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US food and drug administration (FDA) panel endorses islet cell treatment for type 1 diabetes: A pyrrhic victory?

Authors :
Piemonti, Lorenzo
Andres, Axel
Casey, John
Koning, Eelco
Engelse, Marten
Hilbrands, Robert
Johnson, Paul
Keymeulen, Bart
Kerr‐Conte, Julie
Korsgren, Olle
Lehmann, Roger
Lundgren, Torbjörn
Maffi, Paola
Pattou, Francois
Saudek, Frantisek
Shaw, James
Scholz, Hanne
White, Steve
Berney, Thierry
Source :
Transplant International; Jul2021, Vol. 34 Issue 7, p1182-1186, 5p
Publication Year :
2021

Abstract

Summary: Allogeneic islet transplantation is a standard of care treatment for patients with labile type 1 diabetes in many countries around the world, including Japan, the United Kingdom, Australia, much of continental Europe, and parts of Canada. The United States is now endorsing islet cell treatment for type 1 diabetes, but the FDA has chosen to consider islets as a biologic that requires licensure, making the universal implementation of the procedure in the clinic very challenging and opening the manufacture of islet grafts to private companies. The commercialization of human tissues raises significant legal and ethical issues and ironically leads to a situation where treatments developed as a result of the scientific and economic efforts of academia over several decades become exploited exclusively by for‐profit entities. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09340874
Volume :
34
Issue :
7
Database :
Complementary Index
Journal :
Transplant International
Publication Type :
Academic Journal
Accession number :
151570088
Full Text :
https://doi.org/10.1111/tri.13930