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Exagen Inc. Reports Record Q1 2025 Revenue Driven by Growth in Average Selling Price and Testing Volume

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Exagen reported record Q1 2025 revenue of $15.5 million, driven by growth in AVISE CTD test volume and expanded average selling price (ASP). The company's trailing twelve-month ASP increased to $419, up $42 per test compared to Q1 2024. Despite revenue growth, Exagen posted a net loss of $3.75 million and adjusted EBITDA loss of $2.51 million. The company ended Q1 with $11.2 million in cash and secured a $25 million credit facility with Perceptive Advisors in April. Key developments include the launch of new SLE and RA biomarkers, publication of T-cell research, and commercial expansion plans. Exagen provided 2025 guidance of at least $65 million in revenue and expects positive adjusted EBITDA by Q4 2025.

Exagen ha riportato un fatturato record di 15,5 milioni di dollari nel primo trimestre del 2025, trainato dalla crescita del volume dei test AVISE CTD e dall'aumento del prezzo medio di vendita (ASP). L'ASP negli ultimi dodici mesi è salito a 419 dollari, con un incremento di 42 dollari per test rispetto al primo trimestre del 2024. Nonostante la crescita del fatturato, Exagen ha registrato una perdita netta di 3,75 milioni di dollari e una perdita di EBITDA rettificato di 2,51 milioni di dollari. La società ha chiuso il primo trimestre con 11,2 milioni di dollari in contanti e ha ottenuto una linea di credito da 25 milioni di dollari con Perceptive Advisors ad aprile. Tra le principali novità figurano il lancio di nuovi biomarcatori per SLE e AR, la pubblicazione di ricerche sui linfociti T e i piani di espansione commerciale. Exagen ha fornito una previsione per il 2025 di almeno 65 milioni di dollari di ricavi e si aspetta un EBITDA rettificato positivo entro il quarto trimestre del 2025.
Exagen reportó ingresos récord de 15,5 millones de dólares en el primer trimestre de 2025, impulsados por el crecimiento en el volumen de pruebas AVISE CTD y el aumento del precio medio de venta (ASP). El ASP de los últimos doce meses aumentó a 419 dólares, un incremento de 42 dólares por prueba en comparación con el primer trimestre de 2024. A pesar del crecimiento de los ingresos, Exagen registró una pérdida neta de 3,75 millones de dólares y una pérdida de EBITDA ajustado de 2,51 millones de dólares. La compañía terminó el primer trimestre con 11,2 millones de dólares en efectivo y aseguró una línea de crédito de 25 millones de dólares con Perceptive Advisors en abril. Entre los desarrollos clave se incluyen el lanzamiento de nuevos biomarcadores para SLE y AR, la publicación de investigaciones sobre células T y planes de expansión comercial. Exagen proporcionó una proyección para 2025 de al menos 65 millones de dólares en ingresos y espera un EBITDA ajustado positivo para el cuarto trimestre de 2025.
Exagen은 AVISE CTD 테스트 수량 증가와 평균 판매 가격(ASP) 상승에 힘입어 2025년 1분기 매출 기록인 1,550만 달러를 보고했습니다. 최근 12개월간 ASP는 테스트당 419달러로, 2024년 1분기 대비 테스트당 42달러 상승했습니다. 매출 증가에도 불구하고 Exagen은 375만 달러의 순손실과 251만 달러의 조정 EBITDA 손실을 기록했습니다. 회사는 1분기 말에 1,120만 달러의 현금을 보유했으며 4월에 Perceptive Advisors와 2,500만 달러의 신용 한도를 확보했습니다. 주요 발전 사항으로는 새로운 SLE 및 RA 바이오마커 출시, T세포 연구 발표, 상업 확장 계획이 포함됩니다. Exagen은 2025년 매출 최소 6,500만 달러를 목표로 하며 2025년 4분기까지 조정 EBITDA 흑자를 기대하고 있습니다.
Exagen a annoncé un chiffre d'affaires record de 15,5 millions de dollars au premier trimestre 2025, porté par la croissance du volume des tests AVISE CTD et l'augmentation du prix de vente moyen (ASP). L'ASP sur les douze derniers mois a atteint 419 dollars, soit une hausse de 42 dollars par test par rapport au premier trimestre 2024. Malgré cette croissance du chiffre d'affaires, Exagen a enregistré une perte nette de 3,75 millions de dollars et une perte d'EBITDA ajusté de 2,51 millions de dollars. La société a terminé le premier trimestre avec 11,2 millions de dollars de liquidités et a obtenu en avril une ligne de crédit de 25 millions de dollars avec Perceptive Advisors. Parmi les faits marquants figurent le lancement de nouveaux biomarqueurs pour le LES et la polyarthrite rhumatoïde, la publication de recherches sur les cellules T et des plans d'expansion commerciale. Exagen a fourni des prévisions pour 2025 d'au moins 65 millions de dollars de revenus et prévoit un EBITDA ajusté positif d'ici le quatrième trimestre 2025.
Exagen meldete einen rekordverdächtigen Umsatz von 15,5 Millionen US-Dollar im ersten Quartal 2025, angetrieben durch ein Wachstum des AVISE CTD-Testvolumens und einen gestiegenen durchschnittlichen Verkaufspreis (ASP). Der ASP der letzten zwölf Monate stieg auf 419 US-Dollar, ein Anstieg von 42 US-Dollar pro Test im Vergleich zum ersten Quartal 2024. Trotz Umsatzwachstum verzeichnete Exagen einen Nettoverlust von 3,75 Millionen US-Dollar und einen bereinigten EBITDA-Verlust von 2,51 Millionen US-Dollar. Das Unternehmen beendete das erste Quartal mit 11,2 Millionen US-Dollar in bar und sicherte sich im April eine Kreditlinie über 25 Millionen US-Dollar mit Perceptive Advisors. Zu den wichtigsten Entwicklungen gehören die Einführung neuer Biomarker für SLE und RA, die Veröffentlichung von T-Zell-Forschung und Pläne zur kommerziellen Expansion. Exagen gab eine Umsatzprognose für 2025 von mindestens 65 Millionen US-Dollar ab und erwartet bis zum vierten Quartal 2025 ein positives bereinigtes EBITDA.
Positive
  • Record quarterly revenue of $15.5 million, up from $14.4 million in Q1 2024
  • ASP increased by $42 to $419 per test compared to Q1 2024
  • Secured $25 million credit facility with Perceptive Advisors
  • Launched new SLE and RA biomarkers with expected reimbursement of $90 per test
  • Projected combined cash and receivables of $28 million as of April 30, 2025
  • Guidance for 2025 revenue of at least $65 million with positive adjusted EBITDA expected in Q4
Negative
  • Net loss increased to $3.75 million from $3.36 million in Q1 2024
  • Adjusted EBITDA loss widened to $2.51 million from $1.99 million
  • Cash position decreased to $11.2 million from $27.3 million year-over-year
  • Gross margin declined to 58.9% from 59.6% in Q1 2024

Insights

Exagen reports 7.5% revenue growth to $15.5M, but widening losses and reduced cash position offset the positive revenue trajectory.

Exagen's Q1 2025 earnings reveal record revenue of $15.5 million, a 7.5% year-over-year increase from $14.4 million in Q1 2024. This growth was driven by two factors: increased AVISE CTD test volume and a substantial improvement in pricing, with the trailing twelve-month average selling price (ASP) rising to $419, an 11.1% increase from the prior year.

Despite the revenue gains, the company's financial performance shows concerning trends. Net loss widened to $3.75 million from $3.36 million in Q1 2024, representing an 11.7% deterioration. Similarly, adjusted EBITDA loss increased to $2.51 million from $1.99 million, a 25.9% increase. Gross margin saw a slight decline to 58.9% from 59.6% year-over-year.

The company's cash position has substantially decreased, with cash and cash equivalents standing at $11.2 million compared to $27.3 million a year earlier. Exagen explains this is partly due to their strategy of holding insurance claims in Q1 to maximize reimbursement, resulting in accounts receivable of $14.7 million. Following the initial release of held claims in April, the company projects combined cash and receivables of approximately $28 million.

To address financing needs, Exagen closed a $25 million senior secured credit facility with Perceptive Advisors in April 2025, which refinanced existing debt and extended maturity dates. This provides additional financial flexibility and potential growth capital.

On the product front, Exagen has enhanced its AVISE CTD offering with new biomarkers for lupus and rheumatoid arthritis, expected to generate additional reimbursement of $90 per test. The company has also initiated commercial expansion with new sales territories.

Management's forward guidance projects full-year 2025 revenue of at least $65 million and anticipates achieving positive adjusted EBITDA by Q4 2025. Given Q1 revenue of $15.5 million, this suggests stronger performance in upcoming quarters to meet the annual target.

From a biotechnology perspective, Exagen continues to strengthen its position in the specialized autoimmune testing market through both clinical validation and product enhancements. The company's expansion of their AVISE CTD test with new biomarkers for systemic lupus erythematosus (SLE) and rheumatoid arthritis (RA) represents a meaningful advancement in their diagnostic capabilities.

The scientific credibility of Exagen's approach is reinforced by their recently published T-cell research in Frontiers in Immunology, which details the clinical benefits of their new SLE biomarkers. Additionally, their presentation on biomarkers for early kidney damage detection at the Chronic Kidney Disease Drug Development Summit indicates ongoing R&D efforts to expand their diagnostic applications beyond current offerings.

The expected $90 per test reimbursement for the new biomarkers suggests favorable reception from payers who recognize the clinical utility of these enhanced tests. This incremental revenue opportunity, combined with the 11.1% increase in average selling price over the past year, demonstrates the company's ability to extract greater value from their diagnostic platform.

The initiation of commercial expansion with new sales territories signals management's confidence in market demand for their specialized testing solutions. However, the increased operating expenses ($12.5 million vs. $11.6 million year-over-year) and widening losses suggest Exagen remains in an investment phase, prioritizing market penetration and portfolio expansion over immediate profitability.

The company's financial strategy of temporarily holding claims to maximize reimbursement highlights the complexities of the diagnostic reimbursement landscape. While this approach may optimize revenue in the long run, it creates short-term pressure on cash flow that necessitated the recent $25 million credit facility.

Exagen's continued test volume growth and ASP expansion are positive indicators of clinical adoption. The projected timeline to positive adjusted EBITDA by Q4 2025 suggests management sees a clear path to operational efficiency, though execution will be key to achieving this milestone.

CARLSBAD, Calif., May 05, 2025 (GLOBE NEWSWIRE) -- Exagen Inc. (Nasdaq: XGN), a leading provider of autoimmune testing solutions, today reported financial results for the quarter ended March 31, 2025, and recent corporate updates.

  Three Months Ended March 31,
   2025   2024 
(in thousands, except ASP data)  
Revenue $15,498  $14,415 
Gross margin  58.9%  59.6%
Operating expenses $12,488  $11,601 
Operating loss $(3,365) $(3,003)
Net loss $(3,752) $(3,360)
Adjusted EBITDA $(2,508) $(1,992)
Cash and cash equivalents $11,194  $27,267 
Trailing-twelve-month average selling price (ASP) $419  $377 
         

Q1 2025 Highlights and Recent Corporate Updates:

  • Delivered record total revenue of $15.5 million on the strength of continued ASP expansion and AVISE CTD test volume growth.

  • Expanded AVISE CTD trailing twelve-month ASP to $419, an increase of $42 per test over the first quarter of 2024.

  • Enhanced AVISE CTD offering with commercial launch of new systemic lupus erythematosus (SLE) and rheumatoid arthritis (RA) biomarkers; expected reimbursement in line with initial estimates of $90 per test.

  • Ended the first quarter of 2025 with cash, cash equivalents and restricted cash of $11.2 million, with an accounts receivable balance of $14.7 million, driven by the company's strategy to hold claims in the first quarter to maximize reimbursement. Following the initial release of held claims in April 2025, combined cash, cash equivalents and accounts receivable are projected to be approximately $28 million as of April 30, 2025.

  • Closed a senior secured credit facility with Perceptive Advisors on April 25, 2025, with $25 million funded at closing to refinance existing debt and extend maturity; potential additional borrowing capacity for minimally dilutive growth capital available.

  • Published T-cell manuscript in a peer-reviewed journal, Frontiers in Immunology, detailing clinical benefit of new SLE biomarkers.

  • Presented research on biomarkers for early detection of kidney damage at the 7th Annual Chronic Kidney Disease Drug Development Summit in Boston.

  • Initiated commercial expansion with first wave of new sales territories identified.

2025 Guidance 

The company expects 2025 full-year revenue of at least $65 million and anticipates being on-track to deliver positive adjusted EBITDA in the fourth quarter of 2025.

Conference Call

A conference call to review first quarter 2025 financial results and to provide a business update is scheduled for today, May 5, 2025 at 8:30 a.m. ET (5:30 a.m. PT). Interested parties may access the conference call by dialing (201) 389-0918 (U.S.) or (877) 407-0890 (international). Additionally, a link to a live webcast of the call will be available in the Investor Relations section of Exagen's website at investors.exagen.com.

Participants are asked to join a few minutes prior to the call to register for the event. A replay of the conference call will be available until May 19, 2025. Interested parties may access the replay by dialing (201) 612-7415 (U.S.) or (877) 660-6853 (international) using passcode 13753132. A link to the replay of the webcast will also be available in the Investor Relations section of Exagen's website.

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 excludes from net loss interest income (expense), income tax expense (benefit), depreciation and amortization expense, stock-based compensation expense and other expenses or income that management believes are not representative of the company’s operations. 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 our 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 our 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 our 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 syndrome earlier and with greater accuracy. Exagen’s laboratory specializes in the testing of rheumatic diseases, delivering precise and timely results, supported by a full 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, please visit Exagen.com or follow @ExagenInc on X.

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 and/or Exagen’s ability obtain additional funding pursuant to its secured credit facility with Perceptive Advisors (which is subject to milestones and conditions); the potential utility and effectiveness of Exagen’s services and testing solutions; potential shareholder value and growth and full-year 2025 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; 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, 2024, filed with the SEC on March 11, 2025 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.

Contact:
Ryan Douglas
Exagen Inc.
ir@exagen.com
760.560.1525


Exagen Inc.

Unaudited Condensed Statements of Operations
(in thousands, except share and per share data)
  Three Months Ended March 31,
   2025   2024 
   
Revenue $15,498  $14,415 
Cost of revenue  6,375   5,817 
Gross margin  9,123   8,598 
Operating expenses:    
Selling, general and administrative expenses  11,204   10,542 
Research and development expenses  1,284   1,059 
Total operating expenses  12,488   11,601 
Loss from operations  (3,365)  (3,003)
Interest expense  (545)  (549)
Interest income  158   192 
Net loss $(3,752) $(3,360)
Net loss per share, basic and diluted $(0.20) $(0.19)
Weighted-average number of shares used to compute net loss per share, basic and diluted  18,557,390   17,944,438 


Exagen Inc.

Unaudited Condensed Balance Sheets
(in thousands, except share and per share data)
  March 31,
2025
 December 31,
2024
     
Assets    
Current assets:    
Cash and cash equivalents $11,194  $22,036 
Accounts receivable, net  14,728   7,835 
Prepaid expenses and other current assets  6,583   6,584 
Total current assets  32,505   36,455 
Property and equipment, net  5,025   5,283 
Operating lease right-of-use assets  2,168   2,401 
Other assets  596   550 
Total assets $40,294  $44,689 
Liabilities and Stockholders' Equity    
Current liabilities:    
Accounts payable $4,509  $4,137 
Accrued and other current liabilities  4,948   7,117 
Deferred revenue  876   733 
Operating lease liabilities, current  1,127   1,096 
Borrowings, current  2,535   423 
Total current liabilities  13,995   13,506 
Borrowings, non-current, net of discounts and debt issuance costs  18,405   19,822 
Operating lease liabilities, non-current  1,369   1,664 
Other liabilities, non-current  122   157 
Total liabilities  33,891   35,149 
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 March 31, 2025 and December 31, 2024      
Common stock, $0.001 par value; 200,000,000 shares authorized as of March 31, 2025 and December 31, 2024; 17,950,033 and 17,640,328 shares issued and outstanding as of March 31, 2025 and December 31, 2024, respectively  18   18 
Additional paid-in capital  304,468   303,853 
Accumulated deficit  (298,083)  (294,331)
Total stockholders' equity  6,403   9,540 
Total liabilities and stockholders' equity $40,294  $44,689 


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 the company's use of non-GAAP financial measures.

  Three Months Ended March 31,
   2025   2024 
(in thousands)  
Adjusted EBITDA    
Net loss $(3,752) $(3,360)
Other (income) expense  (158)  (192)
Interest expense  545   549 
Depreciation and amortization expense  440   458 
Stock-based compensation expense  417   553 
Adjusted EBITDA (Non-GAAP) $(2,508) $(1,992)

FAQ

What was Exagen's (XGN) revenue in Q1 2025?

Exagen reported record revenue of $15.5 million in Q1 2025, up from $14.4 million in Q1 2024.

What is Exagen's (XGN) revenue guidance for 2025?

Exagen expects full-year 2025 revenue of at least $65 million and anticipates achieving positive adjusted EBITDA in Q4 2025.

How much did Exagen (XGN) secure in the credit facility with Perceptive Advisors?

Exagen secured a $25 million senior secured credit facility with Perceptive Advisors on April 25, 2025, with potential additional borrowing capacity available.

What was Exagen's (XGN) average selling price (ASP) in Q1 2025?

Exagen's trailing twelve-month average selling price (ASP) was $419, an increase of $42 per test compared to Q1 2024.

What was Exagen's (XGN) net loss in Q1 2025?

Exagen reported a net loss of $3.75 million in Q1 2025, compared to a net loss of $3.36 million in Q1 2024.
Exagen Inc.

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