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Treatment of human African trypanosomiasis--present situation and needs for research and development.

机译:非洲人锥虫病的治疗-研究现状和需求

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Human African trypanosomiasis re-emerged in the 1980s. However, little progress has been made in the treatment of this disease over the past decades. The first-line treatment for second-stage cases is melarsoprol, a toxic drug in use since 1949. High therapeutic failure rates have been reported recently in several foci. The alternative, eflornithine, is better tolerated but difficult to administer. A third drug, nifurtimox, is a cheap, orally administered drug not yet fully validated for use in human African trypanosomiasis. No new drugs for second-stage cases are expected in the near future. Because of resistance to and limited number of current treatments, there may soon be no effective drugs available to treat trypanosomiasis patients, especially second-stage cases. Additional research and development efforts must be made for the development of new compounds, including: testing combinations of current trypanocidal drugs, completing the clinical development of nifurtimox and registering it for trypanosomiasis, completing the clinical development of an oral form of eflornithine, pursuing the development of DB 289 and its derivatives, and advancing the pre-clinical development of megazol, eventually engaging firmly in its clinical development. Partners from the public and private sector are already engaged in joint initiatives to maintain the production of current drugs. This network should go further and be responsible for assigning selected teams to urgently needed research projects with funds provided by industry and governments. At the same time, on a long term basis, ambitious research programmes for new compounds must be supported to ensure the sustainable development of new drugs.
机译:非洲非洲锥虫病在1980年代重新出现。然而,在过去的几十年中,在该疾病的治疗方面几乎没有进展。对于第二阶段的病例,一线治疗是美拉索洛,一种自1949年以来就一直使用的有毒药物。最近在一些病灶中报告了很高的治疗失败率。替代品依氟鸟氨酸具有更好的耐受性,但难以给药。第三种药物尼呋替莫是一种廉价的口服药物,尚未完全证实可用于人类非洲锥虫病。在不久的将来,预计不会有用于第二阶段病例的新药。由于对目前治疗方法的耐药性和数量有限,可能很快就没有有效的药物可用于治疗锥虫病患者,尤其是二期病例。为了开发新化合物,还必须进行额外的研究和开发工作,包括:测试现有锥虫病药物的组合,完成尼呋替莫的临床开发并将其注册为锥虫病,完成依氟鸟氨酸口服形式的临床开发,进行开发DB 289及其衍生产品的开发,并推动了兆唑的临床前开发,最终坚定地参与了其临床开发。来自公共和私营部门的合作伙伴已经在采取联合行动,以维持现有药物的生产。该网络应走得更远,并负责利用行业和政府提供的资金,将选定的团队分配给急需的研究项目。同时,从长远来看,必须支持雄心勃勃的新化合物研究计划,以确保新药的可持续发展。

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