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OpenTrials
Completed

NCT Number: NCT02916706

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

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).

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Investigational center

Beijing, China

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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).

Treatment and study plan

Teneligliptin 20mg

Drug

Placebo

Drug

Primary outcomes

  1. Change in HbA1c From Baseline to Week 24

    Time frame: at Day 1(baseline) and Week 24

    The change in HbA1c from baseline to Week 24 in Teneligliptin compared to Placebo was performed on FAS.

Secondary outcomes

  1. The Changes in Fasting Plasma Glucose (FPG) at Week 24

    Time frame: at Day 1(baseline) and Week 24

    The change in FPG from baseline to Week 24 in Teneligliptin compared to Placebo was performed on FAS.

Sponsors and collaborators

Lead sponsor

Tanabe Pharma Corporation

Industry

Registry information

Important dates

Study start
2016
Primary completion
2018
First posted
Sep 27, 2016
Registry last updated
Jan 6, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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