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Edwards Lifesciences Corporation (EW) Welcomes Newly Updated ESC/EACTS Guidelines for Severe Aortic Stenosis (AS)
Yahoo Finance· 2025-09-10 08:52
Group 1 - Edwards Lifesciences Corporation (EW) has positively responded to the updated ESC/EACTS guidelines for severe aortic stenosis (AS), which recommend earlier treatment for asymptomatic patients and lower the TAVR age threshold to 70 [2][4] - The company is the only one with an approved TAVR indication for asymptomatic severe AS in the U.S. and Europe, emphasizing its critical EARLY TAVR trial and the CE Mark for its SAPIEN 3 platform [3][4] - Data from the TRISCEND II study presented at the ESC Congress indicates that the EVOQUE tricuspid valve replacement significantly reduced heart failure hospitalizations at 18 months, reinforcing the company's leadership in structural heart innovation [4] Group 2 - Edwards Lifesciences specializes in structural heart therapies, pioneering innovations in TAVR, mitral, and tricuspid procedures to improve patient outcomes and expand access globally [5]
Edwards' New Late-Breaking Data on Severe AS Expected to Boost Stock
ZACKS· 2025-05-23 13:55
Company Insights - Edwards Lifesciences announced new economic and clinical evidence on severe aortic stenosis (AS) at EuroPCR 2025, indicating that early intervention before symptoms develop can reduce healthcare costs by $36,000 per patient and improve patient outcomes [1][5] - The company has a market capitalization of $44.64 billion and an earnings yield of 3.2%, outperforming the industry average of -2.8% [4] - Edwards' stock closed at $74.79, down 1.7% from the previous close, but the company is expected to maintain positive market sentiment due to its commitment to TAVR innovation and strong clinician adoption of SAPIEN technology [3] Industry Insights - The AS treatment market is projected to reach $8.6 billion in 2024, with a compound annual growth rate (CAGR) of 7.4% by 2034, driven by advancements in medical technology and increased awareness among healthcare professionals and patients [7][8] - The recent FDA approval for the SAPIEN 3 platform for asymptomatic severe AS patients is based on data from the EARLY TAVR trial, which showed superior outcomes compared to traditional clinical surveillance [10] - The company continues to benefit from the strong uptake of its premium RESILIA portfolio in the surgical segment, which includes products like INSPIRIS, MITRIS, and KONECT [3]