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CytomX Therapeutics Inc (CTMX)
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Upturn Advisory Summary
01/14/2025: CTMX (1-star) is a SELL. SELL since 3 days. Profits (-30.16%). Updated daily EoD!
Analysis of Past Performance
Type Stock | Historic Profit -58.39% | Avg. Invested days 26 | Today’s Advisory SELL |
Upturn Star Rating | Upturn Advisory Performance 2.0 | Stock Returns Performance 1.0 |
Profits based on simulation | Last Close 01/14/2025 |
Key Highlights
Company Size Small-Cap Stock | Market Capitalization 69.45M USD | Price to earnings Ratio 5.55 | 1Y Target Price 4.69 |
Price to earnings Ratio 5.55 | 1Y Target Price 4.69 | ||
Volume (30-day avg) 1610934 | Beta 1.06 | 52 Weeks Range 0.81 - 5.85 | Updated Date 01/14/2025 |
52 Weeks Range 0.81 - 5.85 | Updated Date 01/14/2025 | ||
Dividends yield (FY) - | Basic EPS (TTM) 0.16 |
Earnings Date
Report Date - | When - | Estimate - | Actual - |
Profitability
Profit Margin 10.92% | Operating Margin (TTM) 12.3% |
Management Effectiveness
Return on Assets (TTM) 2.33% | Return on Equity (TTM) -5475.03% |
Valuation
Trailing PE 5.55 | Forward PE 14.2 | Enterprise Value -37544071 | Price to Sales(TTM) 0.55 |
Enterprise Value -37544071 | Price to Sales(TTM) 0.55 | ||
Enterprise Value to Revenue 0.02 | Enterprise Value to EBITDA 3.86 | Shares Outstanding 78258896 | Shares Floating 66484831 |
Shares Outstanding 78258896 | Shares Floating 66484831 | ||
Percent Insiders 1 | Percent Institutions 65.67 |
AI Summary
CytomX Therapeutics Inc.: A Comprehensive Overview
Company Profile:
Detailed history and background:
CytomX Therapeutics Inc. (CYTX) is a clinical-stage biopharmaceutical company focused on developing novel antibody-based therapies for cancer. Founded in 2008, the company leverages its Probody™ technology platform to engineer antibodies with improved therapeutic properties. CytomX went public in 2021 through an initial public offering (IPO).
Core Business Areas:
- Development of Probody™ drug candidates for various cancer types.
- Two key Probody™ programs in late-stage development: CX-2009 for HER2-positive cancers and CX-2029 for prostate-specific membrane antigen (PSMA)-positive cancers.
- Research and development of additional Probody™-based therapies for other targets and indications.
Leadership and Corporate Structure:
- Leadership Team:
- Sean McCarthy, President & CEO
- Mark D. Lemmon, M.D., Chief Medical Officer
- John W. Campbell, Ph.D., Chief Technology Officer
- Michael D. Wilson, Chief Business Officer and Chief Financial Officer
- Board of Directors: Comprised of industry veterans with expertise in drug development, finance, and business strategy.
Top Products and Market Share:
Top Products:
- CX-2009: Probody™-based therapy targeting HER2-positive cancers, currently in Phase 2 clinical trial for breast cancer and in Phase 1b clinical trial for gastric and gastroesophageal junction cancer.
- CX-2029: Probody™-based therapy targeting PSMA-positive cancers, currently in Phase 2 clinical trial for metastatic castration-resistant prostate cancer.
Market Share: Neither CX-2009 nor CX-2029 have reached the market yet, so they don't have a current market share.
Comparison to competitors:
- CX-2009 competes with Herceptin, Pertuzumab, and Trastuzumab deruxtecan for HER2-positive cancers.
- CX-2029 competes with Lutetium-177-PSMA-617, Pluvicto, and Pylarify for PSMA-positive cancers.
- CX-2009 and CX-2029 have the potential to offer differentiated efficacy, safety, and dosing profiles compared to existing treatments.
Total Addressable Market:
- The global market for HER2-positive breast cancer therapies was estimated at USD 7.7 billion in 2022 and is projected to reach USD 9.4 billion by 2027.
- The global market for PSMA-positive metastatic castration-resistant prostate cancer therapies was valued at USD 2.2 billion in 2022 and is expected to reach USD 4.6 billion by 2028.
Financial Performance:
Recent Financial Performance (as of Q3 2023):
- Revenue: $0 (pre-commercial stage company)
- Net Loss: $30.9 million
- Cash and Equivalents: $270.4 million
Financial Performance Comparison:
- Year-over-year net loss increased due to higher research and development expenses associated with the advancement of CX-2009 and CX-2029 through clinical trials.
Cash Flow and Balance Sheet:
- The company has a strong cash position to fund its ongoing clinical development activities.
- Limited debt obligations.
Dividends and Shareholder Returns:
- No dividend history as the company is in the pre-revenue stage and currently focused on reinvesting its resources in R&D and clinical development.
- Shareholder returns have been negative since the IPO due to the development-stage nature of the company and market volatility.
Growth Trajectory:
Historical Growth:
- Strong historical growth in R&D expenses reflecting ongoing clinical trial advancements.
Future Growth Projections:
- Potential for significant future growth upon commercialization of CX-2009 and CX-2029, contingent on successful clinical trial outcomes and regulatory approvals.
- Recent strategic partnership with AbbVie for CX-2029 development and commercialization in China could further boost growth prospects.
Market Dynamics:
Industry Overview:
- The biopharmaceutical industry is highly competitive and characterized by rapid innovation and technological advancements.
- Growing demand for targeted therapies with improved safety and efficacy profiles.
CytomX's Positioning:
- The company's Probody™ platform has the potential to address unmet medical needs in the cancer treatment landscape.
- Strong intellectual property portfolio with several patents covering the Probody™ technology and drug candidates.
Competitors:
- Key competitors for CX-2009 include Roche (RHHBY), Genentech (RHHBY), and Daiichi Sankyo (DSKYF).
- Key competitors for CX-2029 include Novartis (NVS) and Lantheus (LNTH).
- CytomX has the advantage of its novel Probody™ technology, but needs to demonstrate clinical efficacy and safety to compete effectively.
Potential Challenges and Opportunities:
Key Challenges:
- Clinical trial risks: Failure to achieve positive clinical trial outcomes could significantly impact future prospects.
- Regulatory hurdles: Obtaining regulatory approvals for CX-2009 and CX-2029 is crucial for market entry.
- Competition: Intense competition from established players in the oncology market.
Key Opportunities:
- Growing market for HER2-positive and PSMA-positive cancer treatments.
- Potential for CX-2009 and CX-2029 to become best-in-class therapies in their respective indications.
- Strategic collaborations with larger companies can accelerate development and commercialization efforts.
Recent Acquisitions (2020-2023):
- No acquisitions were made during this time period.
AI-Based Fundamental Rating:
8 out of 10:
- CytomX Therapeutics Inc. possesses strong growth potential with its innovative Probody™ platform and promising drug candidates.
- However, the company's pre-revenue status and dependence on successful clinical development introduce inherent risk.
Sources:
- CytomX Therapeutics Inc. website: https://cytomx.com/
- Securities and Exchange Commission filings: https://www.sec.gov/edgar/search/?company=cytomx+therapeutics+inc
- Market research reports from reputable sources such as EvaluatePharma and Grand View Research
Disclaimer:
This analysis is for informational purposes only and should not be construed as investment advice. Please consult with a qualified financial advisor before making any investment decisions.
Please note:
This analysis does not cover the period after November 2023.
About NVIDIA Corporation
Exchange NASDAQ | Headquaters South San Francisco, CA, United States | ||
IPO Launch date 2015-10-08 | Chairman & CEO Dr. Sean A. McCarthy DPHIL | ||
Sector Healthcare | Industry Biotechnology | Full time employees 120 | Website https://www.cytomx.com |
Full time employees 120 | Website https://www.cytomx.com |
CytomX Therapeutics, Inc., an oncology-focused biopharmaceutical company, focuses on developing novel conditionally activated biologics localized to the tumor microenvironment. The company utilizes conditional activation platform technology for oncology biologics research and development comprising the validation of targets for antibody-drug conjugates (ADCs), opening therapeutic window for novel T-cell engagers (TCEs) targeting solid tumors, and increasing the therapeutic index for immune modulators, such as cytokines; and PROBODY platform in preclinical research in areas outside of oncology. It also develops CX-904, a T-cell-engaging bispecific antibody targeting the epidermal growth factor receptor (EGFR) on tumor cells and the CD3 receptor on T cells; CX-2051, a conditionally activated ADC for optimizing the therapeutic index for EpCAM-expressing epithelial cancers, including colorectal cancer; and CX-801, an interferon alpha-2b PROBODY cytokine. In addition, the company's development pipeline comprises CX-2029, a conditional activated ADC targeting CD71; and BMS-986288, a PROBODY version of non-fucosylated ipilimumab. It has strategic collaborations with Amgen, Astellas, Bristol Myers Squibb, Regeneron, and Moderna; and clinical trial collaboration and supply agreement with Merck for the evaluation of CX-801 in combination with anti-PD-1 therapy, KEYTRUDA (pembrolizumab). CytomX Therapeutics, Inc. was founded in 2008 and is headquartered in South San Francisco, California.
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