Implementation of highly sophisticated flow cytometry assays in multicenter clinical studies: considerations and guidance

Author:

Sommer Ulrike1,Morales Johanna2,Groenewegen Andrea1,Müller Annemarie1,Naab Julia1,Woerly Gaetane1,Kamphausen Esther1,Marsot Helene1,Bennett Patrick2,Kakkanaiah Vellalore2,Vitaliti Alessandra1

Affiliation:

1. Novartis Institutes for BioMedical Research, Basel, Switzerland

2. Biomarker Laboratories, PPD Inc., Richmond, VA 23230, USA

Abstract

Flow cytometry is increasingly becoming an important technology for biomarkers used in drug discovery and development. Within clinical development flow cytometry is used for the determination of PD biomarkers, disease or efficacy biomarkers or patient stratification biomarkers. Significant differences exist between flow cytometry methodology and other widely used technologies measuring soluble biomarkers including ligand binding and mass spectrometry. These differences include the very heavy reliance on aspects of sample processing techniques as well as sample stabilization to ensure viable samples. These differences also require exploration of new approaches and wider discussion regarding method validation requirements. This paper provides a review of the current challenges, solutions, regulatory environment and recommendations for the application of flow cytometry to measure biomarkers in clinical development.

Publisher

Future Science Ltd

Subject

Medical Laboratory Technology,Clinical Biochemistry,General Pharmacology, Toxicology and Pharmaceutics,General Medicine,Analytical Chemistry

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