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. 2017 Dec 6;18(12):2636. doi: 10.3390/ijms18122636
AE adverse event
AUC0–24 area under the plasma drug concentration-time curve from 0 to 24 h
AUC0–∞ area under the plasma drug concentration-time curve from 0 to infinity
AUC area under the plasma drug concentration-time curve
AUEC area under the effect-time curve
CI confidence interval
CL/F apparent oral clearance
Cmax maximum plasma concentration
Emax maximum effect
ECG electrocardiogram
EDTA ethylene di-amine tetra acetic acid
FEV1 forced expiratory volume in 1 s
FVC forced vital capacity
HR heart rate
LS least squares
o.d. once daily
PD pharmacodynamics
PK pharmacokinetics
S1P sphingosine-1-phosphate
S1P1R S1P1 receptor
SD standard deviation
t1/2 terminal half-life
tmax time to reach maximum concentration
Vss/F apparent volume of distribution at steady-state