<p>The best fit was obtained by models for two subpopulation (A and B), characterized by different F values, relative to the baseline model that included all subjects. Parameters: central and peripheral compartment volumes, total body clearance (CL), inter-compartmental clearance (Q), rate of absorption, and relative bioavailability (F). Note that albendazole was administered in both baseline and interaction phases.</p
An integrated absorption model was developed to describe the small intestinal transit, dissolution, ...
<p>Solid line serves as a reference point of no change of ivermectin bioavailability; dotted line is...
Ivermectin is a worldwide-used antiparasitic drug largely administered to cattle as a topical formul...
A recent drug interaction study reported that when azithromycin was administered with the combinatio...
<p>The solid line represents the fit predicted by the typical pharmacokinetic mixture model paramete...
The anthelminthic ivermectin is receiving new attention as it is being repurposed for new indication...
Objective: To establish the pharmacokinetics of ivermectin in the rabbit model as a basis for future...
Ivermectin is a pivotal drug for the control of onchocerciasis and lymphatic filariasis, which is in...
Ivermectin is a worldwide-used antiparasitic drug largely administered to cattle as a topical formul...
<p>*t = 168 h for IgG, t = 24 h for Fab, BSA and Streptavidin. Notations and abbreviations: distribu...
Ivermectin is a pivotal drug for the control of onchocerciasis and lymphatic filariasis, which is in...
<p>Lower panel: Maximum concentration data from 1000 simulation replicates using the non-mixture mod...
BACKGROUND Ivermectin is an older anthelminthic agent that is being studied more intensely given ...
Plasma concentration-time profiles of (A) ALB-OX, (B) DEC, and (C) IVM, after a single dose of IVM+D...
For orally administered drugs, the rate and extent of absorption are governed by the physiology of t...
An integrated absorption model was developed to describe the small intestinal transit, dissolution, ...
<p>Solid line serves as a reference point of no change of ivermectin bioavailability; dotted line is...
Ivermectin is a worldwide-used antiparasitic drug largely administered to cattle as a topical formul...
A recent drug interaction study reported that when azithromycin was administered with the combinatio...
<p>The solid line represents the fit predicted by the typical pharmacokinetic mixture model paramete...
The anthelminthic ivermectin is receiving new attention as it is being repurposed for new indication...
Objective: To establish the pharmacokinetics of ivermectin in the rabbit model as a basis for future...
Ivermectin is a pivotal drug for the control of onchocerciasis and lymphatic filariasis, which is in...
Ivermectin is a worldwide-used antiparasitic drug largely administered to cattle as a topical formul...
<p>*t = 168 h for IgG, t = 24 h for Fab, BSA and Streptavidin. Notations and abbreviations: distribu...
Ivermectin is a pivotal drug for the control of onchocerciasis and lymphatic filariasis, which is in...
<p>Lower panel: Maximum concentration data from 1000 simulation replicates using the non-mixture mod...
BACKGROUND Ivermectin is an older anthelminthic agent that is being studied more intensely given ...
Plasma concentration-time profiles of (A) ALB-OX, (B) DEC, and (C) IVM, after a single dose of IVM+D...
For orally administered drugs, the rate and extent of absorption are governed by the physiology of t...
An integrated absorption model was developed to describe the small intestinal transit, dissolution, ...
<p>Solid line serves as a reference point of no change of ivermectin bioavailability; dotted line is...
Ivermectin is a worldwide-used antiparasitic drug largely administered to cattle as a topical formul...