Journal
CYTOMETRY PART B-CLINICAL CYTOMETRY
Volume 90, Issue 2, Pages 168-176Publisher
WILEY-BLACKWELL
DOI: 10.1002/cyto.b.21236
Keywords
vedolizumab; pharmacodynamics; MADCAM-1ACT-1; ulcerative colitis; crohn's disease
Categories
Funding
- Millennium Pharmaceuticals, Inc. (d/b/a Takeda Pharmaceuticals International Co.)
- inVentiv Medical Communications
- Takeda Pharmaceuticals International, Inc.
Ask authors/readers for more resources
BackgroundVedolizumab is a monoclonal antibody approved for use in ulcerative colitis and Crohn's disease. By specifically binding to (47) 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. MethodsThe 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 (47) integrin. The MAdCAM-1 assay used a soluble version of the natural ligand for (47) integrin to detect free sites. The assays were validated using a fit-for-purpose approach throughout the clinical development of vedolizumab. ResultsBoth 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. ConclusionsTwo 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. (c) 2015 International Clinical Cytometry Society
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available