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Diasorin — Earnings Release 2025
Jul 31, 2025
4129_rns_2025-07-31_4f1f0056-4753-4edd-a54d-dae8ee833c41.pdf
Earnings Release
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| Informazione Regolamentata n. 0957-42-2025 |
Data/Ora Inizio Diffusione 31 Luglio 2025 16:21:58 |
Euronext Milan | ||
|---|---|---|---|---|
| Societa' | : | DIASORIN | ||
| Identificativo Informazione Regolamentata |
: | 208633 | ||
| Utenza - referente | : | DIASORINN02 - Ragazzo Eugenia | ||
| Tipologia | : | 1.2 | ||
| Data/Ora Ricezione | : | 31 Luglio 2025 16:21:58 | ||
| Data/Ora Inizio Diffusione | : | 31 Luglio 2025 16:21:57 | ||
| Oggetto | : | Revenue Growth and Margin Expansion in H1 2025. FY 2025 Guidance Confirmed |
||
| Testo del comunicato |
Vedi allegato

REVENUE GROWTH AND MARGIN EXPANSION IN H1 2025. FY 2025 GUIDANCE CONFIRMED
- REVENUES: € 619 MILLION, +5% COMPARED TO H1'24 (+6% AT CER, +8% AT CER AND EXCLUDING COVID REVENUES), CONFIRMING THE FY'25 GUIDANCE;
- ADJUSTED1 EBITDA2 : € 214 MILLION, +10% AT CER COMPARED TO H1'24, EQUAL TO 35% OF REVENUES, CONFIRMING THE FY'25 GUIDANCE;
- U.S. FDA 510(K) CLEARANCE FOR LIAISON PLEX® GRAM-POSITIVE BLOOD CULTURE ASSAY, COMPLETING THE PANEL PORTFOLIO TO DIAGNOSE BLOODSTREAM INFECTIONS ON THE MULTIPLEXING PLATFORM LIAISON PLEX®;
- SUBMISSION OF THE MOLECULAR POINT-OF-CARE PLATFORM LIAISON NES® AND ITS FIRST RESPIRATORY PANEL TO THE U.S. FDA FOR 510(K) CLEARANCE AND CLIA WAIVER;
- A PROJECT HAS BEEN INITIATED TO DISCONTINUE INDUSTRIAL OPERATIONS AT THE DIETZENBACH PLANT (GERMANY), AS PART OF THE STRATEGY TO OPTIMIZE THE GLOBAL PRODUCTION FOOTPRINT AND ENHANCE LONG-TERM COMPETITIVENESS.
Saluggia, Italy - July 31, 2025 - The Board of Directors of Diasorin S.p.A. (FTSE MIB: DIA), examined and approved the Group's Consolidated Financial Statements at June 30, 2025.
TABLES OF RESULTS1
| H1 | change | |||||
|---|---|---|---|---|---|---|
| Amounts in millions of euros | 2024 | 2025 | amount | % @ current |
% @ CER |
|
| Revenues | 589 | 619 | +30 | +5% | +6% | |
| ex-COVID Immunodiagnostics | 391 | 418 | +27 | +7% | +8% | |
| ex-COVID Molecular Diagnostics | 100 | 103 | +3 | +3% | +4% | |
| Licensed Technologies | 84 | 91 | +7 | +9% | +10% | |
| COVID | 14 | 7 | -7 | -50% | -49% | |
| Revenues net of Covid | 575 | 612 | +37 | +6% | +8% | |
| Adjusted1 EBITDA2 |
198 | 214 | +16 | +8% | +10% | |
| Adjusted 1 EBITDA 2 margin |
34% | 35% | +89 bps | |||
| EBITDA2 | 196 | 204 | +7 | +4% | +6% | |
| EBITDA 2 margin |
33% | 33% | -43 bps | |||
| Adjusted1 EBIT |
153 | 167 | +14 | +9% | ||
| Adjusted 1 EBIT margin |
26% | 27% | +105 bps | |||
| EBIT | 132 | 138 | +6 | +5% | ||
| EBIT margin | 22% | 22% | -4 bps | |||
| Adjusted1 net profit |
120 | 125 | +5 | +4% | ||
| Adjusted 1 Net profit on Revenues |
20% | 20% | -15 bps | |||
| Net profit | 96 | 99 | +3 | +3% | ||
| Net profit on Revenues | 16% | 16% | -27 bps |
2 EBITDA is defined as the "Operating Result", gross of amortization and depreciation of intangible and tangible asset. EBITDA is a measure used by the Company to monitor and evaluate the Group's operating performance and is not defined as an accounting measure in IFRS therefore shall be considered an alternative measure for assessing the Group's operating result performance.
1 With reference to the indicators Adjusted Gross Margin, Adjusted EBITDA, Adjusted EBIT, and Adjusted Net Income, please refer to the table at the end of this Press Release.

| Q2 | change | |||||
|---|---|---|---|---|---|---|
| Amounts in millions of euros | 2024 | 2025 | amount | % @ current |
% @ CER |
|
| Revenues | 300 | 306 | +6 | +2% | +5% | |
| ex-COVID Immunodiagnostics | 205 | 215 | +10 | +5% | +8% | |
| ex-COVID Molecular Diagnostics | 49 | 47 | -2 | -5% | +1% | |
| Licensed Technologies | 41 | 42 | +0 | +1% | +7% | |
| COVID | 5 | 3 | -3 | -54% | -50% | |
| Revenues net of Covid | 295 | 304 | +9 | +3% | +7% | |
| Adjusted1 EBITDA2 |
102 | 107 | +6 | +6% | +11% | |
| Adjusted 1 EBITDA 2 margin |
34% | 35% | +127 bps | |||
| EBITDA2 | 101 | 97 | -3 | -3% | +2% | |
| EBITDA 2 margin |
34% | 32% | -173 bps | |||
| Adjusted1 EBIT |
79 | 84 | +5 | +6% | ||
| Adjusted 1 EBIT margin |
26% | 28% | +115 bps | |||
| EBIT | 69 | 65 | -3 | -5% | ||
| EBIT margin | 23% | 21% | -145 bps | |||
| Adjusted1 net profit |
61 | 61 | -0 | -0% | ||
| Adjusted 1 Net profit on Revenues |
20% | 20% | -43 bps | |||
| Net profit | 50 | 46 | -3 | -7% | ||
| Net profit on Revenues | 17% | 15% | -140 bps |
COMMENTS ON ECONOMIC RESULTS
REVENUES: € 619 million, +5% (+6% at CER). Excluding the COVID business, H1'25 revenues grew +8% at CER compared to the same period of the previous year, a result in line with the FY'25 guidance.
In Q2'25, revenues grew by +2%, following the unfavorable impact of the significant depreciation of the U.S. Dollar against the Euro and the expected decline in COVID sales. At CER, revenues grew by +5% (+7% excluding the COVID business). This result confirms the strong performance of the immunodiagnostic business line, along with positive contributions from the molecular diagnostics and Licensed Technologies franchises.
The following are the revenue trends of the different business lines:
- Ex-COVID Immunodiagnostics: € 418 million, an increase of € 27 million, equal to +7% (+8% at CER) vs. H1'24, mainly driven by the excellent performance of CLIA specialty tests sales. The strong performance continued also in Q2'25 (+8% at CER), despite tough year-on-year comparable with 2024, which has been characterized by an increase in volumes driven by infectious disease outbreaks. The growth in H1'25 reflects the contribution of the U.S. Hospital Strategy and the increase in sales in Europe, driven by the broad offering of specialty tests, which more than offset the expected contraction of the Chinese market due to Volume-Based Procurement regulations.
- Ex-COVID Molecular Diagnostics: € 103 million, +3% (+4% at CER) vs. H1'24. In Q2'24, business grew by 1% at CER, supported by the "Legacy Diasorin" tests, and by the positive contribution of the multiplexing business. The comparison with the same period of the previous year is affected by the discontinuation of the ARIES platform and by the absence of infectious disease outbreaks that had increased the 2024 sales volumes. Net of these factors, Q2'25 revenues grew by +6% at CER.
- Licensed Technologies: € 91 million, +9% (+10% at CER) vs. H1'24, and +7% at CER in Q2'25. The favorable scheduling of certain major orders positively contributed to the performance of this business line.
- COVID: € 7 million, equal to -50% (-49% at CER) vs. H1'24, in line with expectations, down compared to the same period of last year.
The following is the revenue performance by geographic area, net of the contribution of COVID products:
- North America Direct: € 308 million, +10% (+12% at CER). The sales increase in H1'25 is mainly driven by the excellent performance of the immunodiagnostic business (+14% or +16% at CER), as a result of the success of the U.S. Hospital Strategy, as well as of the broad offering of CLIA specialties; the molecular diagnostic business registered also a positive performance (+5% or +7% at CER).
- Europe Direct: € 217 million, +5% (+4% at CER).

The growth in H1'25 was driven by the positive performance of the Immunodiagnostic business, with a focus on the specialty tests that characterize Diasorin's offerings, despite an unfavorable comparison with the same period in 2024, which benefited by an increase in sales volumes linked to some infectious disease outbreaks in the main European countries.
Rest of the World: € 88 million, -1% (+2% at CER).
The positive performance of the markets in which Diasorin operates both directly and through local distributors has been able to offset the revenue contraction of the Chinese market, mainly due to the Volume-Based Procurement regulations. Net of the contribution of the Chinese market, the geographical area defined as "Rest of the World" registered a growth of +5%.
ADJUSTED1GROSS PROFIT: € 406 million (equal to 66% of revenues), an increase of € 16 million compared to H1'24, confirming the previous year's results.
ADJUSTED1 EBITDA2 : € 214 million (equal to 35% of revenues both at current and constant exchange rates), an increase of € 16 million (+8% or + 10% at CER) compared to H1'24, with a higher incidence on revenues of about 100 bps at current and constant exchange rates. In Q2'25, growth equals to +6% vs. Q2'24 (+11% at CER), with EBITDA margin at 35% (almost 36% at CER). The increase in profitability was driven by a favorable product mix and contained growth in operating expenses, confirming the FY'25 guidance.
ADJUSTED1 EBIT: € 167 million (equal to 27% of revenues), an increase of € 14 million (+9%) vs. H1'24. Q2'25 registered a growth equal to +6% over the same period of 2024.
NET FINANCIAL EXPENSES € 7 million (€ 8 million in 2024); down from H1'24 mainly as a result of the fair value measurement of interest rate hedging financial instruments taken out for the acquisition of Luminex.
INCOME TAXES: € 33 million, with a tax rate of 25%.
ADJUSTED1 NET PROFIT: € 125 million (equal to 20% of revenues), an increase of € 5 million (+4%) vs. H1'24.
COMMENT ON FINANCIAL RESULTS
CONSOLIDATED NET FINANCIAL DEBT: -€ 683 million (-€ 618 million at December 31, 2024).
The net financial position at the end of H1'25 shows a decrease of € 65 million, as a combined effect of the exercise of the withdrawal right by certain shareholders following the approval of the increased voting rights mechanism for € 97 million, the payment of dividends for € 63 million, and the operating cash flow generation during the period.
FREE CASH FLOW3 : € 83 million at June 30, 2025 (€ 91 million at June 30, 2024).
The year-on-year change is attributable to higher taxes paid in H1'25, primarily in the United States, compared to the same period of the previous year, which had benefited from prior-year tax credits.
BUSINESS HIGHLIGHTS
IMMUNODIAGNOSTICS:
510(k) clearance of the LIAISON® MUREX HIV Ab-Ag HT and LIAISON® MUREX Control HIV Ab-Ag HT.
MOLECULAR DIAGNOSTICS:
- ∙ Submission of the molecular diagnostic Point-of-Care platform LIAISON NES® and its respiratory 4-plex panel (Flu A, Flu B, COVID, RSV) to the U.S. FDA for 510(k) clearance and CLIA Waiver;
- ∙ Launch of the full panel portfolio to diagnose bloodstream infections on LIAISON PLEX®, the new multiplexing platform of the Group, following the U.S. FDA 510(k) clearance for the LIAISON PLEX® Gram-Positive Blood Culture Assay, LIAISON PLEX® Gram-Negative Blood Culture Assay, and LIAISON PLEX® Blood Culture Yeast Assay;
- ∙ Launch of a new Measles Virus Primer Pair in the U.S., expanding the growing portfolio of Analyte-Specific Reagents (ASRs);
- ∙ Launch of Simplexa™ C. auris direct assay on the LIAISON® MDX platform for all countries accepting the CE Mark.
3 Free Cash Flow equals net cash flow generated from operating activities including uses for investment and before payment of interest and acquisitions of companies and businesses.

OTHER BUSINESS HIGHLIGHTS
During H1 2025, Diasorin launched a project aimed at discontinuing industrial operations at its Dietzenbach (Germany) plant, as part of the ongoing strategic efforts to optimize the global footprint of its production sites and improve long-term competitiveness. The implementation of this initiative, which is expected to be completed by the end of 2026, will be carried out in compliance with the co-determination and employee participation rights provided for under German law. Once completed, the project is expected to generate operational synergies and annual cost savings estimated at approximately € 7 million. To implement the project, total non-recurring costs not exceeding € 15 million are expected to be incurred, which will be recognized in the consolidated financial statements for 2025 and 2026.
Regarding the introduction of new tariff measures that could potentially impact the Group's business areas, as of today, taking into account the upcoming tariffs imposition and the mitigation measures already implemented, the estimated impact on the Group's profitability for the current year is not expected to be material. Nonetheless, the Company will continue to closely monitor the implementing provisions of the announced tariff measures, any potential changes in the tariff framework, the related impacts on both the import and export of its products, and the procurement of raw materials used in its production processes.
FY 2025 GUIDANCE AT 2024 CER
The Company confirms FY 2025 guidance:
- EX-COVID REVENUES: approx. +8%, approx. +7% including COVID revenues (equal to approx. € 20 million)
- ADJUSTED1 EBITDA2 MARGIN: approx. 34%
***
Mr. Piergiorgio Pedron, the Officer in charge of preparing the corporate accounting documents of DiaSorin S.p.A. declares that, pursuant to paragraph 2, Art. 154 bis of the Consolidated Law on Finance, to the best of his knowledge, the accounting information contained in this Press Release corresponds to the documental results, accounting books and records.
***
This press release is available to the public at the registered office of the Company and is also published on the Company's website (www.diasorin.com) under the section "Investors - Financial Corner - Press Releases" and on the centralized storage system named eMarket STORAGE at .
***
H1'25 results will be presented to the financial community during a conference call on Thursday, July 31, 2025, at 5:00 PM CET. To participate in the conference call, dial the following numbers:
- From Italy + 39 02 8020911
- From U.K. +44 1212 818004
- From U.S.A. +1 718 7058796
Presentation slides will be made available under the section "Investors - Financial Corner - Presentations" on the Company's website (www.diasorin.com) and on the centralized storage system named eMarket STORAGE at prior to the beginning of the conference call.
***
Annex: Financial statements not subject to audit by the Group's Independent Auditors.

ANNEXES
33% 33% -43 bps
CONSOLIDATED INCOME STATEMENT
| H1 | Change | ||||
|---|---|---|---|---|---|
| Amounts in millions of euros | 2024 | 2025 | amount | % | |
| Net Revenues | 589 | 619 | +30 | +5% | |
| Cost of sales | (199) | (213) | -14 | +7% | |
| Gross profit | 390 | 406 | +16 | +4% | |
| 66% | 66% | -63 bps | |||
| Sales and marketing expenses | (141) | (142) | - 1 | +1% | |
| Research and development costs | (43) | (47) | - 4 | +9% | |
| General and administrative expenses | (64) | (61) | +3 | -4% | |
| Total operating expenses | (249) | (251) | -2 | +1% | |
| 42% | 41% | -165 bps | |||
| Other operating income (expense) | (10) | (17) | - 7 | +73% | |
| non recurring amount | (2) | (10) | - 8 | n.m | |
| EBIT | 132 | 138 | +6 | +5% | |
| 22% | 22% | -4 bps | |||
| Net financial income (expense) | (8) | (7) | +1 | -12% | |
| Profit before taxes | 124 | 131 | +7 | +6% | |
| Income taxes | (29) | (33) | - 4 | +15% | |
| Net result | 96 | 99 | +3 | +3% | |
| EBITDA2 | 196 | 204 | +7 | +4% |
| Q2 | Change | ||||
|---|---|---|---|---|---|
| Amounts in millions of euros | 2024 | 2025 | amount | % | |
| Net Revenues | 300 | 306 | +6 | +2% | |
| Cost of sales | (102) | (105) | - 3 | +3% | |
| Gross profit | 198 | 201 | +3 | +1% | |
| 66% | 66% | -28 bps | |||
| Sales and marketing expenses | (71) | (69) | +1 | -2% | |
| Research and development costs | (21) | (23) | - 1 | +7% | |
| General and administrative expenses | (33) | (31) | +2 | -5% | |
| Total operating expenses | (125) | (123) | +2 | -1% | |
| 42% | 40% | -127 bps | |||
| Other operating income (expense) | (5) | (13) | -8 | n.m | |
| non recurring amount | (1) | (9) | -9 | n.m | |
| EBIT | 69 | 65 | -3 | -5% | |
| 23% | 21% | -145 bps | |||
| Net financial income (expense) | (4) | (3) | +1 | -32% | |
| Profit before taxes | 64 | 63 | -2 | -3% | |
| Income taxes | (15) | (16) | - 2 | +10% | |
| Net result | 50 | 46 | -3 | -7% | |
| EBITDA2 | 101 | 97 | -3 | -3% | |
| 34% | 32% | -172 bps |

REVENUES BY TECHNOLOGY
| H1 | |||
|---|---|---|---|
| % of revenues contributed | 2024 | 2025 | Change |
| Immunodiagnostics ex-COVID | 67% | 67% | +95 bps |
| Molecular Diagnostics ex-COVID | 17% | 17% | -37 bps |
| Licensed Technologies | 14% | 15% | +49 bps |
| COVID | 2% | 1% | -126 bps |
| Q2 | |||
|---|---|---|---|
| % of revenues contributed | 2024 | 2025 | Change |
| Immunodiagnostics ex-COVID | 68% | 70% | +215 bps |
| Molecular Diagnostics ex-COVID | 16% | 15% | -106 bps |
| Licensed Technologies | 14% | 14% | -9 bps |
| COVID | 2% | 1% | -99 bps |
REVENUES BY GEOGRAPHY
| H 1 | Change | ||||
|---|---|---|---|---|---|
| Amounts in millions of euros | 2024 2025 |
amount | % | ||
| @ current | @ CER | ||||
| North America Direct | 279 | 308 | +29 | +10% | +12% |
| % on total revenues | 48% | 50% | |||
| Europe Direct | 207 | 217 | +10 | +5% | +4% |
| % on total revenues | 35% | 35% | |||
| Rest of the World | 89 | 88 | -1 | -1% | +2% |
| % on total revenues | 16% | 14% | |||
| COVID | 14 | 7 | -7 | -50% | -49% |
| % on total revenues | 2% | 1% | |||
| Total | 589 | 619 | +30 | +5% | +6% |
| Q2 | Change | ||||
|---|---|---|---|---|---|
| Amounts in millions of euros | 2024 2025 |
amount | % | ||
| @ current | @ CER | ||||
| North America Direct | 144 | 148 | +4 | +3% | +9% |
| % on total revenues | 48% | 48% | |||
| Europe Direct | 105 | 110 | +5 | +5% | +5% |
| % on total revenues | 35% | 36% | |||
| Rest of the World | 46 | 45 | -1 | -1% | +4% |
| % on total revenues | 15% | 15% | |||
| COVID | 5 | 3 | -3 | -54% | -50% |
| % on total revenues | 2% | 1% | |||
| Total | 300 | 306 | +6 | +2% | +5% |

CONSOLIDATED BALANCE SHEET
| Amounts in millions of euros | 12/31/2024 | 06/30/2025 | Change |
|---|---|---|---|
| Goodwill and intangibles assets | 2,028 | 1,817 | -212 |
| Property, plant and equipment | 271 | 256 | -15 |
| Other non-current assets | 34 | 36 | +1 |
| Net working capital | 346 | 356 | +10 |
| Other non-current liabilities | (264) | (249) | +15 |
| Net Invested Capital | 2,417 | 2,216 | -201 |
| Net Financial Debt | (618) | (683) | -66 |
| Total shareholders' equity | 1,799 | 1,532 | -267 |
CONSOLIDATED STATEMENT OF CASH FLOWS
| H1 | ||||
|---|---|---|---|---|
| Amounts in millions of euros | 2024 | 2025 | ||
| Cash and cash equivalents at the beginning of the period | 280 | 344 | ||
| Cash provided by operating activities | 155 | 145 | ||
| Cash provided/(used) in investing activities | (11) | (28) | ||
| Cash provided/(used) in financing activities | (255) | (288) | ||
| Net change in cash and cash equivalents before investments in financial assets | (111) | (171) | ||
| Net change in cash and cash equivalents | (111) | (171) | ||
| Cash and cash equivalents at the end of the period | 170 | 173 |
| Q2 | |||
|---|---|---|---|
| Amounts in millions of euros | 2024 | 2025 | |
| Cash and cash equivalents at the beginning of the period | 308 | 365 | |
| Cash provided by operating activities | 80 | 74 | |
| Cash provided/(used) in investing activities | (50) | (35) | |
| Cash provided/(used) in financing activities | (168) | (231) | |
| Net change in cash and cash equivalents before investments in financial assets | (138) | (192) | |
| Net change in cash and cash equivalents | (138) | (192) | |
| Cash and cash equivalents at the end of the period | 170 | 173 |

OVERVIEW OF THE GROUP'S OPERATING PERFORMANCE AND FINANCIAL POSITION
This press release presents and comments on certain financial indicators that are not identified in the IFRS. These indicators, which are described below, are used to comment on the Group's business performance, in compliance with the requirements of Consob communication of 28 July 2006 (DEM 6064293), as subsequently amended and supplemented (Consob communication 0092543 of 3 December 2015, which incorporates the ESMA Guidelines ESMA/2015/1415).
The alternative performance indicators listed below should be used to supplement the information required by IFRS to help readers of the press release gain a more comprehensive understanding of the Group's economic, financial and operating position, by excluding the result of one-off elements for the Luminex integration from the amortization deriving from the Purchase Price Allocation, and the financial expenses related to the financing of the transaction, including their tax impact. It should be noted that the calculation of these adjusted indicators could differ from those used by other companies.
H1 2025 ADJUSTED INDICATORS
| Amounts in millions of euros | Gross Profit | EBITDA | EBIT | Net Result |
|---|---|---|---|---|
| Financial Statements Measures | 406 | 204 | 138 | 99 |
| % on Revenues | 66% | 33% | 22% | 16% |
| Adjustments | ||||
| "One-off" costs related to non recurring events | - | 10 | 10 | 10 |
| Depreciation of Luminex intangibles identified in the Purchase Price Allocation |
- | - | 19 | 19 |
| Financial charges relating t o debt instruments and t o the convertible bond issued to finance the acquisition of Luminex net of hedging effects |
- | - | - | 6 |
| Total adjustments before tax effect | - | 10 | 29 | 36 |
| Fiscal effect on adjustments | - | - | - | (9) |
| Total Adjustments | - | 10 | 29 | 26 |
| Adjusted Measures | 406 | 214 | 167 | 125 |
H1 2024 ADJUSTED INDICATORS
| Amounts in millions of euros | Gross Profit | EBITDA | EBIT | Net Result |
|---|---|---|---|---|
| Financial Statements Measures | 390 | 196 | 132 | 96 |
| % on Revenues | 66% | 33% | 22% | 16% |
| Adjustments | ||||
| "One-off" costs related to the integration and restructuring of Luminex | - | 2 | 2 | 2 |
| Depreciation of Luminex intangibles identified in the Purchase Price Allocation |
- | - | 19 | 19 |
| Financial charges relating t o debt instruments and t o the convertible bond issued to finance the acquisition of Luminex net of hedging effects |
- | - | - | 10 |
| Total adjustments before tax effect | - | 2 | 21 | 31 |
| Fiscal effect on adjustments | - | - | - | (7) |
| Total Adjustments | - | 2 | 21 | 24 |
| Adjusted Measures | 390 | 198 | 153 | 120 |

OPERATING PERFORMANCE IN H1 2025 AND COMPARISON WITH H1 2024
| Amounts in millions of euros | 06/30/2024 | % on Revenues | 06/30/2025 | % on Revenues |
|---|---|---|---|---|
| Net Revenues | 589 | 100% | 619 | 100% |
| Cost of Sales | (199) | 34% | (213) | 34% |
| Gross Profit | 390 | 66% | 406 | 66% |
| Adjusted1 Gross Profit | 390 | 66% | 406 | 66% |
| Sales and marketing expenses | (141) | 24% | (142) | 23% |
| Research and development expenses | (43) | 7% | (47) | 8% |
| General and administrative expenses | (64) | 11% | (61) | 10% |
| Total operating expenses | (249) | 42% | (251) | 41% |
| Other operating income (expense) | (10) | 2% | (17) | 3% |
| EBIT | 132 | 22% | 138 | 22% |
| Adjusted1 EBIT |
153 | 26% | 167 | 27% |
| Net financial income (expense) | (8) | 1% | (7) | 1% |
| Profit before taxes | 124 | 21% | 131 | 21% |
| Income taxes | (29) | 5% | (33) | 5% |
| Net Profit | 96 | 16% | 99 | 16% |
| Adjusted1 Net Profit | 120 | 20% | 125 | 20% |
| EBITDA2 | 196 | 33% | 204 | 33% |
| Adjusted1 EBITDA2 |
198 | 34% | 214 | 35% |
For additional information, please contact:
INVESTOR RELATIONS
Riccardo Fava Eugenia Ragazzo Corporate Vice President Communication, ESG & Investor Relations Corporate Investor Relations & ESG Senior Analyst [email protected] [email protected]
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