Health Protection Agency Centre for Infections, Department of Healthcare-associated Infection & Antimicrobial Resistance, London NW9 5EQ, UK.
Expert Opin Ther Pat. 2010 Oct;20(10):1389-99. doi: 10.1517/13543776.2010.511177.
Clostridium difficile infection (CDI) is associated with consumption of antibiotics which disrupt the normal microbial flora of the gut, allowing C. difficile to establish itself and produce disease. Currently, only vancomycin or metronidazole are recommended for treatment and many patients suffer from relapse on infection. Hence, there is a need for new treatment options.
This review evaluates five agents in development where the focus is on treatment of CDI.
This review gives up-to-date information on fidaxomicin, REP3123, oritavancin, NVB302 and nitazoxanide and their likelihood of being licensed for the treatment of CDI.
One agent, fidaxomicin, has undergone Phase III clinical trials which show it to be a promising new agent for the treatment of CDI with a low rate of relapse. Nitazoxanide is licensed for the treatment of parasitic intestinal infections but is not licensed for CDI. However, in small scale clinical trials it has been shown to have activity comparable to that of vancomycin and metronidazole. The other agents are all at early stages of development and clinical trials to evaluate their therapeutic potential for CDI have not yet been undertaken.
艰难梭菌感染(CDI)与抗生素的使用有关,抗生素会破坏肠道的正常微生物菌群,使艰难梭菌得以定植并引发疾病。目前,仅万古霉素或甲硝唑被推荐用于治疗,许多患者在感染后会复发。因此,需要新的治疗选择。
本综述评估了五种正在开发中的药物,重点是治疗 CDI。
本综述提供了关于 fidaxomicin、REP3123、oritavancin、NVB302 和硝唑尼特的最新信息,以及它们获得 CDI 治疗许可的可能性。
一种名为 fidaxomicin 的药物已进行 III 期临床试验,结果表明它是一种很有前途的新型 CDI 治疗药物,复发率低。硝唑尼特被批准用于治疗寄生虫性肠道感染,但未被批准用于 CDI。然而,在小规模临床试验中,它已被证明具有与万古霉素和甲硝唑相当的活性。其他药物都处于早期开发阶段,尚未进行临床试验来评估它们治疗 CDI 的潜在疗效。