Nevro Reports Fourth Quarter and Full Year 2020 Financial Results
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REDWOOD CITY, Calif., Feb. 24, 2021 /PRNewswire/ -- Nevro Corp. (NYSE: NVRO), a global medical device company that is providing innovative, evidence-based solutions for the treatment of chronic pain, today reported its financial results for the fourth quarter and full year ended December 31, 2020 and provided 2021 guidance.
- Fourth Quarter 2020 Worldwide Revenue of $109.7 Million; Decrease of 4% Compared to Prior Year
- Fourth Quarter 2020 Net Loss from Operations of $0.9 Million; Fourth Quarter 2020 Non-GAAP Adjusted EBITDA of $15.7 Million
- Company Provides Full-Year 2021 Revenue Guidance of $430 Million to $450 Million
- Company Provides Full-Year 2021 Non-GAAP Adjusted EBITDA Guidance of $0 Million to $15 Million
- Submitted PMA Supplement to FDA in December Seeking Approval of Senza® System for Treatment of Chronic Pain Associated with Painful Diabetic Neuropathy (PDN)
- Senza-PDN and Senza-NSRBP Randomized Clinical Data Presented at 2021 North American Neuromodulation Society Virtual Meeting Reinforce Significant Benefits of Nevro's HF10® Therapy
Fourth Quarter 2020 Financial Overview
Worldwide revenue for the fourth quarter of 2020 was $109.7 million, a decrease of 4% compared to $114.4 million in the prior year period. On a sequential basis, fourth quarter worldwide revenue increased 1% compared to the third quarter of 2020. U.S. revenue in the fourth quarter of 2020 was $94.6 million, a decrease of 3% compared to $97.9 million in the prior year period. On a sequential basis, fourth quarter U.S. revenue increased 4% compared to the third quarter of 2020. In the fourth quarter of 2020, total U.S. permanent implant procedures decreased 1%, with trial procedures declining 8% compared to the prior year period. Nearly 200 scheduled U.S. permanent implant procedures were cancelled in the fourth quarter, with the majority occurring in the month of December. In late November and all of December, reductions in both trials and perms were caused by a combination of patient reluctance to move forward due to COVID-related issues and facility constraints on elective procedures due to COVID resurgence in specific geographies. International revenue was $15.1 million, a decrease of 8% on an as reported basis (14% on a constant currency basis), compared to $16.5 million in the prior year period. Both U.S. and international revenue was meaningfully impacted by the resurgence of COVID activity in the second half of the quarter.
"While the COVID-impacted environment continues to be a difficult one, we believe we continued to capture market share in the core lower back and leg pain market throughout 2020 with our best-in-class HF10 SCS technology, the expanded Omnia platform, superior clinical data and sharpened commercial execution," said D. Keith Grossman, Chairman, CEO and President of Nevro. "I believe we are well positioned for attractive and sustainable growth as the pressure of COVID on our business subsides. We expect pent-up patient demand to come back into the system as infection rates decline, vaccine availability improves and the market reverts to normalcy. In addition, we are excited about expanded growth opportunities to treat Painful Diabetic Neuropathy and Non-Surgical Refractory Back Pain, which will bring our HF10 therapy to potentially many more patients who are unable to find relief with currently available treatment options."
Gross profit for the fourth quarter of 2020 was $78.0 million, a decrease of 4% compared to $81.3 million in the prior year period. The decrease in gross profit was primarily attributable to the year-over-year reduction in revenue. Gross margin was 71% in the fourth quarter of 2020, consistent with the prior year period.
Operating expenses for the fourth quarter of 2020 were $78.9 million, a 15% decrease compared to $92.9 million in the prior year period. The year-over-year decrease in operating expenses was primarily related to a decrease in clinical trial expenses related to PDN and NSRBP studies, lower personnel and travel expenses, as well as management's continued initiatives to drive leverage throughout the business which had begun well before COVID. Legal expenses associated with patent litigation were $5.1 million for the fourth quarter of 2020, compared to $1.7 million in the prior year period.
Net loss from operations for the fourth quarter of 2020 was $0.9 million, a 93% improvement compared to a loss of $11.7 million in the prior year period. Non-GAAP adjusted EBITDA for the fourth quarter of 2020 was $15.7 million, compared to $1.5 million in the prior year period. Non-GAAP adjusted EBITDA excludes certain litigation expenses, interest, taxes, and non-cash items such as stock-based compensation and depreciation and amortization. Please see the financial table below for GAAP to Non-GAAP reconciliations.
Cash, cash equivalents and short-term investments totaled $588.0 million as of December 31, 2020, an increase of $15.1 million in the fourth quarter of 2020.
Full Year 2020
Worldwide revenue for the full year 2020 was $362.0 million, a 7% decrease compared to $390.3 million in the prior year period. U.S. revenue for the full year 2020 was $311.9 million, a 4% decrease compared to $326.0 million in the prior year period. International revenue was $50.2 million, a 22% decrease as reported, or a 24% decrease on a constant currency basis, compared to $64.2 million in the prior year period. Please see financial statements for additional full year 2020 results and GAAP to Non-GAAP reconciliations.
Nevro continues to monitor and evaluate the impact the global response to the COVID pandemic has had, and will continue to have, on its operations and financial results. The guidance provided below is highly sensitive to the company's COVID recovery assumptions, which include an ongoing and steady recovery in the U.S. and key international geographies leading to more normalized case scheduling and elective procedure levels beginning in the second quarter of 2021. This guidance also assumes the impact from COVID will diminish with each sequential quarter this year as vaccine availability improves and patients begin to again seek elective care in typical levels. If these assumptions differ materially from the actual pace of COVID recovery and its impact on the company's markets, then the company may need to change or withdraw this guidance in the future.
Nevro expects first quarter of 2021 worldwide revenue of approximately $84 million to $86 million. This assumes COVID headwinds in the first two months of the first quarter of 2021, with improvement beginning in March of 2021. The company expects operating expenses in the first quarter of 2021 of approximately $83 million to $86 million, including litigation expenses and additional investment in PDN market development.
Nevro expects full year 2021 worldwide revenue of approximately $430 million to $450 million. This range assumes FDA approval of PDN at the beginning of the third quarter of 2021 and a mid-single digit million revenue contribution from PDN in 2021, with the majority generated in the fourth quarter.
For full year 2021, gross margin is expected to be approximately 69%, and operating expenses are expected to be approximately $370 million, including litigation expenses and approximately $22 million of investment in a PDN launch and market development. The company expects full year 2021 non-GAAP adjusted EBITDA of $0 million to $15 million, which compares to a non-GAAP adjusted EBITDA loss of $3.9 million in 2020. Non-GAAP adjusted EBITDA excludes certain litigation expenses, interest, taxes and non-cash items such as stock-based compensation and depreciation and amortization. Please see financial tables for GAAP to Non-GAAP reconciliations.
An investor presentation for the company's fourth quarter and full year 2020 financial results is available in the "Investors" section of Nevro's website at www.nevro.com.
Webcast and Conference Call Information
As previously announced, Nevro management will host a conference call starting at 1:30 pm PT / 4:30 pm ET today. Investors interested in listening to the call may do so by dialing (866) 324-3683 in the U.S. or +1 (509) 844-0959 internationally, using Conference ID: 1353779. A live webcast, as well as an archived recording, will also be available in the "Investors" section of Nevro's website at: www.nevro.com.
Internet Posting of Information
Nevro routinely posts information that may be important to investors in the "Investor Relations" section of its website at www.nevro.com. The company encourages investors and potential investors to consult the Nevro website regularly for important information about Nevro.
Headquartered in Redwood City, California, Nevro is a global medical device company focused on providing innovative products that improve the quality of life of patients suffering from debilitating chronic pain. Nevro has developed and commercialized the Senza spinal cord stimulation (SCS) system, an evidence-based, non-pharmacologic neuromodulation platform for the treatment of chronic pain. HF10 therapy has demonstrated the ability to reduce or eliminate opioids in ≥65% of patients across six peer-reviewed clinical studies. The Senza® System, Senza II™ System, and the Senza® Omnia™ System are the only SCS systems that deliver Nevro's proprietary HF10® therapy. Senza, Senza II, Senza Omnia, HF10, Nevro and the Nevro logo are trademarks of Nevro Corp.
In addition to historical information, this press release contains forward-looking statements reflecting the company's current beliefs and expectations of management made pursuant to the safe harbor provisions of the Private Securities Litigation Reform Act of 1995, including: our belief that we are well positioned for attractive and sustainable growth as the pressure of COVID on our business subsides; our expectation that pent-up patient demand will come back into the system as infection rates decline, vaccine availability improves and the market reverts to normalcy; our belief in our ability to expand growth by treating Painful Diabetic Neuropathy and Non-Surgical Refractory Back Pain patients; our Q1 and full year 2021 financial guidance, including our belief (i) in an ongoing and steady recovery in the U.S. and key international geographies leading to more normalized case scheduling and elective procedure levels beginning in the second quarter of 2021 and (ii) that impact from COVID will diminish with each sequential quarter this year as vaccine availability improves and patients begin to again seek elective care in typical levels. These forward-looking statements are based upon information that is currently available to us or our current expectations, speak only as of the date hereof, and are subject to numerous risks and uncertainties, including our ability to successfully commercialize our products; our ability to manufacture our products to meet demand; the level and availability of third-party payor reimbursement for our products; our ability to effectively manage our anticipated growth and the costs and expenses of operating our business; our ability to protect our intellectual property rights and proprietary technologies; our ability to operate our business without infringing the intellectual property rights and proprietary technology of third parties; competition in our industry; additional capital and credit availability; our ability to attract and retain qualified personnel; and product liability claims. These factors, together with those that are described in greater detail in our Annual Report on Form 10-K that we expect to file on February 24, 2021, as well as any reports that we may file with the Securities and Exchange Commission in the future, may cause our actual results, performance or achievements to differ materially and adversely from those anticipated or implied by our forward-looking statements. We expressly disclaim any obligation, except as required by law, or undertaking to update or revise any such forward-looking statements. Nevro's operating results for the fourth quarter ended December 31, 2020 are not necessarily indicative of our operating results for any future periods.
Consolidated Statements of Operations and Comprehensive Loss
(in thousands, except share and per share data)
Three Months Ended
Cost of revenue
Research and development
Sales, general and administrative
Total operating expenses
Loss from operations
Other income (expense):
Interest income (expense), net
Other income (expense), net
Loss before income taxes
Provision for (benefit from) income taxes
Changes in foreign currency translation
Changes in gains (losses) on short-term
Net change in other comprehensive loss
Net loss per share, basic and diluted
Weighted average shares used to compute
net loss per share, basic and diluted
Consolidated Balance Sheets
(in thousands, except share and per share data)
Cash and cash equivalents
Accounts receivable, net
Prepaid expenses and other current assets
Total current assets
Property and equipment, net
Operating lease assets
Liabilities and stockholders' equity
Accrued liabilities and other
Total current liabilities
Long-term operating lease liabilities
Other long-term liabilities
Common stock, $0.001 par value, 290,000,000 shares authorized,
34,583,064 and 31,544,361 shares issued and outstanding at
December 31, 2020 and 2019, respectively
Additional paid-in capital
Accumulated other comprehensive loss
Total stockholders' equity
Total liabilities and stockholders' equity
GAAP to Non-GAAP Adjusted EBITDA Reconciliation
The following table presents a reconciliation of GAAP net loss, as prepared in accordance with U.S. Generally Accepted Accounting Principles ("GAAP"), to Adjusted EBITDA, a non-GAAP financial measure.
Reconciliation of actual results:
Three Months Ended
GAAP Net loss
Interest (income) expense, net
Provision for income taxes
Depreciation and amortization
Stock-based compensation expense
Litigation related expenses
Reconciliation of guidance:
December 31, 2021
GAAP Net Loss
Management uses certain non-GAAP financial measures, most specifically Adjusted EBITDA, as a supplement to GAAP financial measures to further evaluate the Company's operating performance period over period, analyze the underlying business trends, assess performance relative to competitors and establish operational objectives.
Management believes it is important to provide investors with the same non-GAAP metrics it uses to evaluate the performance and underlying trends of the Company's business operations to facilitate comparisons to its historical operating results and evaluate the effectiveness of its operating strategies. Disclosure of these non-GAAP financial measures also facilitates comparisons of the Company's underlying operating performance with other companies in the industry that also supplement their GAAP results with non-GAAP financial measures.
EBITDA is a non-GAAP financial measure, which is calculated by adding interest income and expense, net; provision for income taxes; and depreciation and amortization to net income. In calculating non-GAAP Adjusted EBITDA, the Company further adjusts for the following items:
- Stock-based compensation expense – The Company excludes non-cash costs related to the Company's stock-based plans, which include stock options, restricted stock units and performance-based restricted stock units as these expenses do not require cash settlement from the Company.
- Litigation related expenses – The Company excludes legal and professional fees associated with certain legal matters which management considers not related to the underlying operating performance of the business.
Full year guidance excludes the impact of foreign currency fluctuations.
The non-GAAP financial measure should not be considered in isolation from, or as a replacement for, the most directly comparable GAAP financial measures, as it is not prepared in accordance with U.S. GAAP.
Amounts may not add due to rounding.
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SOURCE Nevro Corp.
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