Home LiteratureArticle Details
PMID: 12814957 Published · ppublish English Guideline Journal Article

The conduct of in vitro and in vivo drug-drug interaction studies: a Pharmaceutical Research and Manufacturers of America (PhRMA) perspective.

Drug metabolism and disposition: the biological fate of chemicals ·Vol. 31 ·No. 7 ·2003-07-00 ·Pages 815-32

Bjornsson TD, Callaghan JT, Einolf HJ, Fischer V, Gan L, Grimm S, Kao J, King SP, Miwa G, Ni L, Kumar G, McLeod J, Obach RS, Roberts S, Roe A, Shah A, Snikeris F, Sullivan JT, Tweedie D, Vega JM, Walsh J, Wrighton SA, Pharmaceutical Research and Manufacturers of America PhRMA Drug Metabolism/Clinical Pharmacology Technical Working Group, FDA Center for Drug Evaluation and Research CDER

Abstract

Current regulatory guidances do not address specific study designs for in vitro and in vivo drug-drug interaction studies. There is a common desire by regulatory authorities and by industry sponsors to harmonize approaches, to allow for a better assessment of the significance of findings across different studies and drugs. There is also a growing consensus for the standardization of cytochrome P450 (P450) probe substrates, inhibitors and inducers and for the development of classification systems to improve the communication of risk to health care providers and to patients. While existing guidances cover mainly P450-mediated drug interactions, the importance of other mechanisms, such as transporters, has been recognized more recently, and should also be addressed. This article was prepared by the Pharmaceutical Research and Manufacturers of America (PhRMA) Drug Metabolism and Clinical Pharmacology Technical Working Groups and represents the current industry position. The intent is to define a minimal best practice for in vitro and in vivo pharmacokinetic drug-drug interaction studies targeted to development (not discovery support) and to define a data package that can be expected by regulatory agencies in compound registration dossiers.

MeSH Terms
Cytochrome P-450 Enzyme System/classification,metabolism Drug Industry Drug Interactions Research Design
Chemicals
Cytochrome P-450 Enzyme System
Authors & Affiliations
24 authors, click to expand affiliations / ORCID
Bjornsson Thorir D
Wyeth, Collegeville, Pennsylvania, USA.
Callaghan John T
Einolf Heidi J
Fischer Volker
Gan Lawrence
Grimm Scott
Kao John
King S Peter
Miwa Gerald
Ni Lan
Kumar Gondi
McLeod James
Obach R Scott
Roberts Stanley
Roe Amy
Shah Anita
Snikeris Fred
Sullivan John T
Tweedie Donald
Vega Jose M
Walsh John
Wrighton Steven A
Pharmaceutical Research and Manufacturers of America (PhRMA) Drug Metabolism/Clinical Pharmacology Technical Working Group
FDA Center for Drug Evaluation and Research (CDER)
Article Info
Journal
Drug metabolism and disposition: the biological fate of chemicals
Abbr.
Drug Metab Dispos
ISSN
0090-9556
Published
2003-07-00
Pages
815-32
Language
English
Region
United States
NLM ID
9421550
Subset
IM
Corrections
CommentIn
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com