Biologics and biosimilars, such as ADCs and mAbs, hold great promise for treating even rare forms of cancer. However, testing for immunogenicity using these modalities presents a set of specific obstacles to overcome to ensure patient safety in clinical trials and beyond. Industry experts recently met to discuss effective strategies for moving forward.
Read the roundtable summary to explore:
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Bridging immunogenicity assays from the pre-clinical to clinical setting and beyond
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Balancing the complexities and benefits of multi-tier assays
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Applying immunogenicity assays in new biologics and new biosimilars
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Dealing with regulators: CDMO and developer experiences
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Improving results with a flexible approach to neutralizing antibody assay selection
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Looking ahead: The role of tech advances and AI