Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
BO-112 is a synthetic double-stranded RNA (dsRNA) drug candidate designed as a viral mimetic for cancer immunotherapy. It consists of polyinosinic:polycytidylic acid (poly I:C) formulated with the cationic carrier polyethyleneimine (PEI), creating a nanoplexed structure that enhances intracellular delivery and stability against nuclease degradation. Administered intratumorally or intralesionally, BO-112 activates innate immune sensors including Toll-like receptor 3 (TLR3), melanoma differentiation-associated protein 5 (MDA5), and retinoic acid-inducible gene I protein (RIG-I). This activation leads to the induction of type I interferon responses and stimulates cytotoxic cytokine release, promoting tumor cell death through both direct cytotoxicity and immune-mediated mechanisms. Preclinical studies have shown synergy with checkpoint inhibitors such as anti-PD-1 antibodies. Clinically, it is being developed primarily for aggressive solid tumors including basal cell carcinoma, non-small cell lung cancer, gastric cancer, colorectal cancer, malignant melanoma and others. Developed by Highlight Therapeutics and Merck Sharp & Dohme.
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 nanoplexed poly I:C.