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A novel, long-acting glucagon-like peptide receptor-agonist: dulaglutide.

Diabetes Metab Syndr Obes · 2015

Last updated 2026-05-28

Dulaglutide is a once-weekly injectable medication for type 2 diabetes available in two doses: 0.75 mg and 1.5 mg. In four clinical trials, dulaglutide improved blood sugar control more than exenatide, sitagliptin, and insulin glargine, with reductions in HbA1c (a measure of blood sugar) ranging from -0.76% to -1.5% depending on the dose and comparison. More patients reached blood sugar targets with dulaglutide, and weight loss was greater compared to some other treatments. Common side effects included nausea, diarrhea, and vomiting.

AI summary of the abstract below.

JournalDiabetes Metab Syndr Obes, 2015
Citations14
Relative citation ratio0.48
NIH percentile28
Molecules dulaglutide
Conditions studied Type 2 Diabetes, Obesity, Cardiovascular Risk Reduction

Abstract

BACKGROUND: Dulaglutide is a new, long-acting glucagon-like peptide analogue in the treatment of type 2 diabetes. It is available in two doses, 0.75 and 1.5 mg, given by injection once weekly. This systematic review reports the effectiveness and safety of dulaglutide in type 2 diabetes in dual and triple therapy. METHODS: MEDLINE, MEDLINE In-Process and Other Non-Indexed Citations, EMBASE, and conference abstracts were searched from 2005 to August 2014, and updated in January 2015. Company websites and references of included studies were checked for potentially relevant studies. European Medicines Agency and US Food and Drug Administration websites were searched. RESULTS: Four trials were included. All were manufacturer-funded randomized controlled trials from the Assessment of Weekly Administration of Dulaglutide in Diabetes (AWARD) program. AWARD-1 compared dulaglutide 1.5 mg against exenatide 10 µg twice daily and placebo, AWARD-2 compared dulaglutide 0.75 and 1.5 mg against insulin glargine, AWARD-5 compared dulaglutide 0.75 and 1.5 mg against sitagliptin 100 mg and placebo, and AWARD-6 compared dulaglutide 1.5 mg against liraglutide 1.8 mg. The duration of follow-up in the trials ranged from 26 to 104 weeks. The primary outcome of all the included trials was change in HbA1c. At 26 weeks, greater HbA1c reductions were seen with dulaglutide than with twice daily exenatide (dulaglutide 1.5/0.75 mg: -1.5%/-1.3%; exe: 0.99%) and sitagliptin (1.5/0.75 mg -1.22%/-1.01%; sitagliptin: -0.6%). HbA1c change was greater with dulaglutide 1.5 mg (-1.08%) than with glargine (-0.63%), but not with dulaglutide 0.75 mg (-0.76%). Dulaglutide 1.5 mg was found to be noninferior to liraglutide 1.8 mg. More patients treated with dulaglutide achieved HbA1c targets of <7% and ≤6.5%. Reduction in weight was greater with dulaglutide than with sitagliptin and exenatide. Hypoglycemia was infrequent. The main adverse events were nausea, diarrhea, and vomiting. CONCLUSION: Dulaglutide is effective in the treatment of patients with type 2 diabetes but we need long follow-up data for safety concerns.

Verbatim abstract via PubMed 26316788 ↗

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