Office of Critical Path Programs in the Office of the Chief Scientist, US FDA, 10903 New Hampshire Avenue, Building 32, Silver Spring, MD 20993, USA.
Expert Rev Anti Infect Ther. 2011 Jul;9(7):823-31. doi: 10.1586/eri.11.64.
Unique challenges remain in the development of new drugs for the treatment of TB. While existing multidrug treatment regimens are prolonged and difficult for patients to adhere to, they are highly efficacious, setting a high bar for the performance of new agents. Complicating matters more, regulatory standards have changed since the first drugs for TB were introduced, with a rigorous characterization of the effect of a new drug within a combination regimen expected. If these demands are to be satisfied, innovative models will be needed to demonstrate drug efficacy. In the past, mycobacterial cultures performed on solid media at the end of treatment have been used as critical biomarkers of drug efficacy, but their inability to predict long-term outcomes with precision has limited their utility. This article reviews a range of nonclinical and clinical models to characterize the bactericidal and/or sterilizing activity of new compounds. Novel approaches, using in vitro and animal models, sensitive biomarkers, as well as creative new clinical trial designs, are discussed. These promise a timely expansion of our TB treatment armamentarium to include potent new drugs and shorter, simpler treatment regimens.
治疗结核病的新药研发仍面临独特挑战。虽然现有的多药治疗方案时间长且患者难以坚持,但疗效显著,为新药物的疗效设定了很高的标准。更复杂的是,自第一批结核病药物问世以来,监管标准已经发生了变化,人们期望对新药物在联合治疗方案中的作用进行严格的特征描述。如果要满足这些要求,就需要创新的模型来证明药物的疗效。过去,治疗结束时在固体培养基上进行的分枝杆菌培养曾被用作药物疗效的关键生物标志物,但由于其无法精确预测长期结果,因此其用途受到限制。本文综述了一系列非临床和临床模型,用于描述新化合物的杀菌和/或灭菌活性。讨论了使用体外和动物模型、敏感生物标志物以及创造性的新临床试验设计等新颖方法。这些方法有望及时扩大我们的结核病治疗手段,包括强效新药和更短、更简单的治疗方案。