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Long-Term Efficacy and Safety of Ertugliflozin in Patients (Pts) with Type 2 Diabetes Mellitus (T2DM) Inadequately Controlled with Metformin (MET) Monotherapy—104-Week VERTIS MET Trial

Authors :
Bernard Charbonnel
Susan Huyck
Steven G. Terra
Silvina Gallo
Brett Lauring
Allison Goldman
Amanda Darekar
Harry Shi
Source :
Diabetes. 67
Publication Year :
2018
Publisher :
American Diabetes Association, 2018.

Abstract

This Phase 3 randomized, double-blind study in adults with T2DM (A1C 7.0-10.5%) on MET monotherapy (≥1500 mg/day ≥8 weeks) included a 26 week placebo (PBO)-controlled period followed by a 78 week extension where non-rescued PBO pts with fasting finger-stick glucose ≥110 mg/dL received blinded glimepiride (GLIM). Efficacy, safety and effect on bone mineral density (BMD) of ertugliflozin (ERTU) 5 mg and 15 mg QD at week 104 are reported. Pts (N=621) had baseline mean ± SD: age 56.6 ± 8.8 y; T2DM duration 8.0 ± 6.0 y; BMI 31.1 ± 4.7 kg/m2; A1C 8.1 ± 0.9%. 41% were post-menopausal women. At week 104, ERTU 5 mg and ERTU 15 mg reduced A1C, FPG, body weight (BW) and blood pressure (BP) compared to baseline, and increased the proportion of pts with A1C Incidence of female genital mycotic infections was higher in ERTU 5 mg (7.3%; p=0.017) and 15 mg (9.8%; p=0.003) vs. PBO/GLIM (0.9%). Symptomatic hypoglycemia was lower in ERTU 5 mg (5.8%; p=0.009) and 15 mg (5.9%; p=0.009) vs. PBO/GLIM (13.4%). ERTU had no impact on BMD vs. PBO/GLIM, except total hip where BMD reduction was greater for ERTU 15 mg (Table). Fractures occurred in 3, 2 and 7 pts in ERTU 5 mg, 15 mg and PBO/GLIM, respectively. ERTU added to MET in pts with inadequately controlled T2DM improved glycemic control, BW and BP over 104 weeks. ERTU was well tolerated with no clinically meaningful impact on BMD. Table: Change in efficacy (vs baseline) and bone mineral density (vs PBO/GLIM) endpointsERTU 5 mgERTU 15 mg Efficacy endpointsa (change vs baseline)Change from baseline at Wk 104: LS mean (95% CI)bA1C (%)-0.5 (-0.6, -0.4)-0.8 (-0.9, -0.6)FPG (mg/dL)-17.0 (-22.7, -11.3)-26.7 (-32.5, -21.0)Body weight (kg)-3.6 (-4.2, -3.0)-3.5 (-4.1, -2.9)SBP (mmHg)-3.9 (-5.8, -2.0)-2.8 (-4.8, -0.9)DBP (mmHg)-2.3 (-3.6, -1.1)-1.2 (-2.5, 0.0)Proportion of subjects with A1C Disclosure S. Gallo: Employee; Self; Pfizer Inc. B. Charbonnel: Advisory Panel; Self; AstraZeneca. Consultant; Self; AstraZeneca, Boehringer Ingelheim GmbH, Eli Lilly and Company, Merck Sharp & Dohme Corp., Novartis AG, Novo Nordisk A/S, Sanofi, Takeda Development Centre Europe Ltd. A. Goldman: Stock/Shareholder; Self; Merck & Co., Inc.. Employee; Self; Pfizer Inc.. Stock/Shareholder; Self; Pfizer Inc. H. Shi: Employee; Self; Pfizer Inc. S. Huyck: Employee; Self; Merck & Co., Inc. A. Darekar: Employee; Self; Pfizer Inc.. Stock/Shareholder; Self; Pfizer Inc. B. Lauring: Employee; Self; Merck & Co., Inc. S. Terra: Employee; Self; Pfizer Inc..

Details

ISSN :
1939327X and 00121797
Volume :
67
Database :
OpenAIRE
Journal :
Diabetes
Accession number :
edsair.doi...........5d74f9ccf04430644ac063ff659baa37