NeuroPace Reports Second Quarter 2025 Financial Results and Increases 2025 Revenue Guidance
NeuroPace (NASDAQ: NPCE), a medical device company specializing in epilepsy treatment, reported strong Q2 2025 financial results. The company achieved record quarterly revenue of $23.5 million, representing a 22% year-over-year growth. Gross margin improved to 77.1%, up from 73.4% in Q2 2024.
The company increased its 2025 revenue guidance to $94-98 million (18-23% growth) and raised gross margin guidance to 75-76%. Key operational highlights include preliminary data from the NAUTILUS study for IGE therapy, showing a 79% median GTC seizure reduction at 12 months. NeuroPace also secured a new $75 million credit facility with MidCap Financial and maintained favorable CMS reimbursement status for RNS procedures.
NeuroPace (NASDAQ: NPCE), azienda di dispositivi medici specializzata nel trattamento dell'epilessia, ha annunciato solidi risultati finanziari del 2° trimestre 2025. La società ha registrato un fatturato trimestrale record di $23.5 milioni, con una crescita del 22% su base annua. Il margine lordo è salito al 77,1%, rispetto al 73,4% nel Q2 2024.
La società ha aumentato la guidance dei ricavi per il 2025 a $94-98 milioni (crescita 18-23%) e ha alzato la previsione del margine lordo al 75-76%. Tra i principali punti operativi, i dati preliminari dello studio NAUTILUS per la terapia IGE mostrano una riduzione mediana delle crisi GTC del 79% a 12 mesi. NeuroPace ha inoltre ottenuto una nuova linea di credito da $75 milioni con MidCap Financial e ha mantenuto uno status di rimborso favorevole da parte dei CMS per le procedure RNS.
NeuroPace (NASDAQ: NPCE), compañía de dispositivos médicos especializada en el tratamiento de la epilepsia, presentó sólidos resultados financieros del 2T 2025. La empresa alcanzó un récord de ingresos trimestrales de $23.5 millones, lo que representa un crecimiento interanual del 22%. El margen bruto mejoró hasta el 77,1%, frente al 73,4% en el 2T 2024.
La compañía elevó su guía de ingresos para 2025 a $94-98 millones (crecimiento 18-23%) y aumentó la previsión del margen bruto al 75-76%. Entre los aspectos operativos clave, los datos preliminares del estudio NAUTILUS para la terapia IGE muestran una reducción mediana de las convulsiones GTC del 79% a 12 meses. NeuroPace también aseguró una nueva línea de crédito de $75 millones con MidCap Financial y mantuvo un estatus favorable de reembolso por parte de CMS para los procedimientos RNS.
NeuroPace (NASDAQ: NPCE)는 간질 치료를 전문으로 하는 의료기기 회사로, 2025년 2분기 실적에서 견조한 성과를 보고했습니다. 회사는 분기별 최고 매출 $23.5M을 기록하며 전년 동기 대비 22% 성장했습니다. 총이익률은 77.1%로 2024년 2분기의 73.4%에서 개선되었습니다.
회사는 2025년 매출 가이던스를 $94-98M(18-23% 성장)으로 상향 조정하고 총이익률 가이던스도 75-76%로 높였습니다. 주요 운영 하이라이트로는 IGE 치료를 위한 NAUTILUS 연구의 예비 데이터가 12개월 시점에서 GTC 발작 중앙값 79% 감소를 보여준 점이 있습니다. 또한 NeuroPace는 MidCap Financial과 $75M의 신규 신용한도를 확보했으며 RNS 시술에 대한 CMS의 유리한 상환 지위를 유지했습니다.
NeuroPace (NASDAQ: NPCE), société de dispositifs médicaux spécialisée dans le traitement de l'épilepsie, a publié de solides résultats financiers du T2 2025. La société a réalisé un chiffre d'affaires trimestriel record de 23,5 M$, soit une croissance de 22% en glissement annuel. La marge brute s'est améliorée à 77,1%, contre 73,4% au T2 2024.
La société a relevé ses prévisions de revenus pour 2025 à 94-98 M$ (croissance de 18-23%) et augmenté la prévision de marge brute à 75-76%. Parmi les points opérationnels clés figurent des données préliminaires de l'étude NAUTILUS pour la thérapie IGE montrant une réduction médiane des crises GTC de 79% à 12 mois. NeuroPace a également obtenu une nouvelle ligne de crédit de 75 M$ avec MidCap Financial et a conservé un statut de remboursement favorable par les CMS pour les procédures RNS.
NeuroPace (NASDAQ: NPCE), ein Medizintechnikunternehmen mit Schwerpunkt auf Epilepsiebehandlung, meldete starke Finanzergebnisse für Q2 2025. Das Unternehmen erzielte einen rekordverdächtigen Quartalsumsatz von $23,5 Millionen, was einem Jahreswachstum von 22% entspricht. Die Bruttomarge verbesserte sich auf 77,1% gegenüber 73,4% im Q2 2024.
Das Unternehmen hob seine Umsatzprognose für 2025 auf $94–98 Millionen (18–23% Wachstum) an und erhöhte die Prognose für die Bruttomarge auf 75–76%. Wichtige operative Highlights sind vorläufige Daten der NAUTILUS-Studie zur IGE-Therapie, die eine mediane Reduktion generalisierter tonisch-klonischer Anfälle (GTC) um 79% nach 12 Monaten zeigen. NeuroPace sicherte sich außerdem eine neue $75-Millionen-Kreditlinie bei MidCap Financial und behielt eine günstige CMS-Erstattungsposition für RNS-Verfahren bei.
- Record quarterly revenue of $23.5M, up 22% year-over-year
- Strong gross margin improvement to 77.1% from 73.4% year-over-year
- Secured new $75M credit facility at favorable terms
- Increased 2025 revenue guidance to $94-98M
- NAUTILUS study showed 79% median GTC seizure reduction at 12 months
- Maintained favorable CMS reimbursement status for RNS procedures
- Operating expenses increased to $25M from $20.4M year-over-year
- Net loss widened to $8.7M from $7.5M in Q2 2024
- Cash position decreased to $62.1M from $66.3M in previous quarter
- NAUTILUS study did not reach statistical significance on primary effectiveness endpoint
Insights
NeuroPace delivered strong Q2 results with 22% revenue growth and raised 2025 guidance, showing operational momentum despite mixed clinical data.
NeuroPace delivered an impressive quarter with
The company has strengthened its financial position by refinancing its debt into a new
Operating expenses increased to
Management's increased guidance for 2025 revenue to
The favorable CMS decision maintaining the current MS-DRG assignment for RNS procedures is critical for preserving Medicare reimbursement stability, eliminating a potential headwind for adoption in an important patient demographic.
NAUTILUS data shows promising seizure reduction for IGE patients despite missing primary endpoint, potentially expanding NeuroPace's addressable market significantly.
The preliminary one-year data from the NAUTILUS study represents a potentially significant development for drug-resistant epilepsy treatment. While the study didn't meet its primary effectiveness endpoint, the secondary endpoints revealed compelling clinical benefits, particularly the
Even more promising are the preliminary 18-24 month data showing better than
The potential expansion to Idiopathic Generalized Epilepsy (IGE) would be significant as it represents approximately
NeuroPace appears on track to submit this data to the FDA in the second half of 2025 for potential indication expansion. While missing the primary endpoint creates some regulatory uncertainty, the robust secondary endpoints and favorable safety profile provide a compelling case. The company is also advancing its pediatric PMA supplement program, which could further expand the addressable patient population.
The operational metrics showing record highs in both active accounts and prescribers indicate growing physician acceptance of RNS therapy as a standard treatment option for drug-resistant epilepsy. This broader adoption is crucial for reaching the approximately 1.1 million patients with drug-resistant epilepsy in the US who could potentially benefit from this therapy.
-- Reported record quarterly revenue of
-- Increased full-year 2025 revenue guidance to between
-- Remain on track to submit NAUTILUS data to FDA for potential IGE indication expansion
in the second half of 2025—
--CMS maintains current MS-DRG assignment for RNS System® procedures--
MOUNTAIN VIEW, Calif., Aug. 12, 2025 (GLOBE NEWSWIRE) -- NeuroPace, Inc. (Nasdaq: NPCE), a medical device company focused on transforming the lives of people living with epilepsy, today reported financial results for the second quarter ended June 30, 2025, and provided a corporate update.
Second Quarter 2025 Financial Highlights
- Revenue grew
22% year-over-year to$23.5 million - RNS System revenue grew
21% year-over-year for the first half of 2025 compared to the first half of 2024 and16% for the second quarter of 2025 compared to the second quarter of 2024 - Delivered strong gross margin of
77.1% driven by manufacturing efficiencies and positive product mix - Refinanced existing debt into a new
$75 million credit facility with MidCap Financial at favorable terms
Second Quarter 2025 Operational & Strategic Highlights
- Announced compelling one-year preliminary data from the NAUTILUS study evaluating RNS therapy in IGE, demonstrating a statistically significant safety profile but did not reach statistical significance on the primary effectiveness endpoint. The study demonstrated statistically significant and clinically meaningful improvement across multiple prespecified secondary effectiveness endpoints, including
79% median GTC seizure reduction at 12 months, which meaningfully exceeded the44% reduction in seizures at 12 months that was seen in the Company’s pivotal trial in focal epilepsy that led to FDA approval. Data collected to date at 18 and 24 months currently indicate better than80% median GTC seizure reduction. - Built on Project CARE momentum with an increasing contribution in the second quarter compared with the first quarter of 2025
- Achieved record highs in number of both active accounts and prescribers
- Received favorable outcome in CMS’s FY 2026 Inpatient Prospective Payment System (IPPS) final rule, with RNS procedures remaining in MS-DRG 023, preserving reimbursement stability for Medicare patients. The Company will continue constructive engagement with CMS to ensure future policies reflect the full value of RNS therapy
“We are pleased with the continued momentum in our business through the second quarter of 2025, as we made significant progress across a number of key initiatives to position NeuroPace for sustained long-term growth,” said Joel Becker, Chief Executive Officer. “We are advancing our strategy, driving increased access to and adoption of RNS therapy and supporting operating leverage as we scale.”
Becker continued, “We also made important clinical and regulatory and research and development progress in the quarter, including advancing our NAUTILUS and the pediatric PMA supplement programs and advancing our AI software development programs. These efforts reflect our leadership in the field, commitment to addressing unmet patient needs, and setting the standard of care for drug-resistant epilepsy.”
Second Quarter 2025 Financial Results
Total revenue in the second quarter of 2025 grew
Gross margin for the second quarter of 2025 was
Total operating expenses in the second quarter of 2025 were
Sales and marketing expense in the second quarter of 2025 was
Loss from operations was
The Company’s cash, cash equivalents and short-term investments balance as of June 30, 2025, was
Updated Full Year 2025 Financial Guidance
- Increased total revenue guidance for full year 2025 to between
$94 million and$98 million , representing growth of18% –23% versus$79.9 million in 2024, up from previous guidance of between$93 million and$97 million - Increased gross margin guidance to between
75% and76% , up from previous guidance of73% and75% - Maintained total operating expenses range between
$92 million and$95 million , including approximately$11 million in stock-based compensation, a non-cash expense
Webcast and Conference Call Information
NeuroPace will host a conference call to discuss the second quarter 2025 financial results after market close on Tuesday, August 12, 2025, at 4:30 P.M. Eastern Time. Investors interested in listening to the conference call may do so by accessing a live and archived webcast of the event at (click here). Individuals interested in participating in the call via telephone may access the call by dialing +1-877-407-3982 and referencing Conference ID 13754370. The webcast will be archived on the Company’s investor relations website at https://investors.neuropace.com/news-and-events/events and will be available for replay for at least 90 days after the event.
About NeuroPace, Inc.
Based in Mountain View, Calif., NeuroPace is a medical device company focused on transforming the lives of people living with epilepsy by reducing or eliminating the occurrence of debilitating seizures. Its novel and differentiated RNS System is the first and only commercially available, brain-responsive platform that delivers personalized, real-time treatment at the seizure source. This platform can drive a better standard of care for patients living with drug-resistant epilepsy and has the potential to offer a more personalized solution and improved outcomes to the large population of patients suffering from other brain disorders.
Forward Looking Statements
This press release may contain forward-looking statements made pursuant to the safe harbor provisions of the Private Securities Litigation Reform Act of 1995. These statements may be identified by words such as “aims,” “anticipates,” “believes,” “could,” “estimates,” “expects,” “forecasts,” “goal,” “intends,” “may,” “plans,” “possible,” “potential,” “seeks,” “will” and variations of these words or similar expressions that are intended to identify forward-looking statements, although not all forward-looking statements contain these words. NeuroPace may not actually achieve the plans, intentions or expectations disclosed in these forward-looking statements, and you should not place undue reliance on these forward-looking statements. Forward-looking statements in this press release include, but are not limited to, statements regarding: NeuroPace’s expectations, forecasts and beliefs with respect to potential indication expansion for its RNS System and its software, technology and other product development efforts; increasing access to and adoption of RNS therapy; NeuroPace’s ability to maintain or increase the gross margin for its RNS System compared to historical rates; NeuroPace’s ability to execute on its long-term revenue growth strategy, including with respect to sustained revenue growth and long-term value creation; and NeuroPace’s anticipated revenue, gross margin and operating expenses for the year ending 2025. Actual results or events could differ materially from the plans, intentions and expectations disclosed in these forward-looking statements as a result of various factors, including: actual operating results may differ significantly from any guidance provided; uncertainties related to market acceptance and adoption of NeuroPace’s RNS System and impacts to NeuroPace’s revenue for 2025 and in the future; risks that NeuroPace’s operating expenses could be higher than anticipated and that it could use its cash resources sooner than expected; risks that NeuroPace’s gross margin may be lower than forecast; risks related to the pricing of the RNS System and availability of adequate reimbursement for the procedures to implant the RNS System and for clinicians to provide ongoing care for patients treated with the RNS System; risks related to regulatory compliance and expectations for regulatory submissions and approvals to expand the market for NeuroPace’s RNS System, including risks related to the NAUTILUS clinical trial; risks related to product development, including risks related to the development of AI-powered software and the next generation device platform; risks related to NeuroPace’s reliance on contractors and other third parties, including single-source suppliers and vendors; and other important factors. These and other risks and uncertainties include those described more fully in the section titled “Risk Factors” and “Management’s Discussion and Analysis of Financial Condition and Results of Operations” and elsewhere in NeuroPace’s public filings with the U.S. Securities and Exchange Commission (SEC), including its Quarterly Report on Form 10-Q for the quarter ended March 31, 2025, filed with the SEC on May 13, 2025, as well as any other reports that it may file with the SEC in the future. Forward-looking statements contained in this announcement are based on information available to NeuroPace as of the date hereof. NeuroPace undertakes no obligation to update such information except as required under applicable law. These forward-looking statements should not be relied upon as representing NeuroPace’s views as of any date subsequent to the date of this press release and should not be relied upon as a prediction of future events. In light of the foregoing, investors are urged not to rely on any forward-looking statement in reaching any conclusion or making any investment decision about any securities of NeuroPace.
Investor Contact:
Scott Schaper
Head of Investor Relations
sschaper@neuropace.com
investors@neuropace.com
NeuroPace, Inc. Condensed Statements of Operations (unaudited) | |||||||||||||||
Three Months Ended June 30, | Six Months Ended June 30, | ||||||||||||||
(in thousands, except share and per share amounts) | 2025 | 2024 | 2025 | 2024 | |||||||||||
Revenue | $ | 23,520 | $ | 19,256 | $ | 46,044 | $ | 37,380 | |||||||
Cost of goods sold | 5,388 | 5,122 | 10,570 | 9,903 | |||||||||||
Gross profit | 18,132 | 14,134 | 35,474 | 27,477 | |||||||||||
Operating expenses | |||||||||||||||
Sales and marketing | 12,043 | 9,756 | 23,046 | 19,789 | |||||||||||
Research and development | 6,845 | 6,065 | 14,285 | 11,849 | |||||||||||
General and administrative | 6,068 | 4,543 | 10,114 | 9,614 | |||||||||||
Total operating expenses | 24,956 | 20,364 | 47,445 | 41,252 | |||||||||||
Loss from operations | (6,824 | ) | (6,230 | ) | (11,971 | ) | (13,775 | ) | |||||||
Interest income | 718 | 762 | 1,511 | 1,589 | |||||||||||
Interest expense | (2,059 | ) | (2,166 | ) | (4,212 | ) | (4,424 | ) | |||||||
Other income (expense), net | (486 | ) | 120 | (568 | ) | 171 | |||||||||
Net loss and comprehensive loss | $ | (8,651 | ) | $ | (7,514 | ) | $ | (15,240 | ) | $ | (16,439 | ) | |||
Net loss per share attributable to common stockholders, basic and diluted | $ | (0.26 | ) | $ | (0.26 | ) | $ | (0.47 | ) | $ | (0.58 | ) | |||
Weighted-average shares used in computing net loss per share attributable to common stockholders, basic and diluted | 32,863,031 | 28,853,216 | 32,175,789 | 28,569,196 | |||||||||||
NeuroPace, Inc. Condensed Balance Sheets (unaudited) | |||||||
June 30, | December 31, | ||||||
(in thousands, except share and per share amounts) | 2025 | 2024 | |||||
Assets | |||||||
Current assets | |||||||
Cash and cash equivalents | $ | 22,857 | $ | 13,430 | |||
Short-term investments | 39,284 | 39,325 | |||||
Accounts receivable | 13,554 | 12,851 | |||||
Inventory | 16,346 | 13,381 | |||||
Prepaid expenses and other current assets | 1,701 | 2,352 | |||||
Total current assets | 93,742 | 81,339 | |||||
Property and equipment, net | 1,156 | 1,052 | |||||
Operating lease right-of-use asset | 11,007 | 11,843 | |||||
Restricted cash | 122 | 122 | |||||
Deferred offering costs | — | 276 | |||||
Other assets | 87 | 15 | |||||
Total assets | $ | 106,114 | $ | 94,647 | |||
Liabilities and Stockholders’ Equity | |||||||
Current liabilities | |||||||
Accounts payable | $ | 4,721 | $ | 2,954 | |||
Accrued liabilities | 9,740 | 9,787 | |||||
Operating lease liability | 1,986 | 1,860 | |||||
Deferred revenue | 696 | 555 | |||||
Total current liabilities | 17,143 | 15,156 | |||||
Long-term debt | 58,616 | 59,525 | |||||
Operating lease liability, net of current portion | 10,917 | 11,953 | |||||
Total liabilities | 86,676 | 86,634 | |||||
Stockholders’ equity | |||||||
Common stock, | 33 | 30 | |||||
Additional paid-in capital | 565,595 | 538,933 | |||||
Accumulated deficit | (546,190 | ) | (530,950 | ) | |||
Total stockholders’ equity | 19,438 | 8,013 | |||||
Total liabilities and stockholders’ equity | $ | 106,114 | $ | 94,647 | |||
