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Pharmaceutical development of IPI-504, an Hsp90 inhibitor and clinical candidate for the treatment of cancer

机译:Hsp90抑制剂和癌症候选药物IPI-504的药物开发

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摘要

IPI-504 (retaspimycin hydrochloride) is an Hsp90 inhibitor that is the subject of multiple clinical trials for the treatment of cancer. IPI-504 is an aqueous soluble (>200?mg/ml) hydroquinone hydrochloride salt of 17-(allylamino)-17-demethoxygeldanamycin (17-AAG), a quinone derivative also undergoing clinical evaluation, albeit with suboptimal formulations that address its inferior aqueous solubility (~50?μg/ml). IPI-504 interconverts with 17-AAG in vivo through oxidation-reduction reactions that result in a dynamic redox equilibrium. The development challenges associated with redox active molecules are significant due to the pH, oxygen, and temperature sensitivities associated with such chemotypes. The API and sterile drug product manufacturing processes thus warrant the monitoring and control of these key variables. Furthermore, the pharmaceutical development challenges associated with cancer agents that are often fast-tracked due to unmet medical needs mandate a rapid development cycle with associated regulatory hurdles. Drug Dev Res 71: 429–438, 2010. ? 2010 Wiley-Liss, Inc.
机译:IPI-504(盐酸雷帕霉素)是一种Hsp90抑制剂,是多种治疗癌症的临床试验的主题。 IPI-504是17-(烯丙胺基)-17-去甲氧基格尔德霉素(17-AAG)的水溶性氢醌盐酸盐(> 200?mg / ml),醌衍生物也正在接受临床评估,尽管其次优配方存在劣势水溶性(〜50?μg/ ml)。 IPI-504在体内通过氧化还原反应与17-AAG相互转化,从而导致动态氧化还原平衡。由于与这种化学型有关的pH,氧和温度敏感性,与氧化还原活性分子有关的开发挑战是重大的。因此,API和无菌药品生产过程需要对这些关键变量进行监视和控制。此外,与癌症药物相关的药物开发挑战由于医疗需求未得到满足而常常被快速跟踪,这要求快速的开发周期以及相关的监管障碍。 Drug Dev Res 71:429–438,2010年。 2010 Wiley-Liss,Inc.

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