CDMO selection: critical considerations that can make or break your CGT development

Maryam A. Pasdar, Mitchel M. Sivilotti, Peter S. Jaehn, Benham A. Baghbaderani, John Lee,Bruce L. Levine, William D. Milligan

Cytotherapy(2024)

引用 0|浏览0
暂无评分
摘要
With the increase in cell and gene therapy (CGT) clinical trials in recent years has come a subsequent increase in the number of contract development and manufacturing organizations (CDMOs). Successful transition from development and early phase clinical trials to commercialization of a CGT product often depends on selecting the best-suited CDMO. However, many CGT companies are small biotech companies that lack expertise in the field or do not have experience selecting and transferring a process to a CDMO. Given the interest in this topic, a roundtable with CGT developers and CDMO members at the 2023 annual meeting of the International Society of Cell and Gene Therapy Paris discussed these critical aspects of product development including technical expertise, risk sharing, and timing of partnerships. Here, we'll analyze the considerations discussed by the panel and elaborate on other factors crucial for CGT development.
更多
查看译文
关键词
commercialization,technology transfer,cell manufacturing,process development
AI 理解论文
溯源树
样例
生成溯源树,研究论文发展脉络
Chat Paper
正在生成论文摘要