
What is the -2LL or the Log-likelihood Ratio? Blog Post
Understand the 2LL (Log-likelihood Ratio) and its role in statistical analysis. Explore how it aids in model comparison and decision-making with confidence.
Understand the 2LL (Log-likelihood Ratio) and its role in statistical analysis. Explore how it aids in model comparison and decision-making with confidence.
Categorizations of best response observed at week 8 of first-line treatment in two studies of bevacizumab plus chemotherapy in Western and Chinese patients with non-small cell lung cancer were assessed together with baseline prognostic factors in multivariate parametric models to predict overall survival and progression free survival.
One of the most common questions posed by clinical operations experts when including pharmacokinetic sampling in a clinical trial is the following: “What is the time window we should allow…
Linear regression is a common tool that the pharmacokineticist uses to calculate elimination rate constants. Standard linear regression provides estimates for the slope, intercept, and r2, a statistic that helps…
This study sought to determine levels of microsomal protein (MPPGL) and hepatocellularity (HPGL) per gram of human liver and their interindividual variability. Triplicate liver samples were used to determine values…
Ganitumab is an investigational, fully human monoclonal antibody antagonist of the insulin-like growth factor-1 receptor (IGF1R) that has shown trends towards improved progression-free survival and overall survival in a phase…
The phase III trial of pertuzumab plus trastuzumab plus docetaxel versus placebo plus trastuzumab plus docetaxel for first-line treatment of HER2-positive metastatic breast cancer included a substudy to determine whether…
γ-Hydroxybutyrate (GHB), a common drug of abuse, is often coingested with ethanol. Increasing renal clearance via monocarboxylate transporter (MCT) inhibition represents a potential therapeutic strategy in GHB overdose, as does inhibition of…
A prerequisite for the prediction of the magnitude of P-glycoprotein (P-gp)-mediated drug-drug interactions between digoxin and P-gp inhibitors (e.g. verapamil and its metabolite norverapamil) or P-gp inducers (e.g. rifampicin) is…