Abstract
Background: Receptor occupancy, or saturation, assays are often utilized in preclinical and clinical development programs to evaluate the binding of a biologic to a cellular target. These assays provide critical information regarding the dose of drug required to "saturate" the target as well as important pharmacodymamic (PD) data. A flow cytometric method was developed to measure the degree of Semaphorin 4D (SEMA4D; CD100) saturation by VX15/2303, an investigational monoclonal antibody specific for SEMA4D. Methods: The assay detects VX15/2503, a human IgG4 specific for SEMA4D, with an IgG4-specific monoclonal antibody. Results Data generated allowed assessment of two related SEMA4D-specific pharmacodynamic (PD) markers: (1) The measurement of cellular SEMA4D (cSEMA4D) saturation by VX15/2503, and (2) the cell membrane expression levels of cSEMA4D. Conclusions This assay specifically and reproducibly measured cSEMA4D saturation and expression levels. Evaluation of the SEMA4D-specific PD markers were critical in determining the clinical saturation threshold of cSEMA4D by VX15/2503.
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Fisher, T. L., Seils, J., Reilly, C., Litwin, V., Green, L., Salkowitz-Bokal, J., … Zauderer, M. (2016). Saturation monitoring of VX15/2503, a novel semaphorin 4D-specific antibody, in clinical trials. Cytometry Part B - Clinical Cytometry, 90(2), 199–208. https://doi.org/10.1002/cyto.b.21338
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