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Lucid Diagnostics Inc (LUCD)


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Upturn Advisory Summary
10/17/2025: LUCD (1-star) has a low Upturn Star Rating. Not recommended to BUY.
1 Year Target Price $3.75
1 Year Target Price $3.75
4 | Strong Buy |
2 | Buy |
0 | Hold |
0 | Sell |
0 | Strong Sell |
Analysis of Past Performance
Type Stock | Historic Profit -42.7% | Avg. Invested days 18 | Today’s Advisory Consider higher Upturn Star rating |
Upturn Star Rating ![]() | Upturn Advisory Performance ![]() | Stock Returns Performance ![]() |
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Key Highlights
Company Size Small-Cap Stock | Market Capitalization 154.16M USD | Price to earnings Ratio - | 1Y Target Price 3.75 |
Price to earnings Ratio - | 1Y Target Price 3.75 | ||
Volume (30-day avg) 6 | Beta 1.19 | 52 Weeks Range 0.75 - 1.80 | Updated Date 10/19/2025 |
52 Weeks Range 0.75 - 1.80 | Updated Date 10/19/2025 | ||
Dividends yield (FY) - | Basic EPS (TTM) -0.95 |
Earnings Date
Report Date - | When - | Estimate - | Actual - |
Profitability
Profit Margin - | Operating Margin (TTM) -978.85% |
Management Effectiveness
Return on Assets (TTM) -82.33% | Return on Equity (TTM) -463.56% |
Valuation
Trailing PE - | Forward PE - | Enterprise Value 154780120 | Price to Sales(TTM) 35.36 |
Enterprise Value 154780120 | Price to Sales(TTM) 35.36 | ||
Enterprise Value to Revenue 35.5 | Enterprise Value to EBITDA -0.67 | Shares Outstanding 101893255 | Shares Floating 66895979 |
Shares Outstanding 101893255 | Shares Floating 66895979 | ||
Percent Insiders 33.67 | Percent Institutions 15.03 |
Upturn AI SWOT
Lucid Diagnostics Inc

Company Overview
History and Background
Lucid Diagnostics Inc. (formerly PAVmed Inc.) focuses on commercializing technologies for early cancer detection, primarily of esophageal precancer and cancer. Founded in 2018 as a spin-off from PAVmed, they have focused on developing and commercializing their EsoGuardu00ae Esophageal DNA Test and EsoChecku00ae Esophageal Cell Collection Device.
Core Business Areas
- EsoGuardu00ae Esophageal DNA Test: A laboratory-developed test (LDT) that detects biomarkers associated with Barrett's esophagus (BE) and esophageal adenocarcinoma (EAC) from samples collected using EsoChecku00ae.
- EsoChecku00ae Esophageal Cell Collection Device: A non-endoscopic, disposable device that collects esophageal cells for analysis with the EsoGuard test. It is designed to be a less invasive and more convenient alternative to traditional endoscopy.
Leadership and Structure
Lishan Aklog, M.D. serves as Chairman and Chief Executive Officer. The company has a typical organizational structure with departments focusing on research, development, sales, marketing, and operations. The Board of Directors provides oversight and strategic guidance.
Top Products and Market Share
Key Offerings
- EsoGuardu00ae Esophageal DNA Test: EsoGuard is Lucid's primary product, a diagnostic test for Barrett's esophagus. Revenue figures are still relatively low, as the product is in its commercialization phase. Competitors include traditional endoscopy and biopsy. Exact market share is difficult to determine due to fragmented testing methods, but Lucid is working to capture a significant portion of the BE screening market. The number of users continues to increase as the company expands sales and marketing efforts.
- EsoChecku00ae Esophageal Cell Collection Device: EsoCheck is the delivery system for cell samples used in conjunction with EsoGuard. Revenue figures are combined with the revenue from the diagnostic test.
Market Dynamics
Industry Overview
The industry involves early cancer detection, particularly in gastroenterology. There's a growing focus on non-invasive diagnostic methods for various cancers due to increased awareness and demand for preventative healthcare.
Positioning
Lucid Diagnostics is positioned as a disruptor in the esophageal cancer screening market, offering a non-endoscopic alternative to traditional methods. Its competitive advantage lies in the convenience and accessibility of the EsoGuard/EsoCheck system.
Total Addressable Market (TAM)
The estimated TAM for esophageal cancer screening is billions of dollars, considering the prevalence of GERD (gastroesophageal reflux disease), a risk factor for Barrett's esophagus. Lucid is positioned to capture a significant portion of this market with its non-invasive approach.
Upturn SWOT Analysis
Strengths
- Non-invasive and convenient diagnostic method
- Potential to increase early detection rates
- Patented technology
- Experienced leadership team
- First and only FDA-approved non-endoscopic Esophageal Cell Collection Device
Weaknesses
- Limited commercial traction and market penetration
- Reliance on a single core product
- High cash burn rate
- Dependence on reimbursement approvals
- Need for continued clinical validation and acceptance
Opportunities
- Expanding sales and marketing efforts
- Securing favorable reimbursement coverage
- Developing new applications for its technology
- Partnering with healthcare providers
- Increasing awareness of Barrett's esophagus and esophageal cancer
Threats
- Competition from established diagnostic methods
- Regulatory hurdles and reimbursement challenges
- Technological advancements by competitors
- Economic downturn affecting healthcare spending
- Adverse clinical trial results
Competitors and Market Share
Key Competitors
- ENDO
Competitive Landscape
Lucid Diagnostics has a competitive advantage in non-invasive screening but faces challenges from established endoscopic procedures. The company needs to demonstrate cost-effectiveness and clinical utility to gain wider adoption.
Growth Trajectory and Initiatives
Historical Growth: Historical growth has been centered around the commercialization of EsoGuard and EsoCheck, with revenue increasing as adoption rises.
Future Projections: Future projections are contingent on reimbursement approvals, sales expansion, and further clinical validation. Analyst estimates vary but generally project continued revenue growth.
Recent Initiatives: Recent initiatives include expanding the sales force, conducting clinical studies to support reimbursement, and raising capital to fund operations.
Summary
Lucid Diagnostics is pioneering non-invasive cancer diagnostics, offering a convenient alternative to traditional endoscopy. While its technology holds promise, its financial stability relies on increasing adoption and securing reimbursement. The company faces competition from established methods and needs to demonstrate sustained revenue growth. Future success hinges on expanding sales, securing favorable reimbursement, and continued validation of its technology.
Peer Comparison
Sources and Disclaimers
Data Sources:
- Lucid Diagnostics Inc. Investor Relations
- SEC Filings (10-K, 10-Q)
- Analyst Reports
- Company Press Releases
Disclaimers:
This analysis is for informational purposes only and does not constitute investment advice. Financial data and market information are subject to change. Market share is approximate and based on available data.
AI Summarization is directionally correct and might not be accurate.
Summarized information shown could be a few years old and not current.
Fundamental Rating based on AI could be based on old data.
AI-generated summaries may have inaccuracies (hallucinations). Please verify the information before taking action.
About Lucid Diagnostics Inc
Exchange NASDAQ | Headquaters New York, NY, United States | ||
IPO Launch date 2021-10-14 | Chairman & CEO Dr. Lishan Aklog M.D. | ||
Sector Healthcare | Industry Medical Devices | Full time employees 72 | Website https://www.luciddx.com |
Full time employees 72 | Website https://www.luciddx.com |
Lucid Diagnostics Inc. operates as a commercial-stage medical diagnostics technology company in the United States. The company focuses on patients with gastroesophageal reflux disease (GERD) who are at risk of developing esophageal precancer and cancer, primarily highly lethal esophageal adenocarcinoma. Its flagship product, the EsoGuard Esophageal DNA Test performed on samples collected with the EsoCheck Esophageal Cell collection device, a testing tool with the goal of preventing EAC deaths through early detection of esophageal precancer in at-risk GERD patients. The company was incorporated in 2018 and is based in New York, New York. Lucid Diagnostics Inc. operates as a subsidiary of PAVmed Inc.

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