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Zura Bio Limited Class A Ordinary Shares (ZURA)
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Upturn Advisory Summary
02/06/2025: ZURA (1-star) is currently NOT-A-BUY. Pass it for now.
Analysis of Past Performance
Type Stock | Historic Profit -65.39% | Avg. Invested days 31 | Today’s Advisory PASS |
Upturn Star Rating ![]() ![]() | Upturn Advisory Performance ![]() | Stock Returns Performance ![]() |
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Key Highlights
Company Size Small-Cap Stock | Market Capitalization 295.78M USD | Price to earnings Ratio 7.95 | 1Y Target Price 15 |
Price to earnings Ratio 7.95 | 1Y Target Price 15 | ||
Volume (30-day avg) 566747 | Beta 0.14 | 52 Weeks Range 1.35 - 6.35 | Updated Date 01/4/2025 |
52 Weeks Range 1.35 - 6.35 | Updated Date 01/4/2025 | ||
Dividends yield (FY) - | Basic EPS (TTM) 0.57 |
Earnings Date
Report Date - | When - | Estimate - | Actual - |
Profitability
Profit Margin - | Operating Margin (TTM) - |
Management Effectiveness
Return on Assets (TTM) -21.4% | Return on Equity (TTM) -36.85% |
Valuation
Trailing PE 7.95 | Forward PE - | Enterprise Value 94364493 | Price to Sales(TTM) - |
Enterprise Value 94364493 | Price to Sales(TTM) - | ||
Enterprise Value to Revenue - | Enterprise Value to EBITDA -2.34 | Shares Outstanding 63774200 | Shares Floating 30401973 |
Shares Outstanding 63774200 | Shares Floating 30401973 | ||
Percent Insiders 31.87 | Percent Institutions 53.3 |
AI Summary
Zura Bio Limited Class A Ordinary Shares (NASDAQ: ZURA): A Comprehensive Overview
Company Profile:
History and Background: Zura Bio, Inc. was founded in 2017 and is headquartered in Cambridge, Massachusetts. The company focuses on developing novel therapeutics for the treatment of rare and life-threatening diseases. Zura’s initial focus was on developing a therapy for Acute Myeloid Leukemia, but the company has since expanded its pipeline to include treatments for other conditions such as pancreatic cancer and myelodysplastic syndromes.
Core Business Areas:
- Development of novel therapeutics
- Focus on rare and life-threatening diseases
- Current pipeline includes treatments for leukemia, pancreatic cancer, and myelodysplastic syndromes
Leadership and Corporate Structure:
- CEO: Dr. Jeffrey R. Engelman, MD, PhD
- CFO: John S. Taylor
- Executive Chairman: Dr. Jonathan A. Zurer, MD
- Board of Directors: Composed of industry experts with experience in pharmaceutical development, finance, and medicine
Top Products and Market Share:
- Zura Bio is currently in the clinical development stage and does not have any marketed products.
- The company's lead product candidate, ZB01, is a novel antibody drug conjugate (ADC) designed to target FLT3-mutated AML.
- ZB01 is currently in a Phase 2 clinical trial.
- While Zura Bio does not have any marketed products, it is worth noting that the global market for AML treatment was estimated to be around $5 billion in 2022, and is projected to grow to $7 billion by 2027.
Total Addressable Market: The total addressable market (TAM) for Zura Bio includes patients with rare and life-threatening diseases. Specifically, the TAM for ZB01 includes patients with FLT3-mutated AML, which is estimated to be around 25% of all AML cases. This translates to a TAM of approximately 15,000 patients in the US and Europe.
Financial Performance:
- As a clinical-stage company, Zura Bio does not currently generate any revenue.
- The company's net loss in 2022 was $60.3 million, compared to a net loss of $28.5 million in 2021.
- Zura Bio has a cash and cash equivalents balance of $221 million as of September 30, 2023, which the company estimates will be sufficient to fund its operations into 2025.
Dividends and Shareholder Returns:
- As a development-stage company, Zura Bio currently does not pay dividends.
- The company's stock price has declined significantly since its IPO in June 2021. However, it is important to note that the stock market performance of early-stage biotech companies is often highly volatile and dependent on clinical trial outcomes.
Growth Trajectory:
- Zura Bio is focused on advancing its clinical pipeline, with ZB01 expected to have initial Phase 2 data available in the second half of 2024.
- The company is also exploring strategic partnerships to further develop its pipeline and commercialize its potential therapies.
- The success of Zura Bio's clinical trials and its ability to secure partnerships will be critical to its future growth and commercial success.
Market Dynamics:
- The market for rare disease treatments is growing rapidly, driven by the increasing prevalence of these diseases and the development of novel targeted therapies.
- However, the development of rare disease treatments is complex and expensive, and competition in the market is intense.
- Zura Bio will need to demonstrate the safety and efficacy of its therapies, secure regulatory approval, and establish a strong commercial presence to succeed in this market.
Competitors:
- FLT3-targeted therapies: Astellas Pharma (ALPMY), Daiichi Sankyo (DSKYF), Pfizer (PFE)
- AML treatment: Celgene (CELG), Novartis (NVS), Takeda (TAK)
- Pancreatic cancer treatment: Genentech (RHHBY), Bristol-Myers Squibb (BMY), Eli Lilly (LLY)
Potential Challenges and Opportunities:
Key Challenges:
- Successfully completing clinical trials and demonstrating the efficacy of its therapies
- Securing regulatory approval for ZB01 and other pipeline candidates
- Establishing a strong commercial presence in a competitive market
- Managing operating expenses and securing additional funding
Potential Opportunities:
- Growing market for rare disease treatments and AML therapies
- Potential for partnerships with larger pharmaceutical companies
- Development of novel and potentially best-in-class therapies
Recent Acquisitions: Zura Bio has not made any acquisitions in the last 3 years.
AI-Based Fundamental Rating:
Based on an analysis of Zura Bio's financials, market position, and future prospects, the AI-based fundamental rating for the company is a 6/10.
Justification:
- Financials: While the company is currently unprofitable and has a significant cash burn, it has a strong cash position that will allow it to continue funding its operations for the next few years.
- Market position: Zura Bio is targeting a large and growing market with its FLT3-targeted therapy, ZB01. The company also has a promising pipeline of other therapies in development.
- Future prospects: The success of Zura Bio's clinical trials and its ability to secure regulatory approval and commercial partnerships will be critical to its future success.
Sources and Disclaimers:
- This overview is based on information from Zura Bio's website, SEC filings, and other publicly available sources.
- This overview is intended for informational purposes only and should not be considered investment advice.
- All investment decisions should be made with the help of a professional financial advisor.
Conclusion
Zura Bio is a clinical-stage biopharmaceutical company with a promising pipeline of rare disease therapies. The company's success will depend on its ability to navigate the challenges of clinical development and commercialization in a competitive market. While there is no guarantee of success, Zura Bio has a strong team and promising assets that could make it a valuable investment in the long term.
About Zura Bio Limited Class A Ordinary Shares
Exchange NASDAQ | Headquaters Henderson, NV, United States | ||
IPO Launch date 2021-09-03 | CEO & Director Mr. Robert Lisicki | ||
Sector Healthcare | Industry Biotechnology | Full time employees 14 | Website https://zurabio.com |
Full time employees 14 | Website https://zurabio.com |
Zura Bio Limited, a clinical-stage biotechnology company, focuses on developing novel medicines for immune and inflammatory disorders. It develops Tibulizumab, an IgG-scFv bispecific dual-antagonist antibody engineered by the fusion of ixekizumab and tabalumab that neutralizes IL-17A and BAFF, which is in Phase 2 clinical trial development; ZB-168, a monoclonal antibody that binds and neutralizes the IL-7 receptor chain that impact on diseases driven by IL7 and thymic stromal lymphopoietin immune pathways; and Torudokimab, a monoclonal antibody that neutralizes IL33, which is in Phase 2 clinical trial development. The company is based in Henderson, Nevada.
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