Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
CD276 autologous chimeric antigen receptor (CAR) T cells are a form of cell therapy in which a patient's own T lymphocytes are genetically engineered to express a synthetic receptor targeting the tumor-associated antigen CD276 (also known as B7-H3). The engineered T cells recognize and bind to CD276 on the surface of cancer cells via their single-chain variable fragment (scFv), leading to activation and proliferation of the modified T cells. Upon engagement with target-expressing tumor cells, these CAR-Ts mediate anti-tumor effects through cytokine secretion and direct cytolytic activity. Preclinical studies have demonstrated potent activity against various solid tumors such as pancreatic cancer and acute myeloid leukemia[5][7]. The mechanism of action is based on specific recognition and killing of tumor cells expressing high levels of CD276 while sparing normal tissues[1][2][5]. This approach is under investigation for multiple solid tumors due to the overexpression of CD276 in many malignancies.
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 CD276 autologous chimeric antigen receptor T cells.