The George Institute for Global Health, Sydney, Australia.
The Charles Perkins Centre, University of Sydney, Sydney, Australia.
Diabetes Obes Metab. 2017 Jul;19(7):926-935. doi: 10.1111/dom.12924. Epub 2017 Apr 3.
Two large cardiovascular outcome trials of canagliflozin, comprising the CANVAS Program, will complete in early 2017: the CANagliflozin cardioVascular Assessment Study (CANVAS) and the CANagliflozin cardioVascular Assessment Study-Renal (CANVAS-R). Accruing data for the sodium glucose co-transporter 2 (SGLT2) inhibitor class has identified questions and opportunities that were not apparent when the trials were designed. Accordingly, a series of modifications have been made to the planned analyses. These updates will ensure that the data from the CANVAS Program will maximize advances in scientific knowledge and patient care. The specification of the analysis strategy prior to knowledge of the trial results, their design by the independent scientific trial Steering Committee, the detailed a priori definition of the analysis plans, and the external review provided by the US Food and Drug Administration all provide maximally efficient and robust utilization of the data. The CANVAS Program should significantly advance our understanding of the effects of canagliflozin, and the broader SGLT2 inhibitor class, on a range of important efficacy and safety outcomes.
两项大型卡瓦列利诺嗪心血管结局试验,即 CANVAS 计划,将于 2017 年初完成:卡瓦列利诺嗪心血管评估研究(CANVAS)和卡瓦列利诺嗪心血管评估研究-肾脏(CANVAS-R)。钠葡萄糖协同转运蛋白 2(SGLT2)抑制剂类别的累积数据已经确定了在试验设计时不明显的问题和机会。因此,对计划分析进行了一系列修改。这些更新将确保 CANVAS 计划的数据将最大程度地提高科学知识和患者护理的进展。在了解试验结果之前指定分析策略、由独立的科学试验指导委员会设计、详细的预先定义的分析计划以及美国食品和药物管理局提供的外部审查都为数据的高效和稳健利用提供了保障。CANVAS 计划应显著提高我们对卡瓦列利诺嗪和更广泛的 SGLT2 抑制剂类对一系列重要疗效和安全性结果的影响的理解。