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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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 |
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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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