Lucid Diagnostics Awarded U.S. Department of Veterans Affairs Contract for EsoGuard®
Rhea-AI Summary
Lucid Diagnostics (Nasdaq: LUCD) was awarded a contract by the U.S. Department of Veterans Affairs on January 21, 2026 to supply its EsoGuard® Esophageal DNA Test through the VA Federal Supply Schedule.
The contract expands access to esophageal precancer testing across the VA system serving more than 9 million enrolled veterans, uses a single national VA procurement framework, and sets pre-negotiated pricing that matches the established Medicare payment rate as determined by CMS.
Lucid said the selection reflects the clinical evidence for EsoGuard and plans to work with the VA and other integrated health systems to adopt the test into clinical practice.
Positive
- VA contract awarded for EsoGuard nationwide access
- Access expanded to the VA system serving 9 million enrolled veterans
- Pricing pre-negotiated to match Medicare payment rate via CMS
- Single national procurement simplifies VA hospital access
Negative
- None.
News Market Reaction – PAVM
In the Jan 21 session, PAVM gained 94.67%, reflecting a significant positive market reaction. Argus tracked a peak move of +303.7% during that session. Our momentum scanner triggered 59 alerts that day, indicating high trading interest and price volatility. Trading volume was exceptionally heavy at 1593.7x the daily average, suggesting very strong buying interest.
Data tracked by StockTitan Argus on the day of publication.
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The contract is issued under the VA Federal Supply Schedule and includes pre-negotiated pricing for EsoGuard that matches the established Medicare payment rate determined by the Centers for Medicare & Medicaid Services (CMS), enabling VA hospitals and healthcare facilities nationwide to access EsoGuard through a single, national VA procurement framework.
"We are proud to partner with the
About Lucid Diagnostics
Lucid Diagnostics Inc. is a commercial-stage, cancer prevention medical diagnostics company, and subsidiary of PAVmed Inc. (Nasdaq: PAVM). Lucid is focused on the millions of patients with gastroesophageal reflux disease (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, represent the first and only commercially available tools designed with the goal of preventing cancer and cancer deaths through widespread, early detection of esophageal precancer in at-risk patients.
For more information, please visit www.luciddx.com and for more information about its parent company PAVmed, please visit www.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'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 Lucid's common stock; general economic and market conditions; the uncertainties inherent in research and development, including the cost and time required to advance Lucid's products to regulatory submission; whether regulatory authorities will be satisfied with the design of and results from Lucid's clinical and preclinical studies; whether and when Lucid's products are cleared by regulatory authorities; market acceptance of Lucid's products once cleared and commercialized; Lucid's ability to raise additional funding as needed; and other competitive developments. In addition, Lucid continues to monitor the COVID-19 pandemic and the pandemic's impact on Lucid's businesses. These factors are difficult or impossible to predict accurately and many of them are beyond Lucid's 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's future operations, see Part I, Item 1A, "Risk Factors," in 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 Lucid Diagnostics after its most recent Annual Report. Lucid 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