GLPwatch

Evaluation of unmet medical need among Japanese patients with type 2 diabetes mellitus and efficacy of Lixisenatide treatment among Asian type 2 diabetes mellitus patients.

Diabetes Metab Syndr · 2016

Last updated 2026-05-28

In a study of 1,013 Japanese patients with type 2 diabetes, 36% did not achieve good blood sugar control despite having acceptable fasting blood sugar levels. In a separate analysis of 463 Asian patients, adding lixisenatide to basal insulin treatment for 24 weeks improved blood sugar control by 0.6%, reduced fasting blood sugar by 13.3 mg/dL, lowered after-meal blood sugar by 101.4 mg/dL, and led to a small weight loss of 0.5 kg compared to placebo.

AI summary of the abstract below.

JournalDiabetes Metab Syndr, 2016
Citations1
Relative citation ratio0.04
NIH percentile4
Molecules lixisenatide
Conditions studied Type 2 Diabetes

Abstract

AIMS: This study determined the unmet medical need of basal insulin therapy among type 2 diabetes patients who participated in the ALOHA study. Also a meta-analysis of the GetGoal-Duo1, -L, and -L-Asia trials was conducted to examine the impact of lixisenatide add-on treatment to basal insulin therapy ± OADs specifically among Asian type 2 diabetes patients. METHODS: The proportions of Japanese patients with an unmet need of diabetes management, defined as not achieving an HbA1c<7% despite having a fasting plasma glucose (FPG)<130 mg/dL, and without an unmet need, defined as having an endpoint HbA1c<7%, regardless of FPG level, were determined for the ALOHA study population, which was conducted as a post-marketing survey for insulin glargine in Japan. For the meta-analysis, all Asian modified intent-to-treat patients with baseline and endpoint HbA1c measurements reported from the 3 GetGoal trials were included. RESULTS: Among 1013 Japanese type 2 diabetes patients in the ALOHA study, 36% had an unmet need. In the GetGoal-Duo1, -L, and L-Asia trials, 237 Asian patients were treated with lixisenatide add-on treatment to basal insulin and 226 received placebo. Lixisenatide add-on treatment vs. placebo was associated with the following significant mean changes in efficacy outcomes at week 24: HbA1c: -0.6%, p=0.005; FPG: -13.3mg/dL, p=0.004; PPG: -101.4 mg/dL, p<0.001; weight: -0.5 kg, p=0.018; basal insulin dose: -1.6 U, p<0.001. CONCLUSIONS: Lixisenatide add-on treatment may provide a viable option to address the unmet need of basal insulin therapy among Asian type 2 diabetes patients.

Verbatim abstract via PubMed 26341928 ↗

Related research