TIMI Study Group, Cardiovascular Division, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA.
TIMI Study Group, Cardiovascular Division, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA.
Am Heart J. 2018 Aug;202:39-48. doi: 10.1016/j.ahj.2018.03.012. Epub 2018 Mar 29.
Lorcaserin, a selective serotonin 2C receptor agonist, is an effective pharmacologic weight-loss therapy that improves several cardiovascular risk factors. The long-term clinical cardiovascular and metabolic safety and efficacy in patients with elevated cardiovascular risk are unknown.
CAMELLIA-TIMI 61 (NCT02019264) is a randomized, double-blind, placebo-controlled, multinational clinical trial designed to evaluate the safety and efficacy of lorcaserin with regard to major adverse cardiovascular events and progression to diabetes in overweight or obese patients at high cardiovascular risk. Overweight or obese patients either with established cardiovascular disease or with diabetes and at least 1 other cardiovascular risk factor were randomized in a 1:1 ratio to lorcaserin 10 mg twice daily or matching placebo. The primary safety objective is to assess for noninferiority of lorcaserin for the composite end point of cardiovascular death, myocardial infarction, or stroke (major adverse cardiovascular event [MACE]) (with noninferiority defined as the upper bound of a 1-sided 97.5% CI excluding a hazard ratio of 1.4) compared with placebo assessed at an interim analysis with 460 adjudicated events. The efficacy objectives, assessed at study completion, will evaluate the superiority of lorcaserin for the primary composite end point of cardiovascular death, myocardial infarction, stroke, hospitalization for unstable angina, heart failure, or any coronary revascularization (MACE+) and the key secondary end point of conversion to diabetes. Recruitment began in January 2014 and was completed in November 2015 resulting in a total population of 12,000 patients. The trial is planned to continue until at least 1,401 adjudicated MACE+ events are accrued and the median treatment duration exceeds 2.5 years.
CAMELLIA-TIMI 61 is investigating the safety and efficacy of lorcaserin for MACEs and conversion to diabetes in overweight or obese patients with established cardiovascular disease or multiple cardiovascular risk factors.
洛卡塞嗪是一种选择性血清素 2C 受体激动剂,是一种有效的药物减肥疗法,可改善多种心血管危险因素。但其在心血管风险升高的患者中的长期临床心血管和代谢安全性和疗效尚不清楚。
CAMELLIA-TIMI 61(NCT02019264)是一项随机、双盲、安慰剂对照、多国临床试验,旨在评估洛卡塞嗪在超重或肥胖、心血管疾病高危患者中的主要不良心血管事件(MACE)和进展为糖尿病方面的安全性和疗效。超重或肥胖患者无论是否患有已确诊的心血管疾病,只要患有糖尿病和至少 1 种其他心血管危险因素,均以 1:1 的比例随机分为洛卡塞嗪 10mg 每日 2 次或匹配安慰剂组。主要安全性目标是评估洛卡塞嗪在心血管死亡、心肌梗死或中风(主要不良心血管事件 [MACE])复合终点方面的非劣效性(非劣效性定义为 460 例经裁决事件的中间分析中单侧 97.5%CI 的上限排除危险比为 1.4)与安慰剂相比。疗效目标在研究完成时进行评估,将评估洛卡塞嗪在心血管死亡、心肌梗死、中风、不稳定型心绞痛住院、心力衰竭或任何冠状动脉血运重建(MACE+)的主要复合终点以及关键次要终点糖尿病转化方面的优越性。该试验于 2014 年 1 月开始招募,2015 年 11 月完成,共招募了 12000 名患者。该试验计划持续到至少 1401 例经裁决的 MACE+事件累积和中位治疗时间超过 2.5 年。
CAMELLIA-TIMI 61 正在研究洛卡塞嗪在超重或肥胖、患有已确诊心血管疾病或多种心血管危险因素的患者中的 MACE 和糖尿病转化的安全性和疗效。