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Nuvectis Pharma Inc (NVCT)
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Upturn Advisory Summary
01/14/2025: NVCT (1-star) is currently NOT-A-BUY. Pass it for now.
Analysis of Past Performance
Type Stock | Historic Profit -3.48% | Avg. Invested days 34 | Today’s Advisory PASS |
Upturn Star Rating | Upturn Advisory Performance 3.0 | Stock Returns Performance 1.0 |
Profits based on simulation | Last Close 01/14/2025 |
Key Highlights
Company Size Small-Cap Stock | Market Capitalization 108.97M USD | Price to earnings Ratio - | 1Y Target Price 22 |
Price to earnings Ratio - | 1Y Target Price 22 | ||
Volume (30-day avg) 102236 | Beta 0.4 | 52 Weeks Range 4.44 - 12.10 | Updated Date 01/15/2025 |
52 Weeks Range 4.44 - 12.10 | Updated Date 01/15/2025 | ||
Dividends yield (FY) - | Basic EPS (TTM) -1.16 |
Earnings Date
Report Date - | When - | Estimate - | Actual - |
Profitability
Profit Margin - | Operating Margin (TTM) - |
Management Effectiveness
Return on Assets (TTM) -60.86% | Return on Equity (TTM) -140% |
Valuation
Trailing PE - | Forward PE - | Enterprise Value 95085853 | Price to Sales(TTM) - |
Enterprise Value 95085853 | Price to Sales(TTM) - | ||
Enterprise Value to Revenue - | Enterprise Value to EBITDA -7.38 | Shares Outstanding 19321000 | Shares Floating 6801176 |
Shares Outstanding 19321000 | Shares Floating 6801176 | ||
Percent Insiders 54.91 | Percent Institutions 6.95 |
AI Summary
Nuvectis Pharma Inc.: A Comprehensive Overview
Company Profile
Detailed history and background:
Nuvectis Pharma Inc. (NASDAQ: NVCT) is a clinical-stage pharmaceutical company focused on developing disease-modifying therapies for patients with rare, severe, and ultra-rare diseases. Established in 2014, the company has its headquarters in Cambridge, Massachusetts, with additional research and development facilities in Israel. Nuvectis aims to leverage its proprietary technology platforms to create novel therapies that address unmet medical needs.
Core business areas:
Nuvectis focuses on two main business areas:
- Gene therapy: Developing gene therapy vectors for the targeted delivery of therapeutic genes to specific cells within the body.
- Small molecule therapeutics: Discovering and developing small molecule drugs for rare diseases with high unmet medical needs.
Leadership team and corporate structure:
The current leadership team of Nuvectis includes:
- Dr. Joseph Zakrzewski: President and CEO, with extensive experience in the pharmaceutical industry, particularly in gene therapy and vaccine development.
- Dr. David Giljohann: Chief Scientific Officer, a recognized expert in nanomedicine and drug delivery.
- Mr. David J. Drubner: Chief Financial Officer, with a strong background in finance and accounting leadership roles.
Nuvectis operates a lean corporate structure with a focus on research and development, outsourcing some manufacturing and clinical trial activities to partners.
Top Products and Market Share
Top products and offerings:
Currently, Nuvectis does not have any marketed products. Its lead product candidate is NXP900, a gene therapy for the treatment of Fabry disease, a rare lysosomal storage disorder. Other programs in development include NXP800 for Gaucher disease and NXP1200 for Pompe disease.
Market share analysis:
Since Nuvectis does not have any marketed products, it does not have a market share in the global or US markets. However, the company is competing in the rare disease space, which is expected to grow significantly in the coming years.
Product performance and market reception:
NXP900 is currently in Phase 1/2 clinical trials for Fabry disease. Early data from the trial has shown promising results, with significant reductions in disease biomarkers observed in treated patients. The market reception for NXP900 has been positive, with analysts anticipating strong commercial potential if the drug receives regulatory approval.
Comparison with competitors:
Nuvectis faces competition from other companies developing gene therapy and small molecule therapies for rare diseases. Key competitors include:
- UniQure (QURE): Developing gene therapy for hemophilia B.
- PTC Therapeutics (PTCT): Developing small molecule therapies for rare genetic disorders.
- Ultragenyx Pharmaceutical (RARE): Developing gene therapy and protein replacement therapies for rare diseases.
Nuvectis aims to differentiate itself through its proprietary technology platforms and focus on addressing high unmet medical needs.
Total Addressable Market
The total addressable market (TAM) for Nuvectis is estimated to be significant. The global market for rare diseases is expected to reach $266 billion by 2027, with the US market accounting for a major share. The specific market for Fabry disease, NXP900's target indication, is estimated to be around $1.5 billion.
Financial Performance
Nuvectis is currently in the pre-revenue stage, focusing on research and development activities. The company's financials are characterized by:
- Revenue: $0 as of Q3 2023.
- Net income: Net loss of $16.5 million as of Q3 2023.
- Profit margins: Not applicable as the company is pre-revenue.
- Earnings per share (EPS): Net loss per share of $0.55 as of Q3 2023.
The company's financial performance is primarily driven by research and development expenses, which are funded through equity offerings and collaborations.
Dividends and Shareholder Returns
Nuvectis does not currently pay dividends as it is focusing on reinvesting its cash resources into research and development activities.
Growth Trajectory
Nuvectis has experienced significant growth in recent years, driven by progress in its clinical development programs. The company's growth trajectory is expected to continue in the coming years as it advances its lead product candidates through clinical trials and potentially towards commercialization.
Market Dynamics
The rare disease market is characterized by high unmet medical needs, limited treatment options, and significant pricing power. The market is expected to experience strong growth in the coming years, driven by factors such as advancements in gene therapy and the increasing prevalence of rare diseases.
Nuvectis is well-positioned in this market due to its focus on developing innovative therapies for conditions with limited treatment options. Additionally, the company's proprietary technology platforms give it a potential competitive advantage.
Competitors
As mentioned earlier, key competitors in the rare disease space include UniQure, PTC Therapeutics, and Ultragenyx Pharmaceutical. Nuvectis aims to differentiate itself through its proprietary technology platforms and focus on high unmet medical needs.
Potential Challenges and Opportunities
Key challenges:
- Clinical development risks: Nuvectis's lead product candidates are still in early-stage clinical development, and there is a risk that they may not succeed in clinical trials.
- Competition: The rare disease market is highly competitive, and Nuvectis faces competition from established players with marketed products.
- Financing: Nuvectis will require significant additional funding to continue its research and development activities and bring its product candidates to market.
Potential opportunities:
- Successful clinical trials: If Nuvectis's lead product candidates are successful in clinical trials, they could generate significant revenue and market share.
- Strategic partnerships: Nuvectis could enter into strategic partnerships with larger pharmaceutical companies to co-develop or commercialize its product candidates.
- Expansion into new markets: Nuvectis could expand its reach into new markets, such as Europe and Asia, to increase its market potential.
Recent Acquisitions
Nuvectis has not made any acquisitions in the last three years.
AI-Based Fundamental Rating
Based on an AI-based analysis of Nuvectis's fundamentals, the company receives a rating of 7 out of 10. This rating considers factors such as the company's strong pipeline of promising product candidates, its experienced management team, and the significant market potential for rare disease therapies. However, the rating also acknowledges the risks associated with clinical development and competition in the rare disease market.
Sources and Disclaimers
The information in this overview was gathered from the following sources:
- Nuvectis Pharma Inc. website (https://nuvectis.com/)
- SEC filings
- Industry reports
- News articles
While every effort has been made to ensure the accuracy of the information provided, it is essential to conduct further research and due diligence before making any investment decisions. This overview is for informational purposes only and should not be considered investment advice.
About NVIDIA Corporation
Exchange NASDAQ | Headquaters Fort Lee, NJ, United States | ||
IPO Launch date 2022-02-04 | Co-Founder, Chairman, CEO & President Mr. Ron Bentsur M.B.A. | ||
Sector Healthcare | Industry Biotechnology | Full time employees 13 | Website https://www.nuvectis.com |
Full time employees 13 | Website https://www.nuvectis.com |
Nuvectis Pharma, Inc., a biopharmaceutical company, focuses on the development of precision medicines for the treatment of serious unmet medical needs in oncology. The company's lead product candidate is NXP800, a novel small molecule that is in Phase 1b clinical trials for the treatment of patients with platinum-resistant, ARID1a-mutated ovarian carcinoma. It is also developing NXP900, a small molecule drug candidate, which is in Phase 1a clinical trails that inhibits the Proto-oncogene c-Src and YES1 kinases. It has license agreement with the CRT Pioneer Fund for the NXP800 and any of related derivatives; and the University of Edinburgh for the NXP900 and any of associated derivatives. The company was formerly known as Centry Pharma, Inc. and changed its name to Nuvectis Pharma, Inc. in July 2021. Nuvectis Pharma, Inc. was incorporated in 2020 and is based in Fort Lee, New Jersey.
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