Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8513445 | Journal of Pharmaceutical Sciences | 2018 | 62 Pages |
Abstract
The Biophorum Development Group (BPDG) is an industry-wide consortium enabling networking and sharing of best practices for the development of biopharmaceuticals. To gain a better understanding of current industry approaches for establishing biopharmaceutical drug product (DP) robustness, the BPDG-Formulation Point Share group conducted an intercompany collaboration exercise, which included a bench-marking survey and extensive group discussions around the scope, design, and execution of robustness studies. The results of this industry collaboration revealed several key common themes: (1) overall DP robustness is defined by both the formulation and the manufacturing process robustness; (2) robustness integrates the principles of quality by design (QbD); (3) DP robustness is an important factor in setting critical quality attribute control strategies and commercial specifications; (4) most companies employ robustness studies, along with prior knowledge, risk assessments, and statistics, to develop the DP design space; (5) studies are tailored to commercial development needs and the practices of each company. Three case studies further illustrate how a robustness study design for a biopharmaceutical DP balances experimental complexity, statistical power, scientific understanding, and risk assessment to provide the desired product and process knowledge. The BPDG-Formulation Point Share discusses identified industry challenges with regard to biopharmaceutical DP robustness and presents some recommendations for best practices.
Keywords
QTPPCQABLAIEXSECTPPBiopharmaceuticalGMPDOECPPmAbFMEAQbDFDAPCPPPFsMonoclonal antibodyGood Manufacturing PracticeFailure modes and effects analysisIntravenousRelative humiditysubcutaneousFood and Drug AdministrationPrefilled syringeDesign of experimentsManufacturing processFormulationDesign spacetarget product profilequality target product profileICHDrug productRobustnessCritical quality attributecritical process parameterSize exclusion chromatographyhigh performance liquid chromatographyHPLCIon exchange chromatographyInternational Conference on HarmonisationQuality by design
Related Topics
Health Sciences
Pharmacology, Toxicology and Pharmaceutical Science
Drug Discovery
Authors
Sorina Morar-Mitrica, Monica L. Adams, George Crotts, Christine Wurth, Peter M. Ihnat, Tanvir Tabish, Valentyn Antochshuk, Willow DiLuzio, Daniel B. Dix, Jason E. Fernandez, Kapil Gupta, Michael S. Fleming, Bing He, James K. Kranz, Dingjiang Liu,