Methodologies for investigating drug metabolism at the early drug discovery stage: prediction of hepatic drug clearance and P450 contribution
C Emoto, N Murayama… - Current drug …, 2010 - ingentaconnect.com
The attrition rate in drug development is being reduced by continuous advances in science
and technology introduced by various academic institutions and pharmaceutical companies …
and technology introduced by various academic institutions and pharmaceutical companies …
Patient characteristics compete with dose as predictors of acute treatment toxicity in early phase clinical trials
A Rogatko, JS Babb, H Wang, MJ Slifker… - Clinical Cancer Research, 2004 - AACR
Purpose: The purpose of this study was to identify patient characteristics that may be risk
factors or markers of susceptibility to adverse treatment effects in cancer Phase I and II …
factors or markers of susceptibility to adverse treatment effects in cancer Phase I and II …
[引用][C] New anticancer drug adjustment guidelines for kidney disease attempt to filter out mess
C Diamond - Pharmacy Today, 2022 - Elsevier
Anticancer drug dose individualisation: from body surface area to physiology
A Pétain, É Chatelut - Bulletin du Cancer, 2008 - jle.com
The doses of anticancer drugs are usually calculated according to the body surface area.
This practice is based on the hypothesis that clearance is proportional to this morphologic …
This practice is based on the hypothesis that clearance is proportional to this morphologic …
Clinical pharmacology overview
AP Beelen, LD Lewis - Handbook of Anticancer Pharmacokinetics and …, 2004 - Springer
Clinical pharmacology is the branch of pharmacology that focuses on the study of drugs in
humans. A comprehensive understanding of the principles of clinical pharmacology …
humans. A comprehensive understanding of the principles of clinical pharmacology …
Physiologically‐based pharmacokinetic model for alectinib, ruxolitinib, and panobinostat in the presence of cancer, renal impairment, and hepatic impairment
MM Alsmadi, NM AL‐Daoud… - … & drug disposition, 2021 - Wiley Online Library
Renal (RIP) and hepatic (HIP) impairments are prevalent conditions in cancer patients. They
can cause changes in gastric emptying time, albumin levels, hematocrit, glomerular filtration …
can cause changes in gastric emptying time, albumin levels, hematocrit, glomerular filtration …
Pharmacokinetic/pharmacodynamic modeling for drug development in oncology
E Garralda, R Dienstmann, J Tabernero - American Society of Clinical …, 2017 - ascopubs.org
High drug attrition rates remain a critical issue in oncology drug development. A series of
steps during drug development must be addressed to better understand the …
steps during drug development must be addressed to better understand the …
[引用][C] A successful preclinical toxicology package
S Theodore - Drug Metabolism and Pharmacokinetics, 2024 - Elsevier
[PDF][PDF] Inter-individual variation in hepatic drug metabolism: The potential of in vitro assays in unraveling the role of metabolism in drug induced liver toxicity
SP den Braver-Sewradj - 2018 - research.vu.nl
Together with drug excretion, drug metabolism is an important mechanism of drug
elimination from the human body. This is achieved by biotransformation of (lipophilic) drug …
elimination from the human body. This is achieved by biotransformation of (lipophilic) drug …
The effects of impaired liver function on the elimination of antineoplastic agents
G Koren, K Beatty, A Seto… - Annals of …, 1992 - journals.sagepub.com
OBJECTIVE: To critically review available data on the disposition of cancer chemotherapy in
patients with hepatic dysfunction, and to derive at dose recommendation. DATA SOURCES …
patients with hepatic dysfunction, and to derive at dose recommendation. DATA SOURCES …