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Ascendis Pharma (ASND) investor relations material
Ascendis Pharma Q2 2026 earnings summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.Executive summary
Achieved key milestones and strong demand for TransCon products, driving transformation into a leading global biopharma.
Q2 2026 product revenue reached €315 million, up 105% year-over-year, driven by strong demand for YORVIPATH, SKYTROFA, and YUVIWEL.
SKYTROFA, YORVIPATH, and YUVIWEL are positioned as long-term growth drivers, with global commercialization and label expansion opportunities.
Significant pipeline progress included long-term data presentations, completion of pivotal trial enrollment, and regulatory milestones.
Settled all convertible notes and was added to multiple Russell U.S. Indexes.
Financial highlights
Q2 2026 total product revenue reached EUR 315 million, more than doubling year-over-year.
Total Q2 2026 revenue was €339 million, including €24 million in non-product collaboration revenue and a €17 million milestone for TransCon CNP.
YORVIPATH revenue was EUR 252 million, SKYTROFA EUR 55 million, and YUVIWEL EUR 8 million in its first quarter.
Q2 net profit was EUR 207 million; non-IFRS net profit was EUR 61 million.
Cash and cash equivalents as of June 30, 2026, were €812 million, up from €616 million at year-end 2025.
Outlook and guidance
Expect YORVIPATH growth and performance to remain consistent with prior quarters.
SKYTROFA revenue expected to remain stable in the U.S.; UBEGLA showing strong early demand.
On track to achieve EUR 5 billion in revenues by 2030, with potential to exceed EUR 10 billion in the next decades.
Projecting more than EUR 500 million in operating cash flow for 2026.
Anticipates EMA decision on YUVIWEL in Q4 2026 and plans to initiate Phase 3 trials for TransCon CNP monotherapy and combination therapy in H2 and Q4 2026.
- Four-year data show sustained efficacy, improved renal function, and good tolerability for palopegteriparatide.ASND
Study result presentation - Three-year data show sustained efficacy, renal benefits, and good tolerability for palopegteriparatide.ASND
Study result presentation - TransCon CNP sustained growth and improved limb alignment over 104 weeks in achondroplasia.ASND
Study result presentation - TransCon PTH achieved long-term efficacy and safety, enabling independence from conventional therapy.ASND
Study result presentation - TransCon PTH enabled long-term independence from conventional therapy with sustained efficacy and safety.ASND
Study result presentation - Navepegritide provided sustained growth benefits and a favorable safety profile through 104 weeks.ASND
Study result presentation - Combination therapy delivered transformative growth and proportionality benefits in achondroplasia.ASND
Study update presentation - Navepegritide maintained growth velocity and safety in children with achondroplasia through 104 weeks.ASND
Study result presentation - Combination therapy achieved unprecedented growth efficacy and safety, with strong U.S. launch momentum.ASND
Study update presentation
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