CytomX Therapeutics, Inc. (CTMX) Stock

Healthcare · Biotechnology · Member of Other US Stocks

CytomX Therapeutics, Inc. (CTMX) closed at USD 2.23 on 2026-10-14, a change of -32.8 % over the past year, with a market capitalization of USD 525.14M.

CytomX Therapeutics, Inc. recent closing prices

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CytomX Therapeutics, Inc. key figures

Previous close

USD 2.23 (2026-10-14)

1-year change

-32.8 %

Market cap

USD 525.14M

Enterprise value

USD 200.56M

P/E ratio (trailing)

-4.55

P/E ratio (forward)

-5.13

EPS (trailing)

-0.53

EPS (forward)

-0.47

PEG ratio

n/a

Price to book

1.74

Revenue growth

-92.4 %

Earnings growth

n/a

Dividend per share (trailing)

0.00

Short ratio

9.26

Employees

69

Analyst consensus (third-party)

strong_buy

Source: Yahoo Finance via yfinance. Data may be delayed, incomplete or incorrect.

About CytomX Therapeutics, Inc.

CytomX Therapeutics, Inc. operates as an oncology-focused biopharmaceutical company that focuses on developing potent biologics designed to treat 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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