Drug intelligence / Profile preview

BO-112 + pembrolizumab

Development stage
Unknown
Lead developer
Highlight Therapeutics
Modality
Small Molecules, Monoclonal Antibodies → Antibody-Based Therapeutics, Nanoparticles → Drug Delivery Systems
Administration
Intratumoral, Intravenous
01

Overview

BO-112 + pembrolizumab is a combination immunotherapy regimen under investigation for the treatment of advanced melanoma, particularly in patients who have progressed on or after anti-PD1/PD-L1 therapies. BO-112 is a synthetic double-stranded RNA formulated with polyethyleneimine, acting as a viral mimetic that stimulates innate immune responses by targeting pattern recognition receptors such as TLR3, MDA5, and PKR. It is administered intratumorally to induce local and systemic anti-tumor immunity. Pembrolizumab (Keytruda) is an FDA-approved monoclonal antibody that blocks the programmed cell death protein 1 (PD-1) receptor on T cells, thereby enhancing anti-tumor immune activity. The combination has shown clinical benefit in phase 2 trials for PD1-refractory advanced melanoma, achieving objective response rates of approximately 25–28%. The approach leverages both local immune activation by BO-112 and systemic checkpoint inhibition by pembrolizumab[3][5][8].

Other names
BO-112 + Keytruda
02

Targets

IFIH1 (MDA5)EIF2AK2 (Interferon-induced protein kinase R)PDCD1 (Programmed cell death protein 1 receptor)TLR3 (Toll-like receptor 3)

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