This volume of the Springer book series Advances in Experimental
Medicine and Biology covers potency assays, one of the most complex
yet fundamental evaluations that critically influence stem cell
regenerative medicine. Developing potency assays for cell-based
medicinal products comes with numerous challenges due to the highly
specialised nature of the application and purpose. This book
provides the reader with the knowledge necessary to understand
issues governing the successful development of potency assays,
highlighting an international outlook of how the various challenges
raised are being managed. Stakeholders concerned with potency assay
development range from patient and clinician to contract research
organisations, small and medium enterprise, regulatory authorities
and even politicians. The value of potency assays is poised to
increase given the inevitable watershed as early-stage clinical
trials addressing safety progress to trials testing
efficacy. Contributors from clinical, academic, industrial
and regulatory sectors establish a broad point of view for guidance
and timely debate. Potency assays require extensive collaboration
across disciplines and sectors, as well as compromise and the
authors aim to constructively address the many key aspects
involved. Potency assays provide a quantitative measure of the
biological activity of advanced therapy medicinal products (ATMPs)
and thus are required for their market authorization. As the pace
of ATMP development accelerates, the need to develop specific,
accurate, and robust potency assays for each product is also
accelerating. The volume Potency Assays for Stem Cell Advanced
Therapy Medicinal Products presents a broad outlook on the
development, quality attributes, and implementation of potency
assays for ATMPs. The first few chapters introduce a nuanced
historical perspective on the science of potency assay development,
describe specific quality attributes of an idealized potency assay,
indicate pitfalls associated with developing such assays for ATMPs,
and review guidance recommended by regulatory authorities on assay
suitability for product approval. Subsequent chapters highlight
efforts to develop potency assays for specific ATMPs, including
skeletal stem cells, mesenchymal stromal cells, extracellular
vesicles, CAR T-cells, and discuss emerging technologies/platforms
for potency assay design. The volume concludes with a chapter
reviewing potency assays used for the release of commercial ATMP
products, which amalgamates information contained in previous
chapters. Overall, the knowledge contributed from leading
authorities in both academia and industry is an ideal resource for
technicians, scientists, clinicians, process engineers, and
regulators working with ATMPs. —Donald G. Phinney,
PhD Professor, Department of Molecular
Medicine, Herbert Wertheim UF Scripps Institute for
Biomedical Innovation & Technology Â
General
Imprint: |
Springer International Publishing AG
|
Country of origin: |
Switzerland |
Series: |
Advances in Experimental Medicine and Biology, 1420 |
Release date: |
June 2023 |
First published: |
2023 |
Editors: |
Jorge S. Burns
|
Dimensions: |
254 x 178mm (L x W) |
Pages: |
392 |
Edition: |
1st ed. 2023 |
ISBN-13: |
978-3-03-130039-4 |
Categories: |
Books
Promotions
|
LSN: |
3-03-130039-4 |
Barcode: |
9783031300394 |
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