Klein Klara R, Freeman Jennifer L R, Dunn Imogene, Dvergsten Chris, Kirkman M Sue, Buse John B, Valcarce Carmen
Division of Endocrinology and Metabolism, University of North Carolina School of Medicine, Chapel Hill, NC
vTv Therapeutics LLC, High Point, NC.
Diabetes Care. 2021 Apr;44(4):960-968. doi: 10.2337/dc20-2684. Epub 2021 Feb 23.
Despite advances in exogenous insulin therapy, many patients with type 1 diabetes do not achieve acceptable glycemic control and remain at risk for ketosis and insulin-induced hypoglycemia. We conducted a randomized controlled trial to determine whether TTP399, a novel hepatoselective glucokinase activator, improved glycemic control in people with type 1 diabetes without increasing hypoglycemia or ketosis.
SimpliciT1 was a phase 1b/2 adaptive study. Phase 2 activities were conducted in two parts. Part 1 randomly assigned 20 participants using continuous glucose monitors and continuous subcutaneous insulin infusion (CSII). Part 2 randomly assigned 85 participants receiving multiple daily injections of insulin or CSII. In both parts 1 and 2, participants were randomly assigned to 800 mg TTP399 or matched placebo (fully blinded) and treated for 12 weeks. The primary end point was change in HbA from baseline to week 12.
The difference in change in HbA from baseline to week 12 between TTP399 and placebo was -0.7% (95% CI -1.3, -0.07) in part 1 and -0.21% (95% CI -0.39, -0.04) in part 2. Despite a greater decrease in HbA with TTP399, the frequency of severe or symptomatic hypoglycemia decreased by 40% relative to placebo in part 2. In both parts 1 and 2, plasma β-hydroxybutyrate and urinary ketones were lower during treatment with TTP399 than placebo.
TTP399 lowers HbA and reduces hypoglycemia without increasing the risk of ketosis and should be further evaluated as an adjunctive therapy for the treatment of type 1 diabetes.
尽管外源性胰岛素治疗取得了进展,但许多1型糖尿病患者仍未实现可接受的血糖控制,且仍有发生酮症和胰岛素诱导性低血糖的风险。我们进行了一项随机对照试验,以确定新型肝选择性葡萄糖激酶激活剂TTP399是否能改善1型糖尿病患者的血糖控制,同时不增加低血糖或酮症的发生风险。
SimpliciT1是一项1b/2期适应性研究。2期研究分为两个部分。第1部分随机分配20名使用持续葡萄糖监测仪和持续皮下胰岛素输注(CSII)的参与者。第2部分随机分配85名接受每日多次胰岛素注射或CSII的参与者。在第1部分和第2部分中,参与者均被随机分配至800 mg TTP399组或匹配的安慰剂组(完全盲法),并接受12周的治疗。主要终点是从基线到第12周糖化血红蛋白(HbA)的变化。
在第1部分中,TTP399组与安慰剂组从基线到第12周HbA变化的差异为-0.7%(95%置信区间 -1.3,-0.07),在第2部分中为-0.21%(95%置信区间 -0.39,-0.04)。尽管TTP399使HbA降低幅度更大,但在第2部分中,严重或有症状低血糖的发生率相对于安慰剂组降低了40%。在第1部分和第2部分中,TTP399治疗期间血浆β-羟基丁酸和尿酮均低于安慰剂组。
TTP399可降低HbA并减少低血糖,且不增加酮症风险,应作为1型糖尿病治疗的辅助疗法进行进一步评估。