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Saturation monitoring of VX15/2503, a novel semaphorin 4D‐specific antibody, in clinical trials

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 impo...

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Autores principales: Fisher, Terrence L., Seils, Jennifer, Reilly, Christine, Litwin, Virginia, Green, Lisa, Salkowitz‐Bokal, Janelle, Walsh, Robin, Harville, Sarah, Leonard, John E., Smith, Ernest, Zauderer, Maurice
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5064733/
https://www.ncbi.nlm.nih.gov/pubmed/26566052
http://dx.doi.org/10.1002/cyto.b.21338
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author Fisher, Terrence L.
Seils, Jennifer
Reilly, Christine
Litwin, Virginia
Green, Lisa
Salkowitz‐Bokal, Janelle
Walsh, Robin
Harville, Sarah
Leonard, John E.
Smith, Ernest
Zauderer, Maurice
author_facet Fisher, Terrence L.
Seils, Jennifer
Reilly, Christine
Litwin, Virginia
Green, Lisa
Salkowitz‐Bokal, Janelle
Walsh, Robin
Harville, Sarah
Leonard, John E.
Smith, Ernest
Zauderer, Maurice
author_sort Fisher, Terrence L.
collection PubMed
description 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 IgG(4) specific for SEMA4D, with an IgG(4)‐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. © 2015 he Authors Cytometry Part B: Clinical Cytometry Published by Wiley Periodicals, Inc.
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spelling pubmed-50647332016-10-19 Saturation monitoring of VX15/2503, a novel semaphorin 4D‐specific antibody, in clinical trials Fisher, Terrence L. Seils, Jennifer Reilly, Christine Litwin, Virginia Green, Lisa Salkowitz‐Bokal, Janelle Walsh, Robin Harville, Sarah Leonard, John E. Smith, Ernest Zauderer, Maurice Cytometry B Clin Cytom Original Articles 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 IgG(4) specific for SEMA4D, with an IgG(4)‐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. © 2015 he Authors Cytometry Part B: Clinical Cytometry Published by Wiley Periodicals, Inc. John Wiley and Sons Inc. 2015-12-24 2016-03 /pmc/articles/PMC5064733/ /pubmed/26566052 http://dx.doi.org/10.1002/cyto.b.21338 Text en © 2015 he Authors Cytometry Part B: Clinical Cytometry Published by Wiley Periodicals, Inc. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Fisher, Terrence L.
Seils, Jennifer
Reilly, Christine
Litwin, Virginia
Green, Lisa
Salkowitz‐Bokal, Janelle
Walsh, Robin
Harville, Sarah
Leonard, John E.
Smith, Ernest
Zauderer, Maurice
Saturation monitoring of VX15/2503, a novel semaphorin 4D‐specific antibody, in clinical trials
title Saturation monitoring of VX15/2503, a novel semaphorin 4D‐specific antibody, in clinical trials
title_full Saturation monitoring of VX15/2503, a novel semaphorin 4D‐specific antibody, in clinical trials
title_fullStr Saturation monitoring of VX15/2503, a novel semaphorin 4D‐specific antibody, in clinical trials
title_full_unstemmed Saturation monitoring of VX15/2503, a novel semaphorin 4D‐specific antibody, in clinical trials
title_short Saturation monitoring of VX15/2503, a novel semaphorin 4D‐specific antibody, in clinical trials
title_sort saturation monitoring of vx15/2503, a novel semaphorin 4d‐specific antibody, in clinical trials
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5064733/
https://www.ncbi.nlm.nih.gov/pubmed/26566052
http://dx.doi.org/10.1002/cyto.b.21338
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