Phase III, randomized, double-blind, placebo-controlled study to evaluate the efficacy and safety of teneligliptin monotherapy in Chinese patients with type 2 diabetes mellitus inadequately controlled with diet and exercise.

Linong Ji, Jianhua Ma, Weiping Lu, Jingdong Liu, Jiao'e Zeng, Jialin Yang, Wei Li, Xiuzhen Zhang, Xinhua Xiao, Gen Takayanagi, Yi Wang

Journal: Journal of diabetes investigation 2022;12(4):537-545

PMID: 32810383

Abstract

AIMS/INTRODUCTION

Although the efficacy of teneligliptin, a highly selective dipeptidyl peptidase-4 inhibitor, has been amply studied for the treatment of type 2 diabetes, no clinical trials of teneligliptin have been carried out in China. We evaluated the efficacy and safety of teneligliptin monotherapy compared with a placebo in Chinese patients with type 2 diabetes mellitus inadequately controlled with diet and exercise.

MATERIALS AND METHODS

This multicenter, randomized, double-blind, placebo-controlled, parallel-group study, carried out at 42 sites, enrolled type 2 diabetes patients with glycosylated hemoglobin 7.0 to <10.0% and fasting blood glucose <270 mg/dL. Patients were randomly assigned, in a 1:1 ratio, to treatment with 20 mg teneligliptin or a placebo (n = 127, each) administered orally once daily before breakfast for 24 weeks. Change in glycosylated hemoglobin from baseline to week 24 was the primary efficacy end-point. Safety was assessed by the incidence of adverse events and adverse drug reactions.

RESULTS

The least square mean (LSM) change in glycosylated hemoglobin from baseline to week 24 was -0.95% with teneligliptin versus -0.14% with a placebo, yielding an LSM difference (teneligliptin vs placebo) of -0.80% (P < 0.0001). For the secondary end-point, from baseline to week 24, the LSM change in fasting blood glucose was -21.9 mg/dL with teneligliptin versus -1.4 mg/dL with a placebo, yielding an LSM difference (teneligliptin vs placebo) of -20.5 mg/dL (P < 0.0001). The adverse event and adverse drug reaction incidence rates, including hypoglycemia, were similar in both groups.

CONCLUSIONS

At 24 weeks, teneligliptin was generally well tolerated and effective in Chinese patients with type 2 diabetes mellitus inadequately controlled with diet and exercise.

© 2020 The Authors. Journal of Diabetes Investigation published by Asian Association for the Study of Diabetes (AASD) and John Wiley & Sons Australia, Ltd.

Address: Peking University People's Hospital, Beijing, China.; Nanjing First Hospital, Nanjing, Jiangsu, China.; Huai'an First People's Hospital, Huaian, Jiangsu, China.; Jiangxi Province People's Hospital, Nanchang, Jiangxi, China.; Jingzhou Central Hospital, Jingzhou, Hubei, China.; Minhang Central Hospital, Shanghai, China.; The Affiliated Hospital of Xuzhou Medical University, Xuzhou, Jiangsu, China.; Tongji Hospital, Tongji University, Shanghai, China.; The First Affiliated Hospital, University of South China, Hengyang, Hunan, China.; Mitsubishi Tanabe Pharma Development America, Inc., Jersey City, New Jersey, USA.; Mitsubishi Tanabe Pharma Development (Beijing) Co., Ltd., Beijing, China.
Bant logo

© Copyright 2026, Nutrition Evidence

NED wishes to thank the following organisations for their support:

We use cookies to improve your experience and analyze site traffic with Google Analytics. By continuing to use our site, you agree to our use of cookies. Learn more.