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Lucid Diagnostics to Participate in the Needham 21st Annual Healthcare Conference
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Rhea-AI Summary
Lucid Diagnostics Inc. (Nasdaq: LUCD) has announced that Dr. Lishan Aklog, CEO, will speak at the 21st Annual Needham Virtual Healthcare Conference from April 11-14. He is scheduled for a Fireside chat on April 12 from 1:30 - 2:10 pm ET. Lucid focuses on cancer prevention, particularly for patients with gastroesophageal disease (GERD) using its FDA Breakthrough Device-designated EsoGuard® test. The company is actively enrolling participants for clinical trials to support FDA approval, emphasizing its commitment to early detection of esophageal cancer.
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NEW YORK--(BUSINESS WIRE)--
Lucid Diagnostics Inc. (Nasdaq: LUCD) (“Lucid”), a commercial-stage, cancer prevention medical diagnostics company, and majority-owned subsidiary of PAVmed Inc. (Nasdaq: PAVM, PAVMZ) (“PAVmed”), today announced that Dr. Lishan Aklog, Chairman and CEO, has been invited to present at the 21st Annual Needham Virtual Healthcare Conference taking place from April 11 – 14. Dr. Aklog will participate in a Fireside chat on Tuesday, April 12, from 1:30 - 2:10 pm ET. Register to listen to his presentation at https://wsw.com/webcast/needham117/lucd/2239832. In addition, Lucid will host 1x1 investor meetings during the conference. Please contact your Needham representative to schedule a 1x1 meeting.
About Lucid Diagnostics
Lucid Diagnostics Inc. (Nasdaq: LUCD) 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 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 to prevent cancer and cancer deaths through early detection of esophageal precancer in at-risk GERD patients. EsoGuard is commercialized in the U.S. as a Laboratory Developed Test (LDT). EsoCheck is commercialized in the U.S. as a 510(k)-cleared esophageal cell collection device. EsoGuard, used with EsoCheck, was granted FDA Breakthrough Device designation and is the subject of two large, actively enrolling, international multicenter clinical trials to support FDA PMA approval. Lucid is building a network of Lucid Test Centers where at-risk GERD patients can undergo the EsoCheck procedure for EsoGuard testing. For detailed information on EsoGuard, please visit www.EsoGuard.com and follow us on Twitter, Facebook, and Instagram.
Forward-Looking Statements
This press release includes forward-looking statements. 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 has been monitoring the COVID-19 pandemic and the pandemic’s impact on Lucid’s businesses. Lucid expects the significance of the COVID-19 pandemic, including the extent of its effect on its financial and operational results, to be dictated by, among other things, the success of efforts to contain the pandemic and the impact of such efforts 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 Lucid’s Registration Statement No. 333-259721 filed with the Securities and Exchange Commission. 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.
When is Lucid Diagnostics participating in the Needham Virtual Healthcare Conference?
Lucid Diagnostics will participate in the Needham Virtual Healthcare Conference from April 11-14, with Dr. Lishan Aklog's Fireside chat scheduled for April 12 from 1:30 - 2:10 pm ET.
What is the focus of Lucid Diagnostics?
Lucid Diagnostics focuses on cancer prevention, particularly for patients at risk of esophageal cancer due to gastroesophageal disease (GERD).
What is the EsoGuard test developed by Lucid Diagnostics?
EsoGuard is an esophageal DNA test designed for the early detection of esophageal precancer and cancer in at-risk GERD patients.
What is the stock symbol for Lucid Diagnostics and its parent company?
Lucid Diagnostics is traded under the stock symbol LUCD, while its parent company, PAVmed Inc., is traded as PAVM and PAVMZ.
How can I register for the Needham Virtual Healthcare Conference?
You can register to listen to Dr. Aklog's presentation at the Needham Virtual Healthcare Conference by visiting the provided registration link.
