AbstractOral bioavailability is a key consideration in development of drug products, and the use of preclinical species in predicting bioavailability in human has long been debated. In order to clarify whether any correlation between human and animal bioavailability exist, an extensive analysis of the published literature data was conducted. Due to the complex nature of bioavailability calculations inclusion criteria were applied to ensure integrity of the data. A database of 184 compounds was assembled. Linear regression for the reported compounds indicated no strong or predictive correlations to human data for all species, individually and combined.The lack of correlation in this extended dataset highlights that animal bioavailability is ...
Bioequivalence (BE) studies are scientifi c methods that allow comparison of diff erent medicinal pr...
Oral dosing is the most common method of drug administration, and final plasma concentrations of the...
The authors present a comprehensive analysis on the estimation of volume of distribution at steady s...
Oral bioavailability (F) is an essential determinant for the systemic exposure and dosing regimens o...
Objectives: In pharmaceutical drug development, preclinical tests in animal models are essential to ...
A critically evaluated database of human oral bioavailability for 768 chemical compounds is describe...
Various animal models are used to study pharmacokinetics (PK) of drugs in development. Human renal c...
Obtaining information on the metabolic fate of a drug in humans is a key requirement in drug develop...
The aim of this project was to develop a model for prediction of bioavailability of drug compounds f...
A comprehensive analysis on the prediction of human clearance based on intravenous pharmacokinetic d...
Animal use continues to be central to preclinical drug development, in spite of a lack of its demons...
Dogs remain the main non-rodent species in preclinical drug development. Despite the current dearth ...
Purpose To develop and evaluate a tool for the qualitative pre-diction of human oral bioavailability...
Animals are still widely used in drug development and safety tests, despite evidence for their lack ...
Purpose It has been increasingly recognised that there is a need to reduce costly drug development d...
Bioequivalence (BE) studies are scientifi c methods that allow comparison of diff erent medicinal pr...
Oral dosing is the most common method of drug administration, and final plasma concentrations of the...
The authors present a comprehensive analysis on the estimation of volume of distribution at steady s...
Oral bioavailability (F) is an essential determinant for the systemic exposure and dosing regimens o...
Objectives: In pharmaceutical drug development, preclinical tests in animal models are essential to ...
A critically evaluated database of human oral bioavailability for 768 chemical compounds is describe...
Various animal models are used to study pharmacokinetics (PK) of drugs in development. Human renal c...
Obtaining information on the metabolic fate of a drug in humans is a key requirement in drug develop...
The aim of this project was to develop a model for prediction of bioavailability of drug compounds f...
A comprehensive analysis on the prediction of human clearance based on intravenous pharmacokinetic d...
Animal use continues to be central to preclinical drug development, in spite of a lack of its demons...
Dogs remain the main non-rodent species in preclinical drug development. Despite the current dearth ...
Purpose To develop and evaluate a tool for the qualitative pre-diction of human oral bioavailability...
Animals are still widely used in drug development and safety tests, despite evidence for their lack ...
Purpose It has been increasingly recognised that there is a need to reduce costly drug development d...
Bioequivalence (BE) studies are scientifi c methods that allow comparison of diff erent medicinal pr...
Oral dosing is the most common method of drug administration, and final plasma concentrations of the...
The authors present a comprehensive analysis on the estimation of volume of distribution at steady s...