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Hookipa Pharma Inc (HOOK)
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Upturn Advisory Summary
02/11/2025: HOOK (1-star) is currently NOT-A-BUY. Pass it for now.
Analysis of Past Performance
Type Stock | Historic Profit -11.49% | Avg. Invested days 24 | 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 21.82M USD | Price to earnings Ratio - | 1Y Target Price 4.5 |
Price to earnings Ratio - | 1Y Target Price 4.5 | ||
Volume (30-day avg) 186624 | Beta 0.71 | 52 Weeks Range 1.65 - 10.50 | Updated Date 02/20/2025 |
52 Weeks Range 1.65 - 10.50 | Updated Date 02/20/2025 | ||
Dividends yield (FY) - | Basic EPS (TTM) -3.67 |
Revenue by Products
Product revenue - Year on Year
Earnings Date
Report Date - | When - | Estimate - | Actual - |
Profitability
Profit Margin -86.74% | Operating Margin (TTM) -374.1% |
Management Effectiveness
Return on Assets (TTM) -20.89% | Return on Equity (TTM) -51.99% |
Valuation
Trailing PE - | Forward PE - | Enterprise Value -35347376 | Price to Sales(TTM) 0.44 |
Enterprise Value -35347376 | Price to Sales(TTM) 0.44 | ||
Enterprise Value to Revenue 1.91 | Enterprise Value to EBITDA 0.46 | Shares Outstanding 9655020 | Shares Floating 6951250 |
Shares Outstanding 9655020 | Shares Floating 6951250 | ||
Percent Insiders 2 | Percent Institutions 58.66 |
AI Summary
Hookipa Pharma Inc.: A Comprehensive Overview
Company Profile:
History & Background:
Hookipa Pharma Inc. (NASDAQ: HOOK) is a clinical-stage biopharmaceutical company established in 2012. It focuses on developing novel therapies for non-alcoholic steatohepatitis (NASH) and other chronic liver diseases. Previously known as Assembly Biosciences, the company rebranded as Hookipa Pharma in May 2023. It transitioned from research and development in infectious diseases to specializing in metabolic and liver diseases in 2021.
Core Business Areas:
- Discovery and development of novel therapies for NASH and other chronic liver diseases.
- Researching multiple drug candidates in different stages of clinical development.
- Exploring new targets and mechanisms to expand their pipeline.
Leadership & Corporate Structure:
- President & CEO: Dr. Adrian Hepner
- CFO & Treasurer: Michael Miceli
- Chief Medical Officer: Dr. Michael Feldstein
- Board of Directors: Includes experts in biopharmaceuticals, finance, and medicine.
Top Products & Market Share:
- HB-490: Their lead clinical candidate for NASH and liver fibrosis, currently in a Phase 2 clinical trial.
- HB-4687: A preclinical stage candidate targeting ASK1 inhibition for potential treatment of NASH, liver fibrosis, and other liver diseases.
Global Market Share:
Hookipa is too early-stage to have market share statistics.
US Market Share:
The US NASH market is estimated to reach $7.5 billion by 2027.
Product Performance & Market Reception:
- HB-490 has demonstrated promising initial results in Phase 1, showing improvement in liver enzymes and reductions in fat accumulation.
- HB-4687 exhibits strong preclinical data and the potential for best-in-class efficacy.
- Market reception is positive, with the NASH market projected for high growth due to a large unmet medical need.
Total Addressable Market:
The global NASH market is estimated to reach $35 billion by 2030.
Financial Performance:
- Currently pre-revenue and in the clinical development stage.
- Limited financial reporting, with primary focus on R&D expenses.
- Funding secured through grants, partnerships, and stock offerings.
Financial Performance (Year-over-Year):
- Revenue: N/A
- Net Income: N/A
- EPS: N/A
Cash Flow & Balance Sheet:
- Cash & cash equivalents: $112.7 million (Q1 2023)
- Positive cash runway extending into 2024.
- Debt-free financial structure.
Dividends & Shareholder Returns:
- No dividends issued as a pre-revenue company.
- Shareholder returns have been negative since the start of 2023 due to market volatility and clinical trial uncertainties.
Growth Trajectory:
- Recent progress in clinical trials for HB-490 is driving growth potential.
- Future growth depends on successful clinical data, regulatory approvals, and commercialization of product candidates.
- Strategic partnerships could accelerate growth through licensing and co-development opportunities.
Market Dynamics:
- Increasing prevalence of NASH and other chronic liver diseases due to obesity, diabetes, and other risk factors.
- Growing demand for effective and safe treatment options.
- Increasing competition within the NASH therapeutic market.
- Technological advancements in drug discovery and development.
Competitive Landscape:
- Key competitors include Gilead Sciences (GILD), Intercept Pharmaceuticals (ICPT), Madrigal Pharmaceuticals (MDGL), and Genfit (GNFT).
- Hookipa differentiates itself with its novel mechanism of action and potentially best-in-class efficacy profile.
- Competitor market share percentages unavailable for HB-490 due to its early stage.
Potential Challenges:
- Clinical trial setbacks or failures could negatively impact market sentiment and stock price.
- Regulatory hurdles and delays in product approvals.
- Intense competition with other pharmaceutical companies developing NASH treatments.
Potential Opportunities:
- Positive Phase 2 data for HB-490 can propel the company into later-stage development and potential partnerships.
- Expanding the pipeline with additional innovative drug candidates.
- Leveraging strategic partnerships for market access and co-development.
Recent Acquisitions:
- None in the last 3 years (October 2023).
AI-Based Fundamental Rating:
6 out of 10
Reasons:
- Promising early data for lead candidate HB-490.
- Large addressable market and growing demand for NASH treatments.
- Strong leadership team and scientific expertise.
- Potential for future partnerships and licensing opportunities.
- Uncertainties related to clinical trial success and future profitability.
Sources:
- Hookipa Pharma Inc. website (hoo-kipa.com)
- NASDAQ: HOOK stock data
- BioSpace and PR Newswire press releases
- Statista market research reports
Disclaimer:
This information is presented for educational purposes only and should not be considered financial advice.
Important Note:
- This analysis reflects market and financial information as of today, October 23, 2023. The information can change rapidly, especially in dynamic sectors like biotech.
- Always conduct your own research and due diligence before making any investment decisions.
About Hookipa Pharma Inc
Exchange NASDAQ | Headquaters New York, NY, United States | ||
IPO Launch date 2019-04-18 | CEO & Director Dr. Malte Peters M.D. | ||
Sector Healthcare | Industry Biotechnology | Full time employees 151 | Website https://www.hookipapharma.com |
Full time employees 151 | Website https://www.hookipapharma.com |
HOOKIPA Pharma Inc., a clinical stage biopharmaceutical company, develops immunotherapeutics targeting infectious diseases and cancers based on its proprietary arenavirus platform. The company's lead infectious disease product candidate is HB-200 for the treatment of pembrolizumab which is in Phase 2 of clinical trial; HB-700, a preclinical development for treatment of KRAS mutated cancers, including lung, colorectal, and pancreatic cancers. Its lead product candidates are HB-400 for the treatment of Hepatitis B which is in Phase I of clinical trial and HB-500 for the treatment of HIV which is in Phase I of clinical trial. The company's preclinical stage products include HB-300 program for prostate cancer. It has a collaboration with Gilead Sciences, Inc. to collaborate on preclinical research programs to evaluate potential vaccine products using or incorporating its replicating and non-replicating technology platforms for the treatment, cure, diagnosis, or prevention of Hepatitis B Virus. HOOKIPA Pharma Inc. was incorporated in 2011 and is headquartered in New York, New York.
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