When will we have a clone? An industry perspective on the typical CLD timeline

Author:

Clarke Howard1ORCID,Mayer‐Bartschmid Anke2,Zheng Chenxing3,Masterjohn Elizabeth4,Patel Falguni5,Moffat Mark6,Wei Qingxiang3,Liu Ren7ORCID,Emmins Robyn8,Fischer Simon9ORCID,Rieder Stephanie5,Kelly Thomas10

Affiliation:

1. Seagen Inc. Cell Line Development Bothell Washington USA

2. Bayer AG Biologics Development Wuppertal Germany

3. Incyte Corporation Cell Line Development Wilmington Delaware USA

4. Sanofi Cell Line Development Framingham Massachusetts USA

5. AbbVie Inc. S&T Biologics Development & Launch Worcester Massachusetts USA

6. Pfizer Cell Line Development Chesterfield Missouri USA

7. Merck & Co., Inc. Process Cell Sciences Rahway New Jersey USA

8. GSK Medicines and Research Centre Cell Line Development Stevenage UK

9. Boehringer Ingelheim Pharma GmbH & Co. KG Cell Line Development Biberach Germany

10. Janssen R&D Cell Engineering & Analytical Sciences Spring House Pennsylvania USA

Abstract

AbstractCell line development (CLD) represents a complex but highly critical process during the development of a biological drug. To shed light on this crucial workflow, a team of BioPhorum members (authors) has developed and executed surveys focused on the activities and effort involved in a typical CLD campaign. An average of 27 members from different companies that participate in the BioPhorum CLD working group answered surveys covering three distinguishable stages of a standard CLD process: (1) Pre‐transfection, including vector design and construction; (2) Transfection, spanning the initial introduction of vector into cells and subsequent selection and analysis of the pools; and (3) Single Cell Cloning and Lead Clone Selection, comprising methods of isolating single cells and confirming clonal origin, subsequent expansion and screening processes, and methods for identifying and banking lead clones. The surveys were very extensive, including a total of 341 questions split between antibody and complex molecule CLD processes. In this survey review, the authors interpret and highlight responses for antibody development and, where relevant, contrast complex molecule development challenges to provide a comprehensive industry perspective on the typical time and effort required to develop a CHO production cell line.

Publisher

Wiley

Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3