J Clin Pharmacol
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     

Sign In to gain access to subscriptions and/or personal tools.
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Request Reprints
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Web of Science (33)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Randinitis, E. J.
Right arrow Articles by Bockbrader, H. N.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Randinitis, E. J.
Right arrow Articles by Bockbrader, H. N.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?

PHARMACOKINETICS AND PHARMACODYNAMICS

Pharmacokinetics of Pregabalin in Subjects with Various Degrees of Renal Function

Edward J. Randinitis, PhD, Edward L. Posvar, MD, MPH, FCP, Christine W. Alvey, BS, Allen J. Sedman, MD, PhD, Jack A. Cook, PhD and Howard N. Bockbrader, PhD

From the Clinical Sciences Department, Pfizer Global Research and Development, Ann Arbor, Michigan. Dr. Posvar's current affiliation is the Scott and White Clinic, Temple, Texas.

The objectives of this study were to determine the single-dose pharmacokinetics of pregabalin in subjects with various degrees of renal function, determine the relationship between pregabalin clearance and estimated creatinine clearance (CLcr), and measure the effect of hemodialysis on plasma levels of pregabalin. Results form the basis of recommended pregabalin dosing regimens in patients with decreased renal function. Thirty-eight subjects were enrolled to ensure a wide range of renal function (CLcr < 30 mL/min, n = 8; 30-50, n =5; 50-80, n =7; and > 80, n = 6). Also enrolled were 12 subjects with renal impairment requiring hemodialysis. Each subject received 50 mg of pregabalin as two 25-mg capsules in this open-label, parallel-group study. Pregabalin concentrations were measured using previously validated liquid chromatographic methods. Pregabalin pharmacokinetic parameters were evaluated by established noncompartmental methods. Pregabalin was rapidly absorbed in all subjects. Total and renal pregabalin clearance were proportional (56% and 58%, respectively) to CLcr. As a result, area under the plasma concentration-time profile (AUC) and terminal elimination half-life (t1/2) values increased with decreasing renal function. Pregabalin dosage adjustment should be considered for patients with CLcr < 60 mL/min. A 50% reduction in pregabalin daily dose is recommended for patients with CLcr between 30 and 60 mL/min compared to those with CLcr > 60 mL/min. Daily doses should be further reduced by approximately 50% for each additional 50% decrease in CLcr. Pregabalin was highly cleared by hemodialysis. Supplemental pregabalin doses may be required for patients on chronic hemodialysis treatment after each hemodialysis treatment to maintain steady-state plasma pregabalin concentrations within desired ranges.


Address for reprints: Jack A. Cook, PhD, Pfizer Global Research and Development, 2800 Plymouth Road, Ann Arbor, MI 48105.


Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter    What's this?


This article has been cited by other articles:


Home page
Anesth. Analg.Home page
P. F. White, B. Tufanogullari, J. Taylor, and K. Klein
The Effect of Pregabalin on Preoperative Anxiety and Sedation Levels: A Dose-Ranging Study
Anesth. Analg., April 1, 2009; 108(4): 1140 - 1145.
[Abstract] [Full Text] [PDF]


Home page
Anesth. Analg.Home page
N. M. Gajraj
Pregabalin: Its Pharmacology and Use in Pain Management
Anesth. Analg., December 1, 2007; 105(6): 1805 - 1815.
[Abstract] [Full Text] [PDF]


Home page
Am J Health Syst PharmHome page
M. L. Blommel and A. L. Blommel
Pregabalin: An antiepileptic agent useful for neuropathic pain
Am. J. Health Syst. Pharm., July 15, 2007; 64(14): 1475 - 1482.
[Abstract] [Full Text] [PDF]


Home page
The Annals of PharmacotherapyHome page
B. F Shneker and J. W McAuley
Pregabalin: A New Neuromodulator with Broad Therapeutic Indications
Ann. Pharmacother., December 1, 2005; 39(12): 2029 - 2037.
[Abstract] [Full Text] [PDF]


Home page
Arch Gen PsychiatryHome page
K. Rickels, M. H. Pollack, D. E. Feltner, R. B. Lydiard, D. L. Zimbroff, R. J. Bielski, K. Tobias, J. D. Brock, G. L. Zornberg, and A. C. Pande
Pregabalin for Treatment of Generalized Anxiety Disorder: A 4-Week, Multicenter, Double-blind, Placebo-Controlled Trial of Pregabalin and Alprazolam
Arch Gen Psychiatry, September 1, 2005; 62(9): 1022 - 1030.
[Abstract] [Full Text] [PDF]


Home page
J. Pharmacol. Exp. Ther.Home page
T. Z. Su, M. R. Feng, and M. L. Weber
Mediation of Highly Concentrative Uptake of Pregabalin by L-Type Amino Acid Transport in Chinese Hamster Ovary and Caco-2 Cells
J. Pharmacol. Exp. Ther., June 1, 2005; 313(3): 1406 - 1415.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2003 by the American College of Clinical Pharmacology