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Smarter clinical trials for faster drug development.


An August 4 New York New York, state, United States
New York, Middle Atlantic state of the United States. It is bordered by Vermont, Massachusetts, Connecticut, and the Atlantic Ocean (E), New Jersey and Pennsylvania (S), Lakes Erie and Ontario and the Canadian province of
 Times article describes a new approach to clinical trials. The idea, (sometimes called "experimental medicine") is to use modern imaging, genetic, and other technology early, starting with the first patient who ever takes an experimental drug, to get solid indications of whether or not it is working. Researchers and companies make sure the drug is getting to where it is needed in the body, that it has the biochemical bi·o·chem·is·try  
n.
1. The study of the chemical substances and vital processes occurring in living organisms; biological chemistry; physiological chemistry.

2.
 effects intended, and that the dose is appropriate--eliminating losers early and focusing attention and resources on more promising drug candidates. The traditional approach uses the first human trials to pick the largest dose most patients can tolerate tol·er·ate
v.
1. To allow without prohibiting or opposing; permit.

2. To put up with; endure.

3. To have tolerance for a substance or pathogen.
 (which may be more than needed for medical efficacy efficacy /ef·fi·ca·cy/ (ef´i-kah-se)
1. the ability of an intervention to produce the desired beneficial effect in expert hands and under ideal circumstances.

2.
, but is likely to become a standard dose for further research and for approval), and only then runs other trials to start testing whether the drug does anybody any good.

Comment

AIDS is barely mentioned in the article--perhaps because it is no longer in the forefront of clinical-trial design. In AIDS and other diseases the biggest block to finding new treatments seems to be the gap between where academic research stops and where drug development begins. Many good ideas get published in journals, but usually the researchers who developed them do not do human testing, and no one does the next, relatively inexpensive steps to show which ideas have solid potential for practical development now. And usually only one company has the legal rights to a compound, so if anyone else has a good idea for using it, they (and the public as well) are often out of luck. Or nobody has exclusive rights, so no company gets involved. Clearly the current system works very poorly in turning scientific advances into new kinds of treatment, and fundamental rethinking is needed.

References

Andrew Pollack pollack: see cod.
pollack
 or pollock

Either of two commercially important North Atlantic species of food fish in the cod family (Gadidae).
. "In drug research, the guinea pigs guinea pig (gĭn`ē), domesticated form of the cavy, Cavia porcellus, a South American rodent. It is unrelated to the pig; the name may refer to its shrill squeal.  of choice are, well, human." The New York Times, August 4, 2004. Note: to find the article online you can search for "Garabadian" the name of a patient in a cancer trial, on http://www.nytimes.com--however the Times requires payment for online articles older than one week.
COPYRIGHT 2004 John S. James
No portion of this article can be reproduced without the express written permission from the copyright holder.
Copyright 2004, Gale Group. All rights reserved. Gale Group is a Thomson Corporation Company.

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Publication:AIDS Treatment News
Geographic Code:1USA
Date:Jul 23, 2004
Words:357
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