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Lucid Diagnostics Provides Update Regarding World Trade Center Health Program

Key Takeaway: Lucid Diagnostics announced an update regarding the World Trade Center Health Program, noting that the EsoGuard® Esophageal DNA test had been incorrectly listed as a covered benefit due to a clerical error. The company has been directed to engage with Clinical Centers of Excellence to rectify the situation. Despite this setback, Lucid remains dedicated to providing cancer prevention testing for first responders, having tested thousands through their programs. The company aims to ensure access to essential esophageal precancer testing for high-risk groups.

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POSITIVE FACTORS

  • Lucid Diagnostics is committed to making Esophageal DNA testing accessible to at-risk participants.
  • The company has a history of collaborating with first responders on cancer prevention initiatives.
  • Lucid has successfully tested thousands of first responders through its outreach programs.

CONCERNS & RISKS

  • A clerical error by WTCHP initially misclassified the EsoGuard® test as a covered benefit.
  • Uncertainties could arise from the engagement steps with Clinical Centers of Excellence.

Full Press Release Details

NEW YORK, Feb. 16, 2024 /PRNewswire/ -- Lucid Diagnostics Inc. (Nasdaq: LUCD) ("Lucid" or the "Company") a commercial-stage, cancer prevention medical diagnostics company, and majority-owned subsidiary of PAVmed Inc. (Nasdaq: PAVM, PAVMZ) ( "PAVmed"), today announced that it was notified by the World Trade Center Health Program ("WTCHP") that, due to a clerical error, the EsoGuard® Esophageal DNA test was incorrectly listed as a covered benefit. WTCHP advised Lucid on the further steps required, including engaging directly with its Clinical Centers of Excellence. Lucid has a strong record of partnering with firefighters and other first responders on cancer prevention programs targeting these at-risk groups. Lucid has tested thousands of first responders across the country at high-volume #CheckYourFoodTube Precancer Testing Events. As such, Lucid remains deeply committed to working closely with WTCHP to complete the necessary steps to provide its at-risk participants access to esophageal precancer testing.
About Lucid Diagnostics
Lucid Diagnostics Inc. is a commercial-stage medical diagnostics company focused on cancer prevention, 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, is the first and only commercially available diagnostic test capable of serving as a widespread screening tool for at-risk patients to mitigate the risks of cancer and cancer deaths through early detection of esophageal precancer.
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.
SOURCE Lucid Diagnostics

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Frequently Asked Questions

What is the EsoGuard® Esophageal DNA test?

The EsoGuard® test is a diagnostic tool for esophageal precancer, performed noninvasively.

Why was the EsoGuard® test incorrectly listed?

It was mislisted due to a clerical error by the World Trade Center Health Program.

Who does Lucid Diagnostics partner with?

Lucid partners with firefighters and first responders for cancer prevention programs.

What condition does Lucid primarily focus on?

Lucid focuses on gastroesophageal reflux disease (GERD) and its cancer risks.

How is the EsoGuard® test collected?

The test is collected using the EsoCheck Esophageal Cell Collection Device.

Last updated: Feb 16, 2024