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A bosentan pharmacokinetic study to investigate dosing regimens in paediatric patients with pulmonary arterial hypertension: FUTURE‐3
Author(s) -
Berger Rolf M. F.,
Gehin Martine,
Beghetti Maurice,
Ivy Dunbar,
KusicPajic Andjela,
Cornelisse Peter,
Grill Simon,
Bonnet Damien
Publication year - 2017
Publication title -
british journal of clinical pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.216
H-Index - 146
eISSN - 1365-2125
pISSN - 0306-5251
DOI - 10.1111/bcp.13267
Subject(s) - bosentan , pharmacokinetics , confidence interval , medicine , dosing , geometric mean , urology , gastroenterology , endothelin receptor , mathematics , receptor , statistics
Aim The aim of the present study was to investigate whether increasing the bosentan dosing frequency from 2 mg kg –1 twice daily (b.i.d.) to 2 mg kg –1 three times daily (t.i.d.) in children with pulmonary arterial hypertension (PAH) (from ≥3 months to <12 years of age) would increase exposure. Methods An open‐label, prospective, randomized, multicentre, multiple‐dose, phase III study was conducted. Patients ( n = 64) were randomized 1:1 to receive oral doses of bosentan of 2 mg kg –1 b.i.d. or t.i.d. The main pharmacokinetic endpoint was the daily exposure to bosentan over 24 h corrected to the 2 mg kg –1 dose (AUC 0–24C ). The maximum plasma concentration corrected to the 2 mg kg –1 dose (C maxC ), the time to reach the maximum plasma concentration (t max ) and safety endpoints were also assessed. Results The geometric mean [95% confidence interval (CI)] for AUC 0–24C was 8535 h.ng ml –1 (6936, 10 504) and 7275 h.ng ml –1 (5468, 9679) for 2 mg kg –1 b.i.d. and t.i.d., respectively [geometric mean ratio (95% CI) 0.85 (0.61, 1.20)]. The geometric mean (95% CI) for C maxC was 743 ng ml –1 (573, 963) and 528 ng ml –1 (386, 722) for 2 mg kg –1 b.i.d. and t.i.d., respectively [geometric mean ratio (95% CI) 0.71 (0.48, 1.05)]. The median (range) for t max was 3.0 h (0.0–7.5) and 3.0 h (1.0–8.0) for 2 mg kg –1 b.i.d. and t.i.d., respectively. The proportions of patients who experienced ≥1 adverse event were similar in the b.i.d. (66.7%) and t.i.d. (67.7%) groups. Conclusions There appeared to be no clinically relevant difference in exposure to bosentan, or in safety, when increasing the frequency of bosentan dosing from b.i.d. to t.i.d. Therefore, the present study provides no indication that the dosing recommendation should be changed, and 2 mg kg –1 b.i.d. remains the recommended dosing regimen for bosentan in paediatric PAH patients.