Skip to content

Evaluation of pharmacodynamics and safety of teneligliptin in type 2 diabetic patients with chronic renal dysfunction

Evaluation of pharmacodynamics and safety of teneligliptin in type 2 diabetic patients with chronic renal dysfunction - Evaluation of pharmacodynamics and safety of teneligliptin in type 2 diabetic patients with chronic renal dysfunction

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000010343
Enrollment
12
Registered
2013-03-28
Start date
2013-01-18
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patients with Type 2 diabetes [chronic renal dysfunction (CKD Stage:over G3b)]

Interventions

Teneligliptin 20mg/day 1week

Sponsors

Kitano Hospital, The Tazuke Kofukai Medical Research Institute
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Patients agreed to participate in this study with a written consent 2) Gender: agnostic 3) Age: 20 years old or older when obtaining consent 4) Inpatient and outpatient: hospitalization 5) Patients who continued diet and exercise therapy more than 12 weeks before day1. Exercise therapy is not essential if it is prohibited because of the complication. 6) CKD stage over G3b based on serum Cystatin C level within four weeks of day1.

Exclusion criteria

Exclusion criteria: 1)Type 1 diabetes,diabetes arising from the failure of pancreas,or secondary diabetes (eg. Cushing's syndrome and acromegaly) 2) Patient correspond to contraindications of teneligliptin 3) Excessive alcohol addicts: patient who take average net more than 60 g alcohol every single day (more than following: 3 bottles of sake, 1 with shochu, 3 bottles of beer, 3 glasses of whiskey or brandy(double),and 5 glasses of wine) 4) Pregnant, lactating, possible pregnant patient 5) Patient judged as ineligible for this study by the researcher

Design outcomes

Primary

MeasureTime frame
Plasma concentration of teneligliptin Changes in active GLP-1 levels

Secondary

MeasureTime frame
C-peptide- and glucagon-response to the meal test

Countries

Japan

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026