...
首页> 外文期刊>Canadian journal of gastroenterology >Delayed-release oral mesalamine 4.8 g/day (800 mg tablets) compared to 2.4 g/day (400 mg tablets) for the treatment of mildly to moderately active ulcerative colitis: The ASCEND I trial.
【24h】

Delayed-release oral mesalamine 4.8 g/day (800 mg tablets) compared to 2.4 g/day (400 mg tablets) for the treatment of mildly to moderately active ulcerative colitis: The ASCEND I trial.

机译:口服缓释美沙明胺4.8 g /天(800 mg片剂)与2.4 g /天(400 mg片剂)相比,用于治疗轻度至中度活动性溃疡性结肠炎:ASCEND I试验。

获取原文
获取原文并翻译 | 示例
           

摘要

BACKGROUND: Delayed-release oral mesalamine 2.4 g/day to 4.8 g/day has been shown to be effective in treating mildly to moderately active ulcerative colitis (UC), but it is unknown whether an initial dose of 4.8 g/day is more effective than 2.4 g/day in patients with mildly to moderately active UC and in the subgroup with moderate disease. PATIENTS AND METHODS: A six-week, multicentre, randomized, double-blind, controlled trial assessing the safety and clinical efficacy of a new dose (ASCEND I) of medication randomly assigned 301 adults with mildly to moderately active UC to delayed-release oral mesalamine 2.4 g/day (400 mg tablet [n=154]) or 4.8 g/day (800 mg tablet [n=147]). The primary efficacy end point was overall improvement (ie, treatment success), defined as complete remission or response to therapy from baseline to week 6. Primary safety end points were adverse events and laboratory evaluations. Data were also analyzed separately for the prespecified subgroup of patients with moderate UC at baseline. RESULTS: Treatment success was not statistically different between the treatment groups at week 6; 51% of the group (77 of 150) who received delayed-release oral mesalamine 2.4 g/day and 56% of the group (76 of 136) who received 4.8 g/day reached the efficacy end point (P=0.441). Among the moderate disease subgroup, however, the higher initial dose was more effective; 57% of patients (53 of 93) given delayed-release oral mesalamine 2.4 g/day and 72% of patients (55 of 76) given 4.8 g/day achieved treatment success (P=0.0384). Both regimens were well tolerated. CONCLUSIONS: Delayed-release oral mesalamine is an effective and well-tolerated initial therapy in patients with mildly to moderately active UC, and a 4.8 g/day dose may enhance treatment success rates in patients with moderate disease compared with mesalamine 2.4 g/day.
机译:背景:延迟释放的口服美沙拉敏2.4 g /天至4.8 g /天已被证明可有效治疗轻度至中度活动性溃疡性结肠炎(UC),但尚不清楚初始剂量4.8 g /天是否更有效轻度至中度活动性UC患者和中度疾病亚组患者的血脂水平超过2.4 g /天。患者和方法:一项为期六周的多中心,随机,双盲,对照试验,评估了新剂量药物(ASCEND I)的安全性和临床疗效,该药物随机分配了301名中度至中度活动性UC成年人至延迟释放口服美沙拉敏2.4克/天(400毫克片剂[n = 154])或4.8克/天(800毫克片剂[n = 147])。主要疗效终点是总体改善(即治疗成功),定义为从基线到第6周完全缓解或对治疗的反应。主要安全终点是不良事件和实验室评估。还对基线时中度UC患者的预定亚组的数据进行了单独分析。结果:在第6周,各治疗组之间的治疗成功率无统计学差异;每天口服2.4 mg /天的美沙拉敏口服缓释片的人群中有51%(150人中的77人)和每天4.8g /天的口服药物组中的56%(136人中的76人)达到了疗效终点(P = 0.441)。但是,在中度疾病亚组中,较高的初始剂量更有效;每天口服缓释美沙明胺2.4 g /天的患者中有57%(93中的53)和每天4.8g /天的72%的患者(76中的55)获得了成功的治疗(P = 0.0384)。两种方案均耐受良好。结论:缓释口服美沙拉敏是轻度至中度活动性UC患者的有效且耐受良好的初始治疗,与美沙拉敏2.4 g /天相比,4.8 g /天的剂量可提高中度疾病患者的治疗成功率。

著录项

相似文献

  • 外文文献
  • 中文文献
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号