Ascendis Pharma (ASND) Study result presentation summary
Event summary combining transcript, slides, and related documents.
Study result presentation summary
12 Aug, 2026Product overview and mechanism
Navepegritide is a once-weekly prodrug of C-type natriuretic peptide (CNP) designed for continuous exposure, binding NPR-B to counteract FGFR3 signaling in achondroplasia.
Approved by the FDA to increase linear growth in children aged 2 years and older with achondroplasia and open epiphyses.
Trial design and population
Randomized, double-blind trial in treatment-naïve children aged 2–11 years, followed by an open-label extension (OLE) to Week 104.
Subgroup analysis focused on children aged 5 years or older at enrollment.
Baseline demographics were balanced between navepegritide and placebo groups, including age, sex, and height.
Efficacy results
At Week 52, navepegritide significantly increased annualized growth velocity (AGV) compared to placebo: +1.49 cm/year in all children and +1.78 cm/year in those aged ≥5 years (both p<0.0001).
AGV improvements were maintained through Week 104 in both the overall and ≥5-year-old subgroups.
Height Z-scores (achondroplasia-specific and CDC-based) continued to improve through Week 104, with greater gains in children aged ≥5 years.
Latest events from Ascendis Pharma
- Q2 2026 revenue more than doubled to €339 million, with net profit of €207 million.ASND
Q2 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 - 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