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‐...
Saved in:
Published in | British journal of clinical pharmacology Vol. 89; no. 6; pp. 1780 - 1788 |
---|---|
Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
01.06.2023
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
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 |
Author_xml | – sequence: 1 givenname: Sae Im orcidid: 0000-0002-5299-4305 surname: Jeong fullname: Jeong, Sae Im organization: Chungbuk National University Hospital – sequence: 2 givenname: Yun orcidid: 0000-0002-9809-7351 surname: Kim fullname: Kim, Yun organization: Daegu Catholic University – sequence: 3 givenname: Jae Jin surname: Nah fullname: Nah, Jae Jin organization: Daewoong Pharmaceutical Co., Ltd – sequence: 4 givenname: Wan surname: Huh fullname: Huh, Wan organization: Daewoong Pharmaceutical Co., Ltd – sequence: 5 givenname: In‐Jin orcidid: 0000-0002-8384-3139 surname: Jang fullname: Jang, In‐Jin organization: Seoul National University College of Medicine and Hospital – sequence: 6 givenname: Jun Gi orcidid: 0000-0002-0965-0531 surname: Hwang fullname: Hwang, Jun Gi email: jk_hwang@cbnuhctc.com organization: Chungbuk National University Hospital – sequence: 7 givenname: SeungHwan orcidid: 0000-0002-1713-9194 surname: Lee fullname: Lee, SeungHwan email: leejh413@snu.ac.kr organization: Seoul National University College of Medicine and Hospital |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/36496349$$D View this record in MEDLINE/PubMed |
BookMark | eNp1kc1O3DAUhS0EgoF2wQsgL1uJgH9iJ1m2U_ojITELqi4jx7EnLrEdbEdodn0Hln07nqSGmbLjytLVvf7OseRzDPaddwqAU4wucK7LTk4XmHFK9sACU84KggnbBwtEES8YYfgIHMf4GyFMMWeH4IjysuG0bBbg72oQwQrp74xTyUgoXA-n3a7fOGHzzrikgpDJeAe9hl9-rTDPZudQwOh7M9unP4_rcZY-Kih9CsLFyYesgSRrB9OZ5MM5fDBpgGtlzXo0UzLu5S2rkvbB5imfQYkxDRso-nlM8R040GKM6v2un4CfX69ul9-L65tvP5afrgtJCSJFjWpJJKlrITGRuMZalx1jTV9p0iDR5EveI805retKskpK2RFV8k5RpkmH6Qn4sPWdgr-fVUytNVGqcRRO-Tm2pGKUopJXz-jZDp07q_p2CsaKsGn_f2gGPm4BGXyMQelXBKP2Oaw2h9W-hJXZyy37YEa1eRtsPy9XW8U_LuyYQg |
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 |
ContentType | Journal Article |
Copyright | 2022 British Pharmacological Society. |
Copyright_xml | – notice: 2022 British Pharmacological Society. |
DBID | AAYXX CITATION CGR CUY CVF ECM EIF NPM 7X8 |
DOI | 10.1111/bcp.15632 |
DatabaseName | CrossRef Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed MEDLINE - Academic |
DatabaseTitle | CrossRef MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) MEDLINE - Academic |
DatabaseTitleList | MEDLINE MEDLINE - Academic |
Database_xml | – sequence: 1 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database – sequence: 2 dbid: EIF name: MEDLINE url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search sourceTypes: Index Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Pharmacy, Therapeutics, & Pharmacology |
EISSN | 1365-2125 |
EndPage | 1788 |
ExternalDocumentID | 36496349 10_1111_bcp_15632 BCP15632 |
Genre | article Randomized Controlled Trial Research Support, Non-U.S. Gov't Journal Article |
GrantInformation_xml | – fundername: Daewoong Pharmaceutical Co., Ltd |
GroupedDBID | --- .3N .55 .GA .GJ .Y3 05W 0R~ 10A 1OC 23N 24P 2WC 31~ 33P 36B 3O- 3SF 4.4 50Y 50Z 51W 51X 52M 52N 52O 52P 52R 52S 52T 52U 52V 52W 52X 53G 5GY 5HH 5LA 5VS 66C 6J9 702 7PT 8-0 8-1 8-3 8-4 8-5 8UM 930 A01 A03 AAESR AAEVG AAHHS AAHQN AAIPD AAMNL AANLZ AAONW AASGY AAXRX AAYCA AAZKR ABCQN ABCUV ABEML ABOCM ABPVW ABQWH ABXGK ACAHQ ACCFJ ACCZN ACFBH ACGFO ACGFS ACGOF ACMXC ACPOU ACSCC ACXBN ACXQS ADBBV ADBTR ADEOM ADIZJ ADKYN ADMGS ADOZA ADXAS ADZMN ADZOD AEEZP AEGXH AEIGN AEIMD AENEX AEQDE AEUQT AEUYR AFBPY AFEBI AFFPM AFGKR AFPWT AFWVQ AFZJQ AHBTC AIACR AIAGR AITYG AIURR AIWBW AJBDE ALAGY ALMA_UNASSIGNED_HOLDINGS ALUQN ALVPJ AMBMR AMYDB AOIJS ATUGU AZBYB AZVAB BAFTC BAWUL BFHJK BHBCM BMXJE BROTX BRXPI BY8 C45 CAG COF CS3 D-6 D-7 D-E D-F DCZOG DIK DPXWK DR2 DRFUL DRMAN DRSTM DU5 E3Z EBS EJD EMOBN ESX EX3 F00 F01 F04 F5P FIJ FUBAC G-S G.N GODZA GX1 H.X HF~ HGLYW HYE HZI HZ~ IHE IPNFZ IX1 J0M K48 KBYEO LATKE LC2 LC3 LEEKS LH4 LITHE LOXES LP6 LP7 LSO LUTES LW6 LYRES MEWTI MK4 MRFUL MRMAN MRSTM MSFUL MSMAN MSSTM MXFUL MXMAN MXSTM N04 N05 N9A NF~ O66 O9- OIG OK1 OVD P2P P2W P2X P2Z P4B P4D Q.N Q11 QB0 R.K ROL RPM RX1 SUPJJ TEORI TR2 UB1 V8K W8V W99 WBKPD WHWMO WIH WIJ WIK WIN WOHZO WOW WQJ WRC WVDHM WXI WXSBR X7M XG1 YFH YOC YUY ZGI ZXP ZZTAW ~IA ~WT AAYXX AEYWJ AGHNM AGYGG CITATION AAMMB AEFGJ AGXDD AIDQK AIDYY CGR CUY CVF ECM EIF NPM 7X8 |
ID | FETCH-LOGICAL-c3202-808c2c288ac12c181ff4b559d7f290a9c2c6d0f663887c57cccb2e46be35f2b13 |
IEDL.DBID | DR2 |
ISSN | 0306-5251 1365-2125 |
IngestDate | Fri Jul 11 14:26:27 EDT 2025 Mon Jul 21 06:06:40 EDT 2025 Tue Jul 01 01:59:31 EDT 2025 Wed Jan 22 16:21:26 EST 2025 |
IsDoiOpenAccess | false |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 6 |
Keywords | pharmacokinetics drug interactions diabetes pharmacodynamics |
Language | English |
License | http://onlinelibrary.wiley.com/termsAndConditions#vor 2022 British Pharmacological Society. |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c3202-808c2c288ac12c181ff4b559d7f290a9c2c6d0f663887c57cccb2e46be35f2b13 |
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. ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 ObjectType-Undefined-3 |
ORCID | 0000-0002-9809-7351 0000-0002-0965-0531 0000-0002-1713-9194 0000-0002-8384-3139 0000-0002-5299-4305 |
OpenAccessLink | https://onlinelibrary.wiley.com/doi/pdfdirect/10.1111/bcp.15632 |
PMID | 36496349 |
PQID | 2753304671 |
PQPubID | 23479 |
PageCount | 9 |
ParticipantIDs | proquest_miscellaneous_2753304671 pubmed_primary_36496349 crossref_primary_10_1111_bcp_15632 wiley_primary_10_1111_bcp_15632_BCP15632 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | June 2023 2023-06-00 20230601 |
PublicationDateYYYYMMDD | 2023-06-01 |
PublicationDate_xml | – month: 06 year: 2023 text: June 2023 |
PublicationDecade | 2020 |
PublicationPlace | England |
PublicationPlace_xml | – name: England |
PublicationTitle | British journal of clinical pharmacology |
PublicationTitleAlternate | Br J Clin Pharmacol |
PublicationYear | 2023 |
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 e_1_2_11_18_1 e_1_2_11_17_1 e_1_2_11_16_1 e_1_2_11_15_1 e_1_2_11_19_1 |
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 |
SSID | ssj0013165 |
Score | 2.4046674 |
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... |
SourceID | proquest pubmed crossref wiley |
SourceType | Aggregation Database Index Database Publisher |
StartPage | 1780 |
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 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Lb9QwELaqnrjwKK8FWrkIVRw2q43jvMSp9KGKA1qhVvSAFNljp6zKJqtN9rCc-A8c-Xf8EmbsZLcFISGkHPK0E3k8840z8w1jr6Q0OhWgglxHJS3dJIHOlQwgFmCUjUuhHdvn--TsQr67jC-32Js-F8bzQ6wX3GhmOH1NE1zp5sYk1zAfofMRkf6lWC0CRB_E5g9C6MpIEiRGZysOO1YhiuJZP3nbFv0BMG_jVWdwTu-xT_2r-jiT69Gy1SP4-huL439-y312twOi_NBLzgO2ZasddjDxTNarIT_fJGY1Q37AJxuO69VD9qM_vMa-8RauKsPn3Tnjq9xzoqJY-MQJXpf8-OMkJOAz5Io3tZkuZz-_fe9C5jnU7ZpmfcEFPvt5qlHbLIaclor5lZ1Nr76QgqtcXzPbEtzGI9x8MueKOzKR5hG7OD05PzoLujoPAVD1djSSGQgQWaYgFICQoyylRk_HpKXIxyrHi4kZl4iNUCNCnAKAFlYm2kYkS2H0mG1XdWWfMg4WEUwuAeIslTpJdDmWBk2wNgoy9NYG7GU_4sXc03kUvRuEg1C4QRiw_V4WCpxs9AdFVbZeNoVIKRgXbUs4YE-8kKybiRKJykzmA_baDfXf2y_eHk3czrN_v_U5u0OF7n2Q2gu23S6WdhfhUKv3nNz_AsjECaY |
linkProvider | Wiley-Blackwell |
linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Lb9QwEB5V5QAX3o9tKRiEKg6b1cZxXlIv0FItUKoV2opeUGRPnHbVbrLazR6WE_-BI_-OX8LYTnYpCAkh5ZCHYyeyZ-Ybe_wNwAshchVzlF6qgsJM3USeSqXwMOSYSx0WXFm2z-NocCLenYanG7DX7oVx_BCrCTcjGVZfGwE3E9K_SLnCaY-8j4AU8DWT0dsw5x985Os1BN8mkjSgmNyt0G94hUwcz-rVq9boD4h5FbFak3N4Cz63H-siTS56i1r18MtvPI7_-ze34WaDRdkrN3juwIYu78Lu0JFZL7tstN6bNe-yXTZc01wv78H39vKCGqciTJY5mzb3cpfonhk2ipnbO8Gqgh18GvoG-3SZZPMqHy8mP75-a6LmGVb1iml9xji9ez5WpHBmXWZmi9mZnozPLo2OK21bE10bxE1XdLj9nEtm-UTm9-Hk8M1of-A1qR48NAncyU4myJEniUSfI6GOohCKnJ08Lnjalyk9jPJ-QfCIlCKGMSIqrkWkdGCGkx88gM2yKvUjYKgJxKQCMUxioaJIFX2RkxVWucSEHLYOPG-7PJs6Ro-s9YSoEzLbCR141g6GjOTNLKLIUleLecZjE49L5sXvwEM3SlbVBJEgfSbSDry0ff33-rPX-0N7svXvRZ_C9cHow1F29Pb4_TbcMHnvXczaY9isZwu9Q-ioVk-sEPwESrwNwg |
linkToPdf | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Lb9QwELaqIiEuQHkuUDAIVRw2q43jvNQTdFmVh6oItaIHpMge22VVNlntZg_Lif_Asf-OX8LYTnYpCAkh5ZCHYyeyZ-Ybe_wNIc85VzJlIIJcRsZO3SSBzAUPIGaghI4Nk47t8yg5POFvT-PTLbLf7YXx_BDrCTcrGU5fWwGfKfOLkEuYDdD5iFD_XuHJMLd5G0Yf2GYJIXR5JC0mRm8rDltaIRvGs371sjH6A2FeBqzO4oxvkE_dt_pAk_PBspED-PobjeN__sxNcr1FovSlHzo7ZEtXt8he4amsV316vNmZtejTPVpsSK5Xt8lFd3mObWMRKipFZ-095dPcU8tFMfc7J2ht6OhjEVrk06eCLmo1WU5_fPvexsxTqJs1z_qcMnz380Siupn3qZ0rpmd6Ojn7YjVc5dqa6sbibbzCw-_mXFHHJrK4Q07Gr48PDoM20UMANn07WskMGLAsExAyQMxhDJfo6qjUsHwocnyYqKFBcIQqEeIUACTTPJE6soMpjO6S7aqu9H1CQSOEyTlAnKVcJok0Q67QBkslIEN3rUeedT1ezjyfR9n5QdgJpeuEHnnajYUSpc0uoYhK18tFyVIbjYvGJeyRe36QrKuJEo7ajOc98sJ19d_rL18dFO7kwb8XfUKuFqNx-f7N0buH5JpNeu8D1h6R7Wa-1LsIjRr52InATyU9DHE |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Pharmacokinetic+and+pharmacodynamic+interaction+of+DWP16001%2C+a+sodium-glucose+cotransporter+2+inhibitor%2C+with+gemigliptin+and+metformin+in+healthy+adults&rft.jtitle=British+journal+of+clinical+pharmacology&rft.au=Jeong%2C+Sae+Im&rft.au=Kim%2C+Yun&rft.au=Nah%2C+Jae+Jin&rft.au=Huh%2C+Wan&rft.date=2023-06-01&rft.eissn=1365-2125&rft.volume=89&rft.issue=6&rft.spage=1780&rft_id=info:doi/10.1111%2Fbcp.15632&rft_id=info%3Apmid%2F36496349&rft.externalDocID=36496349 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0306-5251&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0306-5251&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0306-5251&client=summon |