Eli Lilly Reports Topline Results from P-III (QWINT-1 and QWINT-3) Studies of Efsitora Alfa (Efsitora) for Type 2 Diabetes
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- QWINT-1 study assessed the safety & efficacy of efsitora (QW) vs insulin glargine (QD) for 52wks. in insulin-naïve T2D adults (n=796) while QWINT-3 trial compared the same b/w efsitora & insulin degludec for 78wks. in T2D adults (n=986) currently on basal insulin
- QWINT-1 reaching its 1EP, depicting non-inferior A1C reduction of 1.31% vs 1.27% (A1C of 6.92% & 6.96%, respectively) in efficacy estimand and 1.19% vs 1.16% (A1C of 7.05% & 7.08%, respectively) in treatment-regimen estimand at wk.52
- QWINT-3 also met its 1EP, showing reduced A1C of 0.86% vs 0.75% (A1C of 6.93% & 7.03%, respectively) in efficacy estimand and 0.81% vs 0.72% (A1C of 6.99% & 7.08%, respectively) in treatment-regimen estimand at wk.26
Ref: Eli Lilly | Image: Eli Lilly
Related News:- Eli Lilly Reports Data from Two P-III (QWINT-2 and QWINT-4) Studies of Efsitora for Treating Type 2 Diabetes
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