Back to Search Start Over

Pharmacokinetics and Safety of a Single Dose and Multiple Doses of Allisartan Isoproxil, an Angiotensin II Receptor Blocker, in Healthy Chinese People.

Authors :
Yi W
Yan P
Lin S
Hao R
Wang Y
Yu J
Fang L
Zhu J
Zhao D
Tong S
Si Y
Ye T
Wu Z
Qin Z
Huang H
Deng C
Sun J
Wang Y
Source :
Clinical pharmacology in drug development [Clin Pharmacol Drug Dev] 2022 Jan; Vol. 11 (1), pp. 43-50. Date of Electronic Publication: 2021 Jul 08.
Publication Year :
2022

Abstract

Allisartan isoproxil (AI) is a blocker of the angiotensin II type 1 receptor. We evaluated the safety and pharmacokinetics of single- and multiple-dose AI in healthy Chinese individuals. Participants were assigned to receive AI or placebo. Plasma concentration of EXP3174 (carboxylic acid derivative) was measured using liquid chromatography-tandem mass spectrometry. Pharmacokinetic parameters were determined by noncompartmental methods. Twelve subjects were enrolled, and the ratio of men to women was 5:1. Main pharmacokinetic parameters of EXP3174 after single and multiple doses of AI were a mean maximum concentration in plasma (C <subscript>max</subscript> ) of 2242 ± 1037 ng/mL and median time to reach C <subscript>max</subscript> (T <subscript>max</subscript> ) of 3.5 hours (2.5-8 hours). The median T <subscript>max,</subscript> at steady state was 4.0 hours (1.5-8 hours). The mean C <subscript>max</subscript> at steady state (C <subscript>max, SS</subscript> ) was 2047 ± 1050 ng/mL. In terms of EXP3174, there was no significant difference in the C <subscript>max, SS</subscript> , area under the curve from time zero to 24 hours of quantifiable concentration at steady state (AUC <subscript>0-24 SS</subscript> ), and AUC <subscript>0-72</subscript> after multiple doses of AI. Serious adverse events did not occur. These data suggest that AI is safe and well tolerated in healthy Chinese individuals at a single dose of 480 or 480 mg once daily for 7 days.<br /> (© 2021, The American College of Clinical Pharmacology.)

Details

Language :
English
ISSN :
2160-7648
Volume :
11
Issue :
1
Database :
MEDLINE
Journal :
Clinical pharmacology in drug development
Publication Type :
Academic Journal
Accession number :
34240572
Full Text :
https://doi.org/10.1002/cpdd.995