Infectious Diseases Department, Vall d'Hebron University Hospital, PROSICS Barcelona, Universitat Autònoma de Barcelona, P° Vall d'Hebron 119, Edifici Mediterrània, VHIR, 08035, Barcelona, Spain.
Departamento de Clínica, Patología y Tratamiento, Instituto Nacional de Parasitología Dr. Mario Fatala Chaben, Ministerio de Salud y Desarrollo Social, Buenos Aires, Argentina.
Trials. 2020 Apr 15;21(1):328. doi: 10.1186/s13063-020-4226-2.
Chagas disease (CD) continues to be a neglected infectious disease with one of the largest burdens globally. Despite the modest cure rates in adult chronic patients and its safety profile, benznidazole (BNZ) is still the drug of choice. Its current recommended dose is based on nonrandomized studies, and efficacy and safety of the optimal dose of BNZ have been scarcely analyzed in clinical trials.
METHODS/DESIGN: MULTIBENZ is a phase II, randomized, noninferiority, double-blind, multicenter international clinical trial. A total of 240 patients with Trypanosoma CD in the chronic phase will be recruited in four different countries (Argentina, Brazil, Colombia, and Spain). Patients will be randomized to receive BNZ 150 mg/day for 60 days, 400 mg/day for 15 days, or 300 mg/day for 60 days (comparator arm). The primary outcome is the efficacy of three different BNZ therapeutic schemes in terms of dose and duration. Efficacy will be assessed according to the proportion of patients with sustained parasitic load suppression in peripheral blood measured by polymerase chain reaction. The secondary outcomes are related to pharmacokinetics and drug tolerability. The follow-up will be 12 months from randomization to end of study participation. Recruitment was started in April 2018.
This is a clinical trial conducted for the assessment of different dose schemes of BNZ compared with the standard treatment regimen for the treatment of CD in the chronic phase. MULTIBENZ may help to clarify which is the most adequate BNZ regimen in terms of efficacy and safety, predicated on sustained parasitic load suppression in peripheral blood.
ClinicalTrials.gov, NCT03191162. Registered on 19 June 2017.
恰加斯病(CD)仍然是一种被忽视的传染病,在全球范围内负担最重。尽管成人慢性患者的治愈率不高,且安全性良好,但苯硝唑(BNZ)仍是首选药物。目前推荐的剂量是基于非随机研究,BNZ 的最佳剂量的疗效和安全性在临床试验中很少被分析。
方法/设计:MULTIBENZ 是一项 II 期、随机、非劣效性、双盲、多中心国际临床试验。将在四个不同国家(阿根廷、巴西、哥伦比亚和西班牙)招募 240 名 CD 慢性期的 Trypanosoma 患者。患者将随机分为三组,分别接受 BNZ 150mg/天治疗 60 天、400mg/天治疗 15 天或 300mg/天治疗 60 天(对照组)。主要结局是三种不同 BNZ 治疗方案在剂量和时间方面的疗效。疗效将根据聚合酶链反应(PCR)测量的外周血寄生虫载量持续抑制的患者比例来评估。次要结局与药代动力学和药物耐受性有关。随访时间为随机分组至研究结束后 12 个月。招募工作于 2018 年 4 月开始。
这是一项评估 BNZ 不同剂量方案与 CD 慢性期标准治疗方案相比的临床试验。MULTIBENZ 可能有助于阐明在基于外周血寄生虫载量持续抑制的疗效和安全性方面,哪种 BNZ 方案最适合。
ClinicalTrials.gov,NCT03191162。于 2017 年 6 月 19 日注册。