Thorough QT study of the effect of intravenous amisulpride on QTc interval in Caucasian and Japanese healthy subjects

被引:39
|
作者
Taubel, Jorg [1 ,4 ]
Ferber, Georg [2 ]
Fox, Gabriel [3 ]
Fernandes, Sara [1 ]
Lorch, Ulrike [1 ]
Camm, A. John [4 ]
机构
[1] St Georges Univ London, Richmond Pharmacol Ltd, Cranmer Terrace, London SW17 0RE, England
[2] Stat Georg Ferber GmbH, Cagliostrostr, Riehen, Switzerland
[3] Acacia Pharma Ltd, Cambridge, England
[4] St Georges Univ London, Cardiovasc & Cell Sci Res Inst, London, England
关键词
amisulpride; Thorough QT study; QTc interval; TORSADE-DE-POINTES; PLASMA AMISULPRIDE; CHANNEL VARIANTS; SODIUM-CHANNEL; CONCISE GUIDE; SCHIZOPHRENIA; PROLONGATION; PHARMACOLOGY; HERG; ANTIPSYCHOTICS;
D O I
10.1111/bcp.13128
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
AIM The D-2/D-3 antagonist amisulpride has shown promising efficacy against postoperative nausea and vomiting (PONV) at low doses. We investigated whether intravenous amisulpride has an effect on the QTc interval in a formal Thorough QT study (TQT). METHODS This was a randomized, double-blind, placebo and positive-controlled, four-way crossover study. Forty healthy Caucasian and Japanese subjects were included to receive a single administration of 5 mg and 40 mg of i.v. amisulpride or a single oral dose of moxifloxacin or placebo per period. RESULTS The therapeutic dose of 5 mg amisulpride was associated with a slight, transient increase in mean Delta Delta QTcF, from 2.0 ms prior to dosing to a peak of 5ms (90% CI: 2.8, 7.1 ms) at 8 min, decreasing to 2.1 ms at 30 min after dosing. The supra-therapeutic dose of 40 mg given at twice the infusion rate was associated with prolongation in Delta Delta QTcF peaking at 23.4 ms (90% CI: 21.3, 25.5 ms) at the end of infusion (8 min), returning below 10 ms within 1.5 h. Assay sensitivity was confirmed; Delta Delta QTcF had increased by 12.3 ms (90% CI 10.1, 14.6 ms) at 4 h post-dose. The PK-PD relationship revealed no differences between Caucasian and Japanese subjects (p-value > 0.5). CONCLUSIONS Amisulpride has a plasma concentration-dependent effect on the QTc interval. The proposed therapeutic dose for management of PONV does not lead to a prolongation of QTcF above the threshold of regulatory concern, while such effect could not be excluded for the supratherapeutic dose.
引用
收藏
页码:339 / 348
页数:10
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