Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Anti-CEA designer T cells are second-generation chimeric antigen receptor (CAR) T cells engineered to target cancers expressing carcinoembryonic antigen (CEA). These autologous T cells are genetically modified using mammalian expression vectors to express a "Tandem" chimeric immune receptor (CIR), designated as IgCD28TCR. This construct consists of a single-chain antibody fragment (sFv) specific for CEA fused to the CD28 costimulatory signaling domain and the CD3-zeta (TCR zeta) signaling chain. By incorporating both Signal 1 (activation) and Signal 2 (costimulation), these modified T cells are designed to resist activation-induced cell death (AICD), enhance cytokine secretion (such as IL-2 and IFN-gamma), and promote sustained proliferation upon tumor contact. Clinical trials have investigated these cells for various CEA-positive malignancies, including colorectal, gastric, breast, and lung cancers, utilizing both systemic intravenous administration and regional delivery methods like intrahepatic arterial infusion for liver metastases.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on anti-CEA designer T cells.