In vitro metabolism, disposition, preclinical pharmacokinetics and prediction of human pharmacokinetics of DNDI-VL-2098, a potential oral treatment for Visceral Leishmaniasis
ALLOMETRY;
ANIMAL EXPERIMENT;
AREA UNDER THE CURVE;
ARTICLE;
CACO 2 CELL LINE;
CONTROLLED STUDY;
DOG;
DRUG BIOAVAILABILITY;
DRUG CLEARANCE;
DRUG DISPOSITION;
DRUG DISTRIBUTION;
DRUG EFFICACY;
DRUG HALF LIFE;
DRUG METABOLISM;
DRUG PENETRATION;
DRUG PROTEIN BINDING;
DRUG SOLUBILITY;
DRUG STABILITY;
DRUG TRANSFORMATION;
HAMSTER;
HUMAN;
HUMAN CELL;
IN VITRO STUDY;
LIVER BLOOD FLOW;
LIVER CELL;
LIVER MICROSOME;
MALE;
MAXIMUM PLASMA CONCENTRATION;
MOUSE;
NONHUMAN;
PHARMACOKINETICS;
PLASMA CLEARANCE;
PLASMA CONCENTRATION-TIME CURVE;
RAT;
RECOMMENDED DRUG DOSE;
TIME TO MAXIMUM PLASMA CONCENTRATION;
TOTAL BODY WATER;
VISCERAL LEISHMANIASIS;
ANIMAL;
BIOAVAILABILITY;
DRUG SCREENING;
HALF LIFE TIME;
LEISHMANIASIS, VISCERAL;
LIVER;
METABOLISM;
ORAL DRUG ADMINISTRATION;
PROCEDURES;
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