Premium
Drug Development Perspective on Pharmacokinetic Studies of New Drugs in Patients With Renal Impairment
Author(s) -
Lalonde RL,
Wagner JA
Publication year - 2009
Publication title -
clinical pharmacology and therapeutics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.941
H-Index - 188
eISSN - 1532-6535
pISSN - 0009-9236
DOI - 10.1038/clpt.2009.182
Subject(s) - clinical pharmacology , medicine , pharmacokinetics , dosing , confusion , pharmacology , intensive care medicine , drug , drug development , renal physiology , clinical trial , population , renal function , psychology , environmental health , psychoanalysis
Severe renal impairment can, through diverse mechanisms, alter the pharmacokinetics (PK) of drugs that are renally eliminated and even of some drugs that are nonrenally eliminated. Consequently, dose adjustment for new molecular entities in patients with renal insufficiency is a critical issue in drug development. Clinical pharmacology studies undertaken in patients with renal impairment are generally quite small. We therefore recommend that all pertinent pharmacokinetic data relating to subjects with different degrees of renal impairment and from different clinical trials, including population pharmacokinetic evaluation, form the basis for dosage recommendations in renal impairment. The Modification of Diet in Renal Disease (MDRD) equation has gained popularity for renal insufficiency classification, but traditional equations such as the Cockcroft–Gault (C–G) formula should enjoy continued use so as to avoid confusion, particularly for drugs for which dosing guidelines have previously been developed. Clinical Pharmacology & Therapeutics (2009) 86 5, 557–561. doi: 10.1038/clpt.2009.182