Press releases

IRVINE, Calif., July 23, 2020 -- Edwards Lifesciences Corporation (NYSE: EW), the global leader in patient-focused innovations for structural heart disease and critical care monitoring, today reported financial results for the quarter ended June 30, 2020.

Second Quarter Highlights and Outlook

• Sales declined 15% to $925 million; underlying¹ sales declined 14%
• TAVR sales declined 12%; underlying¹ sales declined 11%
• Previously announced IP settlement resulted in $368 million charge
• EPS was $(0.20); adjusted¹ EPS decreased 26% to $0.34
• Received FDA approval to initiate EVOQUE tricuspid replacement pivotal trial
• 2020 sales guidance reiterated: $4.0 billion to $4.5 billion
• 2020 adjusted EPS guidance increased: $1.75 to $1.95 from $1.58 to $1.75

"Even with the heroic efforts of the healthcare community, we know that this remains a very difficult time for the patients we serve as they continue to weigh the risk of COVID-19 against the severe effects of progressive heart valve disease.  Edwards is committed to providing the opportunity for faster procedures, shorter hospital stays, and exceptional patient outcomes," said Michael A. Mussallem, chairman and CEO.  "Irrespective of the unpredictable surges of this deadly pandemic, there is growing recognition that valve therapy should not be postponed as these patients have an urgent need."

Second Quarter 2020 Results
Sales for the quarter ended June 30, 2020 were $925 million, a decrease of 15% over the prior year, or down 14% on an underlying basis.  Diluted earnings per share for the quarter were negative $0.20, while adjusted earnings per share decreased 26% to $0.34.

Transcatheter Aortic Valve Replacement (TAVR)

For the quarter, the company reported global TAVR sales of $594 million, a decrease of 12% over the second quarter last year, or down 11% on an underlying basis. Globally, average selling prices were stable.

"As expected, sales were depressed in April as patients and providers turned their focus to the pandemic response.  However, we were encouraged by steady improvement in procedure volumes throughout May and June, when approximately 90% of our active sites performed TAVR cases.  This is a testament to the dedicated heart teams and our committed clinical field teams.  We hear from a number of clinicians that new patients are increasingly entering the system as they seek treatment for severe aortic stenosis," said Mussallem.

Transcatheter Mitral and Tricuspid Therapies (TMTT)

In the mitral position, Edwards is developing repair therapies with PASCAL and Cardioband as well as replacement therapies with the SAPIEN M3 and the EVOQUE system.  In the tricuspid position, the company is pursuing the PASCAL and Cardioband repair therapies and the EVOQUE system for use in tricuspid replacement.  The company has early commercial sales in Europe with several of these therapies, and is advancing each of these platforms, including five pivotal studies underway in the U.S.

Second quarter TMTT sales were $6 million, and Edwards was pleased to recently announce an intellectual property agreement which allows the company to fully dedicate time and resources to helping patients.

As previously announced, last quarter the company temporarily paused new enrollments for its active mitral and tricuspid pivotal clinical trials.  In consultation with investigators and hospitals, more than half of the company's trial sites have been re-activated and are beginning to treat patients.  The company anticipates enrollment in CLASP IID/IIF and CLASP II TR trials will continue to increase in the third and fourth quarters and is still targeting U.S. approval of PASCAL device for patients with degenerative mitral regurgitation in 2022.

The company is pleased to announce FDA approval to initiate a pivotal study for the EVOQUE tricuspid replacement system, which is designed to gain U.S. approval and has breakthrough device designation from the FDA.  The TRISCEND II study is a prospective, multi-center, randomized pivotal clinical trial to evaluate the EVOQUE system compared to optimal medical therapy alone in patients with severe tricuspid regurgitation.

Surgical Structural Heart and Critical Care

Surgical Structural Heart sales for the quarter were $161 million, a decrease of 26% compared to the second quarter of 2019, or down 25% on an underlying basis.  Second quarter sales were primarily impacted by COVID-19, while ongoing adoption of TAVR also contributed to U.S. surgical aortic valve procedure headwinds. The company remains encouraged by clinician enthusiasm for Edwards' resilient tissue valves, both the INSPIRIS RESILIA aortic valve and the recently FDA-approved KONECT RESILIA aortic valved conduit.  Additionally, the company reported successful completion of the first commercial cases of the HARPOON mitral valve repair system in Europe.

Critical Care sales were $164 million for the quarter, representing a decrease of 11% versus the second quarter of 2019, or down 10% on an underlying basis.  Increased demand for TruWave disposable pressure monitoring devices used in the ICU remained strong in the second quarter, but was not sufficient to offset the COVID-driven impact of delayed elective procedures.  The company also experienced a decline in HemoSphere advanced monitoring platform orders in the U.S. as hospitals continue to limit their capital spending as a result of COVID-19.

Additional Financial Results

For the quarter, the company's adjusted gross margin was 74.4%, down from 76.4% in the prior year quarter. This year's rate included incremental costs associated with responding to COVID-19, and a negative impact from foreign exchange.

Selling, general and administrative expenses in the second quarter were $275 million, or 29.7% of sales, compared to $308 million in the prior year. This reduced spending resulted from the impact of COVID-19, which interrupted the company's planned flow of operating expenses.

Research and development expenses in the second quarter were $182 million, or 19.7% of sales, compared to $192 million in the prior year.  This decrease was primarily the result of high clinical spending in the prior year, as well as reduced current year clinical trial activity due to COVID-19.

Free cash flow for the second quarter was $123 million, defined as cash flow from operating activities of $231 million, less capital spending of $108 million.

Cash and investments totaled $1.7 billion at June 30, 2020.  Total debt was $595 million.

Outlook

The company's guidance assumes that a progressive recovery is likely during the second half of the year. The company's sales grew 19% in the second of half of 2019, so year-over-year comparisons will remain challenging. Even so, Edwards expects sales in the third quarter to return to 2019 levels, and for sales to start growing again in the fourth quarter.

Overall, 2020 sales guidance for Edwards continues to be $4.0 to $4.5 billion. For the third quarter of 2020, the company projects total sales to be between $1.0 and $1.2 billion. The company now expects full-year 2020 adjusted earnings per share of $1.75 to $1.95 on a post-split basis, versus previous guidance of $1.58 to $1.75, or on a pre-split basis, $4.75 to $5.25.

"Due to the unpredictability of COVID-19, including additional waves and isolated flare ups and the associated impact on the healthcare system, we are preparing to deal with the ups and downs of this pandemic for the foreseeable future.  Because of the severe condition of the patients we serve and our strong patient-focused team, I remain confident in our ability to continue to successfully deliver during this global crisis," said Mussallem.

About Edwards Lifesciences

Edwards Lifesciences, based in Irvine, Calif., is the global leader of patient-focused medical innovations for structural heart disease and critical care monitoring.  We are driven by a passion for patients, dedicated to improving and enhancing lives through partnerships with clinicians and stakeholders across the global healthcare landscape. For more information, visit Edwards.com and follow us on Facebook, Instagram, LinkedIn, Twitter and YouTube.

Conference Call and Webcast Information

Edwards Lifesciences will be hosting a conference call today at 2:00 p.m. PT to discuss its second quarter results.  To participate in the conference call, dial (877) 704-2848 or (201) 389-0893.  For 72 hours following the call, an audio replay can be accessed by dialing (877) 660-6853 or (201) 612-7415 and using conference number 13705594.  The call will also be available via live or archived webcast on the "Investor Relations" section of the Edwards web site at ir.edwards.com or www.edwards.com.

This news release includes forward-looking statements within the meaning of Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934.  These forward-looking statements can sometimes be identified by the use of words such as "may," "will," "should," "anticipate," "believe," "plan," "project," "estimate," "potential," "predict," "early clinician feedback," "expect," "intend," "guidance," "outlook," "optimistic," "aspire," "confident"  or other forms of these words or similar expressions and include, but are not limited to, statements made by Mr. Mussallem, third quarter and full year 2020 financial guidance, trial enrollment numbers, rate of new patients entering the system, success in navigating the global crisis, future therapy opportunities and information in the Outlook section.  Statements of past performance, efforts, or results about which inferences or assumptions may be made can also be forward-looking statements and are not indicative of future performance or results.  Forward-looking statements are based on estimates and assumptions made by management of the company and are believed to be reasonable, though they are inherently uncertain, difficult to predict, and may be outside of the company's control; these assumptions include, but are not limited to, that the most severe impacts of COVID-19 have passed and that the second half of the year will demonstrate a progressive recovery.  The company's forward-looking statements speak only as of the date on which they are made and the company does not undertake any obligation to update any forward-looking statement to reflect events or circumstances after the date of the statement.  If the company does update or correct one or more of these statements, investors and others should not conclude that the company will make additional updates or corrections.

Forward-looking statements involve risks and uncertainties that could cause actual results or experience to differ materially from that expressed or implied by the forward-looking statements.  Factors that could cause actual results or experience to differ materially from that expressed or implied by the forward-looking statements include risk and uncertainties associated with COVID-19 pandemic, clinical trial or commercial results or new product approvals and therapy adoption, particularly in TAVR and TMTT; unpredictability of product launches; competitive dynamics; changes to reimbursement for the company's products; the company's success in developing new products and avoiding manufacturing and quality issues; the impact of currency exchange rates; the timing or results of R&D and clinical trials; unanticipated actions by the U.S. Food and Drug Administration and other regulatory agencies; unexpected litigation impacts or expenses; and other risks detailed in the company's filings with the Securities and Exchange Commission, including its Annual Report on Form 10-K for the year ended December 31, 2019 and its Quarterly Report on Form 10-Q for the quarter ended March 31, 2020.  These filings, along with important safety information about our products, may be found at edwards.com.

Edwards, Edwards Lifesciences, the stylized E logo, Cardioband, CLASP, EVOQUE, HARPOON, HemoSphere, INSPIRIS, INSPIRIS RESILIA, KONECT, KONECT RESILIA, PASCAL, RESILIA, SAPIEN, SAPIEN M3, TRISCEND, and TruWave are trademarks of Edwards Lifesciences Corporation or its affiliates.  All other trademarks are the property of their respective owners.  This statement is made on behalf of Edwards Lifesciences Corporation and its subsidiaries.

 

 

 

EDWARDS LIFESCIENCES CORPORATION
Non-GAAP Financial Information

To supplement the consolidated financial results prepared in accordance with Generally Accepted Accounting Principles ("GAAP"), the Company uses non-GAAP historical financial measures.  Management makes adjustments to the GAAP measures for items (both charges and gains) that (a) do not reflect the core operational activities of the Company, (b) are commonly adjusted within the Company's industry to enhance comparability of the Company's financial results with those of its peer group, or (c) are inconsistent in amount or frequency between periods (albeit such items are monitored and controlled with equal diligence relative to core operations).  The Company uses the term "adjusted sales" or "underlying growth rate" when referring to non-GAAP sales information, which excludes foreign exchange rate fluctuations and includes the prior year sales results of a business acquired as if the acquisition had occurred at the beginning of the earliest period presented. The Company uses the term "adjusted" to also exclude intellectual property litigation expenses, amortization of intangible assets, fair value adjustments to contingent consideration liabilities arising from acquisitions, significant charges associated with transcatheter aortic valve replacement ("TAVR") inventory write offs, and the purchase of intellectual property.

Management uses non-GAAP financial measures internally for strategic decision making, forecasting future results, and evaluating current performance.  These non-GAAP financial measures are used in addition to, and in conjunction with, results presented in accordance with GAAP and reflect an additional way of viewing aspects of the Company's operations by investors that, when viewed with its GAAP results, provide a more complete understanding of factors and trends affecting the Company's business and facilitate comparability to historical periods.

Non-GAAP financial measures are not prepared in accordance with GAAP; therefore, the information is not necessarily comparable to other companies and should be considered as a supplement to, and not as a substitute for, or superior to, the corresponding measures calculated in accordance with GAAP.  A reconciliation of non-GAAP historical financial measures to the most comparable GAAP measure is provided in the tables below.

Fluctuations in exchange rates impact the comparative results and sales growth rates of the Company's underlying business. Management believes that excluding the impact of foreign exchange rate fluctuations from its sales growth provides investors a more useful comparison to historical financial results. The impact of foreign exchange rate fluctuations has been detailed in the "Reconciliation of Sales by Product Group and Region."

Guidance for sales and sales growth rates is provided on an "underlying basis," and projections for diluted earnings per share, net income and growth, gross profit margin, taxes, and free cash flow are also provided on a non-GAAP basis as adjusted for the items identified above due to the inherent difficulty in forecasting such items.  The Company is not able to provide a reconciliation of the non-GAAP guidance to comparable GAAP measures due to the unknown effect, timing, and potential significance of special charges or gains, and management's inability to forecast charges associated with future transactions and initiatives.

Management considers free cash flow to be a liquidity measure which provides useful information to management and investors about the amount of cash generated by business operations, after deducting payments for capital expenditures, which can then be used for strategic opportunities or other business purposes including, among others, investing in the Company's business, making strategic acquisitions, strengthening the balance sheet, and repurchasing stock.

The items described below are adjustments to the GAAP financial results in the reconciliations that follow:

Litigation Settlement - In the second quarter of 2020, the Company recorded a $367.9 million charge to settle certain patent litigation related to transcatheter mitral and tricuspid repair products.

TAVR Inventory Write Off - In the second quarter of 2019, the Company recorded a $46.2 million charge, primarily comprised of the write off of inventory in response to strategic decisions regarding its TAVR portfolio.

Intellectual Property Litigation Expenses - The Company incurred intellectual property litigation expenses of $12.5 million and $4.6 million in the first quarter of 2020 and 2019, respectively, and $12.0 million and $7.0 million in the second quarter of 2020 and 2019, respectively.

Change in Fair Value of Contingent Consideration Liabilities, net - The Company recorded income of $2.2 million and expense of $6.7 million in the first quarter of 2020 and 2019, respectively, and expenses of $19.6 million and $8.0 million in the second quarter of 2020 and 2019, respectively, related to changes in the fair value of its contingent consideration liabilities arising from acquisitions.

Amortization of Intangible Assets - The Company recorded amortization expense related to developed technology, patents and trademarks in the amount of $1.7 million and $0.5 million in the first quarter of 2020 and 2019, respectively, and $1.3 million and $1.2 million in the second quarter of 2020 and 2019, respectively.

Purchase of Intellectual Property - The Company recorded a $24.0 million charge in the first quarter of 2019 related to the acquisition of early-stage transcatheter intellectual property and associated clinical and regulatory experience.

(Benefit from) Provision for Income Taxes - The income tax impact of the expenses and gains discussed above is based upon the items' forecasted effect upon the Company's full year effective tax rate.  Adjustments to forecasted items unrelated to these expenses and gains, as well as impacts related to interim reporting, will have an effect on the income tax impact of these items in subsequent periods.

 

 

 

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