Lucid Diagnostics Provides Business Update and First Quarter 2024 Financial Results
Lucid Diagnostics Inc., a cancer prevention medical diagnostics company, provided a business update and financial results for the first quarter of 2024. The company reported a 10% increase in EsoGuard test volume, a strengthened balance sheet after a $29.8 million Series B Preferred Stock Offering, and a MolDX pre-submission meeting scheduled for July 17, 2024. Lucid also highlighted revenue growth, clinical study outcomes, and market access strategy.
Quarterly EsoGuard test volume increased by 10%.
Strengthened balance sheet with $29.8 million Series B Preferred Stock Offering.
Successful peer-reviewed publication of positive data from NCI-sponsored clinical validation study.
Secured MolDX pre-submission meeting for Medicare coverage.
Operating expenses were approximately $11.8 million, with GAAP net loss of $18.1 million.
Non-GAAP adjusted loss was approximately $9.4 million for the quarter.
Stock-based compensation expenses were $0.9 million.
Quarterly EsoGuard® test volume increased 10 percent
Strengthened balance sheet following completion of
MolDX pre-submission meeting scheduled for July 17, 2024
Conference call and webcast to be held today, May 13th at 8:30 AM EDT
Conference Call and Webcast
The webcast will take place on Monday, May 13, 2024, 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,
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 Update Highlights
"I am very pleased with the excellent progress Lucid has made on multiple fronts during the first quarter and recent weeks and look forward to exciting very near-term milestones for our business," said Lishan Aklog, M.D., Lucid's Chairman and Chief Executive Officer. "We strengthened our balance sheet closing an approximately
Highlights from the first quarter and recent weeks:
- For the quarter, EsoGuard® revenue was
$1.0M - Lucid's CLIA-certified clinical laboratory performed 2,420 commercial EsoGuard Esophageal DNA Tests in 1Q24, which represents a 10 percent increase sequentially from 4Q23 and a 31 percent annual increase from 1Q23.
- Continuous revenue cycle management improvements, including prior authorization appeals, physician advocacy, etc., while maintaining stable out-of-network allowed amounts averaging
~ .$1,800 - Strengthened balance sheet by completing
$29.8 million - Peer-reviewed publication of positive data from landmark National Cancer Institute (NCI)-sponsored clinical validation study of EsoGuard esophageal precancer testing demonstrating unprecedented early cancer detection. The publication of data strengthens EsoGuard's clinical data supporting ongoing engagement to secure commercial and Medicare payor coverage.
- Secured July 17, 2024 MolDX pre-submission meeting to review data for technical assessment (TA) seeking EsoGuard coverage under its foundational Local Coverage Determination (LCD).
- Robust pipeline of direct contracting engagements with benefits brokers, third-party administrators, and self-insured entities.
- Actively executing on aggressive market access strategy focused on securing medical policy coverage with regional plans in biomarker legislation states and pilots with national plans.
Financial Results
- For the three months ended March 31, 2024, EsoGuard related revenues were
$1.0 million $11.8 million $0.9 million $18.1 million $(0.40) - 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 March 31, 2024 was approximately
$9.4 million $(0.21) - Lucid had cash and cash equivalents of
$24.8 million $18.9 million $11.6 million - The unaudited financial results for the three months ended March 31, 2024, were filed with the SEC on Form 10-Q on May 13, 2024, and available at www.luciddx.com or www.sec.gov.
Lucid Non-GAAP Measures
- To supplement our unaudited 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 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 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 ended March 31, 2024, and 2023 are as follows:
Condensed consolidated statements of operations (unaudited) | ||||
(in thousands except per-share amounts) | For the three months ended March 31, | |||
2024 | 2023 | |||
Revenue | $ 1,001 | $ 446 | ||
Operating expenses | 11,793 | 14,763 | ||
Other (Income) expense | (180) | 1,930 | ||
Net Loss | (10,612) | (16,247) | ||
Net income (loss) per common share, basic and diluted | $ (0.40) | $ (0.40) | ||
Net loss attributable to common stockholders | (18,108) | (16,247) | ||
Preferred Stock dividends and deemed dividends | 7,496 | — | ||
Net income (loss) as reported | (10,612) | (16,247) | ||
Adjustments: | ||||
Depreciation and amortization expense1 | 501 | 612 | ||
Interest expense (income), net2 | (56) | (45) | ||
EBITDA | (10,167) | (15,680) | ||
Other non-cash or financing related expenses: | ||||
Stock-based compensation expense3 | 933 | 3,208 | ||
ResearchDx acquisition paid in stock1 | — | 713 | ||
Change in FV convertible debt2 | (291) | 789 | ||
Offering costs convertible debt2 | — | 1,186 | ||
Debt extinguishments loss - Senior Secured Convertible Note2 | 167 | — | ||
Non-GAAP adjusted (loss) | $ (9,358) | $ (9,784) | ||
Basic and Diluted shares outstanding | 45,014 | 40,971 | ||
Non-GAAP adjusted (loss) income per share | ||||
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 March 31, | |||
2024 | 2023 | |||
Cost of revenues | $ 1,656 | $ 1,338 | ||
Stock-based compensation expense3 | (36) | (19) | ||
Net cost of revenues | 1,620 | 1,319 | ||
Amortization of intangible assets | 372 | 505 | ||
Sales and marketing | 4,194 | 4,127 | ||
Stock-based compensation expense3 | (350) | (356) | ||
Net sales and marketing | 3,844 | 3,771 | ||
General and administrative | 4,070 | 6,900 | ||
Depreciation expense | (129) | (107) | ||
RDx Settlement in Stock | — | (713) | ||
Stock-based compensation expense3 | (330) | (2,668) | ||
Net general and administrative | 3,611 | 3,412 | ||
Research and development | 1,501 | 1,893 | ||
Stock-based compensation expense3 | (217) | (165) | ||
Net research and development | 1,284 | 1,728 | ||
Total operating expenses | 11,793 | 14,763 | ||
Depreciation and amortization expense | (501) | (612) | ||
RDx Settlement in Stock | — | (713) | ||
Stock-based compensation expense3 | (933) | (3,208) | ||
Net operating expenses | $ 10,359 | $ 10,230 | ||
About EsoGuard and EsoCheck
Millions of patients with gastroesophageal reflux disease (GERD) are at risk of developing esophageal precancer and a highly lethal form of esophageal cancer ("EAC"). Over 80 percent of EAC patients die within five years of diagnosis, making it the second most lethal cancer in the
Esophageal precancer screening is already recommended by clinical practice guidelines for the millions of GERD patients with multiple risk factors, including age over 50 years, male sex, White race, obesity, smoking history, and a family history of esophageal precancer or cancer. Unfortunately, fewer than 10 percent of those recommended for screening undergo traditional invasive endoscopic screening. The profound tragedy of an EAC diagnosis is that death could likely have been prevented if the at-risk GERD patient had been screened and then undergone surveillance and curative treatment at the precancer stage.
The only missing element for a viable esophageal cancer prevention program has been the lack of an easily-accessible, in-office screening tool that can detect esophageal precancer. Lucid believes EsoGuard, performed on samples collected non-endoscopically with EsoCheck, is the missing element – the first and only commercially available test capable of serving as a widespread screening tool to prevent esophageal cancer deaths through the early detection of esophageal precancer in at-risk GERD patients. An updated American College of Gastroenterology (ACG) clinical practice guideline and an American Gastroenterological Association (AGA) clinical practice update both endorse non-endoscopic biomarker tests as an acceptable alternative to costly and invasive endoscopy for esophageal precancer screening. EsoGuard is the only such test currently available in
EsoGuard is a Next Generation Sequencing (NGS) based DNA methylation assay performed on surface esophageal cells collected with EsoCheck, which quantifies methylation at 31 sites on two genes, Vimentin (VIM) and Cyclin A1 (CCNA1). The assay was initially evaluated in a 408-patient, multicenter, case-control study published in Science Translational Medicine and showed greater than 90 percent sensitivity and specificity at detecting esophageal precancer and cancer.
EsoCheck is a CE Marked and FDA 510(k) cleared noninvasive swallowable balloon capsule catheter device capable of sampling surface esophageal cells in a less than three-minute office procedure. It consists of a vitamin pill-sized rigid plastic capsule tethered to a thin silicone catheter from which a soft silicone balloon with textured ridges emerges to gently swab surface esophageal cells. When vacuum suction is applied, the balloon and sampled cells are pulled into the capsule, protecting them from contamination and dilution by cells outside of the targeted region during device withdrawal. Lucid believes this proprietary Collect+Protect™ technology makes EsoCheck the only noninvasive esophageal cell collection device capable of such anatomically targeted and protected sampling. The sample is sent by overnight express mail to Lucid's CLIA-certified, CAP-accredited, NYS CLEP approved laboratory, LucidDx Labs, for EsoGuard testing.
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.
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SOURCE Lucid Diagnostics
FAQ
What was the revenue for EsoGuard in the first quarter of 2024?
The revenue for EsoGuard in the first quarter of 2024 was $1.0 million.
What was the increase in EsoGuard test volume compared to the previous quarter?
The EsoGuard test volume increased by 10% compared to the previous quarter.
When is the MolDX pre-submission meeting scheduled?
The MolDX pre-submission meeting is scheduled for July 17, 2024.
What was the amount raised in the Series B Preferred Stock Offering?
The Series B Preferred Stock Offering raised approximately $29.8 million.
Who is Lucid Diagnostics' majority-owned subsidiary?
Lucid Diagnostics' majority-owned subsidiary is PAVmed Inc.
