首页> 外文期刊>International journal of clinical pharmacology and therapeutics >Pharmacokinetic and tolerability of i.m. disodium clodronate 200 mg/lidocaine 1%, given twice monthly, in comparison with i.m. disodium clodronate 100 mg/lidocaine 1%, given weekly, in healthy postmenopausal female patients
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Pharmacokinetic and tolerability of i.m. disodium clodronate 200 mg/lidocaine 1%, given twice monthly, in comparison with i.m. disodium clodronate 100 mg/lidocaine 1%, given weekly, in healthy postmenopausal female patients

机译:i.m.的药代动力学和耐受性氯碘酸二钠200 mg /利多卡因1%,每月两次,与i.m.健康绝经后女性患者每周服用一次氯膦酸二钠100 mg /利多卡因1%

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Background: Clodronate is a bisphosphonate effective in the prevention and treatment of osteoporosis in postmeno-pausal women. Non-adherence to bisphos-phonates, however, is a major issue in clinical practice. Simplifying dose regimens may increase compliance. Objectives: To assess bioequivalence between an intramuscular (i.m.) clodronate 200 mg/lidocaine 1% twice-a-month formulation and a clodronate 100 mg/lidocaine 1% weekly formulation in 32 postmenopausal women. Methods: In this double-blind, randomized, two-way crossover study, test and reference formulations were administered in single dose, with a 2-week wash-out between administrations. The primary endpoint was clodronic acid cumulative excretion in the first 24 hours after injection (Xu0-24h). Cumulative excretion in the 72 hours post-dose (Xu 0-72h) and maximum excretion rate (Ratemax) were also evaluated. Bioequivalence was assumed if the 90% confidence intervals (CIs) of the geometric means ratios of the dose-normalized parameters were within the 80.00 - 125.00% range. Local tolerability was evaluated. Results: Mean Xu 0-24h values were 114.03 ± 23.13 mg and 55.22 ± 9.73 mg for clodronate 200 mg and 100 mg. The 90% CIs for dose-normalized Xu 0-24h, Xu0-72h and Ratemax were 95 - 110%, 94 - 107% and 95 - 113%. Local tolerability of both treatments was good. The differences in pain intensity between formulations were not significantly different at most assessment times. Headache was the only treatment-related adverse event. Conclusions: Bioequivalence of the two formulations was confirmed in terms of dose-normalized rate and amount of clodronic acid excretion. This result, together with the favorable tolerability of the novel 200 mg formulation, suggests the possibility of reducing the number of i.m. administrations from once-a-week to twice-a-month.
机译:背景:氯膦酸盐是一种双膦酸盐,对预防和治疗绝经后妇女的骨质疏松症有效。然而,不遵守双膦酸酯是临床实践中的主要问题。简化剂量方案可以增加依从性。目的:评估32名绝经后妇女的肌内(i.m.)氯膦酸盐200 mg /利多卡因1%每月两次制剂与每周一次氯膦酸盐100 mg /利多卡因1%每周制剂之间的生物等效性。方法:在这项双盲,随机,双向交叉研究中,测试和参考制剂以单剂量给药,两次给药之间需要冲洗2周。主要终点是注射后24小时(Xu0-24h)的氯膦酸累积排泄。还评估了给药后72小时(Xu 0-72h)的累积排泄和最大排泄率(Ratemax)。如果剂量标准化参数的几何平均值比率的90%置信区间(CIs)在80.00-125.00%的范围内,则假定具有生物等效性。评价局部耐受性。结果:对于200 mg和100 mg的氯膦酸盐,Xu 0-24h的平均值分别为114.03±23.13 mg和55.22±9.73 mg。剂量标准化的Xu 0-24h,Xu0-72h和Ratemax的90%CI为95-110%,94-107%和95-113%。两种治疗方法的局部耐受性均良好。在大多数评估时间,制剂之间的疼痛强度差异没有显着差异。头痛是唯一与治疗相关的不良事件。结论:根据剂量标准化率和氯膦酸排泄量证实了两种制剂的生物等效性。该结果与新颖的200mg制剂的良好耐受性一起提示减少i.m的数目的可能性。管理从每周一次到每月两次。

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