Strong Revenue Growth for YORVIPATH
YORVIPATH revenue in Q2 reached EUR 103 million, more than double from Q1 2025, with strong U.S. uptake and continued international growth.
FDA Approval and Expansion for SKYTROFA
SKYTROFA received FDA approval for adult growth hormone deficiency, with Q2 revenue of EUR 51 million, and plans for further label expansion.
Priority Review for TransCon CNP
FDA granted priority review for TransCon CNP with a PDUFA date of November 30, recognizing its potential to significantly improve treatment for achondroplasia.
Progress in Combination Therapy for Achondroplasia
Interim Phase II results showed a boost in linear growth and body proportionality improvement in achondroplasia patients using a combination of TransCon CNP and TransCon Growth Hormone.
Strong Financial Position
Total Q2 product revenue was EUR 153.7 million, with expectations for Ascendis to become cash flow positive on a quarterly basis this year.