Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
BCG-STING is a preclinical recombinant Bacillus Calmette-Guérin (BCG) strain engineered to overexpress the bioactive STING (Stimulator of Interferon Genes) agonist cyclic di-AMP (c-di-AMP). Developed by researchers at Johns Hopkins University, it is designed as an immunotherapy for non-muscle invasive bladder cancer (NMIBC). By combining the inherent immunogenicity of BCG with the potent activation of the STING pathway, BCG-STING enhances the recruitment and activation of tumor-infiltrating CD4+ and CD8+ T cells and inflammatory macrophages within the tumor microenvironment. In preclinical models of urothelial carcinoma, intravesical administration of BCG-STING demonstrated superior antitumor efficacy and higher rates of complete tumor regression compared to wild-type BCG or small-molecule STING agonists like ADU-S100.
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 BCG-STING.