利拉鲁肽
医学
艾塞那肽
不利影响
杜拉鲁肽
恶心
血糖性
2型糖尿病
胰高血糖素样肽1受体
减肥
药理学
内科学
低血糖
糖尿病
2型糖尿病
兴奋剂
胰岛素
内分泌学
受体
肥胖
作者
Giovanna Muscogiuri,Amalia Gastaldelli
出处
期刊:Drugs of Today
日期:2014-01-01
卷期号:50 (10): 665-665
被引量:7
标识
DOI:10.1358/dot.2014.50.10.2214156
摘要
The glucagon-like peptide 1 (GLP-1) receptor agonists are a new class of antidiabetic drugs that provide the benefits of decreasing HbA1c and plasma glucose concentrations, stimulating insulin secretion with a very low risk of hypoglycemia, and promoting weight loss. With the exception of once-weekly exenatide, currently available GLP-1 receptor agonists are administered once or twice daily by injection. Albiglutide is a new GLP-1 receptor agonist recently approved in the U.S. (Tanzeum™) and European Union (Eperzan®) for the treatment of patients with type 2 diabetes with a dosage of 30 mg once weekly, which may be increased to 50 mg if the glycemic response is inadequate. Clinical trials showed that albiglutide once weekly delayed gastric emptying, mildly decreased body weight and had similar efficacy in the reduction of HbA1c as comparators, but it failed to demonstrate noninferiority to liraglutide. Albiglutide exhibits an acceptable safety profile, although it is associated with more frequent gastrointestinal complaints (e.g., nausea, diarrhea, vomiting) and injection-site reactions. Immunogenicity (i.e., testing positive for anti-drug antibody) was observed in 5.5% of subjects but it was not associated with increased adverse events. Long-term studies are needed to fully assess potential adverse events.
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