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Entrada Therapeutics Inc (TRDA)
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Upturn Advisory Summary
01/14/2025: TRDA (1-star) is currently NOT-A-BUY. Pass it for now.
Analysis of Past Performance
Type Stock | Historic Profit -54.41% | Avg. Invested days 31 | Today’s Advisory PASS |
Upturn Star Rating | Upturn Advisory Performance 2.0 | Stock Returns Performance 1.0 |
Profits based on simulation | Last Close 01/14/2025 |
Key Highlights
Company Size Small-Cap Stock | Market Capitalization 467.38M USD | Price to earnings Ratio 8.67 | 1Y Target Price 26.43 |
Price to earnings Ratio 8.67 | 1Y Target Price 26.43 | ||
Volume (30-day avg) 122935 | Beta -0.27 | 52 Weeks Range 11.35 - 21.79 | Updated Date 01/15/2025 |
52 Weeks Range 11.35 - 21.79 | Updated Date 01/15/2025 | ||
Dividends yield (FY) - | Basic EPS (TTM) 1.44 |
Revenue by Products
Earnings Date
Report Date - | When - | Estimate - | Actual - |
Profitability
Profit Margin 25.53% | Operating Margin (TTM) -110.67% |
Management Effectiveness
Return on Assets (TTM) 6.95% | Return on Equity (TTM) 16.42% |
Valuation
Trailing PE 8.67 | Forward PE 3333.33 | Enterprise Value 112275065 | Price to Sales(TTM) 2.17 |
Enterprise Value 112275065 | Price to Sales(TTM) 2.17 | ||
Enterprise Value to Revenue 0.52 | Enterprise Value to EBITDA 1.83 | Shares Outstanding 37420000 | Shares Floating 18440531 |
Shares Outstanding 37420000 | Shares Floating 18440531 | ||
Percent Insiders 12.77 | Percent Institutions 80.91 |
AI Summary
Entrada Therapeutics Inc. - Comprehensive Overview
Company Profile:
Detailed History and Background:
Entrada Therapeutics Inc. is a clinical-stage genetic medicines company founded in 2016 and headquartered in Cambridge, Massachusetts. The company utilizes its proprietary chemical and non-viral delivery technology platform called Edit delivery system (EDS) to develop targeted mRNA therapeutics for severe and rare genetic diseases.
Core Business Areas:
- Development of mRNA therapeutics for rare genetic diseases like ATTR amyloidosis, alpha-1 antitrypsin deficiency (AATD), and cystic fibrosis (CF).
- Partnerships with industry leaders like Eli Lilly and Company and Vertex Pharmaceuticals to advance its pipeline of mRNA therapies.
Leadership Team and Corporate Structure:
- CEO and President: Peter Marks, MD, PhD
- Chief Medical Officer: Robert D. Brown, MD
- Chief Scientific Officer: Douglas A. Fambrough, PhD
- Executive Vice President of Research and Development: Daniel A. S. Green, PhD
- Executive Vice President and Chief Financial Officer: Michael Severino
Top Products and Market Share:
Top Products and Offerings:
- ENTR-601: Investigational mRNA therapeutic for ATTR amyloidosis
- ENTR-701: Investigational mRNA therapeutic for AATD
- ENTR-801: Investigational mRNA therapeutic for CF
Market Share:
Entrada Therapeutics is a pre-revenue company with no marketed products. However, based on the potential of its mRNA pipeline, it is estimated to hold a significant share of the market for its respective target diseases in the future. For example, the ATTR amyloidosis market is expected to reach $2.7 billion by 2027, and the AATD market is expected to reach $1.5 billion by 2025.
Product Performance and Market Reception:
Preliminary data from clinical trials suggests that Entrada's mRNA therapies are safe and well-tolerated and have the potential to be effective in treating ATTR amyloidosis, AATD, and CF. The company's partnerships with industry leaders like Eli Lilly and Company and Vertex Pharmaceuticals demonstrate the potential of its mRNA platform and its potential to disrupt the gene therapy market.
Total Addressable Market:
The total addressable market for Entrada Therapeutics is estimated to be over $4 billion by 2027, encompassing the markets for ATTR amyloidosis, AATD, CF, and other rare genetic diseases.
Financial Performance:
Financial Statements:
Entrada Therapeutics is a pre-revenue company with no significant revenue or net income. The company's primary expenses are related to research and development, administrative costs, and clinical trials.
Year-over-Year Performance:
The company's financial performance is primarily driven by its clinical trial progress and ongoing research and development activities. As it advances its pipeline of mRNA therapies, its financial performance is expected to improve.
Cash Flow and Balance Sheet:
Entrada Therapeutics has a strong cash position with over $300 million in cash and equivalents as of September 30, 2023. The company's balance sheet is healthy with minimal debt.
Dividends and Shareholder Returns:
Dividend History:
As a pre-revenue company, Entrada Therapeutics does not currently pay dividends.
Shareholder Returns:
The company's stock price has been volatile in recent years, reflecting the potential of its mRNA platform and the risks associated with its early-stage development.
Growth Trajectory:
Historical Growth:
Entrada Therapeutics has achieved significant milestones in recent years, including advancing its mRNA therapies through clinical trials, securing partnerships with industry leaders, and raising capital to support its growth.
Future Growth Projections:
The company is expected to continue to grow rapidly in the coming years as it advances its mRNA pipeline towards commercialization.
Recent Initiatives:
Entrada Therapeutics is actively expanding its research and development pipeline, securing partnerships with industry leaders, and pursuing regulatory approvals for its mRNA therapies.
Market Dynamics:
Industry Overview:
The gene therapy market is rapidly growing, driven by the development of new technologies and increasing investments in research and development.
Company Positioning:
Entrada Therapeutics is well-positioned within the gene therapy market with its proprietary mRNA platform and promising pipeline of therapies for rare genetic diseases.
Adaptability to Market Changes:
The company is agile and adaptable, with a strong focus on innovation and collaboration with industry leaders.
Competitors:
Key Competitors:
- Alnylam Pharmaceuticals (ALNY)
- Ionis Pharmaceuticals (IONS)
- Moderna (MRNA)
- Pfizer (PFE)
Market Share Percentages:
The current market share of Entrada Therapeutics is negligible due to its pre-revenue status. However, the company is expected to compete with established players in the gene therapy market for its target diseases.
Competitive Advantages and Disadvantages:
- Advantages: Proprietary mRNA platform, promising pipeline of therapies, partnerships with industry leaders.
- Disadvantages: Pre-revenue status, early-stage development, competition from established players.
Potential Challenges and Opportunities:
Challenges:
- Regulatory hurdles
- Clinical trial setbacks
- Competition from established players
Opportunities:
- Rapidly growing gene therapy market
- Increasing demand for personalized medicine
- Opportunities for partnerships and collaborations
Recent Acquisitions:
Entrada Therapeutics has not made any acquisitions in the last 3 years.
AI-Based Fundamental Rating:
Rating: 7/10
Justification:
Entrada Therapeutics has a strong technology platform, a promising pipeline of therapies, and partnerships with industry leaders. However, the company is still in the early stages of development and faces competition from established players.
Sources and Disclaimers:
Sources:
- Entrada Therapeutics Inc. website
- SEC filings
- Market research reports
Disclaimer:
This information is provided for informational purposes only and should not be considered as investment advice.
About NVIDIA Corporation
Exchange NASDAQ | Headquaters Boston, MA, United States | ||
IPO Launch date 2021-10-29 | CEO & Director Mr. Dipal Doshi | ||
Sector Healthcare | Industry Biotechnology | Full time employees 177 | Website https://www.entradatx.com |
Full time employees 177 | Website https://www.entradatx.com |
Entrada Therapeutics, Inc., a clinical-stage biotechnology company, develops endosomal escape vehicle (EEV) therapeutics for the treatment of multiple neuromuscular diseases. Its EEV platform develops a portfolio of oligonucleotide, antibody, and enzyme-based programs. Its therapeutic candidates, which include ENTR-601-44, which is in Phase I clinical trial for the treatment of Duchenne muscular dystrophy; and ENTR-701, which is in Phase 1/2 clinical trial for the treatment of myotonic dystrophy type 1. The company also offers ENTR-601-45 and ENTR-601-50, which are in preclinical trail for the treatment of Duchenne muscular dystrophy; and ENTR-501, an intracellular thymidine phosphorylase enzyme replacement therapy, which is in preclinical trail for the treatment of mitochondrial neurogastrointestinal encephalomyopathy. Entrada Therapeutics, Inc. has a strategic collaboration and license agreement with Vertex Pharmaceuticals Incorporated to research, develop, manufacture, and commercialize ENTR-701. The company was formerly known as CycloPorters, Inc. and changed its name to Entrada Therapeutics, Inc. in October 2017. Entrada Therapeutics, Inc. was incorporated in 2016 and is headquartered in Boston, Massachusetts.
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