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A greater proportion of participants with type 2 diabetes achieve treatment targets with IDegLira (insulin degludec/liraglutide) vs insulin glargine U100 at 26 weeks: DUAL VIII a randomized trial designed to resemble clinical practice

Diabetes, Obesity and Metabolism Jan 13, 2020

Sesti G, Bardtrum L, Dagdelen S, et al. - Among candidates (n = 1,012) with T2D uncontrolled on oral antidiabetic drugs (OADs), researchers tested the safety and effectiveness of insulin degludec/liraglutide (IDegLira) vs insulin glargine 100 units/mL (IGlar U100) as initial injectable therapy at 26 weeks in the 104-week DUAL VIII durability trial. Study participants were randomized 1:1 to open-label IDegLira or IGlar U100. Weeks 1, 2, 4 and 12, and every three months thereafter, were scheduled to visit. According to results, HbA1c reductions were higher with IDegLira vs IGlar U100 after 26 weeks, as were the percentage of participants with no weight gain and/or hypoglycaemia attaining HbA1c < 53 mmol/mol and HbA1c targets. The rate of hypoglycaemia with IDegLira was 44% lower than with IGlar U100. The results were similar in terms of safety. The authors concluded that more candidates receiving IDegLira than IGlar U100 met treatment targets in a trial resembling clinical practice, supporting the use of IDegLira as initial injectable therapy for people with T2D uncontrolled on OADs and eligible for insulin initiation.
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