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US food and drug administration (FDA) panel endorses islet cell treatment for type 1 diabetes: A pyrrhic victory?
Author(s) -
Piemonti Lorenzo,
Andres Axel,
Casey John,
Koning Eelco,
Engelse Marten,
Hilbrands Robert,
Johnson Paul,
Keymeulen Bart,
KerrConte Julie,
Korsgren Olle,
Lehmann Roger,
Lundgren Torbjörn,
Maffi Paola,
Pattou Francois,
Saudek Frantisek,
Shaw James,
Scholz Hanne,
White Steve,
Berney Thierry
Publication year - 2021
Publication title -
transplant international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.998
H-Index - 82
eISSN - 1432-2277
pISSN - 0934-0874
DOI - 10.1111/tri.13930
Subject(s) - medicine , islet , food and drug administration , licensure , transplantation , diabetes mellitus , family medicine , intensive care medicine , surgery , pharmacology , medical education , endocrinology
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.

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