National Institute of Malaria Research, New Delhi, India.
Clin Infect Dis. 2012 Sep;55(5):663-71. doi: 10.1093/cid/cis475. Epub 2012 May 14.
Artemisinin-based combination therapy is the first-line treatment for uncomplicated falciparum malaria. This study assessed the antimalarial efficacy and safety of a combination of 150 mg of arterolane maleate and 750 mg of piperaquine phosphate (AM-PQP) in comparison to Coartem (artemether and lumefantrine) in patients with acute uncomplicated P. falciparum malaria.
In this open-label, randomized, multicentric, parallel group clinical trial, 240 patients were randomized to receive AM-PQP (160 patients) or Coartem (80 patients). Patients with P. falciparum monoinfection and initial parasite densities ranging from 1000 to 100 000 asexual parasites/µL of blood were followed for 28 days. Polymerase chain reaction-corrected adequate clinical and parasitologic response on day 28, parasite clearance time, and fever clearance time were evaluated.
A total of 151 (94.4%) of 160 patients in the AM-PQP group completed the trial, while 77 (96.3%) of 80 patients in the Coartem group completed the trial. No treatment failure was noted in the AM-PQP group, while one patient receiving Coartem failed treatment on day 28. There was no difference in the median parasite clearance time (30 hours in both groups) or median fever clearance time (24 hours in both groups) after administration of the 2 study treatments.
The available data support the evaluation of a drug combination in a larger population as a fixed-dose combination. Clinical Trials Registration. CTRI/2007/091/000031.
青蒿素类复方疗法是治疗无并发症恶性疟的一线疗法。本研究评估了 150 毫克马来酸蒿甲醚和 750 毫克磷酸哌喹(AM-PQP)联合用药与科泰新(青蒿琥酯和氨酚喹啉)治疗急性无并发症恶性疟原虫疟疾患者的抗疟疗效和安全性。
这是一项开放标签、随机、多中心、平行组临床试验,共 240 例患者被随机分为 AM-PQP 组(160 例)或科泰新组(80 例)。入选患者均为恶性疟原虫单一感染,初始寄生虫密度为 1000 至 100000 个无性体/µL 血液。随访 28 天,评估聚合酶链反应校正后的 28 天临床和寄生虫学应答完全率、寄生虫清除时间和退热时间。
AM-PQP 组 160 例患者中,共有 151 例(94.4%)完成了试验,而科泰新组 80 例患者中,共有 77 例(96.3%)完成了试验。AM-PQP 组无治疗失败病例,而科泰新组有 1 例患者在第 28 天治疗失败。两种研究药物治疗后,寄生虫清除时间的中位数(均为 30 小时)和退热时间的中位数(均为 24 小时)无差异。
现有数据支持在更大人群中评估药物联合作为固定剂量复方。临床试验注册号:CTRI/2007/091/000031。