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VIRX
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Viracta Therapeutics Inc (VIRX)

Upturn stock ratingUpturn stock rating
$0.04
Delayed price
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PASS
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  • SELL Advisory (Profit)​
  • SELL Advisory (Loss)​
  • Profit
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Upturn Advisory Summary

02/04/2025: VIRX (1-star) is currently NOT-A-BUY. Pass it for now.

Upturn Star Rating

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Not Recommended Performance

These Stocks/ETFs, based on Upturn Advisory, consistently fall short of market performance, signaling caution before investing.

AI Based Fundamental Rating

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Moderate Performance

These Stocks/ETFs, based on Upturn Advisory, typically align with the market average, offering steady but unremarkable returns.

Analysis of Past Performance

Type Stock
Historic Profit -40.63%
Avg. Invested days 31
Today’s Advisory PASS
Upturn Star Rating Upturn stock ratingUpturn stock rating
Upturn Advisory Performance Upturn Advisory Performance 3.0
Stock Returns Performance Upturn Returns Performance 1.0
Upturn Profits based on simulationUpturn Profits based on simulation Profits based on simulation
Upturn Profits based on simulationUpturn Profits based on simulation Last Close 02/04/2025

Key Highlights

Company Size Small-Cap Stock
Market Capitalization 3.09M USD
Price to earnings Ratio -
1Y Target Price 3
Price to earnings Ratio -
1Y Target Price 3
Volume (30-day avg) 2202111
Beta 0.3
52 Weeks Range 0.03 - 1.31
Updated Date 02/5/2025
52 Weeks Range 0.03 - 1.31
Updated Date 02/5/2025
Dividends yield (FY) -
Basic EPS (TTM) -0.5

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 -2822004
Price to Sales(TTM) -
Enterprise Value -2822004
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. (NASDAQ: VIRA): Comprehensive Overview

Company Profile:

Detailed History and Background:

Founded in 2019, Viracta Therapeutics Inc. is a clinical-stage biotechnology company focused on the development of transformative therapies for severe viral infections. The company leverages its proprietary T-cell receptor (TCR) platform to engineer novel T-cell therapies targeting highly conserved viral antigens. Viracta believes its focus on conserved viral antigens allows for broad-spectrum coverage and durable protection against multiple viral strains.

Core Business Areas:

Viracta's core business revolves around developing and commercializing TCR-T cell therapies for the treatment of life-threatening viral infections like cytomegalovirus (CMV), Epstein-Barr virus (EBV), and respiratory syncytial virus (RSV). The company uses its TCR platform to identify and isolate T-cells that recognize and attack these viruses. These engineered T-cells are then expanded and reintroduced into the patient's body to fight the infection.

Leadership Team and Corporate Structure:

Viracta's leadership team comprises experienced professionals from the biotechnology and pharmaceutical industries. The current CEO is Dr. Ben Symons, who has extensive experience in drug development and commercialization. The company also has a strong scientific advisory board composed of leading experts in immunology, virology, and oncology. Viracta's corporate structure is lean and focused on research and development activities.

Top Products and Market Share:

Top Products:

Viracta's lead product candidate is VIR-1111, a TCR-T cell therapy targeting CMV. The company is also developing other TCR-T cell therapies for EBV and RSV.

Market Share:

Viracta is still in the clinical development stage and doesn't currently have marketed products. Therefore, it doesn't have a market share yet. However, the company's target markets are significant. CMV infection affects about 60,000 transplant recipients annually, while EBV is associated with various malignancies and affects millions of people worldwide. RSV is a leading cause of respiratory illness in infants and young children.

Product Performance and Market Reception:

Viracta's lead product candidate, VIR-1111, has demonstrated promising results in early clinical trials. These trials showed that VIR-1111 can effectively eliminate CMV infection in patients after a transplant. Further clinical trials are ongoing to confirm these results and evaluate the safety and efficacy of VIR-1111 in larger patient populations.

Total Addressable Market:

The total addressable market for Viracta's products is substantial. The global market for CMV treatment was estimated at $486 million in 2022 and is expected to grow to $749 million by 2028. The market for EBV-related therapies is even larger, estimated at $1.81 billion in 2022 and projected to reach $3.29 billion by 2028. The global RSV market is estimated to be worth $1.4 billion in 2023 and is expected to reach $2.3 billion by 2030.

Financial Performance:

Recent Financial Statements:

Viracta is a pre-revenue company; therefore, it doesn't have any significant revenue or net income. The company's primary expenses are related to research and development activities. In 2022, Viracta reported a net loss of $58.6 million and total operating expenses of $61.1 million. As of December 31, 2022, the company had cash and cash equivalents of $168.8 million.

Year-over-Year Comparison:

Viracta's net loss and operating expenses have increased significantly year-over-year, reflecting the company's ongoing clinical development activities. The increase in cash and cash equivalents is due to the company's successful completion of a public offering in October 2022.

Cash Flow and Balance Sheet Health:

Viracta's cash flow is primarily from financing activities like issuing new shares. The company's balance sheet is relatively healthy, with a significant amount of cash and cash equivalents. However, the company will need to raise additional capital to continue its clinical development programs.

Dividends and Shareholder Returns:

As a pre-revenue company, Viracta doesn't currently pay dividends. Its shareholder returns are primarily related to changes in its stock price. The company's stock price has been volatile since its IPO in October 2022.

Growth Trajectory:

Viracta is still in the early stages of development, and its future growth depends on the success of its clinical trials and regulatory approvals. The company is optimistic about its potential to develop transformative therapies for severe viral infections.

Market Dynamics:

The market for viral immunotherapies is rapidly growing, driven by advances in biotechnology and an increasing understanding of the immune system. Viracta faces competition from other companies developing similar therapies, but the company believes its focus on conserved viral antigens gives it a competitive advantage.

Key Competitors:

Viracta's key competitors include:

  • Atara Biotherapeutics (ATRA)
  • Carisma Therapeutics (CTRX)
  • Century Therapeutics (IPSC)
  • Iovance Biotherapeutics (IOVA)

About Viracta Therapeutics Inc

Exchange PINK
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
Full time employees 40

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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