Diabetes Therapeutics and Research Centre, Institute of Advanced Medical Sciences, Tokushima University, Tokushima, Japan.
Medicine Development Unit-Japan and Medical Affairs, Eli Lilly Japan K.K., Kobe, Japan.
Diabetes Obes Metab. 2020 Jul;22(7):1167-1175. doi: 10.1111/dom.14019. Epub 2020 Apr 12.
To compare nasal glucagon (NG) with intramuscular glucagon (IMG) for the treatment of insulin-induced hypoglycaemia in Japanese patients with type 1 (T1DM) or type 2 diabetes mellitus (T2DM).
This phase 3, randomized, open-label, two-treatment, two-period crossover non-inferiority study enrolled Japanese adults with T1DM or T2DM on insulin therapy, with glycated haemoglobin levels ≤86 mmol/mol (≤10%). After ≥8 hours of fasting, hypoglycaemia was induced with human regular insulin (intravenous infusion). Patients received NG 3 mg or IMG 1 mg approximately 5 minutes after insulin termination. The primary endpoint was the proportion of patients achieving treatment success [plasma glucose (PG) increase to ≥3.9 mmol/L (≥70 mg/dL) or ≥1.1 mmol/L (≥20 mg/dL) increase from the PG nadir within 30 minutes of receiving glucagon]. Non-inferiority was declared if the upper limit of the two-sided 95% confidence interval (CI) of the mean difference in the percentage of patients achieving treatment success (IMG minus NG) was <10%.
Seventy-five patients with T1DM (n = 34) or T2DM (n = 41) were enrolled; 72 patients (50 men, 22 women) received ≥1 study drug dose (T1DM, n = 33; T2DM, n = 39). Sixty-eight patients completed the study and were evaluable. All NG- and IMG-treated patients achieved treatment success (treatment arm difference: 0%; upper limit of two-sided 95% CI 1.47%); NG met prespecified conditions defining non-inferiority versus IMG. Glucagon was rapidly absorbed after both nasal and intramuscular administration; PG profiles were similar between administration routes during the first 60 minutes post dose. Study drug-related treatment-emergent adverse events affecting >2 patients were rhinalgia, increased blood pressure, nausea, ear pain and vomiting in the NG group, and nausea and vomiting in the IMG group.
Nasal glucagon was non-inferior to IMG for successful treatment of insulin-induced hypoglycaemia in Japanese patients with T1DM/T2DM, supporting use of NG as a rescue treatment for severe hypoglycaemia.
比较鼻内给予胰高血糖素(NG)与肌内给予胰高血糖素(IMG)治疗 1 型(T1DM)或 2 型糖尿病(T2DM)日本患者的胰岛素诱导性低血糖。
这是一项 3 期、随机、开放标签、两治疗、两周期交叉非劣效性研究,纳入了正在接受胰岛素治疗、糖化血红蛋白水平≤86mmol/mol(≤10%)的 T1DM 或 T2DM 日本成年患者。禁食≥8 小时后,用重组人胰岛素(静脉输注)诱导低血糖。在胰岛素终止后约 5 分钟,患者接受 NG 3mg 或 IMG 1mg。主要终点是治疗成功的患者比例[血浆葡萄糖(PG)增加≥3.9mmol/L(≥70mg/dL)或从 PG 最低点增加≥1.1mmol/L(≥20mg/dL),在接受胰高血糖素后 30 分钟内]。如果 IMG 与 NG 治疗成功率(IMG 减去 NG)的双侧 95%置信区间(CI)上限的差值的上限<10%,则宣布非劣效性。
纳入了 75 例 T1DM(n=34)或 T2DM(n=41)患者;72 例(50 例男性,22 例女性)患者接受了≥1 次研究药物剂量(T1DM,n=33;T2DM,n=39)。68 例患者完成了研究并可进行评估。所有接受 NG 和 IMG 治疗的患者均达到治疗成功(治疗臂差异:0%;双侧 95%CI 上限 1.47%);NG 符合定义 IMG 非劣效性的预设条件。鼻内和肌内给予后,胰高血糖素均迅速吸收;在给药后 60 分钟内,两种给药途径的 PG 谱相似。影响>2 例患者的与研究药物相关的治疗后出现的不良事件为鼻内给予组的鼻咽炎、血压升高、恶心、耳痛和呕吐,以及肌内给予组的恶心和呕吐。
在日本 T1DM/T2DM 患者中,鼻内给予胰高血糖素与肌内给予胰高血糖素相比,治疗胰岛素诱导性低血糖不劣效,支持将 NG 作为严重低血糖的抢救治疗。