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A novel reflux inhibitor lesogaberan (AZD3355) as add-on treatment in patients with GORD with persistent reflux symptoms despite proton pump inhibitor therapy: a randomised placebo-controlled trial

机译:尽管有质子泵抑制剂治疗,但仍存在持续性反流症状的GORD患者中,一种新型反流抑制剂来沙贝加仑(AZD3355)作为附加治疗:一项随机安慰剂对照试验

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摘要

o evaluate the efficacy and tolerability of add-on treatment with lesogaberan (AZD3355), a novel reflux inhibitor, in patients with persistent gastro-oesophageal reflux disease (GORD) symptoms despite proton pump inhibitor (PPI) therapy. double-blind, placebo-controlled, randomised, parallel-group, multicentre phase IIA study was carried out in outpatient clinics. The study group comprised 244 adult patients with persistent GORD symptoms (heartburn and/or regurgitation) of at least mild intensity and for 3 days of 7 days before enrolment, despite ≥6 weeks of continuous PPI therapy. Patients received either lesogaberan (65 mg twice daily) or placebo in addition to PPI therapy for a period of 4 weeks. Symptom intensity, based on the Reflux Disease Questionnaire, was recorded twice daily. Treatment response (defined as at most one 24 h period with heartburn or regurgitation of not more than mild intensity during the last 7 days of treatment). Time to response, proportion of symptom-free days and measures of tolerability were also analysed. total of 232 (114 lesogaberan- and 118 placebo-treated patients) of the 244 randomised patients were analysed for efficacy. Treatment with lesogaberan, compared with placebo, resulted in a significantly larger proportion of responders to treatment (16% vs 8% of patients; p=0.026) and cumulative proportion of responders over time (log-rank p=0.0195). Lesogaberan was well tolerated: adverse events of mostly mild to moderate intensity were reported in 45% of patients on lesogaberan and in 37% on placebo. esogaberan add-on therapy to PPIs significantly improved heartburn and regurgitation symptoms; however, the proportion of responders was small. Clinical trial number NCT00394472
机译:o对质子泵抑制剂(PPI)治疗后持续存在的胃食管反流病(GORD)症状的患者,使用新的反流抑制剂lesogaberan(AZD3355)进行联合治疗的疗效和耐受性进行评估。在门诊进行了双盲,安慰剂对照,随机分组,平行组,多中心IIA期研究。研究组包括244名成年患者,尽管连续进行PPI治疗≥6周,但其持续性GORD症状(烧心和/或反流)的强度至少为轻度,入组前7天为3天。除PPI治疗外,患者还接受了lesogaberan(每天两次,每次65 mg)或安慰剂,为期4周。每天两次记录基于反流疾病问卷的症状强度。治疗反应(定义为在治疗的最后7天中最多有24小时出现烧心或反流,强度不超过中等强度)。还分析了响应时间,无症状天数的比例和耐受性的度量。分析了244例随机分组患者中的232例(114例接受利索加贝兰治疗的患者和118例接受安慰剂治疗的患者)的疗效。与安慰剂相比,使用莱索加贝兰治疗可显着提高对治疗的反应者比例(16%比8%的患者; p = 0.026)和随时间推移的累积反应者比例(log-rank p = 0.0195)。莱加贝兰的耐受性良好:在莱加贝兰和安慰剂组中,分别有45%和37%的患者报告了轻度至中度强度的不良事件。依索加贝兰对PPI的附加疗法可显着改善胃灼热和反流症状;但是,响应者的比例很小。临床试验编号NCT00394472

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