Carvedilol and the Food and Drug Administration approval process:: An introduction

被引:36
作者
Fisher, LD
Moyé, LA
机构
[1] Univ Washington, Dept Biostat, Seattle, WA 98195 USA
[2] Univ Texas, Sch Publ Hlth, Houston, TX USA
来源
CONTROLLED CLINICAL TRIALS | 1999年 / 20卷 / 01期
关键词
FDA; advisory committee; carvedilol; beta-blocker; alpha-blocker; antioxidant; randomized clinical trial;
D O I
10.1016/S0197-2456(98)00052-X
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
We discuss briefly the new drug carvedilol (Coreg(R)), a beta-blocker, alpha-blocker, and antioxidant. This drug was developed for congestive heart failure in a series of trials, four in the United States and one in Australia and New Zealand, briefly summarized in this document. We also summarize the classical paradigm of the U.S. Food and Drug Administration (FDA) for drug approval and the FDA's use of advisory committees. This document serves as background to the discussion of carvedilol's approval. (C) Elsevier Science Inc. 1999.
引用
收藏
页码:1 / 15
页数:15
相关论文
共 2 条
[1]   Carvedilol and the food and drug administration (FDA) approval process: The FDA paradigm and reflections on hypothesis testing [J].
Fisher, LD .
CONTROLLED CLINICAL TRIALS, 1999, 20 (01) :16-39
[2]   End-point interpretation in clinical trials:: The case for discipline [J].
Moyé, LA .
CONTROLLED CLINICAL TRIALS, 1999, 20 (01) :40-49