Contract development and manufacturing organization selection: critical considerations that can make or break your cell and gene therapy development

被引:0
|
作者
Pasdar, Maryam A. [1 ]
Sivilotti, Mitchel M. [2 ]
Jaehn, Peter S. [3 ]
Baghbaderani, Benham A. [4 ]
Lee, John [5 ]
Levine, Bruce L. [6 ,7 ]
Milligan, William D. [8 ]
机构
[1] Childrens Natl Hosp, Washington, DC 20010 USA
[2] OmniaBio Inc, Toronto, ON, Canada
[3] Catalent Pharma Solut, Gosselies, Hainaut, Belgium
[4] Lonza Biol Inc, Houston, TX USA
[5] Ctr Breakthrough Med, King Of Prussia, PA USA
[6] Univ Penn, Perelman Sch Med, Ctr Cellular Immunotherapies, Philadelphia, PA USA
[7] Univ Penn, Perelman Sch Med, Dept Pathol & Lab Med, Philadelphia, PA USA
[8] Steminent Biotherapeut Inc, Vancouver, BC, Canada
关键词
cell manufacturing; commercialization; process development; technology transfer;
D O I
10.1016/j.jcyt.2024.03.002
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Background aims: 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. Methods: 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. Results and Conclusions: Here, we 'll analyze the considerations discussed by the panel and elaborate on other factors crucial for CGT development. (c) 2024 International Society for Cell & Gene Therapy. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:656 / 659
页数:4
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