A multiexponential allometry (MA) method was devel-oped to predict human drug clearance from preclinical data. Separate data sets containing clearances from human and preclinical species were chosen for the study. Human clearance was estimated using the MA technique according to the equation: CL = aBWb + cBWd, where CL is clearance in milliliters/minute, and a, b, c, and d are con-stants derived from preclinical pharmacokinetic data. Simple allometry (SA) gave the poorest prediction using any data set, and the percentage outliers remained larger than MA or monkey liver blood flow within 1.5-, 2-, and 3-fold error. Analysis of compounds common to both data sets suggested that MA could accurately predict human clearances within approximately ...
<p>Allometric scaling was performed by fitting a linear regression model with the log of animal mass...
Human HIV integrase inhibitors are a novel class of antiretroviral drugs that act by blocking incorp...
Introduction: Successful quantitative prediction of hepatic drug metabolism often requires integrate...
Background: Human pharmacokinetics can be predicted from animal data using the principle of allometr...
Various modified methods have been proposed in response to criticisms regarding the practical applic...
The literature was searched for drugs where adequate data were available on in vitro human metabolis...
To predict human pharmacokinetics such as the clearance and the plasma concentration profile of a ne...
A comprehensive analysis on the prediction of human clearance based on intravenous pharmacokinetic d...
Identifying any extrahepatic excretion phenomenon in preclinical species is crucial for an accurate ...
These days, there is a lot of emphasis on the prediction of human clearance (CL) from a single speci...
Total human clearance is a key determinant for the pharmacokinetic behavior of drug candidates. Our ...
We developed a hybrid method for predicting plasma concentration-time curves in humans by integratin...
The appropriateness of relying on the coefficient of determination (r2) as a statistical metric for ...
Various animal models are used to study pharmacokinetics (PK) of drugs in development. Human renal c...
We describe a comprehensive retrospective analysis in which the abilities of several methods by whic...
<p>Allometric scaling was performed by fitting a linear regression model with the log of animal mass...
Human HIV integrase inhibitors are a novel class of antiretroviral drugs that act by blocking incorp...
Introduction: Successful quantitative prediction of hepatic drug metabolism often requires integrate...
Background: Human pharmacokinetics can be predicted from animal data using the principle of allometr...
Various modified methods have been proposed in response to criticisms regarding the practical applic...
The literature was searched for drugs where adequate data were available on in vitro human metabolis...
To predict human pharmacokinetics such as the clearance and the plasma concentration profile of a ne...
A comprehensive analysis on the prediction of human clearance based on intravenous pharmacokinetic d...
Identifying any extrahepatic excretion phenomenon in preclinical species is crucial for an accurate ...
These days, there is a lot of emphasis on the prediction of human clearance (CL) from a single speci...
Total human clearance is a key determinant for the pharmacokinetic behavior of drug candidates. Our ...
We developed a hybrid method for predicting plasma concentration-time curves in humans by integratin...
The appropriateness of relying on the coefficient of determination (r2) as a statistical metric for ...
Various animal models are used to study pharmacokinetics (PK) of drugs in development. Human renal c...
We describe a comprehensive retrospective analysis in which the abilities of several methods by whic...
<p>Allometric scaling was performed by fitting a linear regression model with the log of animal mass...
Human HIV integrase inhibitors are a novel class of antiretroviral drugs that act by blocking incorp...
Introduction: Successful quantitative prediction of hepatic drug metabolism often requires integrate...