Absolute oral bioavailability of traxoprodil in cytochrome P450 2D6 extensive and poor metabolisers
TJ Taylor, K Diringer, T Russell… - Clinical …, 2006 - Springer
Background Traxoprodil, a substituted 4-phenylpiperidine, is an N-methyl-D-aspartate
(NMDA) receptor antagonist that is selective for receptors containing the NR2B subunit. In …
(NMDA) receptor antagonist that is selective for receptors containing the NR2B subunit. In …
[HTML][HTML] Clinical efficacy and safety of topiroxostat in Japanese hyperuricemic patients with or without gout: a randomized, double-blinded, controlled phase 2b study
T Hosoya, T Sasaki, T Ohashi - Clinical Rheumatology, 2017 - Springer
Topiroxostat, a selective xanthine oxidoreductase inhibitor, is used in Japan for the
treatment of hyperuricemic patients with or without gout. In terms of the effectiveness of …
treatment of hyperuricemic patients with or without gout. In terms of the effectiveness of …
Physiologically based pharmacokinetic–pharmacodynamic modeling for prediction of vonoprazan pharmacokinetics and its inhibition on gastric acid secretion …
W Kong, B Sun, Z Wang, X Zheng, K Zhao… - Acta Pharmacologica …, 2020 - nature.com
Vonoprazan is characterized as having a long-lasting antisecretory effect on gastric acid. In
this study we developed a physiologically based pharmacokinetic (PBPK) …
this study we developed a physiologically based pharmacokinetic (PBPK) …
The impact of genetic variability in urate transporters on oxypurinol pharmacokinetics
HZ Hishe, SL Stocker, LK Stamp… - Clinical and …, 2023 - Wiley Online Library
The genetic determinants of the allopurinol dose‐concentration relationship have not been
extensively studied. We aimed to clarify what factors, including genetic variation in urate …
extensively studied. We aimed to clarify what factors, including genetic variation in urate …
Effects of age and gender on febuxostat pharmacokinetics, pharmacodynamics, and safety in healthy subjects
R Khosravan, M Kukulka, JT Wu… - Clinical …, 2005 - Wiley Online Library
Background Febuxostat is a novel non‐purine selective inhibitor of xanthine oxidase (NP‐
SIXO) being developed for the management of hyperuricemia in patients with gout. Aim The …
SIXO) being developed for the management of hyperuricemia in patients with gout. Aim The …
[HTML][HTML] Predictive performance and verification of physiologically based pharmacokinetic model of propylthiouracil
C Shen, D Liang, X Wang, W Shao, K Geng… - Frontiers in …, 2022 - frontiersin.org
Background: Propylthiouracil (PTU) treats hyperthyroidism and thyroid crisis in all age
groups. A variety of serious adverse effects can occur during clinical use and require …
groups. A variety of serious adverse effects can occur during clinical use and require …
[HTML][HTML] Physiologically based pharmacokinetic modeling of ritonavir-oxycodone drug interactions and its implication for dosing strategy
The concomitant administration of ritonavir and oxycodone may significantly increase the
plasma concentrations of oxycodone. This study was aimed to simulate DDI between …
plasma concentrations of oxycodone. This study was aimed to simulate DDI between …
Assessment of OATP transporter‐mediated drug–drug interaction using physiologically‐based pharmacokinetic (PBPK) modeling–a case example
Y Chen, R Zhu, F Ma, J Mao, EC Chen… - … & Drug Disposition, 2018 - Wiley Online Library
GDC‐0810 was under development as an oral anti‐cancer drug for the treatment of
estrogen receptor‐positive breast cancer as a single agent or in combination. In vitro data …
estrogen receptor‐positive breast cancer as a single agent or in combination. In vitro data …
Pharmacokinetics considerations for gout treatments
P Richette, A Frazier, T Bardin - Expert Opinion on Drug …, 2014 - Taylor & Francis
Introduction: Patients with gout often have comorbid conditions such as renal failure,
cardiovascular disease and metabolic syndrome. The presence and required treatment of …
cardiovascular disease and metabolic syndrome. The presence and required treatment of …
Physiologically based pharmacokinetic (PBPK) modeling of piroxicam with regard to CYP2C9 genetic polymorphism
CK Cho, P Kang, HJ Park, E Ko, CY Mu, YJ Lee… - Archives of Pharmacal …, 2022 - Springer
Piroxicam is a non-steroidal anti-inflammatory drug used to alleviate symptoms of
osteoarthritis and rheumatoid arthritis. CYP2C9 genetic polymorphism significantly …
osteoarthritis and rheumatoid arthritis. CYP2C9 genetic polymorphism significantly …