Hermann Robert, Hellwig Kerstin, Gaikwad Sumedh, Galazka Andrew, Bytyqi Afrim, Jack Dominic, Krebs-Brown Axel, Vetter Claudia, Nolting Axel, Venkatakrishnan Karthik, Dong Jennifer Q
Clinical Research Appliance (Cr Appliance), Gelnhausen, Germany.
Department of Neurology, Katholisches Klinikum, Ruhr University Bochum, Bochum, Germany.
Clin Transl Sci. 2025 Apr;18(4):e70204. doi: 10.1111/cts.70204.
This study assessed the effect of cladribine tablets (CladT) on the pharmacokinetics (PK) of a combined oral contraceptive (COC) in pre-menopausal women with relapsing multiple sclerosis. It was a randomized, double-blind, two-period, two-sequence crossover study to assess steady-state plasma PK (area under the concentration-time curve and peak concentration) of COC (ethinylestradiol [EE] 30 μg and levonorgestrel [LNG] 150 μg) when co-administered with CladT or placebo. Participants received 2 weeks of active CladT treatment per course (Weeks 1 and 5 per year) to have a cumulative dose of 3.5 mg/kg over 2 years as per label. Of the 24 randomized participants, 23 completed the study. The results showed that the concentration-time profiles as well as PK parameters of EE and LNG in the plasma were similar when co-administered with CladT or placebo. Analysis of variance confirmed the bioequivalence of EE and LNG in COC when co-administered with either CladT or placebo. All participants were adequately exposed to cladribine. Repeat-dose administration of CladT had no apparent effect on serum luteinizing hormone, follicle-stimulating hormone, progesterone, or sex hormone-binding globulin concentrations during concomitant treatment with COC. Co-administration with COC did not change the known safety and tolerability profile of CladT and did not alter the PK of EE or LNG in a COC during the study. Therefore, the concomitant use of CladT is not expected to decrease the efficacy of COCs containing EE and LNG. Trial Registration: EudraCT Number: 2018-001015-70.
本研究评估了克拉屈滨片(CladT)对复发型多发性硬化症绝经前女性联合口服避孕药(COC)药代动力学(PK)的影响。这是一项随机、双盲、两周期、两序列交叉研究,旨在评估COC(炔雌醇[EE]30μg和左炔诺孕酮[LNG]150μg)与CladT或安慰剂联合给药时的稳态血浆PK(浓度-时间曲线下面积和峰浓度)。参与者每疗程接受2周的CladT活性治疗(每年第1周和第5周),按照标签要求在2年内累积剂量达到3.5mg/kg。24名随机分组的参与者中,23名完成了研究。结果显示,与CladT或安慰剂联合给药时,血浆中EE和LNG的浓度-时间曲线以及PK参数相似。方差分析证实,与CladT或安慰剂联合给药时,COC中EE和LNG具有生物等效性。所有参与者均充分暴露于克拉屈滨。在与COC同时治疗期间,重复给药CladT对血清促黄体生成素、促卵泡激素、孕酮或性激素结合球蛋白浓度无明显影响。与COC联合给药未改变CladT已知的安全性和耐受性,且在研究期间未改变COC中EE或LNG的PK。因此,预计同时使用CladT不会降低含EE和LNG的COC的疗效。试验注册号:EudraCT编号:2018-001015-70。