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Lonza Group AG

Company Profile Analysis

Ticker: LONN.SW

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Lonza Group AG - Healthcare showcase

Year Founded & Workforce

1897

20,141 Employees

Industry

Healthcare

Services

Global Oilfield Biocides MarketGene Editing
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Lonza Group AG Overview

Lonza is the world's largest and longest-established pure-play contract development and manufacturing organization (CDMO). It sells development, manufacturing and technology services to pharmaceutical and biotechnology companies across the main modalities:

  • mammalian and microbial biologics;

  • small-molecule APIs and drug products;

  • antibody-drug conjugates (ADCs) and bioconjugates;

  • cell and gene therapies;

  • mRNA.

Following the March 2026 agreement to sell Capsules & Health Ingredients (CHI) to Lone Star Funds, Lonza is completing a two-year transformation into a focused CDMO. It now operates three business platforms: Integrated Biologics, Advanced Synthesis and Specialized Modalities. Its differentiation rests on four things:

  • scale, including Visp, Vacaville (the largest US biologics CDMO site) and Portsmouth;

  • an integrated drug-substance-to-drug-product offering;

  • a proprietary toolbox: GS Xceed® expression, Ibex®, Synaffix® ADC linkers and the Nona TfR1 BBB technology;

  • a quality track record across 125+ years of chemical and biological manufacturing.

FY2025 continuing sales were CHF 6.5bn at a 31.6% CORE EBITDA margin. Management guides FY2026 to 11–12% CER growth and a 33–34% margin.


Company's own description. In its 2026 releases Lonza calls itself the world's leading CDMO "dedicated to serving the healthcare industry." It describes a team of around 20,000 people working with pharma and biotech customers to turn breakthrough innovations into viable therapies, using science, smart technology and lean manufacturing (H1 2026 release boilerplate). The FY2025 FYR and AR2025 present the business as three complementary, integrated CDMO Business Platforms "powered by the Lonza Engine®." The Lonza Engine is the company's term for its combined strengths in science, smart technology and lean manufacturing for complex and emerging modalities (6 Mar 2026 release).

What Lonza does. Lonza takes a customer's molecule, from DNA sequence or chemical route, and develops and manufactures it. Work runs from pre-clinical development through clinical supply to commercial launch and lifecycle manufacturing. Revenue comes from four sources:

Development services: Cell-line development, process and analytical development, formulation and regulatory CMC. Typically billed fee-for-service or per milestone.

Clinical and commercial manufacturing: Drug substance and drug product. Usually batch-based or capacity-reservation contracts, often with take-or-pay or minimum-volume features. Large commercial deals are frequently multi-year and sometimes involve customer co-funding of dedicated capacity, as in the Ibex model and the 2026 Stein ADC line backed by a long-term customer commitment.

Technology licensing: GS Xceed® expression system licences, Synaffix ADC technology licences with upfront/milestone/royalty structures, bYlok® and the Nona TfR1 BBB platform.

Products (Bioscience): Cell-culture media, primary cells, transfection systems (Nucleofector™), endotoxin and microbial testing. Sold as consumables and instruments.

Revenue-model mix. Lonza does not publish an exact split between product, service, subscription and licensing revenue. The analyst estimate is that more than 90% of continuing revenue is service-based CDMO revenue (development plus manufacturing). The rest is Bioscience products, reported within Specialized Modalities, and technology licensing. There is no subscription revenue. Licensing is strategically important as a customer-acquisition funnel but financially small; its amount is not separately disclosed.

Value-chain position. Lonza sits between drug innovators (big pharma, mid-cap and small biotech) and patients. It is an outsourced manufacturer that carries large fixed-asset intensity:

  • PP&E of CHF 8.3bn at FY2025 (S&P/StockAnalysis);

  • CapEx of CHF 1.3bn in FY2025, 19.6% of sales (FY2025 FYR).

Its upstream suppliers are equipment, single-use consumable, raw-material and media vendors. Downstream, its customers own the regulatory licences and commercialize the drugs.

Customer types:

  1. Large pharmaceutical companies outsourcing commercial capacity. Examples are the strategic multi-site US biopharma collaboration expanded on 1 Jul 2026 and the Vacaville commercial contracts.

  2. Mid-size and emerging biotech needing integrated DNA-to-IND and clinical supply. Example: the ImmuneOncia late-stage mAb deal, March 2026.

  3. Academic and research customers (Bioscience).

  4. Cell and gene therapy developers (autologous and allogeneic).

End-markets. The main end-markets are:

  • biologic therapeutics (mAbs, bispecifics, fusion proteins);

  • ADCs and bioconjugates in oncology;

  • small-molecule APIs including highly potent APIs (HPAPI);

  • cell and gene therapy;

  • microbial-derived proteins, peptides and enzymes;

  • mRNA/LNP;

  • research tools.

Analyst characterization. Lonza is a capital-heavy, scale-advantaged infrastructure provider to biopharma. Its economics depend on asset utilization:

  • New plants dilute margins during ramp-up. This was visible in FY2023, when the CORE EBITDA margin fell to 29.8%, and in early Vacaville.

  • Mature, full assets earn returns well above group average. Advanced Synthesis reached a 48.1% CORE EBITDA margin in H1 2026.

The CHI exit removes a lower-growth consumer-health and capsule business that lacked CDMO synergy. It turns Lonza into a purer "picks-and-shovels" exposure to biologic and complex-modality pipelines. The key debates are:

  • the pace of capacity absorption at Vacaville and Visp large-scale;

  • competitive intensity from Asian CDMOs and big-pharma insourcing;

  • capital intensity versus free-cash-flow conversion.

Strategy

Stated strategy: "One Lonza." The latest annual report and releases set out four themes:

  1. Become the world-leading pure-play CDMO by exiting non-CDMO and less attractive CDMO offerings. Delivered: CHI, Cocoon, MODA and Monteggio, described as four divestments in under two years.

  2. Operate through three complementary, integrated Business Platforms powered by the Lonza Engine® (science, smart technology, lean manufacturing).

  3. Strengthen customer centricity through a group-wide Strategic Enterprise Account Management team. Lonza reports a significant uplift in an already industry-leading net promoter score (FY2025 FYR).

  4. Drive operational and quality excellence through cross-platform Group Operations and Quality functions, manufacturing productivity, and disciplined CapEx execution.

A newly formed corporate strategy, innovation and M&A team focuses on value creation as a pure-play CDMO, through organic growth and bolt-on acquisitions across current and future Technology Platforms (FY2025 FYR).

CDMO Organic Growth Model (medium-term framework):

  • low-teens organic CER sales growth on average over time;

  • CORE EBITDA growing faster than sales;

  • CapEx intensity in the mid-to-high-teens percent of sales (FY2025 FYR footnote; H1 2026 release).

Capital allocation framework. CHI upfront proceeds (CHF 1.7bn+) go to a discretionary cash pool to fund prioritized organic growth and bolt-on M&A. CHF 500m will be returned through an expedited share buyback after closing (6 Mar 2026 investor presentation; H1 2026 release). Dividend policy is progressive: +25% to CHF 5.00 for FY2025, with 50% paid from capital-contribution reserves free of Swiss withholding tax.

Guidance (latest):

Lonza's earlier mid-term ambitions (from 2023–2024 investor communications) referenced CORE EBITDA margins in the low-to-mid 30s.

Products & Services

Pricing is not publicly disclosed for any CDMO service. Commercial terms are negotiated per contract (batch pricing, capacity reservation, milestone or royalty for technology licences). Sources: lonza.com offering navigation (accessed Oct 2026); Lonza news releases 2023–2026.

Integrated Biologics

OfferingDescription / capabilitiesTarget customerNotes / flagship
GS Xceed® Gene Expression SystemCHO glutamine-synthetase expression system with high-titre cell lines; licensed widely, including within approved drugsBiotech and pharma developing mAbs and recombinant proteinsFlagship licensing franchise; licence plus royalty model (terms not disclosed)
GS piggyBac® Transposon TechnologyTransposon-based integration for faster, higher-expressing cell linesBiologics developersAdd-on to GS platform
GS Effex® Cell LineAfucosylated-antibody CHO host for enhanced ADCCOncology/immunology mAb developersSpecialty host
GS Discovery® Transient ExpressionTransient expression for early materialDiscovery-stage biotechEarly de-risking
bYlok® Bispecific Pairing TechnologyEngineering technology to drive correct heavy/light-chain pairing in bispecificsBispecific developersDifferentiator for complex formats
XS Technologies® PlatformIntegrated cell-line, process and media platform for expressionBiologics developersPlatform bundle
Early De-risking & OptimizationDevelopability, manufacturability, formulatability and immunogenicity/immunotoxicity (in silico and in vitro) assessments; early protein expressionPre-IND biotechFunnel into DNA-to-IND
Integrated DNA-to-IND ProgramsEnd-to-end packages for mAbs, bispecifics, Fab fragments, Fc-fusion proteins, scaffolds and other recombinant proteinsEmerging biotechEnhanced offering announced 8 Jul 2026 (acceleration, de-risking)
Development ServicesBiologics process development, analytical development, formulation and primary-packaging developmentAll biologics customersBasel, Slough, Portsmouth, Singapore
Mammalian Drug Substance ManufacturingClinical to commercial scale, from small/mid-scale to 20,000L-class stainless steel (Vacaville, Visp large-scale, Portsmouth, Singapore, Porriño)Big pharma and late-stage biotechVacaville (acquired 2024) is "one of the world's largest biologics facilities" at ~956,000 sq ft (Pharma Manufacturing, Mar 2026); five significant commercial contracts signed. Visp large-scale started commercial operations in H1 2026.
OptiALTO® Intensified Fed-Batch PlatformProcess-intensification platform to raise volumetric productivityCommercial programsN-1 perfusion and intensification is part of the expanded US biopharma collaboration (Jul 2026)
Drug Product Manufacture / ServicesAseptic fill-finish of vials and syringes; clinical DP in Basel/Stein; large-scale commercial DP facility under construction in Stein (operations now expected 2028, scope expanded to high-value small-molecule DP)Integrated DS–DP customers~USD 514m Stein investment originally announced (Pharmaceutical Commerce)
Tailored License Application Program; Cell Line DevelopmentLicensing and contract cell-line developmentBiologics developers—
Biologics Regulatory AffairsCMC regulatory supportAll customers—
TfR1 Blood-Brain-Barrier Technology (from Nona Biosciences)TfR1-binding single-domain VHH shuttle, usable as an IgG fusion or via GlycoConnect® conjugationCNS therapy developersRights acquired 2 Jul 2026; preclinical data show improved brain delivery versus an industry benchmark in a transgenic model

Advanced Synthesis

OfferingDescription / capabilitiesTarget customerNotes / flagship
Drug Substance / API ServicesEarly-phase through commercial API development and manufacturingSmall-molecule developersVisp, Nansha (CN) and others
Design2Optimize®Model-based process development using DoE and simulation to cut development timeEarly/late-phase small moleculesProprietary method
AI-Enabled Route Scouting ServiceComputational retrosynthesis and route selectionDiscovery/early developmentDigital differentiation
High-Throughput Experimentation; PBPK Modeling; Solid Form Services; Pharmaceutical Method DevelopmentSupporting development scienceSmall-molecule developers—
Highly Potent API (HPAPI) TechnologiesHandling, development and manufacturing at low and high potencyOncology small molecules, ADC payloadsVisp payload-linker expansion announced 30 Jun 2026, operational 2028 (BioAlps)
Bioavailability EnhancementAmorphous solid dispersion, spray-dried dispersion, hot-melt extrusionPoorly soluble moleculesBend, Oregon is the historic centre of excellence
Oral Drug ProductClinical trial material, formulation, preformulation, process optimization, inhalation (dry-powder) development, integrated offeringsSmall-molecule developers—
Regulatory Affairs CMC ServicesCMC development and submissionsAll—
Bioconjugation ServicesEarly development, ADC drug-substance manufacturing, analytical services, targeting agent and carrier protein, process development, clinical and commercial ADC manufacturing, payload developmentADC developersVisp bioconjugate suites (expansion with two suites announced Nov 2024)
Ibex® Design ADC DNA-to-IND ProgramIntegrated ADC development packageEmerging ADC biotechBuilt on Ibex® Visp campus
ADC Technologies Platform (Synaffix)GlycoConnect® site-specific conjugation, HydraSpace® polar spacer, toxSYN® payload-linker platform; licensing model with upfront, milestone and royaltyADC innovatorsAcquired 2023; new licensing deals continue (2026)
Commercial-scale aseptic ADC Drug Product (Stein)Dedicated commercial ADC fill-finish under construction, plus an additional multipurpose ADC filling line announced 22 Jul 2026 (operational 2030), backed by a long-term big-pharma collaborationCommercial ADC customersEnd-to-end ADC chain: mAb (Visp) → payload-linker (Visp) → conjugation (Visp) → DP (Stein)

Specialized Modalities

OfferingDescription / capabilitiesTarget customerNotes / flagship
Cell & Gene: process development and cGMP manufacturingAutologous and allogeneic cell therapies, viral vectors (AAV/LV), exosomesCGT developersPortsmouth NH, Houston TX, Geleen NL. A sixth commercial therapy was approved on the C&G platform in H1 2026.
Cocoon® Platform (Personalized Medicines)Automated closed-system autologous manufacturingPoint-of-care CGTAgreed for divestment to Octane Medical Group (disclosed 6 Mar 2026)
MicrobialStrain development, process development, drug-substance manufacturing, analytics (proteins, peptides, enzymes, plasmid DNA)Biotech and pharmaVisp, Kouřim (CZ). Strong H1 2026 growth after a customer-related plant adaptation.
mRNA/LNPProcess development, analytics, mRNA manufacturing, lipid-nanoparticle encapsulationVaccine and therapeutic mRNA developersLegacy of the Moderna collaboration; partnership with Ethris on intranasal spray-dried mRNA vaccines (2026)
Bioscience ProductsPrimary cells and media, Nucleofector™ transfection (Amaxa), cell-culture media, endotoxin/pyrogen and rapid microbial testing, QC softwareResearch labs, QC labs, manufacturersRobust CER growth throughout 2025 and H1 2026
MODA® software platformQC/manufacturing data and quality-execution softwarePharma QCAgreed for divestment to the parent of STARLIMS (disclosed 6 Mar 2026)

Discontinued: Capsules & Health Ingredients (pending sale to Lone Star)

OfferingDescriptionStatus
Capsugel® hard capsulesGelatin and plant-based (HPMC/pullulan) hard empty capsules for pharma and nutraceuticalDivestment to Lone Star; Lonza retains 40%
Health IngredientsBranded nutritional ingredientsSame
Dosage-form solutionsEncapsulation and formulation servicesSame
FY2025 / H1 2026 metricsFY2025 CER growth +3.9%; CORE EBITDA margin 25.9% (24.7% as discontinued-operation basis). H1 2026 sales CHF 541m (+6.3% CER), margin 26.8%.FY2025 FYR; H1 2026 release

Financial Narrative

Basis. FY2021–FY2023 are group figures including CHI (excluding LSI). FY2024–FY2025 are continuing operations excluding CHI for P&L lines. Balance-sheet lines are group-level (FY2025 CHI assets are in held-for-sale). The data comes from S&P/StockAnalysis standardized statements, Lonza FYR and AR financial highlights, and the FY2025 APM report.

Income statement

Notes on the income statement:

  • FY2024 –18.4% AER is the CHI perimeter break. The FY2024 CER +1.3% is the continuing-basis growth (FY2025 FYR).

  • FY2022 and FY2023 IFRS EBITDA are derived from reported EBITDA margins of 34.4% and 28.9% (Lonza AR2023 financial highlights).

  • FY2021 net income includes the LSI disposal gain.

  • FY2025 net income is a group loss. Continuing operations earned CHF 909m (+51% YoY). Discontinued operations lost CHF 1,184m, mainly a CHF 1,229m goodwill impairment on CHI (AR2025 consolidated statements).

  • Company-defined EBIT (continuing) was CHF 908m in FY2024 and CHF 1,239m in FY2025 (FY2025 FYR). S&P's standardized operating income differs because of classification of certain items.

  • CORE EPS (continuing) was CHF 15.08 basic / 15.03 diluted in FY2025, versus CHF 13.12 / 13.10 in FY2024 (Lonza FY2025 FYR). H1 2026 EPS was CHF 8.14 versus CHF 5.65 in H1 2025 (Simply Wall St summary of H1 2026 report).

Margins (%)

Revenue CAGR. FY2021–FY2025 reported revenue CAGR is ~4.8% (derived; distorted by the CHI exit). On a like-for-like CDMO basis, CER growth averaged in the mid-teens over 2021–2025. Detail: 20% (2021), 15.1% (2022), 10.9% (2023, group), 1.3% (2024, continuing), 21.7% (2025, continuing; low-teens organic ex-Vacaville).

Commentary. Profitability peaked in 2022 at a 32.1% CORE EBITDA margin. That year combined COVID mRNA volumes with high utilization. 2023 was the trough (29.8%, guided down twice): mRNA volumes rolled off, Moderna terminated, biotech funding was tight, capsule demand was weak, and large new assets started depreciating and ramping.

Since 2024 the continuing CDMO business has re-expanded margins steadily: 30.2% (FY2024), 31.6% (FY2025), 34.8% (H1 2026), and guidance of 33–34% for FY2026. The drivers are maturing growth projects, Advanced Synthesis mix and operating leverage, partly offset by Vacaville dilution.

The gap between IFRS and CORE EBITDA narrowed in FY2025: CHF 1,970m versus CHF 2,064m, a 1.4-ppt gap versus 3.7 ppts in FY2024. This reflects lower restructuring and divestiture charges, although one-off environmental and impairment costs persisted.

Balance sheet

Notes on the balance sheet. Short-term debt is the S&P short-term debt plus current portion of LTD, excluding leases. Lonza's own net-debt definition (AR2025 financial highlights) shows net cash in 2021–2022.

FY2025 goodwill and intangibles fell because CHI assets were reclassified to held-for-sale and goodwill was impaired. "Other current assets" of CHF 2,795m at FY2025 are mostly CHI assets held for sale. This also inflates FY2025 working capital.

H1 2026 balance sheet (30 Jun 2026, S&P): cash CHF 487m; total debt CHF 4,167m; equity CHF 8,152m; total assets CHF 18,258m.

Cash flow

Dividends paid are an analyst estimate: prior-year DPS multiplied by approximate shares outstanding. They are not company-reported cash-flow lines.

Lonza-defined cash metrics (FY2025 FYR):

  • Operational free cash flow before acquisitions and divestitures, group: CHF 674m in FY2025 (+42.5%) versus CHF 473m in FY2024.

  • CDMO free cash flow: CHF 545m in FY2025 versus CHF 313m, "nearly doubled."

  • CapEx intensity: 30% of sales in 2022; 25% in 2023; 19.6% in 2025; 15.7% in H1 2026.

  • H1 2026 FCF: CHF 0.4bn (+CHF 0.3bn YoY).

  • S&P TTM to Jun 2026: OCF CHF 1,435m, CapEx CHF 1,228m, FCF CHF 207m.

Ratios

Notes on the ratios:

  • ROE and ROA are derived from net income and year-end balances.

  • The FY2024 and FY2025 net debt/CORE EBITDA ratios conflict between sources. The FY2025 FYR reports 1.4x (FY2025) and 1.5x (FY2024). The AR2025 historical table shows 1.6x and 1.7x. The difference is the perimeter of CORE EBITDA (continuing versus total group including CHI).

  • The FY2024 cash conversion cycle and asset turnover are distorted: the P&L is restated to exclude CHI while the balance sheet still includes CHI.

Trend commentary. The defining financial feature of the period is a deliberate leveraging-up to fund capacity. Lonza went from CHF 958m net cash (2021, post-LSI) to CHF 3.26bn net debt (2025). The drivers were roughly CHF 7.5bn of cumulative CapEx over 2021–2025, the USD 1.2bn Vacaville acquisition, and about CHF 2.5bn of buybacks over 2021–2025 (net repurchases per S&P).

Returns compressed as the asset base grew faster than earnings: PP&E rose 77% from 2021 to 2025. They are now inflecting:

  • CapEx intensity is normalizing toward the mid-to-high-teens range of the CDMO Organic Growth Model.

  • The FY2026 CORE EBITDA margin is guided at 33–34%.

  • The CHI proceeds (CHF 1.7bn upfront) should take leverage "well below" the target range (6 Mar 2026 release).

The FY2025 statutory loss is purely a non-cash CHI write-down and does not reflect continuing-business economics.

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Financial Detail

Business Platform Details

Business PlatformContentsHead

Integrated Biologics (IB)

Mammalian drug substance (clinical and commercial, all scales: Visp, Portsmouth, Vacaville, Slough, Singapore, Porriño and others), biologics drug product (Basel, Stein), expression technologies (GS Xceed®, GS piggyBac®, GS Effex®, bYlok®, XS Technologies®), early de-risking, DNA-to-IND programs

Gordon Bates

Advanced Synthesis (AS)

Small molecules (API/drug substance, HPAPI, bioavailability enhancement, oral drug product; Visp, Bend OR, Nansha/Guangzhou and others), bioconjugates/ADCs (Visp incl. Ibex, conjugation suites), Synaffix ADC technology platform, payload-linkers

Christian Seufert

Specialized Modalities (SM)

Cell & Gene (Portsmouth, Houston/Pearland, Geleen), Microbial (Visp, Kouřim), mRNA/LNP, Bioscience products (research media, cells, Nucleofector™, testing)

Daniel Palmacci

Corporate

Group functions, central hedging program (FY2025 hedging impact on sales CHF 71m, CORE EBITDA CHF 35m), residual activities

—

Discontinued: CHI

Capsugel hard capsules, health ingredients, dosage-form solutions; held for sale pending close with Lone Star

Jean-Christophe Hyvert

Revenue by Segment

Segment (sales, CHF Mn)FY2024FY2025

Integrated Biologics

2,8833,649

Advanced Synthesis

1,3231,611

Specialized Modalities

1,0991,034

Corporate

175237

Total continuing sales

5,4806,531

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Revenue by Segment — Integrated Biologics

Segment (CORE EBITDA, CHF Mn)FY2024FY2025

Integrated Biologics

1,0451,287

Advanced Synthesis

484674

Specialized Modalities

192176

Corporate

-68-73

Total CORE EBITDA

1,6532,064

Segment CORE EBITDA margin (%)

Segment CORE EBITDA margin (%)FY2024FY2025

Integrated Biologics

36.235.3

Advanced Synthesis

36.641.8

Specialized Modalities

17.517.0

Group

30.231.6

Segment growth and mix (%)

Segment growth and mix (%)FY2024FY2025

IB CER growth

032.2

AS CER growth

022.4

SM CER growth

0-3.0

IB share of total sales

52.655.9

AS share of total sales

24.124.7

SM share of total sales

20.115.8

Segment Revenue

PlatformH1 2026 CER growthH1 2026 CORE EBITDA marginChange vs H1 2025

Integrated Biologics

+10.0%36.0%

flat

Advanced Synthesis

+27.7%48.1%

+6.8 ppts

Specialized Modalities

+22.6%28.0%

+10.7 ppts

Group (continuing)

+16.0% (+11.2% AER)

34.8%

+4.4 ppts

Group continuing (CHF Mn)

H1 2025

H1 2026

—

Sales

3,0343,374—

CORE EBITDA

9221,175—

EBITDA

8771,152—

EBIT

573789—

Revenue by Segment (FY2021–FY2023)

Division (sales, CHF Mn)FY2021FY2022FY2023

Biologics

2,6993,2743,719

Small Molecules

767819901

Cell & Gene

602693696

Capsules & Health Ingredients (derived)

1,2041,2661,161

Corporate

137171240

Total group sales

5,4096,2236,717

Revenue by Segment by Division

Division (CORE EBITDA, CHF Mn)FY2021FY2022FY2023

Biologics

9791,2281,294

Small Molecules

215248283

Cell & Gene

10611664

Capsules & Health Ingredients

414418327

Corporate (derived)

-49-1531

Total group CORE EBITDA

1,6651,9951,999

Division CORE EBITDA margin (%)

Division CORE EBITDA margin (%)FY2021FY2022FY2023

Biologics

36.337.534.8

Small Molecules

28.030.331.4

Cell & Gene

17.616.79.2

Capsules & Health Ingredients

34.433.028.2

Income Statement and Margin Analysis (%)

MetricFY2021FY2022FY2023FY2024FY2025

Revenue (CHF Mn)

5,4096,2236,7175,4806,531

Revenue growth AER (%)

20.015.17.9-18.419.2

Revenue growth CER (%)

20.015.110.91.321.7

Gross profit (CHF Mn)

2,1102,4382,4032,0062,349

Operating income, S&P standardized (CHF Mn)

8461,3871,3651,1101,397

EBITDA, IFRS reported (CHF Mn)

1,3652,1411,9411,4521,970

CORE EBITDA (CHF Mn)

1,6651,9951,9991,6532,064

Pre-tax income (CHF Mn, derived from S&P pretax margin)

7601,4487907081,101

Net income attributable (CHF Mn)

2,9441,215654636-275

EPS basic, reported (CHF)

39.5216.348.888.92-3.93

Dividend per share for the fiscal year (CHF)

3.003.504.004.005.00

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Margin Analysis (%)

MetricFY2021FY2022FY2023FY2024FY2025

Gross margin (%)

39.039.235.836.636.0

Operating margin, S&P (%)

15.622.320.320.321.4

EBITDA margin, IFRS (%)

25.234.428.926.530.2

CORE EBITDA margin (%)

30.832.129.830.231.6

Net margin (%)

54.419.59.711.6-4.2

Balance Sheet

MetricFY2021FY2022FY2023FY2024FY2025

Total assets (CHF Mn)

16,45917,35616,84819,73317,907

Cash & short-term investments (CHF Mn)

3,1842,2241,6691,711719

Short-term debt incl. current LTD (CHF Mn)

169678192468309

Long-term debt (CHF Mn)

2,2341,5542,6374,3504,015

Total debt incl. leases, S&P (CHF Mn)

2,7492,5873,1605,2284,679

Net debt, Lonza definition (CHF Mn)

-958-1869222,8593,258

Shareholders' equity incl. minorities (CHF Mn)

9,82310,6659,5129,3887,966

Goodwill (CHF Mn)

2,9862,8632,7523,3701,960

Other intangibles (CHF Mn)

2,4542,2311,9882,002328

Working capital (CHF Mn)

3,5852,6372,1391,8613,209

PP&E (CHF Mn)

4,6946,1206,6178,5328,304

Cash Flow

MetricFY2021FY2022FY2023FY2024FY2025

Operating cash flow (CHF Mn)

1,2171,0201,3881,2741,156

Capital expenditure (CHF Mn)

1,3011,8261,6481,3811,321

Free cash flow, S&P = OCF − CapEx (CHF Mn)

-84-806-260-107-165

Share repurchases, net (CHF Mn)

174511,011717507

Dividends paid (CHF Mn, derived est.)

223223257286282

Cash acquisitions (CHF Mn)

4810931,07556

Returns & Leverage Ratios (%) and Financial Ratios (x)

RatioFY2021FY2022FY2023FY2024FY2025

ROE, year-end equity (%)

30.011.46.96.8-3.5

ROA, year-end assets (%)

17.97.03.93.2-1.5

Current ratio (x)

2.511.861.771.521.89

Debt/equity, total debt (x)

0.280.240.330.560.59

Net debt / CORE EBITDA (x, Lonza AR2025 series)

-0.6-0.10.51.71.6

Asset turnover (x)

0.330.360.400.280.36

Days inventory outstanding (days, derived)

166175134181147

Days sales outstanding (days, derived)

6369628659

Days payables outstanding (days, derived)

5346404945

Cash conversion cycle (days, derived)

176198156218161

Financial Analysis

RatioPeriodValueSource

ROIC

TTM Jun 2026

11.2%

S&P/StockAnalysis

ROE

TTM Jun 2026

12.9% (continuing-earnings basis per S&P)

S&P/StockAnalysis

Interest coverage (EBIT / net financial result)

FY2025

8.9x (1,239 / 140, derived)

FY2025 FYR; AR2025

Interest coverage

FY2024

4.6x (908 / 199, derived)

FY2025 FYR; AR2025

Interest coverage (S&P)

TTM Jun 2026

10.2x

S&P/StockAnalysis

Net debt / equity

FY2025

0.4x (Lonza)

FY2025 FYR

Effective tax rate

TTM

17.8%

S&P/StockAnalysis

Revenue by Region

Region, MarketScreener aggregator (CHF Mn, unreconciled)FY2021FY2022FY2023FY2024FY2025

United States

2,1172,4152,1362,3092,525

Switzerland

6569961,168719963

United Kingdom

170139171239212

Rest of Europe

21820719518332

Rest of Asia

313629288

Share Price and Margin Analysis (%)

MetricFY2022FY2023FY2024FY2025

Year-end share price (CHF)

452.9353.7535.8537.8

Calendar-year price change (%)

-40.6-21.951.50.4

Share Price & Returns

PeriodPerformanceSource

Last price

CHF 565.60 (2 Oct 2026)

S&P/StockAnalysis

YTD 2026

≈ +5.2% (vs 537.8 YE2025, derived)

Derived

1-year

+5.8%

S&P/StockAnalysis

3-year

≈ +60% from YE2023 (353.7) to Oct 2026 (derived; not an exact 36-month figure)

Derived

50-day / 200-day MA

CHF 566.4 / CHF 531.1

S&P/StockAnalysis

Beta (5Y)

0.81

S&P/StockAnalysis

Average daily volume

~133k shares (20-day); 138,868 avg in 2025

S&P; AR2025

Valuation Multiples

MultipleLonza

P/E trailing

36.6x (on S&P earnings basis)

P/E forward

27.9x

EV/EBITDA (TTM)

17.8x

EV/Sales (TTM)

6.3x

P/B

4.85x

P/TBV

6.8x

PEG

1.42

FCF yield

0.5% (S&P FCF basis)

Dividend yield

0.88%

Per-Share Data

MetricFY2021FY2022FY2023FY2024FY2025

Dividend per share (CHF)

3.003.504.004.005.00

Credit Ratings

AgencyRatingOutlookSource

S&P Global Ratings

BBB+

Stable

Lonza bond releases 2024; credit info page (last changed Jan 2019)

Moody's

Not rated / not disclosed

——

Fitch

Not rated / not disclosed

——

Capital Instruments

InstrumentIssuerCouponAmountMaturity

Swiss straight bond

Lonza Swiss Finanz AG

0.35%

CHF 150m

22 Sep 2026 (scheduled)

Term loan (syndicated)

Lonza

Floating

USD 200m

2026

Swiss straight bond

Lonza Swiss Finanz AG

2.25%

CHF 185m

16 May 2028

Swiss straight bond

Lonza Swiss Finanz AG

2.10%

CHF 450m

12 Sep 2029

Eurobond (EMTN)

Lonza Finance International NV

3.25%

EUR 600m

4 Sep 2030

Swiss straight bond

Lonza Swiss Finanz AG

2.60%

CHF 215m

16 May 2031

Eurobond (EMTN)

Lonza Finance International NV

3.875%

EUR 500m

25 May 2033

Eurobond (EMTN)

Lonza Finance International NV

3.50%

EUR 600m

4 Sep 2034

Eurobond (EMTN)

Lonza Finance International NV

3.875%

EUR 1,000m

24 Apr 2036

Revolving credit facility

Lonza

Floating

CHF 1,000m (undrawn headroom)

—

“—” = not publicly disclosed.

Analyst Conclusions

Management guidance (FY2026, as of 22 Jul 2026):

  • CER sales growth of 11–12%;

  • CORE EBITDA margin of 33–34% (raised);

  • FX headwind of –2 to –3% on sales;

  • CapEx intensity in the middle of the mid-to-high-teens range;

  • H2 growth and margins lower than H1 because of AS phasing, Vacaville shutdown and a higher prior-year base;

  • CHI (discontinued): mid-single-digit CER growth; closing before YE2026, then a CHF 500m buyback.

Consensus expectations: about 10.8% p.a. revenue growth and about 20% p.a. EPS growth over three years; average target CHF 688 (S&P/StockAnalysis).

Bull case:

  1. Margin structurally re-based upward. CORE EBITDA margin moved from 29.8% (2023) to 34.8% (H1 2026). AS runs at 41–48% and SM recovered to 28% in H1 2026. As Visp large-scale and Vacaville fill under the five-plus commercial contracts and the multi-billion-CHF US collaboration, operating leverage could push group margins toward the mid-30s sustainably. CapEx intensity falling to the mid-to-high teens would turn FCF (CHF 545m CDMO in FY2025) into a compounding story.

  2. Geopolitics favour Lonza. As the largest US biologics CDMO with Swiss-based ADC integration, Lonza is a prime beneficiary of supply regionalization and of US customers de-risking from Chinese CDMOs. WuXi-type peers face structural headwinds.

  3. Pure-play re-rating and optionality. The CHI exit removes a sub-30%-margin, lower-growth business. It brings CHF 1.7bn upfront plus upside to at least CHF 3bn total, funds bolt-ons and a CHF 500m buyback, and simplifies the equity story toward premium CDMO multiples.

Bear case:

  1. Growth decelerates sharply in H2 2026 and 2027. H1 2026 was flattered by phasing and a low base. Vacaville is flat and goes into shutdown, AS margins normalize, and the shares fell about 4% on H1 results despite a margin beat. With low-teens organic growth as the model, a forward P/E of about 28x and EV/EBITDA of about 18x leave little room for a miss.

  2. Capital intensity and returns remain mediocre. S&P-basis FCF was negative every year from 2021 to 2025. TTM ROIC is about 11% against a WACC of about 8%. Statutory ROE has been single-digit or negative since 2023. The Capsugel round-trip shows a history of capital misallocation, and Vacaville's full potential is a next-decade story.

  3. Execution and leadership risk persists. Cell & Gene performance has been volatile. Big pharma's US in-house CapEx wave and Samsung's capacity build could erode utilization and pricing. Board and executive renewal is rapid (average board tenure about 1.3 years; new CCO from 2027) during a period of complex separation and large project delivery (Stein 2028/2030, Visp 2028).

Concluding analyst verdict.

Lonza enters late 2026 as a cleaner, more profitable and more strategically coherent company than at any point in the past decade. The CHI sale, three smaller divestments and the One Lonza reorganization have turned a conglomerate-tinged supplier into a pure-play CDMO.

The evidence of operating improvement is concrete:

  • continuing sales grew 21.7% CER in FY2025;

  • the CORE EBITDA margin moved from 30.2% to 31.6%, then to 34.8% in H1 2026, with full-year guidance raised to 33–34%;

  • the Advanced Synthesis platform now earns returns rivalling the best in contract manufacturing.

Lonza's strategic positioning is unusually strong. It combines the broadest modality coverage in the industry, the largest US biologics footprint at a time when customers want regional supply, and a vertically integrated Swiss ADC chain backed by customer commitments.

The equity case is not without friction. Statutory returns have lagged the narrative, and S&P-basis free cash flow was negative throughout 2021–2025 as about CHF 7.5bn went into CapEx and a large acquisition. Management's own guidance implies a visibly weaker second half. At about 28x forward earnings and about 18x EV/EBITDA, the shares already discount a good part of the margin story. The July 2026 sell-off on a margin beat shows how sensitive the stock is to growth cadence. Leadership and board renewal has been rapid, and Cell & Gene and Vacaville still need to prove their economics.

Overall, Lonza looks like a high-quality compounder in transition from build to harvest. The decisive variable for the next 12–24 months is cash conversion, not growth. If CapEx intensity normalizes to the mid-to-high teens while margins hold in the 33–35% band, operational FCF should step up materially and justify the premium. The CHI proceeds and buyback provide downside support. The verdict is constructive, with valuation-driven patience. The data supports a positive fundamental stance, but entry discipline around H2 2026 phasing and the first pure-play FY2027 guidance is warranted.


All figures are from public sources as cited and are current as of 7 October 2026.

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Executive Leadership

Executive Leadership Team

NameTitleTenure / key background (where verified)

Dr. Wolfgang Wienand

Chief Executive Officer

CEO since 1 Jul 2024; previously CEO of Siegfried Holding (2019–2024). Age ~54 (Simply Wall St).

Philippe Deecke

Chief Financial Officer

Holds ~0.0049% of shares (Simply Wall St).

Maria Soler Nunez

Chief Quality Officer

Previously led Group Operations (AR2025 references her foundation-laying in Operations).

Nicoleta Baumgärtner

Chief Human Resources Officer

—

Andreas Bohrer

Chief Legal & Corporate Affairs Officer

~11.6 years with Lonza.

Jason Berndt

Head of Group Operations (EVP)

Appointed within the last year (Simply Wall St).

Gordon Bates

Head of Integrated Biologics

Previously President and Head of Small Molecules.

Christian Seufert

Head of Advanced Synthesis

—

Daniel Palmacci

Head of Specialized Modalities

Previously President, Cell & Gene.

Jean-Christophe Hyvert

Head of Capsules & Health Ingredients

Expected to depart with CHI at closing; former President, Biologics and Cell & Gene.

Directors' Remuneration

ItemFY2024FY2025

CEO total compensation (CHF Mn)

6.425.72

Executive Committee aggregate (CHF Mn)

21.623.0

Board of Directors aggregate (CHF Mn)

2.763.34

Board of Directors

NameRoleNotes

Jean-Marc Huët

Chair

Re-elected Chair at AGM 8 May 2026.

Claudia Süssmuth-Dyckerhoff

Vice-Chair (independent)

Elected AGM 2026; healthcare and life-sciences board experience.

Christoph Mäder

Lead Independent Director

—

Juan Andres

Independent

—

Sami Atiya

Independent

Elected AGM 2026.

Eric Drapé

Independent

Elected AGM 2025.

Stephen Fry

Independent

Elected AGM 2026.

Marion Helmes

Independent

—

Angelica Kohlmann

Independent

—

David Meline

Independent

—

Major Shareholders

RankHolderStake (%)Source / date
1

BlackRock, Inc.

9.85 (notified) / 9.91–9.96 (aggregator)

AR2025; Simply Wall St 2026

2

UBS Asset Management / UBS Fund Mgmt (CH)

6.25–6.32

AR2025; Simply Wall St

3

The Vanguard Group

3.0–4.35

Simply Wall St (varies by listing view)

4

Norges Bank Investment Management

~3.15 (below 3% notification threshold by YE2025 per AR)

Simply Wall St; AR2025

5

Invesco Ltd.

~1.2–1.4

Simply Wall St

6

JP Morgan Asset Management

~1.2

Simply Wall St

7

Pictet Asset Management

~1.1–1.2

Simply Wall St

8

Baillie Gifford & Co.

~1.2

Simply Wall St (Aug 2026 view)

9

Amundi Asset Management

~1.0

Simply Wall St

10

Comgest S.A. / Union Investment

~0.8–0.9

Simply Wall St

Competitive Landscape

Peer Comparison

PlatformKey competitors

Integrated Biologics (mammalian DS/DP)

Samsung Biologics (KR); WuXi Biologics (CN); Fujifilm Diosynth Biotechnologies (JP/US/EU); Boehringer Ingelheim BioXcellence (DE); Thermo Fisher Patheon Pharma Services (US); AGC Biologics (JP/US/EU); Celltrion (CMO activity); Rentschler (DE); Celonic (CH/DE); National Resilience (US)

Advanced Synthesis (small molecules, ADC/bioconjugates, HPAPI)

WuXi AppTec / WuXi STA (CN); WuXi XDC (CN, ADC); Siegfried (CH); Cambrex (US, Permira-owned); Asymchem (CN); Piramal Pharma Solutions (IN); Recipharm (SE, EQT); Corden Pharma (DE/CH); Axplora (FR); Catalent (now Novo Holdings, US); Abzena (ADC)

Specialized Modalities (C&G, microbial, mRNA, Bioscience)

Charles River (C&G manufacturing); Minaris (ex-Hitachi/Resonac, now private); Oxford Biomedica (UK, vectors); Catalent Gene Therapy (Novo); AGC Biologics; Fujifilm (microbial); Thermo Fisher (viral vectors; Bioscience reagents); Merck KGaA / MilliporeSigma (Bioscience reagents, ADC Bioconjugates); Sartorius (media, tools)

Peer Comparison FY2025

MetricLonza (FY2025, continuing)Samsung Biologics (FY2024)WuXi Biologics (FY2024)Siegfried (FY2024)

Revenue

CHF 6,531m

~KRW 4.5tn (~CHF 2.9bn)

~RMB 18.7bn (~CHF 2.3bn)

~CHF 1.3bn

Revenue growth

+21.7% CER

~+23%

~+9%

low single digit

Profitability

CORE EBITDA margin 31.6% (H1 2026: 34.8%)

Operating margin ~29%

——

R&D intensity

~1.5–2% (aggregator)

———

Listing

SIX / SGX

KRX

HKEX

SIX

Notes

Broadest modality coverage; largest US biologics CDMO

Pure mammalian scale leader in Asia (Plant 5 onward)

US Biosecure Act exposure

Small molecules / DP only

Company Snapshot

$4,332.2M

Revenue

20,141

Employees

1897

Founded

Basel, Switzerland

Headquarters

SWOT Analysis

Strengths

  • Scale and growth. FY2025 continuing sales of CHF 6,531m, +21.7% CER, with low-teens organic growth excluding Vacaville (FY2025 FYR).
  • Expanding profitability. CORE EBITDA margin rose from 30.2% (FY2024) to 31.6% (FY2025) and 34.8% (H1 2026). FY2026 guidance is 33–34% (H1 2026 release).
  • Advanced Synthesis franchise economics. Margin of 41.8% in FY2025 and 48.1% in H1 2026, with +22.4% and +27.7% CER growth (FY2025 FYR; H1 2026 release).
  • US manufacturing leadership. Largest US biologics CDMO; Vacaville has five significant commercial contracts; multi-billion-CHF US biopharma collaboration (1 Jul 2026).
  • End-to-end ADC integration in Switzerland. Visp payload-linker (2028), Ibex conjugation and Stein ADC DP (2030 line, customer-backed).
  • Balance-sheet capacity. Net debt/CORE EBITDA of 1.4x (FY2025 FYR) and S&P BBB+ stable. CHF 1.7bn CHI upfront proceeds are pending.
  • Shareholder returns. DPS raised 25% to CHF 5.00. About CHF 2.5bn of net buybacks in 2021–2025 (S&P). A CHF 500m buyback follows CHI closing.

Weaknesses

  • Capital intensity and weak S&P FCF. S&P-basis FCF was negative every year in 2021–2025 (FY2025: –CHF 165m). CapEx was CHF 1.3bn in FY2025 (19.6% of sales).
  • Specialized Modalities underperformance. Sales –3.0% CER in FY2025; margin 17.0%; Cell & Gene operational issues (FY2025 FYR).
  • Statutory earnings volatility. FY2025 group net loss of CHF 275m from the CHF 1,229m CHI goodwill impairment (AR2025). This followed a value-destructive round-trip on Capsugel (bought for USD 5.5bn in 2017; sold at EV CHF 2.3bn).
  • Leadership and board churn. Four CEOs and interim CEOs since 2019; board average tenure about 1.3 years (Simply Wall St, Aug 2026).
  • Long working-capital cycle. Derived cash conversion cycle of about 160 days (FY2025), with inventory days of about 147.
  • Vacaville earnings drag. FY2026 Vacaville sales expected flat with an H2 shutdown; full potential not before the next decade.
  • Low statutory ROE. 6.8% (FY2024) and –3.5% (FY2025) on year-end equity (derived).

Opportunities

  • ADC market growth. Lonza has three dedicated expansions (Visp payload-linker, Stein ADC DP and the additional line) backed by long-term agreements.
  • Onshoring and Biosecure. US customers are diversifying away from Chinese CDMOs, and Lonza can serve them from its US sites.
  • Redeployment of CHI proceeds into bolt-on M&A (technologies, DP capacity) under the new strategy and M&A team.
  • Integrated DS+DP deals. An increasing number of integrated agreements (FY2025 FYR) lift share of wallet; Stein large-scale DP starts in 2028.
  • CNS biologics via the TfR1 BBB shuttle (Nona, Jul 2026).
  • Margin upside from asset maturation, as the 2026 guidance raise shows.
  • Value of the retained CHI stake. Total CHI proceeds are expected at or above CHF 3bn including the 40% stake and preferential exit participation.

Threats

  • Big-pharma in-sourcing. Large US CapEx commitments by major pharma (acknowledged in FY2025 FYR outlook discussion).
  • Asian capacity build-out. Samsung Biologics' aggressive plant additions could pressure mAb pricing.
  • FX. Weak USD; about –2 to –3% sales headwind guided for 2026.
  • Customer and program risk. A clinical failure or commercial underperformance of an anchor product can strand capacity, as the 2023 Moderna termination did.
  • Regulatory and quality events. An FDA 483 or warning letter at a key site would hit a quality-sensitive franchise. Vacaville passed its first FDA audit under Lonza.
  • Geopolitics and tariffs. Management currently sees no material impact but is monitoring.
  • Environmental legacy liabilities in Valais (mercury and landfill remediation). One-off environmental costs weighed on FY2025 statutory earnings.

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Key Developments

DateEventSignificance
1 Apr 2025One Lonza operating model implementedNew three-platform structure; basis for restatements
9 May 2025AGM 2025: Juan Andres, Eric Drapé and David Meline elected to BoardBoard renewal
23 Jul 2025H1 2025: CHF 3.6bn sales (+19.0% CER); CDMO outlook raised to 20–21% CER and 30–31% margin; SM CORE EBITDA margin dipped to 17.3%Momentum; C&G weakness visible
H2 2025Fifth significant Vacaville commercial contract signedCapacity absorption
H2 2025US final affirmative antidumping and countervailing determinations on imported hard capsulesSupports CHI pricing; aids sale
Oct 2025Claudia Süssmuth-Dyckerhoff nominated as Vice-ChairGovernance
2025EcoVadis Gold medal awardedESG credential
Jan 2026All purchased electricity in US, Europe and China now renewableESG milestone
13 Jan 2026Presentation at 44th J.P. Morgan Healthcare ConferenceInvestor visibility
28 Jan 2026FY2025 results: CHF 6.5bn (+21.7% CER), CORE EBITDA margin 31.6%; FY2026 guidance 11–12% CER, margin above 32%; dividend +25% proposedBeat on upgraded CDMO outlook
6 Mar 2026CHI sale to Lone Star (EV CHF 2.3bn) plus Cocoon, MODA and Monteggio divestments disclosed; ~CHF 1.3bn impairment flaggedTransformational
30 Mar 2026ImmuneOncia late-stage mAb manufacturing agreementIntegrated DS–DP win
1 Apr 2026AR2025 and Sustainability Report published; FY2025 group net loss CHF 275m (CHI impairment); AGM invitation; three new directors proposedStatutory accounts
–Ethris collaboration on intranasal spray-dried mRNA vaccinesmRNA platform
Early May 2026Q1 2026 qualitative update: guidance confirmed; H1-weighted phasing; FX headwind about –3% (as of early May)No surprises
8 May 2026AGM: all motions approved; Huët re-elected Chair; Süssmuth-Dyckerhoff, Atiya and Fry electedGovernance continuity
15 May 2026CHF 5.00 dividend paid (50% from capital-contribution reserves)Shareholder return
H1 2026Visp large-scale mammalian asset begins commercial operationsKey growth project delivered on time
H1 2026Sixth commercial therapy approved on Cell & Gene platformC&G validation
30 Jun 2026Visp HPAPI/payload-linker expansion (operational 2028)ADC integration
1 Jul 2026Expanded multi-site collaboration with leading US biopharma (multi-billion-CHF potential)Major commercial win
2 Jul 2026Acquisition of Nona TfR1 BBB technology rightsNew modality enabler
8 Jul 2026Enhanced integrated DNA-to-IND programsBiotech funnel
22 Jul 2026H1 2026: CHF 3.374bn (+16.0% CER), CORE EBITDA margin 34.8%, FCF CHF 0.4bn; FY margin guidance raised to 33–34%; Stein ADC line; CHF 500m buyback post-CHIStrong margin beat; slight sales miss
22 Jul 2026Share price falls ~4% to CHF 541.20 on the day despite the beat (The Pharma Letter); revenue slightly below consensus (Parqet)Market focused on H2 deceleration
23 Jul 2026Brokers raise targets: RBC to CHF 760 (Outperform), Goldman Sachs to CHF 680 (Buy); ZKB fair value CHF 766 (cash.ch)Sell-side support
1 Sep 2026New Head of Communications joins (succeeding David Carter)Leadership
H2 2026Samanta Cimitan named Chief Commercial Officer, joining by 1 Jan 2027Commercial leadership
22 Sep 2026Scheduled maturity of CHF 150m 0.35% bond (Lonza Swiss Finanz)Debt service; repayment not separately confirmed
H2 2026Planned Vacaville CDMO-readiness shutdownH2 sales headwind
~28 Oct 2026 (expected)Q3 2026 qualitative business updateNext catalyst

Product Offering

  • Lonza Group AG
    • Global Oilfield Biocides Market
    • Gene Editing

Financial Performance

Explore key financial metrics, segmented revenue, balance sheet health, and performance trends.

Revenue

5 charts
Revenue by Segment (FY2024–FY2025): Total continuing sales rose from CHF 5,480 Mn in FY2024 to CHF 6,531 Mn in FY2025.
Lonza Group AG — Revenue by Segment (FY2024–FY2025)
Series (CHF Mn)FY2024FY2025
Total continuing sales5,4806,531
Integrated Biologics2,8833,649
Advanced Synthesis1,3231,611
Specialized Modalities1,0991,034
Corporate175237

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