Evaluation of pharmacokinetic and pharmacodynamic parameters following single dose of sitagliptin in healthy Indian males
Purpose Sitagliptin, a dipeptidyl peptidase (DPP)-IV inhibitor approved for the treatment of type 2 diabetes, is reported to be more efficacious in Indian patients than non-Indian patient population. The objective of the study was to evaluate pharmacokinetic and pharmacodynamic (PK/PD) parameters of...
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Published in: | European journal of clinical pharmacology Vol. 74; no. 5; pp. 561 - 569 |
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Main Authors: | , , , , , , , , , , , |
Format: | Journal Article |
Language: | English |
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01-05-2018
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Abstract | Purpose
Sitagliptin, a dipeptidyl peptidase (DPP)-IV inhibitor approved for the treatment of type 2 diabetes, is reported to be more efficacious in Indian patients than non-Indian patient population. The objective of the study was to evaluate pharmacokinetic and pharmacodynamic (PK/PD) parameters of single-dose sitagliptin 100 mg (Januvia) in healthy Indian male participants.
Method
In a randomised, single-dose, open-label, three-treatment, three-period, three-sequence, crossover bioavailability study, 18 healthy male participants received single-dose of sitagliptin under fasted and fed conditions. PK parameters (
C
max
,
T
max
, AUC
0-∞
and
t
1/2
) were determined using Phoenix WinNonlin software. PD parameters [DPP-IV inhibition, active glucagon-like peptide-1 (GLP-1) and insulin] were determined using established methods.
Results
PK parameters expressed in mean (SD) were
C
max
491.7 (135.9) ng/mL; AUC
0-∞
4256.1 (509.9) ng· hr/mL,
T
max
2.9 (1.0) hr and
t
1/2
10.4 (3.0) hr. The weighted average (WA) plasma DPP-4 inhibition over 24 h was 89.6% and WA of plasma active GLP-1 over 2 h after standardised meal (geometric mean ratio) was 11.1 (9.9) pM/L which is two- to- four fold higher compared to that reported in other populations. The mean average (SD) AUC of plasma insulin over 2 h of standardised meal was 47.9 (24.9) μIU/mL.
Conclusion
Although, there are differences in pharmacokinetic parameters, no clinically meaningful differences were observed with respect to DPP-IV inhibition between Indian and non-Indian population. |
---|---|
AbstractList | Purpose
Sitagliptin, a dipeptidyl peptidase (DPP)-IV inhibitor approved for the treatment of type 2 diabetes, is reported to be more efficacious in Indian patients than non-Indian patient population. The objective of the study was to evaluate pharmacokinetic and pharmacodynamic (PK/PD) parameters of single-dose sitagliptin 100 mg (Januvia) in healthy Indian male participants.
Method
In a randomised, single-dose, open-label, three-treatment, three-period, three-sequence, crossover bioavailability study, 18 healthy male participants received single-dose of sitagliptin under fasted and fed conditions. PK parameters (
C
max
,
T
max
, AUC
0-∞
and
t
1/2
) were determined using Phoenix WinNonlin software. PD parameters [DPP-IV inhibition, active glucagon-like peptide-1 (GLP-1) and insulin] were determined using established methods.
Results
PK parameters expressed in mean (SD) were
C
max
491.7 (135.9) ng/mL; AUC
0-∞
4256.1 (509.9) ng· hr/mL,
T
max
2.9 (1.0) hr and
t
1/2
10.4 (3.0) hr. The weighted average (WA) plasma DPP-4 inhibition over 24 h was 89.6% and WA of plasma active GLP-1 over 2 h after standardised meal (geometric mean ratio) was 11.1 (9.9) pM/L which is two- to- four fold higher compared to that reported in other populations. The mean average (SD) AUC of plasma insulin over 2 h of standardised meal was 47.9 (24.9) μIU/mL.
Conclusion
Although, there are differences in pharmacokinetic parameters, no clinically meaningful differences were observed with respect to DPP-IV inhibition between Indian and non-Indian population. PurposeSitagliptin, a dipeptidyl peptidase (DPP)-IV inhibitor approved for the treatment of type 2 diabetes, is reported to be more efficacious in Indian patients than non-Indian patient population. The objective of the study was to evaluate pharmacokinetic and pharmacodynamic (PK/PD) parameters of single-dose sitagliptin 100 mg (Januvia) in healthy Indian male participants.MethodIn a randomised, single-dose, open-label, three-treatment, three-period, three-sequence, crossover bioavailability study, 18 healthy male participants received single-dose of sitagliptin under fasted and fed conditions. PK parameters (Cmax, Tmax, AUC0-∞ and t1/2) were determined using Phoenix WinNonlin software. PD parameters [DPP-IV inhibition, active glucagon-like peptide-1 (GLP-1) and insulin] were determined using established methods.ResultsPK parameters expressed in mean (SD) were Cmax 491.7 (135.9) ng/mL; AUC0-∞ 4256.1 (509.9) ng· hr/mL, Tmax 2.9 (1.0) hr and t1/2 10.4 (3.0) hr. The weighted average (WA) plasma DPP-4 inhibition over 24 h was 89.6% and WA of plasma active GLP-1 over 2 h after standardised meal (geometric mean ratio) was 11.1 (9.9) pM/L which is two- to- four fold higher compared to that reported in other populations. The mean average (SD) AUC of plasma insulin over 2 h of standardised meal was 47.9 (24.9) μIU/mL.ConclusionAlthough, there are differences in pharmacokinetic parameters, no clinically meaningful differences were observed with respect to DPP-IV inhibition between Indian and non-Indian population. PURPOSESitagliptin, a dipeptidyl peptidase (DPP)-IV inhibitor approved for the treatment of type 2 diabetes, is reported to be more efficacious in Indian patients than non-Indian patient population. The objective of the study was to evaluate pharmacokinetic and pharmacodynamic (PK/PD) parameters of single-dose sitagliptin 100 mg (Januvia) in healthy Indian male participants.METHODIn a randomised, single-dose, open-label, three-treatment, three-period, three-sequence, crossover bioavailability study, 18 healthy male participants received single-dose of sitagliptin under fasted and fed conditions. PK parameters (Cmax, Tmax, AUC0-∞ and t1/2) were determined using Phoenix WinNonlin software. PD parameters [DPP-IV inhibition, active glucagon-like peptide-1 (GLP-1) and insulin] were determined using established methods.RESULTSPK parameters expressed in mean (SD) were Cmax 491.7 (135.9) ng/mL; AUC0-∞ 4256.1 (509.9) ng· hr/mL, Tmax 2.9 (1.0) hr and t1/2 10.4 (3.0) hr. The weighted average (WA) plasma DPP-4 inhibition over 24 h was 89.6% and WA of plasma active GLP-1 over 2 h after standardised meal (geometric mean ratio) was 11.1 (9.9) pM/L which is two- to- four fold higher compared to that reported in other populations. The mean average (SD) AUC of plasma insulin over 2 h of standardised meal was 47.9 (24.9) μIU/mL.CONCLUSIONAlthough, there are differences in pharmacokinetic parameters, no clinically meaningful differences were observed with respect to DPP-IV inhibition between Indian and non-Indian population. Sitagliptin, a dipeptidyl peptidase (DPP)-IV inhibitor approved for the treatment of type 2 diabetes, is reported to be more efficacious in Indian patients than non-Indian patient population. The objective of the study was to evaluate pharmacokinetic and pharmacodynamic (PK/PD) parameters of single-dose sitagliptin 100 mg (Januvia) in healthy Indian male participants. In a randomised, single-dose, open-label, three-treatment, three-period, three-sequence, crossover bioavailability study, 18 healthy male participants received single-dose of sitagliptin under fasted and fed conditions. PK parameters (C , T , AUC and t ) were determined using Phoenix WinNonlin software. PD parameters [DPP-IV inhibition, active glucagon-like peptide-1 (GLP-1) and insulin] were determined using established methods. PK parameters expressed in mean (SD) were C 491.7 (135.9) ng/mL; AUC 4256.1 (509.9) ng· hr/mL, T 2.9 (1.0) hr and t 10.4 (3.0) hr. The weighted average (WA) plasma DPP-4 inhibition over 24 h was 89.6% and WA of plasma active GLP-1 over 2 h after standardised meal (geometric mean ratio) was 11.1 (9.9) pM/L which is two- to- four fold higher compared to that reported in other populations. The mean average (SD) AUC of plasma insulin over 2 h of standardised meal was 47.9 (24.9) μIU/mL. Although, there are differences in pharmacokinetic parameters, no clinically meaningful differences were observed with respect to DPP-IV inhibition between Indian and non-Indian population. |
Author | Aravindababu, P. Shengule, Sushant A. Sangle, Ganesh V. Kamble, Shantibhushan Baig, Mirza Layeeq Ahmed Patil, Mohan Vuppalavanchu, Kiran Kumar Singh, Geetchandra Deshmukh, Nitin J. Kale, Sushil Shaikh, Javed Tripathi, Jitendra |
Author_xml | – sequence: 1 givenname: Ganesh V. surname: Sangle fullname: Sangle, Ganesh V. email: gsangle@wockhardt.com organization: Diabetes Research Lab, New Drug Discovery, Wockhardt Research Centre – sequence: 2 givenname: Mohan surname: Patil fullname: Patil, Mohan organization: Diabetes Research Lab, New Drug Discovery, Wockhardt Research Centre – sequence: 3 givenname: Nitin J. surname: Deshmukh fullname: Deshmukh, Nitin J. organization: Diabetes Research Lab, New Drug Discovery, Wockhardt Research Centre – sequence: 4 givenname: Sushant A. surname: Shengule fullname: Shengule, Sushant A. organization: Diabetes Research Lab, New Drug Discovery, Wockhardt Research Centre – sequence: 5 givenname: Shantibhushan surname: Kamble fullname: Kamble, Shantibhushan organization: Clinical Pharmacokinetics and Biopharmaceutics Department, Wockhardt Research Centre – sequence: 6 givenname: Kiran Kumar surname: Vuppalavanchu fullname: Vuppalavanchu, Kiran Kumar organization: Clinical Pharmacokinetics and Biopharmaceutics Department, Wockhardt Research Centre – sequence: 7 givenname: Sushil surname: Kale fullname: Kale, Sushil organization: Clinical Pharmacokinetics and Biopharmaceutics Department, Wockhardt Research Centre – sequence: 8 givenname: Mirza Layeeq Ahmed surname: Baig fullname: Baig, Mirza Layeeq Ahmed organization: Clinical Pharmacokinetics and Biopharmaceutics Department, Wockhardt Research Centre – sequence: 9 givenname: Geetchandra surname: Singh fullname: Singh, Geetchandra organization: Clinical Pharmacokinetics and Biopharmaceutics Department, Wockhardt Research Centre – sequence: 10 givenname: Javed surname: Shaikh fullname: Shaikh, Javed organization: Clinical Pharmacokinetics and Biopharmaceutics Department, Wockhardt Research Centre – sequence: 11 givenname: Jitendra surname: Tripathi fullname: Tripathi, Jitendra organization: Clinical Pharmacokinetics and Biopharmaceutics Department, Wockhardt Research Centre – sequence: 12 givenname: P. surname: Aravindababu fullname: Aravindababu, P. organization: Clinical Pharmacokinetics and Biopharmaceutics Department, Wockhardt Research Centre |
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Keywords | Incretins DPP-IV inhibitors Sitagliptin Pharmacodynamics Pharmacokinetics |
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Sitagliptin, a dipeptidyl peptidase (DPP)-IV inhibitor approved for the treatment of type 2 diabetes, is reported to be more efficacious in Indian... Sitagliptin, a dipeptidyl peptidase (DPP)-IV inhibitor approved for the treatment of type 2 diabetes, is reported to be more efficacious in Indian patients... PurposeSitagliptin, a dipeptidyl peptidase (DPP)-IV inhibitor approved for the treatment of type 2 diabetes, is reported to be more efficacious in Indian... PURPOSESitagliptin, a dipeptidyl peptidase (DPP)-IV inhibitor approved for the treatment of type 2 diabetes, is reported to be more efficacious in Indian... |
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SubjectTerms | Asian people Bioavailability Biomedical and Life Sciences Biomedicine Diabetes mellitus Diabetes mellitus (non-insulin dependent) Glucagon Glucagon-like peptide 1 Inhibition Insulin Males Peptidase Pharmacodynamics Pharmacokinetics Pharmacology/Toxicology |
Title | Evaluation of pharmacokinetic and pharmacodynamic parameters following single dose of sitagliptin in healthy Indian males |
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