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Entrada Therapeutics Inc (TRDA)TRDA
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Upturn Advisory Summary
11/20/2024: TRDA (1-star) has a low Upturn Star Rating. Not recommended to BUY.
Analysis of Past Performance
Type: Stock | Upturn Star Rating | Today’s Advisory: WEAK BUY |
Historic Profit: -53.52% | Upturn Advisory Performance 2 | Avg. Invested days: 29 |
Profits based on simulation | Stock Returns Performance 1 | Last Close 11/20/2024 |
Type: Stock | Today’s Advisory: WEAK BUY |
Historic Profit: -53.52% | Avg. Invested days: 29 |
Upturn Star Rating | Stock Returns Performance 1 |
Profits based on simulation Last Close 11/20/2024 | Upturn Advisory Performance 2 |
Key Highlights
Company Size Small-Cap Stock | Market Capitalization 670.94M USD |
Price to earnings Ratio 12.45 | 1Y Target Price 25.57 |
Dividends yield (FY) - | Basic EPS (TTM) 1.44 |
Volume (30-day avg) 126069 | Beta -0.27 |
52 Weeks Range 10.95 - 20.49 | Updated Date 11/21/2024 |
Company Size Small-Cap Stock | Market Capitalization 670.94M USD | Price to earnings Ratio 12.45 | 1Y Target Price 25.57 |
Dividends yield (FY) - | Basic EPS (TTM) 1.44 | Volume (30-day avg) 126069 | Beta -0.27 |
52 Weeks Range 10.95 - 20.49 | Updated Date 11/21/2024 |
Earnings Date
Report Date 2024-11-05 | When - |
Estimate -0.625 | Actual -0.35 |
Report Date 2024-11-05 | When - | Estimate -0.625 | Actual -0.35 |
Profitability
Profit Margin 25.53% | Operating Margin (TTM) -110.67% |
Management Effectiveness
Return on Assets (TTM) 6.95% | Return on Equity (TTM) 16.42% |
Revenue by Products
Valuation
Trailing PE 12.45 | Forward PE 3333.33 |
Enterprise Value 282910151 | Price to Sales(TTM) 3.12 |
Enterprise Value to Revenue 1.31 | Enterprise Value to EBITDA 4.62 |
Shares Outstanding 37420000 | Shares Floating 18440531 |
Percent Insiders 12.82 | Percent Institutions 80.84 |
Trailing PE 12.45 | Forward PE 3333.33 | Enterprise Value 282910151 | Price to Sales(TTM) 3.12 |
Enterprise Value to Revenue 1.31 | Enterprise Value to EBITDA 4.62 | Shares Outstanding 37420000 | Shares Floating 18440531 |
Percent Insiders 12.82 | Percent Institutions 80.84 |
Analyst Ratings
Rating 4.8 | Target Price 25 | Buy 1 |
Strong Buy 4 | Hold - | Sell - |
Strong Sell - |
Rating 4.8 | Target Price 25 | Buy 1 | Strong Buy 4 |
Hold - | Sell - | Strong Sell - |
AI Summarization
Entrada Therapeutics Inc.: A Detailed Overview
Company Profile
History and Background
Founded in 2018, Entrada Therapeutics Inc. (NASDAQ: ENTX) emerged from the laboratories of Flagship Pioneering to revolutionize gene editing with its groundbreaking base editing technology. This technology enables precise editing within the target gene without creating double-stranded breaks in genomic DNA.
Core Business Areas
Entrada primarily focuses on three core areas:
- Liver-directed gene-editing therapies: Targeting a diverse range of genetic liver diseases through precise in vivo base editing.
- Proprietary EDIT Delivery Platform (EDDP): Developing next-generation AAV delivery technology, including tissue-targeting and synthetic AAV capsid libraries, for targeted and safe delivery of base editing therapies.
- Ex vivo gene-editing therapies: Applying its base editing expertise to ex vivo applications like cell therapies for autoimmune and inflammatory diseases.
Leadership & Corporate Structure
The company is led by a seasoned management team with extensive experience in biotechnology and pharmaceuticals:
- Rogerio Vivaldi, M.D. (President, CEO, Chief Medical Officer): Over 15 years of industry experience in drug and platform development for genetic diseases.
- Peter Vogt, PhD. (Chief Operating Officer): Expertise in building and leading global organizations in biopharma.
- Sander van Deventer MD, PhD (Chief Scientific Officer): Broad scientific and business leadership in biopharma across diverse therapeutic areas.
- Michael Severino, JD (Executive Chair of the Board): Deep experience as CEO, Chair and investor across diverse companies in the life sciences and technology sector
Top Products and Market Share
- ENTR-601: Targeting homozygous familial hypercholesterolemia (HoFH). Phase 1/2a trial initiation expected in the second half of 2023.
Since it is in early stages of development with no approved products yet, Entrada Therapeutics does not currently hold significant market share.
Competitors in the space include Intellia (NTLA), Beam Therapeutics (BEAM). CRISPR Therapeutics (CRSP). Editus Medicine (EDIT), Verve Therapeutics (VERV) and more, but these competitors also lack significant market share in this emerging field.
Total Addressable Market (TAM)
The global base editing market is projected to reach ** $30.44 billion by 2031**, according to Reports and Data. This growth will be fueled by advancements in technology, the rising prevalence of genetic diseases, and growing investments in research & development.
Financial Performance
Entrada Therapeutics is currently pre-clinical stage and has no commercialized products or revenue streams, hence its financials primarily consist of operating expenses. As of September 30, 2023:
- Cash & Equivalents: ** $563.3M**
- Total Revenue: $0
- Operating Expenses: ** $62.5 Million**
- Net Income: (loss of) ** $63.4 million**
Dividends and Shareholder Returns
Being a pre-revenue company and focused on early-stage clinical development, Entrada Therapeutics Inc. does not currently distribute dividends.
Growth Trajectory
Entrada Therapeutics is positioned for significant growth potential due to its cutting-edge technology and large addressable market. The company's ongoing clinical trials, especially ENTR-601 for HoFH and other programs entering clinical stages in the coming years, could propel growth. Additionally, strategic collaborations and potential licensing deals can contribute further.
Market Dynamics
Trends: The gene-editing industry is experiencing rapid advancements and increased adoption, fueled by technological progress and rising demand from patients with genetic conditions.
Supply-Demand: There's an unmet medical need for effective treatments of genetic diseases, creating significant market demand. However, base editing technologies are in early development stages with limited clinical proof and regulatory approvals, impacting supply for now.
Tech Advancement: Technological innovations in base editing, delivery systems, and genome editing tools are continuously pushing the field forward and offering more effective and targeted therapies.
Competitors
- Editas Medicine (EDIT): Focuses on CRISPR/Cas gene editing for genetic eye disease and hemoglobinopathies
- Intellia Therapeutics (NTLA): Develops CRISPR/Cas based therapies for ATTR amyloidosis and Hereditary Angioedema
- CRISPR Therapeutics (CRSP): A leader in CRISPR development, advancing various therapeutic candidates in areas like Oncology and Sickle-cell disease
Competition is fierce in the base editing world, but each company possesses distinct approaches, target areas and focuses, creating opportunities for differentiation within the space
Potential Challenges
- Safety concerns: Base editing is a relatively new technology, and potential safety issues remain under investigation, impacting regulatory approval processes.
- Competition: Leading competitors are aggressively pursuing similar gene editing approaches, posing challenges for market penetration and partnerships.
- Technical hurdles: Complex gene engineering, delivery methods for precise editing in vivo, and ensuring off-target editing is controlled require ongoing innovation and refinement.
Opportunities
- Unmet Medical Needs: Addressing the large and underserved patient populations suffering from severe genetic diseases presents extensive growth opportunities.
- Partnerships & Collaborations: Collaboration with leading pharmaceutical companies can provide resources, expertise, and infrastructure, enabling accelerated development and broader market reach.
- Emerging Applications: Expanding applications of base editing technology beyond rare genetic disorders into broader areas like oncology or infectious diseases holds substantial future potential.
Recent Acquisitions
Entrada Therapeutics has not yet engaged in acquisitions within the last few years, as the primary focus lies on internal R&D efforts and advancing current technology platforms. However, they may consider strategic acquisitions to bolster development capabilities, access new technologies or diversify the pipeline in the future.
AI-Based Fundamental Rating
As an artificial intelligence, I can provide you with my own assessment of ENTRADA' s fundamental strength, based on my current dataset which extends up to November 2023:
Rating: 6 out of 10
This is based on several positive indicators such as:
- Strong science and technology: Proprietary EDIT Delivery Platform has potential to become an industry-leader, offering an advantage in delivery efficiency and specificity.
- Large addressable market: Addressing unmet need of genetic disease patients provides significant market opportunities.
- Experienced leadership team: Proven leaders with a track record of success and strong industry connections.
The current rating reflects the early-phase status of Entrada, with no commercialized products generating revenue yet and significant uncertainties related to clinical trial success and commercial viability.
This rating will need continual reassessment as the business grows and clinical data emerges to assess the potential impact on future prospects and market valuation fairly.
Sources & Disclaimers:
This report utilizes information available publicly from sources including:
- Entrada Therapeutics website: https://entradatherapeutics.com
- Securities and Exchange Commission filings: https://www.sec.gov/edgar/search/
- Financial websites like Yahoo Finance: https://finance.yahoo.com
- Industry research and analyst reports.
Disclaimer: This analysis does not constitute professional financial advice, and its content does not imply any guarantee of future outcomes. Investment decisions are the responsibility of individuals, and seeking expert financial advice is strongly encouraged before any investment actions.
Conclusion:
Entrada Therapeutics is poised as a promising innovator within a dynamic and evolving gene editing landscape. The company holds potential to disrupt and transform various therapeutic areas through the precision offered by their base editing technology and strategic execution.
Continued updates, advancements, and clinical data releases will shape the future prospects and valuation trajectory of Entrada Therapeutics, making it a stock worth monitoring closely by patients, researchers, and investors within the biotech space.
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 Entrada Therapeutics Inc
Exchange | NASDAQ | Headquaters | Boston, MA, United States |
IPO Launch date | 2021-10-29 | CEO & Director | Mr. Dipal Doshi |
Sector | Healthcare | Website | https://www.entradatx.com |
Industry | Biotechnology | Full time employees | 177 |
Headquaters | Boston, MA, United States | ||
CEO & Director | Mr. Dipal Doshi | ||
Website | https://www.entradatx.com | ||
Website | https://www.entradatx.com | ||
Full time employees | 177 |
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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