[Clinical application of exenatide in Japanese patients with type 2 diabetes mellitus].
Nihon Rinsho · 2011
Last updated 2026-05-28In Japanese patients with type 2 diabetes, the drug exenatide improved blood sugar control (measured by HbA1c, fasting glucose, and post-meal glucose) over 52 weeks. A 10 microgram dose also led to weight loss, but it slightly reduced HDL-C (often called "good" cholesterol). Side effects included a higher chance of low blood sugar and stomach issues, though most patients tolerated it well.
AI summary of the abstract below.
| Journal | Nihon Rinsho, 2011 |
|---|---|
| Citations | 0 |
| Relative citation ratio | 0.00 |
| NIH percentile | 0 |
| Molecules | exenatide |
| Conditions studied | Type 2 Diabetes |
Abstract
Exenatide belongs to a class of antidiabetic agents called incretin mimetics. In 2005, exenatide was first applied clinical therapy of type 2 diabetes mellitus patients in US, and it has now began to be used in Japanese type 2 diabetes mellitus patients since 2010. Large phase 3 clinical trials in Japan revealed that HbA1c, fasting glucose and postprandial glucose levels were improved with exenatide treatment, which were maintained over 52 weeks. Body weight reduction could be achieved with 10 microg treatment. HDL-C was significantly reduced. Exenatide was generally well tolerated, however incidence of hypoglycemia and gastro-intestinal side effect were elevated. Antibodies to exenatide were observed among approximately half of patients, however had no clinical relevant effects on the efficacy or safety.
Verbatim abstract via PubMed 21595277 ↗
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