Zobrazeno 1 - 10
of 10
pro vyhledávání: '"M. R. Gastonguay"'
Publikováno v:
Drug discoveriestherapeutics. 4(1)
The objective of this analysis was to explore exposure-response modeling of data from a thorough QT (TQT) study of tolterodine in CYP2D6 extensive (EMs) and poor metabolizers (PMs). Crossover treatments of the TQT study included the recommended (2 mg
Publikováno v:
Journal of clinical pharmacology. 51(3)
The population pharmacokinetics of pantoprazole was characterized in pediatric patients from birth to 16 years using NONMEM and evaluated via bootstrap and predictive check. Data were described using a 2-compartment model with a typical parameterized
Autor:
K C, Wade, D, Wu, D A, Kaufman, R M, Ward, D K, Benjamin, J E, Sullivan, N, Ramey, B, Jayaraman, K, Hoppu, P C, Adamson, M R, Gastonguay, J S, Barrett, Celeste, Crouse
Publikováno v:
Antimicrobial agents and chemotherapy. 52(11)
Fluconazole is being increasingly used to prevent and treat invasive candidiasis in neonates, yet dosing is largely empirical due to the lack of adequate pharmacokinetic (PK) data. We performed a multicenter population PK study of fluconazole in 23-
Publikováno v:
Journal of pharmacokinetics and pharmacodynamics. 28(6)
To derive useful pharmacokinetic (PK) and pharmacodynamic (PD) information for guiding the clinical use of sotalol in pediatric patients with supraventricular (SVT) or ventricular tachyarrhythmia (VT).Two studies were conducted in-patients with SVT o
Autor:
M R, Gastonguay, S L, Schwartz
Publikováno v:
Pharmaceutical research. 11(12)
Pharmacokinetic-pharmacodynamic modeling algorithms, in general, rely on hysteresis minimization techniques that assume time-invariant pharmacodynamics (constant biophase concentration-effect relationships). When time-variant pharmacodynamics are obs
Publikováno v:
Nicotine and Related Alkaloids ISBN: 9789401049368
Pharmacokinetic models are used to describe or predict the time-dependent changes in drug concentration in blood and tissues, i.e., concentration × time (C × t) curves. There are two basic approaches to pharmacokinetic modelling. In the first, empi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::52cf6c3818f6ff67aee4e078504d89d8
https://doi.org/10.1007/978-94-011-2110-1_12
https://doi.org/10.1007/978-94-011-2110-1_12
Publikováno v:
Clinical Pharmacology & Therapeutics. 77:P91-P91
Background The residual error of parent and metabolite concentrations in pharmacokinetic (PK) samples can be correlated due to issues such as mislabeled timing, sample extraction, and misspecification, although it is not typically estimated in popula
Autor:
A. El‐Tahtawy, M. R. Gastonguay
Publikováno v:
Clinical Pharmacology & Therapeutics. 77:P2-P2
Aims Bootstrap (BS) parameter distributions are often used to characterize estimation uncertainty and determine confidence intervals (CI) for population pharmacokinetic (PPK) model parameters. These results are used to guide inferences about clinical
Publikováno v:
Clinical Pharmacology & Therapeutics. 77:P89-P89
Aims Efaproxiral (EFP), a synthetic allosteric modifier of hemoglobin (Hb), reduces O2-binding affinity in blood (p50) and is investigated as a radiation therapy sensitizer. The goal of this work was to describe the pharmacokinetics (PK) and pharmaco
Publikováno v:
Anesthesia & Analgesia. 80:SCA106