
Nona Biosciences applied discovery-stage investigative toxicology to address key safety challenges associated with CD40 agonism while preserving antitumor efficacyy. This scientific poster highlights:
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- Early investigative toxicology studies in non-human primates to evaluate potential safety liabilities of an HBICE® PD-L1×CD40 bispecific antibody
- Minimal cytokine release and favorable liver safety findings compared with a clinically relevant CD40 agonist benchmark
- Strong preclinical antitumor efficacy and favorable tolerability in a transgenic mouse model
Download the full poster to explore the preclinical safety and efficacy data and learn how early investigative toxicology informed candidate selection and supported an accelerated path toward IND.
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