Division of Circulatory and Body Fluid Regulation, Department of Internal Medicine, Faculty of Medicine, University of Miyazaki, 5200 Kihara, Miyazaki, Miyazaki, 889-1692, Japan.
Department of Gastroenterology, Fujita Health University School of Medicine, Toyoake, Japan.
J Gastroenterol. 2021 Feb;56(2):147-157. doi: 10.1007/s00535-020-01741-4. Epub 2020 Nov 2.
Adrenomedullin (AM) is a bioactive peptide having many pleiotropic effects, including mucosal healing and immunomodulation. AM has shown beneficial effects in rodent models and in preliminary study for patients with ulcerative colitis (UC). We performed a clinical trial to investigate the efficacy and safety of AM in patients with UC.
This was a multi-center, double-blind, placebo-controlled phase-2a trial evaluating 28 patients in Japan with steroid-resistant UC. Patients were randomly assigned to four groups and given an infusion of 5, 10, 15 ng/kg/min of AM or placebo for 8 h per day for 14 days. The primary endpoint was the change in Mayo scores at 2 weeks. Main secondary endpoints included the change in Mayo scores and the rate of clinical remission at 8 weeks, defined as a Mayo score 0.
No differences in the primary or secondary endpoints were observed among the four groups at 2 weeks. Despite the insufficient tracking rate, the Mayo score at 8 weeks was only significantly decreased in the high-dose AM group (15 ng/kg/min) compared with the placebo group (- 9.3 ± 1.2 vs. - 3.0 ± 2.8, P = 0.035), with its rate of clinical remission at 8 weeks being significantly higher (3/3, 100% vs. 0/2, 0%, P = 0.025). We noted mild but no serious adverse events caused by the vasodilatory effect of AM.
In this double-blind randomized trial, we observed the complete remission at 8 weeks in patients with steroid-resistant UC receiving a high dose of AM.
JAPIC clinical trials information; Japic CTI-205255 (200410115290). https://www.clinicaltrials.jp/cti-user/trial/Search.jsp .
肾上腺髓质素 (AM) 是一种具有多种多效性作用的生物活性肽,包括粘膜愈合和免疫调节。AM 在啮齿动物模型和溃疡性结肠炎 (UC) 患者的初步研究中显示出有益的效果。我们进行了一项临床试验,以研究 AM 在 UC 患者中的疗效和安全性。
这是一项多中心、双盲、安慰剂对照的 2a 期临床试验,在日本评估了 28 例类固醇耐药性 UC 患者。患者被随机分为四组,每天接受 5、10、15ng/kg/min 的 AM 或安慰剂输注 8 小时,共 14 天。主要终点是 2 周时 Mayo 评分的变化。主要次要终点包括 8 周时 Mayo 评分的变化和临床缓解率,定义为 Mayo 评分 0。
在 2 周时,四组之间主要或次要终点均无差异。尽管跟踪率不足,但高剂量 AM 组(15ng/kg/min)的 Mayo 评分在 8 周时仅显著降低(-9.3±1.2 与-3.0±2.8,P=0.035),其 8 周时的临床缓解率也显著升高(3/3,100%与 0/2,0%,P=0.025)。我们注意到 AM 的血管扩张作用引起的轻微但无严重不良事件。
在这项双盲随机试验中,我们观察到接受高剂量 AM 的类固醇耐药性 UC 患者在 8 周时达到完全缓解。
日本临床试验信息; Japic CTI-205255(200410115290)。https://www.clinicaltrials.jp/cti-user/trial/Search.jsp。