New immunotherapies are generating unprecedented clinical response. However, immune activation by I/O agents can also cause notable and potentially fatal clinical toxicity, such as cytokine storms, which is not observed in preclinical studies. Immuno-safety has therefore become a major clinical concern, which needs to be sufficiently addressed in early preclinical drug development.
In order to fully evaluate immunotherapies and de-risk clinical trials, appropriate preclinical models for immuno-safety testing are needed, which have a close species homology to humans and an intact immune system. In this webinar, Dr Thomas Scullion introduces NHPs as a valuable early-stage preclinical platform for exploratory toxicology studies. This webinar reviews how NHPs are used to evaluate immunotherapies and their potential toxicity prior to clinical trials.
Thomas Scullion, PhD - Senior Director of Business Development at Crown Bioscience has extensive experience guiding clients’ early drug discovery work through to clinical trials. At Crown Bioscience, he specializes in pharmacology, toxicology, and bioanalytics using translational animal models. Thomas holds a PhD in Neuropharmacology, and previously worked at Symbiosis Pharmaceutical Services Limited and Charles River Laboratories.
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2023-05-29
2021-11-10
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