Abstract
The outstanding results recently obtained in islet xenotransplantation
suggest that porcine islet clinical trials may soon be scientifically
appropriate. Before the initiation of such clinical studies, however, it
is essential that a series of key ethical and regulatory conditions are
satisfied. As far as ethics is concerned, the fundamental requirements
have been previously reported in a position paper of the Ethics Committee
of the International Xenotransplantation Association. These
include aspects related to the selection of adequately informed, appropriate
recipients; animal breeding and welfare; safety issues and the need
for a favorable risk/benefit assessment based on strong efficacy data in
relevant xenotransplantation studies in the primate.
| Original language | English |
|---|---|
| Pages (from-to) | 203-214 |
| Number of pages | 12 |
| Journal | Xenotransplantation |
| Volume | 16 |
| DOIs | |
| Publication status | Published - 2009 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
-
SDG 3 Good Health and Well-being
Keywords
- ethics
- regulation
- xenotransplantation
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