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心血管复方制剂药物研发中需考虑的问题。

Issues to consider in the pharmaceutical development of a cardiovascular polypill.

作者信息

Guglietta Antonio, Guerrero Marta

机构信息

Center of Investigation and Pharmaceutical Development, Grupo Ferrer Internacional, Barcelona, Spain.

出版信息

Nat Clin Pract Cardiovasc Med. 2009 Feb;6(2):112-9. doi: 10.1038/ncpcardio1424. Epub 2008 Dec 23.

Abstract

The pharmaceutical development of a cardiovascular polypill presents several unique challenges. The selection of the type and number of active drugs to be incorporated requires important consideration of clinical, pharmaceutical and commercial issues, and the final decision with regard to the polypill's components depends on how these issues are prioritized. Once the drug combination has been chosen, developers must determine which pharmaceutical formulation should be used. The most appropriate method of drug delivery can vary markedly and depends on the characteristics of the drugs to be combined. Finally, careful consideration of how to gather the type of information required by regulatory agencies before a particular polypill can be approved for use in the general population is crucial. Although the association of multiple, active ingredients in a single dosage form would represent a major step forward in the prevention of cardiovascular conditions, a careful evaluation of all the above-mentioned variables and a well thought-out development plan is mandatory to maximize the chances of success.

摘要

心血管复方制剂的药物研发面临一些独特的挑战。确定要纳入的活性药物的类型和数量,需要对临床、药学和商业问题进行重要考量,而关于复方制剂成分的最终决定取决于如何对这些问题进行优先级排序。一旦选定了药物组合,研发人员必须确定应采用哪种药物剂型。最合适的给药方法可能会有显著差异,这取决于待组合药物的特性。最后,在某种特定的复方制剂能够获批用于普通人群之前,仔细考虑如何收集监管机构所需的信息类型至关重要。尽管在单一剂型中联合多种活性成分将代表在心血管疾病预防方面向前迈出的重要一步,但对上述所有变量进行仔细评估并制定深思熟虑的研发计划,对于最大化成功几率而言是必不可少的。

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