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Lucid Diagnostics (Nasdaq: LUCD) reports 2025 loss, VA contract win

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(Moderate)
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8-K

Rhea-AI Filing Summary

Lucid Diagnostics Inc. reported fourth quarter and full-year 2025 results and provided a business update centered on its EsoGuard esophageal DNA test. In 4Q25 the company processed 3,664 EsoGuard tests and generated $1.5 million in revenue.

For the quarter, operating expenses were $15.5 million and GAAP net loss attributable to common stockholders was about $16.3 million, or $(0.12) per share. Non-GAAP adjusted loss was $12.6 million, or $(0.10) per share.

For full-year 2025, revenue was $4.7 million and GAAP net loss was $58.0 million. Lucid ended 2025 with $34.7 million in cash and cash equivalents, compared with $22.4 million a year earlier.

The company highlighted a U.S. Department of Veterans Affairs contract that provides Medicare-aligned pricing of $1,938 per EsoGuard test across approximately 170 VA medical centers, and positive real-world data in nearly 12,000 at-risk patients showing a 95% technical success rate for its EsoCheck collection device.

Positive

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Insights

Lucid shows modest revenue growth but continues to post sizable losses.

Lucid Diagnostics reported 4Q25 EsoGuard revenue of $1.5 million and full-year revenue of $4.7 million, modestly above 2024. Test volumes reached 3,664 in the quarter, indicating growing clinical adoption of its esophageal precancer screening offering.

However, operating expenses of $15.5 million in 4Q25 drove a GAAP net loss of $16.3 million for the quarter and $58.0 million for 2025. Even on a non-GAAP basis, adjusted loss was $12.6 million in 4Q25 and $44.0 million for the year, underscoring a heavy cash-burn profile.

The VA contract, with Medicare-aligned pricing of $1,938 per test across roughly 170 medical centers, and real-world data in nearly 12,000 patients may support future revenue growth if converted into higher testing volumes. The $34.7 million year-end cash balance provides some funding runway, but the path to scaling revenue relative to expenses remains a key factor for investors.

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UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

WASHINGTON, DC 20549

 

FORM 8-K

 

CURRENT REPORT

PURSUANT TO SECTION 13 OR 15(d) OF THE

SECURITIES EXCHANGE ACT OF 1934

 

Date of Report (Date of earliest event reported): March 26, 2026

 

LUCID DIAGNOSTICS INC.
(Exact Name of Registrant as Specified in Charter)

 

Delaware   001-40901   82-5488042

(State or Other Jurisdiction

of Incorporation)

 

(Commission

File Number)

 

(IRS Employer

Identification No.)

 

360 Madison Avenue, 25th Floor, New York, New York   10017
(Address of Principal Executive Offices)   (Zip Code)

 

Registrant’s telephone number, including area code: (917) 813-1828

 

N/A
(Former Name or Former Address, if Changed Since Last Report)

 

Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions (see General Instruction A.2. below):

 

Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425).
   
Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12).
   
Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b)).
   
Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c)).

 

Securities registered pursuant to Section 12(b) of the Act:

 

Title of each class   Trading Symbol(s)   Name of each exchange on which registered
Common Stock, Par Value $0.001 Per Share   LUCD   The Nasdaq Stock Market LLC

 

Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§240.12b-2 of this chapter).

 

Emerging growth company

 

If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act.

 

 

 

 

 

 

Item 2.02 Results of Operations and Financial Condition.

 

On March 26, 2026, Lucid Diagnostics Inc. (the “Company”) issued a press release announcing financial results for its fiscal year ended December 31, 2025 and providing a business update. A copy of the press release is attached to this report as Exhibit 99.1 and is incorporated herein by reference.

 

Item 7.01.Regulation FD Disclosure.

 

The disclosure set forth under Item 2.02 is incorporated herein by reference.

 

The information furnished under Items 2.02 and 7.01, including the exhibit related thereto, shall not be deemed “filed” for purposes of Section 18 of the Securities Exchange Act of 1934, nor shall it be deemed incorporated by reference in any disclosure document of the Company, except as shall be expressly set forth by specific reference in such document.

 

Item 9.01.Financial Statements and Exhibits.

 

(d) Exhibits:

 

Exhibit No.   Description
99.1   Press release.
104   Cover Page Interactive Data File (embedded within the Inline XBRL document).

 

2

 

 

SIGNATURE

 

Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.

 

Dated: March 26, 2026 LUCID DIAGNOSTICS INC.
     
  By: /s/ Dennis McGrath
    Dennis McGrath
    Chief Financial Officer

 

3

 

Exhibit 99.1

 

Lucid Diagnostics Provides Business Update and Reports Fourth Quarter and Full Year 2025 Financial Results

 

Processed 3,664 EsoGuard® tests and recognized 4Q25 revenue of $1.5 million

 

Expanded EsoGuard access with U.S. Department of Veterans Affairs contract award and strengthened clinical evidence with positive data from the largest reported real-world experience of esophageal precancer detection

 

Conference call and webcast to be held today, March 26, at 8:30 AM EST

 

NEW YORK, March 26, 2026 - Lucid Diagnostics Inc. (Nasdaq: LUCD) (“Lucid” or the “Company”) a commercial-stage, cancer prevention medical diagnostics company, and subsidiary of PAVmed Inc. (Nasdaq: PAVM) (“PAVmed”), today provided a business update for the Company and reported financial results for the fourth quarter and full year ended December 31, 2025.

 

Conference Call and Webcast

 

The webcast will take place on Thursday, March 26, 2026, at 8:30 AM and will be accessible in the investor relations section of the Company’s website at luciddx.com. Alternatively, to access the conference call by telephone, U.S.-based callers should dial 1-800-836-8184 and international listeners should dial 1-646-357-8785. All listeners should provide the operator with the conference call name “Lucid Diagnostics Business Update” to join.

 

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 luciddx.com.

 

Business Highlights

 

“Throughout 2025, we established a strong commercial foundation for EsoGuard, demonstrating that we can consistently generate and sustain demand, drive physician adoption, and engage effectively with both health systems and commercial payors,” said Lishan Aklog, M.D., Lucid’s Chairman and Chief Executive Officer. “As we move into 2026, our focus is on building on that foundation by converting demand into revenue, with priorities including deepening our relationship with the VA, expanding adoption across health systems, advancing coverage with commercial payors, and securing Medicare coverage, which we still expect in the near-term.”

 

 

 

 

Highlights from the fourth quarter and recent weeks:

 

Processed 3,664 EsoGuard® Esophageal DNA Tests in 4Q25.
   
Recognized $1.5 million in EsoGuard revenue for 4Q25.
   
Awarded U.S. Department of Veterans Affairs (VA) contract for EsoGuard, expanding access across the nation’s largest integrated healthcare system serving approximately nine million veterans. The contract, issued under the VA Federal Supply Schedule, includes Medicare-aligned pricing of $1,938 and spans approximately 170 VA medical centers nationwide under a single national framework.
   
Announced positive data from the largest reported real-world experience of esophageal precancer detection, evaluating Lucid’s EsoGuard and EsoCheck® Esophageal Cell Collection Device in nearly 12,000 at-risk patients. Real-world data demonstrated that EsoCheck achieved a 95% technical success rate and that 95% of procedures were completed in under two minutes, while physicians used EsoGuard appropriately in routine clinical practice.

 

Financial Results

 

For the three months ended December 31, 2025, EsoGuard related revenues were $1.5 million. Operating expenses were approximately $15.5 million, which included stock-based compensation expenses of $1.2 million. GAAP net loss attributable to common stockholders was approximately $16.3 million or $(0.12) per common share.
   
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 for the three months ended December 31, 2025 was approximately $12.6 million or $(0.10) per common share.
   
Lucid had cash and cash equivalents of $34.7 million as of December 31, 2025, compared to $22.4 million as of December 31, 2024.
   
The audited financial results for the year ended December 31, 2025, were filed with the SEC on Form 10-K on March 25, 2026, and available at www.luciddx.com or www.sec.gov.

 

Lucid Non-GAAP Measures

 

To supplement our audited 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 and other non-cash income and expenses, if any. The foregoing non-GAAP financial measures of EBITDA and non-GAAP adjusted loss are not recognized terms under U.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 unaudited 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 months and years ended December 31, 2025, and 2024 are as follows:

 

Condensed consolidated statements of operations (unaudited)
 
(in thousands except per-share amounts)  For the three months ended
December 31,
   For the year ended
December 31,
 
   2025   2024   2025   2024 
                 
Revenue  $1,504   $1,197   $4,706   $4,346 
                     
Operating expenses   15,514    13,571    54,346    50,398 
Other (Income) expense   2,256    (833)   8,370    (523)
Net Loss   (16,266)   (11,541)   (58,010)   (45,529)
Net income (loss) per common share, basic and diluted  $(0.12)  $(0.20)  $(0.69)  $(1.05)
Net loss attributable to common stockholders   (16,266)   (11,541)   (70,569)   (53,025)
Preferred Stock dividends and deemed dividends           12,559    7,496 
Net income (loss) as reported   (16,266)   (11,541)   (58,010)   (45,529)
Adjustments:                    
Depreciation and amortization expense1   210    222    872    1,167 
Interest expense, net2   (104)   (58)   (364)   (296)
EBITDA   (16,160)   (11,377)   (57,502)   (44,658)
                     
Other non-cash or financing related expenses:                    
Stock-based compensation expense3   1,165    1,172    4,491    4,534 
Operating expenses issued in stock1       98    234    346 
Change in FV convertible debt2   2,359    (4,825)   7,656    (5,394)
Debt extinguishments loss - Senior Secured Convertible Note2           1,078     
Equity issuance cost extinguishment       4,050        5,167 
Non-GAAP adjusted (loss)  $(12,636)  $(10,882)  $(44,043)  $(40,005)
Basic and Diluted shares outstanding   131,070    58,378    101,947    50,516 
Non-GAAP adjusted (loss) income per share  $(0.10)  $(0.19)  $(0.43)  $(0.79)

 

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 as follows in the table below by category within operating expenses for the non-GAAP Net operating expenses:

 

 

 

 

Reconciliation of GAAP Operating Expenses to Non-GAAP Net Operating Expenses
 
(in thousands except per-share amounts)  For the three months ended
December 31,
   For the year ended
December 31,
 
   2025   2024   2025   2024 
Cost of revenues  $1,859   $2,145   $6,670   $7,099 
Stock-based compensation expense3   (39)   (42)   (191)   (164)
Net cost of revenues   1,820    2,103    6,479    6,935 
                     
Amortization of intangible assets   106    105    421    688 
                     
Sales and marketing   5,343    4,003    17,710    16,463 
Stock-based compensation expense3   (269)   (300)   (1,021)   (1,365)
Net sales and marketing   5,074    3,703    16,689    15,098 
                     
General and administrative   6,483    5,865    23,867    20,156 
Depreciation expense   (104)   (117)   (451)   (479)
Operating expenses issued in stock       (98)   (234)   (346)
Stock-based compensation expense3   (734)   (691)   (2,795)   (2,330)
Net general and administrative   5,645    4,959    20,387    17,001 
                     
Research and development   1,723    1,453    5,678    5,992 
Stock-based compensation expense3   (123)   (139)   (484)   (675)
Net research and development   1,600    1,314    5,194    5,317 
                     
Total operating expenses   15,514    13,571    54,346    50,398 
Depreciation and amortization expense   (210)   (222)   (872)   (1,167)
Operating expenses issued in stock       (98)   (234)   (346)
Stock-based compensation expense3   (1,165)   (1,172)   (4,491)   (4,534)
Net operating expenses  $14,139   $12,079   $48,749   $44,351 

 

 

 

 

About Lucid Diagnostics

 

Lucid Diagnostics Inc. is a commercial-stage, cancer prevention medical diagnostics company, and subsidiary of PAVmed Inc. Lucid is focused on the millions of patients with GERD, also known as chronic heartburn, who are at risk of developing esophageal precancer and cancer. Lucid’s EsoGuard® Esophageal DNA Test, performed on samples collected in a brief, noninvasive office procedure with its EsoCheck® Esophageal Cell Collection Device - the first and only commercially available tools designed with the goal of preventing esophageal cancer and cancer deaths through widespread, early detection of esophageal precancer in at-risk patients.

 

For more information, please visit luciddx.com and for more information about its parent company PAVmed, please visit pavmed.com.

 

Forward-Looking Statements

 

This press release includes forward-looking statements that involve risk 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 Lucid Diagnostics’ 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 Lucid Diagnostics’ common stock; general economic and market conditions; the uncertainties inherent in research and development, including the cost and time required to advance Lucid Diagnostics’ products to regulatory submission; whether regulatory authorities will be satisfied with the design of and results from Lucid Diagnostics’ clinical and preclinical studies; whether and when Lucid Diagnostics’ products are cleared by regulatory authorities; market acceptance of Lucid Diagnostics’ products once cleared and commercialized; Lucid Diagnostics’ ability to raise additional funding as needed; and other competitive developments. These factors are difficult or impossible to predict accurately and many of them are beyond Lucid Diagnostics’ control. 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 Lucid Diagnostics’ future operations, see Part I, Item 1A, “Risk Factors,” in Lucid Diagnostics’ 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 Lucid Diagnostics after its most recent Annual Report. Lucid Diagnostics disclaims 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.

 

Investor and Media Contact

 

Matt Riley

PAVmed and Lucid Diagnostics

mjr@pavmed.com

 

 

FAQ

How did Lucid Diagnostics (LUCD) perform financially in Q4 2025?

Lucid Diagnostics reported 4Q25 EsoGuard-related revenue of $1.5 million. Operating expenses were about $15.5 million, leading to a GAAP net loss attributable to common stockholders of roughly $16.3 million, or $(0.12) per common share for the quarter.

What were Lucid Diagnostics’ full-year 2025 revenue and net loss?

For 2025, Lucid Diagnostics generated $4.7 million in revenue and reported a GAAP net loss of about $58.0 million. Net loss attributable to common stockholders was approximately $70.6 million, reflecting ongoing investment in commercialization and operations for its EsoGuard esophageal DNA test.

What non-GAAP results did Lucid Diagnostics (LUCD) report for 2025?

Lucid Diagnostics reported a non-GAAP adjusted loss of about $12.6 million, or $(0.10) per share, for 4Q25. For full-year 2025, non-GAAP adjusted loss was roughly $44.0 million, or $(0.43) per share, excluding stock-based compensation and other non-cash or financing-related items.

What is notable about Lucid Diagnostics’ VA contract for EsoGuard?

Lucid Diagnostics was awarded a U.S. Department of Veterans Affairs contract for EsoGuard. The agreement offers Medicare-aligned pricing of $1,938 per test and covers approximately 170 VA medical centers, potentially expanding access across the nation’s largest integrated healthcare system.

How strong is Lucid Diagnostics’ cash position at year-end 2025?

As of December 31, 2025, Lucid Diagnostics held $34.7 million in cash and cash equivalents. This compares with $22.4 million a year earlier, indicating an improved liquidity position to support ongoing commercialization and operational activities for its EsoGuard testing platform.

What clinical data did Lucid Diagnostics highlight for EsoGuard and EsoCheck?

Lucid highlighted real-world data from nearly 12,000 at-risk patients using EsoGuard and its EsoCheck collection device. The data showed EsoCheck achieved about a 95% technical success rate, with 95% of procedures completed in under two minutes in routine clinical practice.

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