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Pharmacokinetic/Pharmacodynamic Interaction Between Evogliptin and Pioglitazone in Healthy Male Subjects
by
Jang, In-Jin
, Kim, Yun
, Yu, Kyung-Sang
, Lee, SeungHwan
, Hwang, Inyoung
, Yoo, Hyounggyoon
in
Acids
/ Adult
/ Care and treatment
/ Confidence intervals
/ Cross-Over Studies
/ Diabetes
/ Diabetes mellitus
/ Diabetes mellitus (non-insulin dependent)
/ Dipeptidyl-peptidase IV
/ Dosage
/ Dose-Response Relationship, Drug
/ Drug dosages
/ drug interaction
/ evogliptin
/ Glucagon
/ Glucose
/ Glucose tolerance
/ Glucose tolerance test
/ Health aspects
/ Healthy Volunteers
/ Humans
/ Inhibitors
/ Insulin
/ Male
/ Metabolites
/ Original Research
/ Peptidase
/ Peptidases
/ Peptides
/ Pharmacodynamics
/ Pharmacokinetics
/ Pharmacology
/ Pioglitazone
/ Pioglitazone - administration & dosage
/ Pioglitazone - metabolism
/ Pioglitazone - pharmacokinetics
/ Piperazines - administration & dosage
/ Piperazines - metabolism
/ Piperazines - pharmacokinetics
/ Plasma
/ Quality control
/ Sample size
/ Steady state
/ Type 2 diabetes
/ Urine
2020
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Pharmacokinetic/Pharmacodynamic Interaction Between Evogliptin and Pioglitazone in Healthy Male Subjects
by
Jang, In-Jin
, Kim, Yun
, Yu, Kyung-Sang
, Lee, SeungHwan
, Hwang, Inyoung
, Yoo, Hyounggyoon
in
Acids
/ Adult
/ Care and treatment
/ Confidence intervals
/ Cross-Over Studies
/ Diabetes
/ Diabetes mellitus
/ Diabetes mellitus (non-insulin dependent)
/ Dipeptidyl-peptidase IV
/ Dosage
/ Dose-Response Relationship, Drug
/ Drug dosages
/ drug interaction
/ evogliptin
/ Glucagon
/ Glucose
/ Glucose tolerance
/ Glucose tolerance test
/ Health aspects
/ Healthy Volunteers
/ Humans
/ Inhibitors
/ Insulin
/ Male
/ Metabolites
/ Original Research
/ Peptidase
/ Peptidases
/ Peptides
/ Pharmacodynamics
/ Pharmacokinetics
/ Pharmacology
/ Pioglitazone
/ Pioglitazone - administration & dosage
/ Pioglitazone - metabolism
/ Pioglitazone - pharmacokinetics
/ Piperazines - administration & dosage
/ Piperazines - metabolism
/ Piperazines - pharmacokinetics
/ Plasma
/ Quality control
/ Sample size
/ Steady state
/ Type 2 diabetes
/ Urine
2020
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Pharmacokinetic/Pharmacodynamic Interaction Between Evogliptin and Pioglitazone in Healthy Male Subjects
by
Jang, In-Jin
, Kim, Yun
, Yu, Kyung-Sang
, Lee, SeungHwan
, Hwang, Inyoung
, Yoo, Hyounggyoon
in
Acids
/ Adult
/ Care and treatment
/ Confidence intervals
/ Cross-Over Studies
/ Diabetes
/ Diabetes mellitus
/ Diabetes mellitus (non-insulin dependent)
/ Dipeptidyl-peptidase IV
/ Dosage
/ Dose-Response Relationship, Drug
/ Drug dosages
/ drug interaction
/ evogliptin
/ Glucagon
/ Glucose
/ Glucose tolerance
/ Glucose tolerance test
/ Health aspects
/ Healthy Volunteers
/ Humans
/ Inhibitors
/ Insulin
/ Male
/ Metabolites
/ Original Research
/ Peptidase
/ Peptidases
/ Peptides
/ Pharmacodynamics
/ Pharmacokinetics
/ Pharmacology
/ Pioglitazone
/ Pioglitazone - administration & dosage
/ Pioglitazone - metabolism
/ Pioglitazone - pharmacokinetics
/ Piperazines - administration & dosage
/ Piperazines - metabolism
/ Piperazines - pharmacokinetics
/ Plasma
/ Quality control
/ Sample size
/ Steady state
/ Type 2 diabetes
/ Urine
2020
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Pharmacokinetic/Pharmacodynamic Interaction Between Evogliptin and Pioglitazone in Healthy Male Subjects
Journal Article
Pharmacokinetic/Pharmacodynamic Interaction Between Evogliptin and Pioglitazone in Healthy Male Subjects
2020
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Overview
Evogliptin is a newly developed oral glucose-lowering medication of the dipeptidyl peptidase 4 (DPP-4) inhibitor class for type 2 diabetes mellitus. The combination of a DPP-4 inhibitor with pioglitazone is a promising therapeutic option. The aim of the present study was to evaluate the pharmacokinetic and pharmacodynamic interaction between evogliptin and pioglitazone.
A randomized, open-label, multiple-dose, three-treatment, three-period, six-sequence crossover study was conducted in healthy Korean male subjects. All subjects received evogliptin 5 mg once daily for 7 days (EVO), pioglitazone 30 mg once daily for 7 days (PIO) and co-administration of evogliptin 5 mg and pioglitazone 30 mg once daily for 7 days (EVO+PIO) according to the assigned sequence and period. Serial blood samples were collected for 24 hours for pharmacokinetic analysis and 3 hours after the oral glucose tolerance test for the pharmacodynamic analysis.
Thirty-four subjects completed the study. EVO+PIO and EVO showed a similar maximum plasma concentration at steady state (C
) and area under the concentration-time curve during the dosing interval at the steady state (AUC
) of evogliptin, with geometric mean ratios (GMRs) (90% confidence interval (CI)) of 1.01 (0.97-1.05) and 1.01 (0.98-1.04), respectively. EVO+PIO and PIO showed a similar C
and AUC
of pioglitazone, with GMRs (90% CI) of 1.07 (0.99-1.17) and 1.08 (0.99-1.17), respectively. Reduction of the glucose level after EVO+PIO was larger compared to PIO and similar with EVO.
Concomitant administration of evogliptin and pioglitazone showed similar glucose-lowering effects with those of evogliptin alone without pharmacokinetic interactions when compared to the intake of each drug alone.
Publisher
Dove Medical Press Limited,Taylor & Francis Ltd,Dove,Dove Medical Press
Subject
/ Adult
/ Diabetes
/ Diabetes mellitus (non-insulin dependent)
/ Dosage
/ Dose-Response Relationship, Drug
/ Glucagon
/ Glucose
/ Humans
/ Insulin
/ Male
/ Peptides
/ Pioglitazone - administration & dosage
/ Pioglitazone - pharmacokinetics
/ Piperazines - administration & dosage
/ Piperazines - pharmacokinetics
/ Plasma
/ Urine
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