Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This combination therapy consists of BO-112, an intratumoral viral mimetic, administered alongside the PD-1 inhibitor nivolumab and stereotactic ablative radiotherapy (SABR). BO-112 is a nanoplexed formulation of polyinosinic:polycytidylic acid (poly I:C) and polyethyleneimine that acts as a double-stranded RNA analog. It triggers an immune response by activating Toll-like receptor 3 (TLR3), melanoma differentiation-associated protein 5 (MDA-5), and protein kinase R (PKR), effectively mimicking a viral infection within the tumor microenvironment. This activation leads to dendritic cell maturation, increased CD8+ T-cell infiltration, and the induction of type I interferons. The combination is specifically being evaluated in Phase Ib/II clinical trials for patients with metastatic non-small cell lung cancer (NSCLC) who have progressed on prior PD-1/PD-L1 checkpoint inhibitor therapy, aiming to overcome resistance by turning "cold" tumors "hot."
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 BO-112 + nivolumab + radiotherapy.