Semaglutide Added to Basal Insulin in Type 2 Diabetes (SUSTAIN 5): A Randomized, Controlled Trial

被引:269
作者
Rodbard, Helena W. [1 ]
Lingvay, Ildiko [2 ]
Reed, John [3 ]
de la Rosa, Raymond [4 ]
Rose, Ludger [5 ]
Sugimoto, Danny [6 ]
Araki, Eiichi [7 ]
Chu, Pei-Ling [8 ]
Wijayasinghe, Nelun [9 ]
Norwood, Paul [10 ]
机构
[1] Endocrine & Metab Consultants, Rockville, MD 20852 USA
[2] Univ Texas Southwestern Med Ctr Dallas, Dept Internal Med, Dallas, TX 75390 USA
[3] Endocrine Res Solut Inc, Roswell, GA 30076 USA
[4] Four Rivers Clin Res, Paducah, KY 42003 USA
[5] Inst Diabet Res, D-48145 Munster, Germany
[6] Cedar Crosse Res Ctr, Chicago, IL 60607 USA
[7] Kumamoto Univ, Dept Metab Med, Kumamoto 8608555, Japan
[8] Novo Nordisk Inc, Plainsboro, NJ 08536 USA
[9] Novo Nordisk AS, DK-2860 Soborg, Denmark
[10] Univ Calif San Francisco, Fresno, CA 93730 USA
关键词
HUMAN GLP-1 ANALOG; PEPTIDE-1 RECEPTOR AGONISTS; PLACEBO-CONTROLLED TRIAL; ONCE-WEEKLY SEMAGLUTIDE; DOUBLE-BLIND; MICROVASCULAR COMPLICATIONS; JAPANESE PATIENTS; NAIVE PATIENTS; OPEN-LABEL; PHASE; 3A;
D O I
10.1210/jc.2018-00070
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context: Combination therapy with insulin and glucagon-like peptide-1 receptor agonists (GLP-1RAs) is important for treating type 2 diabetes (T2D). This trial assesses the efficacy and safety of semaglutide, a GLP-1RA, as an add-on to basal insulin. Objective: To demonstrate the superiority of semaglutide vs placebo on glycemic control as an addon to basal insulin in patients with T2D. Design: Phase 3a, double-blind, placebo-controlled, 30-week trial. Setting: This study included 90 sites in five countries. Patients: We studied 397 patients with uncontrolled T2D receiving stable therapy with basal insulin with or without metformin. Interventions: Subcutaneous semaglutide 0.5 or 1.0 mg once weekly or volume-matched placebo. Main Outcome Measures: Primary endpoint was change in glycated Hb (HbA(1c)) from baseline to week 30. Confirmatory secondary endpoint was change in body weight from baseline to week 30. Results: At week 30, mean HbA(1c) reductions [mean baseline value, 8.4% (67.9 mmol/mol)] with semaglutide 0.5 and 1.0mgwere 1.4%(15.8mmol/mol) and 1.8%(20.2mmol/mol) vs 0.1%(1.0mmol/ mol) with placebo [estimated treatment difference (ETD) vs placebo, -1.35 (14.8 mmol/mol); 95% CI, -1.61 to -1.10 and ETD, -1.75%(19.2 mmol/mol); 95% CI, -2.01 to -1.50; both P < 0.0001]. Severe or blood glucose-confirmed hypoglycemic episodes were reported in 11 patients (17 events) and 14 patients (25 events) with semaglutide 0.5 and 1.0 mg, respectively, vs seven patients (13 events) with placebo (estimated rate ratio vs placebo, 2.08; 95% CI, 0.67 to 6.51 and estimated rate ratio vs placebo, 2.41; 95% CI, 0.84 to 6.96 for 0.5 and 1.0 mg; both P = nonsignificant). Mean body weight decreased with semaglutide 0.5 and 1.0 mg vs placebo from baseline to end of treatment: 3.7, 6.4, and 1.4 kg (ETD, -2.31; 95% CI, -3.33 to -1.29 and ETD, -5.06; 95% CI, -6.08 to -4.04 kg; both P<0.0001). Premature treatment discontinuation due to adverse eventswas higher for semaglutide 0.5 and 1.0mg vs placebo (4.5%, 6.1%, and 0.8%), mainly due to gastrointestinal disorders. Conclusions: Semaglutide, added to basal insulin, significantly reduced HbA(1c) and body weight in patients with uncontrolled T2D vs placebo.
引用
收藏
页码:2291 / 2301
页数:11
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