a numerical trendp = 0.033
Body weight showed a numerical trend towards a benefit with iGlarLixi versus IDegAsp, but a difference between treatment arms was only observed in HOMA‐β Q2 (LSM difference −1.73 kg; p = 0.033). 3.4.
Body weight showed a numerical trend towards a benefit with iGlarLixi versus IDegAsp, but a difference between treatment arms was only observed in HOMA‐β Q2 (LSM difference −1.73 kg; p = 0.033). 3.4.
Across all HOMA‐β quartiles, similar reductions in FPG were observed in the iGlarLixi and IDegAsp arms, while PPG reductions showed a trend towards being greater with iGlarLixi versus IDegAsp. 3.3.
Furthermore, the magnitude of the between‐treatment difference in insulin dose exhibited an increasing trend corresponding to higher β‐cell functional capacity, further emphasising the benefits of iGlarLixi over IDegAsp to provide consistent glycaemic efficacy across all levels of β‐cell function without the need for large increases in insulin dose.