Weekly Semaglutide Vs. Liraglutide Efficacy Profile: A Network Meta-Analysis
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Introduction: Glucagon-like peptide 1 receptor agonist (GLP-1 RA) is a class of hypoglycemic medications. Semaglutide once-weekly (QW) and liraglutide once-daily (OD) significantly improved glycemic control compared to placebo. To date, no long-term phase III trials directly comparing semaglutide and liraglutide are available. This network meta-analysis (NMA) aims to compare the long-term efficacy of semaglutide and liraglutide.
Methods: PubMed, Embase, and Cochrane Library were searched from inception until June 2019 to identify relevant articles. Nine long-term randomized controlled trials comparing once-weekly semaglutide or liraglutide with placebo or other active comparisons were identified. The outcomes of interest were changes in HbA1c and weight after 52 weeks. A Bayesian framework and NMA were used for data synthesis. This is a sub-study of the protocol registered in PROSPERO (number CRD42018091598).
Results: The data showed significant superiority in HbA1c reduction of semaglutide 1 mg QW over liraglutide 1.2 and 1.8 mg with a treatment difference of 0.47% and 0.3%, respectively. Semaglutide 0.5 mg QW was found to be significantly superior to liraglutide 1.2 mg in HbA1c reduction with a treatment difference of 0.17%. Regarding weight reduction analysis, semaglutide 0.5 and 1 mg QW were significantly associated with a greater reduction than liraglutide 0.6 mg with a treatment difference of 2.42 and 3.06 kg, respectively. However, no significant reduction was found in comparison to liraglutide 1.2 and 1.8 mg.
Conclusions: Semaglutide improved the control of blood glucose and body weight. The capacity of long-term glycemic control and body weight control of semaglutide appears to be more effective than other GLP-1 RAs, including liraglutide. However, considering the number of included studies and potential limitations, more large-scale, head-to-head, well-designed randomized-controlled trials (RCTs) are needed to confirm these findings.
Hashmi T, Ahmed M, Haider A, Naseem S, Jafar U, Hussain M Clin Transl Sci. 2025; 18(2):e70127.
PMID: 39930946 PMC: 11811509. DOI: 10.1111/cts.70127.
Christensen J, Anand S, Chertow G, Lyden K, Sarwal A, Bjordahl T Contemp Clin Trials. 2024; 149:107766.
PMID: 39608749 PMC: 11875690. DOI: 10.1016/j.cct.2024.107766.
Ruan Z, Chen X, Song M, Jia R, Luo H, Ung C Diabetes Metab Syndr Obes. 2024; 17:3657-3666.
PMID: 39386037 PMC: 11463179. DOI: 10.2147/DMSO.S483065.
Wen J, Nadora D, Bernstein E, How-Volkman C, Truong A, Akhtar M Cureus. 2024; 16(9):e69008.
PMID: 39385875 PMC: 11463578. DOI: 10.7759/cureus.69008.
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Moore P, Malone K, Vanvalkenburg D, Rando L, Williams B, Matejowsky H Adv Ther. 2022; 40(3):723-742.
PMID: 36566341 DOI: 10.1007/s12325-022-02394-w.