Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
CD40 Ligand (CD40L or CD154) is a recombinant protein and a member of the tumor necrosis factor (TNF) superfamily that serves as a potent immunostimulatory agent. In the clinical development program led by the National Cancer Institute (NCI), CD40L is utilized as a critical component in the production of personalized cancer vaccines for pediatric patients with recurrent Ewing sarcoma and alveolar rhabdomyosarcoma. The agent is used ex vivo to activate and mature autologous antigen-presenting cells (APCs), such as dendritic cells, which are then pulsed with tumor-specific peptides (including EF-1, EF-2, PXFK, and E7) derived from disease-defining fusion proteins like EWS-FLI1 and PAX3-FKHR. By binding to the CD40 receptor on APCs, CD40L triggers the upregulation of co-stimulatory molecules and the secretion of pro-inflammatory cytokines, thereby enhancing the ability of the vaccine to prime and expand tumor-specific cytotoxic T-lymphocytes upon re-infusion into the patient.
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 CD40 Ligand.