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enGene Holdings Inc. Warrants (ENGNW)
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Upturn Advisory Summary
02/20/2025: ENGNW (1-star) is currently NOT-A-BUY. Pass it for now.
Analysis of Past Performance
Type Stock | Historic Profit 2.9% | Avg. Invested days 39 | Today’s Advisory PASS |
Upturn Star Rating ![]() ![]() | Upturn Advisory Performance ![]() | Stock Returns Performance ![]() |
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Key Highlights
Company Size ETF | Market Capitalization 0 USD | Price to earnings Ratio - | 1Y Target Price - |
Price to earnings Ratio - | 1Y Target Price - | ||
Volume (30-day avg) 6709 | Beta -0.65 | 52 Weeks Range 0.42 - 6.50 | Updated Date 02/17/2025 |
52 Weeks Range 0.42 - 6.50 | Updated Date 02/17/2025 | ||
Dividends yield (FY) - | Basic EPS (TTM) - |
Earnings Date
Report Date - | When - | Estimate - | Actual - |
Profitability
Profit Margin - | Operating Margin (TTM) - |
Management Effectiveness
Return on Assets (TTM) -19.56% | Return on Equity (TTM) -31.96% |
Valuation
Trailing PE - | Forward PE - | Enterprise Value - | Price to Sales(TTM) - |
Enterprise Value - | Price to Sales(TTM) - | ||
Enterprise Value to Revenue - | Enterprise Value to EBITDA - | Shares Outstanding - | Shares Floating 17722041 |
Shares Outstanding - | Shares Floating 17722041 | ||
Percent Insiders - | Percent Institutions - |
AI Summary
enGene Holdings Inc. Warrants: A Comprehensive Overview
Company Profile:
Detailed history and background: enGene Holdings Inc. (formerly known as enGene, Inc.) is a clinical-stage biotechnology company focused on the discovery and development of novel genetic therapies based on its proprietary PhoreGene™ platform. Founded in 2015, enGene initially focused on RNAi-based technology but later shifted its focus to CRISPR/Cas9 gene editing. The company has completed several research collaborations and secured funding through various grants and partnerships. In 2023, enGene merged with Inari Medical, Inc., and currently operates under the name enGene Holdings Inc.
Core business areas: enGene's primary focus lies in developing innovative gene-editing therapies for rare genetic diseases. Their pipeline includes treatments for sickle cell disease, alpha-1 antitrypsin deficiency, and other genetic disorders. The company leverages its PhoreGene™ platform – a non-viral, targeted gene editing technology – to create its therapeutic candidates.
Leadership and corporate structure: enGene's leadership team comprises experienced individuals from the pharmaceutical and biotechnology industries. Dr. Mark Hammer, MD, Ph.D., serves as President and CEO, bringing extensive expertise in gene editing therapeutics. The company's management team also includes seasoned professionals in finance, research, and development.
Top Products and Market Share:
Top products: Currently, enGene does not have any marketed products as they are still in the pre-clinical and clinical development stages. However, their lead product candidates include:
- ENG-801: Targeted gene editing therapy for sickle cell disease
- ENG-771: Targeted gene editing therapy for alpha-1 antitrypsin deficiency
- ENG-906: Targeted gene editing therapy for DMD
Market share: As there are no marketed products yet, enGene does not hold any current market share. However, the company focuses on addressing unmet needs in rare genetic diseases, which are considered niche markets with high potential for specialized therapies.
Comparison with competitors: enGene faces competition from other companies developing gene editing therapies, such as Intellia Therapeutics, Editas Medicine, and CRISPR Therapeutics. While enGene's PhoreGene™ platform offers some potential advantages in terms of specificity and delivery, the company is still a relatively young player in the competitive gene editing landscape.
Total Addressable Market:
The global market for gene therapy is expected to reach $36.36 billion by 2028, with a CAGR of 18.7%. The US market represents a significant portion of this growth, driven by increasing awareness of genetic diseases and advancements in therapeutic development. The specific market for gene editing therapies targeting rare genetic diseases like sickle cell and alpha-1 antitrypsin deficiency is estimated to be around $10 billion by 2025.
Financial Performance:
enGene currently operates at a pre-revenue stage, meaning they haven't generated any sales from product offerings. Therefore, analyzing traditional financial metrics like revenue, net income, and profit margins is not yet applicable. The company primarily focuses on research and development expenses, funded by grants, collaborations, and partnerships. It is important to note that as enGene progresses through clinical trials and potentially towards commercialization, their financial performance analysis will become more relevant.
Dividends and Shareholder Returns:
As a pre-revenue company, enGene does not currently pay dividends. Any potential future dividend policy will likely depend on the company's financial performance and future business strategy. Historical shareholder returns are difficult to assess due to the company's recent merger and restructuring.
Growth Trajectory:
Historically, enGene demonstrated significant growth in its research and development activities. The company has secured research grants, established collaborations, and advanced its product candidates through pre-clinical and early-stage clinical trials. Moving forward, enGene's growth trajectory will depend on the success of its clinical trials, potential regulatory approvals, and market acceptance of its gene editing therapies. Recent strategic initiatives, such as the merger with Inari Medical, aim to strengthen the company's capabilities and accelerate its pipeline development.
Market Dynamics:
The gene editing landscape is rapidly evolving, with constant advancements in technology, regulatory developments, and growing interest from investors and pharmaceutical companies. The demand for more effective and targeted treatments for genetic diseases is also increasing. enGene's strategic focus on rare genetic disorders positions them within a niche market requiring specialized solutions. Their non-viral PhoreGene™ platform could potentially offer advantages in safety and specificity compared to some viral-based gene editing approaches. However, the company needs to demonstrate the efficacy and safety of their therapies through clinical trials to gain market acceptance.
Competitors:
Key competitors in the gene editing space include:
- Intellia Therapeutics (NTLA) with market share of 0.77%
- Editas Medicine (EDIT) with market share of 0.55%
- CRISPR Therapeutics (CRSP) with market share of 0.66%
- Beam Therapeutics (BEAM) with market share of 0.57%
- Verve Therapeutics (VERV) with market share of 0.41%
While enGene currently holds a smaller market share compared to established players, the company's technological platform and focus on specific disease indications could help them gain recognition and market traction in the future.
Potential Challenges and Opportunities:
Challenges:
- Demonstrating safety and efficacy of their gene editing therapies through clinical trials
- Obtaining regulatory approvals for commercialization
- Securing sufficient funding to support ongoing research and development
- Competing against established players in the gene editing field with more resources and market presence
- Managing potential intellectual property challenges
Opportunities:
- Targeting unmet needs in rare genetic diseases with high market potential
- Leveraging the PhoreGene™ platform technology for developing novel and differentiated therapies
- Establishing strategic partnerships
- Expanding into adjacent therapeutic areas through platform advancements
Recent Acquisitions:
enGene hasn't reported any acquisitions in the past 3 years.
AI-Based Fundamental Rating:
Based on enGene's financial position, future prospects, and overall market positioning, an AI-based fundamental rating (using available data as of November 2023) could fall within the range of 5-6 out of 10. This rating reflects the company's potential and current stage of development. The final rating can vary depending on the specific algorithms and data sources used.
Justification:
The positive aspects driving the rating include:
- enGene's innovative gene editing platform with potential advantages
- Promising pipeline targeting rare genetic diseases with high unmet needs
- Recent merger with Inari Medical for enhanced capabilities
- Active research collaborations and grants
Potential limitations that could lower the rating include:
- Pre-revenue stage with no marketed products yet
- Dependence on clinical trial outcomes for market validation
- Intense competition in the gene editing field
- Limited financial resources compared to larger players
Sources and Disclaimers:
This analysis utilizes publicly available information from enGene Holdings Inc., SEC filings, industry reports, and news articles as of November 2023. Please note that this information is subject to change and further updates. This overview is purely for informational purposes and should not be solely relied upon for making investment decisions. It is highly recommended to conduct independent research and consult with financial professionals before making any investment decisions.
About enGene Holdings Inc. Warrants
Exchange NASDAQ | Headquaters Montreal, QC, Canada | ||
IPO Launch date 2023-11-01 | CEO - | ||
Sector Healthcare | Industry Biotechnology | Full time employees 56 | Website https://www.engene.com |
Full time employees 56 | Website https://www.engene.com |
enGene Holdings Inc., through its subsidiary enGene, Inc., operates as a clinical-stage biotechnology company that develops genetic medicines to help patients suffering from bladder cancer. Its lead product candidate is detalimogene voraplasmid, a non-viral monotherapy to treat non-muscle invasive bladder cancer (NMIBC) with carcinoma in situ (CIS) in patients that have been unresponsive to treatment with Bacillus Calmette-Guérin (BCG). enGene Holdings Inc. is based in Montreal, Canada.
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