Healthcare & Biotech

SHERIDAN, WYOMING – May 7, 2025 – Baxter International Inc. (NYSE:BAX), a global leader in medical technologies, has announced that its Board of Directors has declared a quarterly cash dividend of $0.17 per share of common stock. This dividend is payable on July 1, 2025, to shareholders of record as of May 30, 2025. The indicated annual dividend rate is set at $0.68 per share.

Strategic Commitment to Shareholders

As part of its ongoing commitment to delivering value to its shareholders, Baxter continues to maintain a strong dividend policy. The company’s decision to declare this quarterly cash dividend reflects both the stability of its financial performance and its dedication to providing consistent returns to its investors.

SHERIDAN, WYOMING – May 7, 2025 – Baxter International Inc. (NYSE: BAX), a leading global medtech company, has announced its first-quarter financial results for 2025, reflecting solid performance driven by strategic transformation initiatives. The company’s results indicate continued growth across its core business segments, positioning Baxter for long-term value creation despite global macroeconomic uncertainty.

Strategic Transformation and Focus on Execution

"Our solid performance in the first quarter of 2025 reflects the ongoing impact of our transformation journey," said Brent Shafer, chair and interim CEO of Baxter. "Baxter today is a more focused and agile organization, well-positioned to drive enhanced value for patients, healthcare providers, customers, and shareholders through our reinvigorated emphasis on execution, innovation, and profitable growth."

SHERIDAN, WYOMING – May 7, 2025 – Baxter International Inc. (NYSE: BAX), a global leader in medical technology, will host a conference call on Thursday, May 8, 2025, at 7:30 a.m. Central Time to discuss its first-quarter 2025 financial results. Investors, analysts, and other stakeholders are invited to participate in the call by pre-registering through the provided link to receive the necessary call-in information.

SHERIDAN, WYOMING – May 7, 2025 – Baxter International Inc., a global leader in advancing surgical innovation, has announced the launch of its Hemopatch Sealing Hemostat with room temperature storage at a symposium in Vienna, Austria. This new product evolution significantly improves accessibility for surgeons, offering a practical and effective solution for controlling bleeding and preventing leakage during surgery. The product is now available for order throughout Europe, marking a key step forward in Baxter’s ongoing commitment to enhancing patient care.

SHERIDAN, WYOMING – May 7, 2025 – Edwards Lifesciences (NYSE: EW), a global leader in structural heart innovation, will announce its operating results for the first quarter ending March 31, 2025, after market close on Wednesday, April 23, 2025. The company will then host a conference call at 5:00 p.m. ET that same day to discuss these results in detail, providing insights into its financial performance and future strategic direction.

Conference Call Details and Participation

Edwards Lifesciences invites all interested parties to join the conference call. To participate, dial (877) 704-2848 or (201) 389-0893. For those unable to attend live, the conference call will be available for replay on the "Investor Relations" section of the Edwards website at ir.edwards.com.

About Edwards Lifesciences

SHERIDAN, WYOMING – May 7, 2025 – Edwards Lifesciences (NYSE: EW) today unveiled new eight-year clinical data, confirming the exceptional long-term performance of its RESILIA tissue technology in aortic surgical valves. The data demonstrate significant improvements in patient outcomes, reinforcing the company's leadership in structural heart solutions.

The new findings, presented at the Heart Valve Society Annual Meeting, provide compelling evidence that patients receiving aortic surgical valves with RESILIA tissue experienced significantly better long-term outcomes compared to those with non-RESILIA tissue valves. These results highlight the value of Edwards’ innovation in delivering superior durability and performance, crucial for improving patient care and reducing the need for reoperations.

SHERIDAN, WYOMING – May 7, 2025 – Edwards Lifesciences (NYSE: EW), a global leader in structural heart innovation, has announced its financial results for the first quarter ended March 31, 2025. The company delivered impressive growth across key product categories, including Transcatheter Aortic Valve Replacement (TAVR) and Transcatheter Mitral and Tricuspid Therapies (TMTT), positioning itself for continued success in the structural heart market.

Strong Sales Growth Drives First Quarter Results

In Q1 2025, Edwards Lifesciences reported total sales of $1.41 billion, reflecting a robust 6.2% increase year-over-year, or 7.9% on an adjusted basis. The company also posted a solid earnings per share (EPS) of $0.622, with adjusted EPS of $0.64, reinforcing its strong financial position.

SHERIDAN, WYOMING – May 7, 2025 – Edwards Lifesciences (NYSE: EW) has announced the U.S. Food and Drug Administration (FDA) approval of its transcatheter aortic valve replacement (TAVR) therapy, the SAPIEN 3 platform, for use in patients with asymptomatic severe aortic stenosis (AS). This groundbreaking approval marks the first-ever FDA authorization for TAVR in asymptomatic patients, potentially transforming the treatment landscape for those with this critical condition.

SHERIDAN, WYOMING – May 7, 2025 – Edwards Lifesciences (NYSE: EW) has announced its participation in the highly anticipated BofA Securities 2025 Health Care Conference, scheduled for Tuesday, May 13, 2025. The company's leadership, including CEO Bernard Zovighian and CFO Scott Ullem, will take part in a fireside chat at 10:40 a.m. Pacific Time. The discussion will be accessible to investors and healthcare professionals through a live webcast available on the Edwards Lifesciences investor relations website at http://ir.edwards.com. An archived version of the session will be accessible later in the day for those unable to attend the live event.

SHERIDAN, WYOMING – May 7, 2025 – A new randomized controlled trial (RCT) has revealed significant advancements in rotator cuff repair, showing that augmentation with the REGENETEN Bioinductive Implant can substantially reduce the risk of re-tears, offering hope for better outcomes in patients undergoing full-thickness rotator cuff repairs. The study's findings have the potential to set a new standard of care in orthopedic surgery.

Understanding the Challenge of Rotator Cuff Repairs

Rotator cuff repairs are among the most commonly performed orthopedic procedures, with an estimated 750,000 surgeries taking place annually in the United States alone. However, the procedure is not without its challenges, as up to 25% of patients experience re-tears, often leading to additional treatments and prolonged recovery times.