earnings per share (EPS) | 2.8 | 2.0 |
| 1.2 | 0.9 | Earnings per share (DEPS), diluted | 2.8 | 2.0 |
| Q2 | Q2 | H1 | H1 | |
|---|---|---|---|---|
| 2025 | 2024 | Amounts in DKKm | 2025 | 2024 |
| 263 | 201 | Net profit | 617 | 433 |
| Other comprehensive income | ||||
| Items that will subsequently be reclassified to the income statement, when specific conditions are met: |
||||
| (114) | 15 | Foreign currency translation adjustment of foreign affiliates | (165) | 42 |
| 149 | 216 | Total comprehensive income | 452 | 475 |

| H1 | H1 | |
|---|---|---|
| Amounts in DKKm | 2025 | 2024 |
| Net profit | 617 | 433 |
| Adjustments for non-cash items (note 3) | 377 | 339 |
| Changes in w orking capital |
(200) | (177) |
| Financial income, received | 62 | 8 |
| Financial expenses, paid | (32) | (10) |
| Income taxes, paid (net) | (115) | (51) |
| Cash flow from operating activities | 709 | 542 |
| Acquisitions of companies and operations | - | (115) |
| Investments in intangible assets | (57) | (23) |
| Investments in tangible assets | (106) | (133) |
| Investments in other financial assets | - | 1 |
| Cash flow from investing activities | (163) | (270) |
| Free cash flow | 546 | 272 |
| Exercised share options, paid | (7) | (37) |
| Repayment of lease liabilities | (32) | (22) |
| Proceeds from borrow ings |
671 | - |
| Repayment of borrow ings |
(1,240) | (270) |
| Cash flow from financing activities | (608) | (329) |
| Net cash flow | (62) | (57) |
| Cash beginning of year | 589 | 474 |
| Unrealised gains/(losses) on cash held in foreign currency and financial | ||
| assets carried as cash | (18) | 3 |
| Net cash flow | (62) | (57) |
| Cash end of period | 509 | 420 |
| Cash end of period | 509 | 420 |
The consolidated statement of cash flow is compiled using the indirect method. As a result, the individual figures in the cash flow statement cannot be reconciled directly to the income statement and the balance sheet.

| 30 Jun | 30 Jun | 31 Dec | |
|---|---|---|---|
| Amounts in DKKm | 2025 | 2024 | 2024 |
| Non-current assets | |||
| Intangible assets | |||
| Goodwill | 455 | 461 | 463 |
| Other intangible assets | 1,342 | 331 | 1,329 |
| 1,797 | 792 | 1,792 | |
| Tangible assets | |||
| Land and buildings | 1,074 | 1,000 | 1,137 |
| Plant and machinery | 676 | 495 | 603 |
| Other fixtures and equipment | 76 | 75 | 79 |
| Property, plant and equipment in progress | 423 | 703 | 528 |
| 2,249 | 2,273 | 2,347 | |
| Other non-current assets | |||
| Prepayments | 30 | 32 | 26 |
| Deferred tax assets | 626 | 661 | 642 |
| Income tax receivables | 120 | 209 | 145 |
| 776 | 902 | 813 | |
| Total non-current assets | 4,822 | 3,967 | 4,952 |
| Current assets | |||
| Inventories | 1,718 | 1,593 | 1,716 |
| Trade receivables | 987 | 846 | 812 |
| Income tax receivables | 12 | 29 | 10 |
| Other receivables | 103 | 34 | 49 |
| Prepayments | 121 | 156 | 118 |
| Cash | 509 | 420 | 589 |
| Total current assets | 3,450 | 3,078 | 3,294 |
| Total assets | 8,272 | 7,045 | 8,246 |

| 30 Jun | 30 Jun | 31 Dec | |
|---|---|---|---|
| Amounts in DKKm | 2025 | 2024 | 2024 |
| Equity | |||
| Share capital | 111 | 111 | 111 |
| Currency translation adjustment | (100) | 24 | 65 |
| Retained earnings | 5,836 | 4,784 | 5,197 |
| Total equity | 5,847 | 4,919 | 5,373 |
| Liabilities | |||
| Non-current liabilities | |||
| Mortgage debt | 159 | 175 | 166 |
| Pensions and similar liabilities | 255 | 249 | 251 |
| Lease liabilities | 256 | 267 | 285 |
| Provisions | 1 | 1 | 1 |
| Deferred tax liabilities | - | 3 | 3 |
| Deferred income | 42 | 46 | 45 |
| Income tax payables | 173 | 231 | 173 |
| 886 | 972 | 924 | |
| Current liabilities | |||
| Mortgage debt | 17 | 19 | 19 |
| Bank loans | 112 | - | 671 |
| Trade payables | 131 | 189 | 165 |
| Lease liabilities | 48 | 46 | 46 |
| Deferred income | 7 | 4 | 4 |
| Provisions | 17 | 29 | 38 |
| Income tax payables | 174 | 116 | 124 |
| Other payables | 1,033 | 751 | 882 |
| 1,539 | 1,154 | 1,949 | |
| Total liabilities | 2,425 | 2,126 | 2,873 |
| Total equity and liabilities | 8,272 | 7,045 | 8,246 |

| Currency | ||||
|---|---|---|---|---|
| Share | translation | Retained | Total | |
| Amounts in DKKm | capital | adjustment | earnings | equity |
| Equity at 1 January 2025 | 111 | 65 | 5,197 | 5,373 |
| Net profit | - | - | 617 | 617 |
| Other comprehensive income | - | (165) | - | (165) |
| Total comprehensive income | - | (165) | 617 | 452 |
| Share-based payments | - | - | 25 | 25 |
| Share options settled | - | - | (7) | (7) |
| Tax related to items recognised directly in equity | - | - | 4 | 4 |
| Other transactions | - | - | 22 | 22 |
| Equity at 30 June 2025 | 111 | (100) | 5,836 | 5,847 |
| Equity at 1 January 2024 | 111 | (18) | 4,354 | 4,447 |
| Net profit | - | - | 433 | 433 |
| Other comprehensive income | - | 42 | - | 42 |
| Total comprehensive income | - | 42 | 433 | 475 |
| Share-based payments | - | - | 30 | 30 |
| Share options settled | - | - | (37) | (37) |
| Tax related to items recognised directly in equity | - | - | 4 | 4 |
| Other transactions | - | - | (3) | (3) |
| Equity at 30 June 2024 | 111 | 24 | 4,784 | 4,919 |

This non-audited interim report for the first six months of 2025 has been prepared in accordance with IAS 34 and the additional Danish regulations for the presentation of quarterly interim reports by listed companies. The Interim report for the first six months of 2025 follows the same accounting policies as the annual report for 2024, except for new, amended or revised accounting standards and interpretations (IFRSs) endorsed by the EU effective for the accounting period beginning on 1 January 2025. These IFRSs have not had any impact on the Group's interim report.
| Europe | North America |
International Markets |
Total | |||||
|---|---|---|---|---|---|---|---|---|
| Amounts in DKKm | H1 2025 | H1 2024 | H1 2025 | H1 2024 | H1 2025 | H1 2024 | H1 2025 | H1 2024 |
| SLIT-tablets | 1,189 | 1,018 | 142 | 115 | 357 | 289 | 1,688 | 1,422 |
| SCIT/SLIT-drops | 759 | 744 | 177 | 175 | 45 | 71 | 981 | 990 |
| Other products and services | 167 | 130 | 196 | 162 | 17 | 21 | 380 | 313 |
| Total revenue | 2,115 | 1,892 | 515 | 452 | 419 | 381 | 3,049 | 2,725 |
| Sale of goods | 2,991 | 2,676 | ||||||
| Royalties Services |
51 7 |
48 1 |
||||||
| Total revenue | 3,049 | 2,725 |
| International North |
|||||||||
|---|---|---|---|---|---|---|---|---|---|
| Europe | America | Markets | Total | ||||||
| Organic | Organic | Organic | Organic | ||||||
| growth local | Growth | growth local | Growth | growth local | Growth | growth local | Growth | ||
| Growth, H1 2025 | currencies | (reported) | currencies | (reported) | currencies | (reported) | currencies | (reported) | |
| SLIT-tablets | 17% | 17% | 27% | 23% | 23% | 24% | 19% | 19% | |
| SCIT/SLIT-drops | 2% | 2% | 3% | 1% | -37% | -37% | -1% | -1% | |
| Other products and services | 27% | 28% | 22% | 21% | -16% | -19% | 21% | 21% | |
| Total revenue | 12% | 12% | 16% | 14% | 10% | 10% | 12% | 12% |
Geographical markets (based on customer location):
o Europe comprises the EU, the UK, Norway and Switzerland
o North America comprises the USA and Canada
o International Markets comprise Japan, China and all other countries

| Europe | North America |
International Markets |
Total | |||||
|---|---|---|---|---|---|---|---|---|
| Amounts in DKKm | Q2 2025 | Q2 2024 | Q2 2025 | Q2 2024 | Q2 2025 | Q2 2024 | Q2 2025 | Q2 2024 |
| SLIT-tablets | 570 | 487 | 76 | 61 | 185 | 168 | 831 | 716 |
| SCIT/SLIT-drops | 350 | 345 | 89 | 92 | 42 | 53 | 481 | 490 |
| Other products and services | 104 | 68 | 104 | 88 | 7 | 12 | 215 | 168 |
| Total revenue | 1,024 | 900 | 269 | 241 | 234 | 233 | 1,527 | 1,374 |
| Sale of goods Royalties |
1,497 24 |
1,350 23 |
||||||
| Services | 6 | 1 | ||||||
| Total revenue | 1,527 | 1,374 |
| North | International | |||||||
|---|---|---|---|---|---|---|---|---|
| Growth, Q2 2025 | Europe Organic growth local currencies |
Growth (reported) |
America Organic growth local currencies |
Growth (reported) |
Markets Organic growth local currencies |
Growth (reported) |
Total Organic growth local currencies |
Growth (reported) |
| SLIT-tablets | 17% | 17% | 32% | 25% | 9% | 10% | 16% | 16% |
| SCIT/SLIT-drops | 1% | 1% | 2% | -3% | -20% | -21% | -1% | -2% |
| Other products and services | 51% | 53% | 23% | 18% | -33% | -42% | 30% | 28% |
| Total revenue | 13% | 14% | 17% | 12% | 1% | 0% | 12% | 11% |
Geographical markets (based on customer location):
o Europe comprises the EU, the UK, Norway and Switzerland
o North America comprises the USA and Canada
o International markets comprise Japan, China and all other countries
| H1 | H1 | |
|---|---|---|
| Amounts in DKKm | 2025 | 2024 |
| Tax on profit | 206 | 145 |
| Financial income and expenses | 21 | 2 |
| Share-based payments | 25 | 30 |
| Depreciation, amortisation and impairment | 146 | 133 |
| Other adjustments | (21) | 29 |
| Total | 377 | 339 |
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