PAVmed Provides Business Update and Reports Second Quarter 2025 Financial Results
PAVmed (NASDAQ: PAVM) reported its Q2 2025 financial results and business updates. Key highlights include Lucid Diagnostics processing 2,756 EsoGuard® tests with revenue of $1.2 million. The company reported a GAAP net loss of $13.3 million, or $(0.74) per share.
Significant developments include Lucid securing a CAC meeting for Medicare LCD coverage, strengthening its balance sheet with a $16.1 million public offering, and initiating testing under its first positive commercial insurance coverage with Highmark Blue Cross Blue Shield. Veris Health completed $2.5 million direct equity financing and established a strategic partnership with Ohio State's James Cancer Hospital.
The company ended Q2 2025 with cash and equivalents of $4.0 million, compared to $1.2 million at the end of 2024. Operating expenses were $4.7 million, including $0.2 million in stock-based compensation.
PAVmed (NASDAQ: PAVM) ha comunicato i risultati finanziari e gli aggiornamenti aziendali relativi al secondo trimestre 2025. Tra i punti principali, Lucid Diagnostics ha processato 2.756 test EsoGuard® con ricavi per 1,2 milioni di dollari. La società ha riportato una perdita netta GAAP di 13,3 milioni di dollari, pari a $(0,74) per azione.
Tra gli sviluppi significativi: Lucid ha ottenuto una convocazione CAC per la copertura Medicare LCD, ha rafforzato il proprio bilancio con un collocamento pubblico da 16,1 milioni di dollari e ha iniziato i test nell'ambito della sua prima copertura assicurativa commerciale positiva con Highmark Blue Cross Blue Shield. Veris Health ha completato un finanziamento azionario diretto da 2,5 milioni di dollari e ha avviato una partnership strategica con il James Cancer Hospital della Ohio State.
Al termine del Q2 2025 la società disponeva di liquidità e mezzi equivalenti per 4,0 milioni di dollari, rispetto a 1,2 milioni alla fine del 2024. Le spese operative sono state di 4,7 milioni di dollari, di cui 0,2 milioni in compensi basati su azioni.
PAVmed (NASDAQ: PAVM) informó sus resultados financieros y actualizaciones comerciales del segundo trimestre de 2025. Entre los aspectos clave, Lucid Diagnostics procesó 2.756 pruebas EsoGuard® con ingresos de 1,2 millones de dólares. La compañía reportó una pérdida neta GAAP de 13,3 millones de dólares, o $(0,74) por acción.
Desarrollos importantes incluyen que Lucid consiguió una reunión del CAC para la cobertura Medicare LCD, reforzó su balance con una emisión pública de 16,1 millones de dólares e inició pruebas bajo su primera cobertura comercial positiva con Highmark Blue Cross Blue Shield. Veris Health completó un financiamiento de capital directo de 2,5 millones de dólares y estableció una alianza estratégica con el James Cancer Hospital de Ohio State.
La compañía terminó el Q2 2025 con efectivo y equivalentes por 4,0 millones de dólares, frente a 1,2 millones al cierre de 2024. Los gastos operativos fueron de 4,7 millones de dólares, incluidos 0,2 millones en compensación basada en acciones.
PAVmed (NASDAQ: PAVM)는 2025년 2분기 재무실적 및 사업 업데이트를 발표했습니다. 주요 내용으로는 Lucid Diagnostics가 EsoGuard® 검사 2,756건을 처리하여 매출 120만 달러를 기록했습니다. 회사는 GAAP 기준 순손실 1,330만 달러, 주당 $(0.74)를 보고했습니다.
주요 진행 사항으로는 Lucid가 Medicare LCD 적용을 위한 CAC 회의를 확보했으며, 1,610만 달러 규모의 공개모집으로 재무구조를 강화했고 Highmark Blue Cross Blue Shield와의 첫 긍정적 상업보험 적용에 따라 검사도 시작했습니다. Veris Health는 250만 달러의 직접 지분 금융을 완료하고 오하이오주립대 James Cancer Hospital과 전략적 파트너십을 체결했습니다.
회사는 2025년 2분기 말 현금 및 현금성 자산으로 400만 달러를 보유했으며, 이는 2024년 말의 120만 달러와 비교됩니다. 영업비용은 470만 달러였고 이 중 20만 달러는 스톡옵션 등 주식기반 보상에 해당합니다.
PAVmed (NASDAQ: PAVM) a publié ses résultats financiers et mises à jour commerciales pour le deuxième trimestre 2025. Points clés : Lucid Diagnostics a traité 2 756 tests EsoGuard® générant des revenus de 1,2 million de dollars. La société a enregistré une perte nette GAAP de 13,3 millions de dollars, soit $(0,74) par action.
Parmi les développements importants, Lucid a obtenu une réunion du CAC pour la couverture Medicare LCD, a renforcé sa situation financière grâce à une offre publique de 16,1 millions de dollars et a lancé des tests dans le cadre de sa première couverture d'assurance commerciale positive avec Highmark Blue Cross Blue Shield. Veris Health a finalisé un financement en capital direct de 2,5 millions de dollars et établi un partenariat stratégique avec le James Cancer Hospital de l'Ohio State.
La société a terminé le T2 2025 avec 4,0 millions de dollars de trésorerie et équivalents, contre 1,2 million à la fin de 2024. Les charges d'exploitation se sont élevées à 4,7 millions de dollars, dont 0,2 million en rémunération en actions.
PAVmed (NASDAQ: PAVM) veröffentlichte die Finanzergebnisse und Geschäftsupdates für das zweite Quartal 2025. Wichtige Punkte: Lucid Diagnostics hat 2.756 EsoGuard®-Tests verarbeitet und dabei Erlöse von 1,2 Mio. USD erzielt. Das Unternehmen meldete einen GAAP-Nettoverlust von 13,3 Mio. USD, bzw. $(0,74) je Aktie.
Zu den wesentlichen Entwicklungen gehört, dass Lucid ein CAC‑Meeting zur Medicare LCD‑Deckung gesichert hat, die Bilanz durch ein öffentliches Angebot über 16,1 Mio. USD gestärkt wurde und Tests unter der ersten positiven kommerziellen Versicherungsdeckung mit Highmark Blue Cross Blue Shield begonnen wurden. Veris Health schloss eine direkte Eigenkapitalfinanzierung in Höhe von 2,5 Mio. USD ab und ging eine strategische Partnerschaft mit dem James Cancer Hospital der Ohio State ein.
Zum Ende des Q2 2025 verfügte das Unternehmen über Barmittel und Zahlungsmitteläquivalente in Höhe von 4,0 Mio. USD, gegenüber 1,2 Mio. USD Ende 2024. Die Betriebsausgaben beliefen sich auf 4,7 Mio. USD, davon 0,2 Mio. USD aktienbasierte Vergütung.
- Lucid processed 2,756 EsoGuard tests with $1.2 million in revenue
- Secured $16.1 million from public offering, extending runway into 2026
- Obtained first positive commercial insurance coverage from Highmark Blue Cross Blue Shield
- Veris completed $2.5 million financing to fund implantable monitor development
- Strategic partnership established with Ohio State's James Cancer Hospital
- Cash position improved to $4.0 million from $1.2 million at year-end 2024
- Reported GAAP net loss of $13.3 million ($0.74 per share)
- Operating expenses of $4.7 million in Q2 2025
- Continued cash burn requiring additional financing rounds
Insights
PAVmed shows modest EsoGuard test growth and improved financing across subsidiaries despite overall negative cash flow and GAAP losses.
PAVmed's Q2 2025 results reveal both progress and challenges across its diversified medical technology portfolio. Lucid Diagnostics processed 2,756 EsoGuard tests, generating
The company's balance sheet has been strengthened through strategic financings at both the subsidiary level and parent company. Lucid raised approximately
However, financial challenges persist. PAVmed reported a GAAP net loss of
The partnership with Highmark Blue Cross Blue Shield marks Lucid's first positive commercial insurance coverage for EsoGuard, potentially accelerating revenue growth. Similarly, the strategic alliance with Hoag healthcare network and OSU-The James Cancer Hospital for Veris shows promising commercialization progress, but full financial impact remains uncertain pending completed integration and deployment.
While PAVmed has stabilized its corporate structure and improved liquidity, the
PAVmed advances diagnostic and monitoring technologies through strategic partnerships and financing despite ongoing profitability challenges.
PAVmed's multi-pronged commercialization strategy is taking shape with distinct progress across its portfolio companies, though significant execution challenges remain. The company is transitioning from pure R&D to commercial operations through a parent-subsidiary structure that allows for focused capital allocation and independent financing events.
Lucid's EsoGuard diagnostic platform has reached an important inflection point with 2,756 tests processed in Q2, demonstrating growing clinical adoption. The scheduled September 4th CAC meeting with Medicare could fundamentally transform EsoGuard's market position, as positive Medicare coverage would likely accelerate private payer adoption beyond the initial Highmark Blue Cross Blue Shield coverage secured in May 2025. The Hoag partnership represents a significant channel expansion opportunity, potentially establishing a replicable deployment model for other regional healthcare networks.
Veris Health's dual-track strategy - advancing both an implantable physiological monitor through regulatory clearance while simultaneously launching a software platform with OSU-The James - represents a sophisticated commercialization approach. The ongoing EHR integration suggests imminent commercial deployment, while the recommitment to the implantable monitor indicates confidence in its long-term market potential. The expansion into AI-enabled clinical decision support signals a potential high-margin recurring revenue opportunity beyond basic monitoring.
The parent company's structural approach to innovation through its shared services model offers operational efficiencies, but the limited revenue at the parent level suggests heavy dependence on subsidiary success. PAVmed's active pursuit of new technologies that leverage existing expertise in esophageal disease indicates recognition that portfolio diversification remains essential to long-term viability.
The financial structure reveals a capital-intensive business still far from profitability. The substantial gap between GAAP losses (
Lucid processed 2,756 EsoGuard® 2Q25 tests, recognized revenue of
and secured CAC meeting on Medicare LCD for EsoGuard to be held on September
4
Veris Health completed 2Q25 financing, relaunched development of implantable
physiological monitor, and initiated integration steps to launch commercial phase with
OSU-The James
Conference call and webcast to be held today, August 14, at 8:30 AM EDT
Conference Call and Webcast
The webcast will take place on Thursday, August 14, 2025, at 8:30 AM and is accessible in the investor relations section of the Company's website at pavmed.com. Alternatively, to access the conference call by telephone,
Following the conclusion of the conference call, a replay will be available for 30 days on the investor relations section of the Company's website at pavmed.com.
Business Update Highlights
"PAVmed has stabilized its corporate structure, strengthened its balance sheet, and is positioned to advance its vision as a diversified commercial life sciences company with multiple independently-financed subsidiaries operating under a shared services model," said Lishan Aklog, M.D., PAVmed's Chairman and Chief Executive Officer. "The successful second quarter financings of both Lucid and Veris reflect investor confidence in their commercial potential and provide each company with capital needed to achieve important near-term milestones. Veris is now aggressively advancing towards final development and regulatory clearance of its implantable monitor, as well as completion the final steps toward full commercial engagement with our strategic partner, OSU-The James. We remain actively engaged in evaluating new opportunities to leverage PAVmed's platform and further diversify our portfolio."
Highlights from the second quarter and recent weeks:
- Lucid Diagnostics announced second quarter 2025 financial results and key business developments, including:
- Recognized
in EsoGuard® Esophageal DNA Test revenue for 2Q25 and processed 2,756 EsoGuard tests.$1.2 million - MolDX‑participating Medicare Administrative Contractors (MACs) to convene medical experts at a Contractor Advisory Committee (CAC) meeting of on September 4, 2025.
- Strengthened balance sheet with underwritten public offering of common stock, netting approximately
.1 million in proceeds, extending runway into 2026.$16 - Initiated patient testing and billing under first positive commercial insurance coverage policy for EsoGuard from Highmark Blue Cross Blue Shield, which became effective May 26, 2025.
- Partnered with Hoag, a nationally-recognized regional healthcare delivery network, to launch a comprehensive EsoGuard esophageal precancer testing program.
- Recognized
- Veris completed a
direct equity financing, supplementing a previous$2.5 million financing at a$2.4 million pre-money valuation and is now sufficiently capitalized to fund development of its implantable physiological monitor through FDA clearance.$35 million - Veris completed a long-term strategic partnership with The Ohio State's James Cancer Hospital. Integration with the hospital's electronic health record (EHR) system is now in process, with full commercial deployment of the Veris Cancer Care Platform to commence thereafter.
- Veris advancing long‑term strategic plan, which includes refining its commercial strategy and model for its implantable physiological monitor, expanding commercial operations following FDA clearance, and broadening its scope of its offering beyond remote patient monitoring to include AI‑enabled clinical decision support.
- PAVmed remains engaged in evaluating new opportunities to leverage its shared services model across diverse sectors, including active discussions with academic medical centers with innovative technologies that would leverage PAVmed and Lucid expertise in esophageal disease.
Financial Results:
- For the three months ended June 30, 2025, Operating expenses were approximately
which include stock-based compensation expenses of$4.7 million . GAAP net loss attributable to common stockholders was approximately$0.2 million , or$13.3 million per common share on a diluted basis.$(0.74) - As shown below and for the purpose of illustrating the effect of stock-based compensation and other non-cash income and expenses on the Company's financial results, the Company's non-GAAP adjusted loss was approximately
or$1.8 million per common share.$(0.11) - PAVmed had cash and cash equivalents of
as of June 30, 2025, compared to$4.0 million as of December 31, 2024.$1.2 million - The unaudited financial results for the three and six months ended June 30, 2025 were filed with the SEC on Form 10-Q on August 14, 2025, and are available at www.pavmed.com or www.sec.gov.
PAVmed Non-GAAP Measures
- To supplement our financial results presented in accordance with
U.S. generally accepted accounting principles (GAAP), management provides certain non-GAAP financial measures of the Company's financial results. These non-GAAP financial measures include net loss before interest, taxes, depreciation, and amortization (EBITDA) and non-GAAP adjusted loss, which further adjusts EBITDA for stock-based compensation expense, loss on the issuance or modification of convertible securities, the periodic change in fair value of convertible securities, and loss on debt extinguishment. The foregoing non-GAAP financial measures of EBITDA and non-GAAP adjusted loss are not recognized terms underU.S. GAAP. - Non-GAAP financial measures are presented with the intent of providing greater transparency to the information used by us in our financial performance analysis and operational decision-making. We believe these non-GAAP financial measures provide meaningful information to assist investors, shareholders, and other readers of our financial statements in making comparisons to our historical financial results and analyzing the underlying performance of our results of operations. These non-GAAP financial measures are not intended to be, and should not be, a substitute for, considered superior to, considered separately from, or as an alternative to, the most directly comparable GAAP financial measures.
- Non-GAAP financial measures are provided to enhance readers' overall understanding of our current financial results and to provide further information for comparative purposes. Management believes the non-GAAP financial measures provide useful information to management and investors by isolating certain expenses, gains, and losses that may not be indicative of our core operating results and business outlook. Specifically, the non-GAAP financial measures include non-GAAP adjusted loss, and its presentation is intended to help the reader understand the effect of the loss on the issuance or modification of convertible securities, the periodic change in fair value of convertible securities, the loss on debt extinguishment and the corresponding accounting for non-cash charges on financial performance. In addition, management believes non-GAAP financial measures enhance the comparability of results against prior periods.
- A reconciliation to the most directly comparable GAAP measure of all non-GAAP financial measures included in this press release for the three and six months ended June 30, 2025 and 2024 are as follows:
Condensed Consolidated Statement of Operations (Unaudited) | ||||||||
For the three months ended June 30, | For the six months ended June 30, | |||||||
2025 | 2024 | 2025 | 2024 | |||||
(in thousands except per-share amounts) | ||||||||
Revenue | $ 6 | $ 979 | $ 14 | $ 1,989 | ||||
Operating expenses | 4,721 | 14,663 | 10,174 | 29,711 | ||||
Other (Income) Expense | 7,609 | 1,230 | (16,460) | 5,704 | ||||
Net (Income) Loss | 12,324 | 14,914 | (6,300) | 33,426 | ||||
Net income (loss) per common share, diluted | $ (0.74) | $ (1.19) | $ 0.13 | $ (3.78) | ||||
Net income (loss) attributable to common stockholders | (13,308) | (10,908) | 4,386 | (33,696) | ||||
Preferred Stock dividends and deemed dividends | 1,387 | 81 | 2,661 | 7,657 | ||||
Net income (loss) as reported | (11,921) | (10,827) | 7,047 | (26,039) | ||||
Adjustments: | ||||||||
Depreciation and amortization expense1 | 22 | 305 | 65 | 891 | ||||
Interest expense, net2 | (4) | (99) | (7) | (156) | ||||
NCI ownership share of Interest and Depreciation | — | (40) | — | (180) | ||||
EBITDA | (11,903) | (10,661) | 7,105 | (25,484) | ||||
Other non-cash or financing related expenses: | ||||||||
Stock-based compensation expense3 | 162 | 1,904 | 1,092 | 3,786 | ||||
Operating expenses issued in stock1 | 53 | 140 | 103 | 163 | ||||
Change in FV equity method investments | 10,643 | — | (10,361) | — | ||||
Change in FV convertible debt2 | 200 | 566 | 249 | 2,728 | ||||
Loss on debt extinguishment2 | — | 763 | 58 | 1,132 | ||||
Debt modification expense | — | — | — | 2,000 | ||||
NCI ownership share of non-GAAP adjustments | — | (363) | — | (602) | ||||
Non-GAAP adjusted (loss) | $ (845) | $ (7,651) | $ (1,754) | $ (16,277) | ||||
Non-GAAP shares outstanding, basic and diluted | 18,085 | 9,153 | 15,992 | 8,924 | ||||
Non-GAAP adjusted (loss) income per share, basic and |
1 | Included in general and administrative expenses in the financial statements. |
2 | Included in other income and expenses. |
3 | Stock-based compensation ("SBC") expense included in operating expenses is detailed |
Reconciliation of GAAP Operating Expenses to Non-GAAP Net Operating Expenses | ||||||||
(in thousands except per-share amounts) | For the three months ended June 30, | For the six months ended June 30, | ||||||
2025 | 2024 | 2025 | 2024 | |||||
Cost of revenue | $ 41 | $ 1,666 | $ 78 | $ 3,411 | ||||
Stock-based compensation expense3 | — | (44) | — | (80) | ||||
Net cost of revenue | 41 | 1,622 | 78 | 3,331 | ||||
Amortization of acquired intangible assets | — | 105 | — | 477 | ||||
Sales and marketing | 220 | 4,242 | 467 | 8,552 | ||||
Stock-based compensation expense3 | (1) | (387) | (46) | (790) | ||||
Net sales and marketing | 219 | 3,855 | 421 | 7,762 | ||||
General and administrative | 3,670 | 7,009 | 8,053 | 13,688 | ||||
Depreciation expense | (22) | (200) | (65) | (414) | ||||
Operating expenses issued in stock | (53) | (140) | (103) | (163) | ||||
Stock-based compensation expense3 | (148) | (1,214) | (944) | (2,292) | ||||
Net general and administrative | 3,447 | 5,455 | 6,941 | 10,819 | ||||
Research and development | 790 | 1,641 | 1,576 | 3,583 | ||||
Stock-based compensation expense3 | (13) | (259) | (102) | (624) | ||||
Net research and development | 777 | 1,382 | 1,474 | 2,959 | ||||
Total operating expenses | 4,721 | 14,663 | 10,174 | 29,711 | ||||
Depreciation and amortization expense | (22) | (305) | (65) | (891) | ||||
Operating expenses issued in stock | (53) | (140) | (103) | (163) | ||||
Stock-based compensation expense3 | (162) | (1,904) | (1,092) | (3,786) | ||||
Net operating expenses | $ 4,484 | $ 12,314 | $ 8,914 | $ 24,871 |
About PAVmed and its Subsidiaries
PAVmed Inc. is a diversified commercial-stage medical technology company operating in the medical device, diagnostics, and digital health sectors. Its subsidiary, Lucid Diagnostics Inc. (NASDAQ: LUCD), is a commercial-stage cancer prevention medical diagnostics company that markets the EsoGuard® Esophageal DNA Test and EsoCheck® Esophageal Cell Collection Device—the first and only commercial tools for widespread early detection of esophageal precancer to mitigate the risks of esophageal cancer deaths. Its other subsidiary, Veris Health Inc., is a digital health company focused on enhanced personalized cancer care through remote patient monitoring using implantable biologic sensors with wireless communication along with a custom suite of connected external devices. Veris is concurrently developing an implantable physiological monitor, designed to be implanted alongside a chemotherapy port, which will interface with the Veris Cancer Care Platform.
For more and for more information about PAVmed, please visit pavmed.com.
For more information about Lucid Diagnostics, please visit luciddx.com.
For more information about Veris Health, please visit verishealth.com.
Forward-Looking Statements
This press release includes forward-looking statements that involve risks and uncertainties. Forward-looking statements are any statements that are not historical facts. Such forward-looking statements, which are based upon the current beliefs and expectations of PAVmed's and Lucid's management, are subject to risks and uncertainties, which could cause actual results to differ from the forward-looking statements. Risks and uncertainties that may cause such differences include, among other things, volatility in the price of PAVmed's and Lucid's common stock; general economic and market conditions; the uncertainties inherent in research and development, including the cost and time required to advance PAVmed's and Lucid's products to regulatory submission; whether regulatory authorities will be satisfied with the design of and results from PAVmed's and Lucid's clinical and preclinical studies; whether and when PAVmed's and Lucid's products are cleared by regulatory authorities; market acceptance of PAVmed's and Lucid's products once cleared and commercialized; PAVmed's and Lucid's ability to raise additional funding as needed; and other competitive developments. In addition, new risks and uncertainties may arise from time to time and are difficult to predict. For a further list and description of these and other important risks and uncertainties that may affect PAVmed's and Lucid's future operations, see Part I, Item 1A, "Risk Factors," in PAVmed's and Lucid's most recent Annual Report on Form 10-K filed with the Securities and Exchange Commission, as the same may be updated in Part II, Item 1A, "Risk Factors" in any Quarterly Report on Form 10-Q filed by PAVmed or Lucid after its most recent Annual Report. PAVmed and Lucid disclaim any intention or obligation to publicly update or revise any forward-looking statement to reflect any change in its expectations or in events, conditions, or circumstances on which those expectations may be based, or that may affect the likelihood that actual results will differ from those contained in the forward-looking statements.
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