Oversea drug trials exploit and kill poor in developing countries and US consumers alike

Wednesday, January 26, 2011 by: Tony Isaacs
Tags: drug trials, developing nations, health news

(NewsTarget) Over the past two decades, drug makers have increasingly shifted trials for drugs intended for the U.S. market to developing countries where it is easier and cheaper to recruit trial patients and where oversight is minimal. While outsourcing drug trials may save significant money for the pharmaceutical companies, the cost in human lives and suffering for both the developing trial participants and American drug users is likely horrendous.

Many have questioned how appropriate and ethical it is to test drugs intended for the American market in developing countries. Duke University`s recent report, "Ethical and Scientific Implications of the Globalization of Clinical Research", labeled developing country trials as scientifically questionable and morally inappropriate. The study noted that genetic and other population differences could render results that did not apply to the target population. The report also raised concerns over the role money might play in recruiting poor volunteers.

Lead study author Dr. Kevin A. Schulman said that such trials imply a kind of imperial exploitation of developing countries. "We don`t want to imagine that lower-income countries are the clinical trial mill for higher-income countries," Schulman said.

Until recent years, almost all of the drugs Americans took were tested primarily either in the United States or, to a lesser extent, in Europe. As recently as 1990, only 271 trials of drugs intended for American use were being conducted in foreign countries. By 2008, the number had risen to 6,485. According to a National Institutes of Health database, 58,788 such foreign trials have been conducted in 173 countries outside the United States since 2000. In 2008 alone, 80 percent of the applications submitted to the FDA for new drugs contained data from foreign clinical trials.

The actual numbers may be much worse because companies are not required to report all overseas studies and often list only a single study where the actual trials are conducted in numerous locations.

The drug industry refers to developing country trial recruits as "drug-naive patients" because they usually are not being treated for any condition nor taking any medications. Such patients are almost sure to yield better test results. The term could also apply to how uninformed the patients are. In many instances, patients are led to believe they are being given a medicine to help them and do not understand that it is experimental or that they may be getting a placebo. Consent may consist of only a thumbprint or scrawled "X".

It is much easier to avoid FDA and other institutional scrutiny and sweep negative trial results - including deaths - under the rug in developing countries. In 2008, the FDA inspected only 0.7 percent of all overseas trial sites. That`s just 45 out of the 6,485 locations.

The drug industry also has a phrase they coined for developing countries used for drug trials: rescue countries. Thanks to an FDA loophole, drug companies whose domestic trials have not yielded favorable results can use the results they get in developing country trials to "rescue" drugs, which otherwise might not have been approved.

Due to restricted press freedom and the ease of suppressing negative results, the true scope of the harm caused to "drug-naive patients" in developing "rescue countries" is not fully known. However, numerous discoveries and reports of drug trial deaths, uninformed patients and other acts of abuse and deception leave no doubt that developing drug trial patients are being killed and abused. Ultimately, so are untold thousands of American patients who are killed or harmed by drugs whose approval has been based on questionable trials.

Sources included:

http://douglassreport.com/2009/03/12/should-...
http://www.vanityfair.com/politics/features/...
http://cardiobrief.org/2010/12/02/vanity-fai...
http://www.twnside.org.sg/title2/health.info...

About the author

Tony Isaacs, is a natural health author, advocate and researcher who hosts The Best Years in Life website for those who wish to avoid prescription drugs and mainstream managed illness and live longer, healthier and happier lives naturally. Mr. Isaacs is the author of books and articles about natural health, longevity and beating cancer including "Cancer's Natural Enemy" and is working on a major book project due to be published later this year. He is also a contributing author for the worldwide advocacy group "S.A N.E.Vax. Inc" which endeavors to uncover the truth about HPV vaccine dangers.
Mr. Isaacs is currently residing in scenic East Texas and frequently commutes to the even more scenic Texas hill country near Austin and San Antonio to give lectures and health seminars. He also hosts the CureZone "Ask Tony Isaacs - featuring Luella May" forum as well as the Yahoo Health Group "Oleander Soup" and he serves as a consultant to the "Utopia Silver Supplement Company".