| Literature DB >> 26886324 |
Joseph Kotarek1, Christine Stuart1, Silvia H De Paoli1, Jan Simak1, Tsai-Lien Lin2, Yamei Gao3, Mikhail Ovanesov1, Yideng Liang1, Dorothy Scott1, Janice Brown4, Yun Bai5, Dean D Metcalfe5, Ewa Marszal6, Jack A Ragheb7.
Abstract
Peginesatide (Omontys(®); Affymax, Inc., Cupertino, CA) was voluntarily withdrawn from the market less than a year after the product launch. Although clinical trials had demonstrated the drug to be safe and efficacious, 49 cases of anaphylaxis, including 7 fatalities, were reported not long after market introduction. Commercialization was initiated with a multiuse vial presentation, which differs in formulation from the single-use vial presentation used in phase 3 studies. Standard physical and chemical testing did not indicate any deviation from product specifications in either formulation. However, an analysis of subvisible particulates using nanoparticle tracking analysis and flow imaging revealed a significantly higher concentration of subvisible particles in the multiuse vial presentation linked to the hypersensitivity cases. Although it is unknown whether the elevated particulate content is causally related to these serious adverse events, this report illustrates the utility of characterizing subvisible particulates not captured by conventional light obscuration.Entities:
Keywords: formulation; particle sizing; peptides; protein aggregation
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Year: 2016 PMID: 26886324 DOI: 10.1016/S0022-3549(15)00180-X
Source DB: PubMed Journal: J Pharm Sci ISSN: 0022-3549 Impact factor: 3.534