Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This therapeutic vaccine is an autologous cell-based immunotherapy designed to elicit a potent anti-tumor immune response. It consists of a patient's own tumor cells that have been genetically modified, typically via an adenoviral vector, to express two key immunomodulatory proteins: granulocyte-macrophage colony-stimulating factor (GM-CSF) and CD40 ligand (CD40L, also known as CD154). The autologous tumor cells provide a comprehensive array of patient-specific tumor-associated antigens. GM-CSF acts locally to recruit and differentiate professional antigen-presenting cells (APCs), such as dendritic cells, to the vaccination site. CD40L subsequently provides a critical activation signal to these APCs by binding to CD40, which induces maturation, upregulates co-stimulatory molecules (e.g., CD80 and CD86), and stimulates the secretion of pro-inflammatory cytokines like IL-12. This dual-action approach aims to bypass tumor-induced immunosuppression and prime a systemic, T-cell-mediated immune attack against both the primary tumor and metastatic lesions. Development has primarily focused on hematologic malignancies and specific solid tumors.
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 granulocyte-macrophage colony-stimulating factor + CD40 ligand + autologous tumor cell vaccine.