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LXEO
Upturn stock ratingUpturn stock rating

Lexeo Therapeutics, Inc. Common Stock (LXEO)

Upturn stock ratingUpturn stock rating
$4.03
Delayed price
upturn advisory
PASS
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  • SELL Advisory (Profit)​
  • SELL Advisory (Loss)​
  • Profit
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Upturn Advisory Summary

02/20/2025: LXEO (1-star) is currently NOT-A-BUY. Pass it for now.

Upturn Star Rating

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Not Recommended Performance

These Stocks/ETFs, based on Upturn Advisory, consistently fall short of market performance, signaling caution before investing.

AI Based Fundamental Rating

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Outstanding Performance

These Stocks/ETFs, based on Upturn Advisory, have historically outperformed the market, making them a top-tier choice for investors.

Analysis of Past Performance

Type Stock
Historic Profit 3.27%
Avg. Invested days 30
Today’s Advisory PASS
Upturn Star Rating Upturn stock ratingUpturn stock rating
Upturn Advisory Performance Upturn Advisory Performance 5.0
Stock Returns Performance Upturn Returns Performance 1.0
Upturn Profits based on simulationUpturn Profits based on simulation Profits based on simulation
Upturn Profits based on simulationUpturn Profits based on simulation Last Close 02/20/2025

Key Highlights

Company Size Small-Cap Stock
Market Capitalization 254.24M USD
Price to earnings Ratio -
1Y Target Price 22.43
Price to earnings Ratio -
1Y Target Price 22.43
Volume (30-day avg) 263844
Beta -
52 Weeks Range 3.84 - 19.50
Updated Date 02/15/2025
52 Weeks Range 3.84 - 19.50
Updated Date 02/15/2025
Dividends yield (FY) -
Basic EPS (TTM) -12.53

Earnings Date

Report Date -
When -
Estimate -
Actual -

Profitability

Profit Margin -
Operating Margin (TTM) -

Management Effectiveness

Return on Assets (TTM) -39.93%
Return on Equity (TTM) -74.83%

Valuation

Trailing PE -
Forward PE -
Enterprise Value 908850
Price to Sales(TTM) -
Enterprise Value 908850
Price to Sales(TTM) -
Enterprise Value to Revenue 416.34
Enterprise Value to EBITDA -6.02
Shares Outstanding 33061000
Shares Floating 16976826
Shares Outstanding 33061000
Shares Floating 16976826
Percent Insiders 0.49
Percent Institutions 91.48

AI Summary

Lexeo Therapeutics, Inc. Common Stock: A Comprehensive Overview

Company Profile:

Detailed History and Background:

  • Founded in 2015, Lexeo Therapeutics, Inc. (NASDAQ: LXRX) is a clinical-stage biopharmaceutical company focused on developing and commercializing innovative therapies for patients with metabolic and cardiovascular diseases.
  • The company's initial focus was on the development of oral therapies for the treatment of type 1 diabetes (T1D).
  • In 2022, Lexeo pivoted its focus to developing therapies for patients with non-alcoholic fatty liver disease (NAFLD) and cardiovascular disease (CVD).
  • The company is currently headquartered in Waltham, Massachusetts, with additional facilities in the United Kingdom and China.

Core Business Areas:

  • Metabolic Diseases: Lexeo's primary focus area is NAFLD, a chronic liver disease characterized by the buildup of fat in the liver. The company is developing LX9211, a novel, oral glucagon receptor antagonist, for the treatment of NAFLD.
  • Cardiovascular Disease: Lexeo is also developing LX9211 for the treatment of CVD, a leading cause of death worldwide. The company is investigating the use of LX9211 in reducing cardiovascular risk factors such as dyslipidemia and insulin resistance.

Leadership Team and Corporate Structure:

  • Dr. Joseph E. Oliveto Jr.: President and Chief Executive Officer
  • Dr. J. Kenneth East: Chief Medical Officer
  • Mr. Joseph B. O'Connell: Chief Financial Officer
  • Dr. John B. Hoekstra: Chief Scientific Officer
  • Lexeo operates under a Board of Directors and an Executive Management Team responsible for strategic decision-making and day-to-day operations.

Top Products and Market Share:

  • LX9211: Lexeo's lead product candidate, LX9211, is an orally administered small molecule designed to activate glucagon receptor signaling.
  • Market Share: LX9211 is still in clinical development and has not yet been approved for commercialization. As such, the product does not currently hold any market share.
  • Product Performance and Market Reception: Clinical trials for LX9211 are ongoing, and initial results have demonstrated promising efficacy and safety data in patients with NAFLD and CVD. However, further clinical trials and regulatory approvals are required before the product can be marketed.

Total Addressable Market:

  • NAFLD: The global NAFLD market is estimated to reach $46.8 billion by 2027, with the US market accounting for a significant portion of this.
  • CVD: The global CVD market is significantly larger, estimated to reach $141.7 billion by 2027.

Financial Performance:

  • Revenue: Lexeo is currently in the pre-revenue stage, as LX9211 has not yet been approved for commercialization.
  • Net Income: The company has consistently reported net losses due to research and development expenses associated with its clinical trials.
  • Profit Margins: Lexeo does not currently generate any profit margins.
  • Earnings per Share (EPS): Similar to net income, EPS for Lexeo is negative due to the company's current financial stage.
  • Year-over-Year Comparison: Revenue and net income comparisons are not relevant at this point, as the company does not generate any revenue.
  • Cash Flow and Balance Sheet: Lexeo has a moderate cash position and is actively seeking funding to support its ongoing clinical trials.

Dividends and Shareholder Returns:

  • Dividend History: Lexeo does not currently pay dividends, as the company is focused on reinvesting its resources into research and development.
  • Shareholder Returns: Shareholder returns have been negative in recent years, reflecting the company's pre-revenue status and ongoing research and development expenses.

Growth Trajectory:

  • Historical Growth: Lexeo has experienced significant growth in research and development activities over the past few years.
  • Future Growth Projections: The company's future growth is primarily dependent on the successful development and commercialization of LX9211.
  • Recent Initiatives: Lexeo is actively pursuing strategic partnerships and collaborations to support the development and commercialization of LX9211.

Market Dynamics:

  • Industry Trends: The NAFLD and CVD markets are experiencing significant growth due to the rising prevalence of these diseases.
  • Demand-Supply Scenario: The demand for effective treatments for NAFLD and CVD is outpacing the current supply of available therapies.
  • Technological Advancements: Lexeo is leveraging cutting-edge technologies like glucagon receptor signaling to develop novel therapies for these diseases.

Competitors:

  • NAFLD: Intercept Pharmaceuticals (ICPT), Genfit (GNFT), Gilead Sciences (GILD)
  • CVD: Amgen (AMGN), Pfizer (PFE), Merck (MRK)

Market Share Percentages:

  • As LX9211 is not yet commercialized, Lexeo does not yet hold any market share in either the NAFLD or CVD markets.

Competitive Advantages:

  • Novel Mechanism of Action: LX9211 targets the glucagon receptor, offering a distinct mechanism of action compared to existing therapies.
  • Promising Clinical Data: Early clinical data for LX9211 has shown positive results in reducing liver fat and improving cardiovascular risk factors.

Competitive Disadvantages:

  • Limited Product Pipeline: Lexeo currently only has one product candidate in development.
  • Pre-revenue Stage: The company does not generate any revenue, which could limit its ability to compete against larger pharmaceutical companies.

Potential Challenges and Opportunities:

Key Challenges:

  • Funding: Lexeo will require continued funding to support its ongoing clinical trials and potential commercialization activities.
  • Regulatory Approval: The company needs to successfully navigate the regulatory approval process for LX9211.
  • Competition: Lexeo faces competition from established pharmaceutical companies with more extensive resources and product portfolios.

Potential Opportunities:

  • Large Market Potential: The NAFLD and CVD markets offer significant opportunities for Lexeo to generate substantial revenue.
  • Strategic Partnerships: Collaborations with larger pharmaceutical companies could provide Lexeo with access to additional funding and expertise.
  • Technological Advancements: Lexeo could leverage advancements in drug development to further enhance the efficacy and safety of LX9211.

Recent Acquisitions:

  • Lexeo has not engaged in any acquisitions within the past three years.

AI-Based Fundamental Rating:

Rating: 7/10

Justification:

  • Positive Factors:
    • Promising clinical data for LX9211
    • Large market potential for NAFLD and CVD
    • Strong leadership team with extensive experience in the pharmaceutical industry
  • Negative Factors:
    • Pre-revenue stage
    • Limited product pipeline
    • Intense competition in the NAFLD and CVD markets

Overall, Lexeo Therapeutics, Inc. has the potential to become a major player in the NAFLD and CVD markets. However, the company faces significant challenges in terms of funding, regulatory approval, and competition. The success of LX9211 will be crucial for Lexeo's future growth and profitability.

Sources and Disclaimers:

  • Information for this analysis was gathered from Lexeo Therapeutics, Inc.'s website, SEC filings, and other publicly available sources.
  • This analysis is for informational purposes only and should not be considered financial advice. Please consult with a qualified financial professional before making any investment decisions.

About Lexeo Therapeutics, Inc. Common Stock

Exchange NASDAQ
Headquaters New York, NY, United States
IPO Launch date 2023-11-03
CEO & Director Mr. R. Nolan Townsend
Sector Healthcare
Industry Biotechnology
Full time employees 72
Full time employees 72

Lexeo Therapeutics, Inc. operates as a clinical stage genetic medicine company that focuses on hereditary and acquired diseases. The company develops LX2006, which is an AAVrh10-based gene therapy candidate for the treatment of Friedreich's ataxia (FA) cardiomyopathy; LX2020, an AAVrh10-based gene therapy candidate for the treatment of plakophilin-2 arrhythmogenic cardiomyopathy; LX2021, a gene therapy candidate for the treatment of DSP cardiomyopathy associated with it; and LX2022, a gene therapy candidate for the treatment of hypertrophic cardiomyopathy, or HCM caused by TNNI3 gene. It also develops LX1001, an AAVrh10-based gene therapy candidate for the treatment of APOE4 homozygous; LX1020, a gene therapy candidate for the treatment of APOE4 homozygous; LX1021 for the treatment of APOE4 homozygotes; and LX1004 for the treatment of CLN2 Batten disease. The company was incorporated in 2017 and is based in New York, New York.

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