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A novel, long-acting glucagon-like peptide receptor-agonist: dulaglutide
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 t...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Dove Medical Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4541559/ https://www.ncbi.nlm.nih.gov/pubmed/26316788 http://dx.doi.org/10.2147/DMSO.S34418 |
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author | Gurung, Tara Shyangdan, Deepson S O’Hare, Joseph Paul Waugh, Norman |
author_facet | Gurung, Tara Shyangdan, Deepson S O’Hare, Joseph Paul Waugh, Norman |
author_sort | Gurung, Tara |
collection | PubMed |
description | 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 HbA(1c). At 26 weeks, greater HbA(1c) 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%). HbA(1c) 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 HbA(1c) 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. |
format | Online Article Text |
id | pubmed-4541559 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-45415592015-08-27 A novel, long-acting glucagon-like peptide receptor-agonist: dulaglutide Gurung, Tara Shyangdan, Deepson S O’Hare, Joseph Paul Waugh, Norman Diabetes Metab Syndr Obes Review 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 HbA(1c). At 26 weeks, greater HbA(1c) 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%). HbA(1c) 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 HbA(1c) 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. Dove Medical Press 2015-08-10 /pmc/articles/PMC4541559/ /pubmed/26316788 http://dx.doi.org/10.2147/DMSO.S34418 Text en © 2015 Gurung et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Review Gurung, Tara Shyangdan, Deepson S O’Hare, Joseph Paul Waugh, Norman A novel, long-acting glucagon-like peptide receptor-agonist: dulaglutide |
title | A novel, long-acting glucagon-like peptide receptor-agonist: dulaglutide |
title_full | A novel, long-acting glucagon-like peptide receptor-agonist: dulaglutide |
title_fullStr | A novel, long-acting glucagon-like peptide receptor-agonist: dulaglutide |
title_full_unstemmed | A novel, long-acting glucagon-like peptide receptor-agonist: dulaglutide |
title_short | A novel, long-acting glucagon-like peptide receptor-agonist: dulaglutide |
title_sort | novel, long-acting glucagon-like peptide receptor-agonist: dulaglutide |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4541559/ https://www.ncbi.nlm.nih.gov/pubmed/26316788 http://dx.doi.org/10.2147/DMSO.S34418 |
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