Edwards Lifesciences Reports Third Quarter Results

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IRVINE, Calif., October 24, 2024--(BUSINESS WIRE)--Edwards Lifesciences (NYSE: EW) today reported financial results for the quarter ended Sept. 30, 2024.

Highlights and Outlook

  • Q3 sales from continuing operations grew 9%; constant currency1 sales grew 10%

  • Q3 TAVR sales grew 6%; constant currency1 sales grew 7%

  • TMTT sales grew 73%; PASCAL and EVOQUE commercial launches continue to progress well

  • Q3 EPS of $5.13; adjusted1 EPS of $0.67

  • Completed sale of Critical Care in Q3, resulting in significant one-time gain

  • Pivotal TAVR and TMTT clinical evidence to be presented next week at TCT

  • Completed enrollment in CLASP IITR trial for PASCAL tricuspid

  • First implants in the JOURNEY pivotal trial with the Edwards J-Valve AR system

  • Reiterated 2024 full year sales guidance ranges for total company, TAVR, TMTT and Surgical

"In the third quarter, we took important actions to sharpen our focus on structural heart by divesting Critical Care and investing in platforms to impact more patients and position Edwards for sustainable growth," said Bernard Zovighian, CEO. "Third quarter total company sales growth from continuing operations of 10% reflected strong contributions from both TAVR and our rapidly growing TMTT product group. Results from continuing operations were slightly ahead of our guidance expectations. As we look ahead, we see expanded opportunities to meet the needs of a highly diverse group of patients suffering from aortic stenosis, aortic regurgitation, mitral and tricuspid disease, and structural heart failure."

Transcatheter Aortic Valve Replacement (TAVR)

In the third quarter, the company reported TAVR sales of $1.0 billion, which grew 6%. Edwards’ strong competitive position and pricing remained stable globally.

In the U.S., Edwards’ year-over-year third quarter TAVR sales growth rate was in-line with the company’s global TAVR constant currency growth rate. Although hospitals and physicians continue to acknowledge heart team capacity constraints nationally, it is encouraging that many hospitals are exploring additional investments to address future workflow needs to manage these patients. In Europe, the company continues its introduction of the SAPIEN 3 Ultra RESILIA valve and continues to be pleased with the exceptional patient outcomes. Additionally, Edwards received CE Mark approval for its Alterra system for congenital heart patients. The company believes this will result in quality-of-life improvements and a reduction in the number of procedures that these younger patients will require over their lifetimes.