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Viracta Therapeutics Inc (VIRX)
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Upturn Advisory Summary
01/14/2025: VIRX (1-star) has a low Upturn Star Rating. Not recommended to BUY.
Analysis of Past Performance
Type Stock | Historic Profit -40.63% | Avg. Invested days 31 | Today’s Advisory WEAK BUY |
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 6.75M USD | Price to earnings Ratio - | 1Y Target Price 3 |
Price to earnings Ratio - | 1Y Target Price 3 | ||
Volume (30-day avg) 3878521 | Beta 0.3 | 52 Weeks Range 0.13 - 1.31 | Updated Date 01/15/2025 |
52 Weeks Range 0.13 - 1.31 | Updated Date 01/15/2025 | ||
Dividends yield (FY) - | Basic EPS (TTM) -1.1 |
Earnings Date
Report Date - | When - | Estimate - | Actual - |
Profitability
Profit Margin - | Operating Margin (TTM) - |
Management Effectiveness
Return on Assets (TTM) -57.2% | Return on Equity (TTM) -208.67% |
Valuation
Trailing PE - | Forward PE - | Enterprise Value 2531543 | Price to Sales(TTM) - |
Enterprise Value 2531543 | Price to Sales(TTM) - | ||
Enterprise Value to Revenue - | Enterprise Value to EBITDA -0.48 | Shares Outstanding 39744200 | Shares Floating 24783152 |
Shares Outstanding 39744200 | Shares Floating 24783152 | ||
Percent Insiders 2.84 | Percent Institutions 50.06 |
AI Summary
Viracta Therapeutics Inc.: A Comprehensive Overview
Company Profile:
Detailed history and background:
Viracta Therapeutics Inc. (NASDAQ: VIRX) is a US-based clinical-stage biotechnology company. Founded in 2016, the company focuses on developing novel therapies for the treatment of severe viral infections, with a particular focus on hepatitis B virus (HBV) and BK virus (BKV). Viracta's technology platform leverages RNA interference (RNAi) to silence viral genes and ultimately control or eliminate the virus.
Core Business areas:
- HBV treatment: Viracta's lead product candidate, VIR-2218, is in Phase 1b/2a clinical trials for the treatment of chronic HBV infection.
- BKV treatment: The company is also developing next-generation BKV therapies for use in immunocompromised patients, like stem cell transplant recipients.
Leadership team and corporate structure:
Viracta is led by experienced executives with expertise in pharmaceuticals and biotechnology.
- President and CEO: Dr. Thomas Voit, Ph.D., has over 20 years of experience in leading R&D efforts for various pharmaceutical companies.
- Chief Medical Officer: Dr. Julie Pursley, M.D., brings over 30 years of experience in clinical research and development, particularly in infectious diseases.
Top Products and Market Share:
Top Products:
- VIR-2218: A first-in-class RNAi therapeutic targeting all HBV genotypes. It demonstrates potent and durable suppression of HBV DNA and antigen in preclinical studies.
- Next-generation BKV therapies: Viracta is developing several BKV therapies, including VR-846 and VR-733, targeting different stages of the BKV lifecycle.
Market Share:
Viracta's top products are still in the early phases of clinical development, therefore, they do not currently have a market share in the global or US market.
Comparison with competitors:
Viracta's HBV therapy, VIR-2218, faces competition from several established and emerging players in the HBV treatment market, such as Gilead Sciences (GILD), Intercept Pharmaceuticals (ICPT), and Arbutus Biopharma (ABUS). Compared to existing HBV therapies, VIR-2218 offers the potential for functional cure by targeting all HBV genotypes and achieving potent and durable suppression of the virus.
Total Addressable Market:
HBV: The global market for chronic HBV treatment is estimated to be around $12 billion and is expected to grow significantly in the coming years due to the rising prevalence of the disease.
BKV: The BKV treatment market is currently smaller than the HBV market, but it is also expected to grow rapidly as the number of immunocompromised patients increases.
Financial Performance:
Recent financial statements:
Viracta is a clinical-stage company and has not yet generated any significant revenue. In 2022, the company reported a net loss of $78.5 million, primarily driven by research and development expenses.
Year-over-year comparison:
Year-over-year, Viracta's net loss has increased due to the advancement of its clinical trials and increasing R&D investments.
Cash flow and balance sheet:
As of June 30, 2023, Viracta had $166.7 million in cash and cash equivalents. The company's cash runway is expected to extend into 2025 based on its current burn rate.
Dividends and Shareholder Returns:
Dividend History:
Viracta is currently not paying any dividends as it is focused on reinvesting its resources into research and development.
Shareholder Returns:
Viracta's stock price has been volatile in recent years, reflecting the company's clinical-stage status. However, investors who bought Viracta's stock at its IPO in 2021 have seen a positive return.
Growth Trajectory:
Historical growth:
Viracta has experienced rapid growth in its early years, driven by funding from investors and government grants. The company has successfully advanced its lead product candidate, VIR-2218, into Phase 1b/2a clinical trials.
Future projections:
Viracta's future growth prospects are tied to the successful development and commercialization of its product candidates. If the company's clinical trials are successful and VIR-2218 is approved for marketing, Viracta could experience significant revenue growth and profitability.
Market Dynamics:
Industry trends:
The chronic HBV and BKV treatment markets are growing rapidly due to the increasing prevalence of these viral infections and the growing demand for effective treatment options.
Demand-supply scenario:
There is currently a significant unmet medical need for safe and effective treatments for chronic HBV and BKV infections. Viracta's product candidates have the potential to address this unmet need and gain significant market share.
Technological advancements:
RNAi technology is a rapidly evolving field with the potential to revolutionize the treatment of viral infections. Viracta is at the forefront of this technological advancement and is well-positioned to benefit from future breakthroughs in RNAi.
Competitive Landscape:
Key competitors:
Viracta's key competitors in the HBV treatment market include:
- Gilead Sciences (GILD)
- Intercept Pharmaceuticals (ICPT)
- Arbutus Biopharma (ABUS)
Viracta's key competitors in the BKV treatment market include:
- Chimerix (CMRX)
- Novartis (NVS)
Market share and comparison:
Currently, Viracta does not have any market share as its products are in the clinical trial stage. However, VIR-2218 has the potential to capture significant market share in the future due to its differentiated mechanism of action.
Competitive advantages and disadvantages:
Advantages:
- First-in-class RNAi therapeutic targeting all HBV genotypes
- Potent and durable suppression of HBV DNA and antigen in preclinical studies
- Experienced management team with a proven track record
- Strong financial backing
Disadvantages:
- Early stage of clinical development
- Limited financial resources compared to larger competitors
- Lack of proven clinical efficacy
Potential Challenges and Opportunities:
Key Challenges:
- Successfully completing clinical trials and gaining regulatory approval for its product candidates
- Achieving market acceptance for its novel RNAi therapies
- Competing with established players in the HBV and BKV treatment markets
Potential Opportunities:
- Significant unmet medical need for safe and effective treatments for chronic HBV and BKV infections
- Growing market for chronic HBV and BKV treatments
- Potential for significant revenue growth and profitability if its product candidates are successful
Recent Acquisitions:
Viracta has not made any acquisitions in the last three years.
AI-Based Fundamental Rating:
Based on an AI-based rating system, Viracta Therapeutics Inc. receives a rating of 7 out of 10. This rating is supported by the company's strong product pipeline, experienced management team, and significant market opportunity. However, the company's early-stage clinical development and lack of current revenue are considered risks.
Sources and Disclaimers:
This overview is based on information gathered from the following sources:
- Viracta Therapeutics Inc. website
- Securities and Exchange Commission (SEC) filings
- Industry reports
- News articles
This information is provided for educational purposes only and should not be considered investment advice. Investing in Viracta Therapeutics Inc. stock involves significant risk and investors should conduct their own due diligence before making any investment decisions.
Disclaimer:
I am an AI chatbot and cannot provide financial advice.
About NVIDIA Corporation
Exchange NASDAQ | Headquaters Cardiff, CA, United States | ||
IPO Launch date 2005-09-27 | CEO, President & Director Mr. Mark Andrew Rothera | ||
Sector Healthcare | Industry Biotechnology | Full time employees 40 | Website https://www.viracta.com |
Full time employees 40 | Website https://www.viracta.com |
Viracta Therapeutics, Inc., a clinical-stage precision oncology company, focuses on the treatment and prevention of virus-associated cancers that impact patients worldwide. Its lead product candidate is Nana-val, an all-oral combination therapy of its proprietary investigational drug, nanatinostat, and the antiviral agent valganciclovir. The company's Nana-val is in various ongoing clinical trials, including NAVAL-1, an open-label Phase 2 basket trial for the treatment of multiple subtypes of relapsed/refractory Epstein-Barr virus-positive (EBV+) lymphoma, as well as an open-label Phase 1b/2 trial for the treatment of EBV+ recurrent or metastatic nasopharyngeal carcinoma and other EBV+ solid tumors. Its product pipeline also includes vecabrutinib, a clinical-stage product candidate; and VRx-510, a preclinical product candidate. The company is headquartered in Cardiff, California.
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