Ascendis Pharma A/S (ASND)
| Market Cap | 13.07B |
| Revenue (ttm) | 998.25M +134.8% |
| Net Income | 571.81M |
| EPS | 9.26 |
| Shares Out | 62.11M |
| PE Ratio | 22.72 |
| Forward PE | 48.49 |
| Dividend | n/a |
| Ex-Dividend Date | n/a |
| Volume | 592,713 |
| Open | 220.51 |
| Previous Close | 218.84 |
| Day's Range | 209.56 - 222.55 |
| 52-Week Range | 209.56 - 250.27 |
| Beta | 0.49 |
| Analysts | Strong Buy |
| Price Target | 295.11 (+40.23%) |
| Earnings Date | May 7, 2026 |
About ASND
Ascendis Pharma A/S, operates as a biopharmaceutical company that focuses on developing TransCon-based therapies for unmet medical needs in Europe, the United States, and internationally. The company offers SKYTROFA for treating pediatric patients with growth hormone deficiency; and YORVIPATH, a once-daily subcutaneous injection for the treatment of adults with chronic hypoparathyroidism. It is also developing a pipeline of three independent endocrinology rare disease product candidates in clinical development, as well as focuses on advancing o... [Read more]
Financial Performance
In 2025, Ascendis Pharma's revenue was 720.13 million, an increase of 98.03% compared to the previous year's 363.64 million. Losses were -228.03 million, -39.69% less than in 2024.
Financial numbers in EUR Financial StatementsAnalyst Summary
According to 17 analysts, the average rating for ASND stock is "Strong Buy." The 12-month stock price target is $295.11, which is an increase of 40.23% from the latest price.
News
Ascendis Pharma Earnings Call Transcript: Q1 2026
Q1 2026 saw rapid revenue growth and profitability, driven by the FDA approval of YUVIWEL and strong uptake of YORVIPATH and SKYTROFA. Total revenue reached EUR 247 million, with robust patient and prescriber growth, and a strengthened balance sheet through asset sales and debt redemption.
Ascendis Pharma Earnings release: Q1 2026
Ascendis Pharma released its Q1 2026 earnings on May 7, 2026, summarizing the period's financial results.
Ascendis Pharma Reports First Quarter 2026 Financial Results
- Q1 2026 revenue of €197 million for YORVIPATH ® and €44 million for SKYTROFA ® - More than 1,000 new patient enrollments for YORVIPATH in the U.S. in Q1 - As of May 1, more than 60 YUVIWEL ® enrollm...
New 2-Year Data from Pivotal ApproaCH Trial of TransCon® CNP (Navepegritide) Show Pronounced Gains in Growth Outcomes in Children with Achondroplasia Aged ≥5 Years
COPENHAGEN, Denmark, May 06, 2026 (GLOBE NEWSWIRE) -- Ascendis Pharma A/S (Nasdaq: ASND) today announced new data from a subgroup analysis showing that children with achondroplasia ≥5 years of age at ...
Ascendis to Report First Quarter 2026 Financial Results and Provide Business Update on May 7, 2026
COPENHAGEN, Denmark, April 30, 2026 (GLOBE NEWSWIRE) -- Ascendis Pharma A/S (Nasdaq: ASND) today announced it plans to report first quarter 2026 financial results and provide a business update on Thur...
Ascendis Announces Redemption of All $575 Million of Outstanding 2.25% Convertible Senior Notes Due 2028
COPENHAGEN, Denmark, April 21, 2026 (GLOBE NEWSWIRE) -- Ascendis Pharma A/S (Nasdaq: ASND) today announced that it has called all $575.0 million aggregate principal amount of its outstanding 2.25% Con...
Ascendis Pharma Announces Commencement of Trading of its Ordinary Shares on Nasdaq
COPENHAGEN, Denmark, April 20, 2026 (GLOBE NEWSWIRE) -- Ascendis Pharma A/S (Nasdaq: ASND) today announced the commencement of trading of its ordinary shares on The Nasdaq Global Select Market (Nasdaq...
Ascendis Pharma to List Ordinary Shares Directly on Nasdaq
- Ordinary shares expected to commence trading on Nasdaq on April 20, 2026 following exchange of all American Depositary Shares (ADSs) - ADS holders will receive one ordinary share listed on Nasdaq f...
New Data from Week 52 of the Ongoing COACH Trial Showed that TransCon® hGH Accelerated TransCon® CNP's Benefits Beyond Linear Growth in Children with Achondroplasia
- Unprecedented improvements in arm span observed with TransCon CNP and TransCon hGH combination therapy, a measure highly meaningful to the achondroplasia community
Ascendis Receives Orphan Drug Exclusivity and Launches YUVIWEL® (Navepegritide) in the United States
- YUVIWEL was granted orphan drug exclusivity by U.S. FDA to increase linear growth in pediatric patients 2 years of age and older with achondroplasia with open epiphyses
New InsiGHTS Trial of TransCon® hGH (Lonapegsomatropin) in Turner Syndrome Demonstrated Comparable Efficacy and Safety to Daily Somatropin at Week 52
- Annualized height velocity of 9.05 cm/year (LS mean) for TransCon hGH-treated children was similar at Week 52 to daily somatropin-treated children - TransCon hGH showed a safety and tolerability pr...
New Two-Year Data from Pivotal ApproaCH Trial Showing Durable Benefits of TransCon® CNP (Navepegritide) in Children with Achondroplasia Shared at ACMG 2026
COPENHAGEN, Denmark, March 16, 2026 (GLOBE NEWSWIRE) -- Ascendis Pharma A/S (Nasdaq: ASND) today announced new data from its pivotal ApproaCH Trial showing that children with achondroplasia treated wi...
Ascendis Pharma Transcript: TD Cowen 46th Annual Health Care Conference
YUVIWEL is set for a U.S. launch in early Q2 following FDA approval, targeting both untreated and switch patients with a differentiated weekly dosing profile and strong safety data. Pricing will reflect its clinical benefits, and international expansion is planned.
Ascendis Pharma to Participate in the TD Cowen 46th Annual Health Care Conference
COPENHAGEN, Denmark, March 02, 2026 (GLOBE NEWSWIRE) -- Ascendis Pharma A/S (Nasdaq: ASND) today announced that company executives will participate in a virtual fireside chat at the TD Cowen 46th Annu...
Ascendis Pharma Transcript: FDA announcement
YUVIWEL received FDA approval as the first once-weekly therapy for children with achondroplasia, showing significant efficacy and safety in clinical trials. Commercial launch is planned for early Q2 2026, with label expansion and international rollout to follow.
Ascendis Pharma Press release: FDA announcement
Ascendis Pharma issued a press release on March 2, 2026, disclosing material business information to investors.
Ascendis Pharma Slides: FDA announcement
Ascendis Pharma has posted slides in relation to its latest quarterly earnings report, which was published on March 2, 2026.
Ascendis wins U.S. approval for therapy for children with dwarfism
The U.S. Food and Drug Administration on Friday approved Ascendis Pharma's once-weekly therapy for children with a rare genetic disorder that causes dwarfism, the company said.
FDA Approves Once-Weekly YUVIWEL® (navepegritide) for Children with Achondroplasia Aged 2 Years and Older
COPENHAGEN, Denmark, Feb. 27, 2026 (GLOBE NEWSWIRE) -- Ascendis Pharma A/S (Nasdaq: ASND) today announced that the U.S. Food & Drug Administration (FDA) has granted approval under the FDA's Accelerate...
Ascendis Pharma Earnings Call Transcript: Q4 2025
Strong 2025 performance with EUR 720M revenue, led by YORVIPATH and SKYTROFA growth, supports a robust outlook for 2026. Pipeline advances, global launches, and a solid cash position underpin targets of EUR 500M operating cash flow in 2026 and EUR 5B annual revenue by 2030.
Ascendis Pharma Annual report: Q4 2025
Ascendis Pharma has published its Q4 2025 annual report on February 11, 2026.
Ascendis Pharma Earnings release: Q4 2025
Ascendis Pharma released its Q4 2025 earnings on February 11, 2026, summarizing the period's financial results.
Ascendis Pharma Reports Fourth Quarter and Full-Year 2025 Financial Results
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...
Ascendis Pharma to Report Full Year 2025 Financial Results and Provide Business Update on February 11, 2026
COPENHAGEN, Denmark, Feb. 04, 2026 (GLOBE NEWSWIRE) -- Ascendis Pharma A/S (Nasdaq: ASND) today announced it plans to report full year 2025 financial results and provide a business update on Wednesday...
Ascendis Pharma Transcript: 44th Annual J.P. Morgan Healthcare Conference
2025 revenue reached $1.86B, with strong cash reserves and no major debt. Elevidys and PMOs drive growth, while next-gen siRNA pipeline advances. Focus in 2026 is on expanding Elevidys access, early intervention, and progressing key R&D milestones.