Mallikaarjun Suresh, Wells Charles, Petersen Carolyn, Paccaly Anne, Shoaf Susan E, Patil Shiva, Geiter Lawrence
Otsuka Pharmaceutical Development & Commercialization, Inc., Princeton, New Jersey, USA
Otsuka Pharmaceutical Development & Commercialization, Inc., Princeton, New Jersey, USA.
Antimicrob Agents Chemother. 2016 Sep 23;60(10):5976-85. doi: 10.1128/AAC.00509-16. Print 2016 Oct.
Delamanid is a medicinal product approved for treatment of multidrug-resistant tuberculosis. Three studies were conducted to evaluate the potential drug-drug interactions between delamanid and antiretroviral drugs, including ritonavir, a strong inhibitor of CYP3A4, and selected anti-TB drugs, including rifampin, a strong inducer of cytochrome P450 (CYP) isozymes. Multiple-dose studies were conducted in parallel groups of healthy subjects. Plasma samples were analyzed for delamanid, delamanid metabolite, and coadministered drug concentrations, and pharmacokinetic (PK) parameters were determined. The magnitude of the interaction was assessed by the ratio of the geometric means and 90% confidence intervals. Coadministration of delamanid with tenofovir or efavirenz did not affect the PK characteristics of delamanid. Coadministration of Kaletra (lopinavir/ritonavir) with delamanid resulted in an approximately 25% higher delamanid area under the concentration-time curve from time 0 to the end of the dosing interval (AUCτ). Tenofovir, efavirenz, lopinavir, and ritonavir exposure were not affected by delamanid. Coadministration of delamanid with the TB drugs (ethambutol plus Rifater [rifampin, pyrazinamide, and isoniazid]) resulted in lower delamanid exposures (47 and 42% for the AUCτ and Cmax [maximum concentration of a drug in plasma] values, respectively), as well as decreased exposure of three primary metabolites (approximately 30 to 50% lower AUCτ values). Delamanid did not affect rifampin, pyrazinamide, and isoniazid exposure; the ethambutol AUCτ and Cmax values were about 25% higher with delamanid coadministration. The lack of clinically significant drug-drug interactions between delamanid and selected antiretroviral agents (including the strong CYP inhibitor ritonavir) and a combination of anti-TB drugs was demonstrated. Although there was a decrease in the delamanid concentrations when coadministered with ethambutol plus Rifater, this is likely related to decreased delamanid absorption and not to CYP induction.
地拉米丁是一种被批准用于治疗耐多药结核病的药品。开展了三项研究,以评估地拉米丁与抗逆转录病毒药物(包括细胞色素P450(CYP)3A4的强效抑制剂利托那韦)以及选定的抗结核药物(包括细胞色素P450同工酶的强效诱导剂利福平)之间潜在的药物相互作用。在健康受试者的平行组中进行了多剂量研究。分析血浆样本中的地拉米丁、地拉米丁代谢物和合用药物浓度,并确定药代动力学(PK)参数。通过几何均值比和90%置信区间评估相互作用的程度。地拉米丁与替诺福韦或依非韦伦合用不影响地拉米丁的PK特性。克力芝(洛匹那韦/利托那韦)与地拉米丁合用导致地拉米丁从给药开始到给药间隔结束的浓度-时间曲线下面积(AUCτ)升高约25%。替诺福韦、依非韦伦、洛匹那韦和利托那韦的暴露不受地拉米丁影响。地拉米丁与抗结核药物(乙胺丁醇加卫非特[利福平、吡嗪酰胺和异烟肼])合用导致地拉米丁暴露降低(AUCτ和Cmax[血浆中药物的最大浓度]值分别降低47%和42%),以及三种主要代谢物的暴露降低(AUCτ值降低约30%至50%)。地拉米丁不影响利福平、吡嗪酰胺和异烟肼的暴露;合用 地拉米丁时,乙胺丁醇的AUCτ和Cmax值升高约25%。已证明地拉米丁与选定的抗逆转录病毒药物(包括强效CYP抑制剂利托那韦)以及抗结核药物组合之间不存在具有临床意义 的药物相互作用。虽然与乙胺丁醇加卫非特合用时地拉米丁浓度降低,但这可能与地拉米丁吸收减少有关,而非与CYP诱导有关。