Overview

NCI Definition [1]:
An anti-glycoprotein A33 (gpA33)/anti-CD3 bispecific humanized monoclonal antibody with potential immunostimulatory and antineoplastic activities. Anti-gpA33/CD3 monoclonal antibody MGD007 possesses two antigen-recognition sites, one for the CD3 complex, a group of T-cell surface glycoproteins that complex with the T-cell receptor (TCR), and one for gpA33, a tumor-associated antigen (TAA) overexpressed on the surface of certain tumor cells. Upon administration of MGD007, this bispecific antibody simultaneously binds to both CD3-expressing T-cells and gpA33-expressing cancer cells, thereby crosslinking cytotoxic T-lymphocytes (CTLs) to gpA33-expressing tumor cells. This may result in CTL-mediated cell lysis of the crosslinked tumor cells. The gpA33 antigen, a member of the immunoglobulin superfamily, is expressed in certain malignancies, including colon and gastrointestinal cancers.

Mgd007 has been investigated in 2 clinical trials, of which 1 is open and 1 is closed. Of the trials investigating mgd007, 1 is phase 1 (0 open) and 1 is phase 1/phase 2 (1 open).

KRAS Mutation is the most frequent biomarker inclusion criterion for mgd007 clinical trials.

Colorectal adenocarcinoma and colorectal carcinoma are the most common diseases being investigated in mgd007 clinical trials [2].

Top Biomarker Inclusion Criteria for Open Clinical Trials Investigating Mgd007
Top Biomarker Inclusion Criteria for Closed Clinical Trials Investigating Mgd007
This graph displays the 20 most frequently occurring biomarkers curated on clinical trials investigating mgd007 and the cancer types associated with these biomarkers. These numbers are derived from a set of 5,956 clinical trials for which biomarker status defines treatment.

Drug Details

Synonyms [2]:
humanized gpa33 x cd3 dart (tm) protein mgd007, humanized gpa33 x cd3 dart™ protein mgd007, anti-gpa33/cd3 monoclonal antibody mgd007
Drug Target(s) [2]:
CD3, GPA33
NCIT ID [1]:
C118442

References

1. National Cancer Institute. NCI Thesaurus Version 18.11d. https://ncit.nci.nih.gov/ncitbrowser/. [2018-07-30] [2018-08-02].

2. All assertions and clinical trial landscape data are curated from primary sources. You can read more about the curation process here.