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CVRx Reports First Quarter 2026 Financial and Operating Results

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CVRx (NASDAQ: CVRX) reported first quarter 2026 revenue of $14.8 million, up 20% year over year, driven by 22% U.S. growth to $13.7 million and 429 U.S. revenue units. Europe revenue was $1.1 million, down 2%.

Gross profit rose to $12.9 million with gross margin improving to 87%. Net loss was $13.1 million ($0.50 per share) versus $13.8 million a year ago. Cash and equivalents were $72.3 million, with $12.3 million used in operating and investing activities.

The BENEFIT-HF trial activated its first site, and the first patient was enrolled in Q2 2026. CVRx maintained 2026 revenue and opex guidance, while raising expected full-year gross margin to 85–87% and guiding Q2 2026 revenue to $15.1–$16.1 million.

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AI-generated analysis. Not financial advice.

Positive

  • Q1 2026 revenue increased 20% year over year to $14.8 million
  • U.S. revenue grew 22% to $13.7 million with 429 revenue units
  • Gross margin improved to 87%, up from 84% in Q1 2025
  • Q1 net loss narrowed to $13.1 million from $13.8 million
  • Cash and cash equivalents totaled $72.3 million at March 31, 2026
  • First site activated and first patient enrolled in BENEFIT-HF trial
  • 2026 gross margin guidance raised to 85–87%
  • 2026 revenue guidance maintained at $63–$67 million

Negative

  • Company reported a Q1 2026 net loss of $13.1 million
  • Q1 operating expenses guided for 2026 at $103–$107 million
  • Europe Q1 2026 revenue declined 2% to $1.1 million
  • Q1 2026 SG&A expenses rose 3% to $22.0 million
  • Q1 2026 R&D expenses increased 23% to $3.1 million
  • Net cash used in operating and investing activities was $12.3 million in Q1 2026
  • Other income decreased to $0.6 million from $1.1 million year over year

News Market Reaction – CVRX

-23.84% 2.8x vol
40 alerts
-23.84% News Effect
-19.9% Trough in 6 hr 24 min
-$54M Valuation Impact
$172.33M Market Cap
2.8x Rel. Volume

On the day this news was published, CVRX declined 23.84%, reflecting a significant negative market reaction. Argus tracked a trough of -19.9% from its starting point during tracking. Our momentum scanner triggered 40 alerts that day, indicating elevated trading interest and price volatility. This price movement removed approximately $54M from the company's valuation, bringing the market cap to $172.33M at that time. Trading volume was elevated at 2.8x the daily average, suggesting increased selling activity.

Data tracked by StockTitan Argus on the day of publication.

Key Figures

Q1 2026 revenue: $14.8M U.S. revenue Q1 2026: $13.7M Gross margin Q1 2026: 87% +5 more
8 metrics
Q1 2026 revenue $14.8M Total revenue, three months ended March 31, 2026; +20% YoY
U.S. revenue Q1 2026 $13.7M U.S. revenue, three months ended March 31, 2026; +22% YoY
Gross margin Q1 2026 87% Gross margin for three months ended March 31, 2026 (vs 84% prior year)
Net loss Q1 2026 $13.1M ($0.50/sh) Net loss and loss per share, three months ended March 31, 2026
Cash & equivalents $72.3M Cash and cash equivalents as of March 31, 2026
Active U.S. centers 257 centers Active implanting centers in U.S. as of March 31, 2026
2026 revenue guidance $63.0M–$67.0M Full-year 2026 total revenue guidance, maintained
NT-proBNP cutoff ≤5,000 pg/mL Eligibility threshold in BENEFIT-HF trial design

Market Reality Check

Price: $5.58 Vol: Volume 176,809 is below t...
low vol
$5.58 Last Close
Volume Volume 176,809 is below the 20-day average 258,911, suggesting muted trading interest into the release. low
Technical Shares at $6.83 are trading below the 200-day MA $8.01, indicating a pre‑existing downtrend before this report.

Peers on Argus

Peer moves are mixed: BSGM up 39.91%, ELMD up 0.64%, SGHT down 0.19%, STIM down ...

Peer moves are mixed: BSGM up 39.91%, ELMD up 0.64%, SGHT down 0.19%, STIM down 10.05%, TLSI up 0.23%. With CVRX down 6.69%, trading appears stock-specific rather than a unified medical device move.

Previous Earnings Reports

5 past events · Latest: Apr 13 (Positive)
Same Type Pattern 5 events
Date Event Sentiment Move Catalyst
Apr 13 Prelim Q1 2026 Positive +9.2% Preliminary Q1 revenue ~20% YoY growth and gross margin near 87%.
Feb 12 Q4 & FY25 results Positive -13.0% Q4 and full‑year 2025 revenue growth and higher gross margins with 2026 guidance.
Jan 12 Prelim Q4 & FY25 Neutral -9.9% Preliminary Q4 and FY25 revenue ranges plus initial 2026 guidance and CPT updates.
Nov 05 Q3 2025 results Positive +2.7% Q3 2025 revenue growth, higher gross margin, more U.S. implanting centers and updated guidance.
Aug 04 Q2 2025 results Positive -9.9% Q2 2025 revenue and U.S. HF growth with higher CMS payment signals but sizable net loss.
Pattern Detected

Earnings reactions have been mixed: out of five recent earnings or guidance updates, three aligned with the news tone while two diverged. Average move around earnings-related headlines has been -4.19%, indicating a tendency toward cautious or negative price responses, even when operational metrics improve.

Recent Company History

Over the past few quarters, CVRx has consistently reported revenue growth and high gross margins, while expanding active U.S. implanting centers and advancing the BENEFIT‑HF trial. Earnings events on Aug 4, 2025, Nov 5, 2025, and preliminary/full‑year updates in Jan–Feb 2026 combined commercial progress with ongoing losses and increased borrowing capacity. The preliminary Q1 2026 release on Apr 13, 2026 highlighted roughly 20% growth and ~87% gross margin, setting expectations largely in line with today’s finalized figures.

Historical Comparison

-4.2% avg move · Across five recent earnings-related releases, CVRX’s average move was -4.19%. Today’s -6.69% reactio...
earnings
-4.2%
Average Historical Move earnings

Across five recent earnings-related releases, CVRX’s average move was -4.19%. Today’s -6.69% reaction to finalized Q1 2026 results is somewhat more negative but directionally consistent.

Successive earnings reports show steady revenue growth, rising gross margins and expansion of U.S. implanting centers, while the BENEFIT‑HF trial and 2026 revenue guidance of $63M–$67M frame a longer-term growth narrative alongside ongoing net losses.

Regulatory & Risk Context

Active S-3 Shelf · $150,000,000
Shelf Active
Active S-3 Shelf Registration 2025-11-06
$150,000,000 registered capacity

The company filed a Form S-3 shelf on Nov 6, 2025 to register up to $150,000,000 of securities, with flexibility across common stock, preferred stock, debt, warrants, rights and units. At least one takedown has occurred via a 424B5 filing on Jan 12, 2026. The shelf is currently marked as not effective in the provided context.

Market Pulse Summary

The stock dropped -23.8% in the session following this news. The decline reflects a pattern where ea...
Analysis

The stock dropped -23.8% in the session following this news. The decline reflects a pattern where earnings news often met operational goals yet saw selling pressure; past earnings-linked moves averaged -4.19%, and today’s -6.69% fall is directionally consistent. Despite 20% revenue growth and an 87% gross margin, the company reported a net loss of $13.1M and provided 2026 guidance of $63M–$67M in revenue. Ongoing losses and prior shelf capacity of up to $150M could remain overhangs after an initial reaction.

Key Terms

neuromodulation, randomized controlled trial, all-cause mortality, heart failure decompensation, +2 more
6 terms
neuromodulation medical
"a commercial-stage medical device company focused on developing, manufacturing and commercializing innovative neuromodulation solutions"
Neuromodulation is the use of devices or targeted treatments to change how nerves or brain circuits send signals, much like adjusting the volume or tuning on an audio system to alter what you hear. For investors, it matters because these therapies can treat chronic conditions (pain, movement disorders, depression) where existing medicines fall short, creating potential markets, regulatory milestones, and durable revenue streams if technologies prove safe and effective.
randomized controlled trial medical
"a landmark randomized controlled trial designed to evaluate Barostim's impact"
A randomized controlled trial is a research method that tests the effects of a new idea or treatment by randomly dividing participants into two groups: one that receives the treatment and one that does not. This approach helps ensure that the results are fair and unbiased, providing clear evidence about whether the treatment actually works. Investors value such trials because they offer reliable information that can influence decision-making and reduce uncertainty.
all-cause mortality medical
"designed to evaluate Barostim's impact on all-cause mortality and heart failure decompensation events"
All-cause mortality is the total number of deaths from any cause within a defined group over a specific time period. For investors, it is a broad safety and outcome measure used in clinical trials and public-health studies—like counting everyone who leaves a club for any reason—because higher or lower all-cause mortality can influence regulatory decisions, product reputation, long-term liability and market value.
heart failure decompensation medical
"impact on all-cause mortality and heart failure decompensation events in an expanded population"
Heart failure decompensation is when a chronic weak heart suddenly cannot keep up with the body's needs, causing symptoms like shortness of breath, fluid buildup, and fatigue; think of a household pump that starts failing and lets water overflow. For investors, these episodes drive demand for hospital care, drugs, monitoring devices and procedures, influence clinical trial results and regulatory decisions, and can significantly affect healthcare costs and company revenue streams.
left ventricular ejection fractions medical
"heart failure patients with left ventricular ejection fractions up to 50%"
Left ventricular ejection fraction (LVEF) is the percentage of blood the heart’s main pumping chamber pushes out with each beat, like how much water a pump expels from a tank each cycle. Investors care because LVEF is a key measure used by regulators, doctors and trial designers to judge disease severity, treatment need and eligibility for drugs or devices, which affects market size, approval odds and healthcare spending.
nt-probnp medical
"left ventricular ejection fractions up to 50% and NT-proBNP levels up to 5,000 pg/mL"
A blood test marker released when the heart is under strain; higher NT‑proBNP levels indicate the heart is working harder or may be failing, similar to a dashboard warning light that signals engine stress. Investors watch NT‑proBNP because changes in the marker can drive clinical trial results, treatment approvals, hospital use, and insurance decisions for heart drugs and devices, all of which affect revenue, adoption and valuation in healthcare companies.

AI-generated analysis. Not financial advice.

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MINNEAPOLIS, May 11, 2026 (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 first quarter of 2026.

Recent Highlights

  • Total revenue for the first quarter of 2026 was $14.8 million, an increase of approximately 20% over the prior year quarter
  • U.S. revenue for the first quarter of 2026 was $13.7 million, an increase of 22% over the prior year quarter
  • Active implanting centers in the U.S. grew to 257 as of March 31, 2026, as compared to 227 as of March 31, 2025
  • First site activated and first patient enrolled in BENEFIT-HF clinical trial

"We delivered a strong start to 2026, with U.S. revenue growing 22% as the investments we made in our team and programs throughout 2025 begin to translate into results," said Kevin Hykes, President and Chief Executive Officer of CVRx. "We are seeing continued progress from our sales organization and the successful activation of the first site and our first patient enrolled in our BENEFIT-HF clinical trial. Together, these developments reinforce our confidence in the path ahead and in our ability to make Barostim more accessible to heart failure patients."

First Quarter 2026 Financial and Operating Results

Revenue was $14.8 million for the three months ended March 31, 2026, an increase of $2.4 million, or 20%, over the three months ended March 31, 2025.

Revenue generated in the U.S. was $13.7 million for the three months ended March 31, 2026, an increase of $2.4 million, or 22%, over the three months ended March 31, 2025. Revenue units in the U.S. totaled 429 and 359 for the three months ended March 31, 2026 and 2025, respectively. The increases were primarily driven by continued growth in the U.S. HF business as a result of the expansion into new sales territories, new accounts, and increased physician and patient awareness of Barostim.

As of March 31, 2026, the Company had a total of 257 active implanting centers in the U.S., as compared to 252 as of December 31, 2025. 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 56 during the three months ended March 31, 2026.

Revenue generated in Europe was $1.1 million for the three months ended March 31, 2026, a decrease of $27,000, or 2%, over the three months ended March 31, 2025. Total revenue units in Europe decreased to 56 for the three months ended March 31, 2026 from 59 in the prior year period. The number of sales territories in Europe remained consistent at five for the three months ended March 31, 2026.

Gross profit was $12.9 million for the three months ended March 31, 2026, an increase of $2.6 million, or 25%, over the three months ended March 31, 2025. Gross margin was 87% and 84% for the three months ended March 31, 2026 and March 31, 2025, respectively.

R&D expenses increased $0.6 million, or 23%, to $3.1 million for the three months ended March 31, 2026 compared to the three months ended March 31, 2025. This change was driven by a $0.4 million increase in consulting expenses, a $0.3 million increase in compensation expenses, and a $0.1 million increase in non-cash stock-based compensation expenses, partially offset by a $0.2 million decrease in clinical trial expenses.

SG&A expenses increased $0.7 million, or 3%, to $22.0 million for the three months ended March 31, 2026, compared to the three months ended March 31, 2025. This change was primarily driven by a $1.0 million increase in compensation expenses and a $0.3 million increase in non-cash stock-based compensation expenses, partially offset by a $0.3 million decrease in consulting expenses and a $0.3 million decrease in advertising expenses.

Interest expense increased $0.1 million for the three months ended March 31, 2026, compared to the three months ended March 31, 2025, driven by the increased borrowings under the term loan agreement with Innovatus Capital Partners.

Other income, net was $0.6 and $1.1 million for the three months ended March 31, 2026 and 2025, respectively. These balances consisted of interest income on our interest-bearing accounts. The decrease was primarily driven by the lower cash balance.

Net loss was $13.1 million, or $0.50 per share, for the three months ended March 31, 2026, compared to a net loss of $13.8 million, or $0.53 per share, for the three months ended March 31, 2025. Net loss per share was based on 26.4 million weighted average shares outstanding for three months ended March 31, 2026 and 25.9 million weighted average shares outstanding for the three months ended March 31, 2025.

As of March 31, 2026, cash and cash equivalents were $72.3 million. Net cash used in operating and investing activities was $12.3 million for the three months ended March 31, 2026 as compared to $12.9 million for the three months ended March 31, 2025.

BENEFIT-HF Clinical Trial Update

On March 31, 2026, the first site was activated in the BENEFIT-HF trial and the first patient was enrolled in the second quarter of 2026. This trial, as previously disclosed, is a landmark randomized controlled trial designed to evaluate Barostim's impact on all-cause mortality and heart failure decompensation events in an expanded population of heart failure patients with left ventricular ejection fractions up to 50% and NT-proBNP levels up to 5,000 pg/mL. If successful, the BENEFIT-HF trial could expand the indicated patient population for Barostim approximately three times, significantly broadening access to this proven neuromodulation-based approach to heart failure management.

Business Outlook

For the full year of 2026, the Company maintained its revenue and expense guidance, and updated its guidance range for gross margin, as follows:

  • Total revenue between $63.0 million and $67.0 million;
  • Gross margin between 85% and 87%, compared to prior guidance of 84% and 86%;
  • Operating expenses between $103.0 million and $107.0 million.

For the second quarter of 2026, the Company expects to report total revenue between $15.1 million and $16.1 million.

Webcast and Conference Call Information

The Company will host a conference call to review its results at 4:30 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 been certified as compliant with the EU Medical Device Regulation (MDR) and holds CE Mark approval 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 second quarter 2026 results), our anticipated growth strategies (including statements regarding the expected timing, enrollment, scope and outcomes of the BENEFIT-HF clinical trial, potential expansion of the Barostim indication, and anticipated benefits of Barostim therapy), 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 expectations regarding enrollment in BENEFIT-HF and the resulting impact on our addressable market; 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 limited commercial sales experience marketing and selling Barostim; our ability to continue demonstrating 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; 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; impacts on adoption and regulatory approvals resulting from additional long-term clinical data about our product, including those resulting from the BENEFIT-HF trial; 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, 2025, 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 Healthcare
443-213-0501
ir@cvrx.com

Media Contact:
Emily Meyers
CVRx, Inc.
763-416-2853
emeyers@cvrx.com

CVRx, INC.

Condensed Consolidated Balance Sheets
(In thousands, except share and per share data)
(Unaudited)
       
  March 31, December 31,
  2026
 2025
Assets      
Current assets:      
Cash and cash equivalents $72,303  $75,708 
Accounts receivable, net of allowances of $869 and $871, respectively  9,104   10,665 
Inventory  12,403   12,205 
Prepaid expenses and other current assets  2,940   3,069 
Total current assets  96,750   101,647 
Property and equipment, net  2,159   2,243 
Operating lease right-of-use asset  793   878 
Other non-current assets  26   26 
Total assets $99,728  $104,794 
Liabilities and Stockholders’ Equity      
Current liabilities:      
Accounts payable $2,998  $3,833 
Accrued expenses  6,488   9,484 
Total current liabilities  9,486   13,317 
Long-term debt  58,490   49,514 
Operating lease liability, non-current portion  544   638 
Other long-term liabilities  2,099   2,001 
Total liabilities  70,619   65,470 
Commitments and contingencies      
Stockholders’ equity:      
Common stock, $0.01 par value, 200,000,000 authorized as of March 31, 2026 and December 31, 2025; 26,428,767 and 26,311,607 shares issued and outstanding as of March 31, 2026 and December 31, 2025, respectively  264   263 
Additional paid-in capital  632,820   629,916 
Accumulated deficit  (603,772)  (590,652)
Accumulated other comprehensive loss  (203)  (203)
Total stockholders’ equity  29,109   39,324 
Total liabilities and stockholders’ equity $99,728  $104,794 


CVRx, INC.
Condensed Consolidated Statements of Operations and Comprehensive Loss
(In thousands, except share and per share data)
(Unaudited)

       
  Three months ended
  March 31,
  2026
 2025
Revenue $14,769  $12,348 
Cost of goods sold  1,888   2,036 
Gross profit  12,881   10,312 
Operating expenses:      
Research and development  3,084   2,517 
Selling, general and administrative  21,958   21,232 
Total operating expenses  25,042   23,749 
Loss from operations  (12,161)  (13,437)
Interest expense  (1,551)  (1,457)
Other income, net  593   1,123 
Loss before income taxes  (13,119)  (13,771)
Benefit (provision) for income taxes  (1)  5 
Net loss  (13,120)  (13,766)
Cumulative translation adjustment      
Comprehensive loss $(13,120) $(13,766)
Net loss per share, basic and diluted $(0.50) $(0.53)
Weighted-average common shares used to compute net loss per share, basic and diluted  26,355,591   25,876,062 

FAQ

How did CVRx (NASDAQ: CVRX) perform financially in Q1 2026?

CVRx reported Q1 2026 revenue of $14.8 million, up 20% year over year. According to CVRx, gross profit reached $12.9 million with an 87% gross margin, while net loss was $13.1 million, or $0.50 per share, slightly improving versus Q1 2025.

What drove CVRx's U.S. revenue growth in the first quarter of 2026?

U.S. revenue rose 22% to $13.7 million in Q1 2026. According to CVRx, growth was supported by expansion into new sales territories, new accounts, increased physician and patient awareness of Barostim, and 429 U.S. revenue units across 257 active implanting centers.

What are CVRx's 2026 revenue and gross margin guidance ranges (CVRX)?

For full-year 2026, CVRx expects total revenue between $63 million and $67 million. According to CVRx, the company now anticipates gross margin between 85% and 87%, up from prior guidance of 84% to 86%, with operating expenses projected at $103–$107 million.

What is the status of CVRx's BENEFIT-HF clinical trial as of Q2 2026?

BENEFIT-HF has its first site activated and first patient enrolled by Q2 2026. According to CVRx, this randomized trial evaluates Barostim in a broader heart failure population and could, if successful, approximately triple the indicated patient population for the therapy.

How much cash does CVRx have, and what was Q1 2026 cash usage?

CVRx ended March 31, 2026 with $72.3 million in cash and cash equivalents. According to CVRx, net cash used in operating and investing activities totaled $12.3 million in Q1 2026, slightly better than the $12.9 million used in the prior-year quarter.

What guidance did CVRx provide for Q2 2026 revenue (ticker CVRX)?

For the second quarter of 2026, CVRx expects total revenue between $15.1 million and $16.1 million. According to CVRx, this outlook follows Q1 2026 revenue of $14.8 million and reflects the company’s ongoing U.S. heart failure business expansion.

How did CVRx's European revenue trend in Q1 2026?

European revenue was $1.1 million in Q1 2026, down 2% year over year. According to CVRx, total revenue units in Europe declined from 59 to 56 versus the prior-year quarter, while the number of sales territories remained steady at five.