Dulaglutide: A Review in Type 2 Diabetes
Autor: | Lesley J. Scott |
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Rok vydání: | 2020 |
Předmět: |
medicine.medical_specialty
Injections Subcutaneous Recombinant Fusion Proteins Glucagon-Like Peptides Type 2 diabetes 03 medical and health sciences 0302 clinical medicine Internal medicine Diabetes mellitus medicine Humans Hypoglycemic Agents Pharmacology (medical) Myocardial infarction business.industry medicine.disease Immunoglobulin Fc Fragments Clinical trial Regimen Diabetes Mellitus Type 2 030220 oncology & carcinogenesis Dulaglutide business 030217 neurology & neurosurgery Mace medicine.drug Kidney disease |
Zdroj: | Drugs. 80:197-208 |
ISSN: | 1179-1950 0012-6667 |
DOI: | 10.1007/s40265-020-01260-9 |
Popis: | Subcutaneous dulaglutide (Trulicity®) is a once-weekly glucagon-like peptide-1 receptor agonist that is approved in numerous countries as an adjunct to diet and exercise for the treatment of adults with type 2 diabetes (T2D). In the clinical trial and real-world settings, once-weekly subcutaneous dulaglutide, as monotherapy or add-on therapy to other antihyperglycaemic agents (including oral antihyperglycaemic drugs and insulin), was an effective and generally well tolerated treatment in adults with inadequately controlled T2D, including in high-risk patients [e.g. obese and elderly patients, those with stage 3 or 4 chronic kidney disease (CKD) and/or cardiovascular (CV) disease]. In the REWIND CV outcomes trial in patients with T2D with or without CV disease, dulaglutide was associated with a significant reduction in the risk of a major adverse cardiac event (MACE; primary composite outcome comprising CV death, nonfatal myocardial infarction or nonfatal stroke) at a median of 5.4 years’ follow-up. Given its durable glycaemic efficacy, beneficial effects on bodyweight and MACE outcomes, low inherent risk of hypoglycaemia and convenient once-weekly regimen, dulaglutide remains an important option in the management of T2D. |
Databáze: | OpenAIRE |
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