Linnebjerg Helle, Lam Eric Chen Quin, Zhang Xin, Seger Mary E, Coutant David, Chua Laiyi, Kapitza Christoph, Heise Tim
Eli Lilly and Company, Indianapolis, Indiana.
Lilly-NUS Centre for Clinical Pharmacology, Singapore, Singapore.
Diabetes Obes Metab. 2017 Jan;19(1):33-39. doi: 10.1111/dom.12759. Epub 2016 Sep 8.
LY2963016 (LY IGlar) and Lantus (IGlar) are insulin glargine products manufactured by distinct processes, but with identical amino acid sequences. This study compared the duration of action of LY IGlar and IGlar in subjects with type 1 diabetes mellitus (T1DM).
This was a randomized, double-blind, single-dose, two-period, crossover study. Twenty subjects underwent 42-hour euglycaemic clamps after a single subcutaneous 0.3-U/kg dose of LY IGlar or IGlar. In this study, the duration of action was defined as the time required for blood glucose levels to rise consistently above a predefined cut-off of 8.3 mmol/L (150 mg/dL) from a state of euglycaemia. Blood samples were collected to measure blood glucose for pharmacodynamic (PD) evaluations.
End of action was reached within 42 hours in 26 of 40 clamps (13 LY IGlar and 13 IGlar). The median duration of action for all subjects was 37.1 and 40.0 hours, and the mean duration of action (calculated using only patients who reached end of action) was 23.8 and 25.5 hours for LY IGlar and IGlar, respectively. The duration of action was demonstrated to be similar between the treatments using time-to-event analysis (log-rank test of equality p = .859). Following administration of LY IGlar and IGlar, the PD parameters of maximum glucose infusion rate (R ) and total glucose infusion during the clamp (G ) were comparable.
LY IGlar and IGlar had similar duration of action and comparable PD parameters in subjects with T1DM.
LY2963016(LY甘精胰岛素)和来得时(甘精胰岛素)是通过不同工艺生产但氨基酸序列相同的甘精胰岛素产品。本研究比较了LY甘精胰岛素和甘精胰岛素在1型糖尿病(T1DM)患者中的作用持续时间。
这是一项随机、双盲、单剂量、两阶段、交叉研究。20名受试者在皮下单次注射0.3 U/kg剂量的LY甘精胰岛素或甘精胰岛素后接受了42小时的血糖正常钳夹试验。在本研究中,作用持续时间定义为血糖水平从血糖正常状态持续升至预先定义的8.3 mmol/L(150 mg/dL)以上所需的时间。采集血样以测量血糖进行药效学(PD)评估。
40次钳夹试验中有26次(13次LY甘精胰岛素和13次甘精胰岛素)在42小时内达到作用终点。所有受试者的中位作用持续时间分别为37.1小时和40.0小时,LY甘精胰岛素和甘精胰岛素的平均作用持续时间(仅使用达到作用终点的患者计算)分别为23.8小时和25.5小时。使用事件发生时间分析(对数秩检验,p = 0.859)表明两种治疗的作用持续时间相似。给予LY甘精胰岛素和甘精胰岛素后,钳夹期间的最大葡萄糖输注速率(R )和总葡萄糖输注量(G )等PD参数具有可比性。
LY甘精胰岛素和甘精胰岛素在T1DM患者中的作用持续时间相似,PD参数具有可比性。