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Dual add-on therapy of gemigliptin and dapagliflozin in patients with type 2 diabetes inadequately controlled with metformin alone: The SOLUTION 2 study

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dc.contributor.authorHan, Kyung Ah-
dc.contributor.authorHwang, You-Cheol-
dc.contributor.authorMoon, Shin Je-
dc.contributor.authorCho, Ho Chan-
dc.contributor.authorYoo, Hye Jin-
dc.contributor.authorChoi, Sung Hee-
dc.contributor.authorChon, Suk-
dc.contributor.authorKim, Kyoung-Ah-
dc.contributor.authorKim, Tae Nyun-
dc.contributor.authorKang, Jun Goo-
dc.contributor.authorPark, Cheol-Young-
dc.contributor.authorWon, Jong Chul-
dc.contributor.authorCho, Eunjoo-
dc.contributor.authorKim, Jeongyun-
dc.contributor.authorPark, Kyong Soo-
dc.date.accessioned2024-08-08T13:01:16Z-
dc.date.available2024-08-08T13:01:16Z-
dc.date.issued2024-09-
dc.identifier.issn1462-8902-
dc.identifier.issn1463-1326-
dc.identifier.urihttps://scholarworks.dongguk.edu/handle/sw.dongguk/22431-
dc.description.abstractAim: To evaluate the efficacy and safety of gemigliptin and dapagliflozin dual add-on therapy (GEMI + DAPA) to metformin in type 2 diabetes (T2D) patients who had inadequate glycaemic control on metformin alone, compared with a single add-on of either gemigliptin (GEMI) or dapagliflozin (DAPA) to metformin. Materials and Methods: In this randomized, double-blind, double-dummy, active-controlled, parallel-group, phase 3 study, 469 T2D patients treated with a stable dose of metformin for 8 weeks or longer were randomized to receive GEMI + DAPA (n = 157) and either GEMI (n = 156) or DAPA (n = 156). The primary endpoint was change in HbA1c levels from baseline at week 24. Results: Baseline characteristics including body mass index and T2D duration were similar among groups. At week 24, the least square mean changes in HbA1c from baseline were -1.34% with GEMI + DAPA, -0.90% with GEMI (difference between GEMI + DAPA vs. GEMI -0.44% [95% confidence interval {CI}: -0.58% to -0.31%], P < .01) and -0.78% with DAPA (difference between GEMI + DAPA vs. DAPA -0.56% [95% CI: -0.69% to -0.42%], P < .01). Both upper CIs were less than 0, demonstrating the superiority of GEMI + DAPA for lowering HbA1c. The rates of responders achieving HbA1c less than 7% and less than 6.5% were greater with GEMI + DAPA (84.9%, 56.6%) than with GEMI (55.3%, 32.2%) and DAPA (49.3%, 15.3%). The incidence rate of adverse events was similar across groups, with low incidence rates of hypoglycaemia, urinary tract infection and genital infection. Conclusions: These results suggest that the addition of GEMI + DAPA to metformin as triple combination therapy was effective, safe and well-tolerated, especially for T2D patients who experienced poor glycaemic control on metformin alone.-
dc.format.extent10-
dc.language영어-
dc.language.isoENG-
dc.publisherJohn Wiley & Sons Ltd-
dc.titleDual add-on therapy of gemigliptin and dapagliflozin in patients with type 2 diabetes inadequately controlled with metformin alone: The SOLUTION 2 study-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1111/dom.15717-
dc.identifier.scopusid2-s2.0-85197684684-
dc.identifier.wosid001265229400001-
dc.identifier.bibliographicCitationDiabetes, Obesity and Metabolism, v.26, no.9, pp 3743 - 3752-
dc.citation.titleDiabetes, Obesity and Metabolism-
dc.citation.volume26-
dc.citation.number9-
dc.citation.startPage3743-
dc.citation.endPage3752-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaEndocrinology & Metabolism-
dc.relation.journalWebOfScienceCategoryEndocrinology & Metabolism-
dc.subject.keywordPlusDIPEPTIDYL PEPTIDASE-4 INHIBITOR-
dc.subject.keywordPlusDOUBLE-BLIND-
dc.subject.keywordPlusCARDIOVASCULAR OUTCOMES-
dc.subject.keywordPlusEFFICACY-
dc.subject.keywordPlusSAFETY-
dc.subject.keywordPlusCOMBINATION-
dc.subject.keywordPlusTRIAL-
dc.subject.keywordPlusEMPAGLIFLOZIN-
dc.subject.keywordPlusMONOTHERAPY-
dc.subject.keywordPlusMULTICENTER-
dc.subject.keywordAuthordapagliflozin-
dc.subject.keywordAuthorDPP-4 inhibitor-
dc.subject.keywordAuthormetformin-
dc.subject.keywordAuthorSGLT-2 inhibitor-
dc.subject.keywordAuthortype 2 diabetes-
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