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Network meta-analysis compares bexagliflozin efficacy and safety with other SGLT2 inhibitors in type 2 diabetes

Network meta-analysis compares bexagliflozin efficacy and safety with other SGLT2 inhibitors in…
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Key Takeaway
Consider bexagliflozin's comparable efficacy to most SGLT2 inhibitors, with specific differences in glycemic control and weight loss.

This is a systematic review and network meta-analysis of sodium-glucose cotransporter 2 (SGLT2) inhibitors for adults with type 2 diabetes mellitus. The analysis included 26,838 patients and compared bexagliflozin with canagliflozin, empagliflozin, dapagliflozin, and placebo.

The authors synthesized that canagliflozin (300 mg, 100 mg) and empagliflozin 25 mg were more effective than bexagliflozin for HbA1c reduction, while bexagliflozin was comparable to other SGLT2 inhibitors. For fasting plasma glucose, canagliflozin 300 mg and empagliflozin 25 mg showed slightly greater effects than bexagliflozin, with no significant differences versus other comparators. For weight loss, bexagliflozin was superior to dapagliflozin 5 mg but slightly inferior to canagliflozin 300 mg, with comparable efficacy to other agents.

For blood pressure, bexagliflozin produced similar systolic and diastolic reductions to other SGLT2 inhibitors, with a significantly greater diastolic effect than empagliflozin 10 mg. For urinary tract infection incidence, bexagliflozin had a lower incidence than dapagliflozin (5 mg, 10 mg) and comparable safety to other agents and placebo.

The authors noted limitations in the network evidence but did not specify them. Practice relevance is restrained, as the analysis provides comparative efficacy and safety rankings without direct trial-level outcomes.

Study Details

Study typeMeta analysis
EvidenceLevel 1
PublishedMay 2026
View Original Abstract ↓
BackgroundBexagliflozin exerts definite efficacy in the treatment of type 2 diabetes mellitus (T2DM). However, whether this novel sodium-glucose cotransporter 2 (SGLT2) inhibitor is superior to other SGLT2 inhibitors remains to be elucidated. We therefore performed this network meta-analysis (NMA) to compare bexagliflozin with other SGLT2 inhibitors and establish an efficacy hierarchy in T2DM management.MethodsWe systematically searched PubMed, Embase, Web of Science and the ClinicalTrials.gov registry for eligible randomized controlled trials (RCTs) published up to January 2026. Statistical analysis was conducted using Stata 14.0. Risk of bias was assessed by the Cochrane tool, evidence certainty was evaluated using the Confidence in Network Meta-Analysis (CINeMA) approach, and intervention ranking was performed using surface under the cumulative ranking curve (SUCRA) values.ResultsThis NMA included 48 studies with 26,838 patients. Bexagliflozin significantly reduced HbA1c, fasting plasma glucose (FPG), body weight, systolic blood pressure (SBP) and diastolic blood pressure (DBP) compared with placebo. For HbA1c reduction, canagliflozin (300 mg, 100 mg) and empagliflozin 25 mg were more effective than bexagliflozin, while bexagliflozin was comparable to other SGLT2 inhibitors. For FPG reduction, canagliflozin 300 mg and empagliflozin 25 mg showed slightly greater effects than bexagliflozin, with no significant differences between bexagliflozin and other comparators. Bexagliflozin was superior to dapagliflozin 5 mg but slightly inferior to canagliflozin 300 mg for weight loss, while showing comparable efficacy to other SGLT2 inhibitors. It achieved similar SBP and DBP reduction to other SGLT2 inhibitors, with a significantly greater DBP-lowering effect than empagliflozin 10 mg. Bexagliflozin had a lower incidence of urinary tract infection than dapagliflozin (5 mg, 10 mg), with comparable safety to other agents and placebo. Canagliflozin 300 mg showed the best efficacy for HbA1c, FPG and weight control.ConclusionBexagliflozin demonstrates comparable efficacy to most SGLT2 inhibitors in T2DM patients, with a relatively prominent benefit in body weight reduction and a similar safety profile. Canagliflozin 300 mg provides more effective glycemic and weight control.
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