CytomX Therapeutics, Inc. (CTMX)
CytomX Therapeutics, Inc. is a United States-based biopharmaceutical company primarily focused on creating treatments for cancer. The company utilizes its proprietary Probody technology platform to engineer targeted antibody therapeutics for oncological applications. Its robust clinical pipeline includes several notable drug candidates. CX-2009, an antibody-drug conjugate (ADC) designed to target CD166, is currently in Phase II clinical trials for treating breast cancer. Another investigational therapy, CX-2029, has also reached Phase II trials, where it is being evaluated for various cancers such as squamous non-small cell lung cancer, head and neck squamous cell carcinoma, esophageal and gastro-esophageal junction cancers, and diffuse large B-cell lymphoma. Additionally, CytomX is progressing two CTLA-4 Probody therapeutics: BMS-986249, which is undergoing Phase I/II clinical trials for metastatic melanoma, and BMS-986288, in Phase I trials for solid tumors. Beyond these, the company is developing CX-2043, a conditionally activated ADC targeting the epithelial cell adhesion molecule, and CX-904, a conditionally activated epidermal growth factor receptor, both aimed at addressing solid tumor conditions. CytomX has forged strategic partnerships with leading pharmaceutical firms, including AbbVie Ireland Unlimited Company, Amgen, Inc., Bristol-Myers Squibb Company, ImmunoGen, Inc., Pfizer Inc., and Astellas Pharma Inc., to collaboratively advance its Probody therapeutics. The company was founded in 2008 and its main office is located in South San Francisco, California.
Sector: Pharmaceutical Preparations
Industry: Biotechnology
CytomX Therapeutics, Inc.
Trials need funding. See this company's dilution risk and cash position.
- Phase 2Terminated
PROCLAIM: CX-072-002: Study of PD-L1 Probody Therapeutic CX-072 in Combination With Other Anticancer Therapy in Adults With Solid Tumors
CX-072, Ipilimumab
Solid Tumor, Unresectable or Metastatic Melanoma
NCT03993379Enrollment3StartNov 2019Primary CompletionMay 2020CompletionMay 2020 - Phase 2Completed
Study to Evaluate the Safety and Antitumor Activity of CX-2009 Monotherapy and in Combination With CX-072 in Advanced Breast Cancer
CX-2009, CX-072
Neoplasms, Breast Neoplasms +3
NCT04596150Enrollment125StartDec 2020Primary CompletionJun 2023CompletionJun 2023 - Phase 1/2Terminated
PROCLAIM-CX-072: A Trial to Find Safe and Active Doses of an Investigational Drug CX-072 for Patients With Solid Tumors or Lymphomas
CX-072, ipilimumab
Solid Tumor, Lymphoma
NCT03013491Enrollment196StartJan 2017Primary CompletionOct 2020CompletionOct 2020 - Phase 1/2Terminated
PROCLAIM-CX-2009: A Trial to Find Safe and Active Doses of an Investigational Drug CX-2009 for Patients With Selected Solid Tumors
CX-2009
Solid Tumor, Adult, Breast Cancer +3
NCT03149549Enrollment99StartJun 2017Primary CompletionSep 2020CompletionSep 2020 - Phase 1/2Completed
PROCLAIM-CX-2029: A Trial to Find Safe and Active Doses of an Investigational Drug CX-2029 for Patients With Solid Tumors or DLBCL
CX-2029
Solid Tumor, Adult, Head and Neck Cancer +3
NCT03543813Enrollment133StartJun 2018Primary CompletionJun 2023CompletionJun 2023 - Phase 1/2Not yet recruiting
Study of Varsetatug Masetecan in Combination With Anti-Cancer Therapies in Colorectal Cancer
varsetatug masetecan, bevacizumab + 5-FU + leucovorin
Colo-rectal Cancer
NCT07900165Enrollment368StartDec 2026est.Primary CompletionFeb 2029est.CompletionFeb 2029est. - Phase 1Withdrawn
PROCLAIM-CX-188: A Trial to Find Safe and Active Doses of an Investigational Drug CX-188 for Patients With Solid Tumors
CX-188
Solid Tumor, Adult
NCT03706274Enrollment0StartJan 2020est.Primary CompletionDec 2020est.CompletionDec 2022est. - Phase 1Terminated
A Trial to Find Safe and Active Doses for an Investigational Drug, CX-904, for Patients With Advanced Solid Tumors
CX-904
Solid Tumors
NCT05387265Enrollment83StartMay 2022Primary CompletionJun 2025CompletionJun 2025 - Phase 1Recruiting
First In Human Study of CX-2051 in Advanced Solid Tumors
CX-2051, Bevacizumab
Solid Tumor, Adult
NCT06265688Enrollment160StartApr 2024Primary CompletionNov 2027est.CompletionMar 2029est. - Phase 1Recruiting
First In Human Study of CX-801 in Advanced Solid Tumors
CX-801, pembrolizumab
Solid Tumor, Adult
NCT06462794Enrollment121StartAug 2024Primary CompletionFeb 2028est.CompletionJun 2029est.
| Drug / Therapy | Link | ||
|---|---|---|---|
| Phase 2 | Terminated | CX-072, Ipilimumab | NCT03993379 |
| Phase 2 | Completed | CX-2009, CX-072 | NCT04596150 |
| Phase 1/2 | Terminated | CX-072, ipilimumab | NCT03013491 |
| Phase 1/2 | Terminated | CX-2009 | NCT03149549 |
| Phase 1/2 | Completed | CX-2029 | NCT03543813 |
| Phase 1/2 | Not yet recruiting | varsetatug masetecan, bevacizumab + 5-FU + leucovorin | NCT07900165 |
| Phase 1 | Withdrawn | CX-188 | NCT03706274 |
| Phase 1 | Terminated | CX-904 | NCT05387265 |
| Phase 1 | Recruiting | CX-2051, Bevacizumab | NCT06265688 |
| Phase 1 | Recruiting | CX-801, pembrolizumab | NCT06462794 |