drugset / Trial / NCT02243176

24-Week, Multicenter, Randomized, Parallel-group, Open-label, Active Controlled Phase IV Study to Assess the Efficacy, Safety and Tolerability of Saxagliptin Compared With Acarbose When in Combination With Metformin in Patients With T2D Inadequately Controlled With Metformin Monotherapy

NCT02243176 ↗

Phase 4 Completed 689 enrolled AstraZeneca
RandomizedParallel-groupOpen-labelTreatment

Summary

SMART Study - A 24-Week, Multicenter, Randomized, Parallel-group, Open-label, Active Controlled Phase IV Study to Assess the Efficacy, Safety and Tolerability of Saxagliptin Compared with Acarbose when in Combination with Metformin in Patients with Type 2 Diabetes Mellitus (T2D) Inadequately Controlled with Metformin Monotherapy

Timeline

Start
2014-09
Primary completion
2015-09
Completion
2015-09

Outcome

Met primary endpoint

paper Saxagliptin was non-inferior to acarbose for glycaemic control [Week 24 HbA1c change: -0.82% and -0.78%, respectively; difference (95% confidence interval): -0.04 (-0.22, 0.13)%] PMID 28296055 ↗

Drugs

EvaluationDrugModalityDoseRoute
Comparator Acarbose Unknown 100 mg —
Subject SAXAGLIPTIN ANHYDROUS Small molecule 5 mg Oral