Efficacy and safety of teneligliptin added to metformin in Chinese patients with type 2 diabetes mellitus inadequately controlled with metformin: A phase 3, randomized, double‐blind, placebo‐controlled study

Abstract Introduction We evaluated the efficacy and safety of teneligliptin compared with placebo when added to metformin therapy in Chinese patients with type 2 diabetes inadequately controlled with metformin monotherapy. Methods This multicentre, randomized, double‐blind, placebo‐controlled, paral...

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Main Authors: Linong Ji, Ling Li, Jianhua Ma, Xuefeng Li, Dongmei Li, Bangzhu Meng, Weiping Lu, Jiao Sun, Yanmei Liu, Gen Takayanagi, Yi Wang
Format: Article
Language:English
Published: Wiley 2021-04-01
Series:Endocrinology, Diabetes & Metabolism
Subjects:
Online Access:https://doi.org/10.1002/edm2.222
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spelling doaj-a2759437d7f24e03b6cd9180d3939d042021-04-08T13:20:50ZengWileyEndocrinology, Diabetes & Metabolism2398-92382021-04-0142n/an/a10.1002/edm2.222Efficacy and safety of teneligliptin added to metformin in Chinese patients with type 2 diabetes mellitus inadequately controlled with metformin: A phase 3, randomized, double‐blind, placebo‐controlled studyLinong Ji0Ling Li1Jianhua Ma2Xuefeng Li3Dongmei Li4Bangzhu Meng5Weiping Lu6Jiao Sun7Yanmei Liu8Gen Takayanagi9Yi Wang10Peking University People's Hospital Beijing ChinaShengjing Hospital of China Medical University Liaoning ChinaNanjing First Hospital Nanjing Jiangsu ChinaShiyan Taihe Hospital Hubei ChinaInner Mongolia People’s Hospital Inner Mongolia ChinaThe Affiliated Hospital of Inner Mongolia University for Nationalities Inner Mongolia ChinaHuai'an First People’s Hospital Nanjing Medical University Nanjing Jiangsu ChinaHuadong Hospital Affiliated to Fudan University Shanghai ChinaYancheng City No.1 People's Hospital Jiangsu ChinaMitsubishi Tanabe Pharma Development America, Inc. Jersey City NJ USAMitsubishi Tanabe Pharma Development (Beijing) Co., Ltd. Beijing ChinaAbstract Introduction We evaluated the efficacy and safety of teneligliptin compared with placebo when added to metformin therapy in Chinese patients with type 2 diabetes inadequately controlled with metformin monotherapy. Methods This multicentre, randomized, double‐blind, placebo‐controlled, parallel‐group study enrolled type 2 diabetes patients with glycosylated haemoglobin (HbA1c) 7.0%−<10.0% and fasting plasma glucose (FPG) <270 mg/dl, receiving a stable metformin dose ≥1000 mg/day. Teneligliptin 20 mg or placebo was administered orally once daily (qd) before breakfast for 24 weeks. The primary efficacy end‐point was change in HbA1c from baseline to Week 24. Safety end‐points included the incidence of adverse events (AEs). Results The least square mean (LSM) change from baseline (standard error [SE]) was −0.72 (0.07) (95% confidence intervals [CI], −0.87, −0.58) for teneligliptin and −0.01 (0.07) (95% CI, −0.16, 0.13) for placebo. The differences (LSM ± SE) between the placebo and teneligliptin groups in HbA1c and FPG were −0.71% ± 0.11% (p < .0001) and −16.5 ± 4.7 mg/dl (p = .0005), respectively. Teneligliptin yielded significant changes in HbA1c (−0.81%; p < .0001) and FPG (−22.2 mg/dl; p < .0001) at Week 12. At Week 24, more patients achieved HbA1c <7.0% with teneligliptin (41.7%) compared with placebo (16.1%; p < .0001). Treatment‐emergent AE incidence was similar with teneligliptin (58.9%) and placebo (68.3%); upper respiratory tract infection, hyperuricaemia and hyperlipidaemia were the most common AEs. Conclusions Teneligliptin 20 mg qd for 24 weeks added to ongoing metformin treatment significantly decreased HbA1c and FPG levels compared with placebo in Chinese type 2 diabetes patients. The combination was safe and tolerable.https://doi.org/10.1002/edm2.222diabetes mellitusdipeptidyl peptidase‐IV inhibitorsmetformintype 2
collection DOAJ
language English
format Article
sources DOAJ
author Linong Ji
Ling Li
Jianhua Ma
Xuefeng Li
Dongmei Li
Bangzhu Meng
Weiping Lu
Jiao Sun
Yanmei Liu
Gen Takayanagi
Yi Wang
spellingShingle Linong Ji
Ling Li
Jianhua Ma
Xuefeng Li
Dongmei Li
Bangzhu Meng
Weiping Lu
Jiao Sun
Yanmei Liu
Gen Takayanagi
Yi Wang
Efficacy and safety of teneligliptin added to metformin in Chinese patients with type 2 diabetes mellitus inadequately controlled with metformin: A phase 3, randomized, double‐blind, placebo‐controlled study
Endocrinology, Diabetes & Metabolism
diabetes mellitus
dipeptidyl peptidase‐IV inhibitors
metformin
type 2
author_facet Linong Ji
Ling Li
Jianhua Ma
Xuefeng Li
Dongmei Li
Bangzhu Meng
Weiping Lu
Jiao Sun
Yanmei Liu
Gen Takayanagi
Yi Wang
author_sort Linong Ji
title Efficacy and safety of teneligliptin added to metformin in Chinese patients with type 2 diabetes mellitus inadequately controlled with metformin: A phase 3, randomized, double‐blind, placebo‐controlled study
title_short Efficacy and safety of teneligliptin added to metformin in Chinese patients with type 2 diabetes mellitus inadequately controlled with metformin: A phase 3, randomized, double‐blind, placebo‐controlled study
title_full Efficacy and safety of teneligliptin added to metformin in Chinese patients with type 2 diabetes mellitus inadequately controlled with metformin: A phase 3, randomized, double‐blind, placebo‐controlled study
title_fullStr Efficacy and safety of teneligliptin added to metformin in Chinese patients with type 2 diabetes mellitus inadequately controlled with metformin: A phase 3, randomized, double‐blind, placebo‐controlled study
title_full_unstemmed Efficacy and safety of teneligliptin added to metformin in Chinese patients with type 2 diabetes mellitus inadequately controlled with metformin: A phase 3, randomized, double‐blind, placebo‐controlled study
title_sort efficacy and safety of teneligliptin added to metformin in chinese patients with type 2 diabetes mellitus inadequately controlled with metformin: a phase 3, randomized, double‐blind, placebo‐controlled study
publisher Wiley
series Endocrinology, Diabetes & Metabolism
issn 2398-9238
publishDate 2021-04-01
description Abstract Introduction We evaluated the efficacy and safety of teneligliptin compared with placebo when added to metformin therapy in Chinese patients with type 2 diabetes inadequately controlled with metformin monotherapy. Methods This multicentre, randomized, double‐blind, placebo‐controlled, parallel‐group study enrolled type 2 diabetes patients with glycosylated haemoglobin (HbA1c) 7.0%−<10.0% and fasting plasma glucose (FPG) <270 mg/dl, receiving a stable metformin dose ≥1000 mg/day. Teneligliptin 20 mg or placebo was administered orally once daily (qd) before breakfast for 24 weeks. The primary efficacy end‐point was change in HbA1c from baseline to Week 24. Safety end‐points included the incidence of adverse events (AEs). Results The least square mean (LSM) change from baseline (standard error [SE]) was −0.72 (0.07) (95% confidence intervals [CI], −0.87, −0.58) for teneligliptin and −0.01 (0.07) (95% CI, −0.16, 0.13) for placebo. The differences (LSM ± SE) between the placebo and teneligliptin groups in HbA1c and FPG were −0.71% ± 0.11% (p < .0001) and −16.5 ± 4.7 mg/dl (p = .0005), respectively. Teneligliptin yielded significant changes in HbA1c (−0.81%; p < .0001) and FPG (−22.2 mg/dl; p < .0001) at Week 12. At Week 24, more patients achieved HbA1c <7.0% with teneligliptin (41.7%) compared with placebo (16.1%; p < .0001). Treatment‐emergent AE incidence was similar with teneligliptin (58.9%) and placebo (68.3%); upper respiratory tract infection, hyperuricaemia and hyperlipidaemia were the most common AEs. Conclusions Teneligliptin 20 mg qd for 24 weeks added to ongoing metformin treatment significantly decreased HbA1c and FPG levels compared with placebo in Chinese type 2 diabetes patients. The combination was safe and tolerable.
topic diabetes mellitus
dipeptidyl peptidase‐IV inhibitors
metformin
type 2
url https://doi.org/10.1002/edm2.222
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