CVRx Reports Third Quarter 2023 Financial and Operating Results
- CVRx reports strong financial results for Q3 2023 with a 70% increase in total revenue compared to the same period last year. U.S. Heart Failure revenue shows significant growth, increasing by 92% YoY. The expansion of active implanting centers in the U.S. is a positive sign, with a 75% increase since September 2022. The CMS Advisory Panel's unanimous non-binding recommendation for higher payment for Barostim in 2024 is a positive development for the company. The updated business outlook for 2023 shows increased revenue and reduced operating expenses.
- None.
MINNEAPOLIS, Oct. 26, 2023 (GLOBE NEWSWIRE) -- CVRx, Inc. (NASDAQ: CVRX) (“CVRx”), a commercial-stage medical device company focused on developing, manufacturing and commercializing innovative neuromodulation solutions for patients with cardiovascular diseases, today announced its financial and operating results for the third quarter of 2023.
Recent Highlights
- Total revenue for the third quarter of 2023 was
$10.5 million , an increase of70% over the prior year quarter - U.S. Heart Failure (HF) revenue for the third quarter of 2023 was
$9.4 million , an increase of92% over the prior year quarter - Active implanting centers in the U.S. grew to 159, an increase of
75% since September 30, 2022 - Cash used in operating and investing activities for the third quarter of 2023 was
$8.2 million , as compared to$11.4 million for the third quarter of 2022, and$13.0 million for the second quarter of 2023 - CMS Advisory Panel on Hospital Outpatient Payment gave a unanimous non-binding recommendation to support the request for Barostim to be mapped to a higher payment level for 2024
“We're pleased with the growth trajectory of our business, which has continued to exceed our expectations throughout 2023. The impressive performance of our U.S. heart failure business has been driven by the expansion of our commercial team and the increased positive impacts of our marketing efforts,” said Nadim Yared, President and Chief Executive Officer of CVRx. “Moving forward, we're focused on maintaining this positive momentum while continuing to expect a reduction in our quarterly cash burn as we exit the year and look towards 2024. I want to express my thanks to our dedicated team for their ongoing commitment to our mission of improving patients' lives.”
Third Quarter 2023 Financial and Operating Results
Revenue was
Revenue generated in the U.S. was
As of September 30, 2023, the Company had a total of 159 active implanting centers, as compared to 140 as of June 30, 2023. Active implanting centers are customers that have completed at least one commercial HF implant in the last 12 months. The number of sales territories in the U.S. increased by three to a total of 35 during the three months ended September 30, 2023.
Revenue generated in Europe was
Gross profit was
R&D expenses increased
SG&A expenses increased
Interest expense increased
Other income, net was
Net loss was
As of September 30, 2023, cash and cash equivalents were
Centers for Medicare & Medicaid Services (CMS) Advisory Panel on Hospital Outpatient Payment Update
In August 2023, the Company delivered a presentation before the CMS Advisory Panel on Hospital Outpatient Payment, resulting in a unanimous non-binding vote in favor of mapping Barostim to the higher paying code, New Technology APC1580, which would offer an average reimbursement of
Business Outlook
For the full year of 2023, the Company now expects:
- Total revenue between
$38.5 million and$39.0 million ; up from previously issued guidance of$37.0 million and$38.5 million - Gross margin between
83.0% and84.0% - Operating expenses between
$77.0 million and$78.0 million ; down from previously issued guidance of$78.0 million and$80.0 million
For the fourth quarter of 2023, the Company expects to report total revenue between
Webcast and Conference Call Information
The Company will host a conference call to review its results at 5:30 p.m. Eastern Time today. A live webcast of the investor conference call will be available online at the investor relations page of the Company’s website at ir.cvrx.com. To listen to the conference call on your telephone, please dial 1-877-704-4453 for U.S. callers, or 1-201-389-0920 for international callers, approximately ten minutes prior to the start time.
About CVRx, Inc.
CVRx is a commercial-stage medical device company focused on developing, manufacturing and commercializing innovative neuromodulation solutions for patients with cardiovascular diseases. Barostim™ is the first medical technology approved by FDA that uses neuromodulation to improve the symptoms of patients with heart failure. Barostim is an implantable device that delivers electrical pulses to baroreceptors located in the wall of the carotid artery. The therapy is designed to restore balance to the autonomic nervous system and thereby reduce the symptoms of heart failure. Barostim received the FDA Breakthrough Device designation and is FDA-approved for use in heart failure patients in the U.S. It has also received the CE Mark for heart failure and resistant hypertension in the European Economic Area. To learn more about Barostim, visit www.cvrx.com.
Forward-Looking Statements
This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. All statements other than statements of historical facts are forward-looking statements, including statements regarding our future financial performance (including our financial guidance regarding full year and fourth quarter 2023 results), our anticipated growth strategies, anticipated trends in our industry, our business prospects and our opportunities. In some cases, you can identify forward-looking statements by terms such as “may,” “will,” “should,” “expect,” “plan,” “anticipate,” “could,” “outlook,” “guidance,” “intend,” “target,” “project,” “contemplate,” “believe,” “estimate,” “predict,” “potential” or “continue” or the negative of these terms or other similar expressions, although not all forward-looking statements contain these words.
The forward-looking statements in this press release are only predictions and are based largely on our current expectations and projections about future events and financial trends that we believe may affect our business, financial condition, and results of operations. These forward-looking statements speak only as of the date of this press release and are subject to a number of known and unknown risks, uncertainties and assumptions, including, but not limited to, our history of significant losses, which we expect to continue; our limited history operating as a commercial company and our dependence on a single product, Barostim; our ability to establish and maintain sales and marketing capabilities; our ability to demonstrate to physicians and patients the merits of our Barostim; any failure by third-party payors to provide adequate coverage and reimbursement for the use of Barostim; our competitors’ success in developing and marketing products that are safer, more effective, less costly, easier to use or otherwise more attractive than Barostim; any failure to receive access to hospitals; our dependence upon third-party manufacturers and suppliers, and in some cases a limited number of suppliers; a pandemic, epidemic or outbreak of an infectious disease in the U.S. or worldwide, including the outbreak of the novel strain of coronavirus, COVID-19; any failure of clinical studies for future indications to produce results necessary to support regulatory clearance or approval in the U.S. or elsewhere; product liability claims; future lawsuits to protect or enforce our intellectual property, which could be expensive, time consuming and ultimately unsuccessful; any failure to retain our key executives or recruit and hire new employees; and other important factors that could cause actual results, performance or achievements to differ materially from those that are found in “Part I, Item 1A. Risk Factors” in our Annual Report on Form 10-K for the year ended December 31, 2022, as such factors may be updated from time to time in our other filings with the Securities and Exchange Commission. Except as required by applicable law, we do not plan to publicly update or revise any forward-looking statements contained herein, whether as a result of any new information, future events, changed circumstances or otherwise.
Investor Contact:
Mark Klausner or Mike Vallie
ICR Westwicke
443-213-0501
ir@cvrx.com
Media Contact:
Laura O’Neill
Finn Partners
402-499-8203
laura.oneill@finnpartners.com
CVRx, INC. | ||||||||
Condensed Consolidated Balance Sheets | ||||||||
(In thousands, except share and per share data) | ||||||||
(Unaudited) | ||||||||
September 30, 2023 | December 31, 2022 | |||||||
Assets | ||||||||
Current assets: | ||||||||
Cash and cash equivalents | $ | 82,993 | $ | 106,194 | ||||
Accounts receivable, net of allowances of | 6,372 | 5,504 | ||||||
Inventory | 10,887 | 6,957 | ||||||
Prepaid expenses and other current assets | 3,345 | 4,223 | ||||||
Total current assets | 103,597 | 122,878 | ||||||
Property and equipment, net | 1,723 | 1,698 | ||||||
Operating lease right-of-use asset | 1,058 | 334 | ||||||
Other non-current assets | 26 | 27 | ||||||
Total assets | $ | 106,404 | $ | 124,937 | ||||
Liabilities and Stockholders’ Equity | ||||||||
Current liabilities: | ||||||||
Accounts payable | $ | 1,133 | $ | 1,719 | ||||
Accrued expenses | 6,274 | 6,369 | ||||||
Total current liabilities | 7,407 | 8,088 | ||||||
Long-term debt | 14,294 | 6,747 | ||||||
Operating lease liability, non-current portion | 916 | 117 | ||||||
Other long-term liabilities | 960 | 805 | ||||||
Total liabilities | 23,577 | 15,757 | ||||||
Commitments and contingencies | ||||||||
Stockholders’ equity: | ||||||||
Common stock, September 30, 2023 and December 31, 2022; 20,813,612 and 20,663,736 shares issued and outstanding as of September 30, 2023 and December 31, 2022, respectively | 208 | 207 | ||||||
Additional paid-in capital | 551,045 | 545,362 | ||||||
Accumulated deficit | (468,218 | ) | (436,182 | ) | ||||
Accumulated other comprehensive loss | (208 | ) | (207 | ) | ||||
Total stockholders’ equity | 82,827 | 109,180 | ||||||
Total liabilities and stockholders’ equity | $ | 106,404 | $ | 124,937 | ||||
CVRx, INC. | ||||||||||||||||
Condensed Consolidated Statements of Operations and Comprehensive Loss | ||||||||||||||||
(In thousands, except share and per share data) | ||||||||||||||||
(Unaudited) | ||||||||||||||||
Three months ended September 30, | Nine months ended September 30, | |||||||||||||||
2023 | 2022 | 2023 | 2022 | |||||||||||||
Revenue | $ | 10,511 | $ | 6,186 | $ | 27,990 | $ | 15,293 | ||||||||
Cost of goods sold | 1,691 | 1,340 | 4,536 | 3,490 | ||||||||||||
Gross profit | 8,820 | 4,846 | 23,454 | 11,803 | ||||||||||||
Operating expenses: | ||||||||||||||||
Research and development | 2,696 | 2,293 | 9,392 | 6,906 | ||||||||||||
Selling, general and administrative | 15,652 | 12,679 | 47,504 | 35,945 | ||||||||||||
Total operating expenses | 18,348 | 14,972 | 56,896 | 42,851 | ||||||||||||
Loss from operations | (9,528 | ) | (10,126 | ) | (33,442 | ) | (31,048 | ) | ||||||||
Interest expense | (499 | ) | — | (1,220 | ) | — | ||||||||||
Other income, net | 1,056 | 328 | 2,734 | 237 | ||||||||||||
Loss before income taxes | (8,971 | ) | (9,798 | ) | (31,928 | ) | (30,811 | ) | ||||||||
Provision for income taxes | (40 | ) | (32 | ) | (108 | ) | (81 | ) | ||||||||
Net loss | (9,011 | ) | (9,830 | ) | (32,036 | ) | (30,892 | ) | ||||||||
Cumulative translation adjustment | (21 | ) | (8 | ) | (1 | ) | (21 | ) | ||||||||
Comprehensive loss | $ | (9,032 | ) | $ | (9,838 | ) | $ | (32,037 | ) | $ | (30,913 | ) | ||||
Net loss per share, basic and diluted | $ | (0.43 | ) | $ | (0.48 | ) | $ | (1.55 | ) | $ | (1.51 | ) | ||||
Weighted-average common shares used to compute net loss per share, basic and diluted | 20,801,350 | 20,576,838 | 20,730,024 | 20,512,254 | ||||||||||||
FAQ
What are CVRx's financial results for Q3 2023?
How much did U.S. Heart Failure revenue increase in Q3 2023?
What is the current number of active implanting centers in the U.S.?
What was the CMS Advisory Panel's recommendation for Barostim in 2024?