|
|
||||||||
Sign In to gain access to subscriptions and/or personal tools. |
|||||||||
PHARMACOKINETICS |
From Amylin Pharmaceuticals Inc, San Diego, California.
Exenatide is an incretin mimetic with potential glucoregulatory activity in type 2 diabetes. This randomized, single-blind, placebo-controlled 6-way crossover study assessed exenatide's effect on acetaminophen pharmacokinetics. Of 40 randomized healthy subjects, 39 completed the study. On the placebo day, acetaminophen (1000 mg) was ingested and placebo injected subcutaneously at 0 hours. On exenatide days, acetaminophen was ingested at -1, 0, +1, +2, and +4 hours, relative to the 10 µg exenatide injected subcutaneously at 0 hours. With exenatide injection, mean plasma acetaminophen AUC0-12 h values were reduced by 11% to 24% (vs placebo). Peak plasma acetaminophen concentrations were similar for the -1-hour and placebo groups and reduced by 37% to 56% at other times. The most frequent adverse events were generally mild to moderate nausea and vomiting. Exenatide treatment concurrent with or preceding acetaminophen ingestion slowed acetaminophen absorption but had minimal effect on the extent of absorption.
Key Words: Exenatide exendin-4 type 2 diabetes pharmacokinetics
Address for reprints: Mark Fineman, Amylin Pharmaceuticals Inc, 9360 Towne Centre Drive, Suite 110, San Diego, CA 92121.
This article has been cited by other articles:
![]() |
A. Cervera, E. Wajcberg, A. Sriwijitkamol, M. Fernandez, P. Zuo, C. Triplitt, N. Musi, R. A. DeFronzo, and E. Cersosimo Mechanism of action of exenatide to reduce postprandial hyperglycemia in type 2 diabetes Am J Physiol Endocrinol Metab, May 1, 2008; 294(5): E846 - E852. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. A. Kellmeyer, N. C. Kesty, Y. Wang, J. P. Frias, and M. S. Fineman Pharmacokinetics of an Oral Drug (Acetaminophen) Administered at Various Times Relative to Subcutaneous Injection of Pramlintide in Subjects With Type 2 Diabetes J. Clin. Pharmacol., July 1, 2007; 47(7): 798 - 805. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. Soon, P. A. Kothare, H. Linnebjerg, S. Park, E. Yuen, K. F. Mace, and S. D. Wise Effect of exenatide on the pharmacokinetics and pharmacodynamics of warfarin in healthy asian men. J. Clin. Pharmacol., October 1, 2006; 46(10): 1179 - 1187. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. K. Yoo, D. M. Triller, and D. J. Yoo Exenatide: A New Option for the Treatment of Type 2 Diabetes Ann. Pharmacother., October 1, 2006; 40(10): 1777 - 1784. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. S. Odegard, S. M. Setter, and J. L. Iltz Update in the pharmacologic treatment of diabetes mellitus: focus on pramlintide and exenatide. The Diabetes Educator, September 1, 2006; 32(5): 693 - 712. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. A. Koehler and D. J. Drucker Activation of glucagon-like Peptide-1 receptor signaling does not modify the growth or apoptosis of human pancreatic cancer cells. Diabetes, May 1, 2006; 55(5): 1369 - 1379. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. M. Bray Exenatide Am. J. Health Syst. Pharm., March 1, 2006; 63(5): 411 - 418. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |