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Commentary on the EMA reflection paper on the pharmaceutical development of medicines for use in the older population
DA. van Riet-Nales, B. van den Bemt, D. van Bodegom, F. Cerreta, B. Dooley, D. Eggenschwyler, B. Hirschlérova, PAF. Jansen, F. Karapinar-Çarkit, A. Moran, J. Span, S. Stegemann, K. Sundberg
Jazyk angličtina Země Velká Británie
Typ dokumentu časopisecké články, práce podpořená grantem
NLK
Europe PubMed Central
od 1974 do Před 1 rokem
Wiley Free Content
od 1997 do Před 1 rokem
PubMed
35141926
DOI
10.1111/bcp.15207
Knihovny.cz E-zdroje
- MeSH
- farmaceutický průmysl * MeSH
- léčivé přípravky MeSH
- lidé MeSH
- multimorbidita MeSH
- polypharmacy * MeSH
- senioři MeSH
- vyvíjení léků MeSH
- Check Tag
- lidé MeSH
- senioři MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
Older people are often affected by impaired organ and bodily functions resulting in multimorbidity and polypharmacy, turning them into the main user group of many medicines. Very often, medicines have not specifically been developed for older people, causing practical medication problems for them like limited availability of easy to swallow formulations, easy to open packaging and dosing instructions for enteral administration. In 2020, the European Medicines Agency (EMA) published a reflection paper 'Pharmaceutical development of medicines for use in the older population', which discusses how the emerging needs of an ageing European population can be addressed by medicines regulation. The paper intends to help industry to better consider the needs of older people during pharmaceutical/clinical medicines development by summarising data on the most relevant topics, providing early suggestions on how to move forward and prompting expert discussions and studies into knowledge gaps. Topics include patient acceptability, (dis)advantages of an administration route, formulation, dosage form, packaging, dosing device and user instruction. While the paper is directed at older people and the pharmaceutical industry, the reflections are also relevant to younger patients with similar disease-related needs and of value to other stakeholders parties, e.g., healthcare professionals, academics, patients and caregivers, as the paper makes clear what can be expected from industry and where collaborative work is needed. This commentary provides an overview of the different steps in the development of the reflection paper, discusses points considered most controversial and/or subject to (multidisciplinary) expert discussions and indicates their value for real world clinical practice.
Department of Chemical Pharmaceutical Assessments Medicines Evaluation Board Utrecht Netherlands
Department of Clinical Pharmacy OLVG Hospital Amsterdam Netherlands
Department of Pharmaceutics and Biotechnology Swedish Medical Products Agency Uppsala Sweden
Department of Pharmacy Radboud University Medical Center Nijmegen Netherlands
Department of Pharmacy Sint Maartenskliniek Ubbergen Netherlands
Department Public Health and Primary Care Leiden University Medical Centre Leiden Netherlands
Expertise Centre Pharmacotherapy in Old Persons Utrecht Netherlands
Geriatric Department University Medical Center Utrecht Netherlands
Institute of Process and Particle Engineering Graz University of Technology Graz Austria
Medicines and Healthcare Products Regulatory Agency London UK
Public Health and Primary Care Leyden Academy on Vitality and Ageing Leiden Netherlands
Citace poskytuje Crossref.org
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