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制药公司向许可机构提交信息的研究。

Study of information submitted by drug companies to licensing authorities.

作者信息

Hemminki E

出版信息

Br Med J. 1980 Mar 22;280(6217):833-6. doi: 10.1136/bmj.280.6217.833.

Abstract

Reports of clinical trials included in applications submitted by drug companies to licensing authorities in Finland and Sweden in four different years were studied. Many reports were submitted, but most of the trials were uncontrolled and of poor quality. Many of the reports were unpublished, and thus, as the submissions are secret, were not available to doctors. These unpublished reports were in most respects as valuable as the published reports. Most of the reports included some information about adverse effects; the information was often deficient, but skilled analysis might increase its value. This study provides support for those who want to see public disclosure of the reports of trials submitted in licensing applications.

摘要

对制药公司在四个不同年份提交给芬兰和瑞典药品许可当局的申请中所包含的临床试验报告进行了研究。提交了许多报告,但大多数试验未设对照且质量较差。许多报告未发表,因此,由于提交的内容是保密的,医生无法获取。这些未发表的报告在大多数方面与已发表的报告一样有价值。大多数报告包含了一些关于不良反应的信息;这些信息往往不足,但经过专业分析可能会增加其价值。这项研究为那些希望看到药品许可申请中提交的试验报告公开披露的人提供了支持。

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