Introduction & Objective: This study aimed to assess the real-world impact of sema OW vs SGLT2i on HbA1c, weight and HCRU outcomes among patients (pts) with T2D in the US.

Methods: This observational study of adults with uncontrolled T2D (HbA1c ≥7%) initiating sema OW or SGLT2i (Jan 2018—Feb 2022; first prescription = index) used data from IQVIA PharMetrics® Plus and Ambulatory Electronic Medical Records databases. Changes in HbA1c, weight, BMI and all-cause medical HCRU outcomes after 1 year were compared among inverse probability of treatment weighting (IPTW) adjusted cohorts.

Results: Post-IPTW (sema OW: n=416; SGLT2i: n=1093) a significantly higher proportion of pts in the sema OW cohort had combined reductions in HbA1c/weight outcomes vs SGLT2i (Figure). The sema OW cohort had significantly greater mean decreases in HbA1c (-1.6 vs -1.2%, p<0.0001), weight (-4.4 vs -3.4 kg, p<0.0001) and BMI (-1.5 vs -1.1 kg/m2, p=0.013) vs SGLT2i. Over 1-yr follow-up, all-cause HCRU was similar between both cohorts (≥1 hospitalization: 6.0 vs 5.7%, p=0.8190; ≥1 ER visit: 15.2 vs 17.6%, p=0.2658; ≥1 physician office visit: 99.7 vs 99.1%, p=0.2134).

Conclusion: Sema OW was associated with greater improvements in HbA1c and weight vs SGLT2i, but with similar HCRU after 1 year.

Disclosure

J. Amamoo: None. R.P. Doshi: None. J. Noone: Employee; Novo Nordisk. L. Xie: None. C.L. Gamble: Employee; Novo Nordisk. M. Guevarra: Stock/Shareholder; Novo Nordisk. V. Divino: Employee; IQVIA Inc. J. Chen: None. A.A. King: Speaker's Bureau; Abbott, MannKind Corporation, Novo Nordisk. Advisory Panel; Novo Nordisk. Speaker's Bureau; Lilly Diabetes. Advisory Panel; Lilly Diabetes. Speaker's Bureau; Dexcom, Inc. Advisory Panel; Dexcom, Inc. Speaker's Bureau; Astellas Pharma Inc.

Funding

Novo Nordisk

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