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Development and validation of receptor occupancy pharmacodynamic assays used in the clinical development of the monoclonal antibody vedolizumab
Author(s) -
Wyant Tim,
Estevam Jose,
Yang Lili,
Rosario Maria
Publication year - 2016
Publication title -
cytometry part b: clinical cytometry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.646
H-Index - 61
eISSN - 1552-4957
pISSN - 1552-4949
DOI - 10.1002/cyto.b.21236
Subject(s) - vedolizumab , monoclonal antibody , pharmacodynamics , occupancy , antibody , medicine , pharmacology , computational biology , immunology , biology , pharmacokinetics , disease , ecology , inflammatory bowel disease
Background Vedolizumab is a monoclonal antibody approved for use in ulcerative colitis and Crohn's disease. By specifically binding to α 4 β 7 integrin, vedolizumab prevents trafficking of lymphocytes to the gut, thereby interfering with disease pathology. During the clinical development program, the pharmacodynamic effect of vedolizumab was evaluated by 2 flow cytometry receptor occupancy assays: act‐1 (ACT‐1) and mucosal addressin cell adhesion molecule‐1 (MAdCAM‐1). Here we describe the development and validation of these assays. Methods The ACT‐1 assay is a receptor occupancy free‐site assay that uses a monoclonal antibody with the same binding epitope as vedolizumab to detect free (unbound) sites on α 4 β 7 integrin. The MAdCAM‐1 assay used a soluble version of the natural ligand for α 4 β 7 integrin to detect free sites. The assays were validated using a fit‐for‐purpose approach throughout the clinical development of vedolizumab. Results Both the ACT‐1 assay and the MAdCAM‐1 assay demonstrated acceptable reproducibility and repeatability. The assays were sufficiently stable to allow for clinical use. During clinical testing the assays demonstrated that vedolizumab was able to saturate peripheral cells at all doses tested. Conclusions Two pharmacodynamic receptor occupancy assays were developed and validated to assess the effect of vedolizumab on peripheral blood cells. The results of these assays demonstrated the practical use of flow cytometry to examine pharmacodynamic response in clinical trials. © 2015 International Clinical Cytometry Society