首页 | 本学科首页   官方微博 | 高级检索  
     


Pharmacokinetic-pharmacodynamic (PK-PD) modeling for a new antihypertensive agent (neutral metalloendopeptidase inhibitor SCH 42354) in patients with mild to moderate hypertension
Authors:Scott H. Fettner  S. Pai  V. Batra  G.-R. Zhu  T. Kosoglou  C. R. Banfield
Affiliation:(1) Department of Drug Metabolism and Pharmacokinetics, Schering-Plough Research Institute, 2015 Galloping Hill Road, K-15-2 (Mailstop 2650), 07033-0530 Kenilworth, NJ, USA;(2) Department of Biostatistics, Schering-Plough Research Institute, 2015 Galloping Hill Road, 07033-0530 Kenilworth, NJ, USA;(3) Department of Clinical Pharmacology, Schering-Plough Research Institute, 2015 Galloping Hill Road, 07033-0530 Kenilworth, NJ, USA;(4) Present address: Center for Drug Evaluation and Research, Food and Drug Administration, 5600 Fishers Lane, 20857 Rockville, MD, USA
Abstract:SCH 42354, a neutral metalloendopeptidase (NEP) inhibitor, is the pharmacologically active form of the prodrug SCH 42495. It exerts antihypertensive effects by potentiating atrial natriuretic peptide (ANP) activity through inhibition of its hydrolysis by NEP. The objective of this study was to characterize the pharmacokinetics (PK) and pharmacodynamics (PD) of SCH 42354 in hypertensive males. SCH 42495 12.5 to 400 mg was administered orally to hypertensive men twice daily in a double-blind, placebo controlled multiple-dose parallel group design. Plasma SCH 42354 concentration and diastolic blood pressure (DBP) data were used to develop a PK-PD model using two approaches. In the first (non-integrated) approach, the ldquolinkrdquo model was used to predict effect-site concentrations, and was applied to data obtained at the 300 and 400 mg BID doses only; data at the other (lower) doses were not amenable to modeling because of high variability. Effect-site concentration and DBP data were then fit to a sigmoid Emax PD model. For the 300 mg BID dose, PD parameters were: maximum effect (Emax), 8.1mmHg; no-drug effect (Eo), 3.6 mmHg; concentration corresponding to 50% of maximum response (EC50), 0.87 mgrg·ml–1; and gamma, 3.9. In the second (time-integrated) approach, plasma SCH 42354 concentration and effect data obtained over the entire dose range were integrated with respect to time. Average plasma concentration and DBP data were then fit to a simple Emax PD model. PD parameters obtained over the dose range were: Emax, 10.3 mmHg; Eo, 2.0 mmHg; and EC50, 0.7 mgrg·ml–1. These were similar to the estimates obtained from the first approach, demonstrating that the integrated (average) data allow PK-PD modeling over the (entire) dose range. The analysis showed that, at steady-state, a 400 mg BID dose of SCH 42495 produced an approximate 10 mmHg decrease in DBP in hypertensive males; the average plasma SCH 42354 concentration attained at this dose was approximately 1.8 mgrg·ml–1.
Keywords:Atrial natriuretic peptide  Hypertension  SCH 42354  blood pressure  neutral metalloendopeptidase  pharmacodynamics  pharmacokinetics
本文献已被 SpringerLink 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号