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CytomX Therapeutics Inc (CTMX)



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Upturn Advisory Summary
09/15/2025: CTMX (4-star) is currently NOT-A-BUY. Pass it for now.
1 Year Target Price $5.75
1 Year Target Price $5.75
2 | Strong Buy |
3 | Buy |
1 | Hold |
0 | Sell |
0 | Strong Sell |
Analysis of Past Performance
Type Stock | Historic Profit 37.99% | Avg. Invested days 33 | 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 329.83M USD | Price to earnings Ratio 4 | 1Y Target Price 5.75 |
Price to earnings Ratio 4 | 1Y Target Price 5.75 | ||
Volume (30-day avg) 6 | Beta 2.17 | 52 Weeks Range 0.40 - 3.10 | Updated Date 09/15/2025 |
52 Weeks Range 0.40 - 3.10 | Updated Date 09/15/2025 | ||
Dividends yield (FY) - | Basic EPS (TTM) 0.5 |
Earnings Date
Report Date - | When - | Estimate - | Actual - |
Profitability
Profit Margin 34.01% | Operating Margin (TTM) -6.89% |
Management Effectiveness
Return on Assets (TTM) 16.13% | Return on Equity (TTM) 108.21% |
Valuation
Trailing PE 4 | Forward PE 14.2 | Enterprise Value 178623812 | Price to Sales(TTM) 2.34 |
Enterprise Value 178623812 | Price to Sales(TTM) 2.34 | ||
Enterprise Value to Revenue 1.27 | Enterprise Value to EBITDA 4 | Shares Outstanding 164912992 | Shares Floating 120279228 |
Shares Outstanding 164912992 | Shares Floating 120279228 | ||
Percent Insiders 0.79 | Percent Institutions 89.75 |
Upturn AI SWOT
CytomX Therapeutics Inc

Company Overview
History and Background
CytomX Therapeutics Inc. was founded in 2008. It is a biopharmaceutical company focused on developing conditionally activated antibody therapeutics for the treatment of cancer. The company's Probody platform is designed to create antibodies that are activated specifically in the tumor microenvironment.
Core Business Areas
- Oncology Drug Development: CytomX develops and commercializes antibody-based therapies that target specific tumor microenvironments. Their focus is on solid tumors and hematological malignancies. Their Probody technology enables drugs to target tumors while sparing healthy tissues.
Leadership and Structure
Sean McCarthy is the CEO. The company has a board of directors and a management team overseeing various departments, including research, development, and commercial operations.
Top Products and Market Share
Key Offerings
- CX-2009 (Probody Drug Conjugate): An investigational Probody drug conjugate (PDC) targeting CD166. It is in clinical development for solid tumors. There is no current market share as it's in clinical trials. Competitors are various companies developing ADCs, such as Seagen and Immunomedics (now part of Gilead).
- CX-904 (Next Generation T-cell engaging bispecific): An investigational Probody T-cell engager targeting the Epidermal Growth Factor Receptor (EGFR). It is in clinical development for solid tumors. There is no current market share as it's in clinical trials. Competitors are companies developing T-cell engagers, such as Amgen and Roche.
Market Dynamics
Industry Overview
The oncology therapeutics market is rapidly growing, driven by increasing cancer incidence and advancements in targeted therapies and immunotherapies. There's a high demand for more effective and less toxic cancer treatments.
Positioning
CytomX aims to differentiate itself through its Probody technology, which offers a potentially safer and more effective approach to cancer therapy by selectively targeting tumors. Their competitive advantage lies in reduced off-target effects.
Total Addressable Market (TAM)
The global oncology market is projected to reach hundreds of billions of dollars. CytomX is positioned to capture a share of this market with its novel targeted therapies, focusing on specific indications within the larger oncology landscape.
Upturn SWOT Analysis
Strengths
- Proprietary Probody technology platform
- Potential for reduced off-target toxicity
- Strong collaborations with pharmaceutical companies
- Experienced management team
Weaknesses
- Dependence on clinical trial success
- High cash burn rate
- Limited number of commercialized products
- Competition in the oncology therapeutics market
Opportunities
- Expansion of Probody platform to new targets
- Potential for strategic partnerships and acquisitions
- Advancements in cancer diagnostics and personalized medicine
- Growing demand for targeted cancer therapies
Threats
- Clinical trial failures
- Regulatory hurdles
- Competition from established pharmaceutical companies
- Economic downturn affecting healthcare spending
Competitors and Market Share
Key Competitors
- MRK
- BMY
- PFE
- AZN
- GILD
- LLY
Competitive Landscape
CytomX faces intense competition from established pharmaceutical companies with greater resources and broader pipelines. CytomX's advantage lies in its novel Probody technology, but it needs to demonstrate clinical superiority to gain significant market share.
Growth Trajectory and Initiatives
Historical Growth: Growth is primarily driven by advancement of pipeline programs and securing partnership agreements.
Future Projections: Future growth hinges on successful clinical trials and regulatory approvals. Analyst estimates vary widely depending on the perceived probability of success for their key programs.
Recent Initiatives: Focusing on advancing lead programs through clinical trials, expanding the Probody platform, and seeking strategic partnerships.
Summary
CytomX Therapeutics is a clinical-stage biopharmaceutical company with a promising Probody technology platform that aims to develop conditionally activated antibody therapeutics. Their clinical progress is critical, and they are currently experiencing a high cash burn rate. Securing strong partnerships is also crucial. Success in clinical trials and regulatory approvals are major milestones to watch for, as well as increased collaboration.
Peer Comparison
Sources and Disclaimers
Data Sources:
- Company website
- SEC filings
- Analyst reports
- Industry publications
Disclaimers:
This analysis is for informational purposes only and does not constitute financial advice. Investment decisions should be based on your own research and due diligence. Market data is approximate.
AI Summarization is directionally correct and might not be accurate.
Summarized information shown could be a few years old and not current.
Fundamental Rating based on AI could be based on old data.
AI-generated summaries may have inaccuracies (hallucinations). Please verify the information before taking action.
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 119 | Website https://www.cytomx.com |
Full time employees 119 | Website https://www.cytomx.com |
CytomX Therapeutics, Inc. operates as an oncology-focused biopharmaceutical company that 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). The company was founded in 2008 and is based in South San Francisco, California.

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