Cossu Maria Vittoria, Cattaneo Dario, Fucile Serena, Pellegrino Paolo, Baldelli Sara, Cozzi Valeria, Capetti Amedeo, Clementi Emilio
Unit of Clinical Pharmacology, Consiglio Nazionale delle Ricerche Institute of Neuroscience, Department of Biomedical and Clinical Sciences, University Hospital "Luigi Sacco", Università di Milano, Milan, Italy.
Unit of Infectious Diseases, University Hospital "Luigi Sacco", Milan, Italy.
Drug Des Devel Ther. 2014 May 2;8:411-9. doi: 10.2147/DDDT.S58803. eCollection 2014.
We designed two Phase I studies that assessed healthy volunteers in order to evaluate the safety and to optimize the dosing of the combination of the drugs isosorbide dinitrate, a nitric oxide donor, and ibuprofen, a nonsteroidal antiinflammatory drug. We designed these studies with the aim of designing a Phase II trial to evaluate the drugs' efficacy in patients affected by Duchenne muscular dystrophy. For the first trial, ISOFEN1, a single-dose, randomized-sequence, open-label, active control, three-treatment cross-over study, was aimed at comparing the pharmacokinetics of ibuprofen 200 mg and isosorbide dinitrate 20 mg when given alone and concomitantly. The pharmacokinetics of ibuprofen given alone versus ibuprofen given concomitantly with isosorbide dinitrate were similar, as documented by the lack of statistically significant differences in the main drug's pharmacokinetic parameters (time to maximal concentration [Tmax], maximal concentration [Cmax], area under the curve [AUC]0-t, and AUC0-∞). Similarly, we found that the coadministration of ibuprofen did not significantly affect the pharmacokinetics of isosorbide dinitrate. No issues of safety were detected. The second trial, ISOFEN2, was a single-site, dose titration study that was designed to select the maximum tolerated dose for isosorbide dinitrate when coadministered with ibuprofen. Eighteen out of the 19 enrolled subjects tolerated the treatment well, and they completed the study at the highest dose of isosorbide dinitrate applied (80 mg/day). One subject voluntarily decided to reduce the dose of isosorbide dinitrate from 80 mg to 60 mg. The treatment-related adverse events recorded during the study were, for the large majority, episodes of headache that remitted spontaneously in 0.5-1 hour - a known side effect of isosorbide dinitrate. These studies demonstrate that the combination of isosorbide dinitrate and ibuprofen does not lead to pharmacokinetic interactions between the two drugs; they also demonstrate that the combination of isosorbide dinitrate and ibuprofen has optimal tolerability and safety profiles that are similar to those previously reported for isosorbide dinitrate and ibuprofen given alone.
我们设计了两项I期研究,对健康志愿者进行评估,以评价一氧化氮供体药物硝酸异山梨酯与非甾体抗炎药布洛芬联合用药的安全性并优化给药剂量。我们开展这些研究的目的是设计一项II期试验,以评估该药物对杜氏肌营养不良患者的疗效。第一项试验ISOFEN1是一项单剂量、随机序列、开放标签、活性对照、三治疗组交叉研究,旨在比较单独给药和联合给药时布洛芬200毫克和硝酸异山梨酯20毫克的药代动力学。单独给予布洛芬与与硝酸异山梨酯联合给予布洛芬的药代动力学相似,主要药物的药代动力学参数(达峰时间 [Tmax]、峰浓度 [Cmax]、曲线下面积 [AUC]0-t和AUC0-∞)缺乏统计学显著差异证明了这一点。同样,我们发现布洛芬的联合给药并未显著影响硝酸异山梨酯的药代动力学。未检测到安全性问题。第二项试验ISOFEN2是一项单中心剂量滴定研究,旨在选择与布洛芬联合使用时硝酸异山梨酯的最大耐受剂量。19名入组受试者中有18名对治疗耐受性良好,并在应用的硝酸异山梨酯最高剂量(80毫克/天)下完成了研究。一名受试者自愿决定将硝酸异山梨酯剂量从80毫克减至60毫克。研究期间记录的与治疗相关的不良事件,绝大多数是头痛发作,在0.5 - 1小时内自发缓解——这是硝酸异山梨酯的已知副作用。这些研究表明,硝酸异山梨酯和布洛芬联合使用不会导致两种药物之间的药代动力学相互作用;它们还表明,硝酸异山梨酯和布洛芬联合使用具有最佳的耐受性和安全性,与之前单独使用硝酸异山梨酯和布洛芬时报告的情况相似。