Evidence map›Paper›PMID 37282359›Full record

Trial reportClinical and translational science2023

Pharmacokinetic and pharmacodynamic drug-drug interactions between evogliptin and empagliflozin or dapagliflozin in healthy male volunteers.

Dasohm Kim, Minkyu Choi, Byung Hak Jin, Taegon Hong, Choon Ok Kim, Byung Won Yoo, Min Soo Park

Open access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Clinical and translational science, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.0field-weighted citation impact, top 22% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Article
  4. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 1 institution in 2 countries.

Dasohm KimDepartment of Clinical Pharmacology, Severance Hospital, Yonsei University College of Medicine, Seoul, South Korea.ORCID 0000-0002-7925-194X
Minkyu ChoiDepartment of Clinical Pharmacology, Severance Hospital, Yonsei University College of Medicine, Seoul, South Korea.ORCID 0000-0003-2407-0057
Byung Hak JinDepartment of Clinical Pharmacology, Severance Hospital, Yonsei University College of Medicine, Seoul, South Korea.ORCID 0000-0002-8655-4076
Taegon HongDepartment of Clinical Pharmacology, Severance Hospital, Yonsei University College of Medicine, Seoul, South Korea.ORCID 0000-0001-7490-0085
Choon Ok KimDepartment of Clinical Pharmacology, Severance Hospital, Yonsei University College of Medicine, Seoul, South Korea.ORCID 0000-0002-2319-1108
Byung Won YooDepartment of Clinical Pharmacology, Severance Hospital, Yonsei University College of Medicine, Seoul, South Korea.ORCID 0000-0001-6895-1484
Min Soo ParkDepartment of Clinical Pharmacology, Severance Hospital, Yonsei University College of Medicine, Seoul, South Korea.ORCID 0000-0002-4395-9938
Yonsei University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Evogliptin (EV) is a novel dipeptidyl peptidase-4 inhibitor (DPP4i) for glycemic control in patients with type 2 diabetes mellitus (T2DM). This study evaluated the pharmacokinetic (PK) and pharmacodynamic (PD) interactions between EV and sodium glucose cotransporter-2 inhibitors (SGLT2i) in healthy volunteers since combination therapy of DPP4i and SGLT2i has been considered as an effective option for T2DM treatment. A randomized, open-label, multiple-dose, two-arm, three-period, three treatments, two-sequence crossover study was conducted in healthy Korean volunteers. In arm 1, subjects were administered 5 mg of EV once daily for 7 days, 25 mg of empagliflozin (EP) once daily for 5 days, and the combination once daily for 5 days (EV + EP). In arm 2, subjects were administered 5 mg of EV once daily for 7 days, 10 mg of dapagliflozin (DP) once daily for 5 days, and the combination once daily for 5 days (EV + DP). Serial blood samples were collected for PK analysis, and oral glucose tolerance tests were conducted for PD analysis. In each arm, a total of 18 subjects completed the study. All adverse events (AEs) were mild with no serious AEs. The geometric mean ratio and confidence interval of the main PK parameters (maximum concentration of the drug in plasma at steady state and area under the plasma drug concentration-time curve within a dosing interval at a steady state) between EV and either EP or DP alone were not significantly altered by co-administration. Administration of EV + EP or EV + DP did not result in significant PD changes, as determined by the glucose-lowering effect. Administration of EV + EP or EV + DP had no significant effects on the PK profiles of each drug. All treatments were well-tolerated.

Indexed as

Diabetes Mellitus, Type 2Dipeptidyl-Peptidase IV InhibitorsBenzhydryl CompoundsCross-Over StudiesDrug InteractionsGlucosidesHealthy VolunteersHumansHypoglycemic AgentsMalePiperazines4-(3-amino-4-(2,4,5-trifluorophenyl)butanoyl)-3-(tert-butoxymethyl)piperazin-2-oneBenzhydryl CompoundsdapagliflozinDipeptidyl-Peptidase IV InhibitorsempagliflozinGlucosidesHypoglycemic AgentsPiperazines

Identifiers

PMID37282359
PMCPMC10432875
OpenAlexW4379600563

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.