Pharmacokinetic and pharmacodynamic interaction of DWP16001, a sodium–glucose cotransporter 2 inhibitor, with gemigliptin and metformin in healthy adults

Aims DWP16001, a novel sodium–glucose cotransporter 2 inhibitor, is under clinical development for the treatment of type 2 diabetes mellitus. This study aimed to explore the pharmacokinetics (PK) and pharmacodynamics interaction of DWP16001 with gemigliptin and metformin. Methods A randomized, open‐...

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Published inBritish journal of clinical pharmacology Vol. 89; no. 6; pp. 1780 - 1788
Main Authors Jeong, Sae Im, Kim, Yun, Nah, Jae Jin, Huh, Wan, Jang, In‐Jin, Hwang, Jun Gi, Lee, SeungHwan
Format Journal Article
LanguageEnglish
Published England 01.06.2023
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Abstract Aims DWP16001, a novel sodium–glucose cotransporter 2 inhibitor, is under clinical development for the treatment of type 2 diabetes mellitus. This study aimed to explore the pharmacokinetics (PK) and pharmacodynamics interaction of DWP16001 with gemigliptin and metformin. Methods A randomized, open‐label, 2‐sequence, 2‐period crossover study was conducted in 34 healthy male subjects. All subjects received a single oral dose of DWP16001 2 mg with and without gemigliptin and metformin (8 days of 50 mg once‐daily dose and 1000 mg twice daily dose for gemigliptin and metformin, respectively). Serial blood samples were collected for PK and serum glucose analysis, and timed urine samples were collected to analyse urine glucose excretion (UGE). The PK and pharmacodynamic parameters were analysed by the noncompartmental method. Results The PK interactions of DWP16001, gemigliptin and metformin were not clinically significant. The geometric mean ratios (with 90% confidence intervals) of coadministration to separate administration for area under the time‐concentration curves were 1.04 (1.02–1.06), 1.03 (0.98–1.09) and 1.17 (1.12–1.22), for gemigliptin, metformin and DWP16001 respectively. The UGE induced by DWP16001 was not affected by the coadministration of gemigliptin and metformin. Conclusion The results suggest that the DWP16001 could be added to metformin and gemigliptin combination therapy without dose adjustment.
AbstractList DWP16001, a novel sodium-glucose cotransporter 2 inhibitor, is under clinical development for the treatment of type 2 diabetes mellitus. This study aimed to explore the pharmacokinetics (PK) and pharmacodynamics interaction of DWP16001 with gemigliptin and metformin. A randomized, open-label, 2-sequence, 2-period crossover study was conducted in 34 healthy male subjects. All subjects received a single oral dose of DWP16001 2 mg with and without gemigliptin and metformin (8 days of 50 mg once-daily dose and 1000 mg twice daily dose for gemigliptin and metformin, respectively). Serial blood samples were collected for PK and serum glucose analysis, and timed urine samples were collected to analyse urine glucose excretion (UGE). The PK and pharmacodynamic parameters were analysed by the noncompartmental method. The PK interactions of DWP16001, gemigliptin and metformin were not clinically significant. The geometric mean ratios (with 90% confidence intervals) of coadministration to separate administration for area under the time-concentration curves were 1.04 (1.02-1.06), 1.03 (0.98-1.09) and 1.17 (1.12-1.22), for gemigliptin, metformin and DWP16001 respectively. The UGE induced by DWP16001 was not affected by the coadministration of gemigliptin and metformin. The results suggest that the DWP16001 could be added to metformin and gemigliptin combination therapy without dose adjustment.
Aims DWP16001, a novel sodium–glucose cotransporter 2 inhibitor, is under clinical development for the treatment of type 2 diabetes mellitus. This study aimed to explore the pharmacokinetics (PK) and pharmacodynamics interaction of DWP16001 with gemigliptin and metformin. Methods A randomized, open‐label, 2‐sequence, 2‐period crossover study was conducted in 34 healthy male subjects. All subjects received a single oral dose of DWP16001 2 mg with and without gemigliptin and metformin (8 days of 50 mg once‐daily dose and 1000 mg twice daily dose for gemigliptin and metformin, respectively). Serial blood samples were collected for PK and serum glucose analysis, and timed urine samples were collected to analyse urine glucose excretion (UGE). The PK and pharmacodynamic parameters were analysed by the noncompartmental method. Results The PK interactions of DWP16001, gemigliptin and metformin were not clinically significant. The geometric mean ratios (with 90% confidence intervals) of coadministration to separate administration for area under the time‐concentration curves were 1.04 (1.02–1.06), 1.03 (0.98–1.09) and 1.17 (1.12–1.22), for gemigliptin, metformin and DWP16001 respectively. The UGE induced by DWP16001 was not affected by the coadministration of gemigliptin and metformin. Conclusion The results suggest that the DWP16001 could be added to metformin and gemigliptin combination therapy without dose adjustment.
DWP16001, a novel sodium-glucose cotransporter 2 inhibitor, is under clinical development for the treatment of type 2 diabetes mellitus. This study aimed to explore the pharmacokinetics (PK) and pharmacodynamics interaction of DWP16001 with gemigliptin and metformin.AIMSDWP16001, a novel sodium-glucose cotransporter 2 inhibitor, is under clinical development for the treatment of type 2 diabetes mellitus. This study aimed to explore the pharmacokinetics (PK) and pharmacodynamics interaction of DWP16001 with gemigliptin and metformin.A randomized, open-label, 2-sequence, 2-period crossover study was conducted in 34 healthy male subjects. All subjects received a single oral dose of DWP16001 2 mg with and without gemigliptin and metformin (8 days of 50 mg once-daily dose and 1000 mg twice daily dose for gemigliptin and metformin, respectively). Serial blood samples were collected for PK and serum glucose analysis, and timed urine samples were collected to analyse urine glucose excretion (UGE). The PK and pharmacodynamic parameters were analysed by the noncompartmental method.METHODSA randomized, open-label, 2-sequence, 2-period crossover study was conducted in 34 healthy male subjects. All subjects received a single oral dose of DWP16001 2 mg with and without gemigliptin and metformin (8 days of 50 mg once-daily dose and 1000 mg twice daily dose for gemigliptin and metformin, respectively). Serial blood samples were collected for PK and serum glucose analysis, and timed urine samples were collected to analyse urine glucose excretion (UGE). The PK and pharmacodynamic parameters were analysed by the noncompartmental method.The PK interactions of DWP16001, gemigliptin and metformin were not clinically significant. The geometric mean ratios (with 90% confidence intervals) of coadministration to separate administration for area under the time-concentration curves were 1.04 (1.02-1.06), 1.03 (0.98-1.09) and 1.17 (1.12-1.22), for gemigliptin, metformin and DWP16001 respectively. The UGE induced by DWP16001 was not affected by the coadministration of gemigliptin and metformin.RESULTSThe PK interactions of DWP16001, gemigliptin and metformin were not clinically significant. The geometric mean ratios (with 90% confidence intervals) of coadministration to separate administration for area under the time-concentration curves were 1.04 (1.02-1.06), 1.03 (0.98-1.09) and 1.17 (1.12-1.22), for gemigliptin, metformin and DWP16001 respectively. The UGE induced by DWP16001 was not affected by the coadministration of gemigliptin and metformin.The results suggest that the DWP16001 could be added to metformin and gemigliptin combination therapy without dose adjustment.CONCLUSIONThe results suggest that the DWP16001 could be added to metformin and gemigliptin combination therapy without dose adjustment.
Author Jang, In‐Jin
Huh, Wan
Jeong, Sae Im
Lee, SeungHwan
Nah, Jae Jin
Kim, Yun
Hwang, Jun Gi
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  organization: Seoul National University College of Medicine and Hospital
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Cites_doi 10.1038/s41598‐018‐22658‐2
10.1111/dom.13795
10.1515/jom‐2020‐0153
10.1016/j.dsx.2018.06.003
10.1517/17425255.2014.907274
10.1097/FPC.0b013e3283559b22
10.1111/bph.15537
10.2165/00003088-200544070-00004
10.1111/j.1463‐1326.2011.01359.x
10.1111/j.1365‐2125.2009.03376.x
10.1080/17425255.2016.1215427
10.3390/pharmaceutics12090865
10.2215/CJN.06080616
10.4093/dmj.2016.40.5.339
10.15420/ecr.2018.33.1
10.1111/bcp.15348
10.1016/S0140‐6736(10)60576‐4
10.3109/00498254.2013.865856
10.1161/CIRCULATIONAHA.108.191305
10.1007/s40119‐016‐0075‐1
10.1007/s40261‐014‐0184‐3
10.1038/nrdp.2015.19
10.2337/dc22‐S009
10.1016/j.dsx.2020.02.012
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Notes The authors confirm that the principal investigator for this paper is In‐Jin Jang and that he had direct clinical responsibility for the subjects.
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References 2015; 1
2017; 6
2009; 68
2019; 14
2022; 45
2020; 14
2011; 13
2020; 12
2022; 88
2021; 121
2009; 119
2005; 44
2014; 44
2016; 12
2018; 8
2021; 178
2022
2019; 21
2020
2010; 376
2017; 12
2016; 40
2018; 12
2012; 22
2014; 34
2014; 10
e_1_2_11_10_1
e_1_2_11_14_1
e_1_2_11_13_1
e_1_2_11_12_1
e_1_2_11_11_1
e_1_2_11_7_1
e_1_2_11_6_1
e_1_2_11_28_1
e_1_2_11_5_1
e_1_2_11_27_1
e_1_2_11_4_1
e_1_2_11_26_1
e_1_2_11_3_1
e_1_2_11_2_1
e_1_2_11_21_1
e_1_2_11_20_1
e_1_2_11_25_1
e_1_2_11_24_1
e_1_2_11_9_1
e_1_2_11_23_1
e_1_2_11_8_1
e_1_2_11_22_1
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References_xml – volume: 119
  start-page: 351
  issue: 2
  year: 2009
  end-page: 357
  article-title: Intensive glycemic control and the prevention of cardiovascular events: implications of the ACCORD, ADVANCE, and VA diabetes trials: a position statement of the American Diabetes Association and a scientific statement of the American College of Cardiology Foundation and the American Heart Association
  publication-title: Circulation
– volume: 8
  start-page: 4466
  issue: 1
  year: 2018
  article-title: Combination of sodium‐glucose cotransporter 2 inhibitor and dipeptidyl peptidase‐4 inhibitor in type 2 diabetes: a systematic review with meta‐analysis
  publication-title: Sci Rep
– volume: 44
  start-page: 522
  issue: 6
  year: 2014
  end-page: 530
  article-title: Absorption, metabolism and excretion of [14C]gemigliptin, a novel dipeptidyl peptidase 4 inhibitor, in humans
  publication-title: Xenobiotica
– volume: 21
  start-page: 2152
  issue: 9
  year: 2019
  end-page: 2162
  article-title: Triple therapy with low‐dose dapagliflozin plus saxagliptin versus dual therapy with each monocomponent, all added to metformin, in uncontrolled type 2 diabetes
  publication-title: Diabetes Obes Metab
– volume: 1
  issue: 1
  year: 2015
  article-title: Type 2 diabetes mellitus
  publication-title: Nat Rev Dis Primers
– volume: 178
  start-page: S1
  issue: Suppl 1
  year: 2021
  end-page: S26
  article-title: The concise guide to pharmacology 2021/22: Introduction and other protein targets
  publication-title: Br J Pharmacol
– volume: 12
  issue: 9
  year: 2020
  article-title: In vitro metabolism of DWP16001, a novel sodium‐glucose cotransporter 2 inhibitor, in human and animal hepatocytes
  publication-title: Pharmaceutics
– volume: 13
  start-page: 357
  issue: 4
  year: 2011
  end-page: 365
  article-title: Pharmacokinetics and pharmacodynamics of dapagliflozin, a novel selective inhibitor of sodium‐glucose co‐transporter type 2, in Japanese subjects without and with type 2 diabetes mellitus
  publication-title: Diabetes Obes Metab
– volume: 40
  start-page: 339
  issue: 5
  year: 2016
  end-page: 353
  article-title: Gemigliptin: an update of its clinical use in the management of type 2 diabetes mellitus
  publication-title: Diabetes Metab J
– volume: 34
  start-page: 383
  issue: 6
  year: 2014
  end-page: 393
  article-title: Pharmacokinetic and pharmacodynamic interaction between gemigliptin and metformin in healthy subjects
  publication-title: Clin Drug Investig
– volume: 45
  start-page: S125
  issue: Suppl 1
  year: 2022
  end-page: S143
  article-title: 9. Pharmacologic approaches to glycemic treatment: standards of medical Care in Diabetes‐2022
  publication-title: Diabetes Care
– volume: 22
  start-page: 820
  issue: 11
  year: 2012
  end-page: 827
  article-title: Metformin pathways: pharmacokinetics and pharmacodynamics
  publication-title: Pharmacogenet Genomics
– volume: 376
  start-page: 419
  issue: 9739
  year: 2010
  end-page: 430
  article-title: Effect of intensive treatment of hyperglycaemia on microvascular outcomes in type 2 diabetes: an analysis of the ACCORD randomised trial
  publication-title: Lancet
– volume: 12
  start-page: 1117
  issue: 6
  year: 2018
  end-page: 1123
  article-title: SGLT2 inhibitors and the kidney: effects and mechanisms
  publication-title: Diabetes Metab Syndr
– volume: 14
  start-page: 50
  issue: 1
  year: 2019
  end-page: 59
  article-title: The role of inflammation in diabetes: current concepts and future perspectives
  publication-title: Eur Cardiol
– volume: 12
  start-page: 1407
  issue: 12
  year: 2016
  end-page: 1417
  article-title: DPP‐4 inhibitor plus SGLT‐2 inhibitor as combination therapy for type 2 diabetes: from rationale to clinical aspects
  publication-title: Expert Opin Drug Metab Toxicol
– volume: 6
  start-page: 129
  issue: 1
  year: 2017
  end-page: 132
  article-title: Does gender influence the cardiovascular benefits observed with sodium glucose co‐transporter‐2 (SGLT‐2) inhibitors? A meta‐regression analysis
  publication-title: Cardiol Ther
– volume: 88
  start-page: 4100
  issue: 9
  year: 2022
  end-page: 4110
  article-title: Dose‐dependent glucosuria of DWP16001, a novel selective sodium‐glucose cotransporter‐2 inhibitor, in healthy subjects
  publication-title: Br J Clin Pharmacol
– volume: 14
  start-page: 181
  issue: 3
  year: 2020
  end-page: 187
  article-title: Gender difference in cardiovascular outcomes with SGLT‐2 inhibitors and GLP‐1 receptor agonist in type 2 diabetes: a systematic review and meta‐analysis of cardio‐vascular outcome trials
  publication-title: Diabetes Metab Syndr
– volume: 44
  start-page: 721
  issue: 7
  year: 2005
  end-page: 729
  article-title: Steady‐state pharmacokinetics of a novel extended‐release metformin formulation
  publication-title: Clin Pharmacokinet
– year: 2022
– year: 2020
– volume: 68
  start-page: 883
  issue: 6
  year: 2009
  end-page: 890
  article-title: Pharmacokinetics and pharmacodynamics of LC15‐0444, a novel dipeptidyl peptidase IV inhibitor, after multiple dosing in healthy volunteers
  publication-title: Br J Clin Pharmacol
– volume: 12
  start-page: 700
  issue: 4
  year: 2017
  end-page: 710
  article-title: SGLT2 inhibition in the diabetic kidney‐from mechanisms to clinical outcome
  publication-title: Clin J Am Soc Nephrol
– volume: 121
  start-page: 229
  issue: 2
  year: 2021
  end-page: 239
  article-title: SGLT2 inhibitors: a narrative review of efficacy and safety
  publication-title: J Osteopath Med
– volume: 10
  start-page: 787
  issue: 6
  year: 2014
  end-page: 812
  article-title: The pharmacokinetic considerations and adverse effects of DDP‐4 inhibitors
  publication-title: Expert Opin Drug Metab Toxicol
– ident: e_1_2_11_7_1
  doi: 10.1038/s41598‐018‐22658‐2
– ident: e_1_2_11_19_1
– ident: e_1_2_11_9_1
  doi: 10.1111/dom.13795
– ident: e_1_2_11_24_1
– ident: e_1_2_11_27_1
  doi: 10.1515/jom‐2020‐0153
– ident: e_1_2_11_10_1
– ident: e_1_2_11_22_1
  doi: 10.1016/j.dsx.2018.06.003
– ident: e_1_2_11_13_1
  doi: 10.1517/17425255.2014.907274
– ident: e_1_2_11_16_1
  doi: 10.1097/FPC.0b013e3283559b22
– ident: e_1_2_11_17_1
  doi: 10.1111/bph.15537
– ident: e_1_2_11_21_1
  doi: 10.2165/00003088-200544070-00004
– ident: e_1_2_11_28_1
  doi: 10.1111/j.1463‐1326.2011.01359.x
– ident: e_1_2_11_18_1
  doi: 10.1111/j.1365‐2125.2009.03376.x
– ident: e_1_2_11_8_1
  doi: 10.1080/17425255.2016.1215427
– ident: e_1_2_11_11_1
  doi: 10.3390/pharmaceutics12090865
– ident: e_1_2_11_6_1
  doi: 10.2215/CJN.06080616
– ident: e_1_2_11_15_1
  doi: 10.4093/dmj.2016.40.5.339
– ident: e_1_2_11_2_1
  doi: 10.15420/ecr.2018.33.1
– ident: e_1_2_11_12_1
  doi: 10.1111/bcp.15348
– ident: e_1_2_11_3_1
  doi: 10.1016/S0140‐6736(10)60576‐4
– ident: e_1_2_11_14_1
  doi: 10.3109/00498254.2013.865856
– ident: e_1_2_11_4_1
  doi: 10.1161/CIRCULATIONAHA.108.191305
– ident: e_1_2_11_25_1
  doi: 10.1007/s40119‐016‐0075‐1
– ident: e_1_2_11_20_1
  doi: 10.1007/s40261‐014‐0184‐3
– ident: e_1_2_11_23_1
  doi: 10.1038/nrdp.2015.19
– ident: e_1_2_11_5_1
  doi: 10.2337/dc22‐S009
– ident: e_1_2_11_26_1
  doi: 10.1016/j.dsx.2020.02.012
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Snippet Aims DWP16001, a novel sodium–glucose cotransporter 2 inhibitor, is under clinical development for the treatment of type 2 diabetes mellitus. This study aimed...
DWP16001, a novel sodium-glucose cotransporter 2 inhibitor, is under clinical development for the treatment of type 2 diabetes mellitus. This study aimed to...
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SubjectTerms Adult
Area Under Curve
Benzofurans - pharmacokinetics
Benzofurans - pharmacology
Cross-Over Studies
diabetes
Diabetes Mellitus, Type 2 - drug therapy
Drug Interactions
Glucose
Healthy Volunteers
Humans
Hypoglycemic Agents
Male
Metformin
pharmacodynamics
pharmacokinetics
Sodium
Sodium-Glucose Transporter 2 Inhibitors - pharmacology
Title Pharmacokinetic and pharmacodynamic interaction of DWP16001, a sodium–glucose cotransporter 2 inhibitor, with gemigliptin and metformin in healthy adults
URI https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fbcp.15632
https://www.ncbi.nlm.nih.gov/pubmed/36496349
https://www.proquest.com/docview/2753304671
Volume 89
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