Ascendis Pharma A/S (FRA:A71)

Germany flag Germany · Delayed Price · Currency is EUR
206.00
+2.00 (0.98%)
Last updated: Apr 17, 2026, 8:00 PM CET
Market Cap12.18B
Revenue (ttm)720.13M +98.0%
Net Income-228.03M
EPS-3.76
Shares Outn/a
PE Ration/a
Forward PE46.31
Dividendn/a
Ex-Dividend Daten/a
Volumen/a
Average Volume3
Open206.00
Previous Close204.00
Day's Range206.00 - 206.00
52-Week Range137.00 - 210.00
Betan/a
RSI58.10
Earnings DateApr 30, 2026

About Ascendis Pharma

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]

Industry Biological Products, Except Diagnostic Substances
Founded 2006
Employees 1,189
Stock Exchange Frankfurt Stock Exchange
Ticker Symbol A71
Full Company Profile

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 Statements

News

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...

2 days ago - GlobeNewsWire

Ascendis Pharma (ASND) Begins Trading on Nasdaq Global Select Market

Ascendis Pharma (ASND) Begins Trading on Nasdaq Global Select Market

3 days ago - GuruFocus

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...

3 days ago - GlobeNewsWire

Ascendis Pharma (ASND) Shifts to Nasdaq Direct Listing

Ascendis Pharma (ASND) Shifts to Nasdaq Direct Listing

15 days ago - GuruFocus

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...

15 days ago - GlobeNewsWire

ASND: Promising Results from Ascendis Pharma's TransCon Therapies in Achondroplasia

ASND: Promising Results from Ascendis Pharma's TransCon Therapies in Achondroplasia

15 days ago - GuruFocus

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

15 days ago - GlobeNewsWire

FDA Grants Orphan Drug Exclusivity To Ascendis Pharma's YUVIWEL In Achondroplasia

(RTTNews) - Ascendis Pharma A/S (ASND), a biopharmaceutical company, announced that its lead asset, YUVIWEL or Navepegritide, in the treatment of Achondroplasia in children aged two years and older, h...

16 days ago - Nasdaq

Ascendis Pharma (ASND) Gains FDA Orphan Drug Exclusivity for Yuviwel

Ascendis Pharma (ASND) Gains FDA Orphan Drug Exclusivity for Yuviwel

17 days ago - GuruFocus

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

17 days ago - GlobeNewsWire

Ascendis Pharma Reports Positive Results From Phase 2 Trial For TransCon HGH In Turner Syndrome

(RTTNews) - Ascendis Pharma A/S (ASND) announced positive topline 52-week results from its Phase 2 trial, dubbed New InsiGHTS, evaluating once-weekly TransCon hGH (Lonapegsomatropin) versus daily soma...

5 weeks ago - Nasdaq

Ascendis Pharma (ASND) Reports Positive Phase 2 Trial Results for Turner Syndrome Treatment

Ascendis Pharma (ASND) Reports Positive Phase 2 Trial Results for Turner Syndrome Treatment

5 weeks ago - GuruFocus

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...

5 weeks ago - GlobeNewsWire

Analyst Jefferies Elevates Ascendis Pharma (ASND) Price Target to $290 | ASND Stock News

Analyst Jefferies Elevates Ascendis Pharma (ASND) Price Target to $290 | ASND Stock News

5 weeks ago - GuruFocus

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...

5 weeks ago - Wallstreet:Online

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...

5 weeks ago - GlobeNewsWire

Ascendis Pharma (ASND) Receives Analyst's Rating Update with Raised Price Target | ASND Stock News

Ascendis Pharma (ASND) Receives Analyst's Rating Update with Raised Price Target | ASND Stock News

7 weeks ago - GuruFocus

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...

7 weeks ago - Wallstreet:Online

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...

7 weeks ago - GlobeNewsWire

Ascendis Wins FDA Approval For Rare Disease Therapy

Ascendis Pharma A/S (NASDAQ: ASND) shares are up during Monday’s premarket session following the FDA’s approval of Yuviwel (navepegritide; developed as TransCon CNP), the first and only once-weekly t...

7 weeks ago - Benzinga

FDA Grants Accelerated Approval To Ascendis Pharma's YUVIWEL For Achondroplasia In Children

(RTTNews) - Ascendis Pharma A/S (ASND) announced that the U.S. Food & Drug Administration (FDA) has granted accelerated approval for YUVIWEL (navepegritide; developed as TransCon CNP), the first and o...

7 weeks ago - Nasdaq

FDA Approves Ascendis Pharma's Yuviwel for Pediatric Dwarfism Treatment

FDA Approves Ascendis Pharma's Yuviwel for Pediatric Dwarfism Treatment

7 weeks ago - GuruFocus

FDA Approves Ascendis Pharma's (ASND) Weekly Treatment for Achondroplasia

FDA Approves Ascendis Pharma's (ASND) Weekly Treatment for Achondroplasia

7 weeks ago - GuruFocus

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.

7 weeks ago - Reuters

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...

7 weeks ago - GlobeNewsWire