医学
异种移植
移植
食品药品监督管理局
临床试验
监管事务
监管机构
重症监护医学
家庭医学
外科
公共行政
病理
药理学
政治学
作者
Andrew Adams,Linda C. Cendales,David K.C. Cooper,Emanuele Cozzi,John S. Gill,Eric Judd,Eliezer Katz,Allan D. Kirk,Jay A. Fishman,Peter P. Reese,Anji Wall,James F. Markmann
标识
DOI:10.1016/j.ajt.2023.05.010
摘要
In June 2022, the US Food and Drug Administration Center for Biologics Evaluation and Research held the 73rd meeting of the Cellular, Tissue, and Gene Therapies Advisory Committee for public discussion of regulatory expectations for xenotransplantation products. The members of a joint American Society of Transplant Surgeons/American Society of Transplantation committee on xenotransplantation compiled a meeting summary focusing on 7 topics believed to be key by the committee: (1) preclinical evidence supporting progression to a clinical trial, (2) porcine kidney function, (3) ethical aspects, (4) design of initial clinical trials, (5) infectious disease issues, (6) industry perspectives, and (7) regulatory oversight.
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