Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Allan Maroli"'
Autor:
Robert M. Day, Osamu Nemoto, Mayumi Komine, Mamitaro Ohtsuki, Allan Maroli, Peng Chen, Yukari Okubo, Rosemary Petric, Shinichi Imafuku
Publikováno v:
The Journal of Dermatology
Apremilast, an oral, small‐molecule phosphodiesterase 4 inhibitor, works intracellularly within immune cells to regulate inflammatory mediators. This phase 2b randomized, placebo‐controlled study evaluated efficacy and safety of apremilast among
Autor:
Shinichi Imafuku, Mayumi Komine, Yukari Okubo, Osamu Nemoto, Mamitaro Ohtsuki, Robert M. Day, Peng Chen, Allan Maroli
Publikováno v:
Journal of Dermatological Science. 86:e8
Publikováno v:
Clinical Pharmacokinetics. 33:39-46
Two phase I trials, each involving 16 healthy adult volunteers, were performed to investigate possible interactions between grepafloxacin and theophylline or warfarin. In the theophylline study, grepafloxacin 600 mg was administered once daily for 10
Autor:
Nathan M. Bass, Steven L. Bramer, Allan Maroli, Erika Wolfe, John F. Flaherty, Constantin Efthymiopoulos, Kenneth A. Somberg
Publikováno v:
Clinical Pharmacokinetics. 33:25-31
The pharmacokinetics of grepafloxacin, a new broad spectrum fluoroquinolone antibiotic, were studied in 2 trials involving 14 healthy volunteers, 10 individuals with mild (Child-Pugh Class A) impairment of liver function, and 12 with moderate (Child-
Publikováno v:
Clinical Pharmacokinetics. 33:1-8
The pharmacokinetics of grepafloxacin in healthy male subjects following single oral administration of doses ranging from 200 to 1200 mg, and following repeated oral administration of 400 and 800 mg doses are reported. Plasma levels of grepafloxacin
Publikováno v:
Clinical Pharmacokinetics. 33:9-17
The effects of age and gender on the pharmacokinetics of the oral fluoroquinolone grepafloxacin were examined in 48 healthy middle-aged and elderly individuals, of whom half were male and half were female. Participants were stratified into 4 groups (
Publikováno v:
Clinical pharmacokinetics. 33
Two open crossover studies were conducted to investigate the effects of food or concomitant treatment with the histamine H2-receptor antagonist famotidine on the pharmacokinetics of the new fluoroquinolone grepafloxacin. Each study involved 16 health
Publikováno v:
Clinical pharmacokinetics. 33
Grepafloxacin is mainly (approximately 90%) excreted by nonrenal mechanisms. The effect of renal impairment on the pharmacokinetics of grepafloxacin was evaluated in an open-label study involving 20 adults, 15 of whom had some degree of renal impairm