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Ascendis Pharma Reports First Quarter 2025 Financial Results Q1 2025 revenue of 44.7 million for YORVIPATH and 51.3 million for SKYTROFA TransCon CNP NDA submitted in Q1 2025; MAA submission planned in Q3 2

Key Takeaway: Ascendis Pharma has reported its financial results for Q1 2025, highlighting a total revenue increase to 101 million, driven by strong sales of YORVIPATH. The company anticipates an inflection point in 2025 with ongoing development of TransCon CNP, expected for approval in children with achondroplasia. However, the quarter also featured a net loss of 94.6 million, largely due to rising operational expenses. The firm plans to submit a marketing authorization application for TransCon CNP in Q3 2025 and is optimistic about its future pipeline and prospects.

Market Sentiment Analysis

POSITIVE FACTORS

  • Significant revenue growth from YORVIPATH, generating 44.7 million.
  • Potential upcoming approvals for TransCon CNP may enhance their product offerings.
  • The company has a strong pipeline and commercial capabilities for future growth.

CONCERNS & RISKS

  • Net loss of 94.6 million reported for Q1 2025, despite revenue growth.
  • Increased R&D and administrative expenses impacted overall financial health.

Full Press Release Details

Ascendis Pharma Reports First Quarter 2025 Financial Results
Q1 2025 revenue of 44.7 million for YORVIPATH and
51.3 million for SKYTROFA
TransCon CNP NDA submitted in Q1 2025; MAA submission planned in Q3 2025
Topline COACH combination trial (TransCon CNP + TransCon hGH) data expected in Q2 2025
Conference call today at 4:30 pm ET
COPENHAGEN, Denmark, May 1, 2025 (GLOBE NEWSWIRE) Ascendis Pharma A/S (Nasdaq: ASND) today announced financial results for
the first quarter ended March 31, 2025, and provided a business update.
The strong global launch of YORVIPATH positions 2025 to be an
inflection point for Ascendis with growing revenue and a path to cashflow breakeven in the near term, said Jan Mikkelsen, Ascendis Pharma s President and Chief Executive Officer. We look forward to potential approvals of our third
product, TransCon CNP, as a monotherapy in children with achondroplasia, and we believe the upcoming topline COACH combination trial data may demonstrate improved outcomes, including growth, compared to TransCon CNP alone. With our diversified
pipeline, robust supply chain, and strong global commercial capabilities we are well-positioned to deliver on our commitment to provide patients with highly differentiated medicines.
Select Highlights & Anticipated 2025 Milestones
(palopegteriparatide, marketed as YORVIPATH)
(lonapegsomatropin, marketed as SKYTROFA)
(navepegritide plus lonapegsomatropin, marketed as SKYTROFA)
First Quarter 2025 Financial Results
Total revenue for the first quarter of 2025 was 101.0 million, compared to 95.9 million during the same period in 2024. The
year-over-year increase in revenue was primarily attributable to an increase in product revenue which reflected a contribution of 44.7 million from YORVIPATH, following its commercial launch.
Non-product revenue decreased to 4.9 million in the first quarter of 2025, compared to 29.4 million for the same period for 2024.
Total Revenue
(In EUR 000s) Three Months Ended March 31,
2025 2024
Revenue
Commercial products 96,028 66,499
Rendering of services and clinical supply 3,524 4,625
Licenses 1,402 24,770
Total revenue 100,954 95,894
Commercial Product Revenue
(In EUR 000s) Three Months Ended March 31,
2025 2024
Revenue from commercial products
SKYTROFA 51,340 65,005
YORVIPATH 44,688 1,494
Total revenue from commercial products 96,028 66,499
Research and development costs for the first quarter of 2025 were 86.6 million, compared to 70.7 million
during the same period in 2024. The first quarter of 2024 was positively impacted by a reversal of prior period write-downs of pre-launch inventories related to TransCon PTH. The first quarter of 2025 was
negatively impacted by an impairment charge related to property, plant and equipment due to change in activities at one of our sites in the U.S.
general, and administrative expenses for the first quarter of 2025 were 101.0 million, compared to 66.8 million during the same period in 2024. The increase was primarily due to the impact from commercial expansion including
global launch activities for YORVIPATH, as well as an impairment charge related to property, plant and equipment due to change in activities at one of our sites in the U.S.
Total operating expenses for the first quarter of 2025 were 187.6 million compared to 137.5 million during the same period in 2024.
Net finance expenses for the first quarter of 2025 was 15.9 million compared to 73.6 million during the same period in 2024. The
decrease was primarily driven by non-cash items.
For the first quarter of 2025, Ascendis Pharma reported a net
loss of 94.6 million, or 1.58 per share (basic and diluted) compared to a net loss of 131.0 million, or 2.30 per share (basic and diluted) for the same period in 2024.
As of March 31, 2025, Ascendis Pharma had cash and cash equivalents totaling 518 million compared to 560 million as of
December 31, 2024. As of March 31, 2025, Ascendis Pharma had 60,970,565 ordinary shares outstanding, including 597,055 ordinary shares represented by ADSs held by the company.
Conference Call and Webcast Information
Ascendis Pharma will host a conference call and webcast today at 4:30 pm Eastern Time (ET) to discuss its first quarter 2025 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. Examples of such statements include, but are not limited to, statements relating to
(i) Ascendis planned MAA submission for TransCon CNP; (ii) the timing and results of clinical trials; (iii) Ascendis expectations with respect to its revenue base and path to cashflow breakeven; (iv) the potential
approval of TransCon CNP as a monotherapy in children with achondroplasia; (v) Ascendis ability to provide patients with highly differentiated medicines; (vi) Ascendis plans for the commercial launch of TransCon PTH in
additional Europe Direct countries; (vii) Ascendis expectations regarding the PDUFA date for the supplemental BLA for TransCon hGH; (viii) Ascendis plans to submit IND applications or similar for a basket trial evaluating
TransCon hGH in additional indications and to investigate TransCon CNP alone or in combination with TransCon hGH for the treatment of hypochondroplasia; (ix) Ascendis ability to apply its TransCon technology platform to make a meaningful
difference for patients, and (x) Ascendis application of its TransCon technologies to develop new therapies that demonstrate best-in-class potential to
address unmet medical needs. 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 the following: dependence on third party manufacturers, distributors and service providers for Ascendis products and product candidates; unforeseen safety or efficacy results
in Ascendis development programs or on-market products; unforeseen expenses related to commercialization of any approved Ascendis products; unforeseen expenses related to Ascendis development
programs; unforeseen selling, general and administrative expenses, other research and development expenses and Ascendis business generally; delays in the development of its programs related to manufacturing, regulatory requirements, speed of
patient recruitment or other unforeseen delays; Ascendis ability to obtain additional funding, if needed, to support its business activities; the impact of international economic, political, legal, compliance, social
and business factors, including tariffs and trade policies. 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 12, 2025, 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 , and
YORVIPATH are trademarks owned by the Ascendis Pharma group. May 2025 Ascendis Pharma A/S.
Investor Contacts: Media Contact:
Scott Smith Melinda Baker
Ascendis Pharma Ascendis Pharma
ir@ascendispharma.com media@ascendispharma.com
Patti Bank
ICR Healthcare
+1 (415) 513-1284
patti.bank@icrhealthcare.com
FINANCIAL TABLES FOLLOW
Ascendis Pharma A/S
Consolidated Statements of Profit or (Loss) and
Comprehensive Income / (Loss) (In EUR 000s, except share and per share data) Three Months Ended March 31,
2025 2024
Consolidated Statement of Profit or (Loss)
Revenue 100,954 95,894
Cost of sales 17,517 7,569
Gross profit 83,437 88,325
Research and development expenses 86,603 70,687
Selling, general, and administrative expenses 101,046 66,783
Operating profit/(loss) (104,212 ) (49,145 )
Share of profit/(loss) of associates 26,579 (5,796 )
Finance income 28,854 3,575
Finance expenses 44,786 77,161
Profit/(loss) before tax (93,565 ) (128,527 )
Income taxes (expenses) (1,061 ) (2,508 )
Net profit/(loss) for the period (94,626 ) (131,035 )
Attributable to owners of the Company (94,626 ) (131,035 )
Basic and diluted earnings/(loss) per share (1.58 ) (2.30 )
Number of shares used for calculation (basic and diluted) 60,018,550 56,883,257
Consolidated Statement of Comprehensive Income or (Loss)
Net profit/(loss) for the period (94,626 ) (131,035 )
Other comprehensive income/(loss)
Items that may be reclassified subsequently to profit or (loss):
Exchange differences on translating foreign operations (75 ) 63
Other comprehensive income/(loss) for the period, net of tax (75 ) 63
Total comprehensive income/(loss) for the period, net of tax (94,701 ) (130,972 )
Attributable to owners of the Company (94,701 ) (130,972 )
Ascendis Pharma A/S
Consolidated Statements of Financial Position
(In EUR 000s) March 31, 2025 December 31, 2024
Assets
Non-current assets
Intangible assets 3,909 4,028
Property, plant and equipment 92,447 98,714
Investments in associates 40,938 13,575
Other receivables 2,657 2,317
139,951 118,634
Current assets
Inventories 293,071 295,609
Trade receivables 66,685 166,280
Income tax receivables 1,614 1,775
Other receivables 8,522 9,385
Prepayments 33,672 28,269
Cash and cash equivalents 517,923 559,543
921,487 1,060,861
Total assets 1,061,438 1,179,495
Equity and liabilities
Equity
Share capital 8,187 8,149
Distributable equity (197,994 ) (113,855 )
Total equity (189,807 ) (105,706 )
Non-current liabilities
Borrowings 357,312 365,080
Contract liabilities 692 5,000
Deferred tax liabilities 7,733 7,258
365,737 377,338
Current liabilities
Convertible notes, matures in April 2028
Borrowings 449,562 458,207
Derivative liabilities 174,581 150,670
624,143 608,877
Other current liabilities
Borrowings 40,398 33,329
Contract liabilities 1,190 936
Trade payables and accrued expenses 84,370 96,394
Other liabilities 38,062 67,956
Income tax payables 1,573 1,222
Provisions 95,772 99,149
261,365 298,986
885,508 907,863
Total liabilities 1,251,245 1,285,201
Total equity and liabilities 1,061,438 1,179,495

Frequently Asked Questions

What were Ascendis Pharma's Q1 2025 revenues?

Ascendis Pharma reported Q1 2025 revenues of 101.0 million.

When is the MAA submission for TransCon CNP planned?

The MAA submission for TransCon CNP is planned for Q3 2025.

What were the main drivers of revenue growth in Q1 2025?

Revenue growth in Q1 2025 was largely driven by the launch of YORVIPATH.

When is the upcoming COACH trial data expected?

Topline data from the COACH trial is expected in Q2 2025.

What was Ascendis Pharma's net loss in Q1 2025?

Ascendis Pharma reported a net loss of 94.6 million in Q1 2025.

Last updated: May 1, 2025