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CRC/EORTC/NCI Joint Formulation Working Party: experiences in the formulation of investigational cytotoxic drugs.

机译:CRC / EORTC / NCI联合制定工作组:研究性细胞毒性药物制定方面的经验。

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摘要

The pharmaceutical formulation of a new anti-tumour agent has often been perceived as the bottleneck in anti-cancer drug development. In order to increase the speed of this essential development step, the Cancer Research Campaign (CRC), the European Organization for Research and Treatment of Cancer (EORTC) and the National Cancer Institute (NCI) agreed in 1987 to form the Joint Formulation Working Party (JFWP). The main goal of the JFWP is to facilitate the rapid progress of a new drug through pharmaceutical developmental to preclinical toxicology and subsequently to phase I clinical trial. Under the auspices of the JFWP around 50 new agents have been developed or are currently in development. In this report we present our formulation experiences since the establishment of the JFWP with a selected number of agents: aphidicolin glycinate, bryostatin 1, carmethizole, carzelesin, combretastatin A4, dabis maleate, disulphonated aluminium phthalocyanine, E.O.9, 4-hydroxyanisole, pancratistatin, rhizoxin, Springer pro-drug, SRI 62-834, temozolomide, trimelamol and V489. The approaches used and problems presented may be of general interest to scientists in related fields and those considering submitting agents for development.
机译:新型抗肿瘤药的药物配方通常被视为抗癌药物开发的瓶颈。为了加快这一重要开发步骤的速度,1987年,癌症研究运动(CRC),欧洲癌症研究和治疗组织(EORTC)和美国国家癌症研究所(NCI)同意组建联合制剂工作组(JFWP)。 JFWP的主要目标是通过药物开发到临床前毒理学以及随后的I期临床试验,促进新药的快速发展。在JFWP的主持下,已经开发了或正在开发约50个新代理。在本报告中,我们介绍了自建立JFWP以来使用以下几种药物的制剂经验:蚜虫碱甘氨酸盐,溴抑他汀1,甲氧苄唑,羧甲基蝶呤,康维他汀A4,达比斯马来酸盐,二磺化酞菁铝,EO9、4-羟基茴香醚,潘克拉汀,根瘤菌素,施普林格前药,SRI 62-834,替莫唑胺,间苯三酚和V489。相关领域的科学家和正在考虑将药物提交开发的人员可能普遍感兴趣使用的方法和提出的问题。

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