Carvedilol and the Food and Drug Administration approval process: an introduction
- PMID: 10027497
- DOI: 10.1016/s0197-2456(98)00052-x
Carvedilol and the Food and Drug Administration approval process: an introduction
Abstract
We discuss briefly the new drug carvedilol (Coreg), 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.
Comment on
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Carvedilol and the Food and Drug Administration (FDA) approval process: the FDA paradigm and reflections on hypothesis testing.Control Clin Trials. 1999 Feb;20(1):16-39. doi: 10.1016/s0197-2456(98)00054-3. Control Clin Trials. 1999. PMID: 10027498
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End-point interpretation in clinical trials: the case for discipline.Control Clin Trials. 1999 Feb;20(1):40-9; discussion 50-1. doi: 10.1016/s0197-2456(98)00051-8. Control Clin Trials. 1999. PMID: 10027499
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