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TRICOM-CEA(6D)

Development stage
Phase 1
Lead developer
National Cancer Institute
Modality
Recombinant Proteins and Enzymes, Oncolytic Viruses → Oncolytic Therapeutics, Vaccines & Immunotherapeutics
Administration
Subcutaneous
01

Overview

A therapeutic cancer vaccine platform consisting of a recombinant viral vector (either vaccinia or fowlpox) engineered to express the tumor-associated antigen carcinoembryonic antigen (CEA) with an enhancer agonist epitope (designated 6D), along with a TRIad of COstimulatory Molecules (B7.1, ICAM‑1, and LFA‑3; collectively called TRICOM). The addition of these costimulatory molecules is designed to enhance antigen-specific T-cell responses and antitumor activity by improving immune recognition and activation against CEA-expressing tumors. The platform has been evaluated in phase I clinical trials for patients with advanced cancers expressing CEA, including colorectal cancer and other carcinomas. It is developed primarily by the National Cancer Institute[1][2][4][7].

Other names
CEA/TRICOM vaccineCEA(6D)/TRICOM
02

Targets

CD80 (T-lymphocyte activation antigen CD80)MUC1 (Mucin-1 Antigen)ICAM1 (Intercellular Adhesion Molecule 1)CD58 (Leukocyte function-associated antigen 3)CEACAM5 (Carcinoembryonic antigen related cell adhesion molecule 5)

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