Skip to main content
An official website of the United States government
Government Funding Lapse
Because of a lapse in government funding, the information on this website may not be up to date, transactions submitted via the website may not be processed, and the agency may not be able to respond to inquiries until appropriations are enacted.

The NIH Clinical Center (the research hospital of NIH) is open. For more details about its operating status, please visit cc.nih.gov.

Updates regarding government operating status and resumption of normal operations can be found at opm.gov.

Technology ID
TAB-4393

Fully Human Antibodies and Antibody Drug Conjugates Targeting CD276 (B7-H3) for the Treatment of Cancer

E-Numbers
E-250-2014-0
Lead Inventors
Dimitrov, Dimiter
Co-Inventors
Zhu, Zhongyu
St. Croix, Brad
Seaman, Steven
Saha, Saurabh
Zhang, Xaioyan
Welsch, Dean
Decrescenzo, Gary
Applications
Therapeutics
Therapeutic Areas
Oncology
Development Stages
Pre-clinical (in vivo)
Lead IC
NCI
ICs
NCI

Angiogenesis is the formation of new blood vessels from pre-existing blood vessels. Angiogenesis occurs during normal growth and development, where it is known as physiological angiogenesis, and during the growth of solid tumors, where it is known as pathological angiogenesis. CD276, also known as B7-H3, is a cell surface tumor endothelial marker that is highly expressed in the tumor vessels of human lung, breast, colon, endometrial, renal, and ovarian cancer, but not in the angiogenic vessels of healthy tissue. This differential expression makes CD276 an attractive target for cancer treatment due to the ability to selectively target pathological angiogenesis without impacting physiological angiogenesis. In fact, CD276-directed therapeutic antibodies may have a higher degree of specificity for tumor vessels than current antiangiogenic agents that cannot distinguish physiological and pathological angiogenesis. Moreover, CD276 protein is also frequently overexpressed on tumor cells. The ability to target the vasculature as well as tumor cells directly makes CD276 a potentially ideal dual-compartment therapeutic target.

Researchers at the National Cancer Institute (NCI) have developed fully human monoclonal antibodies and antibody-drug conjugates (ADCs) that target CD276. The antibodies and ADCs have been tested both in vitro and in vivo and have shown promising data.  Pyrrolobenzodiazepine (PBD)-conjugated CD276 ADCs killed both cancer cells and tumor vasculature, eradicating large established tumors and metastases, and improving long-term overall survival in mouse models. In addition, the ADCs have been evaluated in preliminary toxicology studies where they showed limited, if any, off-target toxicity.

Competitive Advantages:

  • Simultaneously targets both tumor cells and tumor vasculature
  • Potentially superior adverse events profile than existing anti-angiogenic agents due to the differential expression of CD276 on tumor and normal vasculature
  • Fully human antibodies are less likely to be recognized and cleared by the immune system upon repeated administration.   
  • Relevance to a wide range of cancers – representing several major market opportunities.
  • High cellular internalization. 
  • Cross-reactive with mouse, rat, and monkey CD276 making preclinical studies easier and more informative.

Commercial Applications:

  • Antibody-drug conjugates (ADCs) for the treatment of cancer
  • CAR-T cell therapy 
  • Diagnostic agent for detecting and monitoring CD276-expressing malignancies
Licensing Contacts