...
首页> 外文期刊>The American Journal of Tropical Medicine and Hygiene >Malarone (atovaquone and proguanil hydrochloride): a review of its clinical development for treatment of malaria. Malarone Clinical Trials Study Group.
【24h】

Malarone (atovaquone and proguanil hydrochloride): a review of its clinical development for treatment of malaria. Malarone Clinical Trials Study Group.

机译:马拉龙(盐酸阿托伐醌和盐酸胍):综述其治疗疟疾的临床进展。 Malarone临床试验研究小组。

获取原文
获取原文并翻译 | 示例
           

摘要

The continuing spread of drug-resistant malaria emphasizes the need for new antimalarial drugs. Atovaquone is a broad-spectrum antiprotozoal drug with a novel mechanism of action, via inhibition of parasite mitochondrial electron transport, and a favorable safety profile. Early studies with atovaquone alone for treatment of malaria demonstrated good initial control of parasitemia but an unacceptable rate of recrudescent parasitemia. Parasites isolated during recrudescence after treatment with atovaquone alone were resistant to atovaquone in vitro. The combination of atovaquone and proguanil is synergistic in vitro, and clinical studies demonstrated enhanced efficacy of the combination compared to either drug alone for treatment of malaria. Malarone, a fixed-dose combination of 250 mg of atovaquone and 100 mg of proguanil hydrochloride, is available in many countries for treatment of acute, uncomplicated malaria caused by Plasmodium falciparum. At the recommended dose (in adults, four tablets once a day for three days), the overall cure rate was > 98% in more than 500 patients with falciparum malaria. In four randomized, controlled clinical trials, treatment with atovaquone and proguanil hydrochloride was significantly more effective than mefloquine (Thailand), amodiaquine (Gabon), chloroquine (Peru and the Philippines) or chloroquine plus pyrimethamine/sulfadoxine (Philippines). In clinical trials where the comparator drug was highly effective, treatment with atovaquone and proguanil hydrochloride was equally effective. Parasites isolated during recrudescence after treatment with the combination of atovaquone and proguanil were not resistant to atovaquone in vitro. The most commonly reported adverse events in clinical trials (abdominal pain, anorexia, nausea, vomiting, diarrhea and coughing) occurred with similar frequency in patients treated with a comparator drug. Malarone is a safe and effective new agent for treatment of malaria.
机译:耐药性疟疾的持续传播强调了对新抗疟药的需求。 Atovaquone是一种广谱的抗原生动物药物,具有通过抑制寄生虫线粒体电子运输而产生的新作用机制,并具有良好的安全性。早期仅用阿托伐醌治疗疟疾的早期研究表明,对寄生虫病具有良好的初步控制,但复发性寄生虫病的发生率不可接受。单独使用阿托伐醌治疗后在复发期间分离出的寄生虫对体外阿托伐醌具有抗性。 Atovaquone和Proguanil的组合在体外具有协同作用,临床研究表明,与单独使用这两种药物治疗疟疾相比,该组合的疗效增强。马拉洛酮是250毫克阿托伐醌和100毫克盐酸盐酸胍的固定剂量组合,在许多国家/地区均可用于治疗由恶性疟原虫引起的急性,简单的疟疾。在推荐剂量下(成人每天四片,连续三天),超过500例恶性疟疾患者的总治愈率> 98%。在四项随机,对照的临床试验中,用阿托伐醌和盐酸异丙胍治疗的效果明显优于甲氟喹(泰国),氨二喹(加蓬),氯喹(秘鲁和菲律宾)或氯喹加乙胺嘧啶/磺胺多辛(菲律宾)。在比较药物非常有效的临床试验中,用阿托伐醌和盐酸异丙胍治疗同样有效。在用阿托伐醌和异丙胍联合治疗后的再发过程中分离出的寄生虫在体外对阿托伐醌没有抗药性。在临床试验中,最常见的不良事件(腹痛,厌食,恶心,呕吐,腹泻和咳嗽)发生在以比较药物治疗的患者中,发生频率相似。马拉隆是治疗疟疾的安全有效的新药。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号