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Forecast
The analysts' average price target is €7.62 (+284.85%). The median is €7.62 (+284.85%).
| Buy |
Â
17 |
| Hold |
Â
4 |
| Sell |
Â
0 |
News Go to news feed
CytomX focuses strategy on advanced colorectal cancer after positive Varseta‑M data
CytomX presented early phase‑I data for Varseta‑M in advanced colorectal cancer at the Morgan Stanley Healthcare Conference, showing response rates of 20–30% and an estimated median PFS of 6–7 months. The main adverse event was grade‑3 diarrhea; prophylaxis and dose adjustments reduced severe cases from about 30% to around 10%. The company has pro forma roughly $367 million in cash (runway to at least H2 2028) and is simultaneously advancing a masked interferon‑alfa‑2b program for PD‑1‑refractory melanoma, with first data expected in H1 2025. Next steps include dose selection and regulatory study design under Project Optimus, as well as additional combinations and indication expansions. » More on de.investing.com
CytomX reports pipeline progress and prepares registration‑relevant trial for Varseta‑M
CytomX presented positive efficacy data for Varseta‑M in metastatic colorectal cancer at a health conference (ORR 20–30% vs. 1–2% with standard therapy) and emphasized safety‑management improvements, with grade‑3 diarrhea in optimization cohorts falling to about 10%. The company received a $37 million upfront payment from Regeneron, plans a comprehensive data update by the end of 2024, and intends to discuss regulatory strategy with the FDA in 2024. A first registration‑relevant study could start in the first half of 2025; the second lead program, CX‑801, is also expected to deliver initial data in H1 2025. » More on de.investing.com
CytomX focuses on EpCAM‑ADC Varseta‑M and reports solid liquidity
CytomX presented its Probody portfolio at the Wells‑Fargo conference with Varseta‑M as the only known EpCAM‑targeting ADC in development, showing encouraging phase‑1 data in metastatic colorectal cancer and an FDA fast‑track designation. The company has more than $350 million in liquid assets, supported by an expanded collaboration with Regeneron. The second program, CX‑801 (masked interferon alfa‑2b), has shown initial biomarker activity in melanomas. Key milestones include additional phase‑1 data by the end of 2024, combination data with bevacizumab in H1 2025, and the planned start of a registrational study for Varseta‑M in H1 2027. » More on de.investing.com
Historical dividends Dividends
All dividend metrics All metricsFinancials
| (EUR) | September 2026 | YoY |
|---|---|---|
| Revenue | 1.49m | 70.67% |
| Gross profit | 0 | 100.00% |
| Net profit | -17.66m | 45.61% |
| EBITDA | -20.75m | 73.46% |
Fundamentals
| Metric | Value |
|---|---|
Market capitalization | €427.95m |
Number of shares | 217.9m |
52-week high/low | €7.36 - €1.89 |
| Dividends | No |
Beta | 2.20 |
P/E ratio | -4.87 |
PEG ratio | 0.03 |
P/B ratio | 1.68 |
P/S ratio | 34.02 |
Company profile
CytomX Therapeutics, Inc. operates as an oncology-focused biopharmaceutical company in the United States. The company develops antibody therapeutics based on its Probody technology platform for the treatment of cancer. The company's product candidates include CX-2009, an antibody drug conjugates (ADC) against CD166, which is in Phase II clinical trials for the treatment of breast cancer; CX-2029 that is in Phase II clinical trials for the treatment of squamous non-small cell lung cancer, head and neck squamous cell carcinoma, esophageal and gastro-esophageal junction cancers, and diffuse large B-cell lymphoma; BMS-986249, a CTLA-4 Probody therapeutic drug, which is in Phase I/II clinical trials for the treatment of metastatic melanoma; and BMS-986288, an anti-CTLA-4 Probody drug, which is in Phase I clinical trials for the treatment of solid tumors. It also develops CX-2043, a conditionally activated ADC targeting the epithelial cell adhesion molecule, as well as CX-904, a conditionally activated epidermal growth factor receptor for the treatment of solid tumor. The company has strategic collaborations with AbbVie Ireland Unlimited Company, Amgen, Inc., Bristol-Myers Squibb Company, ImmunoGen, Inc., Pfizer Inc., and Astellas Pharma Inc. to develop Probody therapeutics. CytomX Therapeutics, Inc. was founded in 2008 and is headquartered in South San Francisco, California.
| Name | CytomX Therapeutics |
| CEO | Sean A. McCarthy |
| Headquarters | South San Francisco,
ca USA |
| Website | |
| Sector | Materials |
| Industry | Chemicals |
| IPO | 13/07/2021 |
| Employees | 69 |
Ticker symbols
| Exchange | Symbol |
|---|---|
NASDAQ | CTMX |
Frankfurt | 6C1.F |
DĂĽsseldorf | 6C1.DU |
SIX | 6C1.SW |