David Ewing Duncan's blog

Experimenting with Drugs on the Less Fortunate

A Johns Hopkins study suggests that paying volunteers to test new drugs attracts mostly the poor, who, to their own detriment, keep coming back for more.

David Ewing Duncan 04/19/2007

  • 4 Comments

Testing new drugs in humans for the first time is tricky and potentially dangerous. Researchers spend years performing safety and efficacy tests on animals before handing a pill to a human, but what works in mice or rats does not always work the same way in us. No one knows for sure what will happen the first time a person swallows a new remedy for Alzheimer's or diabetes.

Most drugs not given to gravely ill people are tested on volunteers who are paid up to thousands of dollars to participate in studies. Check out a newspaper in a city with a major medical center, and you'll see dozens of ads asking healthy people to participate in trials testing new meds for cash.

Trial managers are required to follow safety protocols, and most volunteers emerge unscathed, though injuries and even deaths do happen. In Britain earlier this year, a group of healthy men were given a new drug that had shown great success in boosting the immune system of mice. Unfortunately, when the volunteers took the drug, their human immune systems went into an almost immediate overdrive that caused their organs to swell and nearly killed them.

With 2,000 compounds in human trials in the United States and more coming all the time, the demand for test subjects is fierce--which is why some trials pay big bucks. (This is also why many pharmaceutical companies are moving overseas to India, South Africa, and Eastern Europe--a topic to be covered in a future blog.)

So, who are these volunteers in the United States?

According to findings in a recent article in the journal Clinical Pharmacology and Therapeutics, test subjects are mostly poor people willing to take a risk for what would seem to be easy money. The study, written by ethicists at Johns Hopkins, discovered that most volunteers are not only lower income, but are also serial volunteers. That is, they join one trial after another. A few of them even join more than one at the same time, a violation of trial rules that can endanger volunteers. Mixing experimental drugs can also skew the trial's results.

According to an article that ran in the Baltimore Sun this week,

Experts in medical ethics say the Hopkins study raises difficult questions about the way research is conducted. Scientists don't know much about the long-term health effects of repeatedly volunteering for such studies. Nor do they have a definitive way to determine if participants violate guidelines that prohibit joining more than one study at a time.

"That could pose a risk to the volunteers, and a risk to the science," said Nancy E. Kass, deputy director for public health at the Johns Hopkins Berman Institute of Bioethics and one of the study's authors.

Bottom line: as more new drugs enter human trials, a crisis is brewing. On the one hand, using cash to lure poor volunteers to test risky drugs, which, having only been tested in lab critters, may fail to predict reactions in humans, is clearly exploitive; on the other hand, there is no substitute for testing drugs in humans.

In the future, computer simulations to test drugs in virtual human systems will be helpful; so will designing tests to further ensure safety. For example, giving very low doses to the first human guinea pigs can lessen negative reactions--something that could have helped prevent the United Kingdom debacle. Perhaps volunteers should be more carefully screened to make sure that they are not on other trials, although this is next to impossible if a volunteer lies.

As for the payments, the problem of poverty and the desperation to make money that drives people to take health risks are much larger than the issue of drug testing. Yet an industry that is creating products to help people, not to mention the physicians and clinicians who are running the trials, need to address the issue of drug testing for cash and come up with creative solutions, if possible.

There need to be more studies about who is volunteering for drug trials. The Hopkins study surveyed only 60 volunteers. A larger sampling is needed so that researchers can learn if the findings of this study hold up.

I am curious to know if anyone reading this has any thoughts or ideas about how to solve the dilemma of how to attract human volunteers for drug trials without resorting to payments that seem to prey on the poor.

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kb

1 Comment

  • 1761 Days Ago
  • 04/20/2007

I am curious if the ethicists at Hopkins payed volunteers for their survey?

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Buckwheat469

34 Comments

  • 1761 Days Ago
  • 04/20/2007

Easy Bandage to the problem

I say Bandage in the subject line because I don't believe that this will actually fix the problem, it's not a solution it's just something to alleviate the problems. We should pay someone to try this fix out... maybe a poor person.

I propose that volunteers must obtain a volunteer ID card which is only issued once per person (an update can be made if something changes or someone loses a card). The patient information will be kept in a single database which has replicas in various medical facilities which can support it (this is to reduce server load on the database). A patient can only enter at most one trial per year, or 1 year past the end date of the trial, or until a specified date from the trial administrators. The last 'or' does not override the 1 year mandatory waiting time.

Explaination:
The trial cards are like drivers licenses for the patients. They should require the patient to have a mailing address for checks (so that payments are mailed and not handed over). They also ensure that identifying a patient and all of the programs that he/she was entered is easy for program admins to review on a computer and print out for legal references.

The time limit ensures that the drugs are completely out of the patients system. Some drugs can have effects for up to 1 year (like some birth controls), so 1 year would be the minimum limit. It also makes sure patients aren't abusing the privilege of being a drug tester. One check (or set of checks) per year is different than 4 or 5 (or as many as the patient can handle).

These two steps may not be the best solution, but in a world where databases can be easily maintained by these research institutes, the data contained in these solutions can be discovered without a big problem. The solutions will help minimize the number of people abusing the studies.

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Sara Gambrill

1 Comment

  • 1758 Days Ago
  • 04/23/2007

Mr. Duncan:

I don’t agree that “a crisis is brewing” in clinical research. There are serious incidents that need to be addressed urgently and learned from.

Also, a few points in your post “Experimenting with Drugs on the Less Fortunate” need clarifying.

First, phase I studies are conducted on healthy volunteers, so people participating in them cannot be so poor that it makes them unhealthy and unable to be tested on. Many college students participate in phase I studies. They may not have incomes, but most would not be considered poor in the sense that you imply in your post.

Because phase I studies are conducted in healthy volunteers and therefore study participants have no chance to receive a medical benefit but are taking a risk, it is important to offer cash benefit to compensate for the lack of medical benefit. Some phase I studies do indeed pay a few thousand dollars, but generally these are studies that require overnight stays of a duration that would be cumbersome and impossible to find volunteers for otherwise. The payments vary, and certainly college students and poorer citizens would find the sums attractive. There are certainly problems in the phase I area of “professional” volunteers and worse, simultaneous volunteers.

The case of TeGenero in the U.K. was an unusual phase I trial as it was studying a biologic, and the results of the animal studies were clearly not a good indication of how the drug would behave in humans. That was a rare case. The mistakes made in that trial will not soon be repeated. There have certainly been other severe injuries and even deaths as well in phase I trials, but I believe they are rare and, arguably, avoidable.

You write about the need to recruit more trial subjects for clinical trials as the reason why pharmaceutical companies are conducting clinical research in emerging markets such as India. They are not going there to conduct first-in-man phase I studies, though, for the most part. Phase I trials only require between 20 and 100 patients. They are relatively short and it makes more sense to conduct them mostly in the West, if it is a trial sponsored by a pharmaceutical company based in the West, where the regulatory approval timeline is short. Canada, for example, has one of the shortest regulatory timelines for phase I. In addition, India does not allow first-in-man phase I studies unless the molecule was developed in-country. That fact is not going to change anytime soon. India does allow bioequivalency/bioavailability phase I studies, which are nearly without risk.

Other emerging markets in clinical research also have protections in the area of first-in-human phase I clinical trials and some have a much longer regulatory approval process for phase I than the U.S. does. But, faster time to market coupled with quality clinical trials data are the driving factors to move a larger percentage of U.S. based clinical research to emerging markets. Phase III clinical trials have become much more complex and are requiring more patients than previously. Emerging countries offer Western-trained physicians as well as large populations of treatment-naïve patients.

As I stated at the beginning, there are certainly incidents that have occurred in phase I that need addressing, and I strongly believe they will be.

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tmcclain

4 Comments

  • 1752 Days Ago
  • 04/29/2007

Exploitation in Clinical Trials

"Using cash to lure poor volunteers to test risky drugs...is clearly exploitive." I disagree. If volunteers who are mentally competent and properly informed of the risks of a trial make the decision, of their own free will, that the reward is worth the risk, then why is it unethical to involve them in that trial? The fact that the volunteers are poor does not mean that they cannot make decisions for themselves. Furthermore, consider the alternatives: expect people to risk their health with no short-term personal incentive or force random people to participate without their consent. No thanks.

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Getting real about the life sciences, medicine and biological discovery.

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