Towards the development of a paediatric biopharmaceutics classification system: Results of a survey of experts

被引:14
作者
Batchelor, Hannah [1 ]
Ernest, Terry [2 ]
Flanagan, Talia [3 ]
Klein, Sandra [4 ]
Turner, Roy [5 ]
Fotaki, Nikoletta [6 ]
Storey, David [7 ]
机构
[1] Inst Clin Sci, Sch Pharm, Robert Aitken Bldg, Edgbaston B15 2TT, W Midlands, England
[2] GlaxoSmithKline, New Frontiers Sci Pk,Third Ave, Harlow CM19 5AW, Essex, England
[3] AstraZeneca R&D, Pharmaceut Dev, Macclesfield, Cheshire, England
[4] Ernst Moritz Arndt Univ Greifswald, Dept Pharm, Greifswald, Germany
[5] Novartis Pharma AG, Basel, Switzerland
[6] Univ Bath, Dept Pharm & Pharmacol, Bath, Avon, England
[7] MSD, Pharmaceut Sci, Hoddesdon, England
关键词
Survey; Paediatric; Biopharmaceutics; Solubility; Dissolution; Permeability; BCS; NATIONAL INSTITUTE; CHILD HEALTH; WORKSHOP;
D O I
10.1016/j.ijpharm.2016.06.115
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The aim of this research survey was to understand current global thinking around the need for and development of a paediatric biopharmaceutics classification system (pBCS) to be used for the development of paediatric medicines and regulatory purposes (e.g. Biowaivers). A literature review highlighted the paucity of data in this area and therefore a survey was developed to better understand this topic to identify areas of common thinking and highlight future research needs. Global experts in paediatric biopharmaceutics were identified from existing networks and public forums. An online survey was developed and circulated broadly to maximise participation. Sixty individuals (including academics, health care professionals, pharmaceutical industry scientists and regulators) completed the survey, bringing together their views on the need for a pBCS. The results highlighted that the area of greatest concern was the definition, of BCS II and IV drugs within this population and additional research is required to generate evidence to underpin this issue. In questions relating to permeability and dissolution consensus was generally reached within the expert population suggesting that little additional research is required to define suitable criteria. More than 90% of those experts who participated agreed that a pBCS would be useful for paediatric populations with a greater need identified for the younger populations (newborn and infants compared to adolescents). The results presented will facilitate further discussion and research into the evidence to underpin a relevant pBCS. These results highlight the need for additional evidence and guidance in this area. (C) 2016 Published by Elsevier B.V.
引用
收藏
页码:1151 / 1157
页数:7
相关论文
共 25 条
[1]   Summary of the National Institute of Child Health and Human Development-Best Pharmaceuticals for Children Act Pediatric Formulation Initiatives Workshop-Pediatric Biopharmaceutics Classification System Working Group [J].
Abdel-Rahman, Susan M. ;
Amidon, Gordon L. ;
Kaul, Ajay ;
Lukacova, Viera ;
Vinks, Alexander A. ;
Knipp, Gregory T. .
CLINICAL THERAPEUTICS, 2012, 34 (11) :S11-S24
[2]   A THEORETICAL BASIS FOR A BIOPHARMACEUTIC DRUG CLASSIFICATION - THE CORRELATION OF IN-VITRO DRUG PRODUCT DISSOLUTION AND IN-VIVO BIOAVAILABILITY [J].
AMIDON, GL ;
LENNERNAS, H ;
SHAH, VP ;
CRISON, JR .
PHARMACEUTICAL RESEARCH, 1995, 12 (03) :413-420
[3]  
[Anonymous], 2015, Draft Guidance. Guidance for industry: waiver of in vivo bioavailability and bioequivalence studies for immediate-release solid oral dosage forms based on a biopharmaceutics classification system
[4]  
[Anonymous], 2002, Ann. ICRP, DOI DOI 10.1016/S0146-6453(03)00002-2
[5]  
Batchelor H. K., 2012, EUPFI ANN M PRAG
[6]  
Batchelor H.K., 2013, EUPFI ANN M BARC
[7]   Paediatric biopharmaceutics classification system: Current status and future decisions [J].
Batchelor, Hannah .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2014, 469 (02) :251-253
[8]   Paediatric oral biopharmaceutics: Key considerations and current challenges [J].
Batchelor, Hannah K. ;
Fotaki, Nikoletta ;
Klein, Sandra .
ADVANCED DRUG DELIVERY REVIEWS, 2014, 73 :102-126
[9]   Application of in vitro biopharmaceutical methods in development of immediate release oral dosage forms intended for paediatric patients [J].
Batchelor, Hannah K. ;
Kendall, Richard ;
Desset-Brethes, Sabine ;
Alex, Rainer ;
Ernest, Terry B. .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2013, 85 (03) :833-842
[10]  
CHMP, 2006, REFL PAP FORM CHOIC