[HTML][HTML] Prediction of the pharmacokinetics and pharmacodynamics of topiroxostat in humans by integrating the physiologically based pharmacokinetic model with the …

Z Luo, G Yu, X Han, T Yang, Y Ji, H Huang… - Biomedicine & …, 2020 - Elsevier
Topiroxostat is a selective xanthine oxidoreductase (XOR) inhibitor for the management of
hyperuricemia in patients with or without gout. In this work, we aim to employ the …

Simulation of febuxostat pharmacokinetics in healthy subjects and patients with impaired kidney function using physiologically based pharmacokinetic modeling

Y Xu, J Chen, Z Ruan, B Jiang, D Yang… - … & Drug Disposition, 2022 - Wiley Online Library
Febuxostat is recommended by the American College of Rheumatology Gout Management
Guidelines as a first‐line therapy for lowering the level of urate in patients with gout. At …

Pharmacokinetic/pharmacodynamic modeling and simulation of dotinurad, a novel uricosuric agent, in healthy volunteers

K Motoki, T Igarashi, K Omura… - Pharmacology …, 2019 - Wiley Online Library
This study aimed to investigate the pharmacokinetic and pharmacodynamic (PK/PD) profiles
of dotinurad, a novel uricosuric agent, and to construct a PK/PD model to predict serum urate …

Model informed development of SIM0295 in patients with gout and hyperuricemia and healthy volunteers using a population pharmacokinetics/pharmacodynamics …

Y Chen, Y Yang, S Xu, C Wang, P Shu… - Expert Opinion on …, 2023 - Taylor & Francis
Background SIM0295, a novel inhibitor of human uric acid transporter 1 (hURAT1), is used
to treat patients with gout and hyperuricemia. This study aimed to develop population …

A semi-mechanistic exposure–response model to assess the effects of verinurad, a potent URAT1 inhibitor, on serum and urine uric acid in patients with …

J Leander, M Sunnåker, D Rekić, S Aksenov… - … of Pharmacokinetics and …, 2021 - Springer
Verinurad, a uric acid transporter 1 (URAT1) inhibitor, lowers serum uric acid by promoting
its urinary excretion. Co-administration with a xanthine oxidase inhibitor (XOI) to …

A possible covalent xanthine oxidase inhibitor TS10: Inhibition mechanism, metabolites identification and PDPK assessment

T Zhang, X Zhang, E Xu, Z Wang, Z Zhang, Q Wang… - Bioorganic …, 2022 - Elsevier
Xanthine oxidase (XO) inhibitors are widely used in the control of serum uric acid levels in
the clinical management of gout. Our continuous efforts in searching novel amide-based XO …

The pharmacokinetics of oxypurinol in people with gout

SL Stocker, AJ McLachlan, RM Savic… - British journal of …, 2012 - Wiley Online Library
WHAT IS ALREADY KNOWN ABOUT THIS SUBJECT• Response to allopurinol in patients
with gout is often suboptimal due to large variability in pharmacokinetics.• The sources of the …

Development of physiologically based pharmacokinetic model for orally administered fexuprazan in humans

YS Jeong, MS Kim, N Lee, A Lee, YJ Chae, SJ Chung… - Pharmaceutics, 2021 - mdpi.com
Fexuprazan is a new drug candidate in the potassium-competitive acid blocker (P-CAB)
family. As proton pump inhibitors (PPIs), P-CABs inhibit gastric acid secretion and can be …

[PDF][PDF] The influence of albumin on the plasma xanthine oxidoreductase inhibitory activity of allopurinol, febuxostat and topiroxostat: insight into extra-urate lowering …

T Nakamura, T Murase, E Satoh, A Miyachi… - Integr Mol …, 2019 - siriusstore.com
Xanthine oxidoreductase (XOR) inhibitors, allopurinol, febuxostat, and topiroxostat are
hyperuricemia and gout therapeutic drugs, which were supposed to be same. However, it …

[HTML][HTML] Effect of experimentally induced hepatic and renal failure on the pharmacokinetics of topiramate in rats

KM Matar, YI Tayem - BioMed research international, 2014 - hindawi.com
We aimed to investigate the effect of induced hepatic and renal failure on the
pharmacokinetics of topiramate (TPM) in rats. Twenty-four Sprague-Dawley rats were used …