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Trials / Completed

CompletedNCT04195919

The Pharmacokinetics/Pharmacodynamics and Safety/Tolerability of Evogliptin in Hemodialysis Patients

A Clinical Study to Investigate the Pharmacokinetics/Pharmacodynamics and Safety/Tolerability of Evogliptin in Hemodialysis Patients

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
17 (actual)
Sponsor
Dong-A ST Co., Ltd. · Industry
Sex
All
Age
20 Years – 80 Years
Healthy volunteers
Accepted

Summary

A clinical study to investigate the pharmacokinetics/ pharmacodynamics and safety/tolerability of Evogliptin in hemodialysis patients

Conditions

Interventions

TypeNameDescription
DRUGEvogliptin 5mgParticipants receive Single oral administration of Evogliptin 5mg on day1
DRUGEvogliptin 5mgPeriod 1(1d,After hemodialysis) → Wash-out period → Period 2(15d,Before hemodialysis) Hemodialysis patients receive Single oral administration of Evogliptin 5mg on day1 and day15 With a 14-day washout period

Timeline

Start date
2020-07-10
Primary completion
2021-05-24
Completion
2021-05-24
First posted
2019-12-12
Last updated
2021-12-01

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT04195919. Inclusion in this directory is not an endorsement.

The Pharmacokinetics/Pharmacodynamics and Safety/Tolerability of Evogliptin in Hemodialysis Patients (NCT04195919) · Clinical Trials Directory