Cell-Based Therapies Formulations: Unintended components
- PMID: 27233803
- PMCID: PMC8277633
- DOI: 10.1208/s12248-016-9935-9
Cell-Based Therapies Formulations: Unintended components
Erratum in
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Correction to: Cell-Based Therapies Formulations: Unintended Components.AAPS J. 2022 Aug 30;24(5):95. doi: 10.1208/s12248-022-00747-5. AAPS J. 2022. PMID: 36125582 Free PMC article. No abstract available.
Abstract
Cell-based therapy is the fastest growing segment of regenerative medicine, a field that promises to cure diseases not treated by other small molecules or biological drugs. The use of living cells as the active medicinal ingredient present great opportunities to deliver treatment that can trigger the body's own capacity to regenerate damaged or diseased tissue. Some of the challenges in controlling the quality of the finished cell-therapy product relate to the use of a variety of raw materials including excipients, process aids, and growth promotion factors. The quality of these materials is critical for ensuring the safety and quality of the finished therapeutic products. This review will discuss some of the challenges and opportunities associated with the qualification of excipients as well as that of the ancillary materials used in manufacturing.
Keywords: ancillary material; cell-based therapy; excipient; formulation.
Comment on
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Bovine apolipoprotein B-100 is a dominant immunogen in therapeutic cell populations cultured in fetal calf serum in mice and humans.Blood. 2007 Jul 15;110(2):501-8. doi: 10.1182/blood-2007-01-066522. Epub 2007 Mar 29. Blood. 2007. PMID: 17395779 Free PMC article.
References
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- <1043> Ancillary materials for cell, gene, and tissue engineered products. In: USP38-NF33. Rockville, MD: US Pharmacopeial Convention; 2016:896.
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- Guidance for FDA Reviewers and Sponsors: Content and Review of Chemistry, Manufacturing, and Control (CMC) Information for Human Somatic Cell Therapy Investigational New Drug Applications (INDs), April 2008. Available at the Food and Drug Administration Web site. http://www.fda.gov, Accessed April 28, 2016
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- Guidance for industry: nonclinical studies for the safety evaluation of pharmaceutical excipients, May 2005. Available at the Food and Drug Administration Web site. http://www.fda.gov, Accessed April 28, 2016
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- International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH) Q8 Pharmaceutical Development (R2), August 2009. Available at the ICH website: http://www.ich.org, Accessed April 28, 2016
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