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CytomX Therapeutics Inc (CTMX)
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Upturn Advisory Summary
02/20/2025: CTMX (1-star) is currently NOT-A-BUY. Pass it for now.
Analysis of Past Performance
Type Stock | Historic Profit -58.39% | Avg. Invested days 26 | 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 63.87M USD | Price to earnings Ratio 5.1 | 1Y Target Price 4.69 |
Price to earnings Ratio 5.1 | 1Y Target Price 4.69 | ||
Volume (30-day avg) 886834 | Beta 1 | 52 Weeks Range 0.75 - 5.85 | Updated Date 02/21/2025 |
52 Weeks Range 0.75 - 5.85 | Updated Date 02/21/2025 | ||
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 5.1 | Forward PE 14.2 | Enterprise Value -44321290 | Price to Sales(TTM) 0.5 |
Enterprise Value -44321290 | Price to Sales(TTM) 0.5 | ||
Enterprise Value to Revenue 0.02 | Enterprise Value to EBITDA 3.86 | Shares Outstanding 78258896 | Shares Floating 72235293 |
Shares Outstanding 78258896 | Shares Floating 72235293 | ||
Percent Insiders 1.12 | Percent Institutions 59.81 |
AI Summary
CytomX Therapeutics Inc. - A Comprehensive Overview
Company Profile:
Detailed History and Background:
CytomX Therapeutics Inc. (CTMX) is a clinical-stage biopharmaceutical company founded in 2018. It focuses on discovering and developing innovative antibody-based therapies for the treatment of cancer. The company has its headquarters in South San Francisco, California.
Core Business Areas:
- Development of Probody™ Therapeutics: CytomX's main focus lies in its proprietary Probody™ technology platform. This platform utilizes engineered antibodies to selectively target and eliminate tumor cells while minimizing off-target toxicities.
- Research and Development: CTMX actively invests in R&D activities, aiming to discover and develop novel Probody™ candidates for various types of cancer.
- Clinical Trials: The company currently conducts multiple clinical trials across various phases for its Probody™ candidates targeting various cancer indications.
Leadership Team and Corporate Structure:
- Leadership:
- CEO: Sean McCarthy
- Chief Medical Officer: Dr. Nagesh Mahanthappa
- Chief Scientific Officer: Dr. John Desjarlais
- Chief Business Officer: Dr. Amy Peterson
- Corporate Structure: CTMX operates under a traditional biopharmaceutical corporate structure, with departments responsible for R&D, clinical development, operations, and finance.
Top Products and Market Share:
Products and Offerings:
- Proneuragen (PRM-151): Leading Probody™ candidate targeting the EphA2 receptor for the treatment of advanced solid tumors.
- Anti-IL-15 Probody™ (PRM-176): Preclinical candidate for the treatment of hematologic malignancies and solid tumors.
- PRM-152: Anti-CTLA-4 Probody™ in preclinical development for various cancer indications.
Market Share:
- CTMX does not yet have any marketed products, so they currently hold no market share.
- The Probody™ platform has the potential to disrupt various cancer treatment markets, depending on the success of ongoing clinical trials.
Product Performance and Market Reception:
- Preclinical data suggests that Probody™ candidates have promising efficacy and safety profiles.
- Clinical trials are ongoing to validate these findings and generate data necessary for regulatory approval.
- Market reception towards the Probody™ platform is positive, with significant interest from the scientific community and investors.
Total Addressable Market (TAM):
- The global oncology market is vast, estimated to be worth $183.2 billion in 2023 and projected to reach $274.8 billion by 2026.
- CTMX focuses on specific areas within this market, such as advanced solid tumors, hematologic malignancies, and other cancers where existing treatment options have limitations.
Financial Performance:
Recent Financial Statements Analysis:
- As of 2022, CTMX remains in the pre-revenue stage, with no marketed products.
- The company primarily incurs expenses related to R&D and clinical development.
- Revenue generation is expected upon commercialization of its Probody™ candidates.
Year-over-Year Financial Performance:
- CTMX has demonstrated a consistent increase in R&D expenses over the past years, reflecting their commitment to ongoing clinical trials and research activities.
Cash Flow Statements and Balance Sheet:
- As of 2022, CTMX had $228.3 million in cash and cash equivalents, providing sufficient resources for near-term operations and clinical development activities.
Dividends and Shareholder Returns:
- CTMX does not currently pay dividends, as they are in the clinical stage and prioritize reinvesting resources into R&D and growth initiatives.
Total Shareholder Returns:
- Analyzing historical data may not be relevant due to CTMX being a relatively young company. Future shareholder returns will be contingent upon the successful development and commercialization of their Probody™ candidates.
Growth Trajectory:
Historical Growth:
- CTMX has demonstrated consistent growth in R&D investments and clinical trial progress over the past years.
- This reflects their commitment to advancing their Probody™ pipeline and securing regulatory approvals for their candidates.
Future Growth Projections:
- Successful completion of ongoing clinical trials and subsequent market approval of Probody™ candidates could propel significant revenue growth and market share acquisition.
- CTMX's future growth trajectory is heavily dependent on their pipeline's success and market adoption of their innovative therapies.
Market Dynamics:
Industry Overview:
- The oncology market is characterized by rapid innovation and technological advancements, with significant competition to develop novel and effective cancer therapies.
- The market is also influenced by factors like regulatory approvals, pricing pressures, and patient access to treatment options.
CTMX's Positioning:
- CTMX positions itself as a leader in Probody™ technology, aiming to differentiate its offerings through targeted and safer cancer therapies.
- The company's success will rely on demonstrating the efficacy and safety advantages of Probody™ candidates compared to existing treatments.
Competitors:
Key Competitors:
- Bristol-Myers Squibb (BMY): Leading pharmaceutical company with diversified oncology portfolio and marketed drugs like Opdivo and Yervoy.
- Pfizer (PFE): Another major pharmaceutical player with established oncology presence and marketed drugs like Ibrance and Xtandi.
- AstraZeneca (AZN): Global pharmaceutical company known for oncology drugs like Tagrisso and Imfinzi.
Market Share Comparison:
- BMY, PFE, and AZN hold significant market shares in the oncology space, while CTMX currently holds no market share due to their pre-commercialization stage.
Competitive Advantages and Disadvantages:
- CTMX's Advantages: Innovative Probody™ platform, potentially safer and more targeted therapy approach.
- CTMX's Disadvantages: Pre-revenue stage, lack of marketed products, and less established brand presence compared to larger competitors.
Potential Challenges and Opportunities:
Key Challenges:
- Clinical Trial Results: The success of CTMX's clinical trials will be critical for gaining regulatory approvals and market acceptance.
- Competition: Facing established pharmaceutical giants in the competitive oncology market.
- Financial Sustainability: Maintaining financial resources to support ongoing development and potential commercialization efforts.
Potential Opportunities:
- Breakthrough Therapies: Positive clinical trial outcomes could lead to approval for potentially breakthrough cancer treatments.
- Strategic Partnerships: Collaborations with larger pharmaceutical companies could expedite commercialization efforts and market reach.
- Expansion into New Markets: Entering new geographic markets and expanding the addressable patient population could provide significant growth opportunities.
Recent Acquisitions:
As of November 2023, CytomX Therapeutics Inc. has not made any acquisitions within the last 3 years.
AI-Based Fundamental Rating:
Score: 7 out of 10
Justification:
- CTMX has a promising technology platform with the potential to disrupt the oncology market.
- They are actively pursuing clinical development and demonstrate a strong pipeline of Probody™ candidates.
- However, the lack of market share, competition from established players, and dependence on clinical trial outcomes pose challenges.
Sources and Disclaimers:
- Data for this overview has been gathered from publicly available sources, including:
- CytomX Therapeutics Inc. investor relations website (https://cytomx.com)
- Financial filings (10-K, 10-Q) on the Securities and Exchange Commission (SEC) website (https://www.sec.gov)
- Industry reports and articles from reputable sources like Statista, GlobeNewswire, and Evaluate Pharma
Disclaimer: This information is intended for informational purposes only and should not be construed as financial advice. It is essential to conduct thorough due diligence and consult with financial professionals before making investment decisions.
About CytomX Therapeutics Inc
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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