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CytomX Therapeutics Inc (CTMX)

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Upturn Advisory Summary
01/08/2026: CTMX (5-star) is a STRONG-BUY. BUY since 72 days. Simulated Profits (46.90%). Updated daily EoD!
1 Year Target Price $7.07
1 Year Target Price $7.07
| 2 | Strong Buy |
| 3 | Buy |
| 1 | Hold |
| 0 | Sell |
| 0 | Strong Sell |
Analysis of Past Performance
Type Stock | Historic Profit 102.7% | Avg. Invested days 40 | Today’s Advisory Strong Buy |
Upturn Star Rating ![]() | Upturn Advisory Performance | Stock Returns Performance |
Key Highlights
Company Size Small-Cap Stock | Market Capitalization 728.57M USD | Price to earnings Ratio 14.33 | 1Y Target Price 7.07 |
Price to earnings Ratio 14.33 | 1Y Target Price 7.07 | ||
Volume (30-day avg) 6 | Beta 2.42 | 52 Weeks Range 0.40 - 4.66 | Updated Date 01/8/2026 |
52 Weeks Range 0.40 - 4.66 | Updated Date 01/8/2026 | ||
Dividends yield (FY) - | Basic EPS (TTM) 0.3 |
Earnings Date
Report Date - | When - | Estimate - | Actual - |
Profitability
Profit Margin 24.66% | Operating Margin (TTM) -264.43% |
Management Effectiveness
Return on Assets (TTM) 9.78% | Return on Equity (TTM) 66.76% |
Valuation
Trailing PE 14.33 | Forward PE 14.2 | Enterprise Value 590542198 | Price to Sales(TTM) 6.41 |
Enterprise Value 590542198 | Price to Sales(TTM) 6.41 | ||
Enterprise Value to Revenue 5.2 | Enterprise Value to EBITDA 24.08 | Shares Outstanding 169435395 | Shares Floating 131773295 |
Shares Outstanding 169435395 | Shares Floating 131773295 | ||
Percent Insiders 0.57 | Percent Institutions 88.83 |
Upturn AI SWOT
CytomX Therapeutics Inc

Company Overview
History and Background
CytomX Therapeutics Inc. was founded in 2007 with the mission to develop best-in-class therapies that harness the power of the immune system. The company is focused on developing a new class of antibody-drug conjugates (ADCs) and antibody-based therapeutics using its Probody platform. Significant milestones include the advancement of its pipeline candidates into clinical trials and strategic partnerships with major pharmaceutical companies.
Core Business Areas
- Proprietary Probody Platform: CytomX utilizes its Probody technology platform to engineer conditionally activated biologics. These Probody therapeutics are designed to be inactive in the bloodstream and only become activated at the tumor site, thereby improving efficacy and reducing systemic toxicity.
- Oncology Therapeutics Development: The company's primary focus is the development of novel oncology therapies. Their pipeline includes multiple drug candidates targeting various solid tumors and hematological malignancies, designed to be activated by specific tumor-associated proteases.
- Strategic Partnerships: CytomX engages in strategic collaborations with leading pharmaceutical companies to co-develop and commercialize its Probody-based drug candidates. These partnerships provide funding, expertise, and broad market access.
Leadership and Structure
CytomX Therapeutics Inc. is led by a management team with extensive experience in biotechnology and drug development. The organizational structure is typical for a biopharmaceutical company, with departments dedicated to research and development, clinical operations, regulatory affairs, manufacturing, and commercial strategy. Specific leadership details (CEO, CFO, CSO, etc.) are publicly available on their corporate website and in SEC filings.
Top Products and Market Share
Key Offerings
- CX-2029 (Acquired by AbbVie): A conditionally activated antibody-drug conjugate (ADC) targeting CD166. This product was previously a key pipeline asset for CytomX but has been acquired by AbbVie. Market share data is not directly applicable as it is now part of AbbVie's portfolio. Competitors include other CD166-targeting ADCs and therapies for the indications it was intended for.
- CX-301 (Seph-ADC, Partnered with Amgen): A conditionally activated ADC targeting EGFR, intended for patients with specific types of cancer. Market share is nascent as it is in clinical development. Competitors include other EGFR-targeting therapies and ADCs in the oncology space.
- CX-801 (Partnered with Bristol Myers Squibb): A conditionally activated antibody targeting IL-12, for potential use in various solid tumors. Market share is not yet established as it is in clinical development. Competitors include other immunotherapies and biologics targeting the tumor microenvironment.
Market Dynamics
Industry Overview
The biopharmaceutical industry, particularly the oncology sector, is characterized by rapid innovation, high R&D costs, and significant unmet medical needs. The development of targeted therapies, immunotherapies, and antibody-drug conjugates are key trends. The market is highly competitive with a strong focus on demonstrating clinical efficacy and safety.
Positioning
CytomX Therapeutics is positioned as an innovator in the field of conditionally activated biologics, leveraging its proprietary Probody platform. Its competitive advantage lies in its ability to potentially deliver potent therapeutic agents directly to tumors while minimizing systemic toxicity, offering a differentiated approach to cancer treatment. Strategic partnerships with larger pharmaceutical companies further solidify its market position and provide access to broader development and commercialization capabilities.
Total Addressable Market (TAM)
The TAM for oncology therapeutics is vast and continually growing, estimated to be in the hundreds of billions of dollars globally. CytomX Therapeutics is positioned to address significant portions of this TAM by developing novel treatments for various cancer types, with its Probody platform offering potential applications across a broad range of therapeutic targets and indications.
Upturn SWOT Analysis
Strengths
- Proprietary Probody technology platform enabling differentiated therapeutic design.
- Strong pipeline of conditionally activated biologics targeting significant unmet needs in oncology.
- Established strategic partnerships with major pharmaceutical companies (e.g., Bristol Myers Squibb, AbbVie, Amgen) providing validation and funding.
- Experienced management team with a track record in drug development.
- Focus on reducing systemic toxicity, a key challenge in current cancer therapies.
Weaknesses
- Relatively early-stage pipeline with limited approved products.
- Reliance on partners for significant portions of development and commercialization.
- High cash burn rate typical of biopharmaceutical R&D companies.
- Clinical trial success is inherently uncertain and can lead to significant setbacks.
Opportunities
- Expansion of Probody platform to new targets and therapeutic areas beyond oncology.
- Successful progression of pipeline candidates through clinical trials and potential regulatory approvals.
- Leveraging partnerships to expand global reach and market access.
- Advancements in companion diagnostics to identify patient populations most likely to benefit from Probody therapies.
- Potential for in-licensing or acquisition of complementary technologies or assets.
Threats
- Failure of pipeline candidates in clinical trials.
- Increased competition from other novel therapeutic modalities and established oncology treatments.
- Changes in regulatory landscapes and approval pathways.
- Adverse market reactions to clinical trial data or company news.
- Patent expirations and the emergence of generic or biosimilar competition for partnered products in the future.
Competitors and Market Share
Key Competitors
- Moderna Inc (MRNA)
- BioNTech SE (BNTX)
- Gilead Sciences Inc (GILD)
- Bristol Myers Squibb Company (BMY)
- Amgen Inc (AMGN)
- Merck & Co., Inc. (MRK)
Competitive Landscape
CytomX Therapeutics competes in the highly dynamic and competitive oncology and immunology drug development space. Its primary competitive advantages lie in its novel Probody platform, which offers a differentiated approach to targeting diseases with potentially improved safety profiles. However, it faces intense competition from established large pharmaceutical companies with extensive R&D budgets and commercial infrastructure, as well as other innovative biotechnology firms developing next-generation therapies. CytomX's reliance on partnerships is a key aspect of its competitive strategy, allowing it to leverage the resources of larger players.
Growth Trajectory and Initiatives
Historical Growth: Historically, CytomX Therapeutics has experienced growth primarily through the expansion of its pipeline, the formation of strategic partnerships, and successful fundraising rounds. Revenue has been largely driven by collaboration milestones rather than product sales. The focus has been on building a robust pipeline of novel drug candidates.
Future Projections: Future growth projections for CytomX Therapeutics are contingent upon the successful clinical development and potential commercialization of its pipeline assets, as well as the performance of its partnered programs. Analyst estimates will vary based on their assessment of clinical trial success probabilities and market potential for specific indications. Key drivers will be the advancement of CX-301, CX-801, and other preclinical candidates.
Recent Initiatives: Recent initiatives likely include the continued advancement of their lead drug candidates in clinical trials, the exploration of new therapeutic applications for the Probody platform, and the ongoing management and expansion of strategic partnerships. They may also focus on operational efficiency to manage their R&D spend.
Summary
CytomX Therapeutics Inc. is an innovative biotechnology company with a promising proprietary Probody platform focused on developing novel oncology therapies. Its strengths lie in its unique technology, strategic partnerships with major pharmaceutical players, and a strong pipeline. However, as a clinical-stage company, it faces significant risks associated with drug development and a high cash burn rate. Future success hinges on successful clinical trials and the ability to translate its platform into approved, marketable drugs. Monitoring pipeline progress and partnership performance will be crucial.
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Sources and Disclaimers
Data Sources:
- CytomX Therapeutics Inc. Official Investor Relations Website
- U.S. Securities and Exchange Commission (SEC) Filings (10-K, 10-Q)
- Financial News Outlets (e.g., Bloomberg, Reuters)
- Biotechnology Industry Research Reports
- Market Data Aggregators (for competitor information and market share estimates)
Disclaimers:
This JSON output is generated based on publicly available information and does not constitute financial advice. The market share figures are estimates and subject to change. Financial performance data is subject to periodic updates in SEC filings. Users should conduct their own due diligence before making any investment decisions. Information regarding pipeline status, partnerships, and clinical trials is dynamic and should be verified with the latest company announcements.
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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