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Exagen Inc. Reports Second Quarter 2026 Financial Results

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Exagen (Nasdaq: XGN) reported second quarter 2026 revenue of $19.9 million, up 16% from $17.2 million in 2025, with record total revenue, test volume and a gross margin of 61.3%. AVISE CTD test volume grew 11% year over year and trailing twelve‑month average selling price rose 4% to $446 per test.

Net loss narrowed to $3.2 million from $4.4 million, while adjusted EBITDA improved to a loss of $0.1 million versus a $1.7 million loss a year earlier. Cash and cash equivalents were approximately $24.6 million at June 30, 2026. The company raised full‑year 2026 revenue guidance to $72–$75 million from $70–$73 million. Exagen also highlighted a published systematic review of over 3,100 patients across 14 medical centers supporting AVISE Lupus performance, showing AVISE CTD correctly identified about 25% of SLE patients missed by conventional markers.

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Positive

  • Revenue +16% YoY to $19.9 million in Q2 2026
  • Gross margin 61.3%, up from 60.4% in Q2 2025
  • Net loss reduced to $3.2 million from $4.4 million YoY
  • Adjusted EBITDA improved to a $0.1 million loss from $1.7 million loss
  • 2026 revenue guidance raised to $72–$75 million from $70–$73 million
  • AVISE CTD volume +11% and trailing ASP up 4% to $446
  • Clinical evidence review showed AVISE CTD detected ~25% of SLE cases missed by conventional markers

Negative

  • Net loss $3.2 million and six‑month loss $7.2 million
  • Operating expenses rose to $13.9 million from $13.0 million YoY
  • Cash balance declined to $24.6 million from $32.2 million at December 31, 2025
  • Interest expense of $1.2 million in Q2 2026
  • Accumulated deficit reached $321.4 million as of June 30, 2026
  • Common shares outstanding increased to 24.2 million from 22.9 million at year‑end 2025

News Explained

The completed quarter reports a higher common share count, reducing existing holders’ percentage ownership absent offsetting changes.

Exagen has completed and reported its second quarter ended June 30, 2026; its reported common shares outstanding increased from $22,911,575 shares at December 31, 2025 to $24,193,101 shares at June 30, 2026, which reduces existing holders’ percentage ownership absent offsetting changes.

Market reaction after 2Q26 earnings report: XGN +34.40%

+34.40% $6.29 4.3x vol
15m delay
+34.40% Vs previous close
+14.5% Peak in 3 min
$6.29 Last Price
$4.69 $6.83 Day Range
$147.09M Market Cap
4.3x Rel. Volume

Following this news, XGN has gained 34.40%, reflecting a significant positive market reaction. Argus tracked a peak move of +14.5% during the session. Our momentum scanner has triggered 26 alerts so far, indicating elevated trading interest and price volatility. The stock is currently trading at $6.29. Trading volume is very high at 4.3x the average, suggesting strong buying interest.

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Market Context

The active S-3 shelf dated 2025-06-20 covers a resale registration for 1,150,000 shares tied to warr...
Analysis

The active S-3 shelf dated 2025-06-20 covers a resale registration for 1,150,000 shares tied to warrant exercise. Against this backdrop, improved guidance and operating metrics warrant monitoring alongside financing-related dilution risk.

Key Figures

Revenue: $19.9 million Revenue growth: 16% Adjusted EBITDA: loss of $0.1 million +5 more
8 metrics
Revenue $19.9 million Q2 2026, up 16% year over year
Revenue growth 16% Q2 2026 compared to Q2 2025
Adjusted EBITDA loss of $0.1 million Q2 2026 versus loss of $1.7 million in Q2 2025
Net loss $3.196 million Three months ended June 30, 2026
Full-year revenue guidance $72 million - $75 million 2026 guidance, increased from $70 million - $73 million
Test volume growth 11% AVISE CTD test volume compared to Q2 2025
Trailing-twelve-month ASP $446 per test Q2 2026, up $18 per test or 4% year over year
Systematic review population and finding over 3,100 patients; approximately 25% 14 medical centers; AVISE CTD identified SLE patients missed by conventional markers

Previous Earnings Reports

5 past events · Latest: May 11 (Positive)
Same Type Pattern 5 events
Date Event Sentiment 24h Move Catalyst
May 11 Q1 earnings report Positive +34.9% Record revenue, volume growth, improved EBITDA loss, and maintained full-year guidance
Jan 11 Preliminary results Positive -6.2% Projected revenue growth, higher ASP, increased cash, and preliminary unaudited results
Nov 04 Q3 earnings report Positive -9.0% Strong revenue growth, improved EBITDA loss, product launch, and reiterated guidance
Jul 29 Q2 earnings report Positive +14.3% Record revenue, higher test volume, expanded ASP, public offering, and guidance
May 05 Q1 earnings report Positive +3.8% Record revenue, higher ASP, testing-volume growth, credit facility, and guidance

24h Move is the share-price change in the day after each event; other market factors may also have contributed.

Pattern Detected

Earnings announcements were positive in content, with three aligned reactions and two divergences over the selected historical period.

Key Terms

adjusted ebitda, non-gaap financial measure, clia-certified, cap-accredited
4 terms
adjusted ebitda financial
"narrowed adjusted EBITDA loss to $0.1 million"
Adjusted EBITDA is a way companies measure how much money they make from their core operations, like running a business, by removing certain costs or income that aren’t part of regular business activities. It helps investors see how well a company is doing without distractions from unusual expenses or gains, making it easier to compare companies or track performance over time.
non-gaap financial measure financial
"adjusted EBITDA, which is not calculated in accordance with GAAP"
A non-GAAP financial measure is a way companies present their financial results that excludes certain expenses or income to show how they believe their core business is performing. It matters because it can give a clearer picture of how the company is really doing, but it can also be used to make results look better than they actually are.
clia-certified regulatory
"Exagen’s CLIA-certified, CAP-accredited laboratory"
CLIA-certified means a laboratory has passed U.S. federal standards for performing tests on human samples, showing its results are accurate, reliable and timely. For investors this matters because certification is often required to sell clinical test services, bill insurers, win hospital or physician partnerships and avoid regulatory penalties — much like a restaurant passing a health inspection or a car getting a safety sticker before it can be sold.
cap-accredited regulatory
"CLIA-certified, CAP-accredited laboratory specializes in the testing"
Cap-accredited means a laboratory or diagnostic service has been inspected and certified by the College of American Pathologists (CAP) for meeting rigorous standards in testing accuracy, quality control, staff qualifications and reporting. For investors, CAP accreditation signals that the lab’s results are more reliable and that the operation meets a well-recognized regulatory benchmark, which can reduce clinical and regulatory risk and support market trust and reimbursement; think of it like a high-score health inspection for a restaurant.

AI-generated analysis. How Rhea-AI works. Not financial advice.

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Achieved record total revenue, test volume and trailing twelve-month ASP

Reduced net loss by nearly 30% and narrowed adjusted EBITDA loss to $0.1 million

Increased full-year revenue guidance to $72 - $75 million

CARLSBAD, Calif., Aug. 04, 2026 (GLOBE NEWSWIRE) -- Exagen Inc. (Nasdaq: XGN), a leading provider of autoimmune testing solutions, today reported financial results for the quarter ended June 30, 2026, and recent corporate updates.

  Three Months Ended June 30, Six Months Ended June 30,
   2026   2025   2026   2025 
Unaudited. In thousands, except
ASP data.
  
Revenue $19,941  $17,202  $37,247  $32,700 
Gross margin  61.3%  60.4%  60.2%  59.7%
Operating expenses $13,939  $13,025  $27,558  $25,513 
Operating loss $(1,722) $(2,630) $(5,136) $(5,995)
Net loss $(3,196) $(4,439) $(7,163) $(8,191)
Adjusted EBITDA $(114) $(1,721) $(2,274) $(4,229)
Trailing-twelve-month average
selling price (ASP)
 $446  $428  $446  $428 
Cash and cash equivalents $24,588  $30,033  $24,588  $30,033 


Second Quarter 2026 and Recent Corporate Highlights:

  • Achieved record total revenue of $19.9 million, an increase of 16% compared to second quarter 2025.
  • Grew AVISE CTD test volume 11% compared to second quarter 2025.
  • Expanded AVISE CTD trailing twelve-month ASP to $446 per test, an increase of $18 per test, or 4% compared to second quarter 2025.
  • Drove a significant improvement in adjusted EBITDA, reporting a loss of $0.1 million compared to a loss of $1.7 million in second quarter 2025.
  • Ended the quarter with approximately $25 million in cash and cash equivalents.
  • Published a systematic review validating strong real-world AVISE Lupus performance in an analysis of over 3,100 patients across 14 medical centers, which demonstrated that use of AVISE CTD correctly identified approximately 25% of SLE patients missed by conventional markers.

“We continue to advance Exagen’s unique mission to bring clarity to autoimmune disease,” said John Aballi, President and Chief Executive Officer. “Second quarter financial results demonstrate the progress we’re making in improving the growth and operating profile of our business, putting us within reach of sustainable profitability and cash generation. At the same time, we are building on Exagen’s leadership in autoimmune diagnostics through continued investment in clinical evidence generation, pipeline innovation and AI-powered tools that support rheumatology workflows to strengthen our role in rheumatology decision-making.”

2026 Guidance   

The Company increased full-year 2026 revenue guidance to $72 million - $75 million compared to previous guidance of $70 million - $73 million.

Conference Call and Webcast

  • Date: August 4, 2026
  • Time: 8:30 a.m. ET/ 5:30 a.m. PT
  • U.S. dial-in: 877-407-0890
  • International dial-in: +1 201-389-0918
  • Webcast: Available via the Exagen Investor Relations website at investors.exagen.com

Replay: A telephone replay will be available until Tuesday, August 18, 2026:

  • U.S. replay: 877-660-6853
  • International replay: +1 201-612-7415
  • Replay passcode: 13760979
  • Webcast: A recording of the webcast will be available one hour after the call concludes via the Exagen Investor Relations website at investors.exagen.com

Use of Non-GAAP Financial Measures (Unaudited)

In addition to the financial results prepared in accordance with generally accepted accounting principles in the United States (GAAP), this press release contains the metric adjusted EBITDA, which is not calculated in accordance with GAAP and is a non-GAAP financial measure. Adjusted EBITDA is defined as net loss adjusted for interest income (expense), income tax expense (benefit), depreciation and amortization expense, stock‑based compensation expense, change in fair value of warrant liability, and certain other non‑cash, unusual or non‑recurring items, including, for example, losses on extinguishment of debt and changes in the fair value of warrant liabilities; we do not exclude normal, recurring, cash operating expenses from this measure. Such items could have a significant impact on the calculation of GAAP net loss.

Exagen uses adjusted EBITDA internally because the company believes these metrics provide useful supplemental information in assessing its operating performance reported in accordance with GAAP. Exagen believes adjusted EBITDA may enhance an evaluation of the operating performance because it excludes the impact of prior decisions made about capital investment, financing, investing and certain expenses the company believes are not indicative of the ongoing performance. However, this non-GAAP financial measure may be different from non-GAAP financial measures used by other companies, even when the same or similarly titled terms are used to identify such measures, limiting their usefulness for comparative purposes.

This non-GAAP financial measure is not meant to be considered in isolation or used as a substitute for net loss reported in accordance with GAAP, should be considered in conjunction with the financial information presented in accordance with GAAP, has no standardized meaning prescribed by GAAP, is unaudited, and is not prepared under any comprehensive set of accounting rules or principles. In addition, from time to time in the future, there may be other items that Exagen may exclude for purposes of these non-GAAP financial measures, and the company may in the future cease to exclude items that it has historically excluded for purposes of these non-GAAP financial measures. Likewise, Exagen may determine to modify the nature of adjustments to arrive at these non-GAAP financial measures. Because of the non-standardized definitions of non-GAAP financial measures, the non-GAAP financial measure as used by the company in this press release and the accompanying reconciliation table have limits in their usefulness to investors and may be calculated differently from, and therefore may not be directly comparable to, similarly titled measures used by other companies. Accordingly, investors should not place undue reliance on non-GAAP financial measures.

A reconciliation of net loss to non-GAAP adjusted EBITDA is provided in the financial schedules that are part of this press release.

About Exagen

Exagen Inc. (Nasdaq: XGN) is a leading provider of autoimmune diagnostics, committed to transforming care for patients with chronic and debilitating autoimmune conditions. Based in San Diego County, California, Exagen’s mission is to provide clarity in autoimmune disease decision-making and improve clinical outcomes through its innovative testing portfolio. The company’s flagship product, AVISE® CTD, enables clinicians to more effectively diagnose complex autoimmune conditions such as lupus, rheumatoid arthritis, and Sjögren’s disease earlier and with greater accuracy. Exagen’s CLIA-certified, CAP-accredited laboratory specializes in the testing of rheumatic diseases, delivering precise and timely results, supported by a suite of AVISE-branded tests for disease diagnosis, prognosis, and monitoring. With a focus on research, innovation, education, and patient-centered care, Exagen is dedicated to addressing the ongoing challenges of autoimmune disease management.

For more information, visit Exagen.com or follow Exagen on LinkedIn.

Forward Looking Statements

Exagen cautions you that statements contained in this press release regarding matters that are not historical facts are forward-looking statements. These statements are based on Exagen’s current beliefs and expectations. Such forward-looking statements include, but are not limited to, statements regarding: Exagen’s goals, strategies, positioning, and ambitions; evaluations and judgments regarding financial results and the potential implications of those results, potential future financial and business performance, including any improvements to adjusted EBITDA, ASP, net loss and potential profitability; the potential utility and effectiveness of Exagen’s services and testing solutions; the impact of Exagen’s revenue cycle management strategy on the timing of collections and cash burn; potential stockholder value and growth and full-year 2026 guidance. The inclusion of forward-looking statements should not be regarded as a representation by Exagen that any of its plans will be achieved. Actual results may differ from those set forth in this press release due to the risks and uncertainties inherent in Exagen’s business, including, without limitation: delays in reimbursement and coverage decisions from Medicare and third-party payors and interactions with regulatory authorities, and delays in ongoing and planned clinical trials involving its tests; the potential effects of inflation and tariffs on Exagen’s margins; and changes in laws and regulations related to Exagen’s regulatory requirements. Exagen’s commercial success depends upon attaining and maintaining significant market acceptance of its testing products among rheumatologists, patients, third-party payors and others in the medical community; Exagen’s ability to successfully execute on its business strategies; and ability to obtain additional funding; third-party payors not providing coverage and adequate reimbursement for Exagen’s testing products, including Exagen’s ability to collect on funds due; Exagen’s ability to obtain and maintain intellectual property protection for its testing products; regulatory developments affecting Exagen’s business; and other risks described in Exagen’s prior press releases and Exagen’s filings with the Securities and Exchange Commission (SEC), including under the heading “Risk Factors” in Exagen’s Annual Report on Form 10-K for the year ended December 31, 2025, filed with the SEC on March 10, 2026, and any subsequent filings with the SEC. You are cautioned not to place undue reliance on these forward-looking statements, which speak only as of the date hereof, and Exagen undertakes no obligation to update such statements to reflect events that occur or circumstances that exist after the date hereof. All forward-looking statements are qualified in their entirety by this cautionary statement, which is made under the safe harbor provisions of the Private Securities Litigation Reform Act of 1995.

Investors:

Tina Jacobsen, CFA
Exagen Inc.
ir@exagen.com

Exagen Inc.

Unaudited Condensed Statements of Operations
(in thousands, except share and per share amounts)

  Three Months Ended June 30, Six Months Ended June 30,
   2026   2025   2026   2025 
   
Revenue $19,941  $17,202  $37,247  $32,700 
Cost of revenue  7,724   6,807   14,825   13,182 
Gross margin  12,217   10,395   22,422   19,518 
Operating expenses:        
Selling, general and administrative expenses  12,513   11,542   24,579   22,746 
Research and development expenses  1,426   1,483   2,979   2,767 
Total operating expenses  13,939   13,025   27,558   25,513 
Loss from operations  (1,722)  (2,630)  (5,136)  (5,995)
Interest expense  (1,201)  (1,124)  (2,468)  (1,669)
Loss on extinguishment of debt     (295)     (295)
Change in fair value of warrant liability  (426)  (438)  456   (438)
Other income (expense), net  153   85   21   243 
Loss before income taxes  (3,196)  (4,402)  (7,127)  (8,154)
Income tax expense     (37)  (36)  (37)
Net loss $(3,196) $(4,439) $(7,163) $(8,191)
Net loss per share, basic and diluted $(0.13) $(0.21) $(0.30) $(0.41)
Weighted-average number of shares used to compute net loss per share, basic and diluted  24,164,569   21,085,749   24,012,761   19,830,265 


Exagen Inc.

Unaudited Condensed Balance Sheets
(in thousands, except share and per share amounts)

  June 30, 2026 December 31, 2025
     
Assets    
Current assets:    
Cash and cash equivalents $24,588  $32,220 
Accounts receivable, net  12,407   10,855 
Prepaid expenses and other current assets  5,862   5,818 
Total current assets  42,857   48,893 
Property and equipment, net  6,565   6,938 
Operating lease right-of-use assets  1,953   1,435 
Other assets  560   756 
Total assets $51,935  $58,022 
Liabilities and Stockholders' Equity    
Current liabilities:    
Accounts payable $4,439  $4,153 
Accrued and other current liabilities  4,939   6,327 
Deferred revenue  1,492   675 
Finance lease liabilities, current  1,091   1,135 
Operating lease liabilities, current  979   1,226 
Borrowings, current  517   643 
Total current liabilities  13,457   14,159 
Borrowings, non-current, net of discounts and debt issuance costs  22,322   22,264 
Finance lease liabilities, non-current  1,617   1,960 
Operating lease liabilities, non-current  1,130   438 
Warrant liability  1,193   1,752 
Total liabilities  39,719   40,573 
Commitments and contingencies (Note 5)    
Stockholders' equity:    
Preferred stock, $0.001 par value; 10,000,000 shares authorized, no shares issued or outstanding as of June 30, 2026 and December 31, 2025      
Common stock, $0.001 par value; 200,000,000 shares authorized as of June 30, 2026 and December 31, 2025; 24,193,101 and 22,911,575 shares issued and outstanding as of June 30, 2026 and December 31, 2025, respectively  24   23 
Additional paid-in capital  333,637   331,708 
Accumulated deficit  (321,445)  (314,282)
Total stockholders' equity  12,216   17,449 
Total liabilities and stockholders' equity $51,935  $58,022 


Exagen Inc.

Reconciliation of Non-GAAP Financial Measures (UNAUDITED)
The table below presents the reconciliation of adjusted EBITDA, which is a non-GAAP financial
measure. See "Use of Non-GAAP Financial Measures (UNAUDITED)" above for further
information regarding Exagen's use of non-GAAP financial measures.
  Three Months Ended June 30, Six Months Ended June 30,
   2026   2025   2026   2025 
(in thousands)  
Adjusted EBITDA        
Net loss $(3,196) $(4,439) $(7,163) $(8,191)
Other (income) expense  (153)  (85)  (21)  (243)
Interest expense  1,201   1,124   2,468   1,669 
Loss on extinguishment of debt     295      295 
Change in fair value of warrant liability  426   438   (456)  438 
Income tax expense (benefit)     37   36   37 
Depreciation and amortization expense  628   466   1,227   906 
Stock-based compensation expense  980   443   1,635   860 
Adjusted EBITDA (Non-GAAP) $(114) $(1,721) $(2,274) $(4,229)
         

FAQ

How did Exagen (XGN) perform financially in Q2 2026?

Exagen reported Q2 2026 revenue of $19.9 million, up 16% year over year. According to Exagen, net loss narrowed to $3.2 million, gross margin reached 61.3%, and adjusted EBITDA improved to a loss of $0.1 million, nearing breakeven.

What guidance did Exagen (XGN) give for full-year 2026 revenue?

Exagen raised its full-year 2026 revenue guidance to $72–$75 million. According to Exagen, this compares with previous guidance of $70–$73 million and reflects record revenue, higher AVISE CTD test volume, and improved average selling price trends in the first half.

Did Exagen (XGN) improve profitability and adjusted EBITDA in Q2 2026?

Yes, profitability metrics improved, though still negative. According to Exagen, net loss decreased to $3.2 million from $4.4 million, and adjusted EBITDA improved to a loss of $0.1 million, compared with a $1.7 million adjusted EBITDA loss in Q2 2025.

What is Exagen’s cash position and debt profile as of June 30, 2026?

Exagen held $24.6 million in cash and cash equivalents at June 30, 2026. According to Exagen, total assets were $51.9 million, with current liabilities of $13.5 million and non‑current borrowings of $22.3 million, plus finance and operating lease obligations.

What clinical evidence did Exagen report for its AVISE Lupus testing in 2026?

Exagen reported a systematic review of over 3,100 patients across 14 medical centers. According to Exagen, AVISE CTD correctly identified approximately 25% of SLE patients missed by conventional markers, supporting the real‑world performance of its AVISE Lupus-focused testing.

How did Exagen’s operating expenses and margins change in Q2 2026?

Operating expenses rose to $13.9 million from $13.0 million year over year. According to Exagen, gross margin improved to 61.3% from 60.4%, reflecting higher revenue and AVISE CTD ASP, while still generating a loss from operations of $1.7 million.