- Q1 2026 revenue of EUR197 million for YORVIPATH$(R)$ and EUR44 million for SKYTROFA(R)
- More than 1,000 new patient enrollments for YORVIPATH in the U.S. in Q1
- As of May 1, more than 60 YUVIWEL(R) enrollments since early April U.S. commercial launch
- Entered into agreement to sell Rare Pediatric Disease Priority Review Voucher for $187.5 million
- Conference call today at 8:00 am ET
COPENHAGEN, Denmark, May 07, 2026 (GLOBE NEWSWIRE) -- Ascendis Pharma A/S (Nasdaq: ASND) today announced financial results for the first quarter ended March 31, 2026, and provided a business update.
"The FDA approval of YUVIWEL, our third consecutive TransCon product, and the robust patient uptake for YORVIPATH are cementing our position as a leading global biopharma," said Jan Mikkelsen, President and Chief Executive Officer of Ascendis Pharma. "Our strong focus on science and making a meaningful difference for patients will continue to be the fundamental driver for our success."
Select Highlights & Anticipated 2026 Milestones
-- YORVIPATH(palopegteriparatide, developed as TransCon PTH)
-- YORVIPATH revenue for the first quarter of 2026 totaled EUR197
million, which for the U.S. includes normal seasonality and the
temporary impact of additional patients supported by free drug, as
well as a one-time impact in Europe Direct related to expanded
market access.
-- In the U.S., more than 1,000 new patient enrollments in the first
quarter of 2026.
-- As of March 31, 2026, more than 6,300 unique patient enrollments
by more than 2,700 prescribing healthcare providers since launch
in the U.S.
-- Outside the U.S., continued expansion of commercial launches with
full reimbursement. Now available commercially or through named
patient programs in 35 countries.
-- Ongoing label expansion trials through PaTHway60 (adults) and
PaTHway Adolescent.
-- YUVIWEL (navepegritide, developed as TransCon CNP)
-- Received U.S. Food & Drug Administration (FDA) accelerated
approval, indicated to increase linear growth in children 2 years
of age and older with achondroplasia with open epiphyses.
-- The FDA granted orphan drug exclusivity for YUVIWEL, which will
run through February 27, 2033.
-- As of May 1, 2026, more than 60 unique patient enrollments by more
than 35 prescribing healthcare providers since U.S. commercial
availability in April 2026.
-- Marketing Authorisation Application remains under review by the
European Medicines Agency, with a decision anticipated in the
fourth quarter of 2026.
-- Label expansion trial in infants with achondroplasia, reACHin, is
ongoing with enrollment completion anticipated in the third
quarter of 2026.
-- Phase 3 trial planned to investigate TransCon CNP monotherapy for
the treatment of hypochondroplasia in the second half of the year.
-- SKYTROFA(lonapegsomatropin, developed as TransCon hGH)
-- SKYTROFA revenue for the first quarter of 2026 totaled EUR44
million.
-- Announced Week 52 data from the Phase 2 New InsiGHTS Trial in
Turner syndrome that demonstrated comparable efficacy and safety
to daily somatropin.
-- Ongoing Phase 3 HighLiGHts basket trial across a range of
established growth disorders including idiopathic short stature
(ISS), SHOX deficiency, Turner syndrome, and small for gestational
age $(SGA)$.
-- TransCon CNP + TransCon hGH Combination Therapy(navepegritide plus
lonapegsomatropin)
-- Announced Phase 2 COACH Trial Week 52 topline results
demonstrating mean annualized growth velocity that exceeded the
97th percentile of average stature children, improvements in body
proportionality, and a safety profile consistent with TransCon CNP
and TransCon hGH monotherapies.
-- Announced additional Week 52 results from COACH demonstrating
meaningful benefits beyond linear growth, including improvements
in spinal canal dimensions and lower limb alignment, along with
unprecedented improvements in arm span compared to monotherapy.
-- Interim Week 78 data from COACH expected in the second quarter of
2026 with Week 104 data expected around year end.
-- Oncology Program(onvapegleukin alfa)
-- In the ongoing Phase 1/2 IL-BELIEVE Trial, TransCon IL-2
<BETA>/<GAMMA> in combination with paclitaxel demonstrated
improved median overall survival (OS) up to 10 months from 6-7
months for historical controls, with a generally well-tolerated
safety profile in patients with late-stage platinum-resistant
ovarian cancer, validating the science behind TransCon IL-2
<BETA>/<GAMMA>.
-- As further internal oncology development does not align with our
strategic focus, we have decided to discontinue internal
development of TransCon IL-2 <BETA>/<GAMMA> in Oncology and will
explore other ways to maximize the value of this asset.
Key Financial Highlights
-- Total revenue for the first quarter of 2026 was EUR247 million, compared
to EUR101 million during the same period in 2025. The year-over-year
increase in revenue was primarily attributable to an increase in product
revenue from YORVIPATH.
-- Operating profit for the first quarter of 2026 totaled EUR25 million,
reflecting a margin of 10.1%. On a non-IFRS basis, operating profit was
EUR55 million*, reflecting a margin of 22.4%*.
-- Net profit for the first quarter of 2026 totaled EUR629 million, or
EUR9.75 per diluted share, including the recognition of previously
unrecognized deferred tax assets of EUR679 million. On a non-IFRS basis,
net profit was EUR18 million*, or EUR0.27 per diluted share*.
-- As of March 31, 2026, Ascendis Pharma had cash and cash equivalents
totaling EUR573 million, which includes the impact of repurchases under
the previously announced share repurchase program of EUR52 million and
the net settlement of certain Restricted Stock Units for EUR8 million,
compared to cash and cash equivalents totaling EUR616 million as of
December 31, 2025.
-- Subsequent to March 31, 2026:
-- On April 20, 2026, the Company's ordinary shares commenced trading
on The Nasdaq Global Select Market, replacing the prior listing of
American Depositary Shares (ADSs).
-- On May 6, 2026, Ascendis redeemed all $575 million aggregate
principal amount of its outstanding 2.25% convertible notes due
2028. Within the redemption period, all holders of the convertible
notes surrendered their notes for conversion, whereupon the
Company delivered 3,635,813 ordinary shares, together with cash in
lieu of any fractional shares. The conversion resulted in the
settlement of the current liabilities of convertible notes,
comprising borrowings and derivative liabilities totaling EUR733
million as of March 31, 2026. The carrying amount as of the
settlement date will be reclassified to equity in the second
quarter of 2026.
-- Entered into agreement to sell its Rare Pediatric Disease Priority
Review Voucher (PRV) to an undisclosed buyer for $187.5 million in
cash, before transaction-related expenses. The PRV was awarded by
the FDA upon approval of YUVIWEL in February 2026. The transaction
is subject to customary closing conditions and is expected to
close in the second quarter of 2026.
* See "Non-IFRS Financial Measures" below for definitions of these non-IFRS measures and a reconciliation to the most directly comparable IFRS measures.
First Quarter 2026 Financial Results
Total revenue for the first quarter of 2026 was EUR247 million, compared to EUR101 million during the same period in 2025. The year-over-year increase in revenue was primarily attributable to an increase in product revenue from YORVIPATH.
Total Revenue Three Months Ended
(In EUR'000s) March 31,
2026 2025
Revenue
Commercial products 240,853 96,028
Services and clinical supply 5,110 3,524
Licenses 638 1,402
Total revenue 246,601 100,954
========= =========
Revenue from Commercial Products Three Months Ended
(In EUR'000s) March 31,
--------------------
2026 2025
Revenue from commercial products
YORVIPATH(R) 196,896 44,688
SKYTROFA(R) 43,957 51,340
Total revenue from commercial products 240,853 96,028
========== ========
Research and development expenses for the first quarter of 2026 were EUR59 million, compared to EUR87 million during the same period in 2025. The decrease was driven primarily by the completion of certain clinical trials and development activities within our Endocrinology Rare Disease and Oncology pipeline and the first quarter of 2026 being positively impacted by a reversal of prior period write-downs of pre-launch inventories related to YUVIWEL.
Selling, general, and administrative expenses for the first quarter of 2026 were EUR145 million, compared to EUR101 million during the same period in 2025. The increase was primarily due to the impact from commercial expansion, including global launch activities.
Total operating expenses for the first quarter of 2026 were EUR204 million compared to EUR188 million during the same period in 2025.
Operating profit for the first quarter of 2026 was EUR25 million, compared to an operating loss of EUR104 million during the same period in 2025. The increase was primarily driven by the increase in product revenue.
Net finance expenses for the first quarter of 2026 were EUR63 million, compared to EUR16 million during the same period in 2025. The increase was primarily driven by non-cash fair-value remeasurement of derivative liabilities associated with our convertible notes.
Income taxes for the first quarter of 2026 included the recognition of previously unrecognized deferred tax assets of EUR679 million.
For the first quarter of 2026, Ascendis Pharma reported net profit of EUR629 million, or EUR10.20 per share basic and EUR9.75 per share (diluted), compared to a net loss of EUR95 million, or EUR1.58 per share (basic and diluted), for the same period in 2025. Net profit for the first quarter of 2026 included the recognition of previously unrecognized deferred tax assets of EUR679 million.
Cash flows used in operating activities for the first quarter of 2026 were EUR8 million compared to EUR14 million used during the same period in 2025. The change primarily reflects the prior-year period benefiting from the $100 million upfront payment received under our exclusive license agreement with Novo Nordisk, which did not recur in the current period, while the current period reflects improved operating performance offset by working capital build.
As of March 31, 2026, Ascendis Pharma had cash and cash equivalents totaling EUR573 million, compared to EUR616 million as of December 31, 2025. As of March 31, 2026, Ascendis Pharma had 62,376,846 ordinary shares outstanding, including 265,251 held by the Company.
Beginning with the first quarter of 2026, Ascendis Pharma is introducing supplemental non-IFRS financial measures that management believes will help investors evaluate the Company's underlying operating performance from period to period and enhance comparability against peer companies. The non-IFRS measures presented are not a substitute for, and should be considered together with, the comparable IFRS measures. See the table below on page 14 for specific reconciling items.
For the first quarter of 2026, non-IFRS operating profit was EUR55 million, compared to a non-IFRS operating loss of EUR79 million for the same period in 2025.
For the first quarter of 2026, non-IFRS net profit was EUR18 million, or EUR0.27 earnings per diluted share, compared to a non-IFRS net loss of EUR73 million, or EUR1.22 loss per diluted share, for the same period in 2025.
Conference Call and Webcast Information
Ascendis Pharma will host a conference call and webcast today at 8:00 am Eastern Time $(ET)$ to discuss its first quarter 2026 financial results.
Those who would like to participate may access the live webcast here, or register in advance for the teleconference here. The link to the live webcast will also be available on the Investors & News section of the Ascendis Pharma website at https://investors.ascendispharma.com. A replay of the webcast will be available in this section of the Ascendis Pharma website shortly after the conclusion of the event for 30 days.
About Ascendis Pharma A/S
Ascendis Pharma is a global biopharmaceutical company focused on applying our innovative TransCon technology platform to make a meaningful difference for patients. Guided by our core values of Patients, Science, and Passion, and following our algorithm for product innovation, we apply TransCon to develop new therapies that demonstrate best-in-class potential to address unmet medical needs. Ascendis is headquartered in Copenhagen, Denmark, and has additional facilities in Europe and the United States. Please visit ascendispharma.com to learn more.
Forward-Looking Statements
This press release contains forward-looking statements that involve substantial risks and uncertainties. All statements, other than statements of historical facts, included in this press release regarding Ascendis' future operations, plans and objectives of management are forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended. Examples of such statements include, but are not limited to, statements relating to (i) Ascendis' evolution into a leading global biopharma, (ii) Ascendis' strong focus on science and making a meaningful difference for patients as the fundamental driver for success, (iii) anticipated timing of a regulatory decision from the European Medicines Agency, (iv) anticipated timing and plans of clinical trials and development activities, (v) Ascendis' ability to apply its TransCon technology platform to make a meaningful difference for patients and (vi) Ascendis' use of TransCon to create new and potentially best-in-class therapies. Ascendis may not actually achieve the plans, carry out the intentions or meet the expectations or projections disclosed in the forward-looking statements and you should not place undue reliance on these forward-looking statements. Actual results or events could differ materially from the plans, intentions, expectations and projections disclosed in the forward-looking statements. Various important factors could cause actual results or events to differ materially from the forward-looking statements that Ascendis makes, including, without limitation: dependence on third--party manufacturers, distributors, and service providers for Ascendis' products and product candidates; risks related to regulatory review and approval, including the possibility of delays, requests for additional data or analyses, restrictions or limitations on use, approval with labeling that is more limited than expected, or failure to obtain approval in the United States, European Union, or other jurisdictions; clinical development risks, including that results from ongoing or future trials may not confirm earlier data; unforeseen safety or efficacy findings in development programs or on--market products; manufacturing, supply chain, quality, or logistics issues that could delay development or commercialization; unforeseen expenses related to commercialization of any approved Ascendis products; unforeseen research and development or selling, general and administrative expenses and other costs impacting Ascendis' business generally; market acceptance, pricing, and reimbursement challenges, including payer coverage decisions and health technology assessments; competitive developments, including new or improved therapies; intellectual property protection, freedom--to--operate, and litigation risks; Ascendis' ability to obtain additional funding, if needed, to support its business activities; cybersecurity, data privacy, and information technology disruptions; and the impact of international economic, political, legal, compliance, public health, and business factors, including tariffs, trade policies, currency fluctuations, and geopolitical events. For a further description of the risks and uncertainties that could cause actual results to differ from those expressed in these forward-looking statements, as well as risks relating to Ascendis' business in general, see Ascendis' Annual Report on Form 20-F filed with the U.S. Securities and Exchange Commission (SEC) on February 11, 2026, and Ascendis' other future reports filed with, or submitted to, the SEC. Forward-looking statements do not reflect the potential impact of any future licensing, collaborations, acquisitions, mergers, dispositions, joint ventures, or investments that Ascendis may enter into or make. Ascendis does not assume any obligation to update any forward-looking statements, except as required by law.
Ascendis, Ascendis Pharma, the Ascendis Pharma logo, the company logo, TransCon, SKYTROFA(R) , YORVIPATH(R) , and YUVIWEL(R) are trademarks owned by the Ascendis Pharma group. (c) May 2026 Ascendis Pharma A/S.
Investor Contacts: Media Contact:
------------------ -----------------
Chad Fugere Melinda Baker
Ascendis Pharma Ascendis Pharma
+1 (650) 519-7494 +1 (650) 709-8875
FINANCIAL TABLES FOLLOW
-----------------------
Ascendis Pharma A/S Unaudited Condensed
Consolidated Statements of Profit or (Loss) and
Comprehensive Income / (Loss) (In EUR'000s, Three Months Ended
except per share data) March 31,
----------------------
2026 2025
--------- -----------
Consolidated Statement of Profit or (Loss)
Revenue 246,601 100,954
Cost of sales (17,515) (17,517)
-------- --------
Gross profit 229,086 83,437
Research and development expenses (59,044) (86,603)
Selling, general, and administrative expenses (145,230) (101,046)
-------- --------
Operating profit/(loss) 24,812 (104,212)
Share of profit/(loss) of associates (10,251) 26,579
Finance income 4,517 28,854
Finance expenses (67,255) (44,786)
-------- --------
Profit/(loss) before tax (48,177) (93,565)
Income taxes (expenses) 677,516 (1,061)
-------- --------
Net profit/(loss) for the period 629,339 (94,626)
======== ========
Attributable to owners of the Company 629,339 (94,626)
-------- --------
Basic earnings/(loss) per share 10.20 (1.58)
Diluted earnings/(loss) per share 9.75 (1.58)
-------- --------
Consolidated Statement of Comprehensive Income
or (Loss)
Net profit/(loss) for the period 629,339 (94,626)
Other comprehensive income/(loss)
Items that may be reclassified subsequently to
profit or (loss):
Exchange differences on translating foreign
operations 3,058 (75)
-------- --------
Other comprehensive income/(loss) for the
period, net of tax 3,058 (75)
-------- --------
Total comprehensive income/(loss) for the
period, net of tax 632,397 (94,701)
======== ========
Attributable to owners of the Company 632,397 (94,701)
-------- --------
Ascendis Pharma A/S Unaudited Condensed
Consolidated Statements of Financial March 31, December 31,
Position (In EUR'000s) 2026 2025
--------- --------------
Assets
Non-current assets
Intangible assets 3,689 3,710
Property, plant and equipment 135,918 146,479
Investments in associates 23,560 32,526
Other receivables 27,367 10,870
Deferred tax assets 690,405 --
880,939 193,585
--------- -----------
Current assets
Inventories 314,342 301,533
Trade receivables 178,676 141,333
Income tax receivables 1,258 1,781
Other receivables 16,673 14,582
Prepayments 38,571 33,715
Cash and cash equivalents 572,820 616,041
--------- -----------
1,122,340 1,108,985
--------- -----------
Total assets 2,003,279 1,302,570
========= ===========
Equity and liabilities
Equity
Share capital 8,380 8,322
Distributable equity 479,593 (171,143)
--------- -----------
Total equity 487,973 (162,821)
--------- -----------
Non-current liabilities
Borrowings 386,106 385,254
Contract liabilities 2,437 1,123
Deferred tax liabilities -- 9,623
--------- -----------
388,543 396,000
--------- -----------
Current liabilities
Convertible notes, due April 2028
Borrowings 448,176 429,391
Derivative liabilities 290,482 256,231
--------- -----------
738,658 685,622
Other current liabilities
Borrowings 62,382 57,141
Contract liabilities 5,364 4,944
Trade payables and accrued expenses 78,588 90,657
Other liabilities 57,316 58,204
Income tax payables 7,805 6,427
Provisions 176,650 166,396
--------- -----------
388,105 383,769
--------- -----------
1,126,763 1,069,391
--------- -----------
Total liabilities 1,515,306 1,465,391
--------- -----------
Total equity and liabilities 2,003,279 1,302,570
========= ===========
Ascendis Pharma A/S Unaudited Condensed
Consolidated Statements of Cash Flow (In Three Months Ended
EUR'000s) March 31,
----------------------
2026 2025
---------- ----------
Operating activities
Net profit/(loss) for the period 629,339 (94,626)
Reversal of finance income (4,517) (28,854)
Reversal of finance expenses 67,255 44,786
Reversal of income taxes (677,516) 1,061
Adjustments for non-cash items:
Non-cash consideration relating to revenue (638) (1,402)
Share of (profit)/loss of associates 10,251 (26,579)
Share-based payment 30,356 25,558
Depreciation and amortization 4,220 4,545
Impairment of property, plant and equipment -- 7,508
Changes in working capital:
Inventories (12,813) 2,538
Receivables (36,377) 98,032
Prepayments (4,852) (5,521)
Contract liabilities 1,735 (4,054)
Trade payables, accrued expenses and other
liabilities (21,051) (40,767)
Provisions 6,534 260
--------- -------
Cash flows generated from/(used in) operations (8,074) (17,515)
Finance income received 4,518 4,208
Finance expenses paid (5,328) (954)
Income taxes received/(paid) 1,163 (52)
Cash flows from/(used in) operating activities (7,721) (14,313)
--------- -------
Investing activities
Payments received under finance leases 959 --
Acquisition of intangible assets and property,
plant and equipment (7,712) (703)
Cash flows from/(used in) investing activities (6,753) (703)
--------- -------
Financing activities
Repayment of borrowings (8,580) (3,066)
Proceeds from exercise of warrants 31,625 13,834
Acquisition of treasury shares (51,857) (17,396)
Payment of withholding taxes under stock
incentive programs (8,021) (11,396)
Cash flows from/(used in) financing activities (36,833) (18,024)
--------- -------
Increase/(decrease) in cash and cash equivalents (51,307) (33,040)
Cash and cash equivalents at January 1 616,041 559,543
Effect of exchange rate changes on balances held
in foreign currencies 8,086 (8,580)
Cash and cash equivalents at March 31 572,820 517,923
--------- -------
Non-IFRS Financial Measures
In addition to the financial information prepared in accordance with IFRS Accounting Standards ("IFRS") as issued by the International Accounting Standards Board and as adopted by the European Union, this press release contains certain non-IFRS financial measures, including Non-IFRS Operating Profit/(Loss), Non-IFRS Net Profit/(Loss), Non-IFRS operating profit/(loss) margin, and Non-IFRS diluted earnings per share ("Non-IFRS Diluted EPS"). These non-IFRS measures are provided as supplemental information and should be considered in addition to, and not as a substitute for or superior to, the comparable measures prepared in accordance with IFRS. Management believes these non-IFRS measures support management's, analysts' and investors' overall understanding of the Company's underlying financial performance and trends and facilitate comparisons among current and past periods.
Since non-IFRS measures do not have standardized definitions and meanings, they may differ from the non-IFRS measures used by other companies, which reduces their usefulness as comparative financial measures. Because of these limitations, you should consider these adjusted financial measures alongside other IFRS financial measures. Because these non-IFRS measures are not prepared in accordance with IFRS, they should not be viewed as superior to IFRS reported measures, nor should they be used on their own or as replacements for the IFRS financial information included in this press release. Additionally, our non-IFRS measures may differ from similarly labeled measures used by other companies due to variations in calculation methods or the size and nature of adjusted items. Investors should note that several of the items excluded from these non-IFRS measures have been recognized in prior periods and may continue to be recognized in future periods.
The Company reports Non-IFRS Operating Profit/(Loss), Non-IFRS Net Profit /(Loss), Non-IFRS operating profit/(loss) margin and Non-IFRS Diluted EPS as non-IFRS measures, which exclude the following specified items:
(i) Share-based compensation expense. Although share-based compensation is a recurring expense, the Company excludes it from non-IFRS measures because the amount and timing of recognition depend on the value of the underlying equity instruments, which can fluctuate based on factors unrelated to the Company's operating performance during the period.
(ii) Share of profit/(loss) of associates. The Company excludes its share of the profit or loss of equity-method investees because these amounts are not within the control of the Company and do not reflect the Company's core operating performance.
(iii) Fair-value remeasurement of derivative liabilities related to the Company's convertible notes. The Company excludes the fair-value remeasurement of derivative liabilities associated with its convertible notes because these amounts depend on movements in the Company's share price and other market inputs and are not indicative of the Company's underlying operating performance.
(iv) Recognition of previously unrecognized deferred tax assets. The Company excludes the one-time recognition of previously unrecognized deferred tax assets because this item reflects a reassessment of the recoverability of historical tax attributes rather than the Company's current period operating performance.
Income taxes related to the foregoing items are adjusted accordingly, considering the individual impact of each item, the relevant tax jurisdiction, applicable tax rates, and the deductibility of the item.
For further details regarding valuation of derivative liabilities, and the recognition of previously unrecognized deferred tax assets, please refer to "Note 3 -- Significant Accounting Judgements and Estimates," contained in our Interim Report on Form 6-K, for the period ended March 31, 2026 and "Note 3 -- Significant Accounting Judgements and Estimates, " contained in our Annual Report on Form 20-F, for the year ended December 31, 2025.
The following table provides a reconciliation of the most directly comparable IFRS measures to Non-IFRS Operating Profit/(Loss), Non-IFRS Net Profit/(Loss) and Non-IFRS Diluted EPS.
Ascendis Pharma A/S
Reconciliation of IFRS to Non-IFRS Financial Information
(unaudited, in EUR'000s, except shares and per share
data)
Three Months Ended
March 31,
2026 2025
-------------- --------------
IFRS operating profit/(loss) 24,812 (104,212)
Share-based compensation costs 30,356 25,558
---------- ----------
Total non-IFRS adjustments to operating
profit/(loss) 30,356 25,558
---------- ----------
Non-IFRS operating profit/(loss) 55,168 (78,654)
========== ==========
IFRS operating profit/(loss) margin
(%)(1) 10.1% (103.2%)
Non-IFRS operating profit/(loss) margin
(%)(1) 22.4% (77.9%)
IFRS Net profit/(loss) 629,339 (94,626)
Share-based compensation costs 30,356 25,558
Share of profit/(loss) of associates 10,251 (26,579)
Remeasurement gain/(loss) of
derivative liabilities 34,251 23,911
Recognition of previously
unrecognized deferred tax assets (679,024) -
Tax effects of adjustments (7,623) (1,640)
Total non-IFRS adjustments to net
profit/(loss) (611,789) 21,250
---------- ----------
Non-IFRS net profit/(loss) 17,550 (73,376)
========== ==========
Net profit/(loss) per diluted share:
IFRS 9.75 (1.58)
Diluted per share impact of total
non-IFRS adjustments (9.48) 0.35
Non-IFRS 0.27 (1.22)
Shares used in diluted per share
calculation:
IFRS 64,521,948 60,018,550
Non-IFRS 64,521,948 60,018,550
(1) Defined as either IFRS or non-IFRS
operating profit/(loss) divided by
total revenue
(END) Dow Jones Newswires
May 07, 2026 07:30 ET (11:30 GMT)