Efficacy and Safety of Teneligliptin in Chinese Patients With Type 2 Diabetes Mellitus

Mitsubishi Tanabe Pharma

Status and phase

Completed

Phase 3

Conditions

Type 2 Diabetes Mellitus

Treatments

Drug: Placebo

Drug: Teneligliptin 20mg

Study type

Interventional

Funder types

Industry

Identifiers

NCT02916706

MP-513-C02

Details and patient eligibility

About

This study is designed as a prospective, multi-centre, parallel group, double-blind randomized, placebo-controlled, phase 3 clinical study to evaluate the efficacy and safety of MP-513 (Teneligliptin).

Enrollment

254 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

A signed and dated informed consent form has been obtained from the subject, in accordance with International Conference on Harmonisation guidelines on Good Clinical Practice (ICH GCP), before any screening or study related procedures take place.
The subject is aged ≥18 years at signature of the informed consent form.
Hospitalization status: outpatient.
The subject has had a documented diagnosis of type 2 diabetes mellitus for at least 3 months at the screening visit (Day -28).
The subject is undergoing diet and exercise therapy, and diet and exercise regimen has not been changed for at least 8 consecutive weeks at the screening visit (Day -28). Subjects who cannot do exercise due to complication are not limited to this criteria.
The subject's glycosylated fraction of haemoglobin(HbA1c) is ≥ 7.0% and < 10.0% at the screening visit (Day -28) and on Day -14.

Exclusion criteria

The subject has a history of type 1 diabetes mellitus or a secondary form of diabetes.
The subject has received insulin within 1 year prior to the screening visit (Day -28), with the exception of insulin therapy during hospitalization or insulin therapy for medical conditions not requiring hospitalization (< 2 weeks' duration).
The subject has received an anti-diabetic drug within 8 weeks prior to the screening visit (Day -28).