Research analysts who have asked questions during Ascendis Pharma earnings calls.
Gavin Clark-Gartner
Evercore ISI
7 questions for ASND
Jessica Fye
JPMorgan Chase & Co.
7 questions for ASND
Tazeen Ahmad
Bank of America
7 questions for ASND
Derek Archila
Wells Fargo
6 questions for ASND
Leland Gershell
Oppenheimer & Co. Inc.
6 questions for ASND
Paul Choi
Goldman Sachs
6 questions for ASND
David Lebowitz
Citigroup Inc.
5 questions for ASND
Luca Issi
RBC Capital Markets
5 questions for ASND
Yaron Werber
TD Cowen
5 questions for ASND
Ellie Merle
UBS Group AG
4 questions for ASND
Joseph Schwartz
Oppenheimer
4 questions for ASND
Li Wang Watsek
Cantor Fitzgerald
4 questions for ASND
Alex Thompson
Stifel Financial Corp.
3 questions for ASND
Daniel Bronder
Cantor Fitzgerald
3 questions for ASND
Maxwell Skor
H.C. Wainwright & Co.
3 questions for ASND
Alexander Thompson
Stifel
2 questions for ASND
Dingding Shi
Jefferies
2 questions for ASND
Faisal Khurshid
Leerink Partners
2 questions for ASND
Kalpit Patel
B. Riley Securities
2 questions for ASND
Kelly Shi
Jefferies
2 questions for ASND
Vikram Purohit
Morgan Stanley
2 questions for ASND
Yun Zhong
Wedbush Securities
2 questions for ASND
Eliana Merle
UBS
1 question for ASND
Heidi Jacobson
Leerink Partners
1 question for ASND
Joori Park
Leerink Partners
1 question for ASND
Jose Lora
Jefferies
1 question for ASND
Kyuwon Choi
Goldman Sachs
1 question for ASND
Simona Stan
Wells Fargo
1 question for ASND
Yun Zheng
Woodbush
1 question for ASND
Recent press releases and 8-K filings for ASND.
- **Ascendis Pharma A/S reported a significant increase in revenue to €720.1 million for the year ended December 31, 2025, up from €363.6 million in the prior year, primarily driven by global sales of YORVIPATH®. **
- **Despite the revenue growth, the company recorded a net loss of €228.0 million for FY 2025, an improvement from a net loss of €378.1 million in FY 2024, with basic earnings per share of (€3.76). **
- **Commercial product revenue for YORVIPATH® surged to €477.4 million in 2025 from €28.7 million in 2024, while SKYTROFA® revenue also increased to €206.2 million. **
- **The company maintained a strong liquidity position with cash and cash equivalents of €616.0 million as of December 31, 2025, and saw cash flows from operating activities improve to €53.9 million for the year. **
- **Strategic developments include the ongoing collaboration with Novo Nordisk, the commercial launch of YORVIPATH in Japan via Teijin Limited in November 2025, and VISEN Pharmaceuticals' IPO in March 2025, which generated a non-cash gain of €35.7 million for Ascendis Pharma A/S. **
- Ascendis Pharma reported Q4 2025 product revenue of €240 million and full-year 2025 product revenue of €684 million, with a Q4 2025 operating profit of €10 million.
- The company recorded a net loss of €34 million for Q4 2025 and a full-year 2025 net loss of €228 million, or €(3.76) per share.
- YORVIPATH revenue totaled €187 million for Q4 2025 and €477 million for the full year 2025, while SKYTROFA revenue was €53 million for Q4 2025 and €206 million for the full year 2025.
- As of December 31, 2025, Ascendis Pharma held a cash balance of €616 million. The company expects to generate approximately €500 million in operating cash flow in 2026 and aims for at least €5 billion in global annual product revenue by 2030.
- TransCon CNP is under FDA Priority Review with a PDUFA action goal date of February 28, 2026 , and SKYTROFA received FDA approval for adult growth hormone deficiency label expansion in July 2025. The company also plans to initiate a $120 million share repurchase program in 2026.
- Ascendis Pharma reported total revenue of EUR 248 million for Q4 2025 and EUR 720 million for the full year 2025, with Europat contributing EUR 187 million and SKYTROFA EUR 53 million in Q4. The company ended 2025 with EUR 616 million in cash and cash equivalents.
- The company expects operating cash flow of around EUR 500 million in 2026 and aspires to achieve at least EUR 5 billion in annual product revenue by 2030.
- The NDA for TransCon CNP in children with achondroplasia is under review in the US with a PDUFA date of February 28. Europat continues its global expansion, with full commercial launches expected in 10 additional new countries in 2026.
- Ascendis Pharma reported total revenue of EUR 248 million for Q4 2025 and EUR 720 million for the full year 2025.
- YORVIPATH revenue reached EUR 187 million in Q4 2025 and EUR 477 million for the full year, while SKYTROFA revenue was EUR 53 million in Q4 and EUR 206 million for the full year.
- The company ended 2025 with EUR 616 million in cash and cash equivalents and projects operating cash flow of approximately EUR 500 million in 2026, with an aspiration for at least EUR 5 billion in annual product revenue by 2030.
- Key regulatory milestones include the U.S. NDA for TransCon CNP remaining under review with a PDUFA date of February 28, and VISEN's approval of SKYTROFA in China in late January 2026.
- Ascendis Pharma reported Q4 2025 total revenue of EUR 248 million and full-year 2025 total revenue of EUR 720 million, driven by Europats revenue of EUR 187 million in Q4 and SKYTROFA revenue of EUR 53 million in Q4.
- The company ended 2025 with EUR 616 million in cash and cash equivalents, and achieved Q4 2025 operating profit of EUR 10 million and operating cash flow of EUR 73 million.
- Ascendis Pharma projects operating cash flow of approximately EUR 500 million in 2026 and aims for at least EUR 5 billion in annual product revenue by 2030.
- The NDA for TransCon CNP in children with achondroplasia has a U.S. PDUFA date of February 28, with a regulatory decision in the EU expected in Q4 2026.
- Ascendis Pharma reported strong financial performance with Q4 product revenue of approximately EUR 240 million and full-year revenue of approximately EUR 683 million.
- The company projects significant future growth, targeting over EUR 5 billion in revenue by 2030, primarily driven by Yorvipath and Skytrofa.
- Key upcoming milestones include the PDUFA date for TransCon CNP in February and a plan to buy back at least $120 million in shares this year.
- Ascendis Pharma anticipates an operating cash flow of at least EUR 500 million and is expanding its European presence for Yorvipath with 10+ new countries expected in 2026.
- Ascendis Pharma (ASND) reported total full-year product revenue of $720 million for 2025, with Yorvipath contributing $477 million and SKYTROFA $206 million. The company anticipates TransCon CNP approval in Q1 2026 and plans a $120 million share buyback. Global peak sales expectations for Yorvipath are $5-$8 billion.
- CRISPR Therapeutics highlighted its approved product Casgevy with multi-billion-dollar revenue potential and pipeline progress, including CTX310 for hypercholesterolemia, CTX611 (Factor XI siRNA) in Phase 2, and a 70% complete response rate for Zugocel (CAR-T) in oncology.
- An unnamed company (Speaker 1) reported total net product revenue of $1.86 billion for FY 2025, including $899 million from Elevidys and $966 million from PMOs. The company ended 2025 with $954 million in cash and expects to be cash flow positive throughout the decade, with biomarker data for FSHD and DM1 programs expected by the end of Q1 2026.
- Ascendis Pharma reported Q4 product revenue of approximately EUR 240 million and full-year 2025 product revenue of about EUR 683 million, primarily from Yorvipath and Skytrofa, and aims for over EUR 5 billion in revenue by 2030. The company also plans to buy back at least $120 million in shares.
- CRISPR Therapeutics announced that its approved product, Casgevy, has achieved over $100 million in revenue and shows strong momentum, with the company also highlighting CTX310 as a potential multi-billion-dollar opportunity in hypercholesterolemia.
- Sarepta Therapeutics reported full-year 2025 total net product revenue of $1.86 billion, with Elevidys contributing $899 million (9% growth) and PMOs $966 million, ending the year with $954 million in cash and cash equivalents.
- Ascendis Pharma reported Q4 2025 product revenue of approximately €240 million and FY 2025 product revenue of approximately €683 million.
- The company aims to achieve over €5 billion in annual revenue by 2030 as part of its Vision 2030 strategy, focusing on worldwide commercialization of its Endocrinology Rare Disease medicines.
- Key product YORVIPATH® (TransCon PTH) generated approximately €477 million in FY 2025 revenue and is expanding commercially in over 30 countries.
- SKYTROFA® (TransCon hGH) is approved for pediatric and adult growth hormone deficiency, with ongoing label and geographic expansion plans.
- TransCon® CNP has an FDA PDUFA date of February 28, 2026, for achondroplasia, with an EU MAA decision anticipated in Q4 2026.
- Ascendis Pharma A/S provided a business and strategic roadmap update on January 9, 2026, outlining planned 2026 key corporate milestones.
- Key regulatory updates include a U.S. PDUFA goal date of February 28, 2026, for TransCon CNP in pediatric achondroplasia, and an anticipated Q1 2026 approval decision from China's NMPA for TransCon hGH in pediatric growth hormone deficiency.
- The company announced positive Week 52 topline results from the Phase 2 COACH Trial for TransCon CNP + TransCon hGH combination therapy on January 8, 2026, demonstrating improvements in annualized growth velocity and body proportionality.
- The Board of Directors authorized a $120 million Share Repurchase Program.
Quarterly earnings call transcripts for Ascendis Pharma.
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