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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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Biotech & Genomic Medicine

CytomX Therapeutics reports Q2 2026 results, advances Varseta-M toward registrational study

CytomX Therapeutics announced second quarter 2026 financial results and a business update highlighted by progress of its lead candidate varsetatug masetecan, or Varseta-M, an EpCAM-directed antibody drug conjugate. The company expects a Phase 1 monotherapy data update in advanced colorectal cancer by the end of 2026 and plans to initiate a registrational study in the first half of 2027. Varseta-M is also being evaluated in combination with bevacizumab in late-line metastatic colorectal cancer, with a Phase 1/2 chemotherapy combination study in second-line disease set to start in the fourth quarter of 2026, and monotherapy expansion cohorts in gastric, pancreatic, and biliary tract cancers are initiating in the third quarter of 2026. CytomX expanded its Regeneron collaboration in masked bispecific immunotherapies, receiving a $37.0 million target selection payment in July 2026 for two additional programs, with total potential milestones under the collaboration now up to approximately $4.0 billion. The company reported cash, cash equivalents and investments of $330.3 million as of June 30, 2026, which does not include the $37.0 million received in July, and expects its cash runway to extend to at least the second half of 2028.
GlobeNewswire·20dRead more ▾
Biotech & Genomic Medicine

CytomX Expands Regeneron Collaboration, Adding $37 Million Payment and Up to $4 Billion in Milestones

CytomX Therapeutics expanded its research collaboration with Regeneron to develop next-generation conditionally-activated bispecific cancer therapies. Under the expanded agreement, CytomX will receive a $37 million target selection payment for two new programs, and Regeneron secured an option for six additional targets, bringing the total potential value of the collaboration to approximately $4 billion in milestones plus tiered royalties. The partnership combines CytomX's PROBODY masking platform with Regeneron's Veloci-Bi technology to create treatments that remain inactive until reaching the tumor microenvironment. Regeneron will fund subsequent preclinical, clinical, and commercialization activities. The expansion builds on the companies' initial 2022 alliance.
Insider Monkey·69dRead more ▾