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From Clinical Trial to Prescription
William T. Carpenter, Jr, MD
Arch Gen Psychiatry. 2002;59:282-285.
There are many steps between drug discovery and prescribing for a patient.
Each step has problems. In this issue of ARCHIVES, Klein and colleagues propose
changes in clinical trials that would result in more meaningful information
for the treating physician. Of particular importance is the gap between what
a physician needs to know and what is produced in the clinical trials that
leads to approval of a new drug by the US Food and Drug Administration (FDA).
Their recommendations for improving clinical trials are cogent, but broad-based
implementation depends on an organizational structure and political effectiveness
not presently in place. Most important, as the authors note, is an effective
work group representing industry, regulatory agencies, and academic and federal
science, addressing clinical trials issues with public participation. While
improved quality and relevance of data from clinical trials will strengthen
the scientific foundation of pharmacotherapy, other problems impede the delivery
of objective information to the treating physician. Most hotly debated is
the role of money in the creation and dissemination of knowledge.
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From the Maryland Psychiatric Research Center, University of Maryland
School of Medicine, Baltimore. The author receives lecture and advisory fees
from several pharmaceutical firms concerned with antipsychotic drugs and is
principal investigator in a science collaboration with Novartis Pharma AG.
He does not receive personal funds from Novartis and does not accept or purchase
pharmaceutical industry stock.
RELATED ARTICLE
Improving Clinical Trials: American Society of Clinical Psychopharmacology Recommendations
Donald F. Klein, Michael E. Thase, Jean Endicott, Lawrence Adler, Ira Glick, Amir Kalali, Steven Leventer, Jeffrey Mattes, Peter Ross, and Alexander Bystritsky
Arch Gen Psychiatry. 2002;59(3):272-278.
ABSTRACT
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