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Ascendis Pharma Reports Fourth Quarter and Full-Year 2025 Financial Results

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Ascendis Pharma (Nasdaq: ASND) reported Q4 2025 product revenue of €240 million and full‑year 2025 product revenue of €684 million. Q4 operating profit was €10 million with operating cash flow of €73 million. Full‑year net loss was €228 million and cash totaled €616 million. Key pipeline milestones include a PDUFA action date of Feb 28, 2026 for TransCon CNP (pediatric achondroplasia) and ongoing TransCon PTH and TransCon hGH label-expansion programs.

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Positive

  • Q4 product revenue of €240 million
  • Full‑year product revenue of €684 million
  • YORVIPATH FY revenue of €477 million
  • Q4 operating cash flow of €73 million
  • Cash balance of €616 million as of Dec 31, 2025
  • PDUFA action date Feb 28, 2026 for TransCon CNP (pediatric achondroplasia)

Negative

  • Full‑year net loss of €228 million
  • SG&A rose to €458 million in 2025
  • Total operating expenses increased to €761 million in 2025
  • Non‑product revenue fell from €138 million in 2024 to €37 million in 2025
  • Net finance expenses increased to €93 million for 2025

Market Reaction

-5.18% $210.02
15m delay 2 alerts
-5.18% Since News
$210.02 Last Price
$207.11 $224.90 Day Range
-$750M Valuation Impact
$13.73B Market Cap
0.0x Rel. Volume

Following this news, ASND has declined 5.18%, reflecting a notable negative market reaction. Our momentum scanner has triggered 2 alerts so far, indicating moderate trading interest and price volatility. The stock is currently trading at $210.02. This price movement has removed approximately $750M from the company's valuation.

Data tracked by StockTitan Argus (15 min delayed). Upgrade to Silver for real-time data.

Key Figures

Q4 2025 product revenue: €240 million FY 2025 product revenue: €684 million Q4 operating profit: €10 million +5 more
8 metrics
Q4 2025 product revenue €240 million Fourth quarter 2025 commercial product revenue
FY 2025 product revenue €684 million Full-year 2025 commercial product revenue
Q4 operating profit €10 million Operating profit in fourth quarter 2025
Q4 operating cash flow €73 million Cash flow from operating activities in Q4 2025
Total revenue 2025 €720 million Full-year 2025 vs €364 million in 2024
R&D expenses 2025 €304 million Full-year 2025 vs €307 million in 2024
Net loss 2025 €228 million Full-year 2025 vs €378 million in 2024
Cash balance €616 million Cash and cash equivalents as of December 31, 2025

Market Reality Check

Price: $221.49 Vol: Volume 975,791 is 1.35x t...
normal vol
$221.49 Last Close
Volume Volume 975,791 is 1.35x the 20-day average of 722,974, indicating elevated trading interest ahead of and around earnings. normal
Technical Shares trade above the 200-day MA, with price at 224.05 versus the 200-day average of 192.97, reflecting a pre-existing uptrend into these results.

Peers on Argus

ASND gained 0.97% while several biotech peers also moved higher: BMRN +2.86%, SM...

ASND gained 0.97% while several biotech peers also moved higher: BMRN +2.86%, SMMT +0.20%, BBIO +0.14%, though EXEL and IONS were modestly negative. The upside in ASND occurs within a mixed but generally constructive biotech tape.

Common Catalyst Earnings-related news across biotech, including peer IONS’ upcoming Q4 and full-year 2025 results webcast.

Previous Earnings Reports

5 past events · Latest: Nov 12 (Positive)
Same Type Pattern 5 events
Date Event Sentiment Move Catalyst
Nov 12 Q3 2025 earnings Positive -1.0% Strong revenue growth and first operating profit but share price slipped modestly.
Aug 07 Q2 2025 earnings Positive +0.6% Significant revenue increase and growing YORVIPATH and SKYTROFA contributions.
May 01 Q1 2025 earnings Positive +2.7% Higher revenue, solid product uptake, and improved net loss versus prior year.
Feb 12 FY 2024 earnings Positive +13.0% Strong 2024 revenue growth and early YORVIPATH and SKYTROFA scaling.
Nov 14 Q3 2024 earnings Positive +1.8% Improving product revenues plus new Novo Nordisk collaboration and guidance.
Pattern Detected

Earnings releases have generally led to positive share reactions, with 4 aligned moves and 1 divergence and an average move of 3.43% around past earnings events.

Recent Company History

Over the past year, Ascendis’ earnings reports have highlighted rapid revenue growth driven by YORVIPATH and SKYTROFA, improving operating metrics, and a still‑negative but narrowing net loss. Events from Q3 2024 through Q3 2025 show total revenue rising from €57.8M to €213.6M, alongside cash balances in the €518–626M range. Regulatory milestones for TransCon CNP and commercial ramp of YORVIPATH have been recurring themes, and today’s full‑year 2025 report extends that trajectory with higher product revenues and improved losses.

Historical Comparison

earnings
+3.4 %
Average Historical Move
Historical Analysis

In the past five earnings releases, ASND showed an average move of 3.43%, usually positive, suggesting investors often reward revenue growth and pipeline progress.

Typical Pattern

Earnings from late 2024 through 2025 show a progression from early YORVIPATH launch to strong global product revenue, improving losses, and repeated confirmation of TransCon CNP regulatory milestones.

Market Pulse Summary

The stock is down -5.2% following this news. A negative reaction despite growing revenues and improv...
Analysis

The stock is down -5.2% following this news. A negative reaction despite growing revenues and improving net losses would fit a pattern where one prior earnings event saw shares fall despite strong fundamentals. With average historical earnings moves of 3.43%, a sharp decline could reflect concerns about sustained spending levels, future profitability, or regulatory timelines rather than the reported 2025 performance itself. Such pullbacks have potential to normalize if subsequent milestones or execution restore confidence.

Key Terms

pdufa, nda, maa, phase 2, +4 more
8 terms
pdufa regulatory
"TransCon® CNP under FDA Priority Review, PDUFA action goal date of February 28, 2026"
PDUFA, short for the Prescription Drug User Fee Act, is a law that allows drug companies to pay fees to the government to speed up the review process for new medicines. This helps bring important drugs to market more quickly, which can impact their availability and pricing. For investors, PDUFA timelines can influence the timing of a drug’s approval and potential market success.
nda regulatory
"TransCon CNP(navepegritide, FDA NDA and EMA MAA filed)"
An NDA, or nondisclosure agreement, is a legal contract that keeps certain information private between parties. It’s like a promise not to share sensitive details, helping protect business ideas, strategies, or data from being leaked or used without permission. For investors, NDAs help ensure that confidential information remains secure, enabling trust and open communication during business discussions.
maa regulatory
"TransCon CNP(navepegritide, FDA NDA and EMA MAA filed)"
MAA stands for Marketing Authorization Application, the formal request a drug developer files with regulators (commonly in the European Union) asking for permission to sell a medicine. Think of it like applying for a driver’s license for a product: approval means the company can market and earn revenue from the drug, while rejection or delays affect expected sales, timelines and the company’s valuation—so investors track MAAs as key risk/reward milestones.
phase 2 medical
"Announced Week 52 topline results from Phase 2 COACH Trial, which demonstrated"
Phase 2 is the mid-stage clinical trial where a new drug or treatment is tested in a larger group of patients to see if it works and to keep checking safety after initial human testing. Think of it as a field test that proves whether a product actually delivers its promised benefit. Investors watch Phase 2 closely because its results strongly influence a medicine’s chances of reaching the market, the size of its potential sales, and the company’s valuation.
phase 3 medical
"regarding a Phase 3 trial of TransCon CNP and TransCon hGH in pediatric"
Phase 3 is the late-stage clinical testing step for a new drug or medical treatment, where the product is given to large groups of patients to confirm effectiveness, monitor side effects, and compare it to standard care. Successful Phase 3 results are often the final scientific hurdle before regulators decide on approval and market launch—like passing a final exam before graduation—and can sharply change a company's valuation and future revenue prospects.
overall survival medical
"Expect to report median overall survival (OS) data for a cohort of 70 patients"
Overall survival is the average or median length of time patients remain alive after starting a treatment or entering a clinical study, measured regardless of cause of death. Investors care because it is a clear, hard measure of a therapy’s real-world benefit — like timing how long a new battery actually runs — and strong improvements in overall survival can drive regulatory approval, market adoption and revenue potential.
basket trial medical
"Initiated Phase 3 basket trial for additional indications: idiopathic short stature"
A basket trial is a type of clinical study that tests one treatment across multiple diseases or patient groups that share a common biological feature, like a genetic marker. Think of it as trying one key in several different locks that use the same mechanism; positive results can speed development and expand a drug’s potential market, while mixed results can raise uncertainty about which patient groups will benefit and how regulators will view approvals.
biologics license application regulatory
"announced that China’s National Medical Products Administration approved its biologics license application for lonapegsomatropin"
A biologics license application is a formal request submitted to regulatory authorities seeking approval to market a new biological medicine, such as vaccines or treatments made from living organisms. It is a comprehensive review process that evaluates the safety, effectiveness, and manufacturing quality of the product. For investors, receiving approval signals that a biological therapy can be sold to the public, potentially leading to revenue growth and market success.

AI-generated analysis. Not financial advice.

  • Q4 2025 product revenue of €240 million and FY 2025 product revenue of €684 million
  • Q4 2025 operating profit of €10 million and cash flow from operating activities of €73 million
  • TransCon® CNP under FDA Priority Review, PDUFA action goal date of February 28, 2026
  • Conference call today at 4:30 pm ET

COPENHAGEN, Denmark, Feb. 11, 2026 (GLOBE NEWSWIRE) -- Ascendis Pharma A/S (Nasdaq: ASND) today announced financial results for the fourth quarter and full year ended December 31, 2025, and provided a business update.

“With a continued focus on making a meaningful difference for patients, we believe Ascendis is entering a steep growth phase as we transform into a leading global biopharma company,” said Jan Mikkelsen, President and CEO of Ascendis Pharma. “With strong execution and the power of our TransCon platform, we are positioned to generate approximately €500 million in operating cash flow in 2026 while aspiring to deliver at least €5 billion in global annual product revenue by 2030. At the same time, we are advancing a growing pipeline of highly differentiated programs to deliver durable, long-term growth.”

Select 2025 Highlights & Anticipated 2026 Milestones

  • TransCon PTH
    (palopegteriparatide, marketed as YORVIPATH)
    • YORVIPATH revenue for the fourth quarter of 2025 totaled €187 million and €477 million for the full year 2025, as previously announced.
    • More than 5,300 unique U.S. patient enrollments, with nearly 2,400 unique prescribing healthcare providers at year end.
    • Outside the U.S., now available commercially or through named patient programs in more than 30 countries, with full commercial launches anticipated in 10 additional countries by year end 2026.
    • Presented pooled analysis of 3-year data from PaTHway and PaTH Forward trials at the American Society of Nephrology (ASN) Kidney Week 2025, reinforcing that treatment with TransCon PTH led to rapid and sustained improvements in kidney function in adults with hypoparathyroidism.
    • Ongoing label expansion trials through PaTHway60 (adults) and PaTHway Adolescent.
    • Confirmed product profile for once-weekly TransCon PTH, targeting patients who have been transitioned from conventional therapy to YORVIPATH and have achieved a stable daily dose.
  • TransCon CNP
    (navepegritide, FDA NDA and EMA MAA filed)
    • In the U.S., PDUFA action goal date of February 28, 2026 for pediatric achondroplasia.
    • Submitted marketing authorization application (MAA) to the European Medicines Agency (EMA) in October 2025, with a regulatory decision on potential use in pediatric achondroplasia anticipated in the fourth quarter of 2026.
    • Label expansion trial in infants with achondroplasia, reACHin, remains ongoing with enrollment completion anticipated later this year.
  • TransCon CNP + TransCon hGH Combination Therapy
    (navepegritide plus lonapegsomatropin)
    • Announced Week 52 topline results from Phase 2 COACH Trial, which demonstrated improvements in annualized growth velocity across both TransCon CNP treatment-naïve and TransCon CNP-treated children that exceeded the 97th percentile of average stature children, along with improvements in body proportionality and in arm span, and a safety profile consistent with those observed for monotherapies of TransCon CNP and TransCon hGH on January 8, 2026.
    • Held a successful end of Phase 2 meeting with the U.S. Food & Drug Administration (FDA) and Scientific Advice meeting in the EU regarding a Phase 3 trial of TransCon CNP and TransCon hGH in pediatric achondroplasia in the fourth quarter of 2025.
    • Week 78 COACH data update anticipated in second quarter of 2026.
    • Planned new trials to support TransCon CNP + TransCon hGH treatment in additional indications.
  • TransCon hGH
    (lonapegsomatropin, marketed as SKYTROFA)
    • SKYTROFA revenue for the fourth quarter of 2025 totaled €53 million and €206 million for the full year 2025, as previously announced.
    • Received first label expansion in July 2025 with FDA approval for adult growth hormone deficiency (GHD).
    • Initiated Phase 3 basket trial for additional indications: idiopathic short stature (ISS), SHOX deficiency, Turner syndrome, and small for gestational age (SGA).
  • Oncology Program
    (onvapegleukin alfa)
    • Expect to report median overall survival (OS) data for a cohort of 70 patients with late-line platinum-resistant ovarian cancer (PROC) from the IL-Believe Trial of TransCon IL-2 β/γ + weekly paclitaxel in the second quarter of this year.
  • Strategic Collaborations & Investments
    • Ongoing multi-product collaboration with Novo Nordisk for TransCon technology-based therapies in obesity and metabolic diseases, with the lead program, TransCon Semaglutide, on track to enter the clinic as anticipated.
    • Eyconis lead program, TransCon aVEGF (EYC-0305), in development for wet AMD and other retinal diseases anticipated to enter the clinic in 2026.
    • On January 26, 2026, VISEN Pharmaceuticals announced that China’s National Medical Products Administration approved its biologics license application for lonapegsomatropin (TransCon hGH) in China for the treatment of pediatric growth hormone deficiency (PGHD).
    • In November 2025, Teijin Limited announced that YORVIPATH is commercially available for prescription in Japan.
  • Financial Update
    • For the fourth quarter of 2025, operating profit was €10 million and cash flow from operating activities was €73 million, primarily driven by continued growth of YORVIPATH revenue globally.
    • Initiating previously announced $120 million share repurchase program in 2026.
    • As of December 31, 2025, our cash balance was €616 million, an increase of €77 million compared to €539 million as of September 30, 2025.

Fourth Quarter and Full-Year 2025 Financial Results
Total revenue for the fourth quarter of 2025 was €248 million, compared to €174 million during the same period for 2024. The increase was primarily attributable to the continued growth of YORVIPATH global product revenue, partially offset by the recognition of a $100 million upfront payment in 2024 that did not recur in 2025.

Total revenue for 2025 was €720 million compared to €364 million in 2024. The increase was primarily attributable to the continued growth of YORVIPATH partially offset by recognition of a $100 million upfront payment in 2024 that did not recur in 2025. Non-product revenue was €37 million in 2025, compared to €138 million in 2024.

Total Revenue
(In EUR'000s)
 Three Months Ended
December 31,

 Twelve Months Ended
December 31,

  2025  2024  2025  2024 
Revenue            
Commercial products 240,092  72,130  683,572  225,728 
Services and clinical supply 4,780  5,933  18,008  15,570 
Licenses 2,628  95,853  5,630  122,343 
Milestones     12,922   
Total revenue 247,500  173,916  720,132  363,641 


Commercial Products Revenue
(In EUR'000s)
 Three Months Ended
December 31,
 Twelve Months Ended
December 31,
  2025  2024  2025  2024 
Revenue from commercial products            
YORVIPATH® 186,677  13,584  477,412  28,727 
SKYTROFA® 53,415  58,546  206,160  197,001 
Total revenue from commercial products 240,092  72,130  683,572  225,728 
             

Research and development (R&D) expenses for the fourth quarter of 2025 were €78 million, compared to €79 million during the same period in 2024. R&D expenses for 2025 were €304 million compared to €307 million in 2024. The lower R&D expenses were driven by the completion of clinical trials and development activities within our Endocrinology Rare Disease pipeline partially offset by reversal (income) of prior period write-downs related to YORVIPATH pre-launch inventory.

Selling, general, and administrative (SG&A) expenses for the fourth quarter of 2025 were €136 million, compared to €80 million during the same period in 2024. SG&A expenses for 2025 were €458 million compared to €291 million in 2024. Higher SG&A expenses were primarily due to the continued impact from global commercial expansion, including global launch activities for YORVIPATH.

Total operating expenses for the fourth quarter of 2025 were €214 million compared to €160 million during the same period in 2024. Total operating expenses for 2025 were €761 million compared to €598 million in 2024.

Net finance expenses were €38 million in the fourth quarter compared to €33 million in the same period in 2024. Net finance expenses for 2025 were €93 million compared to €74 million in 2024. The full year net finance expense increase was driven primarily by non-cash items.

For the fourth quarter of 2025, Ascendis Pharma reported a net loss of €34 million, or €0.55 per share (basic and diluted) compared to a net loss of €38 million, or €0.64 per share (basic and diluted) for the same period in 2024. For the full year 2025, Ascendis Pharma reported a net loss of €228 million, or €3.76 per share (basic and diluted) compared to a net loss of €378 million, or €6.53 per share (basic and diluted) in 2024.

As of December 31, 2025, Ascendis Pharma had cash and cash equivalents totaling €616 million compared to €560 million as of December 31, 2024. As of December 31, 2025, Ascendis Pharma had 61,977,408 ordinary shares outstanding, including 597,096 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 fourth quarter and full year 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 on this section of the Ascendis Pharma website shortly after conclusion of the event for 30 days.

About Ascendis Pharma A/S
Ascendis Pharma is applying its innovative TransCon technology platform to build a leading, fully integrated biopharma company focused on making a meaningful difference in patients’ lives. Guided by its core values of Patients, Science, and Passion, Ascendis uses its TransCon technologies to create new and potentially best-in-class therapies. 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’ expectation for durable, long-term growth, including its expectation to generate approximately €500 million in operating cash flow in 2026 and to deliver at least €5 billion in global annual product revenue by 2030; (ii) Ascendis’ expectations with respect to the commercial launches of TransCon PTH in additional countries; (iii) the PDUFA goal date for FDA review of TransCon CNP; (iv) the timing of EMA’s decision on potential use of TransCon CNP in pediatric achondroplasia; (v) the timing of enrollment completion of the label expansion trial in infants with achondroplasia, reACHin; (vi) the timing of Week 78 COACH data update; (vii) the planned new trials to support TransCon CNP + TransCon hGH treatment in additional indications; (viii) the timing of median OS data for the oncology program; (ix) the clinical entry of TransCon semaglutide; (x) the clinical entry of TransCon aVEGF program in 2026; (xi) Ascendis’ ability to apply its TransCon technology platform to build a leading, fully integrated biopharma company; and (xii) Ascendis’ use of its TransCon technologies 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 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; and the impact of international economic, political, legal, compliance, social and business factors. 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.
© February 2026 Ascendis Pharma A/S. 

Investor Contacts:
Chad Fugere
Ascendis Pharma
ir@ascendispharma.com
Media Contact:
Melinda Baker
Ascendis Pharma
media@ascendispharma.com
  
Patti Bank
ICR Healthcare
patti.bank@icrhealthcare.com
 
  


FINANCIAL TABLES FOLLOW

Ascendis Pharma A/S
Consolidated Statements of Profit or (Loss) and Other Comprehensive Income or (Loss)
(In EUR'000s, except share and per share data)
 Three Months Ended
December 31,
 Twelve Months Ended
December 31,
  2025  2024  2025  2024 
Consolidated Statement of Profit or (Loss)        
Revenue 247,500  173,916  720,132  363,641 
Cost of sales (23,598) (14,023) (94,915) (44,258)
Gross profit 223,902  159,893  625,217  319,383 
Research and development expenses (78,151) (79,294) (303,621) (307,004)
Selling, general, and administrative expenses (135,855) (80,216) (457,867) (291,142)
Operating profit/(loss) 9,896  383  (136,271) (278,763)
Share of profit/(loss) of associates 1,328  (4,575) 16,308  (20,060)
Finance income 24,061  26,233  113,999  25,609 
Finance expenses (61,990) (59,425) (206,687) (100,027)
Profit/(loss) before tax (26,705) (37,384) (212,651) (373,241)
Income taxes (expenses) (6,857) (1,085) (15,383) (4,843)
Net profit/(loss) for the year (33,562) (38,469) (228,034) (378,084)
Attributable to owners of the Company (33,562) (38,469) (228,034) (378,084)
Basic earnings/(loss) per share  (0.55) (0.64) (3.76) (6.53)
Diluted earnings/(loss) per share (0.55) (0.64) (3.76) (6.53)
     
Consolidated Statement of Comprehensive Income or (Loss)        
Net profit/(loss) for the year (33,562) (38,469) (228,034) (378,084)
Other comprehensive income/(loss)        
Items that may be reclassified subsequently to profit or (loss):        
Exchange differences on translating foreign operations (490) 830  (3,538) 1,062 
Other comprehensive income/(loss) for the year, net of tax (490) 830  (3,538) 1,062 
Total comprehensive income/(loss) for the year, net of tax (34,052) (37,639) (231,572) (377,022)
Attributable to owners of the Company (34,052) (37,639) (231,572) (377,022)



Ascendis Pharma A/S
Consolidated Statements of Financial Position
(In EUR'000s)
  December 31,
2025
 December 31,
2024
Assets     
Non-current assets     
Intangible assets  3,710  4,028 
Property, plant and equipment  146,479  98,714 
Investments in associates  32,526  13,575 
Other receivables  10,870  2,317 
   193,585  118,634 
Current assets     
Inventories  301,533  295,609 
Trade receivables  141,333  166,280 
Income tax receivables  1,781  1,775 
Other receivables  14,582  9,385 
Prepayments  33,715  28,269 
Cash and cash equivalents  616,041  559,543 
   1,108,985  1,060,861 
Total assets  1,302,570  1,179,495 
      
Equity and liabilities     
Equity     
Share capital  8,322  8,149 
Distributable equity  (171,143) (113,855)
Total equity  (162,821) (105,706)
      
Non-current liabilities     
Borrowings  385,254  365,080 
Contract liabilities  1,123  5,000 
Deferred tax liabilities  9,623  7,258 
   396,000  377,338 
Current liabilities     
Convertible notes, matures in April 2028     
Borrowings  429,391  458,207 
Derivative liabilities  256,231  150,670 
   685,622  608,877 
Other current liabilities     
Borrowings  57,141  33,329 
Contract liabilities  4,944  936 
Trade payables and accrued expenses  90,657  96,394 
Other liabilities  58,204  67,956 
Income tax payables  6,427  1,222 
Provisions  166,396  99,149 
   383,769  298,986 
   1,069,391  907,863 
Total liabilities  1,465,391  1,285,201 
Total equity and liabilities  1,302,570  1,179,495 

FAQ

What were Ascendis Pharma (ASND) Q4 2025 revenues and operating profit?

Ascendis reported total Q4 2025 revenue of €247.5 million and product revenue of €240 million. According to the company, Q4 operating profit was €10 million, driven primarily by YORVIPATH global sales and related commercial expansion.

What is the PDUFA date for TransCon CNP (ASND) and what does it mean?

The PDUFA action goal date for TransCon CNP is February 28, 2026. According to the company, this is the FDA review deadline for the pediatric achondroplasia NDA and signals a near‑term regulatory decision timeline.

How did YORVIPATH contribute to Ascendis Pharma's 2025 performance (ASND)?

YORVIPATH generated €477 million in product revenue for 2025, the primary driver of revenue growth. According to the company, commercial launches expanded to over 30 countries and supported higher operating cash flow in Q4.

Why did Ascendis Pharma (ASND) report a full‑year net loss in 2025 despite revenue growth?

The company reported a full‑year net loss of €228 million due to higher operating expenses and increased SG&A. According to the company, global commercial expansion and launch activities materially raised SG&A and overall operating expenses.

What is the size and purpose of Ascendis Pharma's 2026 share repurchase program (ASND)?

Ascendis announced a $120 million share repurchase program to begin in 2026. According to the company, the program is intended to return capital and offset dilution while leveraging improving cash flow from commercial products.
Ascendis Pharma

NASDAQ:ASND

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ASND Stock Data

13.70B
60.09M
0.78%
106.97%
4.43%
Biotechnology
Biological Products, (no Disgnostic Substances)
Link
Denmark
ABINGDON, OXFORDSHIRE