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 in: | British journal of clinical pharmacology Vol. 89; no. 6; pp. 1780 - 1788 |
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Main Authors: | , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
England
01-06-2023
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Subjects: | |
Online Access: | Get full text |
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Summary: | 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. |
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Bibliography: | The authors confirm that the principal investigator for this paper is In‐Jin Jang and that he had direct clinical responsibility for the subjects. ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 ObjectType-Undefined-3 |
ISSN: | 0306-5251 1365-2125 1365-2125 |
DOI: | 10.1111/bcp.15632 |