Plasma was separated by centrifugation following collection of blood samples in prechilled glass tubes containing dipotassium ethylenediaminetetraacetic acid. Plasma concentrations of omeprazole were measured using a validated liquid chromatography with tandem mass spectrometry method by Frontage Laboratories, Inc. (Malvern, PA, USA). Omeprazole and omeprazole-d3 were extracted from human plasma by protein precipitation using acetonitrile and separated by reversed-phase high-performance liquid chromatography with a Gemini® C6-Phenyl column

(50x 2 mm, 5 μm; Phenomenex, Torrance, CA, USA) and Shimadzu HPLC pump and autosampler (Shimadzu, Kyoto, Japan), with a flow rate BYL719 ic50 of 0.4 mL/min at room temperature and an elution time of 1.4 min. Mobile phase A was 2 mM ammonium formate in H2O and mobile phase B was 2 mm ammonium formate in MeOH. Omeprazole-d3 was used as the internal standard and the reference standard was omeprazole. Ions were monitored for omeprazole at m/z 346.3–198.1 and for omeprazole-d3 at m/z 349.1–198.1 in positive ionization mode using the API4000™ mass spectrometer

with TurboIonSpray electrospray ion source (AB Sciex, Framingham, MA, USA) at 575 °C and 5,500 V with N2. The dynamic range was 1–1,000 ng/mL with a lower limit of quantitation of 1 ng/mL. The assay accuracy (mean determined concentration/nominal concentration) had a range of 93.0–99.8 % (intra-run) and 96.1–98.5 % (inter-run). The assay precision (coefficient of variation of the mean determined Progesterone concentration) had a range of 0.6–3.7 % (intra-run) and 1.5–4.0 % (inter-run). 2.4 Pharmacokinetic Evaluations and Statistical

MK-0457 cell line Methods WinNonlin version 5.0.1 or higher (Pharsight Corporation Inc., Mountain View, CA, USA) was used to derive PK parameters using standard non-compartmental analysis and actual sampling times. The primary PK endpoint for analysis of drug–drug interaction was the area under the plasma concentration-time curve from time 0 to 24 h (AUC0–24) after multiple doses of omeprazole without (day 7) or with IPE at steady-state concentrations (day 25). Secondary PK endpoints included the maximum observed plasma concentration (C max) and the time of occurrence of C max (T max) for omeprazole. Additional endpoints included elimination half-life (t 1/2) and apparent terminal elimination rate constant (K el). Comparisons of the PK parameters for omeprazole without and with IPE included only subjects with values for the primary PK parameters available for omeprazole from both PK sampling days. The intent-to-treat GSK1120212 datasheet population included all subjects who signed the informed consent form and were included in the study. The PK population included all subjects who had available values for the primary omeprazole PK endpoint parameters from days 7 and 25. The safety population included all subjects who received at least one dose of the study drug.