Focused innovation driving sustainable growth Jefferies Global Healthcare Conference in London 18 November 2025

Mirza, Alzheimer's caregiver



Creating value in growing neuroscience market



Our Focused Innovator strategy

Growth

Secure mid-term growth

Innovation

Lead with focused innovation

Funding

Deliver sustainable Innovation

Disciplined capital allocation



Neuroscience market growth

8% CAGR expected 2022-20281

Neuroscience in top 3 for new drug approvals U.S. and EU2

Well-positioned to secure future success

Multiple new drug modalities

expanding treatment opportunities



Rapidly evolving science and technologies fuel innovation

(1) Evaluate Pharma, CAGR forecast 2022-2028 (only captures CNS); (2) Nature Reviews Drug Discovery, 2023.

Delivering on our Focused Innovator Strategy

Strong performance, advancing innovation, and disciplined capital re-allocation support long-term value

Growth

Innovation

Funding

Strong first nine months of the year


Total revenue +14%

Strategic brands +20%

Scale neuro-specialty position

Vyepti Asia filings advancing for submission Q4 2025 Lu AG09222 (anti-PACAP): Ph IIb HLR expected Q1 2026

Strategic partnering exemplifies disciplined capital re-allocation - raised ambition on track

New commercial model enables reinvestment in long-term

growth opportunities

Strategic brands

Vyepti +57%

Rexulti +26%

Build neuro-rare franchise

Enrollment progressing according to plan for bexicaserin and amlenetug Lu AG22515 (CD40L blocker): Encouraging early data from TED program

Upgraded FY 2025 financial guidance

Revenue: +13% - 14% growth Adjusted EBITDA: +22% - 25% growth

Previous - Revenue: +11% - 13% growth Previous - Adjusted EBITDA: +16% - 21% growth

All growth rates are at constant exchange rates (CER). HLR: Headline Results; PACAP: Pituitary Adenylate Cyclase-Activating Polypeptide; CD40L: CD40 Ligand; TED: Thyroid Eye Disease.

Leveraging Vyepti and Rexulti growth opportunities

Successful AADAD indication drives

increased sales momentum across U.S. market

  • Strengthened overall product profile

  • AADAD to remain the main U.S. growth engine with continued support from MDD

Rexulti monthly claims volume by indication2

40,000

36,000

32,000

28,000

24,000

20,000

16,000

12,000

8,000

4,000

+664% growth since FDA approval

Total TRx (left-hand scale)

AADAD TRx (right-hand scale)

0

Apr-23

Aug-23

Dec-23

Apr-24

Aug-24

Dec-24

Apr-25

Aug-25

180,000

160,000

140,000

120,000

100,000

80,000

60,000

40,000

20,000

0



Re-allocated investments deliver accelerated growth

Vyepti delivers exceptional strong and sustained growth in the U.S.

  • Continued strong performance in key European markets and Canada

  • SUNRISE study supports significant potential in Asia following approval

Vyepti vials volume uptake since launch1

4-week average

Number of vials

2020

2021

2022

2023

2024

2025



AADAD TRx

Total TRx

(1) Wholesale data as of 30 October 2025. (2) IQVIA Source of Business indication-level data in the U.S. through July 2025. AADAD market share within the antipsychotic market. Use of Rexulti for AADAD prior to FDA approval was not promoted by Lundbeck or Otsuka.

Growth Innovation Funding

Progressing as planned to sharpen our commercial focus



80% of the market potential covered by key markets in neuro-specialty and neuro-rare1

Growth Innovation Funding

Total revenue

Share of total revenue 2024

Progressing as planned Increased focus in key markets

17%

83%

On track to complete transition by

1 December 2025

USA

Canada Brazil

France Germany Italy

Spain/Portugal UK/Ireland Australia

China/HK Japan

South Korea

12 Key markets

Rest of world

Business continuity maintained

Continued patient access

Reduced complexity and freed-up capital to re-allocate across our value chain

Maximize growth of Vyepti, Brintellix, Rexuti and Abilify Asimtufii

Strengthening our readiness for upcoming LOEs

Secure the right capabilities for a more neuro-specialty and neuro-rare based model

(1) Evaluate Pharma Report 2025.

Pipeline as the foundation for future growth

Supported by science and innovation

Growth

Innovation

Funding

value drivers1

DKK 3.3bn

+57%

DKK 4.7bn

+26%

DKK 6.3bn

+4%



Current commercial

Future opportunities for expansion

Bexicaserin

USD ~1.5-2bn

Estimated peak sales2

Amlenetug

USD ~1.5-3bn

Potential market size3

Anti-PACAP

USD ~11bn

Potential market size4

(total migraine market)



D1-D2agonist

USD ~6.7bn

Potential market size5

CD40L blocker

USD ~2.2-4bn

Potential market size6

Anti-ACTH

USD >2bn

Potential market size7



(1) 9M 2025 sales; all growth rates at constant exchange rates (CER). (2) Global peak sales potential across Developmental and Epileptic Encephalopathies (DEEs) by loss of exclusivity (LOE) in 2040, assuming a broad label, estimated by Lundbeck. (3) U.S., EU5, and Japan market estimates (Trinity and internal analyses) for 2031. (4) Migraine market estimates for U.S., EU5, and Japan in 2031 (DRG). (5) Market size globally in 2032 based on Evaluate Pharma. (6) Market size for moderate-severe TED in 2034 (Clarivate 2025). (7) Market size in 2031 based on Evaluate Pharma and internal sources. PACAP: Pituitary Adenylate Cyclase-Activating Peptide; TED: Thyroid Eye Disease; ACTH: Adrenocorticotropic Hormone. Bexicaserin, Amlenetug, Anti-PACAP, D1-D2 agonist, CD40L blocker, and Anti-ACTH are investigational compounds not yet approved or assessed by the U.S. FDA.

Advancing a robust and de-risked pipeline toward 2026

Poised to deliver 5 to 6 mid- to late-stage assets with clinically validated biology

Growth

Innovation

Funding

Phase I Phase II Phase III

Pipeline transformation



Robust and clinically de-risked



Asset with clinically de-risked biology

Lu AG092225

HLR expected Q1 2026

Amlenetug

Anti α-synuclein mAb (MSA)

Bexicaserin6

5HT2Cagonist (DEE's)

pipeline allows for multiple shots on goal

Acquisitions & partnerships an integral part of our symbiotic

Lu AF289962

Anti-PACAP mAb (Migraine prevention)

Decision to start Phase II in 2026

internal and external innovation engine

D1-D2agonist (Parkinsons disease)

Lu AG225153

Decision to start Phase II in 2026

CD40L Blocker (TED first indication)

Lu AG139091

Anti-ACTH mAb (CD & CAH)

MAGLi program4

Neurology



(1) ACTH: Adrenocorticotropic hormone. Two phase Ib trials are currently ongoing in Congenital Adrenal Hyperplasia and Cushing's Disease. For technical reasons, the latter has been officially categorized as a Phase II trial to adhere to local requirements in Georgia; (2) Dopamine receptor D1 and D2; (3) Ph1b trial ongoing in TED (Thyroid Eye Disease); (4) MAGLi: Monoacylglycerol lipase ("MAGlipase") inhibitor; (5) PACAP: Pituitary adenylate cyclase activating peptide; (6) Acts as a partial agonist at 5-HT1A and dopamine D2 receptors at similar potency, and an antagonist at 5-HT2A and noradrenaline alpha1B/2C receptors.

Value-creating strategic capital reallocation

We want to deliver long-term sustainable growth in line with leading industry peers

Growth Innovation Funding

Significant capital reallocation program supporting active pipeline build

Impact raised to approx. DKK 1.3-1.5bn by 2027

Commercial operating model

Procure4Growth

US Trintellix modified agreement

Production model optimization

Vyepti & Rexulti growth

Organic sources of capital

Organic uses of capital

Pipeline investments

Longboard acquisition

Focused investments

in key markets



Strategic capital re-allocation

40+ cross-functional workstreams are contributing to strategic capital allocation

Culture

Digital



Current mid-term targets and assumptions1

Mid-single-digit revenue CAGR through 20272

More than 30% adjusted EBITDA margin2

R&D investment increasing to

20-25% of revenue

Improved S&D cost ratio to 30-35% of revenues

(1) Expected. (2) Current mid-term targets.

Guidance for FY 2025

Continued momentum of Vyepti and Rexulti gives room to upgrade the guidance for FY 2025

New guidance

Previous guidance

Driven by

Growth Innovation Funding

Revenue

7% - 10%

11% - 13%

Strategic brand growth

Delayed Gx

FY 2024

Q2 2025

13% - 14%

Q3 2025



Adj. EBITDA

16% - 21%

Gross profit

5% - 11%

Capital re-allocation

R&D investments

FY 2024

Q2 2025

22% - 25%

Q3 2025

Gross profit

Capital re-allocation



In a much stronger position than a year ago

Well-positioned for sustained profitability, innovation-led growth, and long-term value creation

Growth Innovation Funding



Growth

Innovation

Funding

  • Re-allocated investments delivers accelerated growth for Vyepti and Rexulti

  • Strategic partner model sharpens our commercial focus

  • Momentum in both neuro-specialty and neuro-rare

  • Steadily progressing towards 5-6 mid/late-stage pipeline assets in 2026

  • Disciplined capital reallocation and an optimized commercial model freeing resources for innovation and growth

  • Our upgraded FY 2025 guidance reflects a strong financial performance and operating efficiency





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H. Lundbeck A/S published this content on November 18, 2025, and is solely responsible for the information contained herein. Distributed via Public Technologies (PUBT), unedited and unaltered, on November 18, 2025 at 13:29 UTC.